MeSH Browser

MeSH Supplementary: Van der Woude syndrome
Unique ID: C536528
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536528
Entry Term(s): Cleft lip and-or palate with mucous cysts of lower lip; Lip pit syndrome; Lip-Pit Syndrome
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; *Cleft Lip; *Cleft Palate; *Cysts; Lip / *abnormalities
Frequency: 114
Note: An autosomal dominant hereditary developmental disorder characterized by pits and/or sinuses of the lower lip, and cleft lip and/or cleft palate (CL/P, CP). It is the most common cleft syndrome. Mutations in the IRF6 gene have been identified. OMIM: 119300
Date of Entry: 2010/08/25
Revision Date: 2015/11/12

Concept UI: M0530989
Registry Number: 0
Terms: Van der Woude syndrome Preferred Term
Term UI T739616
Date02/24/2009
LexicalTag NON
ThesaurusID; Lip-Pit Syndrome
Term UI T800638
Date11/15/2011
LexicalTag NON
ThesaurusID; Lip pit syndrome
Term UI T739619
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Cleft lip and-or palate with mucous cysts of lower lip
Term UI T000889012
Date11/02/2015
LexicalTag NON
ThesaurusID

Van der Woude syndrome MeSH Supplementary Concept Data 2024