MeSH Browser

MeSH Supplementary: Hemihyperplasia, Isolated
Unique ID: C565524
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565524
Entry Term(s): Hemi 3 Syndrome; Hemihyperplasia; Hemihypertrophy, Isolated
Registry Numbers: 0
Heading Mapped to: *Hyperplasia
Frequency: 37
Note: A hereditary autosomal dominant abnormality of CELL PROLIFERATION leading to asymmetric overgrowth of one or more regions of the body. The incidence of isolated hemihyperplasia is estimated to be 1 in 86,000. Idiopathic hemihypertrophy is associated with increased risk of EMBRYONAL CANCERS in childhood, particularly WILMS TUMOR. Has been mapped to chromosome 11. OMIM: 235000
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Concept UI: M0565824
Registry Numbers: 0
Terms: Hemihyperplasia, Isolated Preferred Term
Term UI T806922
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Hemihyperplasia
Term UI T806923
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Hemihypertrophy, Isolated
Term UI T806924
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Hemi 3 Syndrome
Term UI T826365
Date07/18/2012
LexicalTag NON
ThesaurusID OMIM (2013)

Hemihyperplasia, Isolated MeSH Supplementary Concept Data 2025