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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
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
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 Only initial character 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 Only initial character 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
787876019 Metabolic encephalopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
787876019 Metabolic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
123711000077111 encéphalopathie métabolique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
123711000077111 encéphalopathie métabolique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

46 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Metabolic encephalopathy Is a Metabolic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Metabolic encephalopathy Is a Disorder of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Metabolic encephalopathy Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Metabolic encephalopathy Is a Toxic metabolic encephalopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Hepatic encephalopathy Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Uremic encephalopathy Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Hypertensive encephalopathy (disorder) Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Hypoglycemic encephalopathy Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Dialysis disequilibrium syndrome Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Dialysis dementia Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Anoxia of brain Is a False Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Glucose transporter protein type 1 deficiency syndrome (disorder) Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Myxoedema encephalopathy Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Myxoedema coma Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Encephalopathy due to vitamin deficiency Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Hyponatremic encephalopathy (disorder) Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Secondary amyloid encephalopathy Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Hypermethioninaemia encephalopathy due to adenosine kinase deficiency is a rare inborn error of metabolism disorder characterised by persistent hypermethioninaemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine which manifests with encephalopathy, severe global developmental delay, mild to severe liver dysfunction, hypotonia and facial dysmorphism (most significant is frontal bossing, macrocephaly, hypertelorism and depressed nasal bridge). Epileptic seizures, hypoglycaemia and/or cardiac defects (pulmonary stenosis, atrial and/or ventricular septal defect, coarctation of the aorta) may be associated. Clinical picture may range from neurological symptoms only to multi-organ involvement. Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Progressive polyneuropathy with bilateral striatal necrosis (disorder) Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder) Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)
Renal tubulopathy with encephalopathy and liver failure syndrome Is a True Metabolic encephalopathy Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Description inactivation indicator reference set

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