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| Term | fibrodysplasia ossificans progressiva | ID (Ontology) | DOID:13374 (Human Disease) |
| 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. | ||
| Also Known As | "myositis ossificans progressiva" ; "progressive myositis ossificans" ; "progressive ossifying myositis" (for all, see Synonyms field below) | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ musculoskeletal system disease | |__connective tissue disease___| fibrodysplasia ossificans progressiva 10 rec. |
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| Is a |
autosomal dominant disease connective tissue disease |
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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 |
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