Global Variome shared LOVD

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

Phenotype #0000017686 Individual ID 00019910 Associated disease ID Diagnosis/Initial - Diagnosis/Definite - Inheritance Unknown Phenotype details severe hypotonia, severe motor delay and speech delay, deficient gyration frontal region, mild periventricular white matter abnormalities Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Marianne Vos (LOVD-team) Database submission license No license selected Created by Marianne Vos (LOVD-team) Date created 2014-09-17 10:27:53 +02:00 (CEST) Date last edited 2014-11-08 16:15:30 +01:00 (CET)

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