01
ITGA7
No data
Diseases
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
muscular dystrophy, congenital, due to integrin alpha-7 deficiency
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 1
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
- Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
- Standard Disease Name
- muscular dystrophy, congenital, due to integrin alpha-7 deficiency
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C567850
- OMIM ID
- 612946
- UMLS ID
- C2751878
- 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