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Descriptor English: Anemia, Hemolytic, Congenital Nonspherocytic
Descriptor Spanish: Anemia Hemolítica Congénita no Esferocítica
Descriptor anemia hemolítica congénita no esferocítica
Scope note: Cualquiera de un grupo de anemias hemolíticas congénitas en las que no hay hemoglobina anormal ni esferocitosis y existe un defecto en la glicólisis del eritrocito. Entre las causas frecuentes están el déficit de GLUCOSA-6-FOSFATO ISOMERASA, PIRUVATO CINASA y GLUCOA-6FOSFATO DESHIDROGENASA.
Descriptor Portuguese: Anemia Hemolítica Congênita não Esferocítica
Descriptor French: Anémie hémolytique congénitale non sphérocytaire
Entry term(s): Anemia, Congenital Nonspherocytic Hemolytic
Anemia, Hemolytic Congenital, Nonspherocytic
Congenital Nonspherocytic Hemolytic Anemia
Hemolytic Anemia, Congenital Nonspherocytic
Tree number(s): C15.378.071.141.150.100
C16.320.070.100
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000746
Scope note: Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
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: 91,68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67
Online Note: use ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC to search ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1966-67
History Note: 91(82)68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67
Entry Version: ANEMIA HEMOL CONGEN NONSPHER
DeCS ID: 761
Unique ID: D000746
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1968/01/01
Date of Entry: 1999/01/01
Revision Date: 2011/06/24
Anemia, Hemolytic, Congenital Nonspherocytic - Preferred
Concept UI M0001130
Scope note Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.
Preferred term Anemia, Hemolytic, Congenital Nonspherocytic
Entry term(s) Anemia, Congenital Nonspherocytic Hemolytic
Anemia, Hemolytic Congenital, Nonspherocytic
Congenital Nonspherocytic Hemolytic Anemia
Hemolytic Anemia, Congenital Nonspherocytic



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