| Descriptor English: | Atypical Hemolytic Uremic Syndrome | ||||
| Descriptor Spanish: |
Síndrome Hemolítico Urémico Atípico
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| Descriptor Portuguese: | Síndrome Hemolítico-Urêmica Atípica | ||||
| Descriptor French: | Syndrome hémolytique et urémique atypique | ||||
| Entry term(s): |
Atypical Hemolytic-Uremic Syndrome Atypical Hemolytic-Uremic Syndromes HUS, Non-Shiga-Like Toxin-Associated HUS, Nonenteropathic HUSs, Non-Shiga-Like Toxin-Associated HUSs, Nonenteropathic Hemolytic Uremic Syndrome, Atypical Hemolytic-Uremic Syndrome, Atypical Hemolytic-Uremic Syndromes, Atypical Non Shiga Like Toxin Associated HUS Non Stx Hus Non-Shiga-Like Toxin-Associated HUS Non-Shiga-Like Toxin-Associated HUSs Non-Stx-Hus Nonenteropathic HUS Nonenteropathic HUSs Syndrome, Atypical Hemolytic-Uremic Syndromes, Atypical Hemolytic-Uremic Toxin-Associated HUS, Non-Shiga-Like Toxin-Associated HUSs, Non-Shiga-Like |
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| Tree number(s): |
C12.050.351.968.419.936.463.500 C12.200.777.419.936.463.500 C12.950.419.936.463.500 C15.378.050.141.610.500 C15.378.140.855.925.500.500 C15.378.243.937.925.500.500 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D065766 | ||||
| Scope note: | 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2015; see HEMOLYTIC-UREMIC SYNDROME 2010-2014; |
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| History Note: | 2015; use Hemolytic-Uremic Syndrome 2010-2014 |
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| DeCS ID: | 55579 | ||||
| Unique ID: | D065766 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 2015/01/01 | ||||
| Date of Entry: | 2014/06/26 | ||||
| Revision Date: | 2015/11/23 |
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Atypical Hemolytic Uremic Syndrome
- Preferred
| Concept UI |
M0532727 |
| Scope note | 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. |
| Preferred term | Atypical Hemolytic Uremic Syndrome |
| Entry term(s) |
Atypical Hemolytic-Uremic Syndrome Atypical Hemolytic-Uremic Syndromes HUS, Non-Shiga-Like Toxin-Associated HUS, Nonenteropathic HUSs, Non-Shiga-Like Toxin-Associated HUSs, Nonenteropathic Hemolytic Uremic Syndrome, Atypical Hemolytic-Uremic Syndrome, Atypical Hemolytic-Uremic Syndromes, Atypical Non Shiga Like Toxin Associated HUS Non Stx Hus Non-Shiga-Like Toxin-Associated HUS Non-Shiga-Like Toxin-Associated HUSs Non-Stx-Hus Nonenteropathic HUS Nonenteropathic HUSs Syndrome, Atypical Hemolytic-Uremic Syndromes, Atypical Hemolytic-Uremic Toxin-Associated HUS, Non-Shiga-Like Toxin-Associated HUSs, Non-Shiga-Like |
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