01
ALG1
No data
- 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
- Alg1-Cdg
- Standard Disease Name
- alg1-cdg
- MeSH Tree
- No data
- ICD-10
- E77.8
Identifiers
- DO ID
- No data
- MeSH ID
- C535749
- OMIM ID
- 608540
- UMLS ID
- C2931005
- HPO ID
- No data
Description and Extensions
- Description
- ALG1-CDG is a severe form of congenital disorders of N-linked glycosylation characterized by severe developmental and psychomotor delay, muscular hypotonia, intractable early-onset seizures, and micro
Related
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Related Targets
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