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64855000: Pelizaeus-Merzbacher disease (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
107800019 Pelizaeus-Merzbacher disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
107801015 Sudanophilic leukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
452881000241118 maladie de Pelizaeus-Merzbacher (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
804294011 Pelizaeus-Merzbacher disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
947151000172113 maladie de Pelizaeus-Merzbacher fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
952221000172114 leucodystrophie sudanophile de Pelizaeus-Merzbacher fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelizaeus-Merzbacher disease est un(e) (attribut) Leukodystrophy true Inferred relationship Some
Pelizaeus-Merzbacher disease est un(e) (attribut) trouble du développement false Inferred relationship Some
Pelizaeus-Merzbacher disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Pelizaeus-Merzbacher disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Pelizaeus-Merzbacher disease est un(e) (attribut) Hereditary degenerative disease of central nervous system true Inferred relationship Some
Pelizaeus-Merzbacher disease est un(e) (attribut) X-linked hereditary disease true Inferred relationship Some
Pelizaeus-Merzbacher disease est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Pelizaeus-Merzbacher disease est un(e) (attribut) Inherited metabolic disorder of nervous system false Inferred relationship Some
Pelizaeus-Merzbacher disease est un(e) (attribut) Leucodystrophy without a known biochemical basis false Inferred relationship Some
Pelizaeus-Merzbacher disease est un(e) (attribut) Disorder of lysosomal enzyme false Inferred relationship Some
Pelizaeus-Merzbacher disease morphologie associée (attribut) Myelin sheath alteration false Inferred relationship Some 1
Pelizaeus-Merzbacher disease morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
Pelizaeus-Merzbacher disease morphologie associée (attribut) Myelin sheath alteration true Inferred relationship Some 1
Pelizaeus-Merzbacher disease morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
Pelizaeus-Merzbacher disease localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 1
Pelizaeus-Merzbacher disease localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 1
Pelizaeus-Merzbacher disease survenue (attribut) congénital false Inferred relationship Some 3
Pelizaeus-Merzbacher disease morphologie associée (attribut) Sudanophilic stain reaction false Inferred relationship Some 4
Pelizaeus-Merzbacher disease localisation d'une constatation (attribut) White matter structure of brain and spinal cord (body structure) true Inferred relationship Some 2
Pelizaeus-Merzbacher disease morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 2
Pelizaeus-Merzbacher disease localisation d'une constatation (attribut) Myelinated nerve fiber structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Pelizaeus-Merzbacher disease null syndrome est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some
Pelizaeus-Merzbacher disease in female carrier est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some
Pelizaeus-Merzbacher disease, connatal variant (disorder) est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some
Pelizaeus-Merzbacher disease, classic form est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some
Type III transitional Pelizaeus-Merzbacher disease est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some
Type IV adult Pelizaeus-Merzbacher disease est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some
Type V atypical Pelizaeus-Merzbacher disease est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some
Type VI Cockayne Pelizaeus-Merzbacher disease est un(e) (attribut) True Pelizaeus-Merzbacher disease Inferred relationship Some

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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