Disease #05658 (MYOSCO (myopathy, congenital, progressive, with scoliosis (MYOSCO)), OMIM:618578)

Global Variome shared LOVD

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

Official abbreviation	MYOSCO
Name	myopathy, congenital, progressive, with scoliosis (MYOSCO)
OMIM ID	618578
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PAX7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-10-05 13:28:46 +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.