Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.
Core Information
Disease Name
Isolated Complex I Deficiency
Standard Disease Name
isolated complex i deficiency
MeSH Tree
No data
ICD-10
G71.3
Identifiers
DO ID
No data
MeSH ID
C537475
OMIM ID
252010
UMLS ID
C2936907
HPO ID
No data
Description and Extensions
Description
Isolated complex I deficiency is a rare inborn error of metabolism due to mutations in nuclear or mitochondrial genes encoding subunits or assembly factors of the human mitochondrial complex I (NADH:
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.