01
ALG9
No data
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 10
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
- Alg9-Cdg
- Standard Disease Name
- alg9-cdg
- MeSH Tree
- No data
- ICD-10
- E77.8
Identifiers
- DO ID
- No data
- MeSH ID
- C535750
- OMIM ID
- 263210|608776|608776
- UMLS ID
- C2931006
- HPO ID
- No data
Description and Extensions
- Description
- ALG9-CDG is a form of congenital disorders of N-linked glycosylation characterized by progressive microcephaly, hypotonia, developmental delay, drug-resistant infantile epilepsy, and hepatomegaly. Add
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease1 Targets