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MAP3K7

HGNC ↗

Cardiospondylocarpofacial syndrome (CSCF)

1 article(s) in the watch · Constitutional genetics

Curated publications

6/10

A Novel MAP3K7 Variant Causing Loss of Function Identified in a Family With Cardiospondylocarpofacial Syndrome: Functional Validation and Molecular Insights

Cardiospondylocarpofacial syndrome (CSCF)

Gén.29 April 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.