Global Variome shared LOVD

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

Phenotype #0000239581 Individual ID 00315835 Associated disease ? Diagnosis/Initial Kallmann syndrome, PCWH syndrome Diagnosis/Definite - Phenotype details - Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Veronique Pingault Database submission license No license selected Created by Veronique Pingault Date created 2013-12-19 09:42:23 +01:00 (CET) Date last edited N/A

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