Disease #05239 (CMS19 (myasthenic syndrome, congenital, type 19 (CMS-19)), OMIM:616720)

Official abbreviation CMS19
Name myasthenic syndrome, congenital, type 19 (CMS-19)
OMIM ID 616720
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene COL13A1
Associated tissues -
Disease features -
Remarks -
Date created 2017-03-19 12:35:33 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00406654 24 - - F - - - - - - - CMS19 - - COL13A1 1 1 Martin Krenn
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