Search results for Thalidomide

1100 hits were found for Thalidomide

# Family MCID Name MIFTS Score
1
FTL029 Fetal Thalidomide Syndrome 27 5.827
2
THL020 Thalidomide Susceptibility 6 3.851
3
MYL069 Myeloma, Multiple 85 0.707
4
P NRP001 Neuropathy 56 0.372
5
PLS009 Plasma Cell Neoplasm 51 0.365
6
P PRP019 Peripheral Nervous System Disease 58 0.329
7
HNS001 Hansen's Disease 34 0.302
8
CNS004 Constipation 58 0.295
9
P LPR021 Leprosy 3 69 0.292
10
P EXN002 Exanthem 57 0.213
11
DWN001 Down Syndrome 70 0.211
12
P GRF003 Graft-Versus-Host Disease 72 0.209
13
P NTR004 Neutropenia 63 0.207
14
MYL009 Myelodysplastic Syndrome 70 0.202
15
CRH001 Crohn's Disease 74 0.196
16
P LPS004 Lupus Erythematosus 61 0.180
17
P HPT023 Hepatocellular Carcinoma 100 0.176
18
c RHB024 Rhabdomyosarcoma 2 67 0.167
19
P PLY019 Polyneuropathy 56 0.167
20
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.166
21
GLB015 Glioblastoma Multiforme 75 0.164
22
c THR092 Thrombophilia Due to Thrombin Defect 73 0.164
23
MYL005 Myelofibrosis 70 0.161
24
P LKM002 Leukemia 68 0.157
25
P LYM118 Lymphoma 68 0.156
26
PLS011 Plasmacytoma 56 0.156
27
P PHC014 Phocomelia 24 0.151
28
HMN044 Human Immunodeficiency Virus Type 1 71 0.150
29
P SRC025 Sarcoidosis 1 70 0.145
30
IMM167 Immune Deficiency Disease 78 0.143
31
SNS003 Sensory Peripheral Neuropathy 54 0.143
32
PRR013 Prurigo Nodularis 36 0.143
33
THR024 Thrombosis 57 0.142
34
LYM019 Lymphosarcoma 46 0.140
35
P PRS040 Prostate Cancer 97 0.139
36
c CHR417 Chronic Graft Versus Host Disease 57 0.137
37
DSC009 Discoid Lupus Erythematosus 42 0.134
38
P MLN008 Melanoma 69 0.132
39
c SML038 Small Cell Cancer of the Lung 65 0.132
40
KPS004 Kaposi Sarcoma 75 0.130
41
P LNG032 Lung Cancer 98 0.126
42
P LKM071 Leukemia, Chronic Lymphocytic 79 0.126
43
P THR014 Thrombocytopenia 67 0.126
44
ADL002 Adult Syndrome 70 0.125
45
STM007 Stomatitis 50 0.125
46
FCT007 Factor Vii Deficiency 67 0.123
47
PLM033 Pulmonary Embolism 59 0.123
48
P CTN003 Cutaneous Lupus Erythematosus 53 0.123
49
P AMY004 Amyloidosis 70 0.121
50
SKN019 Skin Melanoma 68 0.121
51
P GLM045 Glioma 63 0.121
52
APH001 Aphthous Stomatitis 57 0.121
53
P INF037 Inflammatory Bowel Disease 54 0.121
54
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.121
55
ANG011 Angiodysplasia 43 0.121
56
GLL048 Glial Tumor 45 0.119
57
P TRN020 Turner Syndrome 67 0.117
58
ACQ007 Acquired Immunodeficiency Syndrome 60 0.117
59
P GLM040 Glioma Susceptibility 1 81 0.115
60
LPR001 Lepromatous Leprosy 50 0.115
61
HST010 Histiocytosis 48 0.115
62
CYT002 Cytokine Deficiency 42 0.115
63
DFC004 Deficiency Anemia 70 0.113
64
P BCL017 B-Cell Lymphoma 58 0.113
65
TLN003 Telangiectasis 52 0.113
66
c PRS136 Prostate Cancer, Hereditary, 6 33 0.113
67
c PRS130 Prostate Cancer, Hereditary, 8 32 0.113
68
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.111
69
SRC014 Sarcoma 65 0.111
70
P ADN016 Adenocarcinoma 64 0.111
71
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.111
72
CRH005 Crohn's Colitis 53 0.111
73
SPN035 Spindle Cell Sarcoma 53 0.111
74
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.111
75
LVR012 Liver Cirrhosis 62 0.109
76
P MYL006 Myeloid Leukemia 60 0.109
77
c MLG068 Malignant Glioma 46 0.109
78
P CLR023 Colorectal Cancer 99 0.107
79
ATM095 Autoimmune Disease 62 0.107
80
MCR004 Macroglobulinemia 49 0.107
81
c LKM061 Leukemia, Acute Myeloid 84 0.105
82
P KDN017 Kidney Cancer 60 0.105
83
LNG108 Langerhans Cell Histiocytosis 58 0.105
84
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.105
85
CNT033 Central Nervous System Cancer 47 0.105
86
LYM133 Lymphoma, Hodgkin, Classic 69 0.103
87
ACT164 Actinic Prurigo 44 0.103
88
c SYS001 Systemic Lupus Erythematosus 86 0.100
89
BRN028 Brain Cancer 74 0.100
90
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.100
91
P DRR001 Diarrhea 55 0.100
92
c ALM001 Al Amyloidosis 50 0.100
93
SPL018 Splenomegaly 48 0.100
94
P THL005 Thalassemia 60 0.098
95
GLS001 Gliosarcoma 54 0.098
96
MXD026 Mixed Glioma 45 0.098
97
P PLM036 Pulmonary Fibrosis 65 0.096
98
CLT003 Colitis 62 0.096
99
PMS001 Poems Syndrome 60 0.096
100
P LCH002 Lichen Planus 53 0.096
101
MNT001 Mantle Cell Lymphoma 69 0.093
102
SFT003 Soft Tissue Sarcoma 56 0.093
103
SKN006 Skin Sarcoidosis 41 0.093
104
P MLG074 Malignant Mesenchymoma 40 0.093
105
48X005 48,xyyy 39 0.093
106
ULC004 Ulcerative Colitis 73 0.091
107
c SPN225 Spondyloarthropathy 1 73 0.091
108
P VSC011 Vasculitis 62 0.091
109
ERY003 Erythema Multiforme 58 0.091
110
PYD001 Pyoderma Gangrenosum 54 0.091
111
GNT002 Giant Cell Glioblastoma 50 0.091
112
PYD002 Pyoderma 50 0.091
113
c LPR022 Leprosy 2 37 0.091
114
P PNM007 Pneumonia 68 0.088
115
ACT058 Active Peptic Ulcer Disease 55 0.088
116
SPN051 Spondylitis 51 0.088
117
INF009 Inflammatory Spondylopathy 31 0.088
118
P OVR042 Ovarian Cancer 88 0.086
119
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.086
120
P ART022 Arthritis 69 0.086
121
MYL031 Myeloproliferative Neoplasm 66 0.086
122
c ACT135 Acute Graft Versus Host Disease 52 0.086
123
P AST007 Astrocytoma 51 0.086
124
SCL025 Scleromyxedema 32 0.086
125
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.083
126
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.083
127
P MNN013 Meningitis 66 0.083
128
P ART005 Arteriovenous Malformation 65 0.083
129
HMT002 Hematologic Cancer 62 0.083
130
LNG031 Lung Benign Neoplasm 51 0.083
131
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.083
132
c PRM038 Primary Agammaglobulinemia 44 0.083
133
P RHM011 Rheumatoid Arthritis 80 0.080
134
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.080
135
WLD007 Waldenstroem's Macroglobulinemia 61 0.080
136
P UVT001 Uveitis 57 0.080
137
IRN002 Iron Metabolism Disease 57 0.080
138
RFR010 Refractory Anemia 48 0.080
139
LYM012 Lymphoplasmacytic Lymphoma 47 0.080
140
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.080
141
HML018 Homologous Wasting Disease 22 0.080
142
c INF071 Inflammatory Bowel Disease 1 67 0.077
143
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.077
144
P PSR002 Psoriasis 62 0.077
145
GRD007 Grade Iii Astrocytoma 59 0.077
146
DFF005 Diffuse Large B-Cell Lymphoma 55 0.077
147
PST011 Pustulosis of Palm and Sole 52 0.077
148
KRT013 Keratolytic Winter Erythema 46 0.077
149
BNM001 Bone Marrow Cancer 43 0.077
150
PRS063 Paresthesia 41 0.077
151
BHC003 Behcet Syndrome 71 0.074
152
SKN016 Skin Disease 63 0.074
153
P LMY004 Leiomyosarcoma 63 0.074
154
P TRM003 Tremor 54 0.074
155
PLS016 Plasma Cell Leukemia 53 0.074
156
NRT004 Neuritis 52 0.074
157
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.074
158
AML065 Amelia 30 0.074
159
P PNC035 Pancreatic Cancer 84 0.071
160
P GST053 Gastric Cancer 83 0.071
161
SVR004 Severe Combined Immunodeficiency 73 0.071
162
P KDN018 Kidney Disease 72 0.071
163
P NRB001 Neuroblastoma 72 0.071
164
CNG034 Congestive Heart Failure 69 0.071
165
P MYC084 Mycobacterium Tuberculosis 1 68 0.071
166
OST159 Osteogenic Sarcoma 66 0.071
167
47X002 47,xyy 49 0.071
168
TBR011 Tuberculous Meningitis 48 0.071
169
UTR043 Uterine Sarcoma 39 0.071
170
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.068
171
c LKM063 Leukemia, Chronic Myeloid 72 0.068
172
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.068
173
P OLG002 Oligodendroglioma 67 0.068
174
P FLL037 Follicular Lymphoma 67 0.068
175
ALL026 Allergic Hypersensitivity Disease 62 0.068
176
c ACT027 Acute Pancreatitis 60 0.068
177
P CHR285 Chronic Myelomonocytic Leukemia 60 0.068
178
LYM027 Lymphopenia 58 0.068
179
CST005 Castleman Disease 57 0.068
180
NRN004 Neuroendocrine Tumor 55 0.068
181
AMN001 Amenorrhea 54 0.068
182
PNC001 Pancytopenia 54 0.068
183
ACR041 Acromelic Frontonasal Dysostosis 52 0.068
184
c FLL041 Follicular Lymphoma 1 49 0.068
185
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.068
186
CRN027 Corneal Neovascularization 47 0.068
187
ANP009 Anaplastic Oligodendroglioma 43 0.068
188
OVR094 Ovarian Epithelial Cancer 38 0.068
189
STT009 Sutton Disease 2 30 0.068
190
ESP021 Esophageal Cancer 90 0.064
191
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.064
192
P HRT032 Heart Disease 75 0.064
193
P HYP086 Hypothyroidism 69 0.064
194
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.064
195
P HMN010 Hemangioma 61 0.064
196
ISC004 Ischemia 58 0.064
197
P LTR001 Lateral Sclerosis 54 0.064
198
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.064
199
ATY042 Atypical Chronic Myeloid Leukemia 49 0.064
200
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.064
201
RTC005 Reticulosarcoma 47 0.064
202
ATX019 Ataxia with Vitamin E Deficiency 42 0.064
203
GST020 Gastric Antral Vascular Ectasia 41 0.064
204
c ADL096 Adult Hepatocellular Carcinoma 40 0.064
205
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.064
206
P AXN001 Axonal Neuropathy 36 0.064
207
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.060
208
P PLM037 Pulmonary Hypertension 67 0.060
209
P HRP006 Herpes Simplex 65 0.060
210
c HPT001 Hepatitis C 62 0.060
211
NTR005 Nutritional Deficiency Disease 62 0.060
212
P PNC044 Pancreatitis 61 0.060
213
P BNG030 Benign Ependymoma 60 0.060
214
P MLN069 Melanoma, Uveal 59 0.060
215
c ACT073 Acute Leukemia 58 0.060
216
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.060
217
CLL010 Cellular Ependymoma 54 0.060
218
MRG003 Marginal Zone B-Cell Lymphoma 52 0.060
219
P RCT021 Rectum Cancer 52 0.060
220
OCL022 Ocular Melanoma 50 0.060
221
MLT113 Multicentric Castleman Disease 47 0.060
222
SYN036 Syncope 45 0.060
223
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.060
224
c SYS043 Systemic Lupus Erythematosus 1 38 0.060
225
c ADL008 Adult Oligodendroglioma 34 0.060
226
P BRS047 Breast Cancer 97 0.057
227
STR067 Stroke, Ischemic 81 0.057
228
P MDL005 Medulloblastoma 77 0.057
229
EWN003 Ewing Sarcoma 69 0.057
230
P LKM062 Leukemia, Acute Lymphoblastic 69 0.057
231
P SYS005 Systemic Scleroderma 68 0.057
232
P INF038 Influenza 68 0.057
233
P HPT021 Hepatitis 67 0.057
234
LNG039 Lung Squamous Cell Carcinoma 66 0.057
235
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.057
236
P END044 Endometriosis 63 0.057
237
c ALP101 Alpha-Thalassemia 62 0.057
238
CRC021 Carcinosarcoma 62 0.057
239
TXC005 Toxic Shock Syndrome 62 0.057
240
DRM006 Dermatitis 61 0.057
241
c PNS012 Paine Syndrome 61 0.057
242
SQM006 Squamous Cell Carcinoma 60 0.057
243
PRT013 Portal Hypertension 59 0.057
244
VSL002 Visual Epilepsy 59 0.057
245
MNT002 Mental Depression 58 0.057
246
CMR002 Coumarin Resistance 56 0.057
247
P SZR006 Seizure Disorder 56 0.057
248
ISL001 Islet Cell Tumor 56 0.057
249
MCS002 Mucositis 56 0.057
250
P LNG035 Lung Large Cell Carcinoma 54 0.057
251
PRP036 Peripheral T-Cell Lymphoma 53 0.057
252
EXT010 Extramedullary Plasmacytoma 45 0.057
253
LTH001 Lethal Midline Granuloma 44 0.057
254
c SRC023 Sarcoidosis 2 43 0.057
255
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.057
256
c PST022 Posterior Uveal Melanoma 42 0.057
257
c OVR114 Ovarian Cancer 1 38 0.057
258
IND003 Indolent Myeloma 36 0.057
259
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.057
260
PRQ002 Paraquat Poisoning 26 0.057
261
MLG164 Malignant Epithelial Tumor of Ovary 26 0.057
262
END057 Endometrial Cancer 74 0.052
263
P EPL164 Epilepsy 71 0.052
264
P ATS364 Autism 70 0.052
265
P LVR013 Liver Disease 68 0.052
266
P CHR012 Chronic Granulomatous Disease 67 0.052
267
CRP001 Carpal Tunnel Syndrome 67 0.052
268
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.052
269
P MTR014 Motor Neuron Disease 65 0.052
270
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.052
271
c JVN010 Juvenile Rheumatoid Arthritis 64 0.052
272
ACT119 Acute Promyelocytic Leukemia 63 0.052
273
INT002 Intermittent Claudication 61 0.052
274
c SCL052 Scleroderma, Familial Progressive 61 0.052
275
UTR024 Uterine Carcinosarcoma 59 0.052
276
P LYM033 Lymphoproliferative Syndrome 59 0.052
277
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.052
278
MCR013 Microphthalmia 57 0.052
279
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.052
280
c BCT007 Bacterial Meningitis 55 0.052
281
CRC006 Carcinoid Syndrome 55 0.052
282
PRP030 Purpura 54 0.052
283
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.052
284
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.052
285
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.052
286
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.052
287
THR004 Thrombocytosis 51 0.052
288
SPL004 Splenic Marginal Zone Lymphoma 51 0.052
289
PNN001 Panniculitis 51 0.052
290
END086 End Stage Renal Disease 51 0.052
291
RSD004 Rosai-Dorfman Disease 51 0.052
292
BNR002 Bone Resorption Disease 48 0.052
293
PRC003 Proctitis 47 0.052
294
P HMN032 Human Herpesvirus 8 47 0.052
295
PLS025 Plasmablastic Lymphoma 47 0.052
296
FCL012 Facial Paralysis 46 0.052
297
P BNG032 Benign Mesothelioma 46 0.052
298
P CHR345 Chronic Pain 44 0.052
299
CVD001 Covid-19 44 0.052
300
ULC007 Ulcerative Stomatitis 39 0.052
301
c DNR003 Duane Retraction Syndrome 1 38 0.052
302
RFR013 Refractory Celiac Disease 35 0.052
303
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.052
304
ADS015 Aids Wasting Syndrome 22 0.052
305
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.052
306
P BLD134 Bladder Cancer 79 0.048
307
P LNG064 Lung Cancer Susceptibility 3 78 0.048
308
ADR007 Adrenoleukodystrophy 75 0.048
309
PLY001 Polycythemia Vera 69 0.048
310
P ESS003 Essential Thrombocythemia 68 0.048
311
BRK010 Burkitt Lymphoma 67 0.048
312
P HYP098 Hypereosinophilic Syndrome 67 0.048
313
P NSP012 Nasopharyngeal Carcinoma 66 0.048
314
P VNW001 Von Willebrand's Disease 65 0.048
315
ANG020 Angiosarcoma 64 0.048
316
P MST009 Mastocytosis 64 0.048
317
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.048
318
c SYS004 Systemic Mastocytosis 63 0.048
319
HLT001 Holt-Oram Syndrome 63 0.048
320
LPP008 Lipoprotein Quantitative Trait Locus 62 0.048
321
P INT143 Interstitial Cystitis 61 0.048
322
INT066 Interstitial Lung Disease 60 0.048
323
LNG099 Lung Disease 60 0.048
324
INS001 Insulinoma 60 0.048
325
IDP011 Idiopathic Interstitial Pneumonia 59 0.048
326
ADN018 Adenoma 59 0.048
327
P PLY006 Polydactyly 59 0.048
328
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.048
329
P PLY018 Polycythemia 56 0.048
330
BCT022 Bacterial Infectious Disease 56 0.048
331
P STR020 Strabismus 55 0.048
332
P PMP001 Pemphigus 54 0.048
333
P EPD016 Epidermolysis Bullosa 53 0.048
334
P HMR003 Hemorrhagic Disease 53 0.048
335
TXC002 Toxic Encephalopathy 53 0.048
336
P BRN035 Brain Stem Glioma 52 0.048
338
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.048
339
c CHR418 Chronic Leukemia 49 0.048
340
ACT029 Acute Interstitial Pneumonia 49 0.048
341
CRC014 Carcinoid Tumors, Intestinal 47 0.048
342
MYX001 Myxopapillary Ependymoma 46 0.048
343
c DRR009 Diarrhea 6 46 0.048
344
APP010 Appendix Cancer 44 0.048
345
PPL001 Papillary Adenoma 44 0.048
346
P EPN001 Ependymoblastoma 44 0.048
347
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.048
348
ARC002 Arachnoiditis 42 0.048
349
MCH006 Mechanical Strabismus 42 0.048
350
LGH004 Light Chain Deposition Disease 40 0.048
351
HST016 Histiocytic Sarcoma 39 0.048
352
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.048
353
UTR037 Uterine Corpus Sarcoma 36 0.048
354
SPN354 Spinal Arachnoiditis 36 0.048
355
HMN016 Hemangioendothelioma 34 0.048
356
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.048
357
MTS005 Metastatic Squamous Neck Cancer with Occult Primary 11 0.048
358
OST012 Osteoarthritis 78 0.043
359
c MNN043 Meningioma, Familial 74 0.043
360
P CNR004 Cone-Rod Dystrophy 2 73 0.043
361
ANX010 Anxiety 73 0.043
362
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.043
363
P MYC007 Myocardial Infarction 70 0.043
364
P MYP004 Myopathy 70 0.043
365
SVR097 Severe Cutaneous Adverse Reaction 69 0.043
366
CHL065 Cholangiocarcinoma 68 0.043
367
GST092 Gastroesophageal Reflux 67 0.043
368
CRB039 Cerebrovascular Disease 67 0.043
369
FLL027 Fallopian Tube Carcinoma 67 0.043
370
MYC006 Mycosis Fungoides 66 0.043
371
P NRV007 Nervous System Disease 66 0.043
372
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.043
373
DPR016 Depression 63 0.043
374
RHB001 Rhabdoid Cancer 63 0.043
375
c HPT003 Hepatitis a 62 0.043
376
PRM126 Primary Peritoneal Carcinoma 62 0.043
377
MNN042 Meningioma, Radiation-Induced 62 0.043
378
P PRM006 Primary Biliary Cirrhosis 62 0.043
379
PSR001 Psoriatic Arthritis 61 0.043
380
OST003 Osteonecrosis 61 0.043
381
P ENC018 Encephalopathy 61 0.043
382
c JVN061 Juvenile Arthritis 60 0.043
383
ORL011 Oral Cancer 60 0.043
384
c HPT016 Hepatitis B 59 0.043
385
THY029 Thyroid Carcinoma 59 0.043
386
P HMN036 Hemangiopericytoma, Malignant 59 0.043
387
IRN001 Iron Deficiency Anemia 59 0.043
388
P ANP001 Anaplastic Large Cell Lymphoma 58 0.043
389
CMP010 Complex Regional Pain Syndrome 58 0.043
390
c DWL002 Dowling-Degos Disease 1 58 0.043
391
P GLL018 Gallbladder Cancer 57 0.043
392
P GLM007 Glomerulonephritis 57 0.043
393
DSS009 Disseminated Intravascular Coagulation 57 0.043
394
c MST023 Mesothelioma, Malignant 57 0.043
395
P CRD246 Cardiovascular System Disease 57 0.043
396
HYP266 Hypoxia 57 0.043
397
P CHN012 Chondrosarcoma 56 0.043
398
PRS047 Prostatitis 56 0.043
399
DNR002 Duane-Radial Ray Syndrome 56 0.043
400
BRN004 Brain Edema 56 0.043
401
P ANT006 Antiphospholipid Syndrome 55 0.043
402
P ALP008 Alopecia 54 0.043
403
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.043
404
DBT010 Diabetic Neuropathy 54 0.043
405
LYM040 Lymphoblastic Lymphoma 54 0.043
406
CLF001 Cleft Lip 53 0.043
407
INT075 Intracranial Hypertension 53 0.043
408
IRD001 Iridocyclitis 53 0.043
409
ART140 Arteries, Anomalies of 52 0.043
410
THY030 Thyroid Gland Disease 52 0.043
411
P THR015 Thrombophilia 51 0.043
412
P CHL066 Cholangitis 51 0.043
413
SPN021 Spinal Meningioma 50 0.043
414
AGG002 Aggressive Systemic Mastocytosis 49 0.043
415
BRN071 Brain Injury 49 0.043
416
FRN020 Frontal Fibrosing Alopecia 49 0.043
417
CRY004 Cryoglobulinemia 48 0.043
418
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.043
419
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.043
420
SXL003 Sexual Disorder 47 0.043
421
ADN009 Adenosquamous Carcinoma 47 0.043
422
ANP006 Anaplastic Ependymoma 46 0.043
423
ORL013 Oral Lichen Planus 45 0.043
424
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.043
425
GRN017 Granulocytopenia 44 0.043
426
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.043
427
P EPT020 Epithelioid Hemangioendothelioma 43 0.043
428
TRP009 Triple X Syndrome 42 0.043
429
c MLG064 Malignant Ependymoma 41 0.043
430
SCR001 Secretory Meningioma 41 0.043
431
ALL014 Allergic Encephalomyelitis 38 0.043
432
EPD022 Epidermolysis Bullosa Pruriginosa 38 0.043
433
ATM052 Autoimmune Disease 1 37 0.043
434
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.043
435
WBR001 Weber Syndrome 35 0.043
436
GRM010 Germ Cells Tumors 34 0.043
437
LTT002 Letterer-Siwe Disease 33 0.043
438
SML008 Small Intestine Lymphoma 33 0.043
439
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.043
440
ERY066 Erythema Multiforme Major 30 0.043
441
c ADL054 Adult Brain Stem Glioma 30 0.043
442
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.043
443
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.043
444
CHL079 Children's Interstitial Lung Disease 26 0.043
445
MNN006 Meninges Hemangiopericytoma 23 0.043
446
c CHR686 Chronic Cutaneous Lupus Erythematosus 19 0.043
447
c MLG023 Malignant Adult Ependymoma 15 0.043
448
c ANK022 Ankylosing Spondylitis 2 15 0.043
449
c ADL045 Adult Ependymoblastoma 14 0.043
450
P ALZ034 Alzheimer Disease 88 0.037
452
GST019 Gastrointestinal Stromal Tumor 78 0.037
453
P APL001 Aplastic Anemia 74 0.037
454
P FML018 Familial Mediterranean Fever 73 0.037
455
ADN011 Adenoid Cystic Carcinoma 70 0.037
456
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.037
457
c CHR684 Chronic Kidney Disease 70 0.037
458
c PNC108 Pancreatitis, Hereditary 70 0.037
459
MST024 Mastocytosis, Cutaneous 69 0.037
460
c BSL007 Basal Cell Carcinoma 68 0.037
461
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.037
462
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.037
463
THY111 Thyroid Carcinoma, Familial Medullary 67 0.037
464
P BLD062 Bile Duct Cancer 67 0.037
465
P MCR115 Microvascular Complications of Diabetes 5 66 0.037
466
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.037
467
P HYD006 Hydrocephalus 66 0.037
468
P DRM053 Dermatitis, Atopic 66 0.037
469
CRN036 Craniopharyngioma 65 0.037
470
TTN003 Tetanus 65 0.037
471
ATH013 Atherosclerosis Susceptibility 65 0.037
472
PRT036 Peritonitis 64 0.037
473
MSC007 Muscle Hypertrophy 64 0.037
474
P CRN300 Coronary Heart Disease 1 63 0.037
475
END041 Endometrial Adenocarcinoma 63 0.037
476
c BRN108 Branchiootic Syndrome 1 62 0.037
477
c SVR001 Severe Acute Respiratory Syndrome 62 0.037
478
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.037
479
P ENC004 Encephalitis 61 0.037
480
P SJG008 Sjogren Syndrome 61 0.037
481
VRL011 Viral Infectious Disease 61 0.037
482
SPN186 Spinal Cord Injury 60 0.037
483
HRP004 Herpes Zoster 60 0.037
484
P NPH012 Nephrotic Syndrome 60 0.037
485
P VNT002 Ventricular Septal Defect 60 0.037
486
VRC005 Varicose Veins 60 0.037
487
CHC001 Chickenpox 60 0.037
488
c ACT071 Acute Kidney Failure 60 0.037
489
P BND020 Bone Disease 59 0.037
490
PRT058 Pure Autonomic Failure 59 0.037
491
P CYS018 Cystitis 59 0.037
492
BRN002 Bronchiolitis 59 0.037
493
MCS006 Macs Syndrome 58 0.037
494
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.037
495
P INF032 Infertility 57 0.037
496
GLS018 Glass Syndrome 57 0.037
497
c CHL119 Cholangitis, Primary Sclerosing 57 0.037
498
P SLV026 Salivary Gland Carcinoma 57 0.037
499
THY122 Thyroid Gland Cancer 57 0.037
500
c SML009 Small Intestine Adenocarcinoma 57 0.037
501
c BSL024 Basal Cell Carcinoma 1 56 0.037
502
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.037
503
P FBR017 Fibrosarcoma 56 0.037
504
HPT046 Hepatic Veno-Occlusive Disease 56 0.037
505
ALL006 Allergic Asthma 56 0.037
506
SPN041 Spinal Cord Disease 56 0.037
507
ANS011 Anus Cancer 56 0.037
508
HMG005 Hemoglobinopathy 56 0.037
509
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.037
510
BRN012 Bronchiolitis Obliterans 55 0.037
511
HYP005 Hypokalemia 55 0.037
512
ZLL002 Zollinger-Ellison Syndrome 55 0.037
513
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.037
514
JVN009 Juvenile Pilocytic Astrocytoma 55 0.037
515
SMT008 Smith-Magenis Syndrome 54 0.037
516
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.037
517
PSD007 Pseudomyxoma Peritonei 54 0.037
518
ANL018 Analbuminemia 54 0.037
519
PPL022 Papilloma 54 0.037
520
PLM012 Pulmonary Sarcoidosis 53 0.037
521
P MNC007 Monocytic Leukemia 53 0.037
522
P CNT005 Central Nervous System Lymphoma 53 0.037
523
c PSR017 Psoriasis 2 53 0.037
524
P INT068 Intestinal Disease 53 0.037
525
c MCR113 Microvascular Complications of Diabetes 3 52 0.037
526
SMT003 Somatostatinoma 52 0.037
527
c PSR023 Psoriasis 1 52 0.037
528
INV006 Inverted Papilloma 52 0.037
529
SRS001 Serous Cystadenocarcinoma 52 0.037
530
PNG002 Pain Agnosia 51 0.037
531
ILS001 Ileus 51 0.037
532
CLR109 Colorectal Adenocarcinoma 51 0.037
533
CYS014 Cystadenocarcinoma 51 0.037
534
c PRM012 Primary Polycythemia 50 0.037
535
P SML016 Small Intestine Cancer 50 0.037
536
P PRT096 Peritoneal Mesothelioma 50 0.037
537
THY125 Thyroid Gland Medullary Carcinoma 50 0.037
538
MCP006 Mucoepidermoid Carcinoma 50 0.037
539
P PNB001 Pineoblastoma 50 0.037
540
VPM001 Vipoma 50 0.037
541
CLR003 Clear Cell Adenocarcinoma 50 0.037
542
HRT011 Heart Septal Defect 50 0.037
543
c THR090 Thrombocythemia 1 49 0.037
544
VRR004 Verrucous Carcinoma 49 0.037
545
GST049 Gastrointestinal System Cancer 49 0.037
546
OLF005 Olfactory Neuroblastoma 48 0.037
547
P SCL009 Sclerosing Cholangitis 48 0.037
548
VTM033 Vitamin K Deficiency Bleeding 48 0.037
549
c PRM226 Primary Central Nervous System Lymphoma 48 0.037
550
SPH010 Sphingolipidosis 47 0.037
551
c PSR032 Psoriasis 11 47 0.037
552
c MCR120 Microvascular Complications of Diabetes 7 47 0.037
553
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.037
554
c INH020 Inherited Metabolic Disorder 47 0.037
555
SRT004 Serotonin Syndrome 47 0.037
556
GST071 Gastrointestinal Carcinoma 47 0.037
557
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.037
558
P CHR573 Choroid Plexus Cancer 46 0.037
559
END031 Endometrial Stromal Sarcoma 46 0.037
560
SBP004 Subependymoma 46 0.037
561
SQM002 Squamous Cell Papilloma 46 0.037
562
BNS007 Bone Sarcoma 45 0.037
563
GST030 Gastrinoma 45 0.037
564
CRB004 Cerebral Artery Occlusion 45 0.037
565
PNC056 Pineocytoma 45 0.037
566
GLC036 Glucagonoma 45 0.037
567
CNT017 Central Nervous System Origin Vertigo 45 0.037
568
c CLR017 Clear Cell Sarcoma 45 0.037
569
MXD023 Mixed Cell Type Cancer 44 0.037
570
CYS009 Cystadenoma 44 0.037
571
APP009 Appendix Adenocarcinoma 44 0.037
572
c PCH010 Pachyonychia Congenita 3 44 0.037
573
c ADL023 Adult Medulloblastoma 44 0.037
574
MRG013 Mirage Syndrome 43 0.037
575
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.037
576
ILC002 Ileocolitis 43 0.037
577
URM005 Uremic Pruritus 42 0.037
578
c PSR028 Psoriasis 7 42 0.037
579
49X006 49, Xxxxy Syndrome 41 0.037
580
c MCR130 Microvascular Complications of Diabetes 6 41 0.037
581
c MCR133 Microvascular Complications of Diabetes 4 41 0.037
582
DFF003 Diffuse Scleroderma 41 0.037
583
PNL014 Pineal Gland Cancer 41 0.037
584
c PSR018 Psoriasis 13 41 0.037
585
P RRT020 Rare Tumor 41 0.037
586
KDN007 Kidney Clear Cell Sarcoma 40 0.037
587
ADN013 Adenoid Squamous Cell Carcinoma 40 0.037
588
NDL003 Nodular Nonsuppurative Panniculitis 39 0.037
589
CRN020 Coronary Restenosis 39 0.037
590
PNC008 Pancreatic Endocrine Carcinoma 39 0.037
591
WLL004 Wallerian Degeneration 39 0.037
592
P MNN007 Meningocele 39 0.037
593
NDL024 Nodal Marginal Zone Lymphoma 38 0.037
594
ADR022 Adrenomyeloneuropathy 38 0.037
595
NCR002 Necrobiosis Lipoidica 38 0.037
596
KDN002 Kidney Rhabdoid Cancer 38 0.037
597
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.037
598
PNC016 Pancreatic Cholera 37 0.037
599
SYS071 Systemic Autoimmune Disease 37 0.037
600
NRS005 Neurosarcoidosis 36 0.037
601
HMM005 Hemimelia 35 0.037
602
UTR042 Uterus Leiomyosarcoma 35 0.037
603
OLG006 Oligoastrocytoma 35 0.037
604
LCL004 Localized Osteosarcoma 35 0.037
605
SML014 Small Intestine Leiomyosarcoma 34 0.037
606
MYC088 Mycobacterium Avium Complex Infections 29 0.037
607
PPM002 Ppoma 29 0.037
608
ANG037 Angiomatosis 28 0.037
609
LRY011 Larynx Verrucous Carcinoma 28 0.037
610
P CNT036 Central Nervous System Germ Cell Tumor 28 0.037
611
PDT027 Pediatric Ulcerative Colitis 28 0.037
612
CYT018 Cytochrome P450 2d6 Variant 27 0.037
613
URT040 Urethral Cancer 23 0.037
614
HDG004 Hodgkin's Granuloma 23 0.037
615
HDG006 Hodgkin's Paragranuloma 22 0.037
616
c ADL025 Adult Pineoblastoma 20 0.037
617
c ADL018 Adult Choroid Plexus Cancer 17 0.037
618
JSS002 Jessner Lymphocytic Infiltration of the Skin 16 0.037
619
c PST032 Posterior Urethra Cancer 15 0.037
620
SML040 Smoldering Systemic Mastocytosis 13 0.037
621
c ANT014 Anterior Urethra Cancer 13 0.037
622
TRN058 Transitional Cell Cancer of the Renal Pelvis and Ureter 12 0.037
623
ESC006 Esco2 Spectrum Disorder 9 0.037
624
c HYP595 Hypertension, Essential 84 0.030
625
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.030
626
LPT014 Leptin Deficiency or Dysfunction 74 0.030
627
c BTT014 Beta-Thalassemia 74 0.030
628
VNH007 Von Hippel-Lindau Syndrome 73 0.030
629
c HYP836 Hypercholesterolemia, Familial, 1 73 0.030
630
P RTN024 Retinoblastoma 73 0.030
631
c HPT073 Hepatitis C Virus 72 0.030
632
P PHC003 Pheochromocytoma 71 0.030
633
PLM001 Pulmonary Tuberculosis 69 0.030
634
P MYS003 Myasthenia Gravis 68 0.030
635
RCK004 Rickets 68 0.030
636
ANG054 Angina Pectoris 66 0.030
637
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.030
638
c WLM013 Wilms Tumor 1 65 0.030
639
BRC012 Brucellosis 64 0.030
640
P PRD008 Periodontitis 64 0.030
641
P RHB003 Rhabdomyosarcoma 63 0.030
642
LSH001 Leishmaniasis 63 0.030
643
CNT061 Conotruncal Heart Malformations 63 0.030
644
TRN015 Transient Cerebral Ischemia 63 0.030
645
c FNC043 Fanconi Anemia, Complementation Group E 62 0.030
646
BLL006 Bullous Pemphigoid 62 0.030
647
P ART023 Arthropathy 62 0.030
648
CHL068 Cholestasis 61 0.030
649
P DRM010 Dermatomyositis 61 0.030
650
HYP066 Hyperglycemia 61 0.030
651
FTT001 Fatty Liver Disease 61 0.030
652
c WLM018 Wilms Tumor 5 61 0.030
653
SZR001 Sezary's Disease 60 0.030
654
P SCL018 Scoliosis 60 0.030
655
HPT019 Hepatic Encephalopathy 60 0.030
656
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.030
657
P ALP009 Alopecia Areata 60 0.030
658
P ATR010 Atrial Heart Septal Defect 60 0.030
659
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.030
660
P PTN014 Patent Ductus Arteriosus 1 60 0.030
661
DSS008 Disease of Mental Health 58 0.030
662
P BNC003 Bone Cancer 58 0.030
663
PMP006 Pemphigus Vulgaris, Familial 57 0.030
664
P HDC001 Headache 57 0.030
665
c ACT075 Acute Myocardial Infarction 57 0.030
666
BLR008 Bilirubin Metabolic Disorder 57 0.030
667
P ADL017 Adult T-Cell Leukemia 56 0.030
668
c ACT134 Acute Liver Failure 56 0.030
669
ATR057 Atrioventricular Block 55 0.030
670
LMB062 Limb Ischemia 55 0.030
671
CPL003 Capillary Leak Syndrome 55 0.030
672
INT007 Intermediate Coronary Syndrome 55 0.030
673
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.030
674
CLF004 Cleft Lip/palate 54 0.030
675
RSC001 Rosacea 54 0.030
676
HMN009 Hemangioblastoma 54 0.030
677
PLM010 Pulmonary Edema 54 0.030
678
P ART021 Arteriosclerosis 54 0.030
679
CLR030 Clear Cell Renal Cell Carcinoma 53 0.030
680
BRN038 Bronchial Disease 53 0.030
681
P ORL007 Oral Cavity Cancer 53 0.030
682
FNG017 Fungal Infectious Disease 53 0.030
683
c FML008 Familial Retinoblastoma 53 0.030
684
CLB010 Coloboma of Macula 52 0.030
685
c VRL010 Viral Hepatitis 52 0.030
686
IMP005 Impotence 52 0.030
687
P MSC003 Muscular Atrophy 52 0.030
688
P NRC002 Narcolepsy 52 0.030
689
P THY032 Thyroiditis 52 0.030
690
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.030
691
THR016 Thrombophlebitis 51 0.030
692
P CPL006 Capillary Hemangioma 51 0.030
693
CCT002 Cicatricial Pemphigoid 51 0.030
694
P HYP077 Hypertrichosis 50 0.030
695
RTN003 Retinal Ischemia 50 0.030
696
BRN009 Burning Mouth Syndrome 50 0.030
697
PRT018 Portal Vein Thrombosis 50 0.030
698
NTR046 Neutrophil Migration 50 0.030
699
PDT042 Pediatric Hepatocellular Carcinoma 49 0.030
700
ADR016 Adrenal Cortical Carcinoma 48 0.030
701
MCR020 Microsporidiosis 48 0.030
702
CHL056 Cheilitis 48 0.030
703
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 0.030
704
PYL006 Pyloric Stenosis 48 0.030
705
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.030
706
ADR040 Adrenal Gland Pheochromocytoma 46 0.030
707
INT253 Intestinal Benign Neoplasm 45 0.030
708
HMR023 Hemorrhagic Cystitis 45 0.030
709
HPT004 Hepatic Coma 45 0.030
710
PRL008 Paralytic Ileus 45 0.030
711
MLK003 Melkersson-Rosenthal Syndrome 45 0.030
712
THR099 Third-Degree Atrioventricular Block 45 0.030
713
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.030
714
TBR006 Tuberculoid Leprosy 44 0.030
715
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.030
716
P PRM001 Primary Cutaneous Amyloidosis 44 0.030
717
RFR003 Refractive Error 43 0.030
718
ORL015 Oral Squamous Cell Carcinoma 43 0.030
719
MCR103 Microtia 43 0.030
720
P AVS003 Avascular Necrosis 42 0.030
721
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.030
722
c MLG079 Malignant Pleural Mesothelioma 42 0.030
723
P KLZ004 Kala-Azar 1 41 0.030
724
P HYP009 Hypertrophic Pyloric Stenosis 41 0.030
725
PST053 Postherpetic Neuralgia 40 0.030
726
THR035 Thrombasthenia 40 0.030
727
ANG049 Angioedema Induced by Ace Inhibitors 40 0.030
728
ERM002 Ear Malformation 39 0.030
729
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.030
730
ORF044 Orofacial Granulomatosis 38 0.030
731
PLY010 Polyclonal Hypergammaglobulinemia 38 0.030
732
SHW001 Shwartzman Phenomenon 37 0.030
733
c WLM011 Wilms Tumor 6 37 0.030
734
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.030
735
FBR002 Fibrosarcoma of Bone 34 0.030
736
VRT016 Vertebral Anomalies and Variable Endocrine and T-Cell Dysfunction 34 0.030
737
c LKM005 Leukemia, T-Cell, Chronic 34 0.030
738
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.030
739
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 33 0.030
740
SML011 Smoldering Myeloma 33 0.030
741
EXF003 Exfoliative Dermatitis 27 0.030
742
NCR009 Necrobiotic Xanthogranuloma 26 0.030
743
MCR093 Microtia-Anotia 25 0.030
744
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.030
745
CNG529 Congenital Femoral Deficiency 15 0.030
747
RFR001 Refractory Plasma Cell Neoplasm 10 0.030
748
NRL016 Neural Tube Defects 82 0.021
749
P ATX030 Ataxia-Telangiectasia 82 0.021
750
c FNC027 Fanconi Anemia, Complementation Group a 81 0.021
751
c DLT002 Dilated Cardiomyopathy 79 0.021
752
INS024 Insulin-Like Growth Factor I 79 0.021
753
CRV035 Cervical Cancer 76 0.021
754
c ATR087 Atrial Standstill 1 75 0.021
755
P RSP003 Respiratory Failure 74 0.021
756
SCK003 Sickle Cell Anemia 74 0.021
757
P OST002 Osteoporosis 74 0.021
758
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.021
759
P MLT020 Multiple Sclerosis 72 0.021
760
c EXD008 Exudative Vitreoretinopathy 1 71 0.021
761
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.021
762
P ANG001 Angelman Syndrome 69 0.021
763
NVS017 Nevus, Epidermal 68 0.021
764
BRN024 Bronchitis 68 0.021
765
CNN005 Connective Tissue Disease 68 0.021
766
P CRD119 Cardiac Arrest 67 0.021
767
P HLP001 Holoprosencephaly 67 0.021
768
ALL003 Allergic Rhinitis 67 0.021
769
P PRP003 Porphyria Cutanea Tarda 67 0.021
770
c ATS007 Autism Spectrum Disorder 67 0.021
771
c MGR028 Migraine with or Without Aura 1 67 0.021
772
LPT001 Leptospirosis 66 0.021
773
ALC007 Alcohol Dependence 66 0.021
774
P DMN002 Dementia 66 0.021
775
GLN010 Glanzmann Thrombasthenia 66 0.021
776
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.021
777
ART001 Arterial Tortuosity Syndrome 66 0.021
778
HYP056 Hypoglycemia 66 0.021
779
AND002 Androgen Insensitivity Syndrome 66 0.021
780
CHG001 Chagas Disease 66 0.021
781
CNC002 Cinca Syndrome 65 0.021
782
PPL049 Papillon-Lefevre Syndrome 65 0.021
783
MSM014 Mismatch Repair Cancer Syndrome 65 0.021
784
BRR014 Barrett Esophagus 65 0.021
785
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.021
786
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.021
787
NRF007 Neurofibroma 64 0.021
788
CLF027 Cleft Palate, Isolated 64 0.021
789
PLM031 Poliomyelitis 64 0.021
790
MGK001 Megakaryocytic Leukemia 64 0.021
791
OST017 Osteomyelitis 64 0.021
792
KRN002 Kearns-Sayre Syndrome 63 0.021
793
BLS001 Blau Syndrome 63 0.021
794
P ANR048 Aniridia 1 63 0.021
795
P VSC007 Vascular Disease 63 0.021
796
c MLG084 Malignant Fibrous Histiocytoma 63 0.021
797
P SHR029 Short Syndrome 63 0.021
798
PTR032 Peters-Plus Syndrome 63 0.021
799
c ACT068 Acute Cystitis 63 0.021
800
ANR007 Anorexia Nervosa 63 0.021
801
c LCL006 Localized Scleroderma 62 0.021
802
LPD008 Lipid Metabolism Disorder 62 0.021
803
P TRC086 Trichohepatoenteric Syndrome 1 62 0.021
804
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.021
805
P ACR001 Aicardi-Goutieres Syndrome 62 0.021
806
HSH003 Hashimoto Thyroiditis 62 0.021
807
P PRP029 Porphyria 62 0.021
808
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.021
809
RCT015 Reactive Arthritis 61 0.021
810
RTN017 Retinal Detachment 61 0.021
811
NRL005 Neurilemmoma 60 0.021
812
PTN001 Patent Foramen Ovale 60 0.021
813
RGH009 Right Atrial Isomerism 60 0.021
814
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.021
815
P TXP001 Toxoplasmosis 60 0.021
816
ACN002 Acanthosis Nigricans 60 0.021
817
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.021
818
P CTR002 Cataract 60 0.021
819
ING001 Inguinal Hernia 60 0.021
820
STT001 Status Epilepticus 60 0.021
821
SPP011 Suppression of Tumorigenicity 12 59 0.021
822
P AXN002 Axenfeld-Rieger Syndrome 59 0.021
823
P GLL022 Guillain-Barre Syndrome 59 0.021
824
CRY005 Cryptococcosis 58 0.021
825
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.021
826
c CHL140 Chilblain Lupus 1 58 0.021
827
CRD132 Cardiac Conduction Defect 58 0.021
828
CHR072 Chordoma 58 0.021
829
c BNG091 Benign Chronic Pemphigus 58 0.021
830
CNT047 Contact Dermatitis 58 0.021
831
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.021
832
P URT039 Urticaria 58 0.021
833
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.021
834
ADL030 Adult-Onset Still's Disease 58 0.021
835
CHL028 Childhood Type Dermatomyositis 58 0.021
836
P CND004 Candidiasis 58 0.021
837
EXT034 Extrinsic Allergic Alveolitis 58 0.021
838
P OPT009 Optic Neuritis 57 0.021
839
CHL067 Cholecystitis 57 0.021
840
P RHN004 Rhinitis 57 0.021
841
MBS002 Moebius Syndrome 57 0.021
842
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 57 0.021
843
FCT006 Factor V Deficiency 57 0.021
844
SCH014 Schistosomiasis 57 0.021
845
PHR003 Pharyngitis 57 0.021
846
P ANG015 Angioedema 57 0.021
847
P MYS005 Myositis 56 0.021
848
TRN018 Transitional Cell Carcinoma 56 0.021
849
ERY051 Erythroleukemia, Familial 56 0.021
850
ALL010 Allergic Contact Dermatitis 56 0.021
851
ANN002 Anencephaly 56 0.021
852
P NRF002 Neurofibromatosis 56 0.021
853
MCR141 Mucormycosis 56 0.021
854
AGN016 Aging 56 0.021
855
P GST044 Gastritis 56 0.021
856
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.021
857
MMB001 Membranoproliferative Glomerulonephritis 55 0.021
858
VSC003 Visceral Leishmaniasis 55 0.021
859
P PTT006 Pituitary Adenoma 55 0.021
860
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.021
861
HDR002 Hidradenitis Suppurativa 55 0.021
862
P HYP076 Hyperthyroidism 55 0.021
863
P ALP106 Alport Syndrome 1, X-Linked 55 0.021
864
P VNS003 Venous Insufficiency 55 0.021
865
P DBT005 Diabetes Insipidus 55 0.021
866
HRY003 Hairy Cell Leukemia 55 0.021
867
GNT003 Genital Herpes 54 0.021
868
SYN007 Synovitis 54 0.021
869
P JNC001 Junctional Epidermolysis Bullosa 54 0.021
870
P SPN052 Spondyloarthropathy 54 0.021
871
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.021
872
RFL001 Reflex Sympathetic Dystrophy 54 0.021
873
THR013 Thoracic Outlet Syndrome 54 0.021
874
c PST005 Posterior Uveitis 54 0.021
875
NNL006 Non-Alcoholic Steatohepatitis 54 0.021
876
LYM022 Lymphangioma 54 0.021
877
P BRC006 Brachydactyly 53 0.021
878
CRY001 Cryptogenic Organizing Pneumonia 53 0.021
879
NVS001 Neovascular Glaucoma 53 0.021
880
LTR009 Lateral Meningocele Syndrome 53 0.021
881
GST023 Gastric Ulcer 53 0.021
882
c CNT035 Central Nervous System Disease 52 0.021
883
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.021
884
P PRG013 Paraganglioma 52 0.021
885
PRP016 Paraplegia 52 0.021
886
GLM004 Gliomatosis Cerebri 52 0.021
887
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.021
888
SCH002 Schnitzler Syndrome 52 0.021
889
P PRR016 Pierre Robin Syndrome 52 0.021
890
HYP088 Hyper-Igd Syndrome 52 0.021
891
THR009 Thrombocytopenia-Absent Radius Syndrome 52 0.021
892
LMY002 Leiomyoma 52 0.021
893
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.021
894
MCR088 Microscopic Polyangiitis 51 0.021
895
LNG095 Lung Abscess 51 0.021
896
ANK001 Ankylosis 51 0.021
897
INT079 Intrahepatic Cholangiocarcinoma 51 0.021
898
TRM010 Traumatic Brain Injury 51 0.021
899
P PRC012 Pericardial Effusion 51 0.021
900
BLL003 Bell's Palsy 51 0.021
901
FBR008 Fibrillary Astrocytoma 51 0.021
902
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.021
903
INT071 Intestinal Perforation 51 0.021
904
SCH012 Schizoaffective Disorder 50 0.021
905
P OVR082 Overgrowth Syndrome 50 0.021
906
P ESN008 Eosinophilic Pneumonia 50 0.021
907
P SCK005 Sickle Cell Disease 50 0.021
908
P PNV001 Panuveitis 50 0.021
909
c LRG001 Large Cell Carcinoma 50 0.021
910
DYS073 Dysphagia 50 0.021
911
RNL078 Renal Dysplasia 50 0.021
912
HYP017 Hypophosphatemia 50 0.021
913
c ACQ017 Acquired Von Willebrand Syndrome 49 0.021
914
ENT004 Enthesopathy 49 0.021
915
PPL021 Papilledema 49 0.021
916
P CRV039 Cervicitis 49 0.021
917
P ART018 Aortic Valve Insufficiency 49 0.021
918
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.021
919
HDR003 Hidradenitis 49 0.021
920
WHP001 Whipple Disease 49 0.021
921
MNN009 Meningoencephalitis 49 0.021
922
P NML001 Nemaline Myopathy 49 0.021
923
SPN405 Spondyloepiphyseal Dysplasia Tarda, X-Linked 49 0.021
924
P CTN015 Cutaneous T Cell Lymphoma 49 0.021
925
WTH001 Withdrawal Disorder 48 0.021
926
ATS010 Autosomal Recessive Disease 48 0.021
927
CLC006 Calcinosis 48 0.021
928
HPT009 Hepatopulmonary Syndrome 48 0.021
929
RGH001 Right Bundle Branch Block 48 0.021
930
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.021
931
P SCL015 Scleritis 48 0.021
932
DGN001 Degenerative Disc Disease 48 0.021
933
P LYM024 Lymphatic System Disease 48 0.021
934
HMP001 Hemopericardium 48 0.021
935
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.021
936
RDT013 Radiation Proctitis 47 0.021
937
CHR031 Chromoblastomycosis 47 0.021
938
MCC002 Mucocutaneous Leishmaniasis 47 0.021
940
CLN019 Colonic Disease 47 0.021
941
P INN002 Inner Ear Disease 47 0.021
942
AST006 Astigmatism 47 0.021
943
RNL077 Renal Fibrosis 47 0.021
944
P DNR001 Duane Retraction Syndrome 47 0.021
945
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.021
946
CHR074 Choriocarcinoma 47 0.021
947
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 47 0.021
948
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.021
949
SMT001 Somatization Disorder 46 0.021
950
FLL008 Folliculitis 46 0.021
951
P MTH007 Methemoglobinemia 46 0.021
952
OBS004 Obstructive Hydrocephalus 46 0.021
953
EPD015 Epidemic Typhus 45 0.021
954
URT010 Ureteral Obstruction 45 0.021
955
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.021
956
SYN005 Synostosis 45 0.021
957
URL001 Urolithiasis 45 0.021
958
NNS002 Nonspecific Interstitial Pneumonia 45 0.021
959
P RDL002 Radioulnar Synostosis 45 0.021
960
CRT015 Carotid Artery Occlusion 45 0.021
961
ATN004 Autonomic Neuropathy 45 0.021
962
c JVN003 Juvenile Xanthogranuloma 44 0.021
963
c DRM054 Dermatitis, Atopic, 2 44 0.021
964
LRY022 Laryngoonychocutaneous Syndrome 44 0.021
965
PLX002 Plexiform Neurofibroma 44 0.021
966
c MCR137 Microphthalmia, Isolated 2 44 0.021
967
SPN119 Spondylarthropathy 44 0.021
968
THR012 Thoracic Cancer 44 0.021
969
HPT082 Hepatic Adenomas, Familial 44 0.021
970
BCT021 Bacterial Sepsis 44 0.021
971
GRN007 Granuloma Annulare 44 0.021
972
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.021
973
LVR002 Liver Angiosarcoma 43 0.021
974
P CRN026 Corneal Edema 43 0.021
975
P DMY001 Demyelinating Polyneuropathy 43 0.021
976
HMP009 Haemophilus Influenzae 43 0.021
977
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.021
978
DRG024 Drug Allergy 42 0.021
979
GST105 Gastroesophageal Adenocarcinoma 42 0.021
980
MNN017 Mononeuropathy 42 0.021
981
BCK006 Back Pain 42 0.021
982
SKN023 Skin Tag 42 0.021
983
FBR019 Fibromatosis 41 0.021
984
PHB001 Phobic Disorder 41 0.021
985
TTT001 Tatton-Brown-Rahman Syndrome 41 0.021
986
PLY021 Polyradiculopathy 41 0.021
987
PCD001 Pica Disease 41 0.021
988
KLB003 Klebsiella Pneumonia 41 0.021
989
MRP001 Morphine Dependence 41 0.021
990
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.021
991
OST115 Osteonecrosis of the Jaw 40 0.021
992
c HYP072 Hypersensitivity Reaction Type Iii Disease 40 0.021
993
IVC001 Ivic Syndrome 40 0.021
994
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 40 0.021
995
GLC008 Glucose Metabolism Disease 40 0.021
996
KLD004 Keloid Disorder 40 0.021
997
SPN221 Spina Bifida Occulta 39 0.021
998
CNT007 Central Nervous System Tuberculosis 39 0.021
999
ALG001 Algoneurodystrophy 39 0.021
1000
ADR004 Adrenal Cortical Adenocarcinoma 39 0.021
1001
MLT016 Multicentric Reticulohistiocytosis 39 0.021
1002
ADP007 Adie Pupil 39 0.021
1003
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.021
1004
FML039 Female Reproductive System Disease 39 0.021
1005
MTR007 Motor Peripheral Neuropathy 39 0.021
1006
c THR111 Thrombocytopenia 3 38 0.021
1007
LWG005 Low-Grade Astrocytoma 38 0.021
1008
ESN006 Eosinophilic Meningitis 38 0.021
1009
ERY017 Erythema Elevatum Diutinum 38 0.021
1010
c MLG157 Malignant Pheochromocytoma 38 0.021
1011
PRP005 Parapsoriasis 38 0.021
1012
OPT010 Optic Papillitis 38 0.021
1013
CDQ001 Cauda Equina Syndrome 38 0.021
1014
ACR005 Acrodermatitis 38 0.021
1015
CRT004 Carotid Artery Thrombosis 38 0.021
1016
BRS004 Breast Angiosarcoma 38 0.021
1017
P PST059 Pustular Psoriasis 37 0.021
1018
AML066 Amelia, Posterior, with Pelvic and Pulmonary Hypoplasia Syndrome 37 0.021
1019
BRN048 Brain Stem Cancer 37 0.021
1020
BLN010 Balanitis 37 0.021
1021
CHR463 Chronic Actinic Dermatitis 37 0.021
1022
SPN331 Spondyloocular Syndrome 36 0.021
1023
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 36 0.021
1024
PLC002 Plica Syndrome 36 0.021
1025
HYP114 Hypertensive Nephropathy 36 0.021
1026
P IDP049 Idiopathic Anterior Uveitis 35 0.021
1027
END072 Endotheliitis 35 0.021
1028
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.021
1029
ATX010 Ataxia Neuropathy Spectrum 34 0.021
1030
MRC002 Marcus Gunn Phenomenon 34 0.021
1031
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.021
1032
c ACQ047 Acquired Methemoglobinemia 34 0.021
1033
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.021
1035
TFR002 Tafro Syndrome 34 0.021
1036
SPN029 Spondylolysis 33 0.021
1037
ALR002 Al-Raqad Syndrome 33 0.021
1038
NNS011 Nonseminomatous Germ Cell Tumor 33 0.021
1039
ACT064 Acute Necrotizing Encephalitis 33 0.021
1040
P CXV002 Coxa Vara 33 0.021
1041
LYM095 Lymphangiomatosis 33 0.021
1042
ORL022 Oral Erosive Lichen 33 0.021
1043
SBV001 Subvalvular Aortic Stenosis 33 0.021
1044
KDN013 Kidney Hypertrophy 32 0.021
1045
c BLD140 Blood Group, I System 32 0.021
1046
RDT001 Radiation Cystitis 32 0.021
1047
PNC059 Punctate Inner Choroidopathy 32 0.021
1048
HGH041 High-Grade Astrocytoma 32 0.021
1049
P RRL003 Rare Lymphatic Malformation 31 0.021
1050
c THR048 Thrombocytopenia 4 31 0.021
1051
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.021
1052
TBL008 Tibial Hemimelia 31 0.021
1053
P ACT028 Acute Closed-Angle Glaucoma 30 0.021
1054
ISL119 Isolated Optic Neuritis 30 0.021
1055
c BNG001 Benign Peritoneal Mesothelioma 30 0.021
1056
FSS001 Fissured Tongue 30 0.021
1057
c INF077 Inflammatory Bowel Disease 19 30 0.021
1058
ANS025 Anus Benign Neoplasm 30 0.021
1059
EPT011 Epithelioid Leiomyosarcoma 30 0.021
1060
MRL006 Meralgia Paraesthetica, Familial 29 0.021
1061
CYS041 Cystic Angiomatosis of Bone, Diffuse 28 0.021
1062
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.021
1063
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.021
1064
EXT059 External Auditory Canal, Bilateral Atresia of, with Congenital Vertical Talus 27 0.021
1065
FBL014 Fibular Hemimelia 27 0.021
1066
ARG006 Aregenerative Anemia 27 0.021
1067
HNM002 Hinman Syndrome 27 0.021
1068
PSD026 Pseudoainhum 27 0.021
1069
BRW006 Brown Syndrome 26 0.021
1070
c CTR182 Cataract 23, Multiple Types 25 0.021
1071
ULN023 Ulnar Hypoplasia 25 0.021
1072
ESN016 Eosinophilic Pustular Folliculitis 25 0.021
1073
ADG002 Audiogenic Seizures 25 0.021
1074
c DMN005 Diamond-Blackfan Anemia 2 25 0.021
1075
UND004 Undetermined Colitis 24 0.021
1076
MCN011 Mucinoses 24 0.021
1077
CRR012 Cirrhotic Cardiomyopathy 24 0.021
1078
c RRH015 Rare Hemorrhagic Disorder 23 0.021
1079
c DKP001 Dk Phocomelia Syndrome 23 0.021
1080
CNG092 Congenital Extrahepatic Portosystemic Shunt 23 0.021
1081
OST008 Osteosclerotic Myeloma 23 0.021
1082
P HYD015 Hydroa Vacciniforme 22 0.021
1083
PLS037 Plasma Cell Tumor 22 0.021
1084
ISL019 Isolated Duane Retraction Syndrome 22 0.021
1085