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loading...| Preferred Name | Van der Woude Syndrome | |
| Synonyms |
Van der Woude Syndrome Van Der Woude Syndrome |
|
| Definitions |
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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| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C74986 |
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| code |
C74986 |
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| Concept_In_Subset | ||
| Contributing_Source |
NICHD |
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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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| FULL_SYN |
Van der Woude Syndrome Van Der Woude Syndrome |
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| label |
Van der Woude Syndrome |
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| Legacy Concept Name |
Van_der_Woude_Syndrome |
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| Preferred_Name |
Van der Woude Syndrome |
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| prefixIRI |
Thesaurus:C74986 |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0175697 |
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| subClassOf |
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