FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

722967008: Ataxia due to mitochondrial mutations (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3334050014 Ataxia due to mitochondrial mutations en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334416014 Ataxia due to mitochondrial mutations (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334050014 Ataxia due to mitochondrial mutations en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334050014 Ataxia due to mitochondrial mutations en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334416014 Ataxia due to mitochondrial mutations (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334416014 Ataxia due to mitochondrial mutations (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5757391000241118 ataxie due à une mutation mitochondriale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5757391000241118 ataxie due à une mutation mitochondriale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ataxia due to mitochondrial mutations Due to Mitochondrial mutation (finding) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ataxia due to mitochondrial mutations Is a Ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
Ataxia due to mitochondrial mutations Is a Movement disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Ataxia due to mitochondrial mutations Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Ataxia due to mitochondrial mutations Interprets Movement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Ataxia due to mitochondrial mutations Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start