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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
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
793441013 Multi-core congenital myopathy (disorder) en Fully specified name Active Entire term 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 Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multi-core congenital myopathy (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Multi-core congenital myopathy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Multi-core congenital myopathy (disorder) est un(e) (attribut) affection d'un muscle squelettique false Inferred relationship Some
Multi-core congenital myopathy (disorder) est un(e) (attribut) Congenital anomaly of skeletal muscle true Inferred relationship Some
Multi-core congenital myopathy (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Multi-core congenital myopathy (disorder) survenue (attribut) congénital false Inferred relationship Some
Multi-core congenital myopathy (disorder) est un(e) (attribut) Congenital myopathy false Inferred relationship Some
Multi-core congenital myopathy (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 1
Multi-core congenital myopathy (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Multi-core congenital myopathy (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Multi-core congenital myopathy (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Multi-core congenital myopathy (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 2
Multi-core congenital myopathy (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Multi-core congenital myopathy (disorder) localisation d'une constatation (attribut) structure de muscle squelettique true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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