Disease #05475 (CMS21 (myasthenic syndrome, congenital, type 21, pre-synaptic (CMS-21)), OMIM:617239)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMS21
Name	myasthenic syndrome, congenital, type 21, pre-synaptic (CMS-21)
OMIM ID	617239
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC18A3
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2018-10-19 17:13:56 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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