Search results for "[genes] HBB"

62 hits were found for '[genes] HBB'

# Family MCID Name MIFTS Score
1
SCK003 Sickle Cell Anemia 72 24.244
2
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 20.172
3
MLR004 Malaria 80 19.019
4
P THL005 Thalassemia 61 17.790
5
HNZ001 Heinz Body Anemia 40 16.471
6
c HMG003 Hemoglobin E Disease 44 16.471
7
THL016 Thalassemias, Alpha- 55 15.036
8
HMG005 Hemoglobinopathy 49 15.036
9
P HML002 Hemolytic Anemia 60 13.448
10
SCK005 Sickle Cell Disease 51 13.448
11
THL018 Thalassemia Major 31 13.448
12
ANM029 Anemia, Sideroblastic, X-Linked 53 11.647
13
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 33 11.647
14
P SCK034 Sickle Beta Thalassemia 33 11.647
15
THL011 Thalassemia-Beta, Dominant Inclusion-Body 22 11.647
16
ANM030 Anemia, Hypochromic Microcytic 37 11.647
17
c HMG001 Hemoglobin C Disease 46 11.647
18
c CNG027 Congenital Hemolytic Anemia 46 11.647
19
ACT017 Acute Chest Syndrome 50 11.647
20
P SDR002 Siderosis 44 11.647
21
P MTH007 Methemoglobinemia 44 11.647
22
SPL006 Splenic Infarction 32 11.647
23
CHL004 Cholelithiasis 48 11.647
24
c HMG004 Hemoglobin D Disease 32 11.647
25
THL017 Thalassemia Intermedia 38 11.647
26
THL010 Thalassemia Minor 38 11.647
27
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 9.509
28
HMG025 Hemoglobin H Disease, Nondeletional 36 9.509
29
GLC009 Glucosephosphate Dehydrogenase Deficiency 38 9.509
30
C3D001 C3 Deficiency 50 9.509
31
BRL010 Buruli Ulcer 47 9.509
32
SPL012 Splenic Disease 48 9.509
33
KLV001 Kluver-Bucy Syndrome 37 9.509
34
IRN002 Iron Metabolism Disease 38 9.509
35
TTN001 Tetanus Neonatorum 32 9.509
36
LYM052 Lymphomatoid Papulosis 45 9.509
37
HMS001 Hemosiderosis 42 9.509
38
OSG001 Osgood-Schlatter's Disease 32 9.509
39
CNG017 Congenital Nonspherocytic Hemolytic Anemia 32 9.509
40
TST007 Testicular Infarct 28 9.509
41
EXT031 Extraosseous Ewing's Sarcoma 40 9.509
42
P HMG026 Hemoglobin E-Beta-Thalassemia Syndrome 14 9.509
43
PLR005 Pleuropneumonia 44 9.509
44
RBS002 Rubeosis Iridis 33 9.509
45
c MLG039 Malignant Essential Hypertension 29 9.509
46
c MLG080 Malignant Secondary Hypertension 28 9.509
47
ANG004 Angioid Streaks 29 9.509
48
ATS009 Autosomal Genetic Disease 38 9.509
49
c INV001 Invasive Aspergillosis 44 9.509
50
SPL007 Splenic Abscess 35 9.509
51
SPL009 Splenic Sequestration 28 9.509
52
P PYR006 Pyridoxine-Responsive Sideroblastic Anemia 15 9.509
53
SCK020 Sickle Cell - Hemoglobin D Disease 23 6.724
54
MTH064 Methemoglobinemia, Beta-Globin Type 29 6.724
55
c HMG027 Hemoglobin C-Beta-Thalassemia Syndrome 11 6.724
56
HMG028 Hemoglobin Lepore-Beta-Thalassemia Syndrome 15 6.724
57
HRD180 Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome 17 6.724
58
HRD183 Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome 21 6.724
59
ATS010 Autosomal Recessive Disease 40 6.724
60
HMG015 Hemoglobin S Beta-Thalassemia 16 6.724
61
P HMG016 Hemoglobin Sd 19 6.724
62
c HMG017 Hemoglobin So 8 6.724