01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
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.
Candidate Ingredients
target disease -> ingredient target8 Ingredients