FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

240082006: Myopathy with abnormality of histochemical fiber type (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
359685013 Myopathy with abnormality of histochemical fibre type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
359686014 Myopathy with abnormality of histochemical fiber type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629176019 Myopathy with abnormality of histochemical fiber type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


14 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Myopathy with type I hypotrophy est un(e) (attribut) True Myopathy with abnormality of histochemical fibre type Inferred relationship Some
Congenital myopathy with fibre type disproportion est un(e) (attribut) True Myopathy with abnormality of histochemical fibre type Inferred relationship Some
Congenital myopathy with uniform fiber type est un(e) (attribut) True Myopathy with abnormality of histochemical fibre type Inferred relationship Some

This concept is not in any reference sets

Back to Start