Phenotype #0000124364

Global Variome shared LOVD

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

Individual ID	00152005
Associated disease	DFNB67
Phenotype details	bilateral profound deafness, walking delay, bilateral vestibular areflexia
Diagnosis/Initial	Usher syndrome
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	DFNB-67
Age/Examination	01y (1 year)
Age/Diagnosis	01y06m
Age/Onset	00y
Phenotype/Onset	0y
Protein	-
Owner name	Justine Lerat
Database submission license	No license selected
Created by	Justine Lerat
Date created	2018-01-31 19:17:21 +01:00 (CET)
Date last edited	2018-04-30 17:14:15 +02:00 (CEST)

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