Global Variome shared LOVD

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

Phenotype #0000093279 Individual ID 00117898 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details hypomyelination, hypodontia, and hypogonadotropic hypogonadism; 4H syndrome Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Gerard C.P. Schaafsma Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2011-12-13 10:21:17 +01:00 (CET) Date last edited N/A

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