Disease #01002 (CMS4C (myasthenic syndrome, congenital, type 4C, associated with acetylcholine receptor deficiency (CMS-4C)), OMIM:608931)

Official abbreviation CMS4C
Name myasthenic syndrome, congenital, type 4C, associated with acetylcholine receptor deficiency (CMS-4C)
OMIM ID 608931
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 11
Phenotype entries for this disease -
Associated with 1 gene CHRNE
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

11 entries on 1 page. Showing entries 1 - 11.
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00406621 2 - - M - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406624 5 - - F - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406625 6 - - F - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406628 9 - - F - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406629 10 - - F - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406643 13 - - F - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406644 14 - - F - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406646 16 - - M - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406649 19 - - M - - - - - - - CMS4C - - CHRNE 2 1 Martin Krenn
00406651 21 - - F - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
00406652 22 - - M - - - - - - - CMS4C - - CHRNE 1 1 Martin Krenn
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