MeSH Browser

MeSH Supplementary: Osseous Heteroplasia, Progressive
Unique ID: C562735
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562735
Entry Term(s): Cutaneous Ossification; Ectopic Ossification, Familial; Osteodermia; Osteoma Cutis; Osteosis Cutis; Progressive Osseous Heteroplasia
Registry Number: 0
Heading Mapped to: *Bone Diseases, Metabolic; *Ossification, Heterotopic; *Skin Diseases, Genetic
Frequency: 106
Note: A rare autosomal dominant disorder characterized by dermal OSTEOGENESIS beginning in infancy, followed by increasing and extensive bone formation in deep muscle and FASCIA. Mutations in the GNAS1 gene have been identified. OMIM: 166350
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Concept UI: M0563035
Registry Number: 0
Terms: Osseous Heteroplasia, Progressive Preferred Term
Term UI T801391
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Ectopic Ossification, Familial
Term UI T801393
Date11/15/2011
LexicalTag NON
ThesaurusID; Osteosis Cutis
Term UI T842338
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Cutaneous Ossification
Term UI T842334
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Osteodermia
Term UI T842337
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Osteoma Cutis
Term UI T801392
Date11/15/2011
LexicalTag NON
ThesaurusID; Progressive Osseous Heteroplasia
Term UI T842333
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Osseous Heteroplasia, Progressive MeSH Supplementary Concept Data 2024