Global Variome shared LOVD

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

Phenotype #0000273605 Individual ID 00379751 Associated disease CSNB Phenotype details HP:0030515, HP:0001123, HP:0000639, HP:0000662 Diagnosis/Initial blindness, night, stationary, congenital (CSNB) Inheritance Familial, X-linked recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jinu Han Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Jinu Han Date created 2021-08-09 04:18:37 +02:00 (CEST) Date last edited 2021-08-11 14:35:53 +02:00 (CEST)

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