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Disease Ontology Browser
fibrodysplasia ossificans progressiva (DOID:13374)
Alliance: disease page
Synonyms: myositis ossificans progressiva; progressive myositis ossificans; progressive ossifying myositis; Stone Man Syndrome
Alt IDs: OMIM:135100, ICD10CM:M61.1, ICD9CM_2006:728.11, ICD9CM:728.11, MESH:D009221, NCI:C3040, ORDO:337, UMLS_CUI:C0016037
Definition: A connective tissue disease that is characterized by progressive ossification of skeletal muscle, fascia, tendons, and ligaments and has_material_basis_in heterozygous mutation in the ACVR1 gene.

Disease References using Mouse Models (10)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory