Disease #04320 (CMS15 (myasthenic syndrome, congenital, type 15, without tubular aggregates (CMS-15)), OMIM:616227)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMS15
Name	myasthenic syndrome, congenital, type 15, without tubular aggregates (CMS-15)
OMIM ID	616227
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALG14
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-08-28 21:42:28 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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