Disease #07178 (UCMD1B (dystrophy, Uhlrich, muscular, congenital, type 1B), OMIM:620727)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	UCMD1B
Name	dystrophy, Uhlrich, muscular, congenital, type 1B
OMIM ID	620727
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive, Digenic
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COL6A2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-09-09 12:25:47 +02:00 (CEST)
Date last edited	N/A

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