Search results for GATA2

103 hits were found for GATA2

# Family MCID Name MIFTS Score
1
MYL009 Myelodysplastic Syndrome 73 6.147
2
IMM078 Immunodeficiency 21 35 6.034
3
EMB016 Emberger Syndrome 28 5.662
4
c LKM061 Leukemia, Acute Myeloid 73 4.758
5
P LYM025 Lymphedema 61 4.329
6
P APL001 Aplastic Anemia 75 4.249
7
P PLM006 Pulmonary Alveolar Proteinosis 48 3.852
8
HMT002 Hematologic Cancer 64 3.779
9
c LKM062 Leukemia, Acute Lymphoblastic 64 3.779
10
c ACT219 Acute Myeloid Leukemia, Flt3-Related 29 3.375
11
c INH015 Inherited Acute Myeloid Leukemia 25 3.303
12
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 4 3.303
13
MYL039 Myelodysplastic Syndrome, Susceptibility, Gata2-Related 2 3.303
14
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 3.273
15
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 60 3.273
16
LKM067 Leukemia, Acute Promyelocytic, Somatic 52 3.273
17
DFN299 Deafness-Lymphedema-Leukemia Syndrome 10 2.963
18
c LYM107 Lymphoproliferative Syndrome 2 50 2.672
19
ACT113 Acute Myeloblastic Leukemia with Maturation 37 2.672
20
P RFR008 Refractory Anemia with Excess Blasts 31 2.672
21
P LKM002 Leukemia 71 0.218
22
P MYL006 Myeloid Leukemia 66 0.187
23
HMT018 Hematopoietic Stem Cell Transplantation 41 0.113
24
P LNG032 Lung Cancer 95 0.080
25
P PRS040 Prostate Cancer 90 0.080
26
P CRN211 Coronary Artery Disease 74 0.080
27
PRM097 Primary Immunodeficiency Disease 60 0.080
28
OCL009 Ocular Cancer 59 0.080
29
P NTR004 Neutropenia 59 0.080
30
PRS047 Prostatitis 56 0.080
31
ART111 Artery Disease 55 0.080
32
P THY032 Thyroiditis 54 0.080
33
C3D001 C3 Deficiency 53 0.080
34
IMM136 Immune System Disease 51 0.080
35
BNM001 Bone Marrow Cancer 51 0.080
36
BCL002 B Cell Deficiency 49 0.080
37
ALN001 Aland Island Eye Disease 45 0.080
38
NTR005 Nutritional Deficiency Disease 36 0.080
39
MRG013 Mirage Syndrome 29 0.080
40
PRM243 Primary Bone Cancer 29 0.080
41
IMM070 Immunodeficiency 13 27 0.080
42
P BRS047 Breast Cancer 100 0.056
43
P CLR023 Colorectal Cancer 97 0.056
44
P HPT023 Hepatocellular Carcinoma 92 0.056
45
P OBS005 Obesity 92 0.056
46
P RNL014 Renal Cell Carcinoma 82 0.056
47
P NRB001 Neuroblastoma 70 0.056
48
SKN016 Skin Disease 66 0.056
49
ATH003 Atherosclerosis 65 0.056
50
P HRP006 Herpes Simplex 65 0.056
51
P THR014 Thrombocytopenia 64 0.056
52
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.056
53
FCT003 Factor X Deficiency 61 0.056
54
ISC004 Ischemia 61 0.056
55
P GLM045 Glioma 60 0.056
56
c ACT073 Acute Leukemia 60 0.056
57
P CLR108 Colorectal Adenoma 60 0.056
58
WLL006 Wells Syndrome 59 0.056
59
BNC003 Bone Cancer 58 0.056
60
CHL071 Child Syndrome 58 0.056
61
SNS001 Sensorineural Hearing Loss 57 0.056
62
LYM027 Lymphopenia 56 0.056
63
KDS001 Kid Syndrome 53 0.056
64
P ACT135 Acute Graft Versus Host Disease 53 0.056
65
CLR030 Clear Cell Renal Cell Carcinoma 53 0.056
66
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.056
67
ALL026 Allergic Hypersensitivity Disease 52 0.056
68
c CHR417 Chronic Graft Versus Host Disease 51 0.056
69
CSY001 C Syndrome 50 0.056
70
ACT098 Acute Erythroid Leukemia 47 0.056
71
VND001 Vein Disease 47 0.056
72
c CHR418 Chronic Leukemia 47 0.056
73
NTR003 Natural Killer Cell Leukemia 47 0.056
74
INC022 Inclusion-Cell Disease 46 0.056
75
GDS001 Good Syndrome 44 0.056
76
PHY002 Physical Disorder 43 0.056
77
LKC003 Leukocyte Disease 43 0.056
78
BLS002 Blastomycosis 42 0.056
79
SMT002 Smooth Muscle Tumor 41 0.056
80
c PRM023 Pre-Malignant Neoplasm 41 0.056
81
MDS022 Mediastinitis 41 0.056
82
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.056
83
NRN002 Neuronitis 41 0.056
84
MYC017 Mycobacterium Kansasii 40 0.056
85
CMM003 Common Wart 39 0.056
86
BNS002 Bone Structure Disease 37 0.056
87
IMM065 Immunodeficiency 10 36 0.056
88
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.056
89
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.056
90
c BRN108 Branchiootic Syndrome 1 34 0.056
91
ENG004 Engraftment Syndrome 32 0.056
92
IMM102 Immunodeficiency 14 31 0.056
93
SKN020 Skin Papilloma 30 0.056
94
IMM066 Immunodeficiency 9 30 0.056
95
IMM096 Immunodeficiency 30 27 0.056
96
IMM063 Immunodeficiency 15 26 0.056
97
HRN022 Hearing Loss/deafness 26 0.056
98
IMM120 Immunodeficiency 40 24 0.056
99
CNT067 Central Cord Syndrome 23 0.056
100
ACT228 Acute Radiation Syndrome 20 0.056
101
IMM142 Immunodeficiency 50 20 0.056
102
DBT019 Diabetes and Hearing Loss 15 0.056
103
HML018 Homologous Wasting Disease 13 0.056
Content
Loading form....