Global Variome shared LOVD

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

Phenotype #0000218568 Individual ID 00284942 Associated disease deafness Phenotype details severe-profound hearing loss, symmetric Diagnosis/Initial deafness, autosomal recessive, non-syndromic Inheritance Isolated (sporadic) Diagnosis/Definite DFNB84A Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Julia Lopez Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2020-02-05 13:36:16 +01:00 (CET) Date last edited 2023-11-08 16:15:39 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.