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722967008: Ataxia due to mitochondrial mutations (disorder)

Status: current, Defined. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

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

0 descendants.

Expanded Value Set

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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