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Summary Literature (0)
DOID:0111535 - progressive osseous heteroplasia


Disease Ontology Definition:A syndrome characterized by infantile onset of dermal ossification followed by progressive bone formation in skeletal muscle and deep fascia that has_material_basis_in heterozygous loss of function mutation in the Gs-alpha isoform of GNAS on chromosome 20q13.32.

Synonyms: POH, ectopic ossification familial type, familial ectopic ossification, osteoma cutis

In OMIM:
OMIM:166350 - OSSEOUS HETEROPLASIA, PROGRESSIVE; POH


Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : gnas

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)