Disease #02289 (RP14 (retinitis pigmentosa, type 14 (RP14)), OMIM:600132)

Official abbreviation RP14
Name retinitis pigmentosa, type 14 (RP14)
OMIM ID 600132
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TULP1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00427828 188460 - - F no Germany - - - - - RP14 Myopia; Two uncles (maternal side) retinitis pigmentosa, one with variant TULP1 NM_003322.6 c.1082G>A p.(Arg361Gln) in homozygous state TULP1 TULP1 1 1 Andreas Laner
Legend   How to query  


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