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

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

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000242720 Rod-cone dystrophy, Retinal dystrophy - - Unknown 18y - - - - Andreas Laner 00324137
0000275974 retinal dystrophy; MIM, 612712 MIM, 612712 - Familial, autosomal recessive - - - - - LOVD 00382132
Legend   How to query  


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