01
KCNJ2
potassium inwardly rectifying channel subfamily J member 2
potassium inwardly rectifying channel subfamily J member 2
Diseases
ATRIAL FIBRILLATION, FAMILIAL, 9
atrial fibrillation, familial, 9
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 1
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- ATRIAL FIBRILLATION, FAMILIAL, 9
- Standard Disease Name
- atrial fibrillation, familial, 9
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C564732
- OMIM ID
- 278740
- UMLS ID
- C1848411
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An autosomal recessive genetic disorder caused by mutations in the DDB2 gene. This disease exhibits the mildest degree of sun sensitivity of all xeroderma pigmentosum complementation groups, although individuals are at high risk for skin cancer.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease1 Targets