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Gene Expression Ontology
Last uploaded:
December 16, 2015
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| Id | http://identifiers.org/omim/123150
http://identifiers.org/omim/123150
|
|---|---|
| Preferred Name | Jackson-Weiss syndrome |
| Definitions |
(JWS) - An autosomal dominant craniosynostosis syndrome characterized by craniofacial abnormalities and abnormality of the feet - broad great toes with medial deviation and tarsal-metatarsal coalescence.
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| Synonyms |
JWS
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | (JWS) - An autosomal dominant craniosynostosis syndrome characterized by craniofacial abnormalities and abnormality of the feet - broad great toes with medial deviation and tarsal-metatarsal coalescence. |
|---|---|
| altLabel |
JWS
|
| prefLabel |
Jackson-Weiss syndrome
|
| notation |
OMIM:123150
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| id |
OMIM:123150
|
| subClassOf | |
| type |
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