Global Variome shared LOVD

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

Phenotype #0000223431 Individual ID 00295955 Associated disease deafness Phenotype details Hearing loss, developmental delay, Kallmann syndrome Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Seungmin Lee Database submission license No license selected Created by Seungmin Lee Date created 2020-03-30 14:08:36 +02:00 (CEST) Date last edited 2020-04-01 03:43:41 +02:00 (CEST)

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