Disease #07109 (CMYO18 (myopathy, congenital, type 18, due to dihydropyridine receptor defect), OMIM:620246)

Global Variome shared LOVD

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Official abbreviation	CMYO18
Name	myopathy, congenital, type 18, due to dihydropyridine receptor defect
OMIM ID	620246
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CACNA1S
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-10-24 13:36:57 +02:00 (CEST)
Date last edited	N/A

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