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722967008: Ataxia due to mitochondrial mutations (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3334050014 Ataxia due to mitochondrial mutations en Synonym Active Entire term case insensitive SNOMED CT core module
3334416014 Ataxia due to mitochondrial mutations (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ataxia due to mitochondrial mutations Due to Mitochondrial mutation true Inferred relationship Existential restriction modifier 1
Ataxia due to mitochondrial mutations Is a Ataxia true Inferred relationship Existential restriction modifier
Ataxia due to mitochondrial mutations Is a Movement disorder true Inferred relationship Existential restriction modifier
Ataxia due to mitochondrial mutations Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 2
Ataxia due to mitochondrial mutations Interprets Movement false Inferred relationship Existential restriction modifier 3
Ataxia due to mitochondrial mutations Interprets Movement true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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