01
ALG3
No data
Diseases
Congenital Disorder of Glycosylation, Type If
congenital disorder of glycosylation, type if
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 2
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
- Congenital Disorder of Glycosylation, Type If
- Standard Disease Name
- congenital disorder of glycosylation, type if
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- No data
- UMLS ID
- C0279655
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An infiltrating adenocarcinoma of the gallbladder characterized by the presence of metaplastic changes of the malignant glandular cells to squamous cells.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease2 Targets