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Osseous Heteroplasia, Progressive MeSH Supplementary Concept Data 2023


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
104
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
Osseous Heteroplasia, Progressive Preferred
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