Elliptocytosis, Hereditary [dědičná eliptocytóza]

topical
6
Terms

dědičná ovalocytóza
eliptocytóza dědičná

 

Ovalocytosis, Hereditary

Persistent link   https://www.medvik.cz/link/D004612
Definition

An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.

Annotation
a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D004612 MeSH Browser
CUI
M0007240
History note
65(64)
Public note
65

Allowable subheadings

BL
blood 2
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 2
DI
diagnosis
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 1
EH
ethnology
ET
etiology
GE
genetics 2
HI
history
IM
immunology
ME
metabolism
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
UR
urine
VE
veterinary
VI
virology

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 976
C15.378.050 Anemia 1 249
C15.378.050.141 Anemia, Hemolytic 258
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 1 215
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

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Disease MeSH Browser

Elliptocytosis 1 Disease MeSH Browser

Elliptocytosis 2 Disease MeSH Browser

Elliptocytosis 3 Disease MeSH Browser

Elliptocytosis 4 Disease MeSH Browser

Elliptocytosis, Atypical Disease MeSH Browser

Glyoxalase II Deficiency Disease MeSH Browser

Ovalocytosis, Hereditary Hemolytic Disease MeSH Browser

Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis Disease MeSH Browser

Pyropoikilocytosis, Hereditary Disease MeSH Browser

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