Search results for "[genes] HBB"

41 hits were found for '[genes] HBB'

# Family MCID Name MIFTS Score
1
SCK003 Sickle Cell Anemia 70 32.570
2
MLR004 Malaria 81 21.322
3
P THL005 Thalassemia 64 20.103
4
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 45 20.103
5
SCK005 Sickle Cell Disease 54 17.409
6
c HMG003 Hemoglobin E Disease 39 14.215
7
HNZ001 Heinz Body Anemia 38 14.215
8
HMG010 Hemoglobinemia 32 14.215
9
c DMN035 Dominant Beta-Thalassemia 15 14.215
10
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 35 12.310
11
TRC008 Trachoma 58 10.051
12
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 57 10.051
13
P MTH007 Methemoglobinemia 51 10.051
14
P SDR002 Siderosis 49 10.051
15
THL016 Thalassemias, Alpha- 48 10.051
16
ACT017 Acute Chest Syndrome 48 10.051
17
BRL010 Buruli Ulcer 46 10.051
18
INV001 Invasive Aspergillosis 44 10.051
19
c CNG027 Congenital Hemolytic Anemia 44 10.051
20
HMG005 Hemoglobinopathy 44 10.051
21
C3D001 C3 Deficiency 38 10.051
22
ANM030 Anemia, Hypochromic Microcytic 34 10.051
23
HMG025 Hemoglobin H Disease, Nondeletional 34 10.051
24
SPL006 Splenic Infarction 32 10.051
25
HMG012 Hemoglobin Constant Spring 25 10.051
26
THL011 Thalassemia-Beta, Dominant Inclusion-Body 10 10.051
27
HRD159 Hereditary Persistence of Fetal Hemoglobin - Beta-Thalassemia 27 7.107
28
c ATS088 Autosomal Dominant Methemoglobinemia 24 7.107
29
c HMG001 Hemoglobin C Disease 24 7.107
30
SCK031 Sickle Cell - Hemoglobin C Disease 23 7.107
31
P HMG021 Hemoglobin E - Beta-Thalassemia 22 7.107
32
HRD111 Hereditary Persistence of Fetal Hemoglobin - Sickle Cell Disease 20 7.107
33
c SCK030 Sickle Cell - Hemoglobin E Disease 19 7.107
34
HMG023 Hemoglobin Lepore - Beta-Thalassemia 16 7.107
35
SCK021 Sickle Cell - Beta-Thalassemia Disease 15 7.107
36
c HMG022 Hemoglobin C - Beta-Thalassemia 15 7.107
37
P SCK020 Sickle Cell - Hemoglobin D Disease 14 7.107
38
c HMG004 Hemoglobin D Disease 14 7.107
39
P HMG016 Hemoglobin Sd 12 7.107
40
HMG015 Hemoglobin S Beta-Thalassemia 9 7.107
41
c HMG017 Hemoglobin So 8 7.107