01
C12ORF65
No data
Diseases
Combined Oxidative Phosphorylation Deficiency 7
combined oxidative phosphorylation deficiency 7
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 3
Basic Information
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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
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