Disease #03881 (CFC3 (cardiofaciocutaneous syndrome, type 3 (CFC-3)), OMIM:615279)

Official abbreviation CFC3
Name cardiofaciocutaneous syndrome, type 3 (CFC-3)
OMIM ID 615279
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 MAP2K1
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

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00433682 253199 - - F no Germany - - - - - CFC3 Global developmental delay MAP2K1 MAP2K1 1 1 Andreas Laner
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