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43152001: Central core disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
71981018 Central core disease en Synonym Active Entire term case insensitive SNOMED CT core module
780131019 Central core disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2966549015 Central core myopathy 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
Central core disease Is a Congenital myopathy false Inferred relationship Existential restriction modifier
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Central core disease Associated morphology Central cores true Inferred relationship Existential restriction modifier 1
Central core disease Is a Congenital anomaly of skeletal muscle true Inferred relationship Existential restriction modifier
Central core disease Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier
Central core disease Occurrence Congenital false Inferred relationship Existential restriction modifier
Central core disease Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Central core disease Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Central core disease Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Central core disease Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Central core disease Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Central core disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Central core disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Central core disease Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier
Central core disease Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Central core disease Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive central core disease Is a True Central core disease Inferred relationship Existential restriction modifier
Autosomal dominant central core disease Is a True Central core disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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