Disease #04317 (CMS3C (myasthenic syndrome, congenital, type 3C, associated with acetylcholine receptor deficiency (CMS-3C)), OMIM:616323)

Official abbreviation CMS3C
Name myasthenic syndrome, congenital, type 3C, associated with acetylcholine receptor deficiency (CMS-3C)
OMIM ID 616323
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CHRND
Associated tissues -
Disease features -
Remarks -
Date created 2015-08-28 20:35:44 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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