01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
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
- Congenital Myotonic Dystrophy
- Standard Disease Name
- congenital myotonic dystrophy
- MeSH Tree
- No data
- ICD-10
- Q87.0
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 101600
- UMLS ID
- No data
- HPO ID
- No data
Description and Extensions
- Description
- Pfeiffer syndrome type 2 (PS2) is a frequent and severe type of Pfeiffer syndrome (PS; see this term), characterized by cloverleaf skull, severe associated functional disorders, and hand/foot and elbo
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients