Disease Browser
|
Parent Node: coenzyme Q10 deficiency (MONDO:0018151) | Parent Node: Leigh disease (MONDO:0018859) | ..Starting node ..Leigh syndrome with nephrotic syndrome ()
| Child Nodes:
| ........coenzyme Q10 deficiency, primary, 1 () L: 00090; | ........coenzyme Q10 deficiency, primary, 3 () L: 00447; |
Sister Nodes: | ..congenital lactic acidosis, Saguenay-Lac-Saint-Jean type () L: 00389;
| ..Leigh syndrome () L: 00015;
| ..Leigh syndrome with nephrotic syndrome ()
| ..necrotizing encephalomyelopathy, subacute, of Leigh, adult () L: 00433;
|
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
|
|
|
Term ID: | 16816 |
Name: | Leigh syndrome with nephrotic syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | |
TreeNumbers: | |
Synonyms: | infantile subacute necrotizing encephalopathy with nephrotic syndrome; Leigh disease with nephrotic syndrome |
Slim Mappings: | |
Reference: |
MedGen:
MeSH:
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
|