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Pediatric Terminology
Last uploaded:
January 25, 2013
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| Preferred Name | Van_Der_Woude_Syndrome | |
| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Van_Der_Woude_Syndrome |
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| ID |
C74986
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| NCI_Definition |
A rare autosomal dominant syndrome caused by mutations in the IRF6 gene. It is characterized by a cleft palate and/or pits on the lower lip. Other signs and symptoms include absent teeth, palate and tongue deformities.
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| NCI_PT |
Van der Woude Syndrome
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| NICHD_Definition |
_
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| prefixIRI |
Van_Der_Woude_Syndrome
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| prefLabel |
Van_Der_Woude_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#Genetic_Disorder |
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