Search Ontology:
Human Disease

cardiofaciocutaneous syndrome 3

Term ID
DOID:0111462
Synonyms
  • CFC3
Definition
A cardiofaciocutaneous syndrome that has_material_basis_in heterozygous mutation in the MAP2K1 gene on chromosome 15q22.31. https://www.ncbi.nlm.nih.gov/pubmed/16439621
References
Ontology
Human Disease   ( DOID:0111462 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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