MeSH Browser

MeSH Supplementary: Parietal Foramina
Unique ID: C566826
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566826
Entry Term(s): Catlin Marks; Cranium Bifidum Occultum; Cranium Bifidum, Hereditary; Enlarged Parietal Foramina; Foramina Parietalia Permagna; Parietal Foramina, Symmetric
Registry Numbers: 0
Heading Mapped to: *Encephalocele
Frequency: 40
Note: Abnormal, symmetric, oval openings in the PARIETAL BONE on each side of the sagittal suture and separated from each other by a narrow bridge of bone. Their size decreases with age and considerable intrafamilial variability is observed. Mutations in the MSX2 and ALX4 genes have been identified for some cases. OMIM: 168500.
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Concept UI: M0567126
Registry Numbers: 0
Terms: Parietal Foramina Preferred Term
Term UI T809187
Date11/15/2011
LexicalTag NON
ThesaurusID; Parietal Foramina, Symmetric
Term UI T809188
Date11/15/2011
LexicalTag NON
ThesaurusID; Foramina Parietalia Permagna
Term UI T809189
Date11/15/2011
LexicalTag NON
ThesaurusID; Catlin Marks
Term UI T809190
Date11/15/2011
LexicalTag NON
ThesaurusID; Cranium Bifidum Occultum
Term UI T809191
Date11/15/2011
LexicalTag NON
ThesaurusID; Cranium Bifidum, Hereditary
Term UI T809192
Date11/15/2011
LexicalTag NON
ThesaurusID; Enlarged Parietal Foramina
Term UI T841329
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Parietal Foramina MeSH Supplementary Concept Data 2025