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GENE - TERM ANNOTATION REPORT

50 Annotations Found.

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:21071502 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:127237550 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760 PMID:34906470

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13785603 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:24474277 PMID:25741868 PMID:26261414 PMID:28492532 PMID:28704921 PMID:29550188

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:11525995 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:20333770 PMID:24938718 PMID:25097241 PMID:25133751 PMID:26787102 PMID:28492532

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:11581375 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:20333770 PMID:24474277 PMID:25741868 PMID:26261414 PMID:28492532 PMID:29550188 PMID:34906470

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:126767077 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25491159 PMID:25741868 PMID:28041643 PMID:28492532 PMID:29074561 PMID:29159838 PMID:32037395

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:127268773|RGD:26913279 (Homo sapiens) & RGD:127268773|RGD:26913279 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:24474277 PMID:25741868 PMID:26261414 PMID:28492532 PMID:29550188

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens) & RGD:127272093|RGD:13785790|RGD:13838629|RGD:151762280|RGD:151797094|RGD:151847378|RGD:156159703|RGD:156291110|RGD:401940813|RGD:401942028|RGD:402509387 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13518176 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:22363543 PMID:24652164 PMID:25741868 PMID:28492532 PMID:28763560

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13445925 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25741868 PMID:28492532 PMID:31456290 PMID:32531858 PMID:33576794 PMID:36764454

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:11640168 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:20237254 PMID:20333770 PMID:20537394 PMID:25741868 PMID:28492532

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:38490715 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:28492532 PMID:29641573

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13785582 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:26667666 PMID:28492532 PMID:29159838 PMID:31213501 PMID:32675063 PMID:33247286 PMID:34178978

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:126745278 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:23591405 PMID:28492532

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:26893539 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:28492532 PMID:30337596

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:11051472 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:22581970 PMID:26872967 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:9480312 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:22302105 PMID:22363543 PMID:24652164 PMID:25324289 PMID:25741868 PMID:26161267 PMID:28492532 PMID:31213501

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:26909361 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:20237254 PMID:25741868 PMID:27208204 PMID:29159838 PMID:32037395 PMID:33749171 PMID:37544434

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:151743778 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:21179430 PMID:25741868 PMID:28492532 PMID:29159838 PMID:31814702

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:151879871 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760 PMID:32037395

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:151889587 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25741868 PMID:28492532 PMID:33090715

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:156351748 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760 PMID:33691693

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:8640540 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:23591405 PMID:23757202 PMID:24474277 PMID:25741868 PMID:26261414 PMID:28492532 PMID:28704921 PMID:29550188

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:21071500 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:20333770 PMID:24474277 PMID:25356976 PMID:25366773 PMID:25741868 PMID:26261414 PMID:28492532 PMID:29550188 PMID:32531858 PMID:33576794 PMID:34906470 PMID:35672425

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:26918616 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:30337596 PMID:32037395

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:26885217 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:30337596 PMID:30804660 PMID:31054281 PMID:34689181

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:156418661 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:28704921 PMID:29159838 PMID:30337596 PMID:31074760 PMID:33090715

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:11634136 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:24474277 PMID:25356976 PMID:25741868 PMID:26261414 PMID:28492532 PMID:29550188

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens) & RGD:127237603|RGD:13612198|RGD:155266482|RGD:155698684|RGD:155698688|RGD:21404358|RGD:401940796|RGD:401940811|RGD:401940828|RGD:401940970|RGD:401940989|RGD:401942049|RGD:401942093|RGD:401942110|RGD:401942125|RGD:401942163|RGD:405868494|RGD:405868664|RGD:405868671|RGD:405868685|RGD:405868688|RGD:407458892|RGD:40814999 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25741868

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13838630|RGD:152982940|RGD:25314813|RGD:407489691 (Homo sapiens) & RGD:13838630|RGD:152982940|RGD:25314813|RGD:407489691 (Homo sapiens) & RGD:13838630|RGD:152982940|RGD:25314813|RGD:407489691 (Homo sapiens) & RGD:13838630|RGD:152982940|RGD:25314813|RGD:407489691 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:401942216 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760 PMID:33576794 PMID:36819107

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:26888827 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25741868 PMID:26787102 PMID:28492532 PMID:31213501 PMID:36819107

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:152046064 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:17011488 PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760 PMID:31144483 PMID:33946315

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:401940990 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:30337596 PMID:30804660 PMID:31054281

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:14698646|RGD:156192116 (Homo sapiens) & RGD:14698646|RGD:156192116 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25741868 PMID:28492532 PMID:30718709 PMID:32037395

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:126756590|RGD:126924247 (Homo sapiens) & RGD:126756590|RGD:126924247 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:28492532 PMID:31814702

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:14394150|RGD:401942236 (Homo sapiens) & RGD:14394150|RGD:401942236 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25356976 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:38464562|RGD:38464987|RGD:38471190|RGD:38493263 (Homo sapiens) & RGD:38464562|RGD:38464987|RGD:38471190|RGD:38493263 (Homo sapiens) & RGD:38464562|RGD:38464987|RGD:38471190|RGD:38493263 (Homo sapiens) & RGD:38464562|RGD:38464987|RGD:38471190|RGD:38493263 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:30337596

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13435012|RGD:13435162 (Homo sapiens) & RGD:13435012|RGD:13435162 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:28041643 PMID:28492532

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens) & RGD:126742340|RGD:126747328|RGD:126749448|RGD:126766747|RGD:126912365|RGD:126912799|RGD:126914657|RGD:127263980|RGD:15113279|RGD:15127843|RGD:26889728|RGD:26889807|RGD:26904443|RGD:26914256|RGD:26914487|RGD:38464123|RGD:38481350|RGD:38486372|RGD:38491205|RGD:38491463|RGD:38494487|RGD:38498302|RGD:38500077 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:28492532

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens) & RGD:11581474|RGD:126768699|RGD:126923848|RGD:127237777|RGD:127237980|RGD:150454205|RGD:38459395|RGD:38476362|RGD:9688660 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13518818 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:30543658 PMID:31074760 PMID:32531858 PMID:34315337 PMID:34426522 PMID:36819107

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:38486283 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:20537394 PMID:25741868 PMID:26667666 PMID:28492532 PMID:29159838 PMID:31074760 PMID:31964843 PMID:34178978 PMID:36819107

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:26899684 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:21069908 PMID:21519034 PMID:25741868 PMID:28492532 PMID:31964843 PMID:32036094 PMID:32531858 PMID:32728228 PMID:36819107

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13785778 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:20333770 PMID:24474277 PMID:25356976 PMID:25741868 PMID:26261414 PMID:28492532 PMID:29550188 PMID:30718709 PMID:3442652

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:14733632 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:24474277 PMID:25741868 PMID:26261414 PMID:27735924 PMID:28492532 PMID:29159838 PMID:29550188 PMID:31074760 PMID:33749171

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:14397257 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:25097241 PMID:25366773 PMID:25741868 PMID:28492532 PMID:30718709 PMID:31725169 PMID:31964843 PMID:32037395 PMID:32728228 PMID:33576794 PMID:36764454

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:8555689 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:21069908 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:31074760 PMID:31589614 PMID:31964843 PMID:32531858 PMID:34327195 PMID:34795310 PMID:34906470 PMID:36460718

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:26921984 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:18976725 PMID:25741868 PMID:28492532 PMID:29159838 PMID:30337596 PMID:30543658 PMID:31074760

An association has been curated linking PHF3 and retinitis pigmentosa 25 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:13785507 (Homo sapiens)
17 RGD objects have been annotated to retinitis pigmentosa 25  (DOID:0110384)
3 papers in RGD have been used to annotate PHF3
Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 25
Original References(s): PMID:20537394 PMID:22363543 PMID:25741868 PMID:28492532 PMID:29068140 PMID:29159838 PMID:30718709 PMID:31087526 PMID:31429209 PMID:31964843 PMID:32531858 PMID:33833316

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