Phenotype #0000319187

Individual ID 00428282
Associated disease DFNB1B
Phenotype details non-syndromic hearing impairment
Diagnosis/Initial non-syndromic hearing impairment
Inheritance Familial, autosomal recessive
Diagnosis/Definite DFN1B
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Yacouba Dia
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Yacouba Dia
Date created 2022-12-30 00:54:11 +01:00 (CET)
Date last edited 2022-12-30 11:18:14 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.