ZFIN Human Disease: cardiofaciocutaneous syndrome 2

OBO ID: DOID:0111461

OBO ID: DOID:0111461

Term Name:	cardiofaciocutaneous syndrome 2	Search Ontology:
Synonyms:	CFC2
Definition:	A cardiofaciocutaneous syndrome that has_material_basis_in heterozygous mutation in the KRAS gene on chromosome 12p12.1. https://www.ncbi.nlm.nih.gov/pubmed/16474404
References:	OMIM:615278
Ontology:	Human Disease ( DOID:0111461 )

Relationships

is a type of:	autosomal dominant disease cardiofaciocutaneous syndrome autosomal dominant disease cardiofaciocutaneous syndrome Show first 5 Terms

OTHER cardiofaciocutaneous syndrome 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KRAS	kras	Cardiofaciocutaneous syndrome 2	615278

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None