Disease #04318 (CMS4A (myasthenic syndrome, congenital, type 4A, slow-channel (CMS-4A)), OMIM:605809)

Official abbreviation CMS4A
Name myasthenic syndrome, congenital, type 4A, slow-channel (CMS-4A)
OMIM ID 605809
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CHRNE
Associated tissues -
Disease features -
Remarks -
Date created 2015-08-28 21:27:12 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00117924 patient 26 de Natera, 2017 - M no Spain - - - - - CMS4A - - CHRNE 1 1 Ana Topf
00309728 - - - M - India - - - - - CMS4A - CHRNE CHRNE 1 1 Anju Shukla
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