Anemia, Hemolytic, Congenital Nonspherocytic [hemolytická nesférocytická kongenitální anemie]

topical
13
Terms

anemie hemolytická kongenitální nesférocytární
anémie hemolytická kongenitální nesférocytární
hemolytická anemie kongenitální nesférocytová
nesférocytová hemolytická kongenitální anemie

 

Anemia, Congenital Nonspherocytic Hemolytic
Anemia, Hemolytic Congenital, Nonspherocytic
Congenital Nonspherocytic Hemolytic Anemia
Hemolytic Anemia, Congenital Nonspherocytic

Persistent link   https://www.medvik.cz/link/D000746
Definition

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.

DUI
D000746 MeSH Browser
CUI
M0001130
History note
91(82)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
Public note
91,68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67

Allowable subheadings

BL
blood 2
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 1
CO
complications
DI
diagnosis 8
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology
EH
ethnology
ET
etiology 3
GE
genetics 7
HI
history
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 3
UR
urine
VE
veterinary
VI
virology

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 975
C15.378.050 Anemia 1 245
C15.378.050.141 Anemia, Hemolytic 257
C15.378.050.141.150 Anemia, Hemolytic, Congenital 48
C15.378.050.141.150.095 Anemia, Dyserythropoietic, Congenital 16
C15.378.050.141.150.100 Anemia, Hemolytic, Congenital Nonspherocytic 13
C15.378.050.141.150.150 Anemia, Sickle Cell 45
C15.378.050.141.150.365 Elliptocytosis, Hereditary 6
C15.378.050.141.150.480 Glucosephosphate Dehydrogenase Deficiency 15
C15.378.050.141.150.490 Hemoglobin C Disease 1
C15.378.050.141.150.785 Spherocytosis, Hereditary 43
C15.378.050.141.150.875 Thalassemia 85
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.070.095 Anemia, Dyserythropoietic, Congenital 16
C16.320.070.100 Anemia, Hemolytic, Congenital Nonspherocytic 13
C16.320.070.150 Anemia, Sickle Cell 45
C16.320.070.365 Elliptocytosis, Hereditary 6
C16.320.070.480 Glucosephosphate Dehydrogenase Deficiency 15
C16.320.070.490 Hemoglobin C Disease 1
C16.320.070.785 Spherocytosis, Hereditary 43
C16.320.070.875 Thalassemia 85

Adenosine Triphosphatase Deficiency, Anemia Due To Disease MeSH Browser

Anemia, Nonspherocytic Hemolytic, associated with Abnormality of Red Cell Membrane Disease MeSH Browser

Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism Disease MeSH Browser

Pyruvate Kinase Deficiency of Red Cells Disease MeSH Browser

Triosephosphate Isomerase Deficiency Disease MeSH Browser

Add