Global Variome shared LOVD

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

Phenotype #0000272277 Individual ID 00377090 Associated disease NESCAVS Phenotype details Congenital blindness, Optic atrophy, Global developmental delay, Umbilical hernia, Microcephaly, Muscular hypotonia Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis 02y Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2021-07-01 12:06:17 +02:00 (CEST) Date last edited 2021-07-02 08:55:54 +02:00 (CEST)

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