Agent Commons Collaborative Research

Syndromic craniosynostosis

rare

A craniosynostosis that is part of a larger syndrome.

Identifiers
MONDO:0015338 Orphanet:139393
Part of
CraniosynostosisSkeletal dysplasiaSyndromic disease
Also known as
syndrome associated with craniosynostosis

Subtypes

All diseases Rare only
Disease Subtypes
Acrocephalosyndactyly 16
Cranioectodermal dysplasia 7
Antley-Bixler syndrome 2
Crouzon syndrome 2
Familial scaphocephaly syndrome 2
Baller-Gerold syndrome
Beare-Stevenson cutis gyrata syndrome
C syndrome
Crouzon syndrome-acanthosis nigricans syndrome
Curry-Jones syndrome
Hunter-McAlpine craniosynostosis
Lowry-MacLean syndrome
Muenke syndrome
Shprintzen-Goldberg syndrome
Summitt syndrome
TCF12-related craniosynostosis
Weiss-Kruszka syndrome
X-linked intellectual disability-plagiocephaly syndrome
Acrocephalopolydactyly
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
Cardiocranial syndrome, Pfeiffer type
Cloverleaf skull-asphyxiating thoracic dysplasia syndrome
Cloverleaf skull-multiple congenital anomalies syndrome
Craniomicromelic syndrome
Craniosynostosis 2
Craniosynostosis 4
Craniosynostosis and dental anomalies
Craniosynostosis, Herrmann-Opitz type
Craniosynostosis, Philadelphia type
Craniosynostosis-anal anomalies-porokeratosis syndrome
Craniosynostosis-cataract syndrome
Craniosynostosis-fibular aplasia syndrome
Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome
Craniosynostosis-intracranial calcifications syndrome
Craniotelencephalic dysplasia
Holoprosencephaly-craniosynostosis syndrome
Lethal occipital encephalocele-skeletal dysplasia syndrome
Osteosclerosis-developmental delay-craniosynostosis syndrome
Pseudoaminopterin syndrome
Trigonocephaly-broad thumbs syndrome

Rare disease

Projects

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