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loading...| Preferred Name | Van der Woude Syndrome | |
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| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Van_der_Woude_Syndrome |
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| 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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| isDefinedBy |
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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| label |
Van der Woude Syndrome |
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| prefixIRI |
Thesaurus:Van_der_Woude_Syndrome |
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| prefLabel |
Van der Woude Syndrome |
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| subClassOf |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Rare_Non-Neoplastic_Disorder |
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