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723307008: Ethylmalonic encephalopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3423999011 Ethylmalonic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3424000013 Ethylmalonic encephalopathy en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ethylmalonic encephalopathy Is a Disorder of brain true Inferred relationship Existential restriction modifier
Ethylmalonic encephalopathy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Ethylmalonic encephalopathy Is a Inborn error of metabolism false Inferred relationship Existential restriction modifier
Ethylmalonic encephalopathy Is a Disorder of organic acid metabolism true Inferred relationship Existential restriction modifier
Ethylmalonic encephalopathy Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Ethylmalonic encephalopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ethylmalonic encephalopathy Finding site Brain structure true Inferred relationship Existential restriction modifier 1
Ethylmalonic encephalopathy Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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