Disease #07251 (CMYO26 (myopathy, congenital, type 26), OMIM:621225)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMYO26
Name	myopathy, congenital, type 26
OMIM ID	621225
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TUBA4A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-04-01 11:01:17 +02:00 (CEST)
Date last edited	N/A

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