Search results for Platinum compounds

651 hits were found for Platinum compounds

# Family MCID Name MIFTS Score
1
P OVR042 Ovarian Cancer 88 0.799
2
P LNG032 Lung Cancer 98 0.573
3
c SML038 Small Cell Cancer of the Lung 65 0.489
4
P NTR004 Neutropenia 63 0.451
5
OVR094 Ovarian Epithelial Cancer 38 0.448
6
c OVR114 Ovarian Cancer 1 38 0.358
7
LNG031 Lung Benign Neoplasm 51 0.303
8
48X005 48,xyyy 39 0.278
9
DWN001 Down Syndrome 70 0.271
10
P NRP001 Neuropathy 56 0.264
11
FLL027 Fallopian Tube Carcinoma 67 0.260
12
P ADN016 Adenocarcinoma 64 0.257
13
ALL026 Allergic Hypersensitivity Disease 62 0.245
14
P CLR023 Colorectal Cancer 99 0.240
15
P BLD134 Bladder Cancer 79 0.237
16
SQM006 Squamous Cell Carcinoma 60 0.231
17
P PRP019 Peripheral Nervous System Disease 58 0.229
18
P BRS047 Breast Cancer 97 0.221
19
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.219
20
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.216
21
P THR014 Thrombocytopenia 67 0.216
22
CRV035 Cervical Cancer 76 0.210
23
P ALP008 Alopecia 54 0.208
24
P LNG064 Lung Cancer Susceptibility 3 78 0.204
25
P GST053 Gastric Cancer 83 0.196
26
P NRB001 Neuroblastoma 72 0.193
27
ANR040 Aneurysm 59 0.189
28
HRW001 Hair Whorl 36 0.188
29
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.187
30
OST159 Osteogenic Sarcoma 66 0.185
31
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.185
32
c PRM038 Primary Agammaglobulinemia 44 0.185
33
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.184
34
MCS002 Mucositis 56 0.181
35
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.179
36
ESP021 Esophageal Cancer 90 0.178
37
c RHB024 Rhabdomyosarcoma 2 67 0.175
38
GLB015 Glioblastoma Multiforme 75 0.172
39
P DRR001 Diarrhea 55 0.171
40
P EXN002 Exanthem 57 0.170
41
P GLM045 Glioma 63 0.169
42
GLL048 Glial Tumor 45 0.167
43
END057 Endometrial Cancer 74 0.163
44
P PNC035 Pancreatic Cancer 84 0.161
45
TRN018 Transitional Cell Carcinoma 56 0.158
46
P HPT023 Hepatocellular Carcinoma 100 0.158
47
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.157
48
P BNG032 Benign Mesothelioma 46 0.154
49
47X002 47,xyy 49 0.149
50
P SPP010 Suppressor of Tumorigenicity 3 51 0.148
51
STM007 Stomatitis 50 0.148
52
TST014 Testicular Cancer 46 0.148
53
CNS004 Constipation 58 0.146
54
P NSP012 Nasopharyngeal Carcinoma 66 0.145
55
FCT007 Factor Vii Deficiency 67 0.144
56
c PCH010 Pachyonychia Congenita 3 44 0.143
57
P PRS040 Prostate Cancer 97 0.141
58
DRM006 Dermatitis 61 0.136
59
P BRS044 Breast Adenocarcinoma 59 0.136
60
HLX001 Helix Syndrome 47 0.132
61
P LKM002 Leukemia 68 0.132
62
SNS003 Sensory Peripheral Neuropathy 54 0.127
63
CNT047 Contact Dermatitis 58 0.126
64
LNG099 Lung Disease 60 0.125
65
P TRN020 Turner Syndrome 67 0.122
66
P FBR017 Fibrosarcoma 56 0.122
67
P LYM118 Lymphoma 68 0.121
68
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.121
69
P ALZ034 Alzheimer Disease 88 0.120
70
SRS001 Serous Cystadenocarcinoma 52 0.119
71
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.118
72
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.115
73
P CRN300 Coronary Heart Disease 1 63 0.115
74
DFC004 Deficiency Anemia 70 0.114
75
LSH001 Leishmaniasis 63 0.114
76
P KLZ004 Kala-Azar 1 41 0.114
77
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.114
78
CYS014 Cystadenocarcinoma 51 0.113
79
c MLG079 Malignant Pleural Mesothelioma 42 0.113
80
P BCL017 B-Cell Lymphoma 58 0.112
81
HYP066 Hyperglycemia 61 0.112
82
P KDN018 Kidney Disease 72 0.111
83
P SML001 Small Cell Carcinoma 52 0.111
84
GST040 Gastric Adenocarcinoma 70 0.109
85
P MLN008 Melanoma 69 0.108
86
SPN035 Spindle Cell Sarcoma 53 0.107
87
CHG001 Chagas Disease 66 0.107
88
P MYL006 Myeloid Leukemia 60 0.107
89
SRC014 Sarcoma 65 0.107
90
ATH013 Atherosclerosis Susceptibility 65 0.106
91
LPP008 Lipoprotein Quantitative Trait Locus 62 0.106
92
ATM095 Autoimmune Disease 62 0.106
93
CLN015 Colon Adenocarcinoma 65 0.106
94
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.106
95
c MST023 Mesothelioma, Malignant 57 0.105
96
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.104
97
HYP056 Hypoglycemia 66 0.103
98
P KDN017 Kidney Cancer 60 0.102
99
HMN044 Human Immunodeficiency Virus Type 1 71 0.101
100
P RHN004 Rhinitis 57 0.100
101
CYT002 Cytokine Deficiency 42 0.100
102
BCT022 Bacterial Infectious Disease 56 0.100
103
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.100
104
ART140 Arteries, Anomalies of 52 0.099
105
P THL005 Thalassemia 60 0.098
106
c LKM061 Leukemia, Acute Myeloid 84 0.098
107
HYP266 Hypoxia 57 0.097
108
CRC021 Carcinosarcoma 62 0.097
109
SKN016 Skin Disease 63 0.096
110
GRM005 Germ Cell Cancer 47 0.096
111
LYM019 Lymphosarcoma 46 0.095
112
c SVR001 Severe Acute Respiratory Syndrome 62 0.095
113
P LVR013 Liver Disease 68 0.093
114
PLS011 Plasmacytoma 56 0.092
115
HYP005 Hypokalemia 55 0.092
116
OVR059 Ovary Adenocarcinoma 53 0.091
117
GRN017 Granulocytopenia 44 0.091
118
SVR004 Severe Combined Immunodeficiency 73 0.091
119
c HYP595 Hypertension, Essential 84 0.091
120
ISC004 Ischemia 58 0.091
121
ATX019 Ataxia with Vitamin E Deficiency 42 0.091
122
TRY001 Trypanosomiasis 50 0.090
123
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.090
124
P SNS001 Sensorineural Hearing Loss 60 0.089
125
ORL011 Oral Cancer 60 0.088
126
c NRF023 Neurofibromatosis, Type Ii 80 0.088
128
SMN007 Seminoma 43 0.087
129
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.087
130
HPT022 Hepatoblastoma 56 0.086
131
PLM033 Pulmonary Embolism 59 0.086
132
SFT003 Soft Tissue Sarcoma 56 0.084
133
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.084
134
SKN019 Skin Melanoma 68 0.084
135
P TRT010 Teratoma 52 0.083
136
GRM010 Germ Cells Tumors 34 0.083
137
P ENC018 Encephalopathy 61 0.083
138
P AST007 Astrocytoma 51 0.083
139
MYL069 Myeloma, Multiple 85 0.083
140
ORL015 Oral Squamous Cell Carcinoma 43 0.083
141
PRT037 Pertussis 65 0.082
142
P URT039 Urticaria 58 0.082
143
c BRN108 Branchiootic Syndrome 1 62 0.082
144
P PLY019 Polyneuropathy 56 0.082
145
c ACT071 Acute Kidney Failure 60 0.081
146
ANG054 Angina Pectoris 66 0.081
147
P VSC007 Vascular Disease 63 0.081
148
P RTN024 Retinoblastoma 73 0.080
149
c FML008 Familial Retinoblastoma 53 0.080
150
P ESP024 Esophagitis 62 0.080
151
ALL010 Allergic Contact Dermatitis 56 0.080
152
P SKN015 Skin Carcinoma 66 0.080
153
P HRT032 Heart Disease 75 0.079
154
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.079
155
IRN002 Iron Metabolism Disease 57 0.078
156
BRN028 Brain Cancer 74 0.078
157
P MSC003 Muscular Atrophy 52 0.077
158
P PHC003 Pheochromocytoma 71 0.077
159
ADR040 Adrenal Gland Pheochromocytoma 46 0.077
160
P RHB003 Rhabdomyosarcoma 63 0.077
161
P RCT021 Rectum Cancer 52 0.077
162
TXC002 Toxic Encephalopathy 53 0.077
163
RTC009 Reticulum Cell Sarcoma 43 0.077
164
RTC005 Reticulosarcoma 47 0.077
165
MYL009 Myelodysplastic Syndrome 70 0.076
166
ADL002 Adult Syndrome 70 0.076
167
P LKM062 Leukemia, Acute Lymphoblastic 69 0.076
168
c LKM063 Leukemia, Chronic Myeloid 72 0.076
169
AST006 Astigmatism 47 0.076
170
P LTR001 Lateral Sclerosis 54 0.075
171
P RSP003 Respiratory Failure 74 0.075
172
DYS073 Dysphagia 50 0.075
173
c MLG068 Malignant Glioma 46 0.075
174
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.075
175
TXC005 Toxic Shock Syndrome 62 0.075
176
CLR109 Colorectal Adenocarcinoma 51 0.075
177
THY022 Thymic Carcinoma 57 0.074
178
IGR001 Ige Responsiveness, Atopic 59 0.074
179
FCL012 Facial Paralysis 46 0.074
180
P CRC039 Coarctation of Aorta 47 0.074
181
CHL065 Cholangiocarcinoma 68 0.073
182
P HYD006 Hydrocephalus 66 0.073
183
P DBT009 Diabetes Mellitus 64 0.073
184
P LKM071 Leukemia, Chronic Lymphocytic 79 0.073
185
THR024 Thrombosis 57 0.073
186
P HYP086 Hypothyroidism 69 0.073
187
ACT119 Acute Promyelocytic Leukemia 63 0.072
188
THY029 Thyroid Carcinoma 59 0.072
189
CNG034 Congestive Heart Failure 69 0.072
190
VCC001 Vaccinia 49 0.071
191
HYP080 Hypogonadism 50 0.071
192
c HYP836 Hypercholesterolemia, Familial, 1 73 0.071
193
INT079 Intrahepatic Cholangiocarcinoma 51 0.070
194
PPL022 Papilloma 54 0.070
195
ERY051 Erythroleukemia, Familial 56 0.070
196
ANX010 Anxiety 73 0.070
197
PST092 Posttransplant Acute Limbic Encephalitis 29 0.070
198
P MYC007 Myocardial Infarction 70 0.070
199
LYM027 Lymphopenia 58 0.069
200
RTN023 Retinitis 46 0.069
201
NRR001 Neuroretinitis 42 0.069
202
P SZR006 Seizure Disorder 56 0.069
203
CRB004 Cerebral Artery Occlusion 45 0.069
204
LPD008 Lipid Metabolism Disorder 62 0.069
205
SQM002 Squamous Cell Papilloma 46 0.069
206
INT066 Interstitial Lung Disease 60 0.068
207
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.068
208
HMS001 Hemosiderosis 54 0.068
209
P RHM011 Rheumatoid Arthritis 80 0.068
210
SLP001 Sleeping Sickness 54 0.067
211
P BND020 Bone Disease 59 0.067
212
P GLM040 Glioma Susceptibility 1 81 0.067
213
P MDL005 Medulloblastoma 77 0.067
214
KRT019 Keratitis, Hereditary 65 0.067
215
c ACT073 Acute Leukemia 58 0.067
216
c CHR684 Chronic Kidney Disease 70 0.067
217
P RTN008 Retinitis Pigmentosa 79 0.066
218
IMM167 Immune Deficiency Disease 78 0.066
219
BNR002 Bone Resorption Disease 48 0.066
220
c PRS136 Prostate Cancer, Hereditary, 6 33 0.066
221
c PRS130 Prostate Cancer, Hereditary, 8 32 0.066
222
P CRD246 Cardiovascular System Disease 57 0.066
223
MLR004 Malaria 81 0.065
224
c BTT014 Beta-Thalassemia 74 0.065
225
P TST026 Testicular Germ Cell Cancer 43 0.065
226
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.065
227
LYM133 Lymphoma, Hodgkin, Classic 69 0.065
228
P CNJ013 Conjunctivitis 65 0.065
229
P MLG074 Malignant Mesenchymoma 40 0.064
230
PRT036 Peritonitis 64 0.064
231
URM002 Uremia 49 0.063
232
P OVR082 Overgrowth Syndrome 50 0.063
233
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.063
234
ADN018 Adenoma 59 0.063
235
P PRN023 Prion Disease 57 0.063
236
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.063
237
NRN004 Neuroendocrine Tumor 55 0.063
238
c FNC027 Fanconi Anemia, Complementation Group a 81 0.062
239
BLD131 Bladder Urothelial Carcinoma 62 0.062
240
c LRG001 Large Cell Carcinoma 50 0.062
241
EMB004 Embryonal Carcinoma 56 0.062
242
BLR013 Biliary Tract Cancer 42 0.062
243
IMP005 Impotence 52 0.062
244
P NRV007 Nervous System Disease 66 0.062
245
LVR012 Liver Cirrhosis 62 0.062
246
P RRH023 Rare Hereditary Hemochromatosis 41 0.062
247
CHR074 Choriocarcinoma 47 0.061
248
DFF005 Diffuse Large B-Cell Lymphoma 55 0.061
249
CRV040 Cervix Carcinoma 51 0.061
250
OST012 Osteoarthritis 78 0.061
251
CLT003 Colitis 62 0.061
252
PPT005 Peptic Ulcer Disease 59 0.061
253
P INT070 Intestinal Obstruction 58 0.061
254
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.061
255
RCK004 Rickets 68 0.061
256
ALL006 Allergic Asthma 56 0.061
257
P PTS002 Ptosis 53 0.061
258
P PLM036 Pulmonary Fibrosis 65 0.061
259
VSL002 Visual Epilepsy 59 0.061
260
AGN016 Aging 56 0.061
261
P GST044 Gastritis 56 0.061
262
c BSL007 Basal Cell Carcinoma 68 0.061
263
P CYS018 Cystitis 59 0.060
264
c DWL002 Dowling-Degos Disease 1 58 0.060
265
P INF032 Infertility 57 0.060
266
c XRD022 Xeroderma Pigmentosum, Complementation Group D 58 0.060
267
c DRR009 Diarrhea 6 46 0.060
268
P THY023 Thymoma 65 0.060
269
c THY107 Thymoma, Familial 52 0.060
270
c THR092 Thrombophilia Due to Thrombin Defect 73 0.060
271
INS024 Insulin-Like Growth Factor I 79 0.059
272
P END044 Endometriosis 63 0.059
273
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.059
274
ADR016 Adrenal Cortical Carcinoma 48 0.059
275
ADR004 Adrenal Cortical Adenocarcinoma 39 0.059
276
P CTR002 Cataract 60 0.059
277
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.059
278
SPN186 Spinal Cord Injury 60 0.058
279
CRB039 Cerebrovascular Disease 67 0.058
280
GT001 Gout 64 0.058
281
PNC129 Pancreatic Adenocarcinoma 68 0.058
282
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.058
283
AST005 Asthma 76 0.057
284
P RRT020 Rare Tumor 41 0.057
285
P OVR049 Ovarian Disease 52 0.057
286
HYP017 Hypophosphatemia 50 0.057
287
P HYP750 Hypertriglyceridemia, Familial 62 0.057
288
PRS063 Paresthesia 41 0.056
289
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.056
290
c HPT001 Hepatitis C 62 0.056
291
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.056
292
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.056
293
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.056
294
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.056
295
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.056
296
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.056
297
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.056
298
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.056
299
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.056
300
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.056
301
GST050 Gastrointestinal System Disease 56 0.056
302
c ATR087 Atrial Standstill 1 75 0.055
303
BLR008 Bilirubin Metabolic Disorder 57 0.055
304
HYP060 Hyperinsulinism 54 0.055
305
P KRT007 Keratoconus 50 0.055
306
c ACT068 Acute Cystitis 63 0.054
307
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.054
308
STR067 Stroke, Ischemic 81 0.054
309
P ART005 Arteriovenous Malformation 65 0.054
310
TTN003 Tetanus 65 0.054
311
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.054
312
P ATX030 Ataxia-Telangiectasia 82 0.053
313
GLC003 Glucose Intolerance 54 0.053
314
c LKM005 Leukemia, T-Cell, Chronic 34 0.053
315
P ART022 Arthritis 69 0.053
316
P HYP098 Hypereosinophilic Syndrome 67 0.053
317
ACQ007 Acquired Immunodeficiency Syndrome 60 0.053
318
P PNM007 Pneumonia 68 0.053
319
P CRV031 Cervical Adenocarcinoma 49 0.053
320
TLN003 Telangiectasis 52 0.053
321
P MTH007 Methemoglobinemia 46 0.053
322
c HPT016 Hepatitis B 59 0.053
323
P ANP001 Anaplastic Large Cell Lymphoma 58 0.053
324
EYD002 Eye Disease 58 0.053
325
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.052
326
CHL079 Children's Interstitial Lung Disease 26 0.052
327
PNC001 Pancytopenia 54 0.052
328
HLC007 Helicobacter Pylori Infection 59 0.052
329
AMN001 Amenorrhea 54 0.052
330
GST019 Gastrointestinal Stromal Tumor 78 0.051
331
SPP011 Suppression of Tumorigenicity 12 59 0.051
332
ENT011 Enterocolitis 51 0.051
333
BRK010 Burkitt Lymphoma 67 0.051
334
P DDN001 Duodenal Ulcer 52 0.051
335
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.051
336
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.051
337
OVR047 Ovarian Cystadenocarcinoma 38 0.051
338
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.051
339
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.051
340
P GLM007 Glomerulonephritis 57 0.050
341
SYN036 Syncope 45 0.050
342
P PLM037 Pulmonary Hypertension 67 0.050
343
P CHR071 Charcot-Marie-Tooth Disease 65 0.050
344
CHL123 Chlamydia 59 0.050
345
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.049
346
TNG007 Tongue Carcinoma 51 0.049
347
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.049
348
ALC007 Alcohol Dependence 66 0.048
349
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.048
350
PTH003 Pathologic Nystagmus 52 0.048
351
TTH006 Tooth Disease 46 0.048
352
P MYC008 Myocarditis 59 0.048
353
c XRD023 Xeroderma Pigmentosum, Complementation Group G 53 0.048
354
P PRT096 Peritoneal Mesothelioma 50 0.048
355
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.048
356
ART016 Aortic Aneurysm 69 0.047
357
NRT004 Neuritis 52 0.047
358
URT010 Ureteral Obstruction 45 0.047
359
TRT001 Teratocarcinoma 45 0.047
360
P HML002 Hemolytic Anemia 63 0.047
361
P SYP003 Syphilis 58 0.047
362
TRP009 Triple X Syndrome 42 0.047
363
HYP014 Hyperuricemia 52 0.047
364
NTR005 Nutritional Deficiency Disease 62 0.047
365
c ACT075 Acute Myocardial Infarction 57 0.047
366
KRT009 Keratosis 51 0.047
367
NWC001 Newcastle Disease 45 0.047
368
MNT001 Mantle Cell Lymphoma 69 0.046
369
P CRD119 Cardiac Arrest 67 0.046
370
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.046
371
BCK006 Back Pain 42 0.046
372
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.046
373
GNG013 Gingivitis 59 0.046
374
AMN003 Amnestic Disorder 54 0.046
375
P AXN001 Axonal Neuropathy 36 0.046
376
P HDC001 Headache 57 0.045
377
P FRD001 Friedreich Ataxia 64 0.045
378
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.045
379
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.045
380
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.045
381
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.045
382
P HML001 Hemolytic-Uremic Syndrome 53 0.045
383
ILS001 Ileus 51 0.045
384
P BNG030 Benign Ependymoma 60 0.044
385
OVR012 Ovarian Serous Cystadenocarcinoma 56 0.044
386
CLL010 Cellular Ependymoma 54 0.044
387
ADN009 Adenosquamous Carcinoma 47 0.044
388
PLY100 Polyploidy 40 0.044
389
c MNN043 Meningioma, Familial 74 0.043
390
PRP027 Peripheral Vascular Disease 71 0.043
391
PLG002 Plague 63 0.043
392
MNN042 Meningioma, Radiation-Induced 62 0.043
393
P ALP009 Alopecia Areata 60 0.043
394
P BNC003 Bone Cancer 58 0.043
395
SPN021 Spinal Meningioma 50 0.043
396
SCR001 Secretory Meningioma 41 0.043
397
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.043
398
49X006 49, Xxxxy Syndrome 41 0.043
399
P RNL007 Renal Tubular Acidosis 51 0.043
400
MTB004 Metabolic Acidosis 50 0.043
401
P PTN014 Patent Ductus Arteriosus 1 60 0.043
402
RYN005 Raynaud Phenomenon 47 0.042
403
ALB002 Albinism 46 0.042
404
P MVM001 Movement Disease 63 0.042
405
CRD223 Cardiac Arrhythmia 60 0.042
406
BRN004 Brain Edema 56 0.042
407
P MRC003 Mercury Poisoning 48 0.042
408
SCK003 Sickle Cell Anemia 74 0.041
409
TYP007 Typhoid Fever 63 0.041
410
INT051 Intussusception 53 0.041
411
OCL069 Ocular Motor Apraxia 51 0.041
412
MST004 Mast Cell Neoplasm 42 0.041
413
EXT007 Extracutaneous Mastocytoma 38 0.041
414
P LPS002 Liposarcoma 65 0.041
415
TRN015 Transient Cerebral Ischemia 63 0.041
416
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.041
417
HRT011 Heart Septal Defect 50 0.041
418
P OCL002 Oculocutaneous Albinism 60 0.041
419
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.041
420
SLC006 Silicosis 56 0.041
421
INT007 Intermediate Coronary Syndrome 55 0.041
422
PLS009 Plasma Cell Neoplasm 51 0.041
423
SKN005 Skin Atrophy 43 0.041
424
ADN011 Adenoid Cystic Carcinoma 70 0.040
425
BRR014 Barrett Esophagus 65 0.040
426
ORP003 Oropharynx Cancer 55 0.040
427
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.040
428
PPL018 Papillary Adenocarcinoma 45 0.040
429
P MLT020 Multiple Sclerosis 72 0.040
430
P GRF003 Graft-Versus-Host Disease 72 0.040
431
P MNN013 Meningitis 66 0.040
432
P ALC033 Alcohol Use Disorder 58 0.040
433
P DBT005 Diabetes Insipidus 55 0.040
434
KLB003 Klebsiella Pneumonia 41 0.040
435
VRL011 Viral Infectious Disease 61 0.039
436
c RNG015 Ring Chromosome 2 26 0.039
437
P NPH012 Nephrotic Syndrome 60 0.039
438
STT001 Status Epilepticus 60 0.039
439
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.039
440
RNL077 Renal Fibrosis 47 0.039
441
MDD018 Middle East Respiratory Syndrome 43 0.039
442
ACT162 Acute Sensory Ataxic Neuropathy 26 0.039
443
c SYS001 Systemic Lupus Erythematosus 86 0.038
444
P HPT021 Hepatitis 67 0.038
445
P LPS004 Lupus Erythematosus 61 0.038
446
LYM040 Lymphoblastic Lymphoma 54 0.038
447
P MNC007 Monocytic Leukemia 53 0.038
448
P LMY004 Leiomyosarcoma 63 0.038
449
VRC005 Varicose Veins 60 0.038
450
P INS002 in Situ Carcinoma 53 0.038
451
EXP004 Exophthalmos 52 0.038
452
RSP021 Respiratory Allergy 45 0.038
453
MYC006 Mycosis Fungoides 66 0.037
454
c FNC043 Fanconi Anemia, Complementation Group E 62 0.037
455
MSL001 Measles 62 0.037
456
OST003 Osteonecrosis 61 0.037
457
P EHL001 Ehlers-Danlos Syndrome 58 0.037
458
c GLL024 Gallbladder Disease 1 53 0.037
459
P THR015 Thrombophilia 51 0.037
460
P CHL066 Cholangitis 51 0.037
461
HVY002 Heavy Metal Poisoning 22 0.037
462
END041 Endometrial Adenocarcinoma 63 0.036
463
P SLV026 Salivary Gland Carcinoma 57 0.036
464
PNM008 Pneumothorax 56 0.036
465
P PRC012 Pericardial Effusion 51 0.036
466
HMP001 Hemopericardium 48 0.036
467
P FLL037 Follicular Lymphoma 67 0.036
468
P CCK001 Cockayne Syndrome 66 0.036
469
P ATR010 Atrial Heart Septal Defect 60 0.036
470
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.036
471
CRN030 Coronary Stenosis 50 0.036
472
FLL008 Folliculitis 46 0.036
473
KPS004 Kaposi Sarcoma 75 0.035
474
PHR003 Pharyngitis 57 0.035
475
P ECL001 Eclampsia 50 0.035
476
INT067 Interstitial Nephritis 48 0.035
477
NND010 Nondisjunction 34 0.035
478
WLS001 Wilson Disease 71 0.034
479
WRN001 Werner Syndrome 69 0.034
480
HMT002 Hematologic Cancer 62 0.034
481
P PLY014 Polycystic Kidney Disease 62 0.034
482
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.034
483
CYT008 Cytomegalovirus Infection 57 0.034
484
P PYL005 Pyelonephritis 56 0.034
485
ATR057 Atrioventricular Block 55 0.034
486
HMP005 Hemiplegia 55 0.034
487
MCR004 Macroglobulinemia 49 0.034
488
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.034
489
URT049 Urate Oxidase, Pseudogene 25 0.034
490
EWN003 Ewing Sarcoma 69 0.034
491
P ANR048 Aniridia 1 63 0.034
492
P VNT002 Ventricular Septal Defect 60 0.034
493
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 52 0.034
494
THR004 Thrombocytosis 51 0.034
495
c FLL041 Follicular Lymphoma 1 49 0.034
496
MXD026 Mixed Glioma 45 0.034
497
CNN005 Connective Tissue Disease 68 0.032
498
PSY004 Psychotic Disorder 67 0.032
499
P INT143 Interstitial Cystitis 61 0.032
500
CHR066 Chronic Fatigue Syndrome 61 0.032
501
P GLL022 Guillain-Barre Syndrome 59 0.032
502
P OPT009 Optic Neuritis 57 0.032
503
GLS001 Gliosarcoma 54 0.032
504
ALL009 Allergic Conjunctivitis 50 0.032
505
P CTN015 Cutaneous T Cell Lymphoma 49 0.032
506
CYN002 Cyanosis, Transient Neonatal 45 0.032
507
ACT003 Acute Kidney Tubular Necrosis 45 0.032
508
c HYP272 Hypercholesterolemia, Familial, 3 44 0.032
509
P CYS017 Cystic Teratoma 41 0.032
510
TBC004 Tobacco Addiction 64 0.031
511
WLD007 Waldenstroem's Macroglobulinemia 61 0.031
512
DSS009 Disseminated Intravascular Coagulation 57 0.031
513
ACS001 Acoustic Neuroma 56 0.031
514
P VNS003 Venous Insufficiency 55 0.031
515
ACT200 Acute Monoblastic Leukemia 52 0.031
516
QDR001 Quadriplegia 48 0.031
517
HMR023 Hemorrhagic Cystitis 45 0.031
518
AML001 Amelanotic Melanoma 39 0.031
519
HRN029 Hearing Loss, Noise-Induced 37 0.031
520
THY111 Thyroid Carcinoma, Familial Medullary 67 0.031
521
LMB062 Limb Ischemia 55 0.031
522
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.031
523
c FNC029 Fanconi Anemia, Complementation Group I 54 0.031
524
BRN038 Bronchial Disease 53 0.031
525
P EMB005 Embryonal Rhabdomyosarcoma 53 0.031
526
P OTS001 Otosclerosis 49 0.031
527
PPL002 Papillary Carcinoma 47 0.031
528
KRT008 Keratopathy 47 0.031
529
CNT033 Central Nervous System Cancer 47 0.031
530
MTR010 Mature Teratoma 44 0.031
531
IDP033 Idiopathic Edema 44 0.031
532
CRT012 Cortical Blindness 37 0.031
533
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.031
534
MST020 Mast Cell Activation Syndrome 26 0.031
535
CRN311 Coronary Ostial Stenosis or Atresia 20 0.031
536
c DBT099 Diabetes Mellitus, Type I 65 0.029
537
P ADL010 Adult Respiratory Distress Syndrome 65 0.029
538
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.029
539
CYS013 Cystinuria 63 0.029
540
c ATM011 Autoimmune Hepatitis 63 0.029
541
HYD002 Hydronephrosis 60 0.029
542
BRN002 Bronchiolitis 59 0.029
543
P PLY017 Polyarteritis Nodosa 58 0.029
544
GLB001 Gilbert Syndrome 58 0.029
545
DSS008 Disease of Mental Health 58 0.029
546
THY122 Thyroid Gland Cancer 57 0.029
547
c LKM070 Leukemia, Acute Monocytic 57 0.029
548
c FML035 Familial Hyperlipidemia 55 0.029
549
MRG003 Marginal Zone B-Cell Lymphoma 52 0.029
550
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.029
551
NRM004 Neuroma 51 0.029
552
P MTR003 Mitral Valve Stenosis 50 0.029
553
P TMP001 Temporal Lobe Epilepsy 50 0.029
554
URN009 Urinary System Disease 48 0.029
555
THY128 Thyroid Tumor 47 0.029
556
P CLL015 Collagen Disease 47 0.029
557
PLS025 Plasmablastic Lymphoma 47 0.029
558
P PRC019 Precocious Puberty 46 0.029
559
OLG001 Oligospermia 45 0.029
560
CRT015 Carotid Artery Occlusion 45 0.029
561
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.029
562
UTR043 Uterine Sarcoma 39 0.029
563
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.029
564
CHR178 Chromosomal Triplication 35 0.029
565
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.029
566
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.029
567
P CHR012 Chronic Granulomatous Disease 67 0.027
568
P TRC086 Trichohepatoenteric Syndrome 1 62 0.027
569
P VSC011 Vasculitis 62 0.027
570
P DRM010 Dermatomyositis 61 0.027
571
P LYM033 Lymphoproliferative Syndrome 59 0.027
572
c LTN004 Late-Onset Retinal Degeneration 59 0.027
573
CHR072 Chordoma 58 0.027
574
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.027
575
BRN012 Bronchiolitis Obliterans 55 0.027
576
CRC006 Carcinoid Syndrome 55 0.027
577
URN010 Urinary Tract Obstruction 55 0.027
578
P CYS039 Cystic Kidney Disease 54 0.027
579
GST009 Gastroschisis 53 0.027
580
SPL004 Splenic Marginal Zone Lymphoma 51 0.027
581
THY125 Thyroid Gland Medullary Carcinoma 50 0.027
582
P OMP004 Omphalocele 50 0.027
583
c INF023 Inflammatory Breast Carcinoma 50 0.027
584
SCT005 Scott Syndrome 49 0.027
585
RCT020 Rectum Adenocarcinoma 48 0.027
586
PRP007 Priapism 47 0.027
587
P RNL015 Renal Hypertension 47 0.027
588
CRD137 Cardiogenic Shock 47 0.027
589
P OVR046 Ovarian Cyst 47 0.027
590
HYP034 Hypertensive Encephalopathy 46 0.027
591
MCR011 Microinvasive Gastric Cancer 43 0.027
592
OCL011 Ocular Motility Disease 42 0.027
593
P ECT005 Ectropion 42 0.027
594
RDN001 Reading Disorder 40 0.027
595
ABD010 Abdominal Wall Defect 36 0.027
596
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.027
597
OCC001 Occupational Dermatitis 29 0.027
598
BRW002 Brown's Tendon Sheath Syndrome 28 0.027
599
OVR104 Ovarian Melanoma 22 0.027
600
c ART115 Aortic Valve Disease 1 75 0.024
601
P OCL013 Oculodentodigital Dysplasia 69 0.024
602
c MCL013 Mucolipidosis Iv 66 0.024
603
c ART101 Aortic Valve Disease 2 65 0.024
604
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.024
605
RHB001 Rhabdoid Cancer 63 0.024
606
SRC027 Sarcoma, Synovial 58 0.024
607
P MTR012 Mitral Valve Disease 58 0.024
608
P MMP001 Mumps 58 0.024
609
MXD005 Mixed Connective Tissue Disease 58 0.024
610
P FNC044 Fanconi Anemia, Complementation Group C 57 0.024
611
P MYM013 Moyamoya Disease 1 57 0.024
612
P URF003 Urofacial Syndrome 1 57 0.024
613
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.024
614
c MCR256 Microphthalmia, Syndromic 9 56 0.024
615
c XRD031 Xeroderma Pigmentosum, Complementation Group F 55 0.024
616
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.024
617
P NRM002 Normal Pressure Hydrocephalus 54 0.024
618
P LNG035 Lung Large Cell Carcinoma 54 0.024
619
CRY001 Cryptogenic Organizing Pneumonia 53 0.024
620
INT075 Intracranial Hypertension 53 0.024
621
ART074 Aortic Dissection 52 0.024
622
ASP003 Aseptic Meningitis 51 0.024
623
ECT026 Ectopic Pregnancy 50 0.024
624
P PNB001 Pineoblastoma 50 0.024
625
PRN014 Paronychia 49 0.024
626
KRT013 Keratolytic Winter Erythema 46 0.024
627
c ACT042 Acute Pyelonephritis 46 0.024
628
LYD001 Leydig Cell Tumor 45 0.024
629
PNC056 Pineocytoma 45 0.024
630
BRN032 Brain Glioma 45 0.024
631
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.024
632
GNG003 Gingival Recession 44 0.024
633
P CRN024 Corneal Disease 44 0.024
634
P RNG032 Ring Chromosome 42 0.024
635
MDS018 Mediastinal Cancer 41 0.024
636
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.024
637
c MSC106 Mosaic Variegated Aneuploidy Syndrome 2 40 0.024
638
c PLM022 Pulmonary Valve Insufficiency 39 0.024
639
c SYS043 Systemic Lupus Erythematosus 1 38 0.024
640
c ATM022 Autoimmune Myocarditis 35 0.024
641
MTH047 Methanol Poisoning 34 0.024
642
MTH086 Methotrexate Toxicity 33 0.024
643
KDN013 Kidney Hypertrophy 32 0.024
644
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.024
645
P CNT036 Central Nervous System Germ Cell Tumor 28 0.024
646
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.024
647
SPC030 Specific Language Disorder 26 0.024
648
c DMN005 Diamond-Blackfan Anemia 2 25 0.024
649
PLS037 Plasma Cell Tumor 22 0.024
650
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.024
651
MTS005 Metastatic Squamous Neck Cancer with Occult Primary 11 0.024
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