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240086009: Myopathy with cytoplasmic inclusions (disorder)

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
359692015 Myopathy with cytoplasmic inclusions en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5036691000241111 myopathie à inclusions cytoplasmiques fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5036691000241111 myopathie à inclusions cytoplasmiques fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myopathy with cytoplasmic inclusions (disorder) Is a Congenital myopathy with abnormal subcellular organelles (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Myopathy with cytoplasmic inclusions (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with cytoplasmic inclusions (disorder) Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier (core metadata concept)
Myopathy with cytoplasmic inclusions (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with cytoplasmic inclusions (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Myopathy with cytoplasmic inclusions (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with cytoplasmic inclusions (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with cytoplasmic inclusions (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Myopathy with cytoplasmic inclusions (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Myopathy with cytoplasmic inclusions (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Myopathy with cytoplasmic inclusions (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with cytoplasmic inclusions (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with cytoplasmic inclusions (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myopathy with cytoplasmic inclusions (disorder) Is a Congenital anomaly of skeletal muscle (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Inclusion body myopathy 2 (disorder) Is a True Myopathy with cytoplasmic inclusions (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) Is a True Myopathy with cytoplasmic inclusions (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Desmin related myopathy with Mallory body-like inclusions (disorder) Is a True Myopathy with cytoplasmic inclusions (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked myopathy with excessive autophagy (disorder) Is a True Myopathy with cytoplasmic inclusions (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a True Myopathy with cytoplasmic inclusions (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Desmin-related myofibrillar myopathy (disorder) Is a True Myopathy with cytoplasmic inclusions (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy type 4 (disorder) Is a True Myopathy with cytoplasmic inclusions (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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