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

717052002: Maternally inherited Leigh syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308295018 Maternally inherited Leigh syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308296017 Maternally inherited Leigh syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308297014 Maternally inherited Leigh disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308298016 Maternally inherited infantile subacute necrotizing encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308299012 Maternally inherited infantile subacute necrotising encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401477010 Maternally inherited Leigh syndrome is a rare subtype of Leigh syndrome characterized clinically by encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay, with onset in infancy or early childhood, and resulting from maternally-inherited mutations in mitochondrial DNA. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401478017 Maternally inherited Leigh syndrome is a rare subtype of Leigh syndrome characterised clinically by encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay, with onset in infancy or early childhood, and resulting from maternally-inherited mutations in mitochondrial DNA. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308295018 Maternally inherited Leigh syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308296017 Maternally inherited Leigh syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308297014 Maternally inherited Leigh disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308298016 Maternally inherited infantile subacute necrotizing encephalopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308298016 Maternally inherited infantile subacute necrotizing encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308299012 Maternally inherited infantile subacute necrotising encephalopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308299012 Maternally inherited infantile subacute necrotising encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308300016 A rare subtype of Leigh syndrome with clinical characteristics of encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay. Onset in infancy or early childhood resulting from maternally-inherited mutations in mitochondrial DNA. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401477010 Maternally inherited Leigh syndrome is a rare subtype of Leigh syndrome characterized clinically by encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay, with onset in infancy or early childhood, and resulting from maternally-inherited mutations in mitochondrial DNA. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401478017 Maternally inherited Leigh syndrome is a rare subtype of Leigh syndrome characterised clinically by encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay, with onset in infancy or early childhood, and resulting from maternally-inherited mutations in mitochondrial DNA. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3443011001000111 Leigh-Syndrom, mitochondriale DNA-assoziiertes de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5477781000241111 encéphalomyopathie nécrosante subaigüe héritée de la mère fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5477781000241111 encéphalomyopathie nécrosante subaigüe héritée de la mère fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3443011001000111 Leigh-Syndrom, mitochondriale DNA-assoziiertes de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Maternally inherited Leigh syndrome Is a Leigh's disease true Inferred relationship Existential restriction modifier (core metadata concept)
Maternally inherited Leigh syndrome Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Maternally inherited Leigh syndrome Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Maternally inherited Leigh syndrome Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Maternally inherited Leigh syndrome Is a Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Maternally inherited Leigh syndrome Occurrence Infancy true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start