Global Variome shared LOVD

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

Phenotype #0000275378 Individual ID 00381528 Associated disease WS2E Phenotype details iris heterochromia, white hair forelock and unilateral hearing loss Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Karina Lezirovitz Mandelbaum Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Karina Lezirovitz Mandelbaum Date created 2021-08-30 16:10:59 +02:00 (CEST) Date last edited 2021-08-30 16:18:45 +02:00 (CEST)

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