Phenotype #0000141832

Global Variome shared LOVD

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

Individual ID	00177015
Associated disease	EE
Phenotype details	HP:0000666 HP:0002451 HP:0001285
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	Epilepsy, hearing loss, and mental retardation syndrome (MIM 616577)
Age/Examination	-
Age/Diagnosis	-
Age/Onset	00y08m
Phenotype/Onset	-
Protein	-
Owner name	Anaïs Begemann
Database submission license	No license selected
Created by	Anaïs Begemann
Date created	2018-08-16 12:01:34 +02:00 (CEST)
Date last edited	2018-08-17 11:41:52 +02:00 (CEST)

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