Global Variome shared LOVD

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

Phenotype #0000054339 Individual ID 00074542 Associated disease OCA1A Phenotype details Generalized hypopigmentation (HP:0007513) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 05y (5 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Pieter Klap Database submission license No license selected Created by Pieter Klap Date created 2016-07-08 10:43:23 +02:00 (CEST) Date last edited 2016-10-11 12:31:54 +02:00 (CEST)

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