SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Leigh's disease

Synonyms

Leighs disease

Leigh syndrome

ID

http://purl.bioontology.org/ontology/SNOMEDCT/29570005

Active

1

altLabel

Leighs disease

SNEM - Subacute necrotizing encephalomyelopathy

Subacute necrotising encephalomyelopathy

Subacute necrotising encephalopathy

SNEM - Subacute necrotising encephalomyelopathy

Infantile necrotising encephalomyelopathy

Subacute necrotizing encephalopathy

Subacute necrotizing encephalomyelopathy

Leigh's disease (disorder)

Leigh disease

Infantile necrotizing encephalomyelopathy

Leigh syndrome

CASE SIGNIFICANCE ID

900000000000448009

900000000000017005

Cause of

http://purl.bioontology.org/ontology/SNOMEDCT/1187533007

CTV3ID

F10y1

cui

C2931891

C0023264

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/107669003

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/12738006

notation

29570005

prefLabel

Leigh's disease

Subset member

6011000124106~MAPTARGET~N04.9

900000000000497000~MAPTARGET~F10y1

6011000124106~MAPTARGET~E88.49

447562003~MAPRULE~TRUE

6011000124106~MAPPRIORITY~4

6011000124106~MAPRULE~IFA 1187520001 | Leigh syndrome due to cytochrome C oxidase deficiency |

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPRULE~IFA 783157004 | Leigh syndrome with nephrotic syndrome |

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

6011000124106~MAPADVICE~IF LEIGH SYNDROME WITH NEPHROTIC SYNDROME CHOOSE G31.82 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 718219002 | Congenital lactic acidosis Saguenay-Lac-Saint-Jean type |

447562003~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF CONGENITAL LACTIC ACIDOSIS SAGUENAY-LAC-SAINT-JEAN TYPE CHOOSE E87.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~ALWAYS G31.82 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPTARGET~G31.82

6011000124106~MAPADVICE~IF CONGENITAL LACTIC ACIDOSIS SAGUENAY-LAC-SAINT-JEAN TYPE CHOOSE E87.22 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPADVICE~IF LEIGH SYNDROME DUE TO CYTOCHROME C OXIDASE DEFICIENCY CHOOSE G31.82 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447639009

447562003~MAPADVICE~ALWAYS G31.8

6011000124106~MAPPRIORITY~1

6011000124106~MAPADVICE~IF LEIGH SYNDROME WITH NEPHROTIC SYNDROME CHOOSE N04.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF LEIGH SYNDROME DUE TO CYTOCHROME C OXIDASE DEFICIENCY CHOOSE E88.49 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~G31.8

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPADVICE~IF CONGENITAL LACTIC ACIDOSIS SAGUENAY-LAC-SAINT-JEAN TYPE CHOOSE G31.82 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~2

6011000124106~MAPTARGET~E87.22

6011000124106~MAPTARGET~E87.2

6011000124106~MAPRULE~IFA 718219002 | Congenital lactic acidosis Saguenay-Lac-Saint-Jean type (disorder) |

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/81308009

http://purl.bioontology.org/ontology/SNOMEDCT/106018006

http://purl.bioontology.org/ontology/SNOMEDCT/230226000

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/SCTSPA/29570005 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/590060 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/256000 OMIM CUI
http://purl.bioontology.org/ontology/MESH/C538590 MESH CUI
http://purl.bioontology.org/ontology/MESH/D007888 MESH CUI
http://purl.bioontology.org/ontology/CSP/5000-0048 CRISP CUI
http://purl.bioontology.org/ontology/OMIM/MTHU039986 OMIM CUI
http://purl.bioontology.org/ontology/MSHFRE/D007888 MSHFRE CUI
http://purl.bioontology.org/ontology/OMIM/590095 OMIM CUI
http://purl.bioontology.org/ontology/SNMI/DA-20161 SNMI CUI
http://purl.bioontology.org/ontology/CSP/1849-5394 CRISP CUI
http://purl.bioontology.org/ontology/MEDDRA/10062950 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10062950 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10062950 MDRGER CUI
http://purl.bioontology.org/ontology/OMIM/590105 OMIM CUI
http://purl.bioontology.org/ontology/SCTSPA/29570005 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/256000 OMIM CUI
http://purl.bioontology.org/ontology/ICD10CM/G31.82 ICD10CM CUI
http://purl.bioontology.org/ontology/CSP/1254-7727 CRISP CUI
http://purl.bioontology.org/ontology/NDFRT/N0000001801 NDFRT CUI
http://purl.bioontology.org/ontology/RCD/F10y1 RCD CUI
http://sbmi.uth.tmc.edu/ontology/ochv#C0023264 OCHV LOOM
http://purl.bioontology.org/ontology/SNMI/DA-20161 SNMI LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Leigh_s_Disease PEDTERM LOOM
http://purl.bioontology.org/ontology/RCTV2/F10y100 RCTV2 LOOM
http://purl.bioontology.org/ontology/ICD10CM/G31.82 ICD10CM LOOM
http://www.gamuts.net/entity#Leigh_disease GAMUTS REST