Phenotype #0000308948

Individual ID 00417462
Associated disease -
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite retinal dystrophy dominated by inner retinal dysfunction and ganglion cell abnormalities
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 2022-09-16 19:13:29 +02:00 (CEST)
Date last edited N/A

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