All individuals with variants in gene POC5

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00151424 FamPatII1;Fam1 PubMed: Weisz Hubshman 2018, Vulto-van Silfhout 2024, submitted 2-generation family, 1 affected, unaffected heterozygous carrier parents/brother F - Morocco Yemenite;Jew - - - - RPar see paper; ..., retinitis pigmentosa (HP:0000510), short stature (HP:0004322), microcephaly (HP:0000252 ), recurrent glomerulonephritis (HP:0000099);height 143cm (SD-3.4), OFC (SD-3.8); best corrected visual acuity 0.5; 6y-myopia; mild central posterior subcapsular cataract; very thin habitus; early fast puberty; recurrent glomerulonephritis ; painful muscle cramps, elevated CK; no skeletal abnormalities; no heart abnormalities; wide mouth, prognathia, midface hypoplasia; normal hair; soft skin 1 1 Johan den Dunnen
00309301 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.