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55133004: Multi-core congenital myopathy (disorder)

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
91653017 Multi-core congenital myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
91654011 Multi-core disease en Synonym Active Entire term case insensitive SNOMED CT core module
793441013 Multi-core congenital myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1231419016 Minicore disease en Synonym Active Entire term case insensitive SNOMED CT core module
1231420010 Multicore disease en Synonym Active Entire term case insensitive SNOMED CT core module
3033415015 Multiminicore disease en Synonym Active Entire term case insensitive SNOMED CT core module
3033531013 Multi-minicore disease en Synonym Active Entire term case insensitive SNOMED CT core module

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 Existential restriction modifier
Multi-core congenital myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Multi-core congenital myopathy Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier
Multi-core congenital myopathy Is a Congenital anomaly of skeletal muscle true Inferred relationship Existential restriction modifier
Multi-core congenital myopathy Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Multi-core congenital myopathy Occurrence Congenital false Inferred relationship Existential restriction modifier
Multi-core congenital myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Multi-core congenital myopathy Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Multi-core congenital myopathy Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Multi-core congenital myopathy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Multi-core congenital myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Multi-core congenital myopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Multi-core congenital myopathy Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Multi-core congenital myopathy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 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 Existential restriction modifier
Congenital multi-minicore disease with external ophthalmoplegia Is a True Multi-core congenital myopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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