Search results for "[genes] HBB"

64 hits were found for '[genes] HBB'

# Family MCID Name MIFTS Score
1
SCK003 Sickle Cell Anemia 71 25.093
2
MLR004 Malaria 83 21.207
3
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 21.207
4
P THL005 Thalassemia 64 18.968
5
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 33 17.743
6
HMG005 Hemoglobinopathy 52 16.427
7
c HMG003 Hemoglobin E Disease 44 16.427
8
HNZ001 Heinz Body Anemia 39 16.427
9
THL011 Thalassemia-Beta, Dominant Inclusion-Body 21 16.427
10
P HML002 Hemolytic Anemia 62 14.996
11
P PLY018 Polycythemia 58 14.996
12
PLS007 Plasmodium Falciparum Malaria 55 14.996
13
SCK005 Sickle Cell Disease 51 14.996
14
THL016 Thalassemias, Alpha- 53 13.413
15
ACT017 Acute Chest Syndrome 48 13.413
16
THL018 Thalassemia Major 48 13.413
17
ANM029 Anemia, Sideroblastic, X-Linked 48 13.413
18
c CNG027 Congenital Hemolytic Anemia 48 13.413
19
c HMG001 Hemoglobin C Disease 47 13.413
20
HMS001 Hemosiderosis 46 13.413
21
P SDR002 Siderosis 44 13.413
22
THL017 Thalassemia Intermedia 40 13.413
23
ANM030 Anemia, Hypochromic Microcytic 36 13.413
24
SPL006 Splenic Infarction 35 13.413
25
c HMG004 Hemoglobin D Disease 31 13.413
26
P SCK034 Sickle Beta Thalassemia 30 13.413
27
P HMG026 Hemoglobin E-Beta-Thalassemia Syndrome 13 13.413
28
DFC004 Deficiency Anemia 64 11.616
29
C3D001 C3 Deficiency 53 11.616
30
BRL010 Buruli Ulcer 48 11.616
31
CHL004 Cholelithiasis 48 11.616
32
ACT098 Acute Erythroid Leukemia 47 11.616
33
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 11.616
34
SPL012 Splenic Disease 46 11.616
35
P MTH007 Methemoglobinemia 45 11.616
36
PLR005 Pleuropneumonia 43 11.616
37
GLC009 Glucosephosphate Dehydrogenase Deficiency 41 11.616
38
EXT031 Extraosseous Ewing's Sarcoma 41 11.616
39
ATS010 Autosomal Recessive Disease 41 11.616
40
HMG025 Hemoglobin H Disease, Nondeletional 39 11.616
41
THL010 Thalassemia Minor 39 11.616
42
KLV001 Kluver-Bucy Syndrome 38 11.616
43
OSG001 Osgood-Schlatter's Disease 35 11.616
44
ATS009 Autosomal Genetic Disease 35 11.616
45
RBS002 Rubeosis Iridis 34 11.616
46
ANG004 Angioid Streaks 30 11.616
47
c MLG039 Malignant Essential Hypertension 29 11.616
48
MTH064 Methemoglobinemia, Beta-Globin Type 29 11.616
49
c MLG080 Malignant Secondary Hypertension 28 11.616
50
c HMG029 Hemoglobin Se Disease 28 11.616
51
SPL009 Splenic Sequestration 28 11.616
52
HMG010 Hemoglobinemia 27 11.616
53
TST007 Testicular Infarct 26 11.616
54
SCK020 Sickle Cell - Hemoglobin D Disease 22 11.616
55
HRD183 Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome 21 11.616
56
HRD180 Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome 16 11.616
57
P PYR006 Pyridoxine-Responsive Sideroblastic Anemia 16 11.616
58
HMG028 Hemoglobin Lepore-Beta-Thalassemia Syndrome 15 11.616
59
HMG015 Hemoglobin S Beta-Thalassemia 14 11.616
60
P HMG016 Hemoglobin Sd 12 11.616
61
c HMG027 Hemoglobin C-Beta-Thalassemia Syndrome 11 11.616
62
c HMG017 Hemoglobin So 8 11.616
63
c HRD192 Hereditary Spherocytosis Type 2 22 9.484
64
P HRD011 Hereditary Spherocytosis 54 6.706