Related MeSH Hierarchy (5)
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Anemia » Anemia, Hemolytic » Hemolytic-Uremic Syndrome » Atypical Hemolytic Uremic Syndrome
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Platelet Disorders » Thrombocytopenia » Thrombotic Microangiopathies » Hemolytic-Uremic Syndrome » Atypical Hemolytic Uremic Syndrome
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Uremia » Hemolytic-Uremic Syndrome » Atypical Hemolytic Uremic Syndrome
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Uremia » Hemolytic-Uremic Syndrome » Atypical Hemolytic Uremic Syndrome
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Uremia » Hemolytic-Uremic Syndrome » Atypical Hemolytic Uremic Syndrome
Description
An hereditary hemolytic uremic syndrome associated with variations in the gene that encodes COMPLEMENT FACTOR H, or the related proteins CFHR1 and CFHR3. Disease often progresses to CHRONIC KIDNEY FAILURE without the prodromal symptoms of ENTEROCOLITIS and DIARRHEA that characterize typical hemolytic uremic syndrome. MeSH
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Approved Indicated Drugs (1)
Phase 3 Indicated Drugs (4)
Phase 2 Indicated Drugs (2)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (2)
Organization Involved with Phase 2 Indications (5)
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