01
Diseases
Hypotonia, Infantile, With Psychomotor Retardation And Characteristic Facies 3
hypotonia, infantile, with psychomotor retardation and characteristic facies 3
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 3
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
- Hypotonia, Infantile, With Psychomotor Retardation And Characteristic Facies 3
- Standard Disease Name
- hypotonia, infantile, with psychomotor retardation and characteristic facies 3
- MeSH Tree
- No data
- ICD-10
- E77.8
Identifiers
- DO ID
- No data
- MeSH ID
- C535745
- OMIM ID
- 607143
- UMLS ID
- C2931001
- HPO ID
- No data
Description and Extensions
- Description
- ALG12-CDG is a form of congenital disorders of N-linked glycosylation characterized by facial dysmorphism (prominent forehead, large ears, thin upper lip), generalized hypotonia, feeding difficulties
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target1 Ingredients