Search results for "[genes] HBB"

68 hits were found for '[genes] HBB'

# Family MCID Name MIFTS Score
1
SCK003 Sickle Cell Anemia 71 24.939
2
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 23.089
3
MLR004 Malaria 72 19.995
4
P THL005 Thalassemia 56 19.995
5
P HML002 Hemolytic Anemia 52 17.634
6
DFC004 Deficiency Anemia 52 14.904
7
THL016 Thalassemias, Alpha- 50 14.904
8
P SCK005 Sickle Cell Disease 49 14.904
9
HMG005 Hemoglobinopathy 40 14.904
10
c CNG027 Congenital Hemolytic Anemia 39 14.904
11
c HMG003 Hemoglobin E Disease 35 14.904
12
P PLY018 Polycythemia 53 13.330
13
PLS007 Plasmodium Falciparum Malaria 52 13.330
14
HNZ001 Heinz Body Anemia 36 13.330
15
c DMN035 Dominant Beta-Thalassemia 17 13.330
16
ANM029 Anemia, Sideroblastic, X-Linked 55 11.544
17
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 46 11.544
18
P MTH007 Methemoglobinemia 44 11.544
19
P SDR002 Siderosis 40 11.544
20
CHL004 Cholelithiasis 40 11.544
21
ACT017 Acute Chest Syndrome 39 11.544
22
c HMG001 Hemoglobin C Disease 36 11.544
23
SPL006 Splenic Infarction 35 11.544
24
ANM030 Anemia, Hypochromic Microcytic 35 11.544
25
THL010 Thalassemia Minor 34 11.544
26
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 33 11.544
27
P HMG021 Hemoglobin E - Beta-Thalassemia 28 11.544
28
P SCK034 Sickle Beta Thalassemia 28 11.544
29
c HMG004 Hemoglobin D Disease 22 11.544
30
P HRD011 Hereditary Spherocytosis 52 9.426
31
BRL010 Buruli Ulcer 43 9.426
32
C3D001 C3 Deficiency 42 9.426
33
ACT098 Acute Erythroid Leukemia 41 9.426
34
HMS001 Hemosiderosis 40 9.426
35
c INV001 Invasive Aspergillosis 40 9.426
36
PLN005 Palindromic Rheumatism 40 9.426
37
PLR005 Pleuropneumonia 38 9.426
38
TRC021 Tricuspid Valve Stenosis 38 9.426
39
SPL012 Splenic Disease 37 9.426
40
OSG001 Osgood-Schlatter's Disease 36 9.426
41
EXT031 Extraosseous Ewing's Sarcoma 36 9.426
42
KLV001 Kluver-Bucy Syndrome 36 9.426
43
SPL007 Splenic Abscess 34 9.426
44
TTN001 Tetanus Neonatorum 33 9.426
45
RBS002 Rubeosis Iridis 31 9.426
46
c ACQ010 Acquired Polycythemia 31 9.426
47
PRS036 Parasitic Protozoa Infectious Disease 31 9.426
48
CHL012 Childhood Disintegrative Disease 30 9.426
49
GST015 Gastric Small Cell Carcinoma 29 9.426
50
HMG025 Hemoglobin H Disease, Nondeletional 28 9.426
51
TST007 Testicular Infarct 28 9.426
52
c MLG039 Malignant Essential Hypertension 28 9.426
53
ACT011 Acute Contagious Conjunctivitis 25 9.426
54
HMG010 Hemoglobinemia 25 9.426
55
SPL009 Splenic Sequestration 23 9.426
56
GLC009 Glucosephosphate Dehydrogenase Deficiency 23 9.426
57
P PYR006 Pyridoxine-Responsive Sideroblastic Anemia 22 9.426
58
c MLG080 Malignant Secondary Hypertension 22 9.426
59
THL011 Thalassemia-Beta, Dominant Inclusion-Body 19 9.426
60
HRD111 Hereditary Persistence of Fetal Hemoglobin - Sickle Cell Disease 16 9.426
61
HRD159 Hereditary Persistence of Fetal Hemoglobin - Beta-Thalassemia 23 6.665
62
c ATS088 Autosomal Dominant Methemoglobinemia 21 6.665
63
c HMG022 Hemoglobin C - Beta-Thalassemia 17 6.665
64
HMG023 Hemoglobin Lepore - Beta-Thalassemia 16 6.665
65
SCK020 Sickle Cell - Hemoglobin D Disease 15 6.665
66
P HMG016 Hemoglobin Sd 12 6.665
67
HMG015 Hemoglobin S Beta-Thalassemia 10 6.665
68
c HMG017 Hemoglobin So 9 6.665