Search results for Sulfate

2207 hits were found for Sulfate

# Family MCID Name MIFTS Score
1
c MCP043 Mucopolysaccharidosis, Type Iiia 61 3.788
2
c EHL076 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1 34 3.727
3
EHL015 Ehlers-Danlos Syndrome Progeroid Type 45 3.712
4
BRC115 Brachyolmia Type 1, Toledo Type 14 3.056
5
c MCP001 Mucopolysaccharidosis Iii 65 2.254
6
c MRQ002 Morquio Syndrome C 13 2.180
7
NMY001 Neomycin Sulfate Allergic Contact Dermatitis 5 2.180
8
CNG363 Congenital Enterocyte Heparan Sulfate Deficiency 10 2.173
10
CLT003 Colitis 62 0.427
11
OST012 Osteoarthritis 78 0.287
12
P LYM118 Lymphoma 68 0.271
13
LYM019 Lymphosarcoma 46 0.269
14
c PRC016 Pre-Eclampsia 63 0.262
15
ULC004 Ulcerative Colitis 73 0.260
16
P INF037 Inflammatory Bowel Disease 54 0.252
17
HMN044 Human Immunodeficiency Virus Type 1 71 0.236
18
P ECL001 Eclampsia 50 0.232
19
48X005 48,xyyy 39 0.216
20
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.210
21
PNG002 Pain Agnosia 51 0.206
22
IRN002 Iron Metabolism Disease 57 0.203
23
P LKM002 Leukemia 68 0.202
24
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.196
25
DFC004 Deficiency Anemia 70 0.194
26
LYM133 Lymphoma, Hodgkin, Classic 69 0.193
27
ADL002 Adult Syndrome 70 0.189
28
c RHB024 Rhabdomyosarcoma 2 67 0.189
29
c CHR684 Chronic Kidney Disease 70 0.188
30
DWN001 Down Syndrome 70 0.182
31
P LKM062 Leukemia, Acute Lymphoblastic 69 0.182
32
P KDN018 Kidney Disease 72 0.178
33
P HRP006 Herpes Simplex 65 0.174
34
ACQ007 Acquired Immunodeficiency Syndrome 60 0.173
35
LYM040 Lymphoblastic Lymphoma 54 0.171
36
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.170
37
IMM167 Immune Deficiency Disease 78 0.169
38
IRN001 Iron Deficiency Anemia 59 0.162
39
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.159
40
c SVR005 Severe Pre-Eclampsia 50 0.156
41
c EXS019 Exostoses, Multiple, Type I 53 0.150
42
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.148
43
P TRN020 Turner Syndrome 67 0.147
44
c PNS012 Paine Syndrome 61 0.147
45
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.147
46
CRB037 Cerebral Palsy 69 0.147
47
AST005 Asthma 76 0.143
48
P CLR023 Colorectal Cancer 99 0.139
49
MTH071 Methane Production 26 0.139
50
P BCL017 B-Cell Lymphoma 58 0.137
51
P NRB001 Neuroblastoma 72 0.136
52
P BRS047 Breast Cancer 97 0.124
53
CNT047 Contact Dermatitis 58 0.124
54
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.124
55
SRC014 Sarcoma 65 0.123
56
P ADN016 Adenocarcinoma 64 0.123
57
SPN035 Spindle Cell Sarcoma 53 0.123
58
SPN186 Spinal Cord Injury 60 0.121
59
P CYS018 Cystitis 59 0.120
60
CNS004 Constipation 58 0.118
61
P DRR001 Diarrhea 55 0.118
62
c HYP595 Hypertension, Essential 84 0.117
63
DRM006 Dermatitis 61 0.116
64
P SZR006 Seizure Disorder 56 0.116
65
SFT003 Soft Tissue Sarcoma 56 0.116
66
c HYP836 Hypercholesterolemia, Familial, 1 73 0.116
67
CHL068 Cholestasis 61 0.116
68
P CHR345 Chronic Pain 44 0.114
69
P MLG074 Malignant Mesenchymoma 40 0.113
70
NTR005 Nutritional Deficiency Disease 62 0.112
71
P INT143 Interstitial Cystitis 61 0.111
72
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.111
73
P NRP001 Neuropathy 56 0.111
74
c PRM038 Primary Agammaglobulinemia 44 0.111
75
c EXS020 Exostoses, Multiple, Type Ii 40 0.111
76
ATH013 Atherosclerosis Susceptibility 65 0.109
77
CYT002 Cytokine Deficiency 42 0.109
78
P MLN008 Melanoma 69 0.108
79
P GLM045 Glioma 63 0.108
80
ALL026 Allergic Hypersensitivity Disease 62 0.108
81
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.107
82
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.107
83
P CHN012 Chondrosarcoma 56 0.106
84
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.106
85
VSL002 Visual Epilepsy 59 0.105
86
PLS025 Plasmablastic Lymphoma 47 0.105
87
GLL048 Glial Tumor 45 0.105
88
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.105
89
ARG004 Argyria 27 0.104
90
BRK010 Burkitt Lymphoma 67 0.103
91
OST017 Osteomyelitis 64 0.103
92
CNT033 Central Nervous System Cancer 47 0.103
93
P SRC025 Sarcoidosis 1 70 0.102
94
RTC005 Reticulosarcoma 47 0.102
95
P PRC031 Preeclampsia/eclampsia 1 38 0.102
96
P ALZ034 Alzheimer Disease 88 0.101
97
c SYS001 Systemic Lupus Erythematosus 86 0.101
98
P AMY004 Amyloidosis 70 0.101
99
P FLL037 Follicular Lymphoma 67 0.101
100
47X002 47,xyy 49 0.101
101
c FLL041 Follicular Lymphoma 1 49 0.101
102
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.101
103
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.101
104
CVD001 Covid-19 44 0.101
105
P VSC007 Vascular Disease 63 0.100
106
DFF005 Diffuse Large B-Cell Lymphoma 55 0.099
107
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.097
108
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.097
109
HDG004 Hodgkin's Granuloma 23 0.097
110
HDG006 Hodgkin's Paragranuloma 22 0.097
111
P LVR013 Liver Disease 68 0.096
112
ADN018 Adenoma 59 0.096
113
MCP033 Mucopolysaccharidoses 38 0.096
114
P PHC003 Pheochromocytoma 71 0.095
115
ATM095 Autoimmune Disease 62 0.095
116
DST005 Diastrophic Dysplasia 58 0.095
117
HLX001 Helix Syndrome 47 0.095
118
ADR040 Adrenal Gland Pheochromocytoma 46 0.095
119
c SVR001 Severe Acute Respiratory Syndrome 62 0.094
120
P CNR004 Cone-Rod Dystrophy 2 73 0.093
121
P HYP086 Hypothyroidism 69 0.093
122
ISC004 Ischemia 58 0.093
123
P MDL005 Medulloblastoma 77 0.091
124
MNT001 Mantle Cell Lymphoma 69 0.091
125
P FBR017 Fibrosarcoma 56 0.091
126
49X006 49, Xxxxy Syndrome 41 0.091
127
c LKM005 Leukemia, T-Cell, Chronic 34 0.091
128
EWN003 Ewing Sarcoma 69 0.090
129
c FML021 Familial Hypercholesterolemia 66 0.090
130
END086 End Stage Renal Disease 51 0.090
131
GLB015 Glioblastoma Multiforme 75 0.089
132
FCT007 Factor Vii Deficiency 67 0.089
133
LVR012 Liver Cirrhosis 62 0.089
134
HYP066 Hyperglycemia 61 0.089
135
MCL075 Macular Dystrophy, Corneal 54 0.089
136
c MCR120 Microvascular Complications of Diabetes 7 47 0.089
137
CHL079 Children's Interstitial Lung Disease 26 0.089
138
P OVR042 Ovarian Cancer 88 0.088
139
P NTR004 Neutropenia 63 0.088
140
P GLM007 Glomerulonephritis 57 0.088
141
c MCR113 Microvascular Complications of Diabetes 3 52 0.088
142
IRR003 Irritant Dermatitis 49 0.088
143
c MCR130 Microvascular Complications of Diabetes 6 41 0.088
144
c MCR133 Microvascular Complications of Diabetes 4 41 0.088
145
P ANP001 Anaplastic Large Cell Lymphoma 58 0.086
146
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.086
147
PLM010 Pulmonary Edema 54 0.086
148
KPS004 Kaposi Sarcoma 75 0.085
149
c THR092 Thrombophilia Due to Thrombin Defect 73 0.085
150
P ART022 Arthritis 69 0.085
151
CMR002 Coumarin Resistance 56 0.085
152
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.085
153
P HRD001 Hereditary Multiple Exostoses 46 0.085
154
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.084
155
P DNG005 Dengue Virus 59 0.084
156
P PRP019 Peripheral Nervous System Disease 58 0.084
157
P ADL017 Adult T-Cell Leukemia 56 0.084
158
HYP005 Hypokalemia 55 0.084
159
c MLG068 Malignant Glioma 46 0.084
160
MST004 Mast Cell Neoplasm 42 0.084
161
c HRD104 Hereditary Multiple Osteochondromas 39 0.084
162
EXT007 Extracutaneous Mastocytoma 38 0.084
163
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.084
164
CYS001 Cystic Fibrosis 81 0.082
165
P ATR011 Atrial Fibrillation 66 0.082
166
P ENC018 Encephalopathy 61 0.082
167
P LPS004 Lupus Erythematosus 61 0.082
168
HYP266 Hypoxia 57 0.082
169
STM007 Stomatitis 50 0.082
170
BRN071 Brain Injury 49 0.082
171
URM002 Uremia 49 0.082
172
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.081
173
P LNG032 Lung Cancer 98 0.080
174
MYL069 Myeloma, Multiple 85 0.080
175
MLR004 Malaria 81 0.080
176
P GLM040 Glioma Susceptibility 1 81 0.080
177
INS024 Insulin-Like Growth Factor I 79 0.080
178
P RHB003 Rhabdomyosarcoma 63 0.080
179
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.080
180
P PLY011 Polycystic Ovary Syndrome 56 0.080
181
NPH009 Nephrolithiasis 55 0.080
182
BNR002 Bone Resorption Disease 48 0.080
183
ATX019 Ataxia with Vitamin E Deficiency 42 0.080
184
BRN028 Brain Cancer 74 0.078
185
P MTC003 Metachromatic Leukodystrophy 70 0.078
186
LSH001 Leishmaniasis 63 0.078
187
DPR016 Depression 63 0.078
188
P ART023 Arthropathy 62 0.078
189
LNG099 Lung Disease 60 0.078
190
VRC005 Varicose Veins 60 0.078
191
MXD026 Mixed Glioma 45 0.078
192
P KLZ004 Kala-Azar 1 41 0.078
193
P HPT023 Hepatocellular Carcinoma 100 0.077
194
P RHM011 Rheumatoid Arthritis 80 0.077
195
CNG034 Congestive Heart Failure 69 0.077
196
P PNM007 Pneumonia 68 0.077
197
P PLM037 Pulmonary Hypertension 67 0.077
198
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.077
199
BRN024 Bronchitis 68 0.075
200
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.075
201
TRM010 Traumatic Brain Injury 51 0.075
202
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.075
203
P PNC035 Pancreatic Cancer 84 0.074
204
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.074
205
PRT036 Peritonitis 64 0.074
206
P CRN300 Coronary Heart Disease 1 63 0.074
207
P ENC004 Encephalitis 61 0.074
208
P LKD001 Leukodystrophy 59 0.074
209
MCS002 Mucositis 56 0.074
210
HYP060 Hyperinsulinism 54 0.074
211
P ICH004 Ichthyosis 54 0.074
212
ICH054 Ichthyosis, X-Linked 53 0.074
213
c ACH042 Achondrogenesis, Type Ib 49 0.074
214
P HMN032 Human Herpesvirus 8 47 0.074
215
P HRT032 Heart Disease 75 0.072
216
CRB039 Cerebrovascular Disease 67 0.072
217
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.072
218
c ACT071 Acute Kidney Failure 60 0.072
219
CHL123 Chlamydia 59 0.072
220
c ACT073 Acute Leukemia 58 0.072
221
MNT002 Mental Depression 58 0.072
222
BCT022 Bacterial Infectious Disease 56 0.072
223
BRN004 Brain Edema 56 0.072
224
PLS009 Plasma Cell Neoplasm 51 0.072
225
P AST007 Astrocytoma 51 0.072
226
PPL052 Papillomatosis, Confluent and Reticulated 33 0.072
227
OST159 Osteogenic Sarcoma 66 0.071
228
ALL010 Allergic Contact Dermatitis 56 0.071
229
P OVR082 Overgrowth Syndrome 50 0.071
230
P CRN025 Corneal Dystrophy 49 0.071
231
STR067 Stroke, Ischemic 81 0.069
232
P LKM071 Leukemia, Chronic Lymphocytic 79 0.069
233
TTN003 Tetanus 65 0.069
234
P GST044 Gastritis 56 0.069
235
P ACH011 Achondrogenesis 50 0.069
236
CHL018 Childhood Medulloblastoma 49 0.069
237
DWR001 Dwarfism 44 0.069
238
c ATL015 Atelosteogenesis, Type Ii 40 0.069
239
HRW001 Hair Whorl 36 0.069
240
RCK004 Rickets 68 0.067
241
P DRM053 Dermatitis, Atopic 66 0.067
242
P PLM036 Pulmonary Fibrosis 65 0.067
243
c ACT068 Acute Cystitis 63 0.067
244
c FNC043 Fanconi Anemia, Complementation Group E 62 0.067
245
LPP008 Lipoprotein Quantitative Trait Locus 62 0.067
246
P NPH012 Nephrotic Syndrome 60 0.067
247
P NRF002 Neurofibromatosis 56 0.067
248
AGN016 Aging 56 0.067
249
STT002 Status Asthmaticus 50 0.067
250
P HMR005 Hemorrhoid 46 0.067
251
P PRS040 Prostate Cancer 97 0.066
252
c LKM061 Leukemia, Acute Myeloid 84 0.066
253
P BLD134 Bladder Cancer 79 0.066
254
P THR014 Thrombocytopenia 67 0.066
255
HYP056 Hypoglycemia 66 0.066
256
P PRD008 Periodontitis 64 0.066
257
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.066
258
CHN016 Cohen Syndrome 63 0.066
259
P RHN004 Rhinitis 57 0.066
260
c ACT075 Acute Myocardial Infarction 57 0.066
261
GST050 Gastrointestinal System Disease 56 0.066
262
VCC001 Vaccinia 49 0.066
263
c DRR009 Diarrhea 6 46 0.066
264
TRP009 Triple X Syndrome 42 0.066
265
ANX004 Anoxia 40 0.066
266
SCR011 Scrapie 39 0.066
267
c CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 33 0.066
268
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.064
269
P RSP003 Respiratory Failure 74 0.064
270
END057 Endometrial Cancer 74 0.064
271
P RTN024 Retinoblastoma 73 0.064
272
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.064
273
P MYC007 Myocardial Infarction 70 0.064
274
CLN015 Colon Adenocarcinoma 65 0.064
275
P DBT009 Diabetes Mellitus 64 0.064
276
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.064
277
c WLM018 Wilms Tumor 5 61 0.064
278
CHL014 Cholera 59 0.064
279
GST045 Gastroenteritis 59 0.064
280
P HDC001 Headache 57 0.064
281
THR024 Thrombosis 57 0.064
282
MTH009 Mouth Disease 56 0.064
283
c FML008 Familial Retinoblastoma 53 0.064
284
LNG031 Lung Benign Neoplasm 51 0.064
285
URL001 Urolithiasis 45 0.064
287
P EPN001 Ependymoblastoma 44 0.064
288
P ATL001 Atelosteogenesis 34 0.064
289
c MLT031 Multiple Epiphyseal Dysplasia, Recessive 19 0.064
290
c NRF024 Neurofibromatosis, Type I 77 0.062
291
SVR004 Severe Combined Immunodeficiency 73 0.062
292
c SML038 Small Cell Cancer of the Lung 65 0.062
293
CTN007 Cutaneous Leishmaniasis 62 0.062
294
TXC005 Toxic Shock Syndrome 62 0.062
295
P EHL001 Ehlers-Danlos Syndrome 58 0.062
296
P EXN002 Exanthem 57 0.062
297
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.062
298
P LTR001 Lateral Sclerosis 54 0.062
299
P INT068 Intestinal Disease 53 0.062
300
SBC016 Subacute Delirium 44 0.062
301
c NRF023 Neurofibromatosis, Type Ii 80 0.060
302
ANX010 Anxiety 73 0.060
303
SCH036 Scheie Syndrome 72 0.060
304
P GRF003 Graft-Versus-Host Disease 72 0.060
305
P ATS364 Autism 70 0.060
306
PLM001 Pulmonary Tuberculosis 69 0.060
307
SKN019 Skin Melanoma 68 0.060
308
P CRD119 Cardiac Arrest 67 0.060
309
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.060
310
PRT037 Pertussis 65 0.060
311
c WLM013 Wilms Tumor 1 65 0.060
312
P PSR002 Psoriasis 62 0.060
313
c HPT003 Hepatitis a 62 0.060
314
P BNG030 Benign Ependymoma 60 0.060
315
P CTR002 Cataract 60 0.060
316
PRN019 Perinatal Necrotizing Enterocolitis 59 0.060
317
P PRN023 Prion Disease 57 0.060
318
SYN007 Synovitis 54 0.060
319
P ALP008 Alopecia 54 0.060
320
CLL010 Cellular Ependymoma 54 0.060
321
GST023 Gastric Ulcer 53 0.060
322
PST011 Pustulosis of Palm and Sole 52 0.060
323
P DDN001 Duodenal Ulcer 52 0.060
324
MRG003 Marginal Zone B-Cell Lymphoma 52 0.060
325
OCL069 Ocular Motor Apraxia 51 0.060
326
ENT011 Enterocolitis 51 0.060
327
CHR005 Chorioamnionitis 51 0.060
328
NTR046 Neutrophil Migration 50 0.060
329
ALL014 Allergic Encephalomyelitis 38 0.060
330
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 37 0.060
331
PLC002 Plica Syndrome 36 0.060
332
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 30 0.060
333
CRH001 Crohn's Disease 74 0.058
334
c HPT073 Hepatitis C Virus 72 0.058
335
P HPT021 Hepatitis 67 0.058
336
P MCR115 Microvascular Complications of Diabetes 5 66 0.058
337
HRL003 Hurler Syndrome 65 0.058
338
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.058
339
SKN016 Skin Disease 63 0.058
340
P HYP750 Hypertriglyceridemia, Familial 62 0.058
341
P MYL006 Myeloid Leukemia 60 0.058
342
P KDN017 Kidney Cancer 60 0.058
343
c ACT027 Acute Pancreatitis 60 0.058
344
P BND020 Bone Disease 59 0.058
345
c HPT016 Hepatitis B 59 0.058
346
AMB001 Amebiasis 55 0.058
347
P ART021 Arteriosclerosis 54 0.058
348
P TRM003 Tremor 54 0.058
349
DYS015 Dysentery 52 0.058
350
PLC007 Placental Abruption 48 0.058
351
KRT002 Keratomalacia 47 0.058
352
CHR074 Choriocarcinoma 47 0.058
353
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.058
354
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.058
355
BCK006 Back Pain 42 0.058
356
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.056
357
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.056
358
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.056
359
P DMN002 Dementia 66 0.056
360
P MSC005 Muscular Dystrophy 66 0.056
361
P PNC044 Pancreatitis 61 0.056
362
SQM006 Squamous Cell Carcinoma 60 0.056
363
BRN002 Bronchiolitis 59 0.056
364
PPT005 Peptic Ulcer Disease 59 0.056
365
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.056
366
JPN002 Japanese Encephalitis 57 0.056
367
EMB004 Embryonal Carcinoma 56 0.056
368
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.056
369
P EMB005 Embryonal Rhabdomyosarcoma 53 0.056
370
TXC002 Toxic Encephalopathy 53 0.056
371
ART140 Arteries, Anomalies of 52 0.056
372
HYP043 Hyperandrogenism 48 0.056
373
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.056
374
RNL077 Renal Fibrosis 47 0.056
375
OPD001 Opioid Abuse 46 0.056
376
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.056
377
ACR005 Acrodermatitis 38 0.056
378
c WLM011 Wilms Tumor 6 37 0.056
379
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.056
380
CYT018 Cytochrome P450 2d6 Variant 27 0.056
381
P GST053 Gastric Cancer 83 0.054
382
P OST002 Osteoporosis 74 0.054
383
PRP027 Peripheral Vascular Disease 71 0.054
384
P INF038 Influenza 68 0.054
385
c MGR028 Migraine with or Without Aura 1 67 0.054
386
KHL003 Kohlschutter-Tonz Syndrome 65 0.054
387
c FML001 Familial Atrial Fibrillation 65 0.054
388
P CNJ013 Conjunctivitis 65 0.054
389
c DBT099 Diabetes Mellitus, Type I 65 0.054
390
NRF007 Neurofibroma 64 0.054
391
LPD008 Lipid Metabolism Disorder 62 0.054
392
c HPT001 Hepatitis C 62 0.054
393
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 0.054
394
P CRD246 Cardiovascular System Disease 57 0.054
395
P PLY019 Polyneuropathy 56 0.054
396
PRT082 Preterm Premature Rupture of the Membranes 54 0.054
397
PRV004 Periventricular Leukomalacia 52 0.054
398
HND002 Hand, Foot and Mouth Disease 51 0.054
399
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.054
400
P BNG032 Benign Mesothelioma 46 0.054
401
NWC001 Newcastle Disease 45 0.054
402
TST015 Testicular Disease 43 0.054
403
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.054
404
ENT007 Enteropathica 26 0.054
406
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.052
407
CRV035 Cervical Cancer 76 0.052
408
c ATR087 Atrial Standstill 1 75 0.052
409
P ASP006 Aspergillosis 69 0.052
410
HYL004 Hyaline Fibromatosis Syndrome 67 0.052
411
P OLG002 Oligodendroglioma 67 0.052
412
PPL049 Papillon-Lefevre Syndrome 65 0.052
413
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.052
414
PLM031 Poliomyelitis 64 0.052
415
RHB001 Rhabdoid Cancer 63 0.052
416
c MCP047 Mucopolysaccharidosis, Type Iva 61 0.052
417
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.052
418
CRD223 Cardiac Arrhythmia 60 0.052
419
P BRS044 Breast Adenocarcinoma 59 0.052
420
P MLT007 Multiple Epiphyseal Dysplasia 58 0.052
421
P URT039 Urticaria 58 0.052
422
EYD002 Eye Disease 58 0.052
423
DSS009 Disseminated Intravascular Coagulation 57 0.052
424
P HYP076 Hyperthyroidism 55 0.052
425
PPL022 Papilloma 54 0.052
426
BRN038 Bronchial Disease 53 0.052
427
LYS002 Lysosomal Storage Disease 52 0.052
428
PLS007 Plasmodium Falciparum Malaria 52 0.052
429
P RCT021 Rectum Cancer 52 0.052
430
TLN003 Telangiectasis 52 0.052
431
MTB004 Metabolic Acidosis 50 0.052
432
EXS001 Exostosis 46 0.052
433
SQM002 Squamous Cell Papilloma 46 0.052
434
BRS050 Breast Cyst 40 0.052
435
c ACT004 Acute Diarrhea 39 0.052
436
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 0.052
437
PDT014 Pediatric Ependymoma 32 0.052
438
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.052
439
ESP021 Esophageal Cancer 90 0.050
440
P LNG064 Lung Cancer Susceptibility 3 78 0.050
441
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.050
442
P MJR001 Major Depressive Disorder 68 0.050
443
ALL003 Allergic Rhinitis 67 0.050
444
CHG001 Chagas Disease 66 0.050
445
FTT001 Fatty Liver Disease 61 0.050
446
VRL011 Viral Infectious Disease 61 0.050
447
THY029 Thyroid Carcinoma 59 0.050
448
GLS018 Glass Syndrome 57 0.050
449
CMM005 Common Cold 57 0.050
450
BLR008 Bilirubin Metabolic Disorder 57 0.050
451
ALL006 Allergic Asthma 56 0.050
452
HYP781 Hypoascorbemia 51 0.050
453
P SCK005 Sickle Cell Disease 50 0.050
454
BLR001 Biliary Atresia 50 0.050
455
MCR004 Macroglobulinemia 49 0.050
456
c INV001 Invasive Aspergillosis 49 0.050
457
DGN001 Degenerative Disc Disease 48 0.050
458
SKL017 Skeletal Dysplasias 40 0.050
459
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.050
460
CRB026 Cerebellar Astrocytoma 37 0.050
461
P MRQ003 Morquio Syndrome 37 0.050
462
PDT015 Pediatric Supratentorial Ependymoma 24 0.050
463
PDT016 Pediatric Infratentorial Ependymoma 22 0.050
464
CHL065 Cholangiocarcinoma 68 0.048
465
P MNN013 Meningitis 66 0.048
466
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.048
467
OST003 Osteonecrosis 61 0.048
468
STT001 Status Epilepticus 60 0.048
469
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.048
470
c MCP004 Mucopolysaccharidosis Iv 57 0.048
471
CYT008 Cytomegalovirus Infection 57 0.048
472
PLS011 Plasmacytoma 56 0.048
473
ATR057 Atrioventricular Block 55 0.048
474
RSC001 Rosacea 54 0.048
475
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.048
476
ILS001 Ileus 51 0.048
477
P LCT001 Lactic Acidosis 51 0.048
478
INT079 Intrahepatic Cholangiocarcinoma 51 0.048
479
P MMB011 Membranous Nephropathy 50 0.048
480
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.048
481
CHD004 Chudley-Mccullough Syndrome 46 0.048
482
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.048
483
P GNG009 Gangliosidosis 44 0.048
484
CRN322 Coronavirus Infectious Disease 40 0.048
485
c HNT011 Huntington Disease-Like 3 38 0.048
486
c INT059 Internal Hemorrhoid 34 0.048
487
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.048
488
CHL009 Childhood Cerebral Astrocytoma 14 0.048
489
P PRK057 Parkinson Disease, Late-Onset 78 0.045
490
ODN023 Odontochondrodysplasia 68 0.045
491
P SYS005 Systemic Scleroderma 68 0.045
492
ALC007 Alcohol Dependence 66 0.045
493
P SKN015 Skin Carcinoma 66 0.045
494
c MCR129 Microvascular Complications of Diabetes 1 66 0.045
495
P HYD006 Hydrocephalus 66 0.045
496
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.045
497
DPH001 Diphtheria 60 0.045
498
P SCL018 Scoliosis 60 0.045
499
PLM033 Pulmonary Embolism 59 0.045
500
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.045
501
P INT070 Intestinal Obstruction 58 0.045
502
P ALC033 Alcohol Use Disorder 58 0.045
503
P INF032 Infertility 57 0.045
504
ISL001 Islet Cell Tumor 56 0.045
505
PRP030 Purpura 54 0.045
506
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.045
507
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.045
508
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.045
509
OPT003 Opiate Dependence 50 0.045
510
WTH001 Withdrawal Disorder 48 0.045
511
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.045
512
IGG001 Iga Glomerulonephritis 48 0.045
513
PYL006 Pyloric Stenosis 48 0.045
514
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.045
515
HPR003 Heparin-Induced Thrombocytopenia 48 0.045
516
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.045
517
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.045
518
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.045
519
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.045
520
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.045
521
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.045
522
CRB004 Cerebral Artery Occlusion 45 0.045
523
P END039 Endodermal Sinus Tumor 44 0.045
524
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.045
525
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.045
526
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.045
527
P HYP009 Hypertrophic Pyloric Stenosis 41 0.045
528
TST018 Testicular Yolk Sac Tumor 39 0.045
529
c SYS043 Systemic Lupus Erythematosus 1 38 0.045
530
PLY150 Polykaryocytosis Inducer 31 0.045
531
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.043
532
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.043
533
LPT014 Leptin Deficiency or Dysfunction 74 0.043
534
MSC157 Muscular Dystrophy, Duchenne Type 72 0.043
535
P MLT020 Multiple Sclerosis 72 0.043
536
c LKM063 Leukemia, Chronic Myeloid 72 0.043
537
c ATS007 Autism Spectrum Disorder 67 0.043
538
ANG054 Angina Pectoris 66 0.043
539
P NRV007 Nervous System Disease 66 0.043
540
KRT019 Keratitis, Hereditary 65 0.043
541
HMT002 Hematologic Cancer 62 0.043
542
P VSC011 Vasculitis 62 0.043
543
WLD007 Waldenstroem's Macroglobulinemia 61 0.043
544
RTN017 Retinal Detachment 61 0.043
545
HPT019 Hepatic Encephalopathy 60 0.043
546
P MLN069 Melanoma, Uveal 59 0.043
547
RBS001 Rabies 58 0.043
548
CRD132 Cardiac Conduction Defect 58 0.043
549
CHL067 Cholecystitis 57 0.043
550
APH001 Aphthous Stomatitis 57 0.043
551
PHR003 Pharyngitis 57 0.043
552
TRN018 Transitional Cell Carcinoma 56 0.043
553
c FML035 Familial Hyperlipidemia 55 0.043
554
P MYP006 Myopia 55 0.043
555
P SBS003 Substance Abuse 55 0.043
556
END040 Endogenous Depression 55 0.043
557
AMN003 Amnestic Disorder 54 0.043
558
CRT017 Cartilage Disease 54 0.043
559
GLC003 Glucose Intolerance 54 0.043
560
MST005 Mastitis 53 0.043
561
FNG017 Fungal Infectious Disease 53 0.043
562
P BRN035 Brain Stem Glioma 52 0.043
563
SPS003 Spastic Diplegia 51 0.043
564
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.043
565
c MCP046 Mucopolysaccharidosis, Type Iiid 51 0.043
566
KRT009 Keratosis 51 0.043
567
SPL004 Splenic Marginal Zone Lymphoma 51 0.043
568
P OBS001 Obstructive Jaundice 50 0.043
569
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.043
570
DYS073 Dysphagia 50 0.043
571
HYP080 Hypogonadism 50 0.043
572
SLF014 Sulfite Oxidase Deficiency, Isolated 49 0.043
573
ATS010 Autosomal Recessive Disease 48 0.043
574
c PRM226 Primary Central Nervous System Lymphoma 48 0.043
575
GRM005 Germ Cell Cancer 47 0.043
576
RSP021 Respiratory Allergy 45 0.043
577
HPT004 Hepatic Coma 45 0.043
578
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.043
579
P OST028 Osteochondroma 45 0.043
580
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.043
581
SPR126 Superior Semicircular Canal Dehiscence 40 0.043
582
P MSC134 Musculocontractural Ehlers-Danlos Syndrome 40 0.043
583
ENT001 Enterocele 39 0.043
584
c HMG029 Hemoglobin Se Disease 39 0.043
585
KSH004 Kashin-Beck Disease 38 0.043
586
GRM010 Germ Cells Tumors 34 0.043
587
CHL057 Childhood Brain Stem Glioma 32 0.043
588
STT009 Sutton Disease 2 30 0.043
589
SCK003 Sickle Cell Anemia 74 0.040
590
c EXD008 Exudative Vitreoretinopathy 1 71 0.040
591
P EPL164 Epilepsy 71 0.040
592
CRT072 Creutzfeldt-Jakob Disease 70 0.040
593
P MYC084 Mycobacterium Tuberculosis 1 68 0.040
594
CNN005 Connective Tissue Disease 68 0.040
595
PNC129 Pancreatic Adenocarcinoma 68 0.040
596
c INF071 Inflammatory Bowel Disease 1 67 0.040
597
MYC006 Mycosis Fungoides 66 0.040
598
P CLC063 Celiac Disease 1 66 0.040
599
P NSP012 Nasopharyngeal Carcinoma 66 0.040
600
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.040
601
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.040
602
P HML002 Hemolytic Anemia 63 0.040
603
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.040
604
P KLL001 Kallmann Syndrome 61 0.040
605
CHR066 Chronic Fatigue Syndrome 61 0.040
606
P HMN010 Hemangioma 61 0.040
607
P TXP001 Toxoplasmosis 60 0.040
608
CHC001 Chickenpox 60 0.040
609
P PTN014 Patent Ductus Arteriosus 1 60 0.040
610
P OPT006 Optic Nerve Disease 60 0.040
611
c DNG003 Dengue Disease 59 0.040
612
PRT058 Pure Autonomic Failure 59 0.040
613
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.040
614
AVN001 Avian Influenza 59 0.040
615
c MCP044 Mucopolysaccharidosis, Type Iiib 59 0.040
616
ANR040 Aneurysm 59 0.040
617
DSS008 Disease of Mental Health 58 0.040
618
c DWL002 Dowling-Degos Disease 1 58 0.040
619
THY122 Thyroid Gland Cancer 57 0.040
620
P PLY018 Polycythemia 56 0.040
621
MLT135 Multiple Sulfatase Deficiency 56 0.040
622
MCR141 Mucormycosis 56 0.040
623
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.040
624
HRL004 Hurler-Scheie Syndrome 55 0.040
625
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.040
626
HMS001 Hemosiderosis 54 0.040
627
P RTN016 Retinal Degeneration 53 0.040
628
P CNT005 Central Nervous System Lymphoma 53 0.040
629
NRT001 Neurotic Disorder 53 0.040
630
DNT012 Dental Caries 53 0.040
631
P TRT010 Teratoma 52 0.040
632
CLB002 Clubfoot 51 0.040
633
c HNT004 Huntington Disease-Like 2 50 0.040
634
c AMY009 Amyloidosis Aa 50 0.040
635
P KRT007 Keratoconus 50 0.040
636
HYP017 Hypophosphatemia 50 0.040
637
PLP001 Pulpitis 49 0.040
638
HST010 Histiocytosis 48 0.040
639
SPL018 Splenomegaly 48 0.040
640
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.040
641
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.040
642
P CRN035 Cranial Nerve Palsy 42 0.040
643
P RRH023 Rare Hereditary Hemochromatosis 41 0.040
644
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.040
645
RDN001 Reading Disorder 40 0.040
646
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.040
647
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.040
648
c BCT006 Bacterial Conjunctivitis 37 0.040
649
PSD088 Pseudobulbar Affect 36 0.040
650
CHL006 Childhood Oligodendroglioma 31 0.040
651
INT082 Intraocular Retinoblastoma 30 0.040
652
P HRM021 Hair Morphology 2 22 0.040
653
CHL016 Childhood Malignant Mesenchymoma 8 0.040
654
P SCH015 Schizophrenia 74 0.037
655
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.037
656
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.037
657
P LNG028 Long Qt Syndrome 66 0.037
658
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.037
659
P ADL010 Adult Respiratory Distress Syndrome 65 0.037
660
c BRN108 Branchiootic Syndrome 1 62 0.037
661
BLD131 Bladder Urothelial Carcinoma 62 0.037
662
MSL001 Measles 62 0.037
663
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.037
664
c SCL052 Scleroderma, Familial Progressive 61 0.037
665
SZR001 Sezary's Disease 60 0.037
666
DNG002 Dengue Hemorrhagic Fever 60 0.037
667
ORL011 Oral Cancer 60 0.037
668
ING001 Inguinal Hernia 60 0.037
669
P THL005 Thalassemia 60 0.037
670
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.037
671
PNM001 Pneumocystosis 59 0.037
672
IGR001 Ige Responsiveness, Atopic 59 0.037
673
FBR047 Fibromyalgia 58 0.037
674
NWB001 Newborn Respiratory Distress Syndrome 58 0.037
675
P CND004 Candidiasis 58 0.037
676
LNG108 Langerhans Cell Histiocytosis 58 0.037
677
P UVT001 Uveitis 57 0.037
678
P PLV020 Pelvic Organ Prolapse 57 0.037
679
CHK001 Chikungunya 57 0.037
680
c MST023 Mesothelioma, Malignant 57 0.037
681
SCH014 Schistosomiasis 57 0.037
682
HPT022 Hepatoblastoma 56 0.037
683
ADR008 Adrenal Adenoma 55 0.037
684
ZLL002 Zollinger-Ellison Syndrome 55 0.037
685
VSC003 Visceral Leishmaniasis 55 0.037
686
P GRV001 Graves' Disease 55 0.037
687
CHR100 Chronic Ulcer of Skin 55 0.037
688
P VNS003 Venous Insufficiency 55 0.037
689
HRY003 Hairy Cell Leukemia 55 0.037
690
GNT003 Genital Herpes 54 0.037
691
P RST001 Restless Legs Syndrome 54 0.037
692
AMN001 Amenorrhea 54 0.037
693
LYM022 Lymphangioma 54 0.037
694
GTR002 Goiter 53 0.037
695
c MCP048 Mucopolysaccharidosis, Type Ivb 52 0.037
696
P NRC002 Narcolepsy 52 0.037
697
FDL002 Food Allergy 51 0.037
698
CLR109 Colorectal Adenocarcinoma 51 0.037
699
P IGN003 Iga Nephropathy 1 49 0.037
700
VRC001 Varicocele 49 0.037
701
LYM012 Lymphoplasmacytic Lymphoma 47 0.037
702
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.037
703
ASP004 Asphyxia Neonatorum 46 0.037
704
P MTH007 Methemoglobinemia 46 0.037
705
URT010 Ureteral Obstruction 45 0.037
706
c PCH010 Pachyonychia Congenita 3 44 0.037
707
P HYP265 Hypotonia 43 0.037
708
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.037
709
MLT162 Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects 42 0.037
710
c MCR112 Microvascular Complications of Diabetes 2 41 0.037
711
PLC009 Placenta Praevia 39 0.037
712
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.037
713
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.037
714
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 33 0.037
715
c CHR064 Chronic Monocytic Leukemia 33 0.037
716
c PRS136 Prostate Cancer, Hereditary, 6 33 0.037
717
c PRS130 Prostate Cancer, Hereditary, 8 32 0.037
718
DPH003 Diphyllobothriasis 32 0.037
719
TST003 Testicular Leukemia 27 0.037
720
HML018 Homologous Wasting Disease 22 0.037
721
c ADL020 Adult Malignant Mesenchymoma 11 0.037
722
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.034
723
P FML011 Familial Adenomatous Polyposis 72 0.034
724
MYL005 Myelofibrosis 70 0.034
725
ADN011 Adenoid Cystic Carcinoma 70 0.034
726
P MYP004 Myopathy 70 0.034
727
ACR008 Acrocallosal Syndrome 69 0.034
728
P TYS001 Tay-Sachs Disease 69 0.034
729
P OCL013 Oculodentodigital Dysplasia 69 0.034
730
ART016 Aortic Aneurysm 69 0.034
731
c HMP004 Hemophilia B 68 0.034
732
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.034
733
ANG020 Angiosarcoma 64 0.034
734
CLF027 Cleft Palate, Isolated 64 0.034
735
TYP007 Typhoid Fever 63 0.034
736
PLG002 Plague 63 0.034
737
P END044 Endometriosis 63 0.034
738
c GM1007 Gm1 Gangliosidosis 62 0.034
739
P DRM010 Dermatomyositis 61 0.034
741
INT002 Intermittent Claudication 61 0.034
742
YLL002 Yellow Fever 61 0.034
743
RCT015 Reactive Arthritis 61 0.034
744
P TST021 Testicular Germ Cell Tumor 60 0.034
745
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.034
746
P GLL022 Guillain-Barre Syndrome 59 0.034
747
LYM027 Lymphopenia 58 0.034
748
MCR013 Microphthalmia 57 0.034
749
P FCL005 Focal Segmental Glomerulosclerosis 57 0.034
750
AYM001 Ayme-Gripp Syndrome 57 0.034
751
ERY051 Erythroleukemia, Familial 56 0.034
752
INT030 Intracranial Aneurysm 56 0.034
753
LMB062 Limb Ischemia 55 0.034
754
P ANT006 Antiphospholipid Syndrome 55 0.034
755
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.034
756
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.034
757
HLL004 Hellp Syndrome 54 0.034
758
PRS045 Prostatic Hypertrophy 53 0.034
759
P EPD016 Epidermolysis Bullosa 53 0.034
760
PRP036 Peripheral T-Cell Lymphoma 53 0.034
761
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.034
762
HMC014 Homocysteinemia 53 0.034
763
PRP080 Peripheral Artery Disease 53 0.034
764
P RTN018 Retinal Disease 53 0.034
765
EXP004 Exophthalmos 52 0.034
766
MCN017 Meconium Ileus 52 0.034
767
c VRL010 Viral Hepatitis 52 0.034
768
IMP005 Impotence 52 0.034
769
THY030 Thyroid Gland Disease 52 0.034
770
P OVR049 Ovarian Disease 52 0.034
771
DSM007 Desmoplastic Small Round Cell Tumor 52 0.034
772
P HMP007 Hemophilia 51 0.034
773
P RNL007 Renal Tubular Acidosis 51 0.034
774
HYP081 Hypolipoproteinemia 51 0.034
775
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.034
776
PLC008 Placenta Disease 50 0.034
777
ENT004 Enthesopathy 49 0.034
778
CCN002 Cocaine Abuse 49 0.034
779
ADR016 Adrenal Cortical Carcinoma 48 0.034
780
INT067 Interstitial Nephritis 48 0.034
781
RYN005 Raynaud Phenomenon 47 0.034
782
CLN045 Colonic Benign Neoplasm 46 0.034
783
P CHR573 Choroid Plexus Cancer 46 0.034
784
HDN002 Head Injury 46 0.034
785
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.034
786
TRT001 Teratocarcinoma 45 0.034
787
CYN002 Cyanosis, Transient Neonatal 45 0.034
788
INT253 Intestinal Benign Neoplasm 45 0.034
789
IMM136 Immune System Disease 45 0.034
790
PRT019 Protein-Losing Enteropathy 45 0.034
791
P PRL003 Proliferative Glomerulonephritis 44 0.034
792
P CRN024 Corneal Disease 44 0.034
793
SPN369 Spinal Disease 43 0.034
794
MDD018 Middle East Respiratory Syndrome 43 0.034
795
IDP070 Idiopathic Scoliosis 42 0.034
796
ANG049 Angioedema Induced by Ace Inhibitors 40 0.034
797
ACT011 Acute Contagious Conjunctivitis 40 0.034
798
ADR004 Adrenal Cortical Adenocarcinoma 39 0.034
799
OVR094 Ovarian Epithelial Cancer 38 0.034
800
GLM044 Glomerular Disease 37 0.034
801
THR123 Thrombotic Microangiopathy 36 0.034
802
ACT149 Acetaminophen Metabolism 35 0.034
803
c ADL008 Adult Oligodendroglioma 34 0.034
804
EXT025 Extragonadal Germ Cell Cancer 32 0.034
805
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.034
806
P RRL003 Rare Lymphatic Malformation 31 0.034
807
EXN003 Exencephaly 31 0.034
808
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.034
809
CHL015 Childhood Choroid Plexus Cancer 16 0.034
810
P LTH050 Lethal Chondrodysplasia 14 0.034
811
P RTN008 Retinitis Pigmentosa 79 0.030
812
GST019 Gastrointestinal Stromal Tumor 78 0.030
813
c BTT014 Beta-Thalassemia 74 0.030
814
P HNT016 Huntington Disease 72 0.030
815
MYL009 Myelodysplastic Syndrome 70 0.030
816
PLY001 Polycythemia Vera 69 0.030
817
SND001 Sandhoff Disease 68 0.030
818
PSY004 Psychotic Disorder 67 0.030
819
P CNG001 Congenital Myasthenic Syndrome 66 0.030
820
c MCL013 Mucolipidosis Iv 66 0.030
821
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.030
822
P LPS002 Liposarcoma 65 0.030
823
IRR002 Irritable Bowel Syndrome 65 0.030
824
LYM017 Lyme Disease 64 0.030
825
c DPH024 Diaphragmatic Hernia, Congenital 63 0.030
826
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.030
827
c MLG084 Malignant Fibrous Histiocytoma 63 0.030
828
c GLC092 Glaucoma, Primary Open Angle 62 0.030
829
P PLY014 Polycystic Kidney Disease 62 0.030
830
CRC021 Carcinosarcoma 62 0.030
831
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.030
832
ALV005 Alveolar Soft Part Sarcoma 61 0.030
833
P SJG008 Sjogren Syndrome 61 0.030
834
GST033 Gestational Diabetes 61 0.030
835
INT066 Interstitial Lung Disease 60 0.030
836
P ALP009 Alopecia Areata 60 0.030
837
P MYC008 Myocarditis 59 0.030
838
P SLP005 Sleep Disorder 59 0.030
839
GRD007 Grade Iii Astrocytoma 59 0.030
840
SRC027 Sarcoma, Synovial 58 0.030
841
P SYP003 Syphilis 58 0.030
842
GLB001 Gilbert Syndrome 58 0.030
843
BRS051 Breast Disease 58 0.030
844
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.030
845
BRN056 Bronchopulmonary Dysplasia 57 0.030
846
HMR039 Hemorrhage, Intracerebral 57 0.030
847
PGM001 Pigmented Villonodular Synovitis 56 0.030
848
P BPL003 Bipolar Disorder 56 0.030
849
TCK001 Tick-Borne Encephalitis 56 0.030
850
HPT046 Hepatic Veno-Occlusive Disease 56 0.030
851
ORL005 Oral Candidiasis 56 0.030
852
P HYP024 Hypoparathyroidism 56 0.030
853
P MLN007 Male Infertility 55 0.030
854
ANG005 Anogenital Venereal Wart 55 0.030
855
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.030
856
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.030
857
DBT010 Diabetic Neuropathy 54 0.030
858
P LCH002 Lichen Planus 53 0.030
859
HRT012 Heart Valve Disease 53 0.030
860
KRT006 Keratoconjunctivitis 53 0.030
861
CRH005 Crohn's Colitis 53 0.030
862
OCL006 Ocular Hypertension 53 0.030
863
c PRD040 Periodontitis, Chronic 53 0.030
864
c CNT035 Central Nervous System Disease 52 0.030
865
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.030
866
OST011 Osteomalacia 52 0.030
867
PRP016 Paraplegia 52 0.030
868
PRS030 Persistent Fetal Circulation Syndrome 52 0.030
869
c ACT135 Acute Graft Versus Host Disease 52 0.030
870
P SPP010 Suppressor of Tumorigenicity 3 51 0.030
871
PRS021 Prostatic Adenoma 51 0.030
872
MYL020 Myelomeningocele 51 0.030
873
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.030
874
SPN019 Spondylolisthesis 51 0.030
875
FBR008 Fibrillary Astrocytoma 51 0.030
876
P PST095 Post-Thrombotic Syndrome 51 0.030
877
BHR001 Behr Syndrome 51 0.030
878
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.030
879
P CHL066 Cholangitis 51 0.030
880
INT071 Intestinal Perforation 51 0.030
881
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.030
882
OCL022 Ocular Melanoma 50 0.030
883
P OTS001 Otosclerosis 49 0.030
884
P MYT002 Myotonic Dystrophy 49 0.030
885
KRT001 Keratoconjunctivitis Sicca 49 0.030
886
c CHR431 Chronic Venous Insufficiency 49 0.030
887
PRS129 Prostatic Hyperplasia, Benign 49 0.030
888
P OPN001 Open-Angle Glaucoma 49 0.030
889
SCT005 Scott Syndrome 49 0.030
890
CHL004 Cholelithiasis 49 0.030
891
P CRV031 Cervical Adenocarcinoma 49 0.030
892
MNN009 Meningoencephalitis 49 0.030
893
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.030
894
P MCL001 Mucolipidosis 48 0.030
895
SXL003 Sexual Disorder 47 0.030
896
PPL002 Papillary Carcinoma 47 0.030
897
TTR011 Tetraploidy 47 0.030
898
ANV001 Anovulation 47 0.030
899
ANP006 Anaplastic Ependymoma 46 0.030
900
P MYC033 Myoclonus 46 0.030
901
ANR004 Anuria 46 0.030
902
RTR008 Root Resorption 45 0.030
903
LYM051 Lymphomatoid Granulomatosis 45 0.030
904
GRD001 Giardiasis 45 0.030
905
TNS007 Taeniasis 45 0.030
906
c CLR017 Clear Cell Sarcoma 45 0.030
907
SPS057 Spasticity 45 0.030
908
CYS009 Cystadenoma 44 0.030
909
GRN017 Granulocytopenia 44 0.030
910
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.030
911
GNG003 Gingival Recession 44 0.030
912
P FBR003 Fibrous Histiocytoma 44 0.030
913
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.030
914
SPN040 Spinal Cancer 44 0.030
915
c HYP272 Hypercholesterolemia, Familial, 3 44 0.030
916
c ADL023 Adult Medulloblastoma 44 0.030
917
ANP009 Anaplastic Oligodendroglioma 43 0.030
918
PRM237 Primary Hypomagnesemia 43 0.030
919
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.030
920
P TST026 Testicular Germ Cell Cancer 43 0.030
921
RFR003 Refractive Error 43 0.030
922
MCR011 Microinvasive Gastric Cancer 43 0.030
923
LWC001 Low Compliance Bladder 43 0.030
924
c MLG064 Malignant Ependymoma 41 0.030
925
DFF003 Diffuse Scleroderma 41 0.030
926
c MJR024 Major Affective Disorder 9 41 0.030
927
PRS063 Paresthesia 41 0.030
928
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.030
929
NNT008 Neonatal Abstinence Syndrome 41 0.030
930
KDN007 Kidney Clear Cell Sarcoma 40 0.030
931
PYR004 Pyuria 40 0.030
932
WLL004 Wallerian Degeneration 39 0.030
933
FML039 Female Reproductive System Disease 39 0.030
934
c CHR682 Chronic Bilirubin Encephalopathy 39 0.030
935
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.030
936
c OVR114 Ovarian Cancer 1 38 0.030
937
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.030
938
c MJR022 Major Affective Disorder 8 38 0.030
939
SHW001 Shwartzman Phenomenon 37 0.030
940
EST003 Eastern Equine Encephalitis 37 0.030
941
SPN331 Spondyloocular Syndrome 36 0.030
942
CYC001 Cycloplegia 35 0.030
943
CHR178 Chromosomal Triplication 35 0.030
944
MYT011 Myotonia 34 0.030
945
c RST012 Restless Legs Syndrome 1 34 0.030
946
LTT002 Letterer-Siwe Disease 33 0.030
947
SML008 Small Intestine Lymphoma 33 0.030
948
CNG064 Congenital Chloride Diarrhea 32 0.030
949
CYT004 Cytomegalic Inclusion Disease 31 0.030
950
ANP008 Anaplastic Oligoastrocytoma 30 0.030
951
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 30 0.030
952
c TST046 Testicular Germ Cell Tumor 1 29 0.030
953
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.030
954
FSH003 Fish Allergy 28 0.030
955
EXT029 Extraocular Retinoblastoma 24 0.030
956
P SLF001 Sulfhemoglobinemia 23 0.030
957
CRB054 Cerebellar Astrocytoma, Childhood 9 0.030
958
NRL016 Neural Tube Defects 82 0.026
959
P ATX030 Ataxia-Telangiectasia 82 0.026
960
c DLT002 Dilated Cardiomyopathy 79 0.026
961
ADR007 Adrenoleukodystrophy 75 0.026
962
c MNN043 Meningioma, Familial 74 0.026
963
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.026
964
P ALG028 Alagille Syndrome 1 73 0.026
965
ACR007 Acromegaly 71 0.026
966
P HYP061 Hypertrophic Cardiomyopathy 70 0.026
967
P SLP006 Sleep Apnea 69 0.026
968
P LPR021 Leprosy 3 69 0.026
969
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.026
970
CST001 Costello Syndrome 68 0.026
971
PCK003 Pick Disease of Brain 68 0.026
972
c NMN015 Niemann-Pick Disease, Type C1 68 0.026
973
P ESS003 Essential Thrombocythemia 68 0.026
974
GST092 Gastroesophageal Reflux 67 0.026
975
c HMP029 Hemophilia a 67 0.026
976
P HYP098 Hypereosinophilic Syndrome 67 0.026
977
c PRM196 Premature Ovarian Failure 1 67 0.026
978
MYX005 Myxoid Liposarcoma 66 0.026
979
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.026
980
MYL031 Myeloproliferative Neoplasm 66 0.026
981
P MTR014 Motor Neuron Disease 65 0.026
982
CLR108 Colorectal Adenoma 64 0.026
983
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.026
984
P HYP069 Hyperparathyroidism 63 0.026
985
ANR007 Anorexia Nervosa 63 0.026
986
c ALP101 Alpha-Thalassemia 62 0.026
987
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.026
988
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.026
989
MNN042 Meningioma, Radiation-Induced 62 0.026
990
MDD011 Mood Disorder 62 0.026
991
P PRM006 Primary Biliary Cirrhosis 62 0.026
992
ASP002 Aspartylglucosaminuria 62 0.026
993
FCS002 Fucosidosis 61 0.026
994
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.026
995
NRL005 Neurilemmoma 60 0.026
996
HRP004 Herpes Zoster 60 0.026
997
ACN002 Acanthosis Nigricans 60 0.026
998
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.026
999
P CHR285 Chronic Myelomonocytic Leukemia 60 0.026
1000
VGN017 Vaginal Cancer 60 0.026
1001
P RBL001 Rubella 59 0.026
1002
P BRN022 Bronchiectasis 59 0.026
1003
SPN027 Spinal Stenosis 59 0.026
1004
P NMN002 Niemann-Pick Disease 59 0.026
1005
VLV032 Vulva Cancer 59 0.026
1006
PST028 Post-Traumatic Stress Disorder 58 0.026
1007
P HYP726 Hypercalcemia, Infantile, 1 58 0.026
1008
MCS006 Macs Syndrome 58 0.026
1009
SPT004 Septic Arthritis 58 0.026
1010
CCC001 Coccidioidomycosis 58 0.026
1011
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.026
1012
ADR005 Adrenal Carcinoma 58 0.026
1013
P GLL018 Gallbladder Cancer 57 0.026
1014
P END033 Endocarditis 57 0.026
1015
CHR177 Chromophobe Renal Cell Carcinoma 57 0.026
1016
P URF003 Urofacial Syndrome 1 57 0.026
1017
PLC005 Placental Insufficiency 57 0.026
1018
P ANG015 Angioedema 57 0.026
1019
P PYL005 Pyelonephritis 56 0.026
1020
P MLT074 Multiple Endocrine Neoplasia 56 0.026
1021
EXF001 Exfoliation Syndrome 56 0.026
1022
SPN041 Spinal Cord Disease 56 0.026
1023
ICH001 Ichthyosis Vulgaris 55 0.026
1024
GLC012 Galactosialidosis 55 0.026
1025
NRG002 Neurogenic Bladder 55 0.026
1026
P PLM034 Pulmonary Emphysema 55 0.026
1027
URN010 Urinary Tract Obstruction 55 0.026
1028
INT007 Intermediate Coronary Syndrome 55 0.026
1029
P SLM003 Salmonellosis 55 0.026
1030
GLS001 Gliosarcoma 54 0.026
1031
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.026
1032
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.026
1033
CRY003 Cryptosporidiosis 54 0.026
1034
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.026
1035
WST005 West Nile Virus 54 0.026
1036
MYM001 Myoma 54 0.026
1037
SNS003 Sensory Peripheral Neuropathy 54 0.026
1038
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.026
1039
CLL003 Cellulitis 54 0.026
1040
ABL002 Ablepharon-Macrostomia Syndrome 53 0.026
1041
P MNC007 Monocytic Leukemia 53 0.026
1042
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.026
1043
P SHR001 Short Bowel Syndrome 53 0.026
1044
P HMR003 Hemorrhagic Disease 53 0.026
1045
P PTS002 Ptosis 53 0.026
1046
INT075 Intracranial Hypertension 53 0.026
1047
PRN011 Pernicious Anemia 53 0.026
1048
TRC003 Trichomoniasis 53 0.026
1049
c GLL024 Gallbladder Disease 1 53 0.026
1050
P CNG436 Congenital Disorder of Deglycosylation 52 0.026
1051
P MSC003 Muscular Atrophy 52 0.026
1052
P THY032 Thyroiditis 52 0.026
1053
PTH003 Pathologic Nystagmus 52 0.026
1054
c VRL005 Viral Pneumonia 52 0.026
1055
LMY002 Leiomyoma 52 0.026
1056
OLG003 Oligohydramnios 51 0.026
1057
CYS014 Cystadenocarcinoma 51 0.026
1058
ESP002 Esophageal Varix 51 0.026
1059
GNG012 Gingival Overgrowth 51 0.026
1060
c ALM001 Al Amyloidosis 50 0.026
1061
PLR007 Pleural Empyema 50 0.026
1062
c PRM012 Primary Polycythemia 50 0.026
1063
TMT002 Temtamy Preaxial Brachydactyly Syndrome 50 0.026
1064
SPN021 Spinal Meningioma 50 0.026
1065
PST021 Postpartum Depression 50 0.026
1066
CRN030 Coronary Stenosis 50 0.026
1067
P TMP001 Temporal Lobe Epilepsy 50 0.026
1068
TRY001 Trypanosomiasis 50 0.026
1069
P PNB001 Pineoblastoma 50 0.026
1070
ISL003 Isolated Growth Hormone Deficiency 49 0.026
1071
URT001 Urethritis 49 0.026
1072
c THR090 Thrombocythemia 1 49 0.026
1073
AMB002 Amblyopia 49 0.026
1074
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.026
1075
LRN003 Learning Disability 49 0.026
1076
QDR001 Quadriplegia 48 0.026
1077
INT017 Intestinal Schistosomiasis 48 0.026
1078
INT054 Intraocular Lymphoma 48 0.026
1079
c DSB006 Desbuquois Dysplasia 1 48 0.026
1080
CCN001 Cocaine Dependence 48