Phenotype #0000308435

Individual ID 00416924
Associated disease EVR2
Phenotype details whole family description: congenital blindness and hearing loss; diagnosed as having Norrie disease
Diagnosis/Initial -
Inheritance Familial, X-linked
Diagnosis/Definite familial exudative vitreoretinopathy
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 2022-09-10 20:47:00 +02:00 (CEST)
Date last edited N/A

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