MeSH Browser

MeSH Supplementary: Orofacial Cleft 1
Unique ID: C566121
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566121
Entry Term(s): Cleft Lip with or without Cleft Palate, Nonsyndromic, 1; Cleft Lip-Palate, Nonsyndromic; OFC1; Orofacial Cleft, Nonsyndromic
Registry Number: 0
Heading Mapped to: Brain / *abnormalities; *Cleft Lip; *Cleft Palate
Frequency: 127
Note: Isolated cleft lip with or without cleft palate (CL/P) is genetically heterogeneous and most cases (>75%) are isolated. Brain abnormalities, including enlarged anterior regions of the CEREBRUM, and decreased volumes of the posterior cerebrum and CEREBELLUM also occur, the left TEMPORAL LOBE is also frequently affected. OFC1 exhibits autosomal dominant inheritance and has been mapped to chromosome 6. OMIM: 119530
Date of Entry: 2012/11/05
Revision Date: 2015/11/10

Concept UI: M0566421
Registry Number: 0
Terms: Orofacial Cleft 1 Preferred Term
Term UI T807946
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Cleft Lip-Palate, Nonsyndromic
Term UI T000889611
Date11/02/2015
LexicalTag NON
ThesaurusID OMIM (2013); Cleft Lip with or without Cleft Palate, Nonsyndromic, 1
Term UI T826721
Date07/25/2012
LexicalTag NON
ThesaurusID OMIM (2013); Orofacial Cleft, Nonsyndromic
Term UI T807947
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); OFC1
Term UI T000883480
Date07/16/2015
LexicalTag NON
ThesaurusID OMIM (2016)

Orofacial Cleft 1 MeSH Supplementary Concept Data 2024