Global Variome shared LOVD

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

Phenotype #0000277068 Individual ID 00383282 Associated disease DFNB7 Phenotype details bilateral symmetric severe group one hearing loss Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis 03y Age/Onset - Phenotype/Onset - Protein - Owner name David Baux Database submission license Creative Commons Attribution 4.0 International Created by David Baux Date created 2021-09-28 17:11:58 +02:00 (CEST) Date last edited N/A

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