Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000255790 Individual ID 00360385 Associated disease - Phenotype details visual acuity: OD = 0,8, OS = 0,9. Retinal phenotype: confluence of STGD1‐like lesions and patches of atrophy in posterior pole, OD slight peripheral pigmentary changes. Diagnosis/Initial multifocal pattern dystrophy Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Manon Peeters Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-04-06 16:50:09 +02:00 (CEST) Date last edited N/A

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