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Cell Cycle Ontology
Last uploaded:
June 26, 2014
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| Id | http://purl.obolibrary.org/obo/OMIM_123500
http://purl.obolibrary.org/obo/OMIM_123500
|
|---|---|
| Preferred Name | Crouzon syndrome |
| 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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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| 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. |
|---|---|
| label |
Crouzon syndrome
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| prefLabel |
Crouzon syndrome
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| notation |
OMIM:123500
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| id |
OMIM:123500
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| has_obo_namespace |
cell_cycle_ontology
|
| subClassOf | |
| type | |
| treeView |
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