Disease #00419 (MWKS (Marden Walker syndrome (MWKS)), OMIM:248700)

Official abbreviation MWKS
Name Marden Walker syndrome (MWKS)
OMIM ID 248700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PIEZO2
Associated tissues -
Disease features -
Remarks -
Date created 2014-06-16 13:07:26 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00049838 - PubMed: McMillin 2014, Journal: McMillin 2014 2-generation family, 1 affected, unaffected non-carrier parents M - - - - - - - MWKS contractures hand/feet PIEZO2 PIEZO2 1 1 Johan den Dunnen
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