01
Diseases
Combined Oxidative Phosphorylation Deficiency 7
combined oxidative phosphorylation deficiency 7
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 13
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
- Combined Oxidative Phosphorylation Deficiency 7
- Standard Disease Name
- combined oxidative phosphorylation deficiency 7
- MeSH Tree
- No data
- ICD-10
- D58.8
Identifiers
- DO ID
- No data
- MeSH ID
- C563785
- OMIM ID
- 609153
- UMLS ID
- C1836705
- HPO ID
- No data
Description and Extensions
- Description
- Familial pseudohyperkalemia (FP) is an inherited, mild, non-hemolytic subtype of hereditary stomatocytosis that is associated with a temperature-dependent anomaly in red cell membrane permeability to
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target3 Ingredients