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
- PARAGANGLIOMAS 3
- Standard Disease Name
- paragangliomas 3
- MeSH Tree
- No data
- ICD-10
- Q87.8
Identifiers
- DO ID
- No data
- MeSH ID
- C538070
- OMIM ID
- 229850
- UMLS ID
- C0220730
- HPO ID
- No data
Description and Extensions
- Description
- Fryns syndrome (FS) is a multiple congenital anomaly syndrome characterized by dysmorphic facial features, congenital diaphragmatic hernia, pulmonary hypoplasia, and distal limb hypoplasia, in additio
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.