Global Variome shared LOVD

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

Phenotype #0000273160 Individual ID 00378013 Associated disease LCA Phenotype details HP:0001141, HP:0000639, HP:0001483, HP:0003745 Diagnosis/Initial Leber congenital amaurosis (LCA) Inheritance Familial, autosomal 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 2021-08-03 03:36:48 +02:00 (CEST) Date last edited 2021-08-06 16:17:22 +02:00 (CEST)

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