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 |
|---|---|---|---|---|---|---|
| APOL1 | APOL1:c.1200T>G(p.Ile400Met) | Pleiotropy | Presence of albuminuria | P=0.048 | Associated with the presence of albuminuria.more | more |
| ANXA2 | ANXA2:n.60609430C>T | Expressivity | Risk factor | Bayesian approach | ANXA2 (rs11853426),TEK (rs489347), and TGFBR3 (rs284875) variants were associated with increased stroke riskmore | more |
| ALOX5AP | ALOX5AP:c.*3192G>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 |
| ALOX5AP:c.494+154T>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 | |
| ALOX5AP:c.494+3269T>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 | |
| ALOX5AP:rs12019512 | 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 | |
| AK9 | AK9:rs10499052 | Expressivity | Altered white blood cell counts | P=0.000088 | Associated with WBC(white blood cell) and ANC(absolute neutrophil count).more | more |
| AGT | AGT:c.803T>C(p.Met268Thr) | Pleiotropy | Alter the occurrence of stroke | OR=14.05, 95% CI: 3.82-28.91; P=0.001 | M235T genotype was a significant independent factor related to the occurrence of stroke among patients with SCDmore | more |
| AGGF1 | AGGF1:c.604G>C(p.Val202Leu) | Expressivity | Altered glomerular filtration rate | P=0.0014 | AGGF1, CYP4B1, CUBN, TOR2A,PKD1L2, and CD163 variants affecting the glomerular filtration ratemore | more |
| ADRB2 | ADRB2:c.79C>G(p.Gln27Glu) | Pleiotropy | Altered stroke susceptibility | Large-vessel stroke: or±se = 0.53±0.16, P=0.033 | Specific polymorphisms in the IL4R 503, TNF (-308), and ADRB2 28 genes were independently associated with stroke susceptibility in the LV stroke subgroupmore | more |