Myositis Ossificans
Disease ID: disease_node_5377
Connections displayed (default: 10).
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| Dbxref | GARD:6445, ICD10CM:M61.1, ICD9CM:728.11, MESH:D009221, MIM:135100, NCI:C3040, ORDO:337, SNOMEDCT_US_2023_03_01:82725007, UMLS_CUI:C0016037 |
|---|---|
| Subclassof | DOID_0050736, DOID_65 |
| Data Source | DOID, MESH |
| Synonyms | Stone Man Syndrome, myositis ossificans progressiva, progressive myositis ossificans, progressive ossifying myositis |
| Mesh Id | D009221 |
| Mesh Label | Myositis Ossificans |
| Mesh Subclassof | D009220 |
| Doid Label | fibrodysplasia ossificans progressiva |
| Doid Description | 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. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_5377 |
| Doid Id | DOID_13374 |
| Label | Myositis Ossificans |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Connective Tissue Diseases(ID:disease_node_2242) (Disease)