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Disease

Cardiofaciocutaneous syndrome 3

Also known as MAP2K1 cardiofaciocutaneous syndrome, cardiofaciocutaneous syndrome caused by mutation in MAP2K1, cardiofaciocutaneous syndrome type 3, CFC3.

2
Associated genes
1
Related proteins

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Associated genes

2 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

MAP2K10.81SNAPC50.18

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Dual specificity mitogen-activated protein kinase kinase 1via MAP2K10.81

Reference

Authoritative identity, definition & identifiers.

Synonyms

MAP2K1 cardiofaciocutaneous syndrome, cardiofaciocutaneous syndrome caused by mutation in MAP2K1, cardiofaciocutaneous syndrome type 3, CFC3

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.