Search results for TG

2447 hits were found for TG

# Family MCID Name MIFTS Score
1
c FML297 Familial Thyroid Dyshormonogenesis 47 77.764
2
c THY056 Thyroid Dyshormonogenesis 3 32 55.464
3
c ATM050 Autoimmune Thyroid Disease 3 21 31.812
4
c CNG006 Congenital Hypothyroidism 63 30.881
5
P HYP086 Hypothyroidism 69 25.370
6
THY029 Thyroid Carcinoma 54 20.283
7
GTR002 Goiter 52 18.168
8
P THY032 Thyroiditis 56 18.165
9
HSH003 Hashimoto Thyroiditis 60 17.509
10
P GRV001 Graves' Disease 54 17.360
11
P HYP076 Hyperthyroidism 53 13.434
12
ATM095 Autoimmune Disease 61 12.902
13
PPL002 Papillary Carcinoma 46 12.714
14
DFF036 Differentiated Thyroid Carcinoma 51 12.542
15
ADN018 Adenoma 58 12.525
16
PRM013 Premature Menopause 57 12.414
17
c TYP008 Type 1 Diabetes Mellitus 77 11.965
18
P DBT009 Diabetes Mellitus 67 11.823
19
NDL007 Nodular Goiter 48 11.463
20
FLL031 Follicular Adenoma 40 11.363
21
THY122 Thyroid Gland Cancer 59 11.222
22
P MLT008 Multinodular Goiter 42 10.878
23
c SBC007 Subacute Thyroiditis 43 10.826
24
NNT010 Nontoxic Goiter 32 10.616
25
PND002 Pendred Syndrome 57 10.355
26
P TRN020 Turner Syndrome 67 10.274
27
c CHR708 Chronic Urticaria 42 10.257
28
P STR021 Struma Ovarii 39 10.248
29
P MLT074 Multiple Endocrine Neoplasia 58 10.167
30
P PRG013 Paraganglioma 57 10.141
31
MCP006 Mucoepidermoid Carcinoma 48 9.927
32
THY030 Thyroid Gland Disease 50 9.896
33
P HYP750 Hypertriglyceridemia, Familial 62 9.762
34
c THY102 Thyroid Cancer, Nonmedullary, 2 54 9.556
35
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 9.460
36
LPD008 Lipid Metabolism Disorder 61 9.377
37
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 54 9.336
38
P CLC063 Celiac Disease 1 66 9.304
39
THY111 Thyroid Carcinoma, Familial Medullary 67 8.877
40
END028 Endemic Goiter 36 8.858
41
THY121 Thyroid Gland Anaplastic Carcinoma 66 8.711
42
PPL035 Papillary Thyroid Microcarcinoma 39 8.687
43
PLM011 Plummer's Disease 34 8.607
44
MYX004 Myxedema 43 8.527
45
PRN011 Pernicious Anemia 52 8.520
46
TXC004 Toxic Diffuse Goiter 23 8.476
47
EXP004 Exophthalmos 50 8.408
48
c MLG059 Malignant Struma Ovarii 31 8.345
49
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 46 8.291
50
THY022 Thymic Carcinoma 56 8.237
51
P ATM019 Autoimmune Polyendocrine Syndrome 46 8.213
52
c BNG093 Benign Teratoma 39 8.106
53
HYP780 Hypoadrenocorticism, Familial 61 8.106
54
THY123 Thyroid Gland Follicular Carcinoma 53 7.477
55
c GRV008 Graves Disease 1 54 7.356
56
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.926
57
FTT001 Fatty Liver Disease 61 6.908
58
THY125 Thyroid Gland Medullary Carcinoma 48 6.473
59
ATH010 Athyreosis 34 6.233
60
DSS008 Disease of Mental Health 74 6.139
61
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 41 6.117
62
FTL005 Fetal Adenoma 21 6.004
63
ETH004 Euthyroid Sick Syndrome 38 5.958
64
OVR109 Ovarian Germ Cell Teratoma 32 5.932
65
c HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 51 5.917
66
OVR112 Ovarian Germ Cell Cancer 41 5.901
67
PST014 Postsurgical Hypothyroidism 28 5.901
68
PPL010 Papillary Follicular Thyroid Adenocarcinoma 10 5.901
69
SBC005 Subacute Lymphocytic Thyroiditis 27 5.883
70
c ACT053 Acute Thyroiditis 28 5.839
71
EPT007 Epithelial Malignant Thymoma 27 5.839
72
MCH006 Mechanical Strabismus 40 5.839
73
THY009 Thyroid Lymphoma 44 5.807
74
LRN001 Laurence-Moon Syndrome 45 5.807
75
c BNG029 Benign Struma Ovarii 33 5.807
76
PRT030 Parathyroid Gland Disease 45 5.807
77
TLL001 Tall Cell Variant Papillary Carcinoma 26 5.807
78
SPN279 Spindle Epithelial Tumor with Thymus-Like Differentiation Tumor 19 5.732
79
ATM014 Autoimmune Disease of Endocrine System 24 5.732
80
END036 Endocrine Organ Benign Neoplasm 24 5.732
81
PLM007 Pulmonary Aspergilloma 29 5.732
82
ASP036 Aspirin Allergy 27 5.732
83
OVR041 Ovarian Benign Neoplasm 30 5.732
84
THY096 Thyroid Carcinoma, Hurthle Cell 24 5.732
85
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 54 5.732
86
c TYP053 Type 1 Diabetes Mellitus 20 39 5.732
87
ADR010 Adrenal Cortical Hypofunction 31 5.732
88
THY001 Thyroid Crisis 30 5.732
89
MTR011 Mature Teratoma of the Ovary 25 5.732
90
IMM005 Immature Teratoma of Ovary 34 5.732
91
IDN001 Iodine Hypothyroidism 24 5.732
92
NNN001 Nonencapsulated Sclerosing Carcinoma 25 5.732
93
ECT003 Ectopic Thymus 25 5.732
94
UTR042 Uterus Leiomyosarcoma 33 5.732
95
MDD004 Middle Ear Adenocarcinoma 25 5.732
96
MDD009 Middle Ear Carcinoma 28 5.732
97
THY126 Thyroid Gland Mucoepidermoid Carcinoma 17 5.732
98
ATR073 Atrophic Glossitis 28 5.732
99
SPP005 Suppurative Thyroiditis 32 5.732
100
SBS002 Substernal Goiter 26 5.732
101
THY013 Thyrotoxic Exophthalmos 23 5.732
102
END034 Endocrine Exophthalmos 30 5.732
103
ANL005 Anal Spasm 28 5.732
104
NSL005 Nasal Cavity Olfactory Neuroblastoma 27 5.732
105
P ACT046 Acute Apical Periodontitis 24 5.732
106
DND003 Dendritic Cell Thymoma 23 5.732
107
ADR009 Adrenal Cortex Disease 36 5.732
108
TRB001 Trabecular Follicular Adenocarcinoma 9 5.732
109
THY127 Thyroid Gland Hurthle Cell Carcinoma 19 5.732
110
ATY007 Atypical Follicular Adenoma 19 5.732
111
CLR014 Clear Cell Adenoma 27 5.732
112
ORB013 Orbital Disease 42 5.732
113
PPL015 Papillary Thymic Adenocarcinoma 19 5.732
114
OVR057 Ovarian Serous Adenofibroma 27 5.732
115
THY004 Thyroid Angiosarcoma 27 5.732
116
THY031 Thyroid Sarcoma 26 5.732
117
CRT001 Carotid Body Cancer 25 5.732
118
CLL011 Colloid Adenoma 18 5.732
119
BRS037 Breast Cystic Hypersecretory Carcinoma 21 5.732
120
MLT005 Multicentric Papillary Thyroid Carcinoma 17 5.732
121
END013 Endometrial Small Cell Carcinoma 29 5.732
122
OVR002 Ovarian Serous Cystadenofibroma 26 5.732
123
CYC003 Cyclotropia 22 5.732
124
IST001 Isthmus Cancer 14 5.732
125
P LVR013 Liver Disease 68 5.606
126
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 5.446
127
c HPT001 Hepatitis C 61 5.171
128
RPD005 Rapidly Involuting Congenital Hemangioma 48 5.032
129
c TYP009 Type 2 Diabetes Mellitus 92 4.732
130
P ALZ034 Alzheimer Disease 87 4.394
131
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.311
132
P LYM118 Lymphoma 69 4.145
133
c HYP836 Hypercholesterolemia, Familial, 1 73 4.107
134
c THY109 Thyroid Cancer, Nonmedullary, 1 55 4.086
135
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.974
136
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 3.974
137
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.974
138
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.974
139
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 3.974
140
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.974
141
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.974
142
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.974
143
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 3.974
144
P HPT021 Hepatitis 68 3.864
145
c HPT073 Hepatitis C Virus 71 3.698
146
P CRN300 Coronary Heart Disease 1 73 3.680
147
ATH013 Atherosclerosis Susceptibility 63 3.589
148
P LKM002 Leukemia 66 3.559
149
NNL006 Non-Alcoholic Steatohepatitis 54 3.531
150
HYP066 Hyperglycemia 60 3.510
151
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.321
152
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.318
153
LPP008 Lipoprotein Quantitative Trait Locus 65 3.265
154
ART140 Arteries, Anomalies of 52 3.233
155
c AMY091 Amyotrophic Lateral Sclerosis 1 88 3.220
156
P LTR001 Lateral Sclerosis 58 3.220
157
P PRS040 Prostate Cancer 95 3.215
158
P ANR048 Aniridia 1 66 3.162
159
P BCL017 B-Cell Lymphoma 57 3.161
160
LYM019 Lymphosarcoma 46 3.149
161
48X005 48,xyyy 39 3.147
162
c HPT003 Hepatitis a 63 3.144
163
LYM133 Lymphoma, Hodgkin, Classic 74 3.047
164
P LKM071 Leukemia, Chronic Lymphocytic 74 3.024
165
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.994
166
SVR004 Severe Combined Immunodeficiency 71 2.900
167
DRM006 Dermatitis 62 2.877
168
c ATR087 Atrial Standstill 1 74 2.855
169
GLC003 Glucose Intolerance 53 2.717
170
P HRP006 Herpes Simplex 65 2.677
171
P DRM053 Dermatitis, Atopic 65 2.674
172
c ACT027 Acute Pancreatitis 60 2.646
173
P PNM007 Pneumonia 64 2.630
174
LYM143 Lymphoma, Non-Hodgkin, Familial 79 2.628
175
MYL069 Myeloma, Multiple 77 2.622
176
CYS001 Cystic Fibrosis 77 2.575
178
CNG021 Congenital Toxoplasmosis 55 2.510
179
c HYP595 Hypertension, Essential 84 2.469
180
CYT002 Cytokine Deficiency 43 2.460
181
AGN016 Aging 54 2.458
182
P SRC025 Sarcoidosis 1 70 2.446
183
PRT251 Proteinuria, Chronic Benign 58 2.434
184
c HNT004 Huntington Disease-Like 2 51 2.388
185
P ALC033 Alcohol Use Disorder 67 2.370
186
P VSC007 Vascular Disease 62 2.354
187
c CHR684 Chronic Kidney Disease 74 2.354
188
HYP060 Hyperinsulinism 53 2.350
189
P CLR023 Colorectal Cancer 100 2.340
190
ALC007 Alcohol Dependence 65 2.331
191
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.301
192
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.295
193
P PLY011 Polycystic Ovary Syndrome 57 2.288
194
P HMN038 Human Coronavirus Sensitivity 30 2.281
195
HMN044 Human Immunodeficiency Virus Type 1 76 2.272
196
P NRB001 Neuroblastoma 66 2.250
197
P GST053 Gastric Cancer 82 2.242
198
P MYC007 Myocardial Infarction 69 2.241
199
TRC064 Trochlear Dysplasia 12 2.240
200
HDG004 Hodgkin's Granuloma 22 2.219
201
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 2.219
202
HDG006 Hodgkin's Paragranuloma 21 2.219
203
c MCR133 Microvascular Complications of Diabetes 4 41 2.207
204
c MCR113 Microvascular Complications of Diabetes 3 52 2.207
205
c MCR130 Microvascular Complications of Diabetes 6 41 2.207
206
c MCR120 Microvascular Complications of Diabetes 7 47 2.207
207
IMM167 Immune Deficiency Disease 77 2.198
208
P BRS047 Breast Cancer 97 2.134
209
c PRC016 Pre-Eclampsia 64 2.117
210
CLT003 Colitis 63 2.115
211
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 50 2.108
212
P ART022 Arthritis 70 2.102
213
PLS009 Plasma Cell Neoplasm 64 2.076
214
47X002 47,xyy 48 2.076
215
BCT022 Bacterial Infectious Disease 56 2.018
216
P PRN023 Prion Disease 60 2.008
217
HLX001 Helix Syndrome 47 1.986
218
P PRD008 Periodontitis 64 1.983
219
P AMY004 Amyloidosis 69 1.939
220
BNR002 Bone Resorption Disease 47 1.937
221
RCK004 Rickets 65 1.916
222
P HRT032 Heart Disease 84 1.893
223
P OVR082 Overgrowth Syndrome 42 1.856
224
ALL014 Allergic Encephalomyelitis 34 1.852
225
P LPS004 Lupus Erythematosus 61 1.846
226
LVR012 Liver Cirrhosis 62 1.832
227
P GRF003 Graft-Versus-Host Disease 71 1.820
228
OST012 Osteoarthritis 77 1.804
229
P INF037 Inflammatory Bowel Disease 53 1.796
230
HYP014 Hyperuricemia 51 1.787
231
P KDN018 Kidney Disease 72 1.780
232
c DLT002 Dilated Cardiomyopathy 79 1.778
233
c SYS001 Systemic Lupus Erythematosus 86 1.748
234
ADL002 Adult Syndrome 69 1.737
235
P MYP004 Myopathy 67 1.734
236
c HNT011 Huntington Disease-Like 3 33 1.722
237
P INF038 Influenza 68 1.719
238
GST033 Gestational Diabetes 61 1.696
239
PRP027 Peripheral Vascular Disease 71 1.696
240
PRT036 Peritonitis 65 1.678
241
P TXP001 Toxoplasmosis 60 1.663
242
P GLM007 Glomerulonephritis 59 1.662
243
END086 End Stage Renal Disease 54 1.662
244
SCR011 Scrapie 39 1.652
245
IRN002 Iron Metabolism Disease 56 1.639
246
P PNC044 Pancreatitis 61 1.638
247
ISC004 Ischemia 61 1.628
248
P ENC004 Encephalitis 61 1.609
249
c PRM196 Premature Ovarian Failure 1 58 1.609
250
P HYP838 Hyperlipidemia, Familial Combined, 3 61 1.601
251
PPL022 Papilloma 53 1.597
252
SQM002 Squamous Cell Papilloma 45 1.597
253
P SLP006 Sleep Apnea 69 1.593
254
c MCR115 Microvascular Complications of Diabetes 5 65 1.585
255
ALL029 Allergic Disease 61 1.579
256
RHB024 Rhabdomyosarcoma 2 65 1.569
257
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.567
258
P MLN008 Melanoma 75 1.564
259
c LKM005 Leukemia, T-Cell, Chronic 33 1.550
260
FML035 Familial Hyperlipidemia 55 1.544
261
CRB039 Cerebrovascular Disease 65 1.541
262
CRN030 Coronary Stenosis 50 1.532
263
P MYC033 Myoclonus 46 1.528
264
CNG034 Congestive Heart Failure 69 1.524
265
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.521
266
P HYP061 Hypertrophic Cardiomyopathy 69 1.509
267
c MGR028 Migraine with or Without Aura 1 64 1.503
268
CHD004 Chudley-Mccullough Syndrome 47 1.500
269
P MSC003 Muscular Atrophy 52 1.499
270
P ENC018 Encephalopathy 62 1.496
271
BRN071 Brain Injury 50 1.442
272
HPT025 Hepatic Lipase Deficiency 47 1.414
273
DPR016 Depression 65 1.414
274
P RTN016 Retinal Degeneration 52 1.411
275
P ECL001 Eclampsia 52 1.407
276
ALL006 Allergic Asthma 56 1.405
277
HYP081 Hypolipoproteinemia 49 1.400
278
P THL005 Thalassemia 56 1.393
279
NTR005 Nutritional Deficiency Disease 60 1.382
280
ART004 Aortic Atherosclerosis 46 1.378
281
c THR092 Thrombophilia Due to Thrombin Defect 74 1.378
282
CNT047 Contact Dermatitis 57 1.378
283
P RTN008 Retinitis Pigmentosa 79 1.371
284
INS024 Insulin-Like Growth Factor I 77 1.370
285
NRR001 Neuroretinitis 42 1.362
286
RTN023 Retinitis 45 1.362
287
TRM010 Traumatic Brain Injury 50 1.358
288
P EPL164 Epilepsy 70 1.355
289
MLD018 Mild Cognitive Impairment 48 1.344
290
KRT019 Keratitis, Hereditary 66 1.344
291
CHL014 Cholera 62 1.341
292
VCC001 Vaccinia 49 1.339
293
VRL011 Viral Infectious Disease 60 1.336
294
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.334
295
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.329
296
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.329
297
c PRM038 Primary Agammaglobulinemia 47 1.329
298
DPH001 Diphtheria 59 1.320
299
P LKM062 Leukemia, Acute Lymphoblastic 69 1.319
300
P HPT023 Hepatocellular Carcinoma 95 1.306
301
ORL011 Oral Cancer 60 1.301
302
c FML021 Familial Hypercholesterolemia 71 1.299
303
SYN007 Synovitis 54 1.287
304
PLC002 Plica Syndrome 35 1.287
305
P BLD134 Bladder Cancer 79 1.266
306
P MYL006 Myeloid Leukemia 60 1.265
307
P FML023 Familial Hemiplegic Migraine 53 1.259
308
HYP266 Hypoxia 56 1.254
309
MNT002 Mental Depression 56 1.250
310
LYM009 Lymphocytic Choriomeningitis 46 1.250
311
LPT014 Leptin Deficiency or Dysfunction 77 1.246
312
P LNG032 Lung Cancer 98 1.239
313
P ACN011 Acne 55 1.238
314
ATS010 Autosomal Recessive Disease 42 1.230
315
P HLP001 Holoprosencephaly 69 1.226
316
HYP080 Hypogonadism 49 1.222
317
LYM021 Lymphadenitis 56 1.221
318
MLT157 Multiple System Atrophy 1 69 1.218
319
GST040 Gastric Adenocarcinoma 66 1.218
320
P AST005 Asthma 76 1.214
321
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.209
322
P RTN024 Retinoblastoma 72 1.209
323
END057 Endometrial Cancer 71 1.200
324
P EPS003 Episodic Ataxia 59 1.197
325
P PNC035 Pancreatic Cancer 86 1.185
326
P LYM033 Lymphoproliferative Syndrome 59 1.185
327
HRW001 Hair Whorl 35 1.185
328
ANX010 Anxiety 70 1.181
329
P MJR001 Major Depressive Disorder 68 1.176
330
NDL013 Nodular Regenerative Hyperplasia 46 1.176
331
c HPT016 Hepatitis B 62 1.167
332
LNG099 Lung Disease 62 1.167
333
P NPH012 Nephrotic Syndrome 62 1.162
334
c BTT014 Beta-Thalassemia 72 1.159
335
P GST044 Gastritis 55 1.159
336
ACQ007 Acquired Immunodeficiency Syndrome 58 1.154
337
c EPS035 Episodic Ataxia, Type 2 63 1.146
338
TTN003 Tetanus 64 1.141
339
P LNG064 Lung Cancer Susceptibility 3 70 1.138
340
P MLN007 Male Infertility 56 1.136
341
CHR178 Chromosomal Triplication 34 1.127
342
AZS001 Azoospermia 45 1.125
343
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 1.124
344
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.122
345
P RHM011 Rheumatoid Arthritis 81 1.112
346
OCL022 Ocular Melanoma 54 1.110
347
GLS018 Glass Syndrome 60 1.109
348
CRB004 Cerebral Artery Occlusion 46 1.109
349
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 1.108
350
SQM006 Squamous Cell Carcinoma 59 1.108
351
AST006 Astigmatism 46 1.103
352
HPT046 Hepatic Veno-Occlusive Disease 55 1.103
353
CMB007 Combined Immunodeficiency 56 1.098
354
P EXN002 Exanthem 58 1.088
355
PST028 Post-Traumatic Stress Disorder 59 1.083
356
P MYC084 Mycobacterium Tuberculosis 1 68 1.073
357
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.073
358
P THY061 Thyroid Dyshormonogenesis 2a 30 1.070
359
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.067
360
P RHN004 Rhinitis 57 1.063
361
STR067 Stroke, Ischemic 79 1.062
362
THY128 Thyroid Tumor 33 1.062
363
P ART021 Arteriosclerosis 53 1.059
364
P HMN010 Hemangioma 61 1.058
365
P NSP012 Nasopharyngeal Carcinoma 60 1.058
366
P SCH015 Schizophrenia 74 1.056
367
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.053
368
c ATM011 Autoimmune Hepatitis 62 1.053
369
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.047
370
ACT088 Acute Insulin Response 39 1.036
371
KRT009 Keratosis 52 1.036
372
c LKM056 Leukemia, Chronic Lymphocytic 2 47 1.026
373
P KRT007 Keratoconus 50 1.025
374
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 1.017
375
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 1.017
376
c SML038 Small Cell Cancer of the Lung 69 1.014
377
SPN186 Spinal Cord Injury 61 1.003
378
HYP017 Hypophosphatemia 49 1.003
379
TLN003 Telangiectasis 51 1.003
380
CRT072 Creutzfeldt-Jakob Disease 67 1.001
381
THP005 Thiopurines, Poor Metabolism of, 2 17 1.000
382
INT007 Intermediate Coronary Syndrome 53 0.995
383
SKN016 Skin Disease 62 0.992
384
P SYP003 Syphilis 59 0.985
385
ALL003 Allergic Rhinitis 66 0.979
386
MSL001 Measles 61 0.979
387
P ADL017 Adult T-Cell Leukemia 54 0.972
388
c LKM061 Leukemia, Acute Myeloid 83 0.972
389
P SLP005 Sleep Disorder 62 0.966
390
LSC001 Lesch-Nyhan Syndrome 62 0.965
391
ANG020 Angiosarcoma 63 0.964
392
P HYD006 Hydrocephalus 63 0.960
393
HMC014 Homocysteinemia 52 0.960
394
P CRD246 Cardiovascular System Disease 55 0.960
395
P PLM037 Pulmonary Hypertension 69 0.957
396
HYP056 Hypoglycemia 65 0.957
397
ACT119 Acute Promyelocytic Leukemia 62 0.953
398
FCL014 Focal Epilepsy 53 0.951
399
P ATX030 Ataxia-Telangiectasia 80 0.940
400
CRT013 Carotid Stenosis 51 0.940
401
c ACT075 Acute Myocardial Infarction 55 0.939
402
SRC014 Sarcoma 64 0.933
403
P EYD002 Eye Disease 57 0.929
404
P KDN017 Kidney Cancer 60 0.927
405
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.927
406
PRT037 Pertussis 49 0.926
407
MTH009 Mouth Disease 57 0.920
408
c PNC106 Pancreatic Agenesis 1 51 0.920
409
STM007 Stomatitis 52 0.920
410
HYP020 Hyperprolactinemia 63 0.913
411
ORL015 Oral Squamous Cell Carcinoma 43 0.913
412
P WSK001 Wiskott-Aldrich Syndrome 72 0.913
413
SPN035 Spindle Cell Sarcoma 51 0.913
414
P HNT016 Huntington Disease 73 0.911
415
P THR014 Thrombocytopenia 66 0.911
416
BRS099 Breast Ductal Carcinoma 61 0.909
417
P TMR010 Tumor Predisposition Syndrome 69 0.905
418
MYL009 Myelodysplastic Syndrome 67 0.905
419
P HMP007 Hemophilia 52 0.898
420
ALL010 Allergic Contact Dermatitis 56 0.898
421
BLD173 Bladder Small Cell Carcinoma 44 0.897
422
EXC002 Exocrine Pancreatic Insufficiency 42 0.891
423
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.889
424
ANG054 Angina Pectoris 65 0.885
425
P KLZ004 Kala-Azar 1 41 0.883
426
LSH001 Leishmaniasis 63 0.883
427
SYS071 Systemic Autoimmune Disease 35 0.883
428
SPL018 Splenomegaly 47 0.872
429
P PLM036 Pulmonary Fibrosis 65 0.869
430
MNN009 Meningoencephalitis 48 0.867
431
IRR001 Irregular Astigmatism 32 0.867
432
SKN019 Skin Melanoma 70 0.867
434
MCR011 Microinvasive Gastric Cancer 41 0.866
435
P INF032 Infertility 60 0.866
436
P ESP024 Esophagitis 60 0.866
437
P SKN015 Skin Carcinoma 71 0.859
438
MSC007 Muscle Hypertrophy 64 0.856
439
CRH001 Crohn's Disease 80 0.852
440
IGR001 Ige Responsiveness, Atopic 59 0.851
441
c ACT068 Acute Cystitis 61 0.851
442
c MJR024 Major Affective Disorder 9 40 0.849
443
c MJR022 Major Affective Disorder 8 37 0.849
444
P BPL003 Bipolar Disorder 56 0.849
445
ESP021 Esophageal Cancer 84 0.842
446
P BNG032 Benign Mesothelioma 53 0.842
447
HYP005 Hypokalemia 55 0.842
448
RNL077 Renal Fibrosis 46 0.839
449
THR024 Thrombosis 56 0.839
450
ANK001 Ankylosis 51 0.833
451
KRT008 Keratopathy 46 0.833
452
CYS042 Cystic Fibrosis and Congenital Absence of the Vas Deferens 14 0.833
453
CRD132 Cardiac Conduction Defect 59 0.832
454
c GLL024 Gallbladder Disease 1 53 0.829
455
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.826
456
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.826
457
P RTN018 Retinal Disease 53 0.824
458
c DRM054 Dermatitis, Atopic, 2 46 0.818
459
P NRP001 Neuropathy 59 0.808
460
LNG039 Lung Squamous Cell Carcinoma 57 0.806
461
P TYS001 Tay-Sachs Disease 69 0.801
462
P PSD015 Pseudohypoparathyroidism 54 0.801
463
DWN001 Down Syndrome 70 0.801
464
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.801
465
P ATR011 Atrial Fibrillation 66 0.797
466
P OST002 Osteoporosis 77 0.793
467
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.793
468
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.793
469
P DMN002 Dementia 65 0.793
470
P HYP098 Hypereosinophilic Syndrome 66 0.790
471
c WLM013 Wilms Tumor 1 65 0.785
472
MYL031 Myeloproliferative Neoplasm 66 0.785
473
TXC005 Toxic Shock Syndrome 62 0.779
474
c PRD040 Periodontitis, Chronic 52 0.775
475
CHL068 Cholestasis 61 0.775
476
P BRN076 Bronchiectasis with or Without Elevated Sweat Chloride 1 33 0.774
477
BTT017 Beta-Thalassemia Major 53 0.774
478
P CRN037 Craniosynostosis 67 0.774
479
P TMP001 Temporal Lobe Epilepsy 49 0.774
480
P PRK057 Parkinson Disease, Late-Onset 79 0.771
481
TRG002 Trigeminal Neuralgia 61 0.771
482
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.771
483
PPT001 Peptic Esophagitis 51 0.771
484
c HMP029 Hemophilia a 69 0.764
485
FCT001 Factor Viii Deficiency 62 0.764
486
PST011 Pustulosis of Palm and Sole 52 0.764
487
P PSR002 Psoriasis 63 0.764
488
P MDL005 Medulloblastoma 75 0.763
489
VSC003 Visceral Leishmaniasis 54 0.763
491
c SCL052 Scleroderma, Familial Progressive 60 0.760
492
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.756
493
P ADN016 Adenocarcinoma 63 0.756
494
PFF001 Pfeiffer Syndrome 77 0.752
495
DRY001 Dry Eye Syndrome 49 0.752
496
CMM004 Common Variable Immunodeficiency 72 0.752
497
SKN020 Skin Papilloma 40 0.752
498
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.750
499
HYP555 Hypertriglyceridemia, Transient Infantile 38 0.750
500
c HYP841 Hypoalphalipoproteinemia, Primary, 1 50 0.750
501
CHR028 Chronic Wasting Disease 33 0.749
502
P ALP008 Alopecia 53 0.745
503
P HYP121 Hypoalphalipoproteinemia 42 0.745
504
SCT005 Scott Syndrome 51 0.739
505
c ATM101 Autoimmune Gastritis 40 0.739
506
MTH071 Methane Production 25 0.739
507
HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.739
508
P PRP019 Peripheral Nervous System Disease 57 0.729
509
P MYC008 Myocarditis 59 0.729
510
PHN003 Phenylketonuria 76 0.726
511
HMP009 Haemophilus Influenzae 41 0.726
512
P STC001 Stickler Syndrome 60 0.725
513
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.725
514
c STC013 Stickler Syndrome, Type Ii 36 0.725
515
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.722
516
c SPN225 Spondyloarthropathy 1 70 0.718
517
SPN051 Spondylitis 51 0.718
518
URM002 Uremia 47 0.718
519
INF009 Inflammatory Spondylopathy 30 0.718
520
P HDC001 Headache 56 0.714
521
IMM003 Immunoglobulin Alpha Deficiency 44 0.712
522
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.712
523
c SPR086 Spermatogenic Failure 3 47 0.712
524
PLL009 Pellucid Marginal Degeneration 21 0.712
525
EPD015 Epidemic Typhus 44 0.710
526
P HYP768 Hyperlipoproteinemia, Type I 67 0.710
527
FRN006 Frontotemporal Dementia 68 0.706
528
P CHR345 Chronic Pain 50 0.706
529
GT001 Gout 63 0.701
530
GLM045 Glioma 62 0.701
531
GLL048 Glial Tumor 52 0.701
532
NWC001 Newcastle Disease 48 0.698
533
OCL009 Ocular Cancer 55 0.698
534
CHL045 Choline Deficiency Disease 39 0.698
535
HYP043 Hyperandrogenism 47 0.697
536
ULC004 Ulcerative Colitis 74 0.697
537
P SCK005 Sickle Cell Disease 56 0.697
538
P SZR006 Seizure Disorder 69 0.693
539
PLY028 Polycystic Bone Disease 17 0.681
540
P PRK039 Parkinsonism 55 0.677
541
TRN015 Transient Cerebral Ischemia 62 0.672
542
DMY004 Demyelinating Disease 50 0.672
543
HLC007 Helicobacter Pylori Infection 67 0.668
544
SPT005 Spotted Fever 49 0.668
545
CHC001 Chickenpox 56 0.664
546
LYN004 Lynch Syndrome I 60 0.664
547
SND001 Sandhoff Disease 66 0.664
548
P KRT005 Keratoacanthoma 47 0.664
549
DFC004 Deficiency Anemia 74 0.659
550
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.655
551
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.655
552
IMP005 Impotence 52 0.646
553
P ICH004 Ichthyosis 56 0.642
554
PPL052 Papillomatosis, Confluent and Reticulated 34 0.637
555
IGG001 Iga Glomerulonephritis 50 0.637
556
RST023 Resting Heart Rate, Variation in 40 0.633
557
P MSC005 Muscular Dystrophy 66 0.633
558
PRP080 Peripheral Artery Disease 54 0.628
559
P CND004 Candidiasis 57 0.624
560
NKC002 Nk Cell Deficiency 31 0.619
561
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.619
562
BLL004 Bullous Keratopathy 47 0.619
563
END041 Endometrial Adenocarcinoma 63 0.619
564
P CHR012 Chronic Granulomatous Disease 69 0.619
565
c RTN041 Retinitis Pigmentosa 11 43 0.619
566
MCR013 Microphthalmia 60 0.619
567
ATR057 Atrioventricular Block 54 0.610
568
P FBR017 Fibrosarcoma 55 0.610
569
P MLT020 Multiple Sclerosis 79 0.600
570
BRN004 Brain Edema 54 0.596
571
CNS004 Constipation 56 0.596
572
P MTR014 Motor Neuron Disease 65 0.596
573
P SNS001 Sensorineural Hearing Loss 59 0.591
574
EXS001 Exostosis 49 0.591
575
P UVT001 Uveitis 57 0.591
576
ATX049 Ataxia with Vitamin 3 Deficiency 52 0.588
577
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.588
578
P MLN069 Melanoma, Uveal 59 0.588
579
ATX019 Ataxia with Vitamin E Deficiency 44 0.588
580
CLS049 Classic Phenylketonuria 42 0.588
581
P HYP069 Hyperparathyroidism 62 0.586
582
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.581
583
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.581
584
HYP732 Hyperalphalipoproteinemia 1 52 0.581
585
c VRL010 Viral Hepatitis 52 0.581
586
c ACT073 Acute Leukemia 59 0.581
587
INS001 Insulinoma 59 0.581
588
OST159 Osteogenic Sarcoma 66 0.581
589
PRT013 Portal Hypertension 59 0.576
590
P OPN001 Open-Angle Glaucoma 55 0.571
591
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.571
592
c PNC108 Pancreatitis, Hereditary 68 0.571
593
LYM027 Lymphopenia 56 0.571
594
ART016 Aortic Aneurysm 69 0.571
595
THR004 Thrombocytosis 52 0.571
596
LPD009 Lipid Storage Disease 45 0.571
597
ADN011 Adenoid Cystic Carcinoma 68 0.567
598
ADN089 Adenosquamous Lung Carcinoma 49 0.567
599
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.567
600
P VSC011 Vasculitis 61 0.566
601
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.561
602
SCH014 Schistosomiasis 56 0.561
603
DMP001 Dumping Syndrome 43 0.561
604
P TRM003 Tremor 50 0.561
605
DBT010 Diabetic Neuropathy 54 0.561
606
TNG002 Tangier Disease 64 0.556
607
c BRN108 Branchiootic Syndrome 1 63 0.556
608
P BND020 Bone Disease 60 0.556
609
CHL004 Cholelithiasis 48 0.556
610
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.551
611
MDD018 Middle East Respiratory Syndrome 44 0.551
612
P OVR042 Ovarian Cancer 88 0.551
613
GST092 Gastroesophageal Reflux 60 0.545
614
APN008 Apnea, Obstructive Sleep 66 0.545
615
P HYP024 Hypoparathyroidism 55 0.545
616
HMS001 Hemosiderosis 48 0.545
617
P NTR004 Neutropenia 62 0.545
618
CRT015 Carotid Artery Occlusion 45 0.545
619
P RRH023 Rare Hereditary Hemochromatosis 53 0.545
620
c ACT134 Acute Liver Failure 57 0.545
621
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.540
622
P RSP003 Respiratory Failure 74 0.540
623
P TRT010 Teratoma 50 0.540
624
GRW007 Growth Hormone Deficiency 47 0.540
625
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.540
626
ACT098 Acute Erythroid Leukemia 55 0.535
627
GLB002 Glioblastoma 67 0.535
628
c BLD140 Blood Group, I System 47 0.531
629
P VSC018 Visceral Steatosis 32 0.531
630
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.531
631
P SYS005 Systemic Scleroderma 73 0.529
632
PRP030 Purpura 54 0.529
633
P PLY018 Polycythemia 56 0.529
634
PLC008 Placenta Disease 49 0.529
635
LYM116 Lymph Node Disease 42 0.524
636
c ATS007 Autism Spectrum Disorder 72 0.519
637
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.519
638
P ANT006 Antiphospholipid Syndrome 55 0.519
639
VSC002 Vascular Dementia 59 0.519
640
THR123 Thrombotic Microangiopathy 40 0.519
641
CRV035 Cervical Cancer 72 0.513
642
MCS002 Mucositis 55 0.513
643
PLY150 Polykaryocytosis Inducer 29 0.513
644
ACR007 Acromegaly 70 0.513
645
P URT039 Urticaria 57 0.513
646
BTT013 Beta-Thalassemia, Dominant Inclusion Body Type 35 0.512
647
HND015 Hand Skill, Relative 29 0.512
648
c SVR005 Severe Pre-Eclampsia 50 0.507
649
MYX013 Myxofibrosarcoma 44 0.504
650
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.504
651
SZR001 Sezary's Disease 60 0.504
652
P LNG028 Long Qt Syndrome 63 0.502
653
P HML002 Hemolytic Anemia 62 0.502
654
MDD011 Mood Disorder 62 0.502
655
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.502
656
c GLC092 Glaucoma, Primary Open Angle 61 0.496
657
CHL067 Cholecystitis 59 0.496
658
FML026 Familial Lipoprotein Lipase Deficiency 52 0.496
659
MSC157 Muscular Dystrophy, Duchenne Type 79 0.496
660
c HNT010 Huntington Disease-Like 1 55 0.496
661
HPT022 Hepatoblastoma 54 0.496
662
ABT001 Abetalipoproteinemia 68 0.490
663
OST003 Osteonecrosis 61 0.490
664
OTT002 Otitis Media 71 0.490
665
MTB004 Metabolic Acidosis 48 0.490
666
PRP016 Paraplegia 52 0.490
667
P DYS154 Dystonia 64 0.490
668
CRD016 Cardiac Rupture 34 0.490
669
P CHL066 Cholangitis 51 0.490
670
PLT004 Platelet Glycoprotein Iv Deficiency 56 0.484
671
P MYS005 Myositis 56 0.484
672
c OPT053 Optic Atrophy 1 62 0.484
673
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.484
674
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.484
675
P END044 Endometriosis 62 0.484
676
SVR001 Severe Acute Respiratory Syndrome 68 0.484
677
INT066 Interstitial Lung Disease 60 0.484
678
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.484
679
SCK003 Sickle Cell Anemia 74 0.478
680
URT010 Ureteral Obstruction 45 0.478
681
DSS009 Disseminated Intravascular Coagulation 56 0.478
682
P ART023 Arthropathy 60 0.478
683
P MYS003 Myasthenia Gravis 68 0.472
684
ACN002 Acanthosis Nigricans 56 0.472
685
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.472
686
PLP001 Pulpitis 48 0.472
687
CHL123 Chlamydia 58 0.472
688
P GLY013 Glycogen Storage Disease 59 0.472
689
P THY023 Thymoma 64 0.472
690
c THY107 Thymoma, Familial 42 0.472
691
P NRC002 Narcolepsy 55 0.472
692
PLM033 Pulmonary Embolism 58 0.472
693
PLY001 Polycythemia Vera 69 0.466
694
P VNW001 Von Willebrand's Disease 64 0.466
695
ANR040 Aneurysm 60 0.466
696
OVR094 Ovarian Epithelial Cancer 39 0.466
697
P CTR002 Cataract 59 0.466
698
DWR001 Dwarfism 45 0.466
699
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.460
700
P PRL003 Proliferative Glomerulonephritis 43 0.460
701
P ESS003 Essential Thrombocythemia 68 0.460
702
P THR015 Thrombophilia 51 0.460
703
P ADL010 Adult Respiratory Distress Syndrome 71 0.460
704
TRG022 Triglyceride Deposit Cardiomyovasculopathy 19 0.460
705
c THR082 Thrombophilia Due to Activated Protein C Resistance 58 0.454
706
P PLY014 Polycystic Kidney Disease 71 0.454
707
P PHC003 Pheochromocytoma 70 0.454
708
CNN005 Connective Tissue Disease 66 0.454
709
HDN002 Head Injury 44 0.454
710
P FML011 Familial Adenomatous Polyposis 71 0.447
711
ILT001 Ileitis 49 0.447
712
PLM031 Poliomyelitis 62 0.447
713
BRC012 Brucellosis 66 0.441
714
PRS045 Prostatic Hypertrophy 52 0.441
715
BRN056 Bronchopulmonary Dysplasia 57 0.441
716
c PRM316 Primary Congenital Hypothyroidism 31 0.441
717
ARG004 Argyria 26 0.441
718
P RCT021 Rectum Cancer 54 0.435
719
c ACT071 Acute Kidney Failure 60 0.435
720
P HMC002 Homocystinuria 52 0.435
721
P FTL002 Fatal Familial Insomnia 50 0.428
722
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.428
723
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.428
724
c CRD087 Cardiomyopathy, Familial Hypertrophic, 10 36 0.428
725
P MTR004 Maturity-Onset Diabetes of the Young 66 0.428
726
BRN024 Bronchitis 67 0.428
727
HYP006 Hypertensive Heart Disease 48 0.428
728
c DRM040 Dermatitis Herpetiformis, Familial 35 0.428
729
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.428
730
P DRM007 Dermatitis Herpetiformis 54 0.428
731
NRM001 Neuromyelitis Optica 60 0.428
732
SLD003 Sialadenitis 47 0.421
733
MLR004 Malaria 78 0.421
734
SCR008 Scrub Typhus 57 0.421
735
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.414
736
ADR040 Adrenal Gland Pheochromocytoma 45 0.414
737
SPS057 Spasticity 43 0.414
739
P MYT002 Myotonic Dystrophy 51 0.414
740
P PMP001 Pemphigus 55 0.414
741
OCL069 Ocular Motor Apraxia 57 0.407
742
c LKM063 Leukemia, Chronic Myeloid 71 0.407
743
LMB062 Limb Ischemia 55 0.407
744
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.407
745
CRD223 Cardiac Arrhythmia 63 0.407
746
MST005 Mastitis 52 0.407
747
PRS021 Prostatic Adenoma 43 0.407
748
P GLL022 Guillain-Barre Syndrome 59 0.407
749
LYS002 Lysosomal Storage Disease 51 0.407
750
PRM329 Premature Aging 36 0.407
751
ESP027 Esophagus Squamous Cell Carcinoma 45 0.401
752
OST011 Osteomalacia 52 0.400
753
P GLM040 Glioma Susceptibility 1 70 0.400
754
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.400
755
MLG169 Malignant Astrocytoma 57 0.400
756
HMG005 Hemoglobinopathy 55 0.400
757
P CNJ013 Conjunctivitis 66 0.400
758
P FCL005 Focal Segmental Glomerulosclerosis 57 0.400
759
AMN001 Amenorrhea 53 0.400
760
CHN055 Chanarin-Dorfman Syndrome 60 0.400
761
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.400
762
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.400
763
P SPP010 Suppressor of Tumorigenicity 3 51 0.393
764
KWS002 Kawasaki Disease 65 0.393
765
DFF005 Diffuse Large B-Cell Lymphoma 55 0.393
766
c PCH010 Pachyonychia Congenita 3 43 0.393
767
P SCL048 Sclerosteosis 58 0.393
768
PCK003 Pick Disease of Brain 69 0.393
769
P SPN046 Spinal Muscular Atrophy 62 0.393
770
CRS001 Crescentic Glomerulonephritis 42 0.393
771
ACT084 Acute Stress Disorder 53 0.393
772
KRT002 Keratomalacia 54 0.393
773
LYS012 Lysosomal Acid Lipase Deficiency 64 0.393
774
ADR016 Adrenal Cortical Carcinoma 61 0.386
775
DSS032 Disease by Infectious Agent 55 0.386
776
c SCN007 Secondary Hyperparathyroidism 51 0.386
777
P HYP265 Hypotonia 42 0.386
778
P PLM034 Pulmonary Emphysema 58 0.386
779
LBS001 Lubs X-Linked Mental Retardation Syndrome 49 0.378
780
CHR710 Chronic Spontaneous Urticaria 45 0.378
781
P DRM010 Dermatomyositis 61 0.378
782
HPT004 Hepatic Coma 43 0.378
783
P ATS364 Autism 72 0.378
784
P TBR001 Tuberous Sclerosis 69 0.378
785
NPH009 Nephrolithiasis 54 0.378
786
P OVR046 Ovarian Cyst 44 0.378
787
RTN020 Retinal Vascular Disease 45 0.378
788
HPT019 Hepatic Encephalopathy 59 0.378
789
NRM005 Neuromuscular Disease 63 0.378
790
HML018 Homologous Wasting Disease 21 0.378
791
ANX004 Anoxia 40 0.378
792
DYS073 Dysphagia 53 0.378
793
THR035 Thrombasthenia 48 0.378
794
GLM044 Glomerular Disease 34 0.378
795
PRS129 Prostatic Hyperplasia, Benign 48 0.371
796
c ANM038 Anemia, Autoimmune Hemolytic 63 0.371
797
PNG002 Pain Agnosia 51 0.371
798
VTM002 Vitamin B12 Deficiency 48 0.371
799
P HRS035 Hirschsprung Disease 1 66 0.371
800
ANL018 Analbuminemia 52 0.371
801
P DRR001 Diarrhea 55 0.371
802
P GND004 Gonadal Dysgenesis 46 0.371
803
IRN001 Iron Deficiency Anemia 58 0.371
804
PNC129 Pancreatic Adenocarcinoma 65 0.371
805
CRT033 Corticobasal Degeneration 48 0.371
806
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.371
807
c ACT135 Acute Graft Versus Host Disease 51 0.371
808
MYL005 Myelofibrosis 70 0.363
809
c ATM099 Autoimmune Uveitis 44 0.363
810
STT001 Status Epilepticus 58 0.363
811
P DDN001 Duodenal Ulcer 53 0.363
812
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.363
813
WLL004 Wallerian Degeneration 38 0.363
814
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.363
815
P NRV007 Nervous System Disease 66 0.363
816
WLF001 Wolff-Parkinson-White Syndrome 63 0.355
817
FCT002 Factor Xi Deficiency 61 0.355
819
P APL001 Aplastic Anemia 73 0.355
820
PSR001 Psoriatic Arthritis 61 0.355
821
P MMB011 Membranous Nephropathy 50 0.355
822
SNL009 Senile Plaque Formation 28 0.355
823
P SBS003 Substance Abuse 54 0.355
824
c PRM005 Primary Hyperparathyroidism 59 0.355
825
GST023 Gastric Ulcer 52 0.355
826
PRD004 Prediabetes Syndrome 52 0.355
827
P BRS044 Breast Adenocarcinoma 58 0.355
828
SDD008 Sudden Sensorineural Hearing Loss 41 0.355
829
P CLS010 Cluster Headache 42 0.355
830
PTT037 Pituitary Tumors 44 0.355
831
SYS003 Systolic Heart Failure 49 0.355
832
c JVN010 Juvenile Rheumatoid Arthritis 66 0.355
833
ACH005 Achalasia 54 0.355
834
P PRC019 Precocious Puberty 49 0.355
835
c INH032 Inherited Human Prion Disease 23 0.355
836
STR077 Streptococcal Toxic-Shock Syndrome 34 0.355
837
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 0.347
838
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.347
839
TND005 Tendinitis 54 0.347
840
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.347
841
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 0.347
842
PMP006 Pemphigus Vulgaris, Familial 58 0.347
843
P PRD006 Prader-Willi Syndrome 60 0.347
844
BRS051 Breast Disease 58 0.347
845
SFT003 Soft Tissue Sarcoma 57 0.347
846
FTL021 Fetal Macrosomia 40 0.347
847
GLY014 Glycerol Kinase Deficiency 48 0.338
848
TND004 Tendinopathy 45 0.338
849
c CHR711 Chronic Asthma 41 0.338
850
c FNC027 Fanconi Anemia, Complementation Group a 81 0.338
851
AML029 Ameloblastoma 46 0.338
852
NRL016 Neural Tube Defects 81 0.338
853
ACT003 Acute Kidney Tubular Necrosis 46 0.338
854
c NPH055 Nephrotic Syndrome, Type 1 52 0.338
855
SGN002 Signet Ring Cell Adenocarcinoma 46 0.338
856
BCK006 Back Pain 43 0.338
857
P INS002 in Situ Carcinoma 53 0.338
858
AML004 Ameloblastic Carcinoma 39 0.338
859
P INT070 Intestinal Obstruction 57 0.338
860
CHL061 Childhood Leukemia 47 0.338
861
P ALP009 Alopecia Areata 59 0.338
862
GNT167 Genetic Obesity 32 0.338
863
P SHR001 Short Bowel Syndrome 53 0.330
864
BCL014 B-Cell Growth Factor 32 0.330
865
P FML018 Familial Mediterranean Fever 73 0.330
866
SXL003 Sexual Disorder 49 0.330
867
P CRD119 Cardiac Arrest 68 0.330
868
c LNG048 Long Qt Syndrome 3 53 0.330
869
HNC001 Henoch-Schoenlein Purpura 56 0.330
870
P MYP006 Myopia 55 0.330
871
OVR063 Overnutrition 42 0.330
872
c BSL007 Basal Cell Carcinoma 68 0.330
873
P OST001 Osteopetrosis 70 0.330
874
PRM236 Primary Biliary Cholangitis 62 0.330
875
P PYL005 Pyelonephritis 56 0.330
876
CLN015 Colon Adenocarcinoma 64 0.330
877
PSY004 Psychotic Disorder 66 0.330
878
PPL018 Papillary Adenocarcinoma 44 0.330
879
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.330
880
HRT012 Heart Valve Disease 53 0.330
881
ATN005 Autonomic Dysfunction 45 0.330
882
ILS001 Ileus 49 0.330
883
P HYP083 Hypopituitarism 52 0.330
884
PRX035 Paroxysmal Dyskinesia 30 0.330
885
P MCH002 Machado-Joseph Disease 63 0.321
886
VRC005 Varicose Veins 59 0.321
887
c HMP004 Hemophilia B 68 0.321
888
P CRN024 Corneal Disease 43 0.321
889
ART074 Aortic Dissection 53 0.321
890
P ANP001 Anaplastic Large Cell Lymphoma 61 0.321
891
BCT021 Bacterial Sepsis 43 0.321
892
HYP540 Hypertension, Diastolic 37 0.321
893
XNT003 Xanthomatosis 48 0.321
894
c TBR025 Tuberous Sclerosis 1 84 0.321
895
LMY002 Leiomyoma 51 0.321
896
PNC001 Pancytopenia 52 0.321
897
MMB001 Membranoproliferative Glomerulonephritis 56 0.321
898
PLM001 Pulmonary Tuberculosis 69 0.321
899
P INT068 Intestinal Disease 53 0.321
900
OLG001 Oligospermia 45 0.321
901
GNG013 Gingivitis 59 0.321
902
FDL002 Food Allergy 47 0.321
903
ANV001 Anovulation 46 0.321
904
LNT001 Linitis Plastica 29 0.321
905
HYP835 Hypothalamic Obesity 38 0.321
906
P PLY188 Polyendocrinopathy 29 0.321
907
PRX085 Preaxial Hallucal Polydactyly 28 0.312
908
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.312
909
INT067 Interstitial Nephritis 47 0.312
910
P STS003 Sitosterolemia 53 0.312
911
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.312
912
P MCR129 Microvascular Complications of Diabetes 1 68 0.312
913
c SPN294 Spinocerebellar Ataxia 1 53 0.312
914
PRP009 Peripartum Cardiomyopathy 54 0.312
915
GRS011 Gerstmann-Straussler Disease 55 0.312
916
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.312
917
THY006 Thymus Lymphoma 27 0.312
918
CRN019 Coronary Artery Vasospasm 47 0.312
919
BRX001 Bruxism 51 0.312
920
TCL003 T Cell Deficiency 44 0.312
921
P GCH001 Gaucher's Disease 69 0.312
922
CHR073 Choreatic Disease 53 0.312
923
GNG003 Gingival Recession 50 0.312
924
P TCD001 Tic Disorder 50 0.312
925
MCL006 Macular Retinal Edema 56 0.312
926
ADR004 Adrenal Cortical Adenocarcinoma 38 0.312
927
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.312
928
HMG002 Hemoglobinuria 50 0.312
929
CCN002 Cocaine Abuse 49 0.312
930
OCL006 Ocular Hypertension 53 0.312
931
PRM315 Permanent Congenital Hypothyroidism 26 0.312
932
P PRG139 Progeroid Syndrome 29 0.312
933
RFS006 Refsum Disease, Classic 63 0.303
934
CLB022 Coloboma, Ocular, Autosomal Recessive 29 0.303
935
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.303
936
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 52 0.303
937
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.303
938
LMY014 Leiomyoma, Uterine 55 0.303
939
HYD002 Hydronephrosis 58 0.303
940
RBS001 Rabies 58 0.303
941
NRT004 Neuritis 53 0.303
942
DYS015 Dysentery 50 0.303
943
P CRN025 Corneal Dystrophy 49 0.303
944
QFV001 Q Fever 61 0.303
945
CHG001 Chagas Disease 65 0.303
946
DBT008 Diabetic Angiopathy 47 0.303
947
CRT016 Carotid Artery Disease 52 0.303
948
P EPD016 Epidermolysis Bullosa 53 0.303
949
ACT058 Active Peptic Ulcer Disease 55 0.303
950
FML304 Familial Isolated Dilated Cardiomyopathy 51 0.303
951
ACT162 Acute Sensory Ataxic Neuropathy 24 0.303
952
IRR002 Irritable Bowel Syndrome 65 0.303
953
FML037 Female Breast Cancer 51 0.293
954
CLR108 Colorectal Adenoma 63 0.293
955
c SPN266 Spinocerebellar Ataxia 35 39 0.293
956
P HML001 Hemolytic-Uremic Syndrome 52 0.293