01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 22
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
- Granuloma Eosinophilic
- Standard Disease Name
- granuloma eosinophilic
- MeSH Tree
- No data
- ICD-10
- K13.4|C96.6
Identifiers
- DO ID
- No data
- MeSH ID
- D004803
- OMIM ID
- No data
- UMLS ID
- C0014461
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A clinical variant of Langerhans cell histiocytosis characterized by unifocal involvement of a bone (most often), skin, or lung. Patients are usually older children or adults usually presenting with a lytic bone lesion. The etiology is unknown. Morphologically, eosinophilic granuloma is characterized by the presence of Langerhans cells in a characteristic milieu which includes histiocytes, eosinophils, neutrophils, and small, mature lymphocytes.|MSH2017_2016_08_12:The most benign and common form of Langerhans-cell histiocytosis which involves localized nodular lesions predominantly of the bones but also of the gastric mucosa, small intestine, lungs, or skin, with infiltration by EOSINOPHILS.|CSP2006:most benign clinical form of Langerhans-cell histiocytosis, which involves localized nodular lesions of the gastric mucosa, small intestine, bones, lungs, or skin, with infiltration by eosinophils; the proliferating cell that appears to be responsible for the clinical manifestations is the Langerhans cell.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients