Cure My Disease

Don't miss your cure!

 Log in / Sign up

Acrocephalosyndactyly

MONDO:0019796

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.

Also known as: ACS, acrocephalosyndactylia, acrocephalosyndactyly

14 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Apert syndrome (11) Saethre-Chotzen syndrome (3) Pfeiffer syndrome (1) Acrocephalopolysyndactyly (0) Carpenter syndrome (0) FGFR1-related Pfeiffer syndrome (0) FGFR2-related Pfeiffer syndrome (0) Goodman syndrome (0) Jackson-Weiss syndrome (0) Maroteaux Fonfria syndrome (0) MEGF8-related Carpenter syndrome (0) Pfeiffer syndrome type 1 (0) Pfeiffer syndrome type 2 (0) Pfeiffer syndrome type 3 (0) RAB23-related Carpenter syndrome (0) Sakati-Nyhan syndrome (0)

Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Syndromic disease (25) Craniosynostosis (15) Human disease (14) Developmental defect during embryogenesis (8) Skeletal system disorder (4) Congenital limb malformation (3)
Trials to join now! 3 Not yet recruiting 1 Not yet finished but already full! 3 Completed 3 Terminated 4
Sort by