RGD Annotation Report for nephrotic syndrome type 2Rat Genome Database

GENE - TERM ANNOTATION REPORT

92 Annotations Found.

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10042206 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:14675423 PMID:14978175 PMID:15042551 PMID:15059485 PMID:15253708 PMID:15322893 PMID:16810518 PMID:17899208 PMID:18216321 PMID:19067903 PMID:19371226 PMID:19674119 PMID:20507940 PMID:20798252 PMID:23013956 PMID:25741868 PMID:26211502 PMID:26467025 PMID:26467726 PMID:28385484 PMID:28492532 PMID:30655312

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred from experiment (EXP)
The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: CTD Direct Evidence: marker/mechanism
Original References(s): PMID:21171529 PMID:24509478

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13792122 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:14978175 PMID:17576681 PMID:18443213 PMID:18709391 PMID:23242530 PMID:25741868 PMID:28492532 PMID:9536098

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10042220 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:11805166 PMID:15253708 PMID:15327385 PMID:18823551 PMID:19406966 PMID:20947785 PMID:21355056 PMID:24509478 PMID:24742477 PMID:25741868 PMID:28492532 PMID:30655312 PMID:32581362 PMID:8589695

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13786666 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:11729243 PMID:14701729 PMID:14978175 PMID:15253708 PMID:15322893 PMID:15327385 PMID:18216321 PMID:19674119 PMID:20001346 PMID:23595123 PMID:25741868 PMID:25903641 PMID:28204945 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8591259 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2, susceptibility to
Original References(s): PMID:11805166 PMID:14978175 PMID:17899208 PMID:18216321 PMID:21171529 PMID:22578956 PMID:23242530 PMID:23645318 PMID:24033266 PMID:24742477 PMID:24856380 PMID:25741868 PMID:28492532 PMID:30295827

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from OMIM Disease Annotation Pipeline
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11544345 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:11805166 PMID:12707396 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11551455 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:15968559 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:38460917 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:11854170 PMID:14701729 PMID:15253708 PMID:23595123 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11544555 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:12707396 PMID:15253708 PMID:16481888 PMID:17942957 PMID:18823551 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13470260 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:14675423 PMID:15253708 PMID:20507940 PMID:20947785 PMID:21415313 PMID:22565185 PMID:23595123 PMID:24413855 PMID:25349199 PMID:25741868 PMID:26420286 PMID:26467025 PMID:26594346 PMID:28492532 PMID:28658201 PMID:30450462

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13799262 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:11805166 PMID:12464671 PMID:14978175 PMID:15253708 PMID:15769810 PMID:16354237 PMID:16898497 PMID:18823551 PMID:19145239 PMID:19876656 PMID:20947785 PMID:21355056 PMID:21415313 PMID:23349334 PMID:23515051 PMID:24227627 PMID:24509478 PMID:25741868 PMID:26211502 PMID:26420286 PMID:26467025 PMID:28492532 PMID:29982877 PMID:32604935

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596781 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:11805168 PMID:12644922 PMID:14570703 PMID:14701729 PMID:15253708 PMID:16291839 PMID:17109732 PMID:17899208 PMID:20798252 PMID:23595123 PMID:25525159 PMID:25741868 PMID:26211502 PMID:26467025 PMID:26467726 PMID:28492532 PMID:28658201 PMID:33532864 PMID:8589695

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596785 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:11805166 PMID:12707396 PMID:14675423 PMID:15253708 PMID:15327385 PMID:15496146 PMID:17218332 PMID:17899208 PMID:18216321 PMID:18823551 PMID:21125408 PMID:23595123 PMID:24072147 PMID:25349199 PMID:25741868 PMID:26467025 PMID:28492532 PMID:8606597

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12740238 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:24227627 PMID:25741868

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13782521 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:26820844

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13786920 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25741868 PMID:28204945

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13790365 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:14978175 PMID:18216321

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596784 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13783051 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:12776285

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:41406997 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25741868 PMID:33532864

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13788252 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:17899208 PMID:24742477

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13810578 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13785922 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:12464671 PMID:18216321 PMID:18823551 PMID:24509478 PMID:25349199 PMID:26413278 PMID:26467025 PMID:29660491 PMID:30260545 PMID:30406062

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596783 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:8589695

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13791012 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:18823551 PMID:25349199

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12738779 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:15253708 PMID:15817495 PMID:23515051 PMID:24227627 PMID:25741868 PMID:28492532 PMID:29660491 PMID:30013592

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13785235 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:17899208

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10042271 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:14978175 PMID:15253708 PMID:16199547 PMID:23595123 PMID:24509478 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13788030 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:24227627

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13784782 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:23645318 PMID:24227627

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151872552 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: NPHS2-related condition
Original References(s): PMID:14978175 PMID:17371932 PMID:17576681 PMID:22565185 PMID:25741868 PMID:28492532 PMID:9536098

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:127258893 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:17371932 PMID:17899208 PMID:23349334 PMID:23515051 PMID:23645318 PMID:25741868 PMID:28492532 PMID:28780565 PMID:29660491

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13485336 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: NPHS2-related condition
Original References(s): PMID:23913389 PMID:25573908 PMID:25741868 PMID:26211502 PMID:26467025

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151733567 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25349199 PMID:25741868 PMID:29127259

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:15170555 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:17216259 PMID:26820844 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596780 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:11729243 PMID:11805166 PMID:11854170 PMID:12649741 PMID:14570703 PMID:14675423 PMID:14978175 PMID:15253708 PMID:17371932 PMID:17942957 PMID:18216321 PMID:18443213 PMID:19371226 PMID:19406966 PMID:20798252 PMID:20947785 PMID:21171529 PMID:21415313 PMID:23242530 PMID:24089165 PMID:24227627 PMID:24500309 PMID:24856380 PMID:25349199 PMID:25741868 PMID:25852895 PMID:26467025 PMID:28492532 PMID:28780565 PMID:29049388 PMID:29127259 PMID:29382718 PMID:29982877 PMID:32129207 PMID:32581362 PMID:8589695

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13785183 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:18726620 PMID:18823551 PMID:25741868

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:127268076 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25741868 PMID:28492532 PMID:28780565

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13785331 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:18823551 PMID:24511133 PMID:25741868

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12738530 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:18823551 PMID:19145239 PMID:23595123 PMID:24227627 PMID:24509478 PMID:25349199 PMID:25525159 PMID:25741868 PMID:25852895 PMID:26467025 PMID:28492532 PMID:28658201

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13836686 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:14978175 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:34895522 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:11729243 PMID:11805166 PMID:14701729 PMID:15253708 PMID:20507940 PMID:23595123 PMID:25741868 PMID:28385484 PMID:28492532 PMID:29127259

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13786101 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:14675423 PMID:1523708 PMID:15253708 PMID:15264208 PMID:16810518 PMID:21636722 PMID:23515051 PMID:24072147 PMID:24509478 PMID:25349199 PMID:25525159 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11548077 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:15954915 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10042243 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:14675423 PMID:15042551 PMID:15059485 PMID:15253708 PMID:18596732 PMID:24072147 PMID:25741868 PMID:26467726 PMID:28385484 PMID:28492532 PMID:30721404 PMID:32604935

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13785189 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:17899208 PMID:25741868

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13787110 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:12608558 PMID:15253708 PMID:15769810 PMID:15817495 PMID:18443213 PMID:23645318 PMID:25741868 PMID:26211502 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151842947 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13810575 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:25741868 PMID:26467025 PMID:28780565

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:126745620 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:22763815 PMID:24509478 PMID:25741868

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13519543 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:23595123 PMID:25741868 PMID:28117080 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13470778 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:20947785 PMID:24227627 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30260545

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151849059 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:11729243 PMID:12707396 PMID:14978175 PMID:18216321 PMID:19406966 PMID:20947785 PMID:21415313 PMID:25741868 PMID:28492532 PMID:32129207

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151733576 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:18823551 PMID:23595123 PMID:25741868 PMID:28492532 PMID:29127259 PMID:29982877

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:38471710 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:14675423 PMID:15253708 PMID:15264208 PMID:15496146 PMID:16810518 PMID:23515051 PMID:24072147 PMID:25741868 PMID:28492532 PMID:29382718 PMID:29660491 PMID:30013592

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13791962 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:12464671 PMID:12707396 PMID:17576681 PMID:19145239 PMID:24227627 PMID:24509478 PMID:25741868 PMID:26413278 PMID:28492532 PMID:28780565 PMID:9536098

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10042233 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:11733557 PMID:14701729 PMID:15253708 PMID:15780077 PMID:23595123 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13788825 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:17699384 PMID:17942957 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12740030 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:23595123 PMID:24227627 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596786 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:11805166 PMID:12464671 PMID:14675423 PMID:14978175 PMID:15327385 PMID:15496146 PMID:15769810 PMID:15817495 PMID:18823551 PMID:24509478 PMID:25349199 PMID:25741868 PMID:26668027 PMID:28476686 PMID:28492532 PMID:29660491 PMID:30260545 PMID:31027891 PMID:31308032 PMID:36167728 PMID:8589695

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596785 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:11805166 PMID:12707396 PMID:14675423 PMID:15253708 PMID:15327385 PMID:15496146 PMID:17218332 PMID:17899208 PMID:18216321 PMID:18823551 PMID:21125408 PMID:23595123 PMID:24072147 PMID:25349199 PMID:25741868 PMID:25741915 PMID:26467025 PMID:28492532 PMID:8606597

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:405281778 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25741914

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13481876 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:15253708 PMID:15954915 PMID:17216259 PMID:18216321 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13785236 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:12707396 PMID:15817495 PMID:19406966 PMID:25741868 PMID:28780565

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:10042252 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:14978175 PMID:15015071 PMID:15327385 PMID:17371932 PMID:18216321 PMID:18443213 PMID:23242530 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12738545 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:12464671 PMID:12707396 PMID:19145239 PMID:20798252 PMID:23515051 PMID:23645318 PMID:24509478 PMID:25349199 PMID:25741868 PMID:26413278 PMID:28492532 PMID:28780565 PMID:29382718 PMID:29644057 PMID:29660491 PMID:33102883

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:40903447 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:20947785 PMID:25741868 PMID:28476686 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13792315 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:16199547 PMID:18216321 PMID:23595123 PMID:25349199 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13784357 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25349199 PMID:25741916

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens) & RGD:11581702\|RGD:11582259\|RGD:11582325\|RGD:126767083\|RGD:127300786\|RGD:15169370\|RGD:15169863\|RGD:15170529\|RGD:15172873\|RGD:28879600\|RGD:28879609\|RGD:28890183\|RGD:28895157\|RGD:40904482 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2 \| ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:156404931 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25741868 PMID:28492532 PMID:33428103 PMID:34031707

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:150530720 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:14978175 PMID:20798252 PMID:24509478 PMID:25741868 PMID:28492532 PMID:30260545

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151760224 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:14978175 PMID:17576681 PMID:23645318 PMID:24509478 PMID:25741868 PMID:26668027 PMID:28492532 PMID:9536098

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13792052 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:14978175 PMID:17576681 PMID:18216321 PMID:23645318 PMID:24227627 PMID:24509478 PMID:25525159 PMID:25741868 PMID:26668027 PMID:28492532 PMID:9536098

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13532148 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:11805166 PMID:14978175 PMID:16721582 PMID:24033266 PMID:24742477 PMID:25741868 PMID:30609409

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens) & RGD:11050259\|RGD:11051372\|RGD:11580976\|RGD:11582368\|RGD:11588465\|RGD:11594527\|RGD:11651229\|RGD:11651537\|RGD:12739533\|RGD:12740379\|RGD:12740504\|RGD:12854204\|RGD:13786140\|RGD:13787426\|RGD:13787664\|RGD:13788374\|RGD:13789160\|RGD:13790024\|RGD:13790988\|RGD:13838582\|RGD:13838583\|RGD:14698738\|RGD:14698740\|RGD:150453436\|RGD:155725283\|RGD:155729799\|RGD:155735418\|RGD:155736526\|RGD:155736556\|RGD:155736600\|RGD:21070516\|RGD:21075003\|RGD:21075004\|RGD:28879287\|RGD:28884771\|RGD:28884777\|RGD:28884782\|RGD:28890180\|RGD:405280305\|RGD:40904480\|RGD:40904481 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2 \| ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens) & RGD:11075109\|RGD:11544194\|RGD:11547253\|RGD:11547691\|RGD:11550591\|RGD:11578059\|RGD:11579112\|RGD:11580200\|RGD:127263930\|RGD:127279750\|RGD:127298434\|RGD:127322565\|RGD:12740294\|RGD:15168515\|RGD:15168771\|RGD:15168802\|RGD:15170210\|RGD:15170623\|RGD:15170690\|RGD:152064304\|RGD:28879605\|RGD:28885084 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: NPHS2-related condition \| ClinVar Annotator: match by term: Nephrotic syndrome, type 2 \| ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596782 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:12707396 PMID:12776285 PMID:14978175 PMID:15042551 PMID:15253708 PMID:15496146 PMID:15769810 PMID:15954915 PMID:16286890 PMID:16810518 PMID:16900088 PMID:17899208 PMID:17942957 PMID:18683072 PMID:19406966 PMID:19812541 PMID:20333530 PMID:20947785 PMID:22578956 PMID:23349334 PMID:23595123 PMID:24227627 PMID:25741868 PMID:26211502 PMID:26467025 PMID:27885584 PMID:28492532 PMID:28712774 PMID:28780565 PMID:32581362

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13785775 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:12464671 PMID:19145239 PMID:20947785 PMID:21415313 PMID:24509478 PMID:25349199 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8596787 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2, susceptibility to
Original References(s): PMID:11805166 PMID:11854170 PMID:12464671 PMID:15327385 PMID:15954915 PMID:16481888 PMID:16900088 PMID:17371932 PMID:17942957 PMID:18216321 PMID:18499321 PMID:18823551 PMID:19145239 PMID:19268410 PMID:19520069 PMID:20798252 PMID:20947785 PMID:21355056 PMID:21415313 PMID:21722858 PMID:22228437 PMID:22578956 PMID:23242530 PMID:23349334 PMID:23515051 PMID:23645318 PMID:23800802 PMID:24227627 PMID:24509478 PMID:24715228 PMID:24969201 PMID:25599733 PMID:25741868 PMID:26138234 PMID:26211502 PMID:26413278 PMID:26420286 PMID:26467025 PMID:28492532 PMID:28529802 PMID:29869118 PMID:30241959 PMID:30260545 PMID:30348286 PMID:31027891 PMID:31738409 PMID:32129207 PMID:32467597 PMID:33193607 PMID:33532864 PMID:34405919 PMID:34853150

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13784785 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:23595123 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:151778431 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:17699384 PMID:19145239 PMID:20507940 PMID:23515051 PMID:24509478 PMID:25720465 PMID:25741868 PMID:26420286 PMID:28492532 PMID:28658201 PMID:30348286 PMID:33305316

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11040033 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:14675423 PMID:14978175 PMID:15253708 PMID:15264208 PMID:15504144 PMID:17899208 PMID:24596097 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13792440\|RGD:152999306 (Homo sapiens) & RGD:13792440\|RGD:152999306 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:15253708 PMID:25741868

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:127268344\|RGD:156117635\|RGD:156311694\|RGD:401947770\|RGD:42723996 (Homo sapiens) & RGD:127268344\|RGD:156117635\|RGD:156311694\|RGD:401947770\|RGD:42723996 (Homo sapiens) & RGD:127268344\|RGD:156117635\|RGD:156311694\|RGD:401947770\|RGD:42723996 (Homo sapiens) & RGD:127268344\|RGD:156117635\|RGD:156311694\|RGD:401947770\|RGD:42723996 (Homo sapiens) & RGD:127268344\|RGD:156117635\|RGD:156311694\|RGD:401947770\|RGD:42723996 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2 \| ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:23595123 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13469935 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:20507940 PMID:23595123 PMID:24856380 PMID:25060053 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13782566\|RGD:38460569 (Homo sapiens) & RGD:13782566\|RGD:38460569 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:16199547 PMID:23595123 PMID:25741868 PMID:28204945 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11551002\|RGD:13810581 (Homo sapiens) & RGD:11551002\|RGD:13810581 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2 \| ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:34891297 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Steroid-resistant nephrotic syndrome
Original References(s): PMID:10742096 PMID:14701729 PMID:15253708 PMID:18216321 PMID:18380020 PMID:23595123 PMID:24227627 PMID:24509478 PMID:25349199 PMID:25720465 PMID:25741868 PMID:28492532

An association has been curated linking NPHS2 and nephrotic syndrome type 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens) & RGD:11050255\|RGD:11050257\|RGD:11050258\|RGD:11051371\|RGD:11590543\|RGD:127274362\|RGD:12739992\|RGD:12740278\|RGD:150332815\|RGD:150332817\|RGD:243057529\|RGD:329954546\|RGD:401856652\|RGD:401919858\|RGD:401942848\|RGD:401942851\|RGD:401943107\|RGD:401947541\|RGD:401947543\|RGD:401947554\|RGD:401947558\|RGD:401947561\|RGD:401947768\|RGD:401947771\|RGD:401947774\|RGD:401947775 (Homo sapiens)
22 RGD objects have been annotated to nephrotic syndrome type 2 (DOID:0080379)
7 papers in RGD have been used to annotate NPHS2
Curation Notes: ClinVar Annotator: match by term: Nephrotic syndrome, type 2
Original References(s): PMID:25741868

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92 Annotations Found.