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240086009: Myopathy with cytoplasmic inclusions (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions

\Muscle finding\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions

\Musculoskeletal finding\Disorder of musculoskeletal system\...

\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions

\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions
\Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

359692015 Myopathy with cytoplasmic inclusions en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

629180012 Myopathy with cytoplasmic inclusions (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1586331000052114 myopati med cytoplastmatiska inklusioner sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Myopathy with cytoplasmic inclusions	Is a	Congenital myopathy with abnormal subcellular organelles	false	Inferred relationship	Some
Myopathy with cytoplasmic inclusions	Finding site	Skeletal muscle structure	true	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Is a	Disorder of skeletal muscle	false	Inferred relationship	Some
Myopathy with cytoplasmic inclusions	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Occurrence	Congenital	false	Inferred relationship	Some
Myopathy with cytoplasmic inclusions	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Occurrence	Congenital	false	Inferred relationship	Some	2
Myopathy with cytoplasmic inclusions	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	2
Myopathy with cytoplasmic inclusions	Finding site	Skeletal muscle structure	false	Inferred relationship	Some	2
Myopathy with cytoplasmic inclusions	Occurrence	Congenital	true	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Inclusion body myopathy 2 (disorder)	Is a	True	Myopathy with cytoplasmic inclusions	Inferred relationship	Some
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)	Is a	True	Myopathy with cytoplasmic inclusions	Inferred relationship	Some
Desmin related myopathy with Mallory body-like inclusions (disorder)	Is a	True	Myopathy with cytoplasmic inclusions	Inferred relationship	Some
X-linked myopathy with excessive autophagy (disorder)	Is a	True	Myopathy with cytoplasmic inclusions	Inferred relationship	Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder)	Is a	True	Myopathy with cytoplasmic inclusions	Inferred relationship	Some
Desmin-related myofibrillar myopathy (disorder)	Is a	True	Myopathy with cytoplasmic inclusions	Inferred relationship	Some
Hereditary inclusion body myopathy type 4 (disorder)	Is a	True	Myopathy with cytoplasmic inclusions	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
359692015	Myopathy with cytoplasmic inclusions	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
629180012	Myopathy with cytoplasmic inclusions (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1586331000052114	myopati med cytoplastmatiska inklusioner	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)