Disease #05334 (CSCF (cardiospondylocarpofacial syndrome (CSCF)), OMIM:157800)

Official abbreviation CSCF
Name cardiospondylocarpofacial syndrome (CSCF)
OMIM ID 157800
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 MAP3K7
Associated tissues -
Disease features -
Remarks -
Date created 2017-10-21 23:51:06 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00132079 - PubMed: Morlino 2018, Journal: Morlino 2018 2-generation family, 1 affected F no Italy white - - - - CSCF see paper; ..., soft/dystrophic skin, extreme joint hypermobility, polyvalvular heart disease, upper gastrointestinal dismotility MAP3K7 MAP3K7 1 1 Marco Ritelli
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