Disease #03182 (LCA13;RP53 (Leber congenital amaurosis, type 13 (LCA13, retinitis pigmentosa, type 53 (RP53))), OMIM:612712)

Official abbreviation LCA13;RP53
Name Leber congenital amaurosis, type 13 (LCA13, retinitis pigmentosa, type 53 (RP53))
OMIM ID 612712
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene RDH12
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

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     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00324137 172672 - - M - - - - - - - LCA13;RP53 Rod-cone dystrophy, Retinal dystrophy RDH12 RDH12 1 1 Andreas Laner
00382132 7 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - LCA13;RP53 retinal dystrophy; MIM, 612712 RDH12 RDH12 1 1 LOVD
Legend   How to query  


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