Search results for "[genes] IL2RA"

89 hits were found for '[genes] IL2RA'

# Family MCID Name MIFTS Score
1
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 19.198
2
P RHM011 Rheumatoid Arthritis 88 15.675
3
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 14.310
4
c JVN010 Juvenile Rheumatoid Arthritis 64 14.310
5
P GRV001 Graves' Disease 51 14.310
6
DPH001 Diphtheria 47 14.310
7
P HYP071 Hypersensitivity Reaction Type Ii Disease 38 14.310
8
BNN003 Bone Inflammation Disease 33 14.310
9
GLC008 Glucose Metabolism Disease 30 14.310
10
P ACQ009 Acquired Metabolic Disease 27 14.310
11
c SYS001 Systemic Lupus Erythematosus 90 12.799
12
P AST005 Asthma 77 12.799
13
c CHR090 Chronic Lymphocytic Leukemia 70 12.799
14
MYC006 Mycosis Fungoides 60 12.799
15
P HMP002 Hemophagocytic Lymphohistiocytosis 59 12.799
16
TTN003 Tetanus 55 12.799
17
P ALP009 Alopecia Areata 52 12.799
18
CNN005 Connective Tissue Disease 49 12.799
19
P UVT001 Uveitis 49 12.799
20
c ADL017 Adult T-Cell Leukemia 48 12.799
21
P HYP076 Hyperthyroidism 48 12.799
22
PLM012 Pulmonary Sarcoidosis 46 12.799
23
P CTN015 Cutaneous T Cell Lymphoma 45 12.799
24
LYM027 Lymphopenia 43 12.799
25
c INT064 Intermediate Uveitis 38 12.799
26
c PST005 Posterior Uveitis 37 12.799
27
DBT074 Diabetes, Mellitus, Insulin-Dependent 10 13 12.799
28
P ATM006 Autoimmune Lymphoproliferative Syndrome 65 11.084
29
CMM004 Common Variable Immunodeficiency 64 11.084
30
c SRC025 Sarcoidosis 1 60 11.084
31
c SYS004 Systemic Mastocytosis 56 11.084
32
HCL001 Hcl-V 52 11.084
33
TRP002 Tropical Spastic Paraparesis 51 11.084
34
P MMP001 Mumps 49 11.084
35
VGT001 Vogt-Koyanagi-Harada Disease 48 11.084
36
SZR001 Sezary's Disease 48 11.084
37
P MST009 Mastocytosis 48 11.084
38
EXT034 Extrinsic Allergic Alveolitis 44 11.084
39
P ACT135 Acute Graft Versus Host Disease 44 11.084
40
DMY004 Demyelinating Disease 43 11.084
41
P TCL004 T-Cell Leukemia 40 11.084
42
THY030 Thyroid Gland Disease 35 11.084
43
ATM014 Autoimmune Disease of Endocrine System 21 11.084
44
LYM115 Lymphoma, Non-Hodgkin 62 9.050
45
ACQ007 Acquired Immunodeficiency Syndrome 55 9.050
46
ALP001 Alopecia Universalis 54 9.050
47
HMT002 Hematologic Cancer 53 9.050
48
WLL006 Wells Syndrome 48 9.050
49
BLL003 Bell's Palsy 46 9.050
50
GRF001 Graft-Versus-Host Disease, Protection Against 44 9.050
51
GMM002 Gamma Chain Deficiency 44 9.050
52
CLS010 Cluster Headache 44 9.050
53
PLR001 Pleural Tuberculosis 43 9.050
54
PRR002 Pure Red-Cell Aplasia 43 9.050
55
P CRV039 Cervicitis 42 9.050
56
LMT001 Limited Scleroderma 42 9.050
57
RDC002 Radiculopathy 41 9.050
58
c CHR417 Chronic Graft Versus Host Disease 41 9.050
59
FLL008 Folliculitis 40 9.050
60
SMT006 Somatoform Disorder 39 9.050
61
GGR001 Geographic Tongue 38 9.050
62
ACN010 Acanthoma 38 9.050
63
P IDP064 Idiopathic Neutropenia 38 9.050
64
PNN001 Panniculitis 37 9.050
65
STR072 Stromal Keratitis 36 9.050
66
TCL002 T-Cell Large Granular Lymphocyte Leukemia 36 9.050
67
FCH002 Fuchs' Heterochromic Uveitis 36 9.050
68
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 9.050
69
P CLR001 Clear Cell Acanthoma 35 9.050
70
P BCL005 B Cell Prolymphocytic Leukemia 35 9.050
71
ILC002 Ileocolitis 35 9.050
72
TXC020 Toxic Oil Syndrome 34 9.050
73
ATR073 Atrophic Glossitis 33 9.050
74
URT008 Urticaria Pigmentosa 32 9.050
75
INT040 Intrinsic Asthma 31 9.050
76
P ATM020 Autoimmune Enteropathy 30 9.050
77
LRG008 Large Granular Lymphocyte Leukemia 30 9.050
78
VRN001 Vernal Conjunctivitis 30 9.050
79
ADN064 Adenohypophysitis 29 9.050
80
HTL002 Htlv-1 Associated Myelopathy 29 9.050
81
BLC015 Balo Concentric Sclerosis 28 9.050
82
HYP015 Hyperlucent Lung 28 9.050
83
INT029 Interleukin-7 Receptor Alpha Deficiency 19 9.050
84
IMM122 Immunodeficiency 41 with Lymphoproliferation and Autoimmunity 19 9.050
85
IMM112 Immunodeficiency Due to Cd25 Deficiency 7 9.050
86
P DYS007 Dyskeratosis Congenita 60 6.399
87
PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 36 6.399
88
OLG015 Oligoarticular Juvenile Arthritis 33 6.399
89
INT106 Interleukin 2 Receptor Alpha Chain Deficiency 4 6.399