Acrocephalosyndactyly

rare

Acrocephalosyndactyly (ACS) syndromes represent a group of inherited congenital malformation disorders characterized by craniosynostosis and fusion or webbing of the fingers or toes, often with other associated manifestations.

Identifiers: MONDO:0019796 Orphanet:946
Part of: Congenital limb malformation Syndromic craniosynostosis
Also known as: acrocephalosyndactylia · ACS

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Acrocephalopolysyndactyly	MONDO:0000078	11
Apert syndrome	MONDO:0007041	1	FGFR2
Jackson-Weiss syndrome	MONDO:0007400
Saethre-Chotzen syndrome	MONDO:0007042

Rare disease

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