Disorder "Sickle Cell Anemia"
Found 352 records
Disorder information
Disorder name:
Sickle Cell Anemia 
Disoder ID:
OMIM entry:
Synonyms:
Hb SC disease,Hb-S/Hb-C disease,Hb-SS disease without crisis,Hemoglobin S disease without crisis,Sickle-cell/Hb-C disease without crisis,drepanocytosis,hemoglobin SC disease 
Definition:
Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur. 
Modifier statisitcs
Record:
352 
Gene:
110 
Variant:
291 
Reference:
43 
Effect type:
Expressivity(325) ,Pleiotropy(22) ,Penetrance(4) ,Dominance(1)  
Modifier effect:
Risk factor(104) ,Altered HbF levels(76) ,Altered response to hydroxyurea(32) ,Altered HbF production(25) ,Altered severity(17) ,Bacteremia-prone phenotype(13) ,Altered white blood cell counts(11) ,Altered baseline HbF level(10) ,Altered hemoglobin level(9) ,Altered fetal hemoglobin (HbF) levels(8) ,Altered levels of fetalhemoglobin and pain crisis(8) ,Altered glomerular filtration rate(6) ,Altered stroke susceptibility(6) ,Altered anemia, leukocytosis, and thrombocytosis(4) ,Altered incidence(4) ,Altered level of Fetal hemoglobin(3) ,Altered levels of HbF(3) ,Altered susceptibility(2) ,Altered serum levels(2) ,Presence of albuminuria(2) ,Alter the occurrence of stroke(1) ,Altered HbF levele(1) ,Altered bilirubin level(1) ,Altered immune response(1) ,Altered level of fetal hemoglobin(1) ,Altered rate of hospitalization(1) ,Heterozygote susceptibility(1)  
Modifier gene Variant Effect type Modifier effect Evidence Effect PubMed ID
OR10G9 OR10G9:rs12366219 Expressivity  Altered white blood cell counts  P=0.00042  Associated with WBC(white blood cell) and ANC(absolute neutrophil count).more more
NOX3 NOX3:c.1308+1182T>C Expressivity  Altered HbF levels  Bayesian approach  Different genes might modulate the rate of decline of HbF and the final level of HbF levels in sickle cell anemia.more more
NOX3:c.1308+3904G>A Expressivity  Altered HbF levels  Bayesian approach  Different genes might modulate the rate of decline of HbF and the final level of HbF levels in sickle cell anemia.more more
NOX3:c.1308+4060A>C Expressivity  Altered HbF levels  Bayesian approach  Different genes might modulate the rate of decline of HbF and the final level of HbF levels in sickle cell anemia.more more
NOX3:c.487-914C>A Expressivity  Altered HbF levels  Bayesian approach  Different genes might modulate the rate of decline of HbF and the final level of HbF levels in sickle cell anemia.more more
NOS3 NOS3:c.786T>C Expressivity  Altered severity  P<0.0001  ENOS gene polymorphisms are associated with SCD patients in India and may act as a genetic modifier of the phenotypic variation of SCD patients.more more
NOS3:c.894T>G(p.Asp298Glu) Expressivity  Altered severity  P<0.0001  ENOS gene polymorphisms are associated with SCD patients in India and may act as a genetic modifier of the phenotypic variation of SCD patients.more more
NOS3:c.*4682C>A Expressivity  Altered HbF levels  Bayesian approach  Different genes might modulate the rate of decline of HbF and the final level of HbF levels in sickle cell anemia.more more
NOS3:c.*5496G>A Expressivity  Altered HbF levels  Bayesian approach  Different genes might modulate the rate of decline of HbF and the final level of HbF levels in sickle cell anemia.more more
NOS3:c.T-786C Expressivity  Altered susceptibility  P=0.0076, 95% CI: 1.761-42.920  ENOS T-786C is a gender-specific genetic modifier that is associated with increased susceptibility to ACS in female SCD patients.more more
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