RGD Annotation Report for Joubert syndrome 9Rat Genome Database

GENE - TERM ANNOTATION REPORT

55 Annotations Found.

An association has been curated linking CC2D2A and Joubert syndrome 9 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
5 additional annotations were made from Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: DNA:mutations: :multiple

An association has been curated linking CC2D2A and Joubert syndrome 9 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
5 additional annotations were made from Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Qualifier: no_association
Curation Notes: DNA:mutations: :multiple

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448773 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:22241855 PMID:25741868 PMID:26092869 PMID:28492532 PMID:30055837 PMID:33502066

An association has been curated linking CC2D2A and Joubert syndrome 9 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from Noor A, etal., Am J Hum Genet. 2008 Nov;83(5):656.
2 additional annotations were made from Noor A, etal., Am J Hum Genet. 2008 Nov;83(5):656.
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: DNA:splice-site mutation:intron:IVS19+1G>C (human)

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448802 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741868 PMID:26092869 PMID:26310553 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8617044 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:16199547 PMID:19466712 PMID:19777577 PMID:25741868 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8555799 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18387594 PMID:18950740

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448737 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8595124 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19574260 PMID:22241855 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448718 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from OMIM Disease Annotation Pipeline
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10406539 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:25741868 PMID:26673778 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8602372 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9/15, digenic
Original References(s): PMID:22246503 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8591119 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8591117 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18414213 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8591111 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18414213 PMID:21068128 PMID:21370303 PMID:22241855 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10049072 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:21370303 PMID:22241855 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448715 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:25741868 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:26903765 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:16199547 PMID:19777577 PMID:25741868 PMID:28492532 PMID:34906502

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448771 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:22241855 PMID:22425360 PMID:23012439 PMID:24033266 PMID:25741868 PMID:26092869 PMID:26477546 PMID:26485645 PMID:26673778 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448709 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18950740 PMID:19777577 PMID:22241855 PMID:25741868 PMID:26092869 PMID:27081510 PMID:27082236 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8617041 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:21068128 PMID:24706459 PMID:25741868 PMID:26092869 PMID:26729329 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448799 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:17576681 PMID:26092869 PMID:28492532 PMID:9536098

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8617035 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18950740 PMID:19466712 PMID:19574260 PMID:19777577 PMID:22241855 PMID:25741868 PMID:26092869 PMID:28125082 PMID:28492532 PMID:32488064

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8595123 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9/15, digenic
Original References(s): PMID:19574260 PMID:19777577 PMID:22246503 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8617036 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19466712 PMID:19777577 PMID:25741868 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448688 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:21068128 PMID:22241855 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:13811427 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:23692786 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448758 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:17576681 PMID:22241855 PMID:26092869 PMID:28492532 PMID:9536098

An association has been curated linking CC2D2A and Joubert syndrome 9 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:150530851 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:25741868 PMID:28492532 PMID:30091983

An association has been curated linking CC2D2A and Joubert syndrome 9 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:14706114 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:25741868 PMID:27848944 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: CTD Direct Evidence: marker/mechanism

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8595120 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18950740 PMID:25741868 PMID:25741914 PMID:26092869 PMID:28492532 PMID:29620724

An association has been curated linking CC2D2A and Joubert syndrome 9 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:9692751 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:16199547 PMID:19777577 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens) & RGD:11544025\|RGD:11550263\|RGD:127238176\|RGD:13612097\|RGD:13703288\|RGD:13827673\|RGD:14695870\|RGD:150408055\|RGD:150408425\|RGD:150452502\|RGD:150530930\|RGD:150532051\|RGD:155795141\|RGD:156436043\|RGD:401940226\|RGD:405280623\|RGD:8591113\|RGD:8591114\|RGD:8591115\|RGD:8591116\|RGD:8591118\|RGD:8591122\|RGD:8591124\|RGD:8591126 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741868

An association has been curated linking CC2D2A and Joubert syndrome 9 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:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens) & RGD:11345769\|RGD:11580612\|RGD:11585400\|RGD:11585884\|RGD:11589492\|RGD:11589688\|RGD:11591010\|RGD:11591781\|RGD:11592215\|RGD:11593587\|RGD:11593598\|RGD:11595405\|RGD:11640877\|RGD:11642562\|RGD:11646130\|RGD:11646340\|RGD:11646775\|RGD:11649076\|RGD:11650880\|RGD:11651865\|RGD:11656908\|RGD:11657871\|RGD:11659467\|RGD:12836986\|RGD:12898829\|RGD:12900473\|RGD:12913204\|RGD:13519334\|RGD:13524038\|RGD:13835530\|RGD:13837586\|RGD:14730546\|RGD:26897165\|RGD:28869398\|RGD:28872790\|RGD:28876208\|RGD:28880720\|RGD:28881398\|RGD:28883561\|RGD:28903673\|RGD:9692755 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens) & RGD:10050408\|RGD:10050409\|RGD:10050479\|RGD:10050480\|RGD:10052980\|RGD:10405447\|RGD:10405517\|RGD:10408104\|RGD:11347843\|RGD:11349155\|RGD:11349891\|RGD:11350040\|RGD:11549744\|RGD:11550703\|RGD:11551461\|RGD:11580349\|RGD:11590920\|RGD:11591085\|RGD:11592228\|RGD:11594416\|RGD:11638997\|RGD:11640242\|RGD:11643026\|RGD:11652247\|RGD:11653254\|RGD:12899224\|RGD:12899844\|RGD:12913703\|RGD:13515899\|RGD:13540215\|RGD:13837643\|RGD:14695775\|RGD:151235353\|RGD:151349626\|RGD:151768671\|RGD:26887463\|RGD:28869898\|RGD:38491631\|RGD:8591112\|RGD:8591120\|RGD:8591123\|RGD:8591130\|RGD:8591131\|RGD:8640450\|RGD:9692752\|RGD:9692754 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448741 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:22241855 PMID:26092869 PMID:28125082 PMID:28497568 PMID:29146704 PMID:30055837

An association has been curated linking CC2D2A and Joubert syndrome 9 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:40814892 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741913

An association has been curated linking CC2D2A and Joubert syndrome 9 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:11636144\|RGD:11639458 (Homo sapiens) & RGD:11636144\|RGD:11639458 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741868 PMID:28492532 PMID:28518168 PMID:32461654

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10045205\|RGD:126741088 (Homo sapiens) & RGD:10045205\|RGD:126741088 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741868 PMID:25741916

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448699 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:22241855 PMID:25741914 PMID:26092869 PMID:27894351 PMID:28492532 PMID:34645488

An association has been curated linking CC2D2A and Joubert syndrome 9 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:28871853 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19466712 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8595122 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18950740 PMID:19777577 PMID:25525159 PMID:25741868 PMID:26092869 PMID:27959436 PMID:28492532 PMID:31618753 PMID:3631907

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448796 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:22241855 PMID:25741868 PMID:26092869 PMID:28492532 PMID:8253763

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448776 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:17576681 PMID:18950740 PMID:26092869 PMID:28492532 PMID:9536098

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448778 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:22241855 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10405509 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18414213 PMID:19777577 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:8595121 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:18950740 PMID:19574260 PMID:25741868 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10405503\|RGD:8591110 (Homo sapiens) & RGD:10405503\|RGD:8591110 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:22241855 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448721\|RGD:10448787 (Homo sapiens) & RGD:10448721\|RGD:10448787 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:22241855 PMID:26092869 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens) & RGD:11595376\|RGD:11644974\|RGD:11645084\|RGD:11646551\|RGD:11647977\|RGD:11650088\|RGD:11651513\|RGD:11651731\|RGD:11654124\|RGD:11654996\|RGD:11655707\|RGD:11656040\|RGD:28869659\|RGD:28873873\|RGD:28874166\|RGD:28875672\|RGD:28878582\|RGD:28880713\|RGD:28883563\|RGD:28904546\|RGD:28904549\|RGD:28905211 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448695\|RGD:10448711\|RGD:10448739\|RGD:10448745\|RGD:10448751\|RGD:10448762 (Homo sapiens) & RGD:10448695\|RGD:10448711\|RGD:10448739\|RGD:10448745\|RGD:10448751\|RGD:10448762 (Homo sapiens) & RGD:10448695\|RGD:10448711\|RGD:10448739\|RGD:10448745\|RGD:10448751\|RGD:10448762 (Homo sapiens) & RGD:10448695\|RGD:10448711\|RGD:10448739\|RGD:10448745\|RGD:10448751\|RGD:10448762 (Homo sapiens) & RGD:10448695\|RGD:10448711\|RGD:10448739\|RGD:10448745\|RGD:10448751\|RGD:10448762 (Homo sapiens) & RGD:10448695\|RGD:10448711\|RGD:10448739\|RGD:10448745\|RGD:10448751\|RGD:10448762 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:26092869

An association has been curated linking CC2D2A and Joubert syndrome 9 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:127246120\|RGD:151799402 (Homo sapiens) & RGD:127246120\|RGD:151799402 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:19777577 PMID:25741868 PMID:28492532

An association has been curated linking CC2D2A and Joubert syndrome 9 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:10448730\|RGD:10448794 (Homo sapiens) & RGD:10448730\|RGD:10448794 (Homo sapiens)
6 RGD objects have been annotated to Joubert syndrome 9 (DOID:0111004)
8 papers in RGD have been used to annotate CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s): PMID:25741868 PMID:26092869

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GENE - TERM ANNOTATION REPORT

55 Annotations Found.