Preferred Name |
Crouzon syndrome |
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Synonyms |
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Definitions |
(CS): An autosomal dominant syndrome characterized by craniosynostosis, hypertelorism, exophthalmos and external strabismus, parrot-beaked nose, short upper lip, hypoplastic maxilla, and a relative mandibular prognathism. |
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ID |
http://purl.obolibrary.org/obo/OMIM_123500 |
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definition |
(CS): An autosomal dominant syndrome characterized by craniosynostosis, hypertelorism, exophthalmos and external strabismus, parrot-beaked nose, short upper lip, hypoplastic maxilla, and a relative mandibular prognathism. |
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has_obo_namespace |
cell_cycle_ontology |
|
id |
OMIM:123500 |
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label |
Crouzon syndrome |
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notation |
OMIM:123500 |
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prefLabel |
Crouzon syndrome |
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treeView | ||
subClassOf |
Create mapping