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50122000: Metabolic encephalopathy (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
123711000077111 encéphalopathie métabolique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
396041000077118 encéphalopathie métabolique (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
787876019 Metabolic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
83497018 Metabolic encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
83498011 Metabolic brain syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


45 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
encéphalopathie métabolique est un(e) (attribut) trouble métabolique true Inferred relationship Some
encéphalopathie métabolique est un(e) (attribut) Disorder of brain (disorder) false Inferred relationship Some
encéphalopathie métabolique est un(e) (attribut) Toxic metabolic encephalopathy (disorder) true Inferred relationship Some
encéphalopathie métabolique localisation d'une constatation (attribut) structure de l'encéphale true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder) est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder) est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
encéphalopathie hépatique est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Uremic encephalopathy est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
encéphalopathie hypertensive (trouble) est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Hypoglycemic encephalopathy est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Dialysis disequilibrium syndrome est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Dialysis dementia est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Anoxia of brain est un(e) (attribut) False encéphalopathie métabolique Inferred relationship Some
Glucose transporter protein type 1 deficiency syndrome (disorder) est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Myxoedema encephalopathy est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Myxedema coma est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Encephalopathy due to vitamin deficiency est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Hyponatraemic encephalopathy est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Secondary amyloid encephalopathy est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Progressive external ophthalmoplegia, myopathy, emaciation syndrome est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some
Progressive polyneuropathy with bilateral striatal necrosis est un(e) (attribut) True encéphalopathie métabolique Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

GB English

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