Phenotype #0000157539

Global Variome shared LOVD

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

	Curator: Global Variome, with Curator vacancy

Individual ID	00208932
Associated disease	EAOH
Phenotype details	-
Diagnosis/Initial	Ataxia-ocular apraxia type 1
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	EAOH
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Sergio Piñeiro
Database submission license
Created by	Rick van Minkelen
Date created	2013-06-07 11:18:43 +02:00 (CEST)
Date last edited	N/A

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