Phenotype #0000015164

Individual ID 00016548
Associated disease RP
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details characteristic arRP with hypopigmented macular atrophy and bear track changes; bilateral congenital subclinical renal cysts; mild cognitive impairment
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Heleen Arts
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-05-02 11:08:51 +02:00 (CEST)
Date last edited 2014-05-02 11:22:17 +02:00 (CEST)

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