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702366001: Childhood myocerebrohepatopathy spectrum (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2995211018 Childhood myocerebrohepatopathy spectrum (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2995462018 Childhood myocerebrohepatopathy spectrum 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
Childhood myocerebrohepatopathy spectrum Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier
Childhood myocerebrohepatopathy spectrum Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Childhood myocerebrohepatopathy spectrum Occurrence Childhood true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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