Search results for "[genes] HBB"

64 hits were found for '[genes] HBB'

# Family MCID Name MIFTS Score
1
SCK003 Sickle Cell Anemia 71 25.178
2
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 22.318
3
MLR004 Malaria 80 19.033
4
P THL005 Thalassemia 62 19.033
5
HNZ001 Heinz Body Anemia 39 16.483
6
P HML002 Hemolytic Anemia 59 15.047
7
THL016 Thalassemias, Alpha- 55 15.047
8
P SCK005 Sickle Cell Disease 53 15.047
9
HMG005 Hemoglobinopathy 48 15.047
10
c HMG003 Hemoglobin E Disease 45 15.047
11
PLS007 Plasmodium Falciparum Malaria 58 13.458
12
P PLY018 Polycythemia 57 13.458
13
DFC004 Deficiency Anemia 62 11.655
14
P HRD011 Hereditary Spherocytosis 54 11.655
15
ANM029 Anemia, Sideroblastic, X-Linked 53 11.655
16
c HMG001 Hemoglobin C Disease 50 11.655
17
P MTH007 Methemoglobinemia 49 11.655
18
ACT017 Acute Chest Syndrome 48 11.655
19
P SDR002 Siderosis 47 11.655
20
HMS001 Hemosiderosis 47 11.655
21
CHL004 Cholelithiasis 46 11.655
22
THL010 Thalassemia Minor 43 11.655
23
SPL006 Splenic Infarction 43 11.655
24
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 36 11.655
25
ANM030 Anemia, Hypochromic Microcytic 34 11.655
26
c HMG004 Hemoglobin D Disease 34 11.655
27
P SCK034 Sickle Beta Thalassemia 30 11.655
28
c DMN035 Dominant Beta-Thalassemia 18 11.655
29
ACT098 Acute Erythroid Leukemia 52 9.516
30
BRL010 Buruli Ulcer 51 9.516
31
c CNG027 Congenital Hemolytic Anemia 50 9.516
32
LYM052 Lymphomatoid Papulosis 48 9.516
33
PLR005 Pleuropneumonia 46 9.516
34
C3D001 C3 Deficiency 44 9.516
35
EXT031 Extraosseous Ewing's Sarcoma 43 9.516
36
SPL012 Splenic Disease 43 9.516
37
ACT011 Acute Contagious Conjunctivitis 43 9.516
38
FVS001 Favism 42 9.516
39
ATS009 Autosomal Genetic Disease 41 9.516
40
OSG001 Osgood-Schlatter's Disease 41 9.516
41
GLC009 Glucosephosphate Dehydrogenase Deficiency 41 9.516
42
KLV001 Kluver-Bucy Syndrome 38 9.516
43
SPL007 Splenic Abscess 38 9.516
44
TTN001 Tetanus Neonatorum 36 9.516
45
c MLG039 Malignant Essential Hypertension 35 9.516
46
c ACQ010 Acquired Polycythemia 35 9.516
47
TST007 Testicular Infarct 33 9.516
48
RBS002 Rubeosis Iridis 32 9.516
49
c MLG080 Malignant Secondary Hypertension 29 9.516
50
HMG010 Hemoglobinemia 28 9.516
51
SPL009 Splenic Sequestration 27 9.516
52
P PYR006 Pyridoxine-Responsive Sideroblastic Anemia 23 9.516
53
P HMG026 Hemoglobin E-Beta-Thalassemia Syndrome 17 9.516
54
THL011 Thalassemia-Beta, Dominant Inclusion-Body 16 9.516
55
ATS010 Autosomal Recessive Disease 43 6.729
56
c ATS088 Autosomal Dominant Methemoglobinemia 26 6.729
57
HRD183 Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome 23 6.729
58
P HMG016 Hemoglobin Sd 22 6.729
59
SCK020 Sickle Cell - Hemoglobin D Disease 22 6.729
60
HMG015 Hemoglobin S Beta-Thalassemia 20 6.729
61
HRD180 Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome 17 6.729
62
HMG028 Hemoglobin Lepore-Beta-Thalassemia Syndrome 15 6.729
63
c HMG027 Hemoglobin C-Beta-Thalassemia Syndrome 12 6.729
64
c HMG017 Hemoglobin So 10 6.729