01
KCNJ11
potassium inwardly rectifying channel subfamily J member 11
potassium inwardly rectifying channel subfamily J member 11
Diseases
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
autosomal dominant hyperinsulinism due to kir6.2 deficiency
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 1
Basic Information
Grouped by core information, identifiers, and descriptions.
Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.
Core Information
- Disease Name
- Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- Standard Disease Name
- autosomal dominant hyperinsulinism due to kir6.2 deficiency
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- No data
- UMLS ID
- No data
- HPO ID
- No data
Description and Extensions
- Description
- No data
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease1 Targets