Preferred Name | mitochondrial disease | |
Synonyms |
|
|
ID |
http://purl.obolibrary.org/obo/MONDO_0044970 |
|
curated_content_resource |
https://search.clinicalgenome.org/kb/conditions/MONDO:0044970 |
|
database_cross_reference |
MEDGEN:155901 UMLS:C0751651 NANDO:2100163 NANDO:1200173 |
|
disease has basis in dysfunction of | ||
exactMatch | ||
id |
MONDO:0044970 |
|
in taxon | ||
in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#clingen http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#rare_grouping |
|
label |
mitochondrial disease |
|
notation |
MONDO:0044970 |
|
preferred label |
mitochondrial disease |
|
prefLabel |
mitochondrial disease |
|
see also |
https://www.epilepsydiagnosis.org/aetiology/metabolic-groupoverview.html#mitochondrial |
|
subClassOf |
Create mapping