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1201861004: Autosomal dominant central core disease (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4945365014 Autosomal dominant central core disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4945366010 Autosomal dominant central core disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4945367018 Autosomal dominant central core myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7852571000241113 myopathie à axe central autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7852591000241112 maladie à axe central autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant central core disease (disorder) Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
Autosomal dominant central core disease (disorder) Is a Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy. true Inferred relationship Some
Autosomal dominant central core disease (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant central core disease (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal dominant central core disease (disorder) Associated morphology Central cores true Inferred relationship Some 1
Autosomal dominant central core disease (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant central core disease (disorder) Interprets Motor function true Inferred relationship Some 4
Autosomal dominant central core disease (disorder) Finding site Structure of central nervous system (body structure) true Inferred relationship Some 2
Autosomal dominant central core disease (disorder) Finding site Peripheral nervous system structure true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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