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

82077006: Myotubular 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
136147016 Myotubular myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
136148014 Centronuclear myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
472651000241112 myopathie myotubulaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
537561000172110 myopathie myotubulaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
823423014 Myotubular myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Myotubular myopathy with type I atrophy est un(e) (attribut) True Myotubular myopathy Inferred relationship Some
Severe X-linked myotubular myopathy (disorder) est un(e) (attribut) True Myotubular myopathy Inferred relationship Some
Autosomal recessive centronuclear myopathy est un(e) (attribut) True Myotubular myopathy Inferred relationship Some
Autosomal dominant centronuclear myopathy (disorder) est un(e) (attribut) True Myotubular myopathy Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

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)

GB English

US English

Back to Start