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702366001: Childhood myocerebrohepatopathy spectrum (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2995211018 Childhood myocerebrohepatopathy spectrum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995462018 Childhood myocerebrohepatopathy spectrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
10057371000172117 spectre myocérébrohépatopathique chez l'enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
10057381000172119 syndrome myocérébrohépatopathie pédiatrique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4808931000172112 myocerebrohepatopathisch spectrum op kinderleeftijd nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood myocerebrohepatopathy spectrum (disorder) Is a Mitochondrial cytopathy (disorder) true Inferred relationship Some
Childhood myocerebrohepatopathy spectrum (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Childhood myocerebrohepatopathy spectrum (disorder) Occurrence Childhood true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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