Autosomal dominant hereditary disorder
Autosomal dominant hereditary disorder
Congenital myopathy
Degenerative disorder of musculoskeletal system
Disorder of skeletal muscle
Disorder of skeletal muscle
Ectopic bone tissue, congenital
Ectopic bone tissue, congenital
Hereditary disorder of musculoskeletal system
Hereditary disorder of musculoskeletal system
Hereditary myopathy
Heterotopic ossification of soft tissue
Muscular ossification
Muscular ossification
Soft tissue lesion
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Progressive myositis ossificans (disorder)
Progressive myositis ossificans
Fibrodysplasia ossificans congenita
FOP - Fibrodysplasia ossificans progressiva
Myositis ossificans progressiva
Fibrodysplasia ossificans progressiva
Diffuse progressive ossifying polymyositis
Münchmeyer disease
progressieve myositis ossificans
FOP
Fibrodysplasia ossificans progressiva; zeldzame erfelijke aandoening waarin bot wordt gevormd in spieren, pezen, gewrichtsbanden en ander bindweefsel.
Id82725007
StatusDefined
Associated morphologyOsseous metaplasia
Associated morphologyOsseous metaplasia
Finding siteSkeletal muscle structure
Finding siteSkeletal muscle structure
OccurrenceCongenital
OccurrenceCongenital
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetM61.19
RuleTRUE
AdviceALWAYS M61.19
CorrelationSNOMED CT source code to target map code correlation not specified