Disease #04171 (STRMK (Stormorken syndrome (STRMK)), OMIM:185070)

Official abbreviation STRMK
Name Stormorken syndrome (STRMK)
OMIM ID 185070
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene STIM1
Associated tissues -
Disease features -
Remarks -
Date created 2015-01-18 10:53:36 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00029011 - PubMed: Nesin 2014 3-generation family, 1 affected M ? United States - - - - - STRMK see paper; congenital miosis, bleeding diathesis, thrombocytopenia, proximal muscle weakness KRTAP1-1, RERE, STIM1 KRTAP1-1, RERE, STIM1 3 1 Johan den Dunnen
00029012 - PubMed: Nesin 2014 2-generation family, 1 affected M - United States - - - - - STRMK see paper; congenital miosis, bleeding diathesis, thrombocytopenia, proximal muscle weakness STIM1 STIM1 1 1 Johan den Dunnen
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