Phenotype #0000288756

Individual ID 00395558
Associated disease -
Phenotype details cataract, optic atrophy, photophobia, rod-cone dystrophy, hearing impairment
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite retinitis pigmentosa, optic atrophy, cataracts, hearing impairment
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-12-08 14:12:08 +01:00 (CET)
Date last edited N/A

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