Phenotype #0000034252

Individual ID 00046458
Associated disease CORD
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details visual loss (HP:0000572), photophobia (HP:0000613), pendular nystagmus (HP:0012043), rod-cone dystrophy (HP:0000510)
Protein -
Owner name Csilla Lazar
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-07-10 20:26:42 +02:00 (CEST)
Date last edited 2017-01-04 12:01:36 +01:00 (CET)

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