Search results for sle susceptibility

209 hits were found for sle susceptibility

# Family MCID Name MIFTS Score
1
c SYS001 Systemic Lupus Erythematosus 86 5.278
2
P LPS004 Lupus Erythematosus 69 0.609
3
ATM095 Autoimmune Disease 66 0.371
4
P ART022 Arthritis 77 0.339
5
CNN005 Connective Tissue Disease 65 0.323
6
IMM136 Immune System Disease 57 0.313
7
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.259
8
P RHM011 Rheumatoid Arthritis 91 0.248
9
P MYC084 Mycobacterium Tuberculosis 1 69 0.198
10
P MLT020 Multiple Sclerosis 85 0.192
11
c BLD140 Blood Group, I System 37 0.176
12
P SCH015 Schizophrenia 71 0.175
13
P LKM002 Leukemia 75 0.170
14
P HPT021 Hepatitis 75 0.169
15
P CLR023 Colorectal Cancer 98 0.168
16
RHM027 Rheumatic Disease 62 0.150
17
P THY032 Thyroiditis 56 0.150
18
END072 Endotheliitis 46 0.149
19
AGN016 Aging 65 0.148
20
CRH001 Crohn's Disease 80 0.130
21
CRB009 Cerebritis 41 0.129
22
P LYM118 Lymphoma 71 0.129
23
ATM052 Autoimmune Disease 1 30 0.128
24
ENT004 Enthesopathy 38 0.126
25
P INF038 Influenza 77 0.125
26
P PNC044 Pancreatitis 64 0.121
27
MLR004 Malaria 86 0.121
28
P HRT032 Heart Disease 80 0.120
29
P PNM007 Pneumonia 70 0.119
30
P ENC004 Encephalitis 66 0.119
31
P GLM007 Glomerulonephritis 61 0.118
32
P ART023 Arthropathy 68 0.117
33
SKN016 Skin Disease 68 0.116
34
VSC011 Vasculitis 66 0.116
35
c SCL052 Scleroderma, Familial Progressive 60 0.113
36
P CLL015 Collagen Disease 53 0.112
37
P CTN003 Cutaneous Lupus Erythematosus 53 0.112
38
ART140 Arteries, Anomalies of 51 0.111
39
P CRN018 Coronary Artery Anomaly 69 0.110
40
P ANT006 Antiphospholipid Syndrome 59 0.110
41
P EPL164 Epilepsy 70 0.109
42
NRN002 Neuronitis 43 0.108
43
SKN027 Skin Conditions 48 0.108
44
P INF037 Inflammatory Bowel Disease 52 0.106
45
c HPT016 Hepatitis B 68 0.103
46
DRM006 Dermatitis 67 0.102
47
P LYM026 Lymphoblastic Leukemia 66 0.102
48
JNT002 Joint Disorders 60 0.101
49
P MYC007 Myocardial Infarction 81 0.098
50
P OST002 Osteoporosis 75 0.098
51
ANR040 Aneurysm 61 0.098
52
P KDN018 Kidney Disease 69 0.093
53
P MNN013 Meningitis 71 0.092
54
P CRN300 Coronary Heart Disease 1 57 0.092
55
P HYP086 Hypothyroidism 62 0.091
56
DSC009 Discoid Lupus Erythematosus 48 0.090
57
C1Q001 C1q Deficiency 40 0.090
58
VRL011 Viral Infectious Disease 64 0.089
59
THR024 Thrombosis 61 0.088
60
P THR014 Thrombocytopenia 65 0.088
61
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.087
62
P LVR013 Liver Disease 76 0.087
63
P HML002 Hemolytic Anemia 62 0.085
64
P SCL057 Scoliosis, Isolated 1 28 0.083
65
MYL001 Myelitis 52 0.082
66
HYP266 Hypoxia 61 0.082
67
LYM027 Lymphopenia 56 0.080
68
HSH003 Hashimoto Thyroiditis 67 0.080
69
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.079
70
c ATM011 Autoimmune Hepatitis 63 0.079
71
PRP030 Purpura 61 0.079
72
P ART021 Arteriosclerosis 62 0.079
73
URN009 Urinary System Disease 58 0.079
74
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.078
75
P DRM053 Dermatitis, Atopic 68 0.077
76
CMP009 Complement Deficiency 41 0.076
77
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.075
78
LNG099 Lung Disease 67 0.075
79
MST005 Mastitis 56 0.075
80
HRP004 Herpes Zoster 61 0.074
81
P MYS003 Myasthenia Gravis 73 0.074
82
c MYS011 Myasthenia Gravis Congenital 28 0.073
83
P HRP006 Herpes Simplex 70 0.073
84
c PRC016 Pre-Eclampsia 65 0.072
85
P ECL001 Eclampsia 57 0.072
86
P INF032 Infertility 59 0.071
87
STL001 St. Louis Encephalitis 43 0.070
88
MXD005 Mixed Connective Tissue Disease 66 0.070
89
P PLY019 Polyneuropathy 58 0.069
90
BRC012 Brucellosis 71 0.068
91
PLS007 Plasmodium Falciparum Malaria 59 0.066
92
MNT002 Mental Depression 60 0.066
93
P NTR004 Neutropenia 60 0.066
94
ART016 Aortic Aneurysm 70 0.065
95
P GRF003 Graft-Versus-Host Disease 72 0.064
96
ANX010 Anxiety 72 0.064
97
OST003 Osteonecrosis 63 0.064
98
P RNG031 Ring Chromosome Y Syndrome 29 0.064
99
P SJG008 Sjogren Syndrome 58 0.064
100
PRC013 Pericarditis 55 0.064
101
P DMY001 Demyelinating Polyneuropathy 46 0.064
102
LVR012 Liver Cirrhosis 73 0.064
103
ISC004 Ischemia 66 0.064
104
P PMP001 Pemphigus 55 0.064
105
ACR006 Aceruloplasminemia 65 0.062
106
P TRN034 Transverse Myelitis 53 0.062
107
MYL069 Myeloma, Multiple 86 0.061
108
P MYP004 Myopathy 69 0.061
109
P MJR001 Major Depressive Disorder 70 0.060
110
P GRM010 Germ Cells Tumors 37 0.060
111
CRB039 Cerebrovascular Disease 68 0.060
112
P MYS005 Myositis 63 0.060
113
P PLY041 Polymyositis 57 0.060
114
P PRS038 Personality Disorder 65 0.058
115
SYN007 Synovitis 61 0.058
116
BRD004 Borderline Personality Disorder 50 0.058
117
P NRP001 Neuropathy 63 0.058
118
PMP004 Pemphigus Foliaceus 46 0.058
119
ACT049 Acute Disseminated Encephalomyelitis 52 0.058
120
MNN009 Meningoencephalitis 49 0.058
121
c HPT003 Hepatitis a 63 0.057
122
VSC007 Vascular Disease 71 0.055
123
P EXN002 Exanthem 62 0.055
124
LYM019 Lymphosarcoma 58 0.055
125
P PLM037 Pulmonary Hypertension 79 0.054
126
P NPH012 Nephrotic Syndrome 60 0.054
127
P TCL004 T-Cell Leukemia 50 0.054
128
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.054
129
c LCL006 Localized Scleroderma 66 0.053
130
c CHR417 Chronic Graft Versus Host Disease 65 0.053
131
PLR008 Pleurisy 52 0.053
132
CTS005 Catastrophic Antiphospholipid Syndrome 45 0.053
133
c ACT027 Acute Pancreatitis 61 0.053
134
CRY005 Cryptococcosis 54 0.053
135
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.053
136
c LKM062 Leukemia, Acute Lymphoblastic 64 0.051
137
P DRM010 Dermatomyositis 65 0.049
138
P ACT074 Acute Lymphocytic Leukemia 61 0.049
139
SWN001 Swine Influenza 46 0.049
140
IMM003 Immunoglobulin Alpha Deficiency 37 0.049
141
WGN006 Wegener Granulomatosis 71 0.049
142
P PRP034 Purpura Fulminans 44 0.049
143
ANC002 Anca-Associated Vasculitis 42 0.049
144
CHR073 Choreatic Disease 40 0.049
145
c SBC035 Subacute Cutaneous Lupus Erythematosus 37 0.049
146
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.049
147
c CTR119 Cataract 32, Multiple Types 32 0.049
148
PSD084 Pseudo-Meigs Syndrome 22 0.049
149
P THR015 Thrombophilia 58 0.048
150
TRY001 Trypanosomiasis 55 0.048
151
CHC001 Chickenpox 48 0.048
152
SLP001 Sleeping Sickness 48 0.048
153
P NRV007 Nervous System Disease 75 0.046
154
ISC006 Ischemic Heart Disease 73 0.046
155
P CMR001 Camurati-Engelmann Disease 62 0.046
156
c ATR087 Atrial Standstill 1 59 0.046
157
P HRT035 Heart Block, Congenital 45 0.046
158
NCR004 Nocardiosis 43 0.046
159
IMM001 Immune-Complex Glomerulonephritis 39 0.046
160
P STR035 Streptococcal Group a Invasive Disease 28 0.046
161
TRY004 Trypanosomiasis, Human East-African 23 0.046
162
P MYL005 Myelofibrosis 75 0.043
163
P HYD006 Hydrocephalus 68 0.043
164
INC002 Inclusion Body Myositis 64 0.043
165
DMY004 Demyelinating Disease 58 0.043
166
SPS003 Spastic Diplegia 55 0.043
167
PNN001 Panniculitis 48 0.043
168
c TRC078 Trichohepatoenteric Syndrome 2 34 0.043
169
SYS068 Systemic Lupus Erythematosus with Hemolytic Anemia 1 10 0.043
170
P FML018 Familial Mediterranean Fever 73 0.041
171
CHR066 Chronic Fatigue Syndrome 67 0.041
172
CRD119 Cardiac Arrest 63 0.041
173
NRM005 Neuromuscular Disease 60 0.041
174
IDP024 Idiopathic Inflammatory Myopathy 49 0.041
175
HYD002 Hydronephrosis 49 0.041
176
HYP063 Hypersplenism 49 0.041
177
LYM067 Lymphoid Leukemia 43 0.041
178
CMP095 Complement Component 4a Deficiency 23 0.041
179
CMP060 Complement Component 9 Deficiency 18 0.041
180
P SYS005 Systemic Scleroderma 67 0.037
181
P THY023 Thymoma 65 0.037
182
HYP020 Hyperprolactinemia 64 0.037
183
KRT001 Keratoconjunctivitis Sicca 63 0.037
184
LYM021 Lymphadenitis 62 0.037
185
P HMP007 Hemophilia 61 0.037
186
P HYP076 Hyperthyroidism 56 0.037
187
DSS009 Disseminated Intravascular Coagulation 56 0.037
188
KRT006 Keratoconjunctivitis 56 0.037
189
STR008 Strongyloidiasis 54 0.037
190
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.037
191
HLL004 Hellp Syndrome 53 0.037
192
c PNS012 Paine Syndrome 52 0.037
193
PLS009 Plasma Cell Neoplasm 51 0.037
194
PRN011 Pernicious Anemia 50 0.037
195
SCB001 Scabies 50 0.037
196
INT303 Intracranial Hypertension, Idiopathic 49 0.037
197
HYP077 Hypertrichosis 49 0.037
198
PLY020 Polyradiculoneuropathy 48 0.037
199
c CHL140 Chilblain Lupus 1 46 0.037
200
CRY014 Cryptococcal Meningitis 45 0.037
201
c ACT159 Acute Transverse Myelitis 45 0.037
202
MCR225 Macrophage Activation Syndrome 44 0.037
203
PRL019 Prolidase Deficiency 41 0.037
204
P PRC031 Preeclampsia/eclampsia 1 41 0.037
205
P CHR084 Chromosomal Disease 40 0.037
206
MLR002 Miliary Tuberculosis 40 0.037
207
P CRB088 Cerebral Atrophy 38 0.037
208
SPL006 Splenic Infarction 34 0.037
209
GRN033 Granulomatous Mastitis 27 0.037
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