Phenotype #0000272868

Individual ID 00377717
Associated disease -
Phenotype details oculocutaneous albinism, which caused nystagmus and reduced visual acuity from early infancy.
Diagnosis/Initial cone-rod dystrophy
Inheritance Familial
Diagnosis/Definite -
Age/Examination 6m
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-08-02 20:37:33 +02:00 (CEST)
Date last edited N/A

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