703544004: Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Musculoskeletal finding\Musculoskeletal disorder\...
• \Hereditary disorder of musculoskeletal system\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Myopathy\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Developmental disorder\Developmental hereditary disorder\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia

Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3009059013	Lower motor neuron degeneration with Paget-like bone disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3009150010	Pagetoid amyotrophic lateral sclerosis	en	Synonym	Active	Case sensitive	SNOMED CT core
3009177018	Muscular dystrophy limb-girdle with Paget disease of bone	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3009459019	Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3009478019	Pagetoid neuroskeletal syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3009492013	Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3009710019	IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia	en	Synonym	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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