Search results for mip

1657 hits were found for mip

# Family MCID Name MIFTS Score
1
c CTR116 Cataract 15, Multiple Types 26 45.113
2
ERL027 Early-Onset Non-Syndromic Cataract 31 37.962
3
P CTR002 Cataract 59 25.000
4
LRN006 Laurin-Sandrow Syndrome 46 18.055
5
CRL001 Cerulean Cataract 26 15.920
6
BRN004 Brain Edema 54 15.223
7
CYS001 Cystic Fibrosis 77 14.265
8
MCR013 Microphthalmia 60 12.819
9
INT323 Intraocular Pressure Quantitative Trait Locus 63 11.332
10
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 11.185
11
BLL004 Bullous Keratopathy 47 10.662
12
MNR012 Meniere Disease 55 10.618
13
RFR003 Refractive Error 41 10.514
14
PRS025 Presbyopia 39 10.478
15
P INN002 Inner Ear Disease 50 10.393
16
c CTR145 Cataract 44 35 7.904
17
ERL037 Early-Onset Lamellar Cataract 16 7.904
18
ERL040 Early-Onset Sutural Cataract 16 7.904
19
P ERL043 Early-Onset Nuclear Cataract 28 7.904
20
c ERL044 Early-Onset Posterior Polar Cataract 22 7.904
21
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 7.590
22
P LNS003 Lens Disease 33 7.434
23
MTR001 Mature Cataract 27 7.434
24
ATM100 Autoimmune Optic Neuritis 28 7.349
25
EYC003 Eye Accommodation Disease 18 7.349
26
HYD003 Hydrarthrosis 32 7.349
27
IMM002 Immature Cataract 28 7.349
28
DYS030 Dysferlinopathy 38 7.349
29
PRP007 Priapism 46 7.349
30
P PRS040 Prostate Cancer 95 6.732
31
CYT002 Cytokine Deficiency 43 5.172
32
PRS047 Prostatitis 58 4.834
33
c PRS130 Prostate Cancer, Hereditary, 8 32 4.505
34
c PRS136 Prostate Cancer, Hereditary, 6 33 4.505
35
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.829
36
MYL069 Myeloma, Multiple 77 3.366
37
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 3.317
38
CHL123 Chlamydia 58 3.183
39
P HYP069 Hyperparathyroidism 62 3.052
40
c PRM005 Primary Hyperparathyroidism 59 2.990
41
IMM167 Immune Deficiency Disease 77 2.903
42
HMN044 Human Immunodeficiency Virus Type 1 76 2.879
43
P PRD008 Periodontitis 64 2.822
44
LGN006 Legionnaire Disease 52 2.775
45
P BND020 Bone Disease 60 2.759
46
P MLN008 Melanoma 75 2.731
47
BNR002 Bone Resorption Disease 47 2.727
48
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.626
49
P ADN016 Adenocarcinoma 63 2.505
50
ALL014 Allergic Encephalomyelitis 34 2.497
51
PRT037 Pertussis 49 2.439
52
HLX001 Helix Syndrome 47 2.402
53
P PLM036 Pulmonary Fibrosis 65 2.360
54
P BRS047 Breast Cancer 97 2.229
55
PRT036 Peritonitis 65 2.206
56
ADN018 Adenoma 58 2.172
57
48X005 48,xyyy 39 2.171
58
P NPH012 Nephrotic Syndrome 62 2.138
59
P MYC008 Myocarditis 59 2.112
60
P PNC035 Pancreatic Cancer 86 2.087
61
P DRM053 Dermatitis, Atopic 65 2.079
62
P INF037 Inflammatory Bowel Disease 53 2.036
63
DMY004 Demyelinating Disease 50 2.015
64
c ACT027 Acute Pancreatitis 60 1.970
65
P DNG005 Dengue Virus 55 1.950
66
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.920
67
P GLM007 Glomerulonephritis 59 1.888
68
ALL029 Allergic Disease 61 1.885
69
VCC001 Vaccinia 49 1.885
70
P MYL006 Myeloid Leukemia 60 1.881
71
c LKM063 Leukemia, Chronic Myeloid 71 1.875
72
P PNC044 Pancreatitis 61 1.833
73
VRL011 Viral Infectious Disease 60 1.833
74
P MYC084 Mycobacterium Tuberculosis 1 68 1.822
75
CLT003 Colitis 63 1.818
76
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.818
77
c LKM005 Leukemia, T-Cell, Chronic 33 1.818
78
PTH003 Pathologic Nystagmus 52 1.804
79
P SRC025 Sarcoidosis 1 70 1.799
80
SVR004 Severe Combined Immunodeficiency 71 1.792
81
DRM006 Dermatitis 62 1.780
82
P MNN013 Meningitis 65 1.777
83
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.768
84
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.768
85
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.768
86
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.768
87
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.768
88
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.768
89
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.768
90
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.768
91
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.768
92
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.768
93
DNG003 Dengue Disease 65 1.754
94
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.752
95
P LTR001 Lateral Sclerosis 58 1.752
96
BRN071 Brain Injury 50 1.720
97
CRT013 Carotid Stenosis 51 1.712
98
P HYP098 Hypereosinophilic Syndrome 66 1.693
99
KRT019 Keratitis, Hereditary 66 1.681
100
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 64 1.679
101
BRN002 Bronchiolitis 57 1.675
102
CRB004 Cerebral Artery Occlusion 46 1.674
103
P PNM007 Pneumonia 64 1.630
104
PRT251 Proteinuria, Chronic Benign 58 1.630
105
P LNG032 Lung Cancer 98 1.630
106
TXC005 Toxic Shock Syndrome 62 1.625
107
MLR004 Malaria 78 1.624
108
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.621
109
ALL006 Allergic Asthma 56 1.618
110
PST028 Post-Traumatic Stress Disorder 59 1.594
111
RBS001 Rabies 58 1.592
112
SPN186 Spinal Cord Injury 61 1.587
113
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.570
114
SKN019 Skin Melanoma 70 1.562
115
c LKM061 Leukemia, Acute Myeloid 83 1.540
116
c SCL052 Scleroderma, Familial Progressive 60 1.504
117
PLM001 Pulmonary Tuberculosis 69 1.491
118
P LKM002 Leukemia 66 1.489
119
P RSP003 Respiratory Failure 74 1.473
120
c BCT007 Bacterial Meningitis 55 1.472
121
LYM017 Lyme Disease 63 1.467
122
ATM095 Autoimmune Disease 61 1.448
123
P LYM118 Lymphoma 69 1.431
124
P UVT001 Uveitis 57 1.424
125
P ADL017 Adult T-Cell Leukemia 54 1.419
126
BRN024 Bronchitis 67 1.419
127
P GST044 Gastritis 55 1.419
128
LGN002 Legionellosis 61 1.418
129
P AGG001 Aggressive Periodontitis 55 1.418
130
HYP266 Hypoxia 56 1.409
131
P PSR002 Psoriasis 63 1.405
132
GNG013 Gingivitis 59 1.398
133
P INF038 Influenza 68 1.388
134
c PRD040 Periodontitis, Chronic 52 1.384
135
LYM133 Lymphoma, Hodgkin, Classic 74 1.378
136
STR067 Stroke, Ischemic 79 1.372
137
P LPS004 Lupus Erythematosus 61 1.372
138
PST011 Pustulosis of Palm and Sole 52 1.370
139
ISC004 Ischemia 61 1.368
140
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.363
141
DNG002 Dengue Hemorrhagic Fever 59 1.363
142
P MLT020 Multiple Sclerosis 79 1.361
143
c MJR024 Major Affective Disorder 9 40 1.356
144
c MJR022 Major Affective Disorder 8 37 1.356
145
P BPL003 Bipolar Disorder 56 1.356
146
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.351
147
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.349
148
DSS032 Disease by Infectious Agent 55 1.349
149
SCH014 Schistosomiasis 56 1.349
150
CRH001 Crohn's Disease 80 1.349
151
GLM044 Glomerular Disease 34 1.349
152
TRM010 Traumatic Brain Injury 50 1.344
153
ULC004 Ulcerative Colitis 74 1.344
154
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.342
155
P NSP012 Nasopharyngeal Carcinoma 60 1.327
156
EXT034 Extrinsic Allergic Alveolitis 56 1.327
157
c SYS001 Systemic Lupus Erythematosus 86 1.321
158
DRY001 Dry Eye Syndrome 49 1.312
159
P END044 Endometriosis 62 1.304
160
P VSC007 Vascular Disease 62 1.298
161
PRT029 Parathyroid Adenoma 51 1.289
162
P HMN032 Human Herpesvirus 8 47 1.277
163
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.273
164
P HYP726 Hypercalcemia, Infantile, 1 58 1.273
165
STT001 Status Epilepticus 58 1.259
166
QFV001 Q Fever 61 1.250
167
P HRP006 Herpes Simplex 65 1.247
168
KPS004 Kaposi Sarcoma 76 1.247
169
P CND004 Candidiasis 57 1.247
170
CRS001 Crescentic Glomerulonephritis 42 1.238
171
IDP091 Idiopathic Nephrotic Syndrome 49 1.221
172
HMP009 Haemophilus Influenzae 41 1.220
173
SQM006 Squamous Cell Carcinoma 59 1.213
174
P ENC004 Encephalitis 61 1.213
175
PLM010 Pulmonary Edema 54 1.208
176
c HPT001 Hepatitis C 61 1.203
177
KRT006 Keratoconjunctivitis 53 1.200
178
NRT004 Neuritis 53 1.198
179
LST001 Listeriosis 59 1.198
180
P ALZ034 Alzheimer Disease 87 1.183
181
P MYC007 Myocardial Infarction 69 1.183
182
P GCH001 Gaucher's Disease 69 1.183
183
NRM005 Neuromuscular Disease 63 1.182
184
HYP066 Hyperglycemia 60 1.171
185
c SML038 Small Cell Cancer of the Lung 69 1.166
186
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.160
187
MNN009 Meningoencephalitis 48 1.160
188
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 1.160
189
P LKM071 Leukemia, Chronic Lymphocytic 74 1.152
190
CHL014 Cholera 62 1.150
191
TNG009 Tongue Squamous Cell Carcinoma 43 1.144
192
CHG001 Chagas Disease 65 1.144
193
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.144
194
P MYP004 Myopathy 67 1.139
195
NSS002 Neisseria Meningitidis Infection 47 1.136
196
HRW001 Hair Whorl 35 1.133
197
P FBR017 Fibrosarcoma 55 1.128
198
P NRB001 Neuroblastoma 66 1.128
199
P DBT005 Diabetes Insipidus 54 1.128
200
c MCR115 Microvascular Complications of Diabetes 5 65 1.121
201
P GRF003 Graft-Versus-Host Disease 71 1.121
202
P GLL022 Guillain-Barre Syndrome 59 1.119
203
c HPT073 Hepatitis C Virus 71 1.116
204
P RHN004 Rhinitis 57 1.116
205
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.110
206
P HPT021 Hepatitis 68 1.086
207
LNG099 Lung Disease 62 1.085
208
P KLZ004 Kala-Azar 1 41 1.080
209
SKN016 Skin Disease 62 1.080
210
LSH001 Leishmaniasis 63 1.080
211
c MCR133 Microvascular Complications of Diabetes 4 41 1.073
212
ALL003 Allergic Rhinitis 66 1.073
213
c MCR113 Microvascular Complications of Diabetes 3 52 1.073
214
c MCR130 Microvascular Complications of Diabetes 6 41 1.073
215
c MCR120 Microvascular Complications of Diabetes 7 47 1.073
216
P SYS005 Systemic Scleroderma 73 1.073
217
AGN016 Aging 54 1.066
218
OST159 Osteogenic Sarcoma 66 1.054
219
DFC004 Deficiency Anemia 74 1.048
220
HLC007 Helicobacter Pylori Infection 67 1.041
221
MNT002 Mental Depression 56 1.034
222
P RTN018 Retinal Disease 53 1.032
223
c MGR028 Migraine with or Without Aura 1 64 1.021
224
P AST005 Asthma 76 1.014
225
BCT022 Bacterial Infectious Disease 56 1.009
226
MNT001 Mantle Cell Lymphoma 65 1.009
227
TRY001 Trypanosomiasis 50 1.009
228
c HPT016 Hepatitis B 62 1.007
229
c ACT075 Acute Myocardial Infarction 55 1.007
230
BRN012 Bronchiolitis Obliterans 56 1.000
231
SLP001 Sleeping Sickness 56 0.997
232
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.997
233
MYL013 Myeloperoxidase Deficiency 44 0.992
234
STM007 Stomatitis 52 0.992
235
DPR016 Depression 65 0.992
236
P BCL017 B-Cell Lymphoma 57 0.985
237
PNC001 Pancytopenia 52 0.984
238
KRT001 Keratoconjunctivitis Sicca 49 0.984
239
P OPN001 Open-Angle Glaucoma 55 0.978
240
PLS007 Plasmodium Falciparum Malaria 52 0.978
241
CRN030 Coronary Stenosis 50 0.978
242
SPL018 Splenomegaly 47 0.978
243
c VRL010 Viral Hepatitis 52 0.970
244
GT001 Gout 63 0.970
245
P URN019 Urinary Tract Infection 49 0.962
246
PNM013 Pneumococcal Meningitis 43 0.962
247
P CNJ013 Conjunctivitis 66 0.958
248
HYP056 Hypoglycemia 65 0.958
249
LVR012 Liver Cirrhosis 62 0.955
250
IRD001 Iridocyclitis 54 0.955
251
SPP011 Suppression of Tumorigenicity 12 61 0.947
252
P MSC003 Muscular Atrophy 52 0.947
253
P CHR345 Chronic Pain 50 0.930
254
GLM045 Glioma 62 0.930
255
GLL048 Glial Tumor 52 0.930
256
PPL022 Papilloma 53 0.922
257
SQM002 Squamous Cell Papilloma 45 0.922
258
P OVR082 Overgrowth Syndrome 42 0.922
259
LPD008 Lipid Metabolism Disorder 61 0.914
260
P ESN008 Eosinophilic Pneumonia 50 0.913
261
P ART023 Arthropathy 60 0.913
262
PLR007 Pleural Empyema 51 0.913
263
c BRN108 Branchiootic Syndrome 1 63 0.912
264
ALV005 Alveolar Soft Part Sarcoma 61 0.911
265
INC003 Inclusion Conjunctivitis 35 0.911
266
c TYP009 Type 2 Diabetes Mellitus 92 0.904
267
CNT047 Contact Dermatitis 57 0.904
268
P ADL010 Adult Respiratory Distress Syndrome 71 0.900
269
ING001 Inguinal Hernia 59 0.895
270
c HYP836 Hypercholesterolemia, Familial, 1 73 0.895
271
BNG077 Benign Idiopathic Neonatal Seizures 22 0.886
272
P ART005 Arteriovenous Malformation 65 0.877
273
IRN002 Iron Metabolism Disease 56 0.877
274
P KDN018 Kidney Disease 72 0.877
275
P HDC001 Headache 56 0.873
276
P LKM062 Leukemia, Acute Lymphoblastic 69 0.867
277
PNC129 Pancreatic Adenocarcinoma 65 0.867
278
P NRP001 Neuropathy 59 0.867
279
P HML001 Hemolytic-Uremic Syndrome 52 0.857
280
FRM003 Farmer's Lung 41 0.857
281
P PYL005 Pyelonephritis 56 0.857
282
MCL006 Macular Retinal Edema 56 0.857
283
PRP002 Periapical Granuloma 38 0.850
284
c ACT068 Acute Cystitis 61 0.847
285
P HMP007 Hemophilia 52 0.847
286
AVN001 Avian Influenza 61 0.847
287
PST021 Postpartum Depression 50 0.840
288
MLD018 Mild Cognitive Impairment 48 0.837
289
P HYP750 Hypertriglyceridemia, Familial 62 0.837
290
MYL057 Myelopathy, Htlv-1-Associated 39 0.837
291
TRP002 Tropical Spastic Paraparesis 48 0.837
292
SPS019 Spastic Paraparesis 38 0.837
293
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.837
294
CTN007 Cutaneous Leishmaniasis 61 0.837
295
P RHM011 Rheumatoid Arthritis 81 0.828
296
ABR009 Abruzzo-Erickson Syndrome 45 0.827
297
c DFN360 Deafness, Autosomal Dominant 69 34 0.827
298
c DFN243 Deafness, Autosomal Recessive 88 24 0.827
299
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.826
300
MLD001 Melioidosis 67 0.826
301
c GLC092 Glaucoma, Primary Open Angle 61 0.826
302
P INF032 Infertility 60 0.826
303
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.826
304
MCS002 Mucositis 55 0.815
305
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.815
306
GLB002 Glioblastoma 67 0.815
307
P MLN007 Male Infertility 56 0.815
308
P MTR014 Motor Neuron Disease 65 0.815
309
P ALP008 Alopecia 53 0.815
310
ANX010 Anxiety 70 0.810
311
P ART022 Arthritis 70 0.806
312
c ACT073 Acute Leukemia 59 0.803
313
TLN003 Telangiectasis 51 0.803
314
DSS009 Disseminated Intravascular Coagulation 56 0.803
315
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 0.803
316
P MSC005 Muscular Dystrophy 66 0.802
317
ADR040 Adrenal Gland Pheochromocytoma 45 0.793
318
P PHC003 Pheochromocytoma 70 0.793
319
c ATM099 Autoimmune Uveitis 44 0.791
320
ORL015 Oral Squamous Cell Carcinoma 43 0.791
321
TRC008 Trachoma 53 0.791
322
NWC001 Newcastle Disease 48 0.791
323
HML018 Homologous Wasting Disease 21 0.791
324
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 35 0.791
325
CRT015 Carotid Artery Occlusion 45 0.791
326
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.788
327
P LNG064 Lung Cancer Susceptibility 3 70 0.784
328
OST012 Osteoarthritis 77 0.784
329
ANG054 Angina Pectoris 65 0.779
330
OST003 Osteonecrosis 61 0.779
331
DBT006 Diabetic Macular Edema 48 0.779
332
c ACT135 Acute Graft Versus Host Disease 51 0.779
333
SYN007 Synovitis 54 0.770
334
PLC002 Plica Syndrome 35 0.770
335
P FTL001 Fetal Alcohol Syndrome 55 0.766
336
BHC003 Behcet Syndrome 71 0.766
337
CHL131 Chlorpropamide-Alcohol Flushing 21 0.766
338
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.766
339
SGN002 Signet Ring Cell Adenocarcinoma 46 0.766
340
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 0.766
341
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.766
342
AGG012 Aggressive Nk-Cell Leukemia 47 0.755
344
LYM011 Lymphogranuloma Venereum 32 0.752
345
P CNT004 Centronuclear Myopathy 56 0.752
346
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.752
347
VSC002 Vascular Dementia 59 0.752
348
PLM035 Pulmonary Eosinophilia 49 0.752
349
MYC006 Mycosis Fungoides 65 0.737
350
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.737
351
PRP036 Peripheral T-Cell Lymphoma 52 0.737
352
RSP021 Respiratory Allergy 41 0.737
353
SCK003 Sickle Cell Anemia 74 0.737
354
P WSK001 Wiskott-Aldrich Syndrome 72 0.737
355
P LFR001 Li-Fraumeni Syndrome 73 0.737
356
c VRL007 Viral Encephalitis 50 0.737
357
JPN002 Japanese Encephalitis 61 0.737
358
P ART021 Arteriosclerosis 53 0.737
359
KRN002 Kearns-Sayre Syndrome 63 0.737
360
CRB079 Cerebrospinal Fluid Leak 36 0.737
361
CLR109 Colorectal Adenocarcinoma 50 0.722
362
OST017 Osteomyelitis 63 0.722
363
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.711
364
P LPR021 Leprosy 3 71 0.706
365
MSC157 Muscular Dystrophy, Duchenne Type 79 0.706
366
HNS001 Hansen's Disease 32 0.706
367
P MMB011 Membranous Nephropathy 50 0.705
368
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.705
369
CNN005 Connective Tissue Disease 66 0.705
370
P BRD002 Bardet-Biedl Syndrome 66 0.705
371
HYP014 Hyperuricemia 51 0.705
372
CHR074 Choriocarcinoma 46 0.705
373
THR123 Thrombotic Microangiopathy 40 0.705
374
c BCT013 Bacterial Pneumonia 47 0.696
375
P OST002 Osteoporosis 77 0.687
376
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.687
377
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.687
378
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.687
379
P OPT006 Optic Nerve Disease 57 0.687
380
OLG001 Oligospermia 45 0.687
381
PNN001 Panniculitis 52 0.687
382
INT007 Intermediate Coronary Syndrome 53 0.687
383
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.670
384
CNG034 Congestive Heart Failure 69 0.669
385
ANR040 Aneurysm 60 0.669
386
c NRB015 Neuroblastoma 2 28 0.667
387
c BRD016 Bardet-Biedl Syndrome 4 44 0.667
388
c SCH079 Schizophrenia 1 44 0.667
389
CRD137 Cardiogenic Shock 56 0.667
390
INT066 Interstitial Lung Disease 60 0.653
391
P CRN024 Corneal Disease 43 0.647
392
c GLY008 Glycogen Storage Disease Ii 72 0.647
393
INT146 Intervertebral Disc Disease 61 0.644
394
SPN392 Spondylosis, Cervical 30 0.644
395
P PST016 Posterior Polar Cataract 26 0.644
396
SPN020 Spondylosis 46 0.644
397
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.644
398
TRC023 Trichinosis 53 0.644
399
47X002 47,xyy 48 0.642
400
ACQ007 Acquired Immunodeficiency Syndrome 58 0.619
401
CRB086 Cerebral Aneurysms 40 0.619
402
MYL009 Myelodysplastic Syndrome 67 0.617
403
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.617
404
CHR710 Chronic Spontaneous Urticaria 45 0.617
405
SWN001 Swine Influenza 45 0.617
406
INT394 Intermittent Asthma 21 0.617
407
DMP001 Dumping Syndrome 43 0.617
408
P URT039 Urticaria 57 0.617
409
VRN004 Vernal Keratoconjunctivitis 47 0.617
410
CHR176 Chromophil Renal Cell Carcinoma 23 0.617
411
CLR112 Clear Cell Papillary Renal Cell Carcinoma 24 0.617
412
OST115 Osteonecrosis of the Jaw 40 0.617
413
DYS073 Dysphagia 53 0.613
414
BRN056 Bronchopulmonary Dysplasia 57 0.613
415
P VSC011 Vasculitis 61 0.607
416
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.585
417
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.585
418
HYP458 Hyper Ige Syndrome 60 0.585
419
c PRG018 Paragangliomas 1 59 0.585
420
HMR039 Hemorrhage, Intracerebral 57 0.585
421
DSS008 Disease of Mental Health 74 0.585
422
P PRG013 Paraganglioma 57 0.585
423
CHL079 Children's Interstitial Lung Disease 26 0.585
424
P PHC019 Pheochromocytoma-Paraganglioma 35 0.585
425
TCK001 Tick-Borne Encephalitis 59 0.582
426
ART016 Aortic Aneurysm 69 0.576
427
P HPT023 Hepatocellular Carcinoma 95 0.570
428
PRP027 Peripheral Vascular Disease 71 0.570
429
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.551
430
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.551
431
c HRD173 Hereditary Late-Onset Parkinson Disease 50 0.551
432
P PLM037 Pulmonary Hypertension 69 0.544
433
P MNC007 Monocytic Leukemia 48 0.538
434
ATH013 Atherosclerosis Susceptibility 63 0.531
435
P HYP040 Hypospadias 51 0.531
436
P SCL018 Scoliosis 57 0.524
437
ACN019 Acanthamoeba Keratitis 30 0.524
438
P MYS003 Myasthenia Gravis 68 0.510
439
CHR005 Chorioamnionitis 50 0.503
440
P HRT032 Heart Disease 84 0.503
441
FNG016 Fungal Keratitis 39 0.503
442
P ANP001 Anaplastic Large Cell Lymphoma 61 0.497
443
P OVR046 Ovarian Cyst 44 0.497
444
GST033 Gestational Diabetes 61 0.497
445
P MLT074 Multiple Endocrine Neoplasia 58 0.496
446
P MYS005 Myositis 56 0.488
447
P ASP006 Aspergillosis 71 0.488
448
KLB003 Klebsiella Pneumonia 49 0.488
449
P THR014 Thrombocytopenia 66 0.488
450
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.481
451
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.481
452
INT030 Intracranial Aneurysm 55 0.481
453
GTR002 Goiter 52 0.481
454
PLM033 Pulmonary Embolism 58 0.481
455
PLM012 Pulmonary Sarcoidosis 53 0.473
456
P SCH015 Schizophrenia 74 0.466
457
VRC005 Varicose Veins 59 0.466
458
P HYP024 Hypoparathyroidism 55 0.466
459
P CLR023 Colorectal Cancer 100 0.458
460
P NTR004 Neutropenia 62 0.458
461
CRN027 Corneal Neovascularization 47 0.458
462
SLC006 Silicosis 55 0.458
463
OTT002 Otitis Media 71 0.450
464
SND001 Sandhoff Disease 66 0.450
465
QDR001 Quadriplegia 49 0.450
466
P THY032 Thyroiditis 56 0.450
467
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.450
469
P APL001 Aplastic Anemia 73 0.442
470
ACT098 Acute Erythroid Leukemia 55 0.442
471
MST005 Mastitis 52 0.442
472
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.442
473
BRK010 Burkitt Lymphoma 66 0.433
474
c ATM022 Autoimmune Myocarditis 36 0.433
475
P DRR001 Diarrhea 55 0.433
476
CMP010 Complex Regional Pain Syndrome 59 0.425
477
END086 End Stage Renal Disease 54 0.425
478
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.416
479
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.416
480
RTN017 Retinal Detachment 60 0.416
481
LMB062 Limb Ischemia 55 0.416
482
P SJG008 Sjogren Syndrome 61 0.416
483
HSH003 Hashimoto Thyroiditis 60 0.416
484
SVR001 Severe Acute Respiratory Syndrome 68 0.416
485
CRB039 Cerebrovascular Disease 65 0.416
486
MCL003 Macular Holes 44 0.416
487
MSL001 Measles 61 0.416
488
ART140 Arteries, Anomalies of 52 0.408
489
P MJR001 Major Depressive Disorder 68 0.408
490
CRY005 Cryptococcosis 61 0.408
491
PLR008 Pleurisy 49 0.408
492
P DBT009 Diabetes Mellitus 67 0.408
493
INT395 Intracranial Meningioma 48 0.399
494
MST021 Meester-Loeys Syndrome 38 0.399
495
P SPN046 Spinal Muscular Atrophy 62 0.399
496
SPN051 Spondylitis 51 0.399
497
INF009 Inflammatory Spondylopathy 30 0.399
498
PLS011 Plasmacytoma 56 0.399
499
c SCN007 Secondary Hyperparathyroidism 51 0.399
500
MNN043 Meningioma, Familial 79 0.399
501
SCR001 Secretory Meningioma 40 0.399
502
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.399
503
SML019 Smallpox 55 0.399
504
P CHL066 Cholangitis 51 0.399
505
P SCK005 Sickle Cell Disease 56 0.399
506
c ACT134 Acute Liver Failure 57 0.399
507
c MCR112 Microvascular Complications of Diabetes 2 42 0.390
508
PRT013 Portal Hypertension 59 0.390
509
ART074 Aortic Dissection 53 0.390
510
P DRM010 Dermatomyositis 61 0.390
511
ENT011 Enterocolitis 55 0.390
512
VLV047 Volvulus of Midgut 55 0.390
513
P MCR129 Microvascular Complications of Diabetes 1 68 0.390
514
P GLM040 Glioma Susceptibility 1 70 0.390
515
MLG169 Malignant Astrocytoma 57 0.390
516
FTT001 Fatty Liver Disease 61 0.390
517
DWN001 Down Syndrome 70 0.380
518
VRL003 Variola Major 43 0.380
519
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.380
520
c SPN225 Spondyloarthropathy 1 70 0.380
521
BCT021 Bacterial Sepsis 43 0.380
522
CHL068 Cholestasis 61 0.380
523
P RTN022 Retinal Vein Occlusion 54 0.380
524
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.380
525
ESP021 Esophageal Cancer 84 0.370
526
OCL069 Ocular Motor Apraxia 57 0.370
527
P PLY041 Polymyositis 59 0.370
528
IMP005 Impotence 52 0.370
529
P CRD246 Cardiovascular System Disease 55 0.370
530
ONC002 Onchocerciasis 50 0.370
531
P LVR013 Liver Disease 68 0.370
532
P EYD002 Eye Disease 57 0.370
533
P PLM034 Pulmonary Emphysema 58 0.370
534
ANT024 Anthrax Disease 58 0.370
535
CCN002 Cocaine Abuse 49 0.370
536
P GST053 Gastric Cancer 82 0.361
537
CMB007 Combined Immunodeficiency 56 0.361
538
P SLP006 Sleep Apnea 69 0.361
539
SRC014 Sarcoma 64 0.361
540
CHL039 Choledocholithiasis 37 0.361
541
CRT016 Carotid Artery Disease 52 0.361
542
SPN035 Spindle Cell Sarcoma 51 0.361
543
c CHR684 Chronic Kidney Disease 74 0.361
544
c ATM024 Autoimmune Pancreatitis 52 0.350
545
P OVR042 Ovarian Cancer 88 0.350
546
c TYP008 Type 1 Diabetes Mellitus 77 0.350
547
c ATS007 Autism Spectrum Disorder 72 0.350
548
PNG002 Pain Agnosia 51 0.350
549
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.350
550
PPL052 Papillomatosis, Confluent and Reticulated 34 0.350
551
PRP016 Paraplegia 52 0.350
552
ALC006 Alcoholic Hepatitis 61 0.350
553
VSC003 Visceral Leishmaniasis 54 0.350
554
P BRN022 Bronchiectasis 59 0.350
555
IRR002 Irritable Bowel Syndrome 65 0.350
556
INV001 Invasive Aspergillosis 48 0.340
557
LPP008 Lipoprotein Quantitative Trait Locus 65 0.340
558
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.340
559
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.340
560
LYM027 Lymphopenia 56 0.340
561
P RPD001 Rapidly Progressive Glomerulonephritis 43 0.340
562
RST023 Resting Heart Rate, Variation in 40 0.340
563
BCK006 Back Pain 43 0.340
564
PPT005 Peptic Ulcer Disease 58 0.340
565
P MYT002 Myotonic Dystrophy 51 0.340
566
P BLD134 Bladder Cancer 79 0.329
568
c PRC016 Pre-Eclampsia 64 0.329
569
CVD001 Covid-19 58 0.329
570
P ATS364 Autism 72 0.329
571
LMY002 Leiomyoma 51 0.329
572
FBR047 Fibromyalgia 58 0.329
573
DNT012 Dental Caries 53 0.329
574
RTN020 Retinal Vascular Disease 45 0.329
575
ASP003 Aseptic Meningitis 51 0.329
576
P TRT010 Teratoma 50 0.329
577
P CRN300 Coronary Heart Disease 1 73 0.329
578
SPT004 Septic Arthritis 58 0.329
579
CHR178 Chromosomal Triplication 34 0.329
580
ILS001 Ileus 49 0.329
581
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 0.318
582
c ATR087 Atrial Standstill 1 74 0.318
583
CRY001 Cryptogenic Organizing Pneumonia 53 0.318
584
LMY014 Leiomyoma, Uterine 55 0.318
585
P CRC039 Coarctation of Aorta 46 0.318
586
FBR032 Fibromuscular Dysplasia 47 0.318
587
URT010 Ureteral Obstruction 45 0.318
588
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.318
589
LPT001 Leptospirosis 66 0.318
590
P HMN010 Hemangioma 61 0.318
591
P HYP086 Hypothyroidism 69 0.318
592
P DDN001 Duodenal Ulcer 53 0.318
593
END028 Endemic Goiter 36 0.318
594
c ACT071 Acute Kidney Failure 60 0.318
595
LYS002 Lysosomal Storage Disease 51 0.318
596
P END047 Endophthalmitis 53 0.318
597
STC004 Stachybotrys Chartarum 33 0.318
598
THY029 Thyroid Carcinoma 54 0.318
599
CRV035 Cervical Cancer 72 0.306
600
KWS002 Kawasaki Disease 65 0.306
601
GLC003 Glucose Intolerance 53 0.306
602
NNL006 Non-Alcoholic Steatohepatitis 54 0.306
603
CHL147 Chlamydia Pneumonia 47 0.306
604
PRT010 Parathyroid Carcinoma 68 0.306
605
PSR001 Psoriatic Arthritis 61 0.306
606
c PRG020 Paragangliomas 3 39 0.306
607
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.306
608
P ESP024 Esophagitis 60 0.306
609
PRM236 Primary Biliary Cholangitis 62 0.306
610
FLR002 Filariasis 55 0.306
611
GST023 Gastric Ulcer 52 0.306
612
PSY004 Psychotic Disorder 66 0.306
613
P BNG032 Benign Mesothelioma 53 0.306
614
PHN003 Phenylketonuria 76 0.306
615
P INS002 in Situ Carcinoma 53 0.306
616
P LCH002 Lichen Planus 55 0.306
617
P VTR007 Vitreoretinopathy 45 0.306
618
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.294
619
ALC007 Alcohol Dependence 65 0.294
620
HYP060 Hyperinsulinism 53 0.294
621
URM002 Uremia 47 0.294
622
KRT008 Keratopathy 46 0.294
623
PNM008 Pneumothorax 54 0.294
624
CRB037 Cerebral Palsy 67 0.294
625
P GRV001 Graves' Disease 54 0.294
626
INS001 Insulinoma 59 0.294
627
HGH041 High-Grade Astrocytoma 36 0.294
629
CHK001 Chikungunya 60 0.282
630
c FNC027 Fanconi Anemia, Complementation Group a 81 0.282
631
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.282
632
CHL065 Cholangiocarcinoma 58 0.282
633
CHL122 Cholesteatoma of Middle Ear 51 0.282
634
P EPL164 Epilepsy 70 0.282
635
INT079 Intrahepatic Cholangiocarcinoma 51 0.282
636
PHM001 Phimosis 38 0.282
637
P RCT021 Rectum Cancer 54 0.282
638
P SCL009 Sclerosing Cholangitis 46 0.282
639
ART006 Arthus Reaction 40 0.282
640
P THY023 Thymoma 64 0.282
641
c THY107 Thymoma, Familial 42 0.282
642
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.282
643
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 0.282
644
OVR094 Ovarian Epithelial Cancer 39 0.282
645
HRP004 Herpes Zoster 60 0.282
646
SNL007 Senile Cataract 40 0.282
647
P TXP001 Toxoplasmosis 60 0.282
648
P RTN008 Retinitis Pigmentosa 79 0.269
649
DFF005 Diffuse Large B-Cell Lymphoma 55 0.269
650
NRR001 Neuroretinitis 42 0.269
651
P LKD001 Leukodystrophy 58 0.269
652
SLD003 Sialadenitis 47 0.269
653
c VRL005 Viral Pneumonia 52 0.269
654
P MLN069 Melanoma, Uveal 59 0.269
655
DCT002 Ductal Carcinoma in Situ 58 0.269
656
IDP070 Idiopathic Scoliosis 41 0.269
657
PRT082 Preterm Premature Rupture of the Membranes 56 0.269
658
c EXD008 Exudative Vitreoretinopathy 1 71 0.269
659
HYD002 Hydronephrosis 58 0.269
660
P CRP001 Carpal Tunnel Syndrome 66 0.269
661
IGR001 Ige Responsiveness, Atopic 59 0.269
662
CHR100 Chronic Ulcer of Skin 57 0.269
663
P PLY019 Polyneuropathy 53 0.269
664
c FML021 Familial Hypercholesterolemia 71 0.269
665
P INT068 Intestinal Disease 53 0.269
666
LYM009 Lymphocytic Choriomeningitis 46 0.269
667
ALL010 Allergic Contact Dermatitis 56 0.269
668
HST010 Histiocytosis 49 0.269
669
RTN023 Retinitis 45 0.269
670
WLL004 Wallerian Degeneration 38 0.269
671
GST045 Gastroenteritis 58 0.269
672
PLR022 Pleural Disease 45 0.269
673
P HYP265 Hypotonia 42 0.269
674
CRV002 Cervix Uteri Carcinoma in Situ 48 0.269
675
NRV004 Nerve Compression Syndrome 47 0.269
676
HDN002 Head Injury 44 0.269
677
CRV045 Cervical Intraepithelial Neoplasia 38 0.269
678
P RTN016 Retinal Degeneration 52 0.269
679
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.269
680
PRN019 Perinatal Necrotizing Enterocolitis 60 0.269
681
HRD223 Hereditary Melanoma 37 0.269
682
FML168 Familial Isolated Pituitary Adenoma 32 0.269
683
ORL013 Oral Lichen Planus 45 0.269
684
P ACT105 Acute Mountain Sickness 52 0.269
685
ARG004 Argyria 26 0.269
686
P SPP010 Suppressor of Tumorigenicity 3 51 0.255
687
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.255
688
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.255
689
ACT119 Acute Promyelocytic Leukemia 62 0.255
690
P CHR071 Charcot-Marie-Tooth Disease 64 0.255
691
PLR001 Pleural Tuberculosis 49 0.255
692
URL001 Urolithiasis 45 0.255
693
PMP014 Pemphigoid 49 0.255
694
CYS005 Cysticercosis 60 0.255
695
RNL077 Renal Fibrosis 46 0.255
696
ERY003 Erythema Multiforme 56 0.255
697
P HNT016 Huntington Disease 73 0.255
698
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.255
699
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.255
700
c HPT003 Hepatitis a 63 0.255
701
VLV011 Vulvovaginal Candidiasis 49 0.255
702
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.255
703
P PLY011 Polycystic Ovary Syndrome 57 0.255
704
P SYP003 Syphilis 59 0.255
705
BCT002 Bacterial Vaginosis 53 0.255
706
TLR001 Tularemia 56 0.255
707
FCL014 Focal Epilepsy 53 0.255
708
ANX004 Anoxia 40 0.255
709
P HYP076 Hyperthyroidism 53 0.255
710
NRF007 Neurofibroma 64 0.255
711
KLB004 Klebsiella Infection 26 0.255
712
CNN002 Cannabis Abuse 44 0.255
713
ORL011 Oral Cancer 60 0.255
714
MSC007 Muscle Hypertrophy 64 0.240
715
EPD015 Epidemic Typhus 44 0.240
716
P SNS001 Sensorineural Hearing Loss 59 0.240
717
CRY014 Cryptococcal Meningitis 48 0.240
718
c VRL012 Viral Meningitis 46 0.240
719
P PRK057 Parkinson Disease, Late-Onset 79 0.240
720
PLY150 Polykaryocytosis Inducer 29 0.240
721
c GCH015 Gaucher Disease, Type I 67 0.240
722
c HYP595 Hypertension, Essential 84 0.240
723
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 54 0.240
724
IMM224 Immunodeficiency 68 36 0.240
725
MLT157 Multiple System Atrophy 1 69 0.240
726
FNG017 Fungal Infectious Disease 54 0.240
727
THR024 Thrombosis 56 0.240
728
PTN001 Patent Foramen Ovale 62 0.240
729
P ACN011 Acne 55 0.240
730
URN010 Urinary Tract Obstruction 55 0.240
731
P DMY001 Demyelinating Polyneuropathy 41 0.240
732
ESP002 Esophageal Varix 51 0.240
733
P ECL001 Eclampsia 52 0.240
734
SCR008 Scrub Typhus 57 0.240
735
P RNV001 Renovascular Hypertension 49 0.240
736
P CYS018 Cystitis 59 0.240
737
P OBS001 Obstructive Jaundice 49 0.240
738
HMS001 Hemosiderosis 48 0.240
739
P HRN001 Horner's Syndrome 45 0.240
740
RTN001 Retinal Vasculitis 46 0.240
741
P LPS002 Liposarcoma 64 0.240
742
PLG002 Plague 58 0.240
743
STP004 Staphylococcal Toxic Shock Syndrome 44 0.240
745
P ENC018 Encephalopathy 62 0.240
746
c RNG008 Ring Chromosome 13 30 0.240
747
BWN006 Bowen's Disease 32 0.240
748
MLR002 Miliary Tuberculosis 47 0.240
749
GNT003 Genital Herpes 54 0.240
750
c CHR417 Chronic Graft Versus Host Disease 55 0.240
751
P RRH023 Rare Hereditary Hemochromatosis 53 0.240
752
STP007 Staphylococcal Scarlet Fever 16 0.240
753
WST005 West Nile Virus 55 0.225
754
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.225
755
RCK004 Rickets 65 0.225
756
MDD018 Middle East Respiratory Syndrome 44 0.225
757
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.225
758
P KRB001 Krabbe Disease 69 0.225
759
MTB004 Metabolic Acidosis 48 0.225
760
LNG108 Langerhans Cell Histiocytosis 57 0.225
761
c HYP243 Hyperparathyroidism 1 48 0.225
762
NRL016 Neural Tube Defects 81 0.225
763
P MYM013 Moyamoya Disease 1 60 0.225
764
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.225
765
c LKM070 Leukemia, Acute Monocytic 56 0.225
766
c ACT249 Acute Asthma 40 0.225
767
HYP457 Hypertrophic Scars 42 0.225
768
PRV004 Periventricular Leukomalacia 52 0.225
769
P SBS003 Substance Abuse 54 0.225
770
ART017 Aortic Disease 49 0.225
771
P BNG030 Benign Ependymoma 51 0.225
772
ACT084 Acute Stress Disorder 53 0.225
773
PLM031 Poliomyelitis 62 0.225
774
GNG011 Gingival Disease 53 0.225
775
ECH003 Echinococcosis 52 0.225
776
PCD001 Pica Disease 38 0.225
777
FLR001 Filarial Elephantiasis 59 0.225
778
PNM001 Pneumocystosis 60 0.225
779
IRR003 Irritant Dermatitis 47 0.225
780
FDL002 Food Allergy 47 0.225
781
NRL005 Neurilemmoma 60 0.225
782
P PLY006 Polydactyly 58 0.225
783
TBR011 Tuberculous Meningitis 48 0.225
784
P TRC031 Trichorhinophalangeal Syndrome 37 0.225
785
CLL010 Cellular Ependymoma 58 0.225
786
ACT200 Acute Monoblastic Leukemia 40 0.225
787
GST050 Gastrointestinal System Disease 55 0.225
788
DRG003 Drug Dependence 46 0.225
789
MLL001 Molluscum Contagiosum 48 0.225
790
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.208
791
PRS129 Prostatic Hyperplasia, Benign 48 0.208
792
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 65 0.208
793
MYL005 Myelofibrosis 70 0.208
794
GRN037 Granulomatosis with Polyangiitis 67 0.208
795
MCN017 Meconium Ileus 52 0.208
796
c PCH010 Pachyonychia Congenita 3 43 0.208
797
P PNM006 Pneumoconiosis 55 0.208
798
P PRK039 Parkinsonism 55 0.208
799
PRM013 Premature Menopause 57 0.208
800
PPL049 Papillon-Lefevre Syndrome 65 0.208
801
SVR097 Severe Cutaneous Adverse Reaction 68 0.208
802
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 0.208
803
INC002 Inclusion Body Myositis 57 0.208
804
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.208
805
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.208
806
CRD223 Cardiac Arrhythmia 63 0.208
807
c DPH024 Diaphragmatic Hernia, Congenital 64 0.208
808
TBC004 Tobacco Addiction 63 0.208
809
ANT011 Antisocial Personality Disorder 47 0.208
810
P PRS038 Personality Disorder 65 0.208
811
c CNG012 Congenital Generalized Lipodystrophy 65 0.208
812
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.208
813
c HRD202 Hereditary Lymphedema I 55 0.208
814
PRS021 Prostatic Adenoma 43 0.208
815
ANR004 Anuria 44 0.208
816
NPH009 Nephrolithiasis 54 0.208
817
P PRL003 Proliferative Glomerulonephritis 43 0.208
818
c ACT042 Acute Pyelonephritis 45 0.208
819
SPT005 Spotted Fever 49 0.208
820
PRS045 Prostatic Hypertrophy 52 0.208
821
TYP007 Typhoid Fever 63 0.208
822
LYM021 Lymphadenitis 56 0.208
823
c DLT002 Dilated Cardiomyopathy 79 0.208
824
NDL007 Nodular Goiter 48 0.208
825
P HYD006 Hydrocephalus 63 0.208
826
TTH006 Tooth Disease 51 0.208
827
P PLM006 Pulmonary Alveolar Proteinosis 53 0.208
828
IRN001 Iron Deficiency Anemia 58 0.208
829
ANT018 Anthracosis 51 0.208
830
P CHN059 Chondrocalcinosis 51 0.208
831
TTN003 Tetanus 64 0.208
832
MTH009 Mouth Disease 57 0.208
833
RTN003 Retinal Ischemia 48 0.208
834
P PLY020 Polyradiculoneuropathy 47 0.208
835
PPL002 Papillary Carcinoma 46 0.208
836
THR013 Thoracic Outlet Syndrome 46 0.208
837
GST019 Gastrointestinal Stromal Tumor 78 0.208
838
c HMN022 Human T-Cell Leukemia Virus Type 2 33 0.208
839
PRP013 Paraphimosis 28 0.208
840
BLL006 Bullous Pemphigoid 61 0.208
841
MCC002 Mucocutaneous Leishmaniasis 47 0.208
842
P NRV007 Nervous System Disease 66 0.208
843
BRR012 Berardinelli-Seip Congenital Lipodystrophy 26 0.208
844
P NRF002 Neurofibromatosis 60 0.208
845
P GNG009 Gangliosidosis 44 0.208
846
OCL025 Ocular Toxoplasmosis 39 0.208
847
MNN020 Meningococcal Infection 45 0.208
848
NRN047 Neuroendocrine Neoplasm of Pancreas 19 0.208
849
GST092 Gastroesophageal Reflux 60 0.190
850
c HMP029 Hemophilia a 69 0.190
851
PLY001 Polycythemia Vera 69 0.190
852
P TMR010 Tumor Predisposition Syndrome 69 0.190
853
c JVN061 Juvenile Arthritis 56 0.190
854
OCC016 Occupational Asthma 33 0.190
855
P KRT007 Keratoconus 50 0.190
856
P END033 Endocarditis 58 0.190
857
P FML018 Familial Mediterranean Fever 73 0.190
858
TRG002 Trigeminal Neuralgia 61 0.190
859
ALX002 Alexithymia 37 0.190
860
KRN001 Korean Hemorrhagic Fever 34 0.190
861
HYP017 Hypophosphatemia 49 0.190
862
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.190
863
PLL012 Pollen Allergy 44 0.190
864
PNB004 Panbronchiolitis, Diffuse 34 0.190
865
FCT001 Factor Viii Deficiency 62 0.190
866
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.190
867
HYP346 Hypotrichosis and Recurrent Skin Vesicles 28 0.190
868
c CHL119 Cholangitis, Primary Sclerosing 57 0.190
869
PLP001 Pulpitis 48 0.190
870
URT020 Ureterocele 36 0.190
871
HMP005 Hemiplegia 53 0.190
872
BRC012 Brucellosis 66 0.190
873
P ALC033 Alcohol Use Disorder 67 0.190
874
ECT026 Ectopic Pregnancy 47 0.190
875
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.190
876
PRN009 Paranoid Schizophrenia 49 0.190
877
IGG001 Iga Glomerulonephritis 50 0.190
878
INT003 Intracranial Hypotension 36 0.190
879
ADN012 Adenocarcinoma in Situ 42 0.190
880
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.190
881
P MTR003 Mitral Valve Stenosis 53 0.190
882
P CRN025 Corneal Dystrophy 49 0.190
883
P FCL005 Focal Segmental Glomerulosclerosis 57 0.190
884
PPT001 Peptic Esophagitis 51 0.190
885
P NMN002 Niemann-Pick Disease 60 0.190
886
PRM024 Primary Angle-Closure Glaucoma 38 0.190
887
LYM022 Lymphangioma 54 0.190
888
CRM001 Crimean-Congo Hemorrhagic Fever 51 0.190
889
FCH001 Fuchs' Endothelial Dystrophy 48 0.190
890
PLC005 Placental Insufficiency 56 0.190
891
P BRS044 Breast Adenocarcinoma 58 0.190
892
THR016 Thrombophlebitis 50 0.190
893
VGN023 Vaginitis 56 0.190
894
c CNT035 Central Nervous System Disease 53 0.190
895
MDD011 Mood Disorder 62 0.190
896
CNS004 Constipation 56 0.190
897
MMM001 Mammary Paget's Disease 53 0.190
898
MMM006 Mammographic Density 39 0.190
899
c RTN047 Retinitis Pigmentosa 18 45 0.190
900
ASP026 Asplenia, Isolated Congenital 43 0.190
901
PRC002 Paracoccidioidomycosis 53 0.190
902
SNG003 Single Ventricular Heart 30 0.190
903
P RRL003 Rare Lymphatic Malformation 31 0.190
904
P SZR006 Seizure Disorder 69 0.190
905
SYN036 Syncope 44 0.190
906
P PLY018 Polycythemia 56 0.190
907
DYS032 Dystrophinopathies 47 0.190
908
NCR004 Nocardiosis 52 0.190
909
RSC001 Rosacea 55 0.190
910
P PLM064 Pulmonary Sequestration 22 0.190
911
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 0.190
912
INH023 Inherited Cancer-Predisposing Syndrome 53 0.190
913
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.190
914
ERY066 Erythema Multiforme Major 29 0.190
915
SPN340 Spontaneous Intracranial Hypotension 27 0.190
916
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.190
917
P MCH002 Machado-Joseph Disease 63 0.170
918
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.170
919
P JBR020 Joubert Syndrome 1 74 0.170
920
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.170
921
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 0.170
922
TKY002 Takayasu Arteritis 61 0.170
923
CTS003 Coats Disease 52 0.170
924
c PRM196 Premature Ovarian Failure 1 58 0.170
925
c DMN005 Diamond-Blackfan Anemia 2 28 0.170
926
JPN001 Japanese Spotted Fever 21 0.170
927
CMB076 Combined Oxidative Phosphorylation Deficiency 31 24 0.170
928
P STR022 Stargardt Disease 61 0.170
929
c JBR024 Joubert Syndrome 14 41 0.170
930
LBR036 Leber Plus Disease 67 0.170
931
PNM005 Pneumonic Plague 47 0.170
932
DNT010 Dentin Caries 31 0.170
933
P PLY014 Polycystic Kidney Disease 71 0.170
934
c CHR711 Chronic Asthma 41 0.170
935
ASY002 Asymptomatic Neurosyphilis 41 0.170
936
APN008 Apnea, Obstructive Sleep 66 0.170
937
c ART115 Aortic Valve Disease 1 72 0.170
938
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.170
939
P CNR004 Cone-Rod Dystrophy 2 75 0.170
940
HYP781 Hypoascorbemia 52 0.170
941
P SPN301 Spinocerebellar Ataxia 2 59 0.170
942
P CLC063 Celiac Disease 1 66 0.170
943
ARM010 Arima Syndrome 56 0.170
944
P MCK013 Meckel Syndrome, Type 1 64 0.170
945
P CRD119 Cardiac Arrest 68 0.170
946
P LFT003 Left Ventricular Noncompaction 57 0.170
947
ILT001 Ileitis 49 0.170
948
DNG001 Dengue Shock Syndrome 40 0.170
949
MST019 Mastoiditis 41 0.170
950
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 52 0.170
951
c JBR004 Joubert Syndrome 2 48 0.170
952
c SPN101 Spinocerebellar Ataxia 29 58 0.170
953
c MST023 Mesothelioma, Malignant 56 0.170
954
c FML253 Familial Cold Autoinflammatory Syndrome 3 49 0.170
955
HPT004 Hepatic Coma 43 0.170
956
HMF011 Hemifacial Spasm, Familial 33 0.170
957
STR039 Sturge-Weber Syndrome 60 0.170
958
c THR092 Thrombophilia Due to Thrombin Defect 74 0.170
959
P TTR001 Tetralogy of Fallot 69 0.170