01
EPB42
No data
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 2
Basic Information
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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.
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