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Descriptor English: Atypical Hemolytic Uremic Syndrome
Descriptor Spanish: Síndrome Hemolítico Urémico Atípico
Descriptor síndrome hemolítico urémico atípico
Scope note: Síndrome hemolítico urémico hereditario asociado a variaciones del gen que codifica el FACTOR H DEL COMPLEMENTO o las proteínas relacionadas CFHR1 y CFHR3. La enfermedad con frecuencia progresa a INSUFICIENCIA RENAL CRÓNICA, sin los síntomas prodrómicos de ENTEROCOLITIS y DIARREA que caracterizan al síndrome hemolítico urémico típico.
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
Tree number(s): C12.050.351.968.419.936.463.500
C12.200.777.419.936.463.500
C12.950.419.936.463.500
C15.378.071.141.610.500
C15.378.140.855.925.500.500
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.
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
Public MeSH Note: 2015; see HEMOLYTIC-UREMIC SYNDROME 2010-2014;
History Note: 2015; use Hemolytic-Uremic Syndrome 2010-2014
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
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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