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55133004: Multi-core congenital myopathy (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
91653017 Multi-core congenital myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91654011 Multi-core disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
793441013 Multi-core congenital myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231419016 Minicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231420010 Multicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3033415015 Multiminicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3033531013 Multi-minicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91653017 Multi-core congenital myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
91653017 Multi-core congenital myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91654011 Multi-core disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
91654011 Multi-core disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
793441013 Multi-core congenital myopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
793441013 Multi-core congenital myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231419016 Minicore disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231419016 Minicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231420010 Multicore disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231420010 Multicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3033415015 Multiminicore disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3033415015 Multiminicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3033531013 Multi-minicore disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3033531013 Multi-minicore disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3414121001000114 Multiminicore-Myopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4570451000241114 myopathie à multiminicores fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4570451000241114 myopathie à multiminicores fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3414121001000114 Multiminicore-Myopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multi-core congenital myopathy (disorder) Is a Congenital myopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Multi-core congenital myopathy (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multi-core congenital myopathy (disorder) Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier (core metadata concept)
Multi-core congenital myopathy (disorder) Is a Congenital anomaly of skeletal muscle (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Multi-core congenital myopathy (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multi-core congenital myopathy (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Multi-core congenital myopathy (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multi-core congenital myopathy (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multi-core congenital myopathy (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Multi-core congenital myopathy (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Multi-core congenital myopathy (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Multi-core congenital myopathy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multi-core congenital myopathy (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multi-core congenital myopathy (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Antenatal multi-minicore disease with arthrogryposis multiplex congenita Is a True Multi-core congenital myopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital multi-minicore disease with external ophthalmoplegia (disorder) Is a True Multi-core congenital myopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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