01
ALG3
No data
- 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
- Alg3-Cdg
- Standard Disease Name
- alg3-cdg
- MeSH Tree
- No data
- ICD-10
- E77.8
Identifiers
- DO ID
- No data
- MeSH ID
- C535742
- OMIM ID
- 601110
- UMLS ID
- C1832736
- HPO ID
- No data
Description and Extensions
- Description
- ALG3-CDG is a form of congenital disorders of N-linked glycosylation characterized by severe neurological involvement, including hypotonia, developmental delay, intellectual disability, postnatal micr
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease1 Targets