Disease #00571 (CMS1B (myasthenic syndrome, congenital, type 1B, fast-channel (CMS-1B)), OMIM:608930)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMS1B
Name	myasthenic syndrome, congenital, type 1B, fast-channel (CMS-1B)
OMIM ID	608930
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	CHRNA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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