Search results for gata2

165 hits were found for gata2

# Family MCID Name MIFTS Score
1
IMM078 Immunodeficiency 21 41 16.376
2
MYL009 Myelodysplastic Syndrome 70 7.005
3
LYM094 Lymphedema, Primary, with Myelodysplasia 38 6.685
4
c LKM061 Leukemia, Acute Myeloid 83 5.438
5
P MYL006 Myeloid Leukemia 60 4.779
6
P LKM002 Leukemia 66 4.544
7
P LNG032 Lung Cancer 97 3.991
8
P LYM025 Lymphedema 53 3.469
9
P PLM006 Pulmonary Alveolar Proteinosis 52 3.267
10
P CHR285 Chronic Myelomonocytic Leukemia 59 3.253
11
P APL001 Aplastic Anemia 74 3.168
12
c ACT073 Acute Leukemia 58 3.102
13
P HMP002 Hemophagocytic Lymphohistiocytosis 54 2.617
14
P LKM062 Leukemia, Acute Lymphoblastic 68 2.595
15
P THR014 Thrombocytopenia 68 2.571
16
c FNC027 Fanconi Anemia, Complementation Group a 81 2.510
17
c LKM063 Leukemia, Chronic Myeloid 71 2.510
18
MYL005 Myelofibrosis 67 2.510
19
HMT002 Hematologic Cancer 62 2.510
20
MYC017 Mycobacterium Kansasii 37 1.850
21
WHM001 Whim Syndrome 59 1.818
22
P EPD083 Epidermodysplasia Verruciformis 1 57 1.818
23
ACT098 Acute Erythroid Leukemia 48 1.818
24
P DMN001 Diamond-Blackfan Anemia 69 1.775
25
P DYS007 Dyskeratosis Congenita 66 1.775
26
P SHW006 Shwachman-Diamond Syndrome 1 66 1.775
27
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 56 1.775
28
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 1.775
29
CBP001 Cebpa-Associated Familial Acute Myeloid Leukemia 30 1.775
30
c INF085 Inflammatory Bowel Disease 27 29 1.775
31
c HRD100 Hereditary Lymphedema Ic 28 1.775
32
c HRD204 Hereditary Lymphedema Ia 25 1.775
33
c PRM327 Primary Lymphedema 38 0.146
34
IMM167 Immune Deficiency Disease 78 0.136
35
LYM027 Lymphopenia 57 0.136
36
c BRN108 Branchiootic Syndrome 1 61 0.126
37
P PRS040 Prostate Cancer 97 0.115
38
P GRF003 Graft-Versus-Host Disease 71 0.115
39
P NTR004 Neutropenia 63 0.115
40
c SVR003 Severe Congenital Neutropenia 59 0.115
41
PNC001 Pancytopenia 54 0.115
42
P HYP086 Hypothyroidism 68 0.103
43
P LYM031 Lymphocytic Leukemia 55 0.103
45
DFC004 Deficiency Anemia 75 0.089
46
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.089
47
P HRP006 Herpes Simplex 65 0.089
48
PPL022 Papilloma 54 0.089
49
SQM002 Squamous Cell Papilloma 42 0.089
50
MYC088 Mycobacterium Avium Complex Infections 29 0.089
51
WRT007 Warts-Immunodeficiency-Lymphedema-Anogenital Dysplasia Syndrome 10 0.089
52
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.073
53
P NRB001 Neuroblastoma 71 0.073
54
P PLM037 Pulmonary Hypertension 68 0.073
55
P CRN018 Coronary Artery Anomaly 63 0.073
56
P SNS001 Sensorineural Hearing Loss 61 0.073
57
MCS006 Macs Syndrome 58 0.073
58
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.073
59
BCT022 Bacterial Infectious Disease 56 0.073
60
ART140 Arteries, Anomalies of 53 0.073
61
CKT002 Cakut 49 0.073
62
SPL018 Splenomegaly 48 0.073
63
c CNG439 Congenital Lymphedema 32 0.073
64
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 32 0.073
65
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.073
66
RRD019 Rare Deficiency Anemia 23 0.073
67
P HYD015 Hydroa Vacciniforme 23 0.073
68
P CLR023 Colorectal Cancer 98 0.051
69
P OVR042 Ovarian Cancer 89 0.051
70
P GST053 Gastric Cancer 83 0.051
71
PFF001 Pfeiffer Syndrome 79 0.051
72
P BLD134 Bladder Cancer 78 0.051
73
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.051
74
P PRK057 Parkinson Disease, Late-Onset 76 0.051
75
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.051
76
GLB015 Glioblastoma Multiforme 75 0.051
77
c THR092 Thrombophilia Due to Thrombin Defect 73 0.051
78
c HYP836 Hypercholesterolemia, Familial, 1 72 0.051
79
P CNR004 Cone-Rod Dystrophy 2 71 0.051
80
MLN008 Melanoma 69 0.051
81
P MYC084 Mycobacterium Tuberculosis 1 68 0.051
82
P INF038 Influenza 68 0.051
83
P PNM007 Pneumonia 68 0.051
84
KRT019 Keratitis, Hereditary 67 0.051
85
P HPT021 Hepatitis 67 0.051
86
LKC009 Leukocyte Adhesion Deficiency, Type I 67 0.051
87
c CHR684 Chronic Kidney Disease 66 0.051
88
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.051
89
MRK001 Merkel Cell Carcinoma 66 0.051
90
MYC006 Mycosis Fungoides 66 0.051
91
c SML038 Small Cell Cancer of the Lung 65 0.051
92
P AGM001 Agammaglobulinemia 65 0.051
93
MYL031 Myeloproliferative Neoplasm 65 0.051
94
CLR108 Colorectal Adenoma 64 0.051
95
c PRC016 Pre-Eclampsia 63 0.051
96
DGR001 Digeorge Syndrome 63 0.051
97
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.051
98
P MST009 Mastocytosis 63 0.051
99
P GLM045 Glioma 63 0.051
100
P NPH012 Nephrotic Syndrome 63 0.051
101
P END044 Endometriosis 62 0.051
102
P PRD008 Periodontitis 62 0.051
103
P VSC011 Vasculitis 62 0.051
104
P ENC004 Encephalitis 61 0.051
105
P TXP001 Toxoplasmosis 60 0.051
106
MCR013 Microphthalmia 60 0.051
107
CHC001 Chickenpox 60 0.051
108
P THL005 Thalassemia 60 0.051
109
HYD002 Hydronephrosis 59 0.051
110
c HPT016 Hepatitis B 59 0.051
111
P SYP003 Syphilis 59 0.051
112
PLM033 Pulmonary Embolism 59 0.051
113
VLV032 Vulva Cancer 59 0.051
114
HLC007 Helicobacter Pylori Infection 59 0.051
115
c CHR417 Chronic Graft Versus Host Disease 56 0.051
116
CYT008 Cytomegalovirus Infection 56 0.051
117
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.051
118
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.051
119
c FML035 Familial Hyperlipidemia 55 0.051
120
P DBT005 Diabetes Insipidus 55 0.051
121
WST005 West Nile Virus 55 0.051
122
P ART021 Arteriosclerosis 54 0.051
123
P MNC007 Monocytic Leukemia 54 0.051
124
c ACT020 Acute T Cell Leukemia 53 0.051
125
CLR030 Clear Cell Renal Cell Carcinoma 53 0.051
126
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.051
127
P RTN022 Retinal Vein Occlusion 52 0.051
128
P TRT010 Teratoma 51 0.051
129
c ACT135 Acute Graft Versus Host Disease 51 0.051
130
CHL061 Childhood Leukemia 50 0.051
131
P SCK005 Sickle Cell Disease 50 0.051
132
P CHR345 Chronic Pain 50 0.051
133
P OVR082 Overgrowth Syndrome 50 0.051
134
c CNT016 Central Retinal Vein Occlusion 49 0.051
135
PNN001 Panniculitis 49 0.051
136
BLS002 Blastomycosis 49 0.051
137
P SDR003 Sideroblastic Anemia 49 0.051
138
LKC005 Leukocyte Adhesion Deficiency, Type Iii 49 0.051
139
RFR010 Refractory Anemia 48 0.051
140
P LYM024 Lymphatic System Disease 48 0.051
141
ERY004 Erysipelas 48 0.051
142
ATX019 Ataxia with Vitamin E Deficiency 48 0.051
143
PLS025 Plasmablastic Lymphoma 47 0.051
144
CRD001 Cardiac Tamponade 46 0.051
145
P PLY020 Polyradiculoneuropathy 46 0.051
146
LNT004 Lentigines 46 0.051
147
GLL048 Glial Tumor 45 0.051
148
c MLG068 Malignant Glioma 45 0.051
149
CYT002 Cytokine Deficiency 44 0.051
150
c HYP829 Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive 41 0.051
151
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.051
152
SMT002 Smooth Muscle Tumor 37 0.051
153
CHN040 Choanal Atresia and Lymphedema 36 0.051
154
LNT002 Lentigo Maligna Melanoma 35 0.051
155
CHR178 Chromosomal Triplication 35 0.051
156
c CHR064 Chronic Monocytic Leukemia 34 0.051
157
P INH011 Inherited Bone Marrow Failure Syndromes 33 0.051
158
PST092 Posttransplant Acute Limbic Encephalitis 29 0.051
159
FLL042 Folliculotropic Mycosis Fungoides 28 0.051
160
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.051
161
DCK002 Dock8 Immunodeficiency Syndrome 20 0.051
162
CHL084 Cholesterol Pneumonia 19 0.051
163
HYD045 Hydroa Vacciniforme-Like Lymphoma 16 0.051
164
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 12 0.051
165
c FML317 Familial Monosomy 7 Syndrome 10 0.051
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