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230670003: Familial infantile myasthenia (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
345607015 Familial infantile myasthenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
345608013 FIM - Familial infantile myasthenia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
618510019 Familial infantile myasthenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
345607015 Familial infantile myasthenia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
345607015 Familial infantile myasthenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
345608013 FIM - Familial infantile myasthenia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
618510019 Familial infantile myasthenia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
618510019 Familial infantile myasthenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
563461000172110 myasthénie infantile familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
563461000172110 myasthénie infantile familiale 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
Familial infantile myasthenia (disorder) Is a Genetically determined myasthenia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Is a Myasthenia gravis, juvenile form true Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Finding site Structure of immune system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Finding site Neuromuscular junction false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Pathological process (attribute) Autoimmune process false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Due to réaction d'hypersensibilité immunitaire false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Due to Hypersensitivity reaction false Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Pathological process (attribute) Hypersensitivity process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial infantile myasthenia (disorder) Is a Congenital myasthenic syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile myasthenia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial infantile myasthenia (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial infantile myasthenia (disorder) Finding site Neuromuscular junction true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial infantile myasthenia (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial infantile myasthenia (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Acetylcholine resynthesis deficiency Is a False Familial infantile myasthenia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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