702382000: Inclusion body myopathy 2 (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 2
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy 2
• \Musculoskeletal finding\Musculoskeletal disorder\...
• \Hereditary disorder of musculoskeletal system\Inclusion body myopathy 2
• \Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy 2
• \Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy 2
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Inclusion body myopathy 2
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Inclusion body myopathy 2
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Inclusion body myopathy 2
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Inclusion body myopathy 2
• \Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Inclusion body myopathy 2
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy 2
• \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 2
• \Disease\Myopathy\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy 2
• \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 2
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\Inclusion body myopathy 2
• \Disease\Developmental disorder\Developmental hereditary disorder\Inclusion body myopathy 2
• \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 2

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2995199011	Hereditary inclusion body myopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
2995276019	Inclusion body myopathy 2 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2995349016	Rimmed vacuole myopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
2995564015	Inclusion body myopathy 2	en	Synonym	Active	Case insensitive	SNOMED CT core
2995724017	Distal myopathy with rimmed vacuoles	en	Synonym	Active	Case insensitive	SNOMED CT core
2995749018	Quadricep sparing inclusion body myopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
2995887019	Nonaka myopathy	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

Back to Start