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