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240086009: Myopathy with cytoplasmic inclusions (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
359692015 Myopathy with cytoplasmic inclusions en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629180012 Myopathy with cytoplasmic inclusions (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


7 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Inclusion body myopathy 2 (disorder) est un(e) (attribut) True Myopathy with cytoplasmic inclusions Inferred relationship Some
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) est un(e) (attribut) True Myopathy with cytoplasmic inclusions Inferred relationship Some
Desmin related myopathy with Mallory body-like inclusions (disorder) est un(e) (attribut) True Myopathy with cytoplasmic inclusions Inferred relationship Some
X-linked myopathy with excessive autophagy (disorder) est un(e) (attribut) True Myopathy with cytoplasmic inclusions Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) est un(e) (attribut) True Myopathy with cytoplasmic inclusions Inferred relationship Some
Desmin-related myofibrillar myopathy (disorder) est un(e) (attribut) True Myopathy with cytoplasmic inclusions Inferred relationship Some
myopathie à corps d'inclusion héréditaire type 4 est un(e) (attribut) True Myopathy with cytoplasmic inclusions Inferred relationship Some

This concept is not in any reference sets

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