Disease #01947 (CMS6 (myasthenic syndrome, congenital, type 6, presynaptic (CMS-6)), OMIM:254210)

Official abbreviation CMS6
Name myasthenic syndrome, congenital, type 6, presynaptic (CMS-6)
OMIM ID 254210
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease -
Associated with 1 gene CHAT
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)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00117930 patient 61 de Natera, 2017 - F no Spain - - - - - CMS6 - - CHAT 2 1 Ana Topf
00117931 patient 62 de Natera, 2017 - M no Spain - - - - - CMS6 - - CHAT 1 1 Ana Topf
00406622 3 - - M - - - - - - - CMS6 - - CHAT 2 1 Martin Krenn
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