Phenotype #0000055849

Individual ID 00076074
Associated disease CORD
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset 10y
Phenotype/Onset unknown
Phenotype details cone-rod dystrophy (HP:0000510); Reduced cone and rod ERGs, OD: 0.02, OS: 0.02, Chorioidal sclerosis
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-02-22 12:22:09 +01:00 (CET)
Date last edited N/A

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