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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


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multi-core congenital myopathy Is a Congenital myopathy false Inferred relationship Some
Multi-core congenital myopathy Finding site Skeletal muscle structure true Inferred relationship Some 1
Multi-core congenital myopathy Is a Disorder of skeletal muscle false Inferred relationship Some
Multi-core congenital myopathy Is a Congenital anomaly of skeletal muscle true Inferred relationship Some
Multi-core congenital myopathy Associated morphology Congenital anomaly false Inferred relationship Some 1
Multi-core congenital myopathy Occurrence Congenital false Inferred relationship Some
Multi-core congenital myopathy Finding site Skeletal muscle structure false Inferred relationship Some 1
Multi-core congenital myopathy Associated morphology Congenital anomaly false Inferred relationship Some 1
Multi-core congenital myopathy Occurrence Congenital false Inferred relationship Some 2
Multi-core congenital myopathy Associated morphology Developmental anomaly false Inferred relationship Some 2
Multi-core congenital myopathy Finding site Skeletal muscle structure false Inferred relationship Some 2
Multi-core congenital myopathy Occurrence Congenital true Inferred relationship Some 1
Multi-core congenital myopathy Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Multi-core congenital myopathy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Antenatal multi-minicore disease with arthrogryposis multiplex congenita Is a True Multi-core congenital myopathy Inferred relationship Some
Congenital multi-minicore disease with external ophthalmoplegia (disorder) Is a True Multi-core congenital myopathy Inferred relationship Some

This concept is not in any reference sets

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