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 | ||
CTV3ID |
F10y1 |
|
cui |
C2931891 C0023264 |
|
DEFINITION STATUS ID |
900000000000074008 |
|
Effective time |
20020131 |
|
Has associated morphology | ||
Has finding site | ||
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 |