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240086009: Myopathy with cytoplasmic inclusions (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

\Muscle finding\Disorder of skeletal AND/OR smooth 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 skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions
\Disease\Congenital disease\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. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

359692015 Myopathy with cytoplasmic inclusions en Synonym Active Entire term case insensitive SNOMED CT core module

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

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	Existential restriction modifier
Myopathy with cytoplasmic inclusions	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1
Myopathy with cytoplasmic inclusions	Is a	Disorder of skeletal muscle	false	Inferred relationship	Existential restriction modifier
Myopathy with cytoplasmic inclusions	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Myopathy with cytoplasmic inclusions	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Myopathy with cytoplasmic inclusions	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Myopathy with cytoplasmic inclusions	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	1
Myopathy with cytoplasmic inclusions	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Myopathy with cytoplasmic inclusions	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Myopathy with cytoplasmic inclusions	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	2
Myopathy with cytoplasmic inclusions	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Myopathy with cytoplasmic inclusions	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Myopathy with cytoplasmic inclusions	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Myopathy with cytoplasmic inclusions	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Existential restriction modifier

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

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
359692015	Myopathy with cytoplasmic inclusions	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
629180012	Myopathy with cytoplasmic inclusions (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module