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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Cloverleaf skull - asphyxiating thoracic dysplasia 
Cloverleaf skull - multiple congenital anomalies 
Craniofacial dysplasia-osteopenia syndrome 
Craniofrontonasal dysplasia - Poland anomaly 
Craniosynostosis - anal anomalies - porokeratosis 
Craniosynostosis - cataract 
Craniosynostosis - Dandy-Walker malformation - hydrocephalus 
Craniosynostosis - fibular aplasia 
Craniosynostosis - hydrocephalus - Arnold-Chiari malformation type I - radioulnar synostosis 
Craniosynostosis - intracranial calcifications 
Craniosynostosis, Boston type 
Crouzon disease 
Crouzon disease is characterized by craniosynostosis and facial hypoplasia.
Crouzon syndrome - acanthosis nigricans 
Cutis gyrata - acanthosis nigricans - craniosynostosis 
Dysostosis of genetic origin with limb anomaly as a major feature +  
Dysostosis with predominant vertebral and costal involvement +  
Familial chondromalacia patellae 
Familial Scheuermann disease 
fgfr2 related craniosynostosis 
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome 
Holoprosencephaly - craniosynostosis 
Hyaluronidase deficiency 
Hypertelorism, Teebi type 
Hypertrichotic osteochondrodysplasia, Cantu type 
Inverse Klippel-Trénaunay syndrome 
Klippel-Trénaunay syndrome 
Mandibulofacial dysostosis - macroblepharon - macrostomia 
metopic craniosynostosis  
Multiple sulfatase deficiency 
Primary bone dysplasia +  
Primary intraosseous vascular malformation 
Rare bone disease related to a common gene or pathway defect +  
Rare hereditary disease with avascular necrosis +  
sialidosis type II +  
Trigonocephaly - broad thumbs 
Trigonocephaly - short stature - developmental delay 
X-linked intellectual disability - plagiocephaly 

Synonyms
Exact Synonyms: Crouzon craniofacial dysostosis
Xrefs: ICD10:Q75.1 ;   MIM:123500

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