Skip to main content
Diseases

Granuloma Eosinophilic

granuloma eosinophilic

Entity Type
Diseases
Relation Groups
1
Relation Preview
6

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

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

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease6 Targets
01
BRAF
B-Raf proto-oncogene, serine/threonine kinase
B-Raf proto-oncogene, serine/threonine kinase