Disease #00084 (FSHD1 (dystrophy, muscular, facioscapulohumeral, type 1 (FSHD-1)), OMIM:158900)

Global Variome shared LOVD

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

Official abbreviation	FSHD1
Name	dystrophy, muscular, facioscapulohumeral, type 1 (FSHD-1)
OMIM ID	158900
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DUX4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-12 15:13:39 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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