01
EPB42
No data
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 18
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
- Spherocytosis, Type 5
- Standard Disease Name
- spherocytosis, type 5
- MeSH Tree
- No data
- ICD-10
- D69.0
Identifiers
- DO ID
- No data
- MeSH ID
- D011695
- OMIM ID
- MTHU027843|MTHU018874
- UMLS ID
- C0034152
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NICHD_1602D:A systemic, usually self-limited immune complex vasculitis, characterized by immunoglobulin A deposition in the small vessels and kidneys. It is manifested with small hemorrhages in the skin, gastrointestinal symptoms, arthritis, and nephropathy.|NCI2016_02D:A systemic, usually self-limited immune complex vasculitis, characterized by immunoglobulin A deposition in the small vessels and kidneys. It is manifested with small hemorrhages in the skin, gastrointestinal symptoms, arthritis, and nephropathy.|MSH2017_2016_08_12:A systemic non-thrombocytopenic purpura caused by HYPERSENSITIVITY VASCULITIS and deposition of IGA-containing IMMUNE COMPLEXES within the blood vessels throughout the body, including those in the kidney (KIDNEY GLOMERULUS). Clinical symptoms include URTICARIA; ERYTHEMA; ARTHRITIS; GASTROINTESTINAL HEMORRHAGE; and renal involvement. Most cases are seen in children after acute upper respiratory infections.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease2 Targets