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loading...| Preferred Name |
Crouzon_Syndrome |
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| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Crouzon_Syndrome |
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| ID |
C84653 |
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| NCI_Definition |
A syndrome inherited in an autosomal dominant pattern. It is characterized by early fusion of the bones of the skull and face. Patients have a distinctive facial appearance which includes low-set ears, brachycephaly, hypertelorism, exophthalmos, and mandibular prognathism. |
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| NCI_PT |
Craniofacial Dysostosis |
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| NICHD_Definition |
_ |
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| prefixIRI |
Crouzon_Syndrome |
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| prefLabel |
Crouzon_Syndrome |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Musculoskeletal_System_Disorder |
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