Phenotype #0000347209

Individual ID 00458779
Associated disease RS1
Phenotype details see paper; ..., retinoshisis, macular schisis, no macular atrophy, no retinal tear
Diagnosis/Initial retinoschisis
Inheritance Familial, X-linked recessive
Diagnosis/Definite RS1
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-12-20 16:21:00 +01:00 (CET)
Date last edited N/A

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