Search results for MBP

1515 hits were found for MBP

# Family MCID Name MIFTS Score
1
P MLT020 Multiple Sclerosis 79 17.379
2
ALL014 Allergic Encephalomyelitis 34 17.164
3
MNN034 Mannose-Binding Lectin Deficiency 45 15.146
4
ATM095 Autoimmune Disease 61 15.026
5
DMY004 Demyelinating Disease 50 14.887
6
NRT004 Neuritis 53 12.717
7
P OPT009 Optic Neuritis 57 12.404
8
c SCN036 Secondary Progressive Multiple Sclerosis 55 12.062
9
RLP002 Relapsing-Remitting Multiple Sclerosis 56 11.954
10
P PLY019 Polyneuropathy 53 11.807
11
P ATS364 Autism 72 11.547
12
P MYS003 Myasthenia Gravis 68 11.457
13
P OLG002 Oligodendroglioma 66 11.447
14
P PLZ001 Pelizaeus-Merzbacher Disease 65 11.116
15
P GLL022 Guillain-Barre Syndrome 59 10.750
16
NRM001 Neuromyelitis Optica 60 10.718
17
P SCH015 Schizophrenia 74 10.699
18
VSC002 Vascular Dementia 59 10.642
19
c PRM108 Primary Progressive Multiple Sclerosis 51 10.452
20
AGN016 Aging 54 10.415
21
P CHR071 Charcot-Marie-Tooth Disease 64 10.387
22
CNT025 Central Pontine Myelinolysis 42 10.212
23
TTN003 Tetanus 64 9.793
24
PRV004 Periventricular Leukomalacia 52 9.729
25
ACT049 Acute Disseminated Encephalomyelitis 53 9.689
26
IMM167 Immune Deficiency Disease 77 9.676
27
P NRP001 Neuropathy 59 9.510
28
CHR382 Chromosome 18q Deletion Syndrome 40 9.313
29
P HYD006 Hydrocephalus 63 8.886
30
STR067 Stroke, Ischemic 79 8.847
31
SBC001 Subacute Sclerosing Panencephalitis 53 8.841
32
PRG009 Progressive Multifocal Leukoencephalopathy 58 8.785
33
MLT157 Multiple System Atrophy 1 69 8.762
34
NRL005 Neurilemmoma 60 8.762
35
c CNT035 Central Nervous System Disease 53 8.746
36
MYL001 Myelitis 49 8.730
37
INT323 Intraocular Pressure Quantitative Trait Locus 63 8.686
38
ACQ007 Acquired Immunodeficiency Syndrome 58 8.606
39
P TRN034 Transverse Myelitis 47 8.570
40
c VRL007 Viral Encephalitis 50 8.570
41
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 8.570
42
P KRB001 Krabbe Disease 69 8.543
43
MNN009 Meningoencephalitis 48 8.529
44
TTH006 Tooth Disease 51 8.529
45
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 8.514
46
P PRK057 Parkinson Disease, Late-Onset 79 8.462
47
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 8.462
48
P RTT002 Rett Syndrome 79 8.462
49
AKN002 Akinetic Mutism 36 8.418
50
OPT007 Optic Nerve Glioma 40 8.390
51
P NMN002 Niemann-Pick Disease 60 8.390
52
P OLV001 Olivopontocerebellar Atrophy 51 8.390
53
P PLY020 Polyradiculoneuropathy 47 8.390
54
c NMN013 Niemann-Pick Disease, Type a 63 8.390
55
BRN028 Brain Cancer 73 8.354
56
CHR629 Charcot-Marie-Tooth Disease and Deafness 54 8.266
57
NRX001 Neuroaxonal Dystrophy 38 8.266
58
c ATM017 Autoimmune Disease of the Nervous System 37 8.266
59
BRN071 Brain Injury 50 6.991
60
P PRP019 Peripheral Nervous System Disease 57 6.874
61
TRM010 Traumatic Brain Injury 50 6.704
62
CRT015 Carotid Artery Occlusion 45 6.439
63
P NRV007 Nervous System Disease 66 6.247
64
DSS008 Disease of Mental Health 74 6.149
65
SPN041 Spinal Cord Disease 54 6.122
66
P MTC003 Metachromatic Leukodystrophy 71 6.093
67
P OPT006 Optic Nerve Disease 57 6.093
68
HYP141 Hyperphenylalaninemia 42 6.093
69
INT042 Internuclear Ophthalmoplegia 32 6.077
70
PST007 Post-Vaccinal Encephalitis 24 6.060
71
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 6.060
72
PRN006 Parenchymatous Neurosyphilis 16 6.041
73
MNN005 Meningovascular Neurosyphilis 31 6.041
74
c HRD088 Hereditary Neuropathies 34 6.041
75
VLV015 Vulvar Dystrophy 29 6.020
76
ISL119 Isolated Optic Neuritis 26 6.020
77
ATM100 Autoimmune Optic Neuritis 28 5.997
78
DYS016 Dysgammaglobulinemia 33 5.997
79
CNV004 Canavan Disease 61 5.969
80
c ATM007 Autoimmune Disease of Central Nervous System 30 5.969
81
CRB033 Cerebral Degeneration 36 5.933
82
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 5.845
83
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 48 5.845
84
CLR009 Color Agnosia 26 5.845
85
FNG001 Finger Agnosia 19 5.845
86
ATM105 Autoimmune Disease of Peripheral Nervous System 25 5.845
87
BLC015 Balo Concentric Sclerosis 37 5.845
88
LKN001 Leukoencephalopathy with Vanishing White Matter 63 5.845
89
NWF001 Newfoundland Rod-Cone Dystrophy 35 5.845
90
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 52 5.845
91
ENC005 Encephalomalacia 43 5.845
92
OCC005 Occlusion Precerebral Artery 28 5.845
93
CRN031 Cranial Nerve Disease 37 5.845
94
PST109 Postinfectious Encephalitis 25 5.845
95
ACT038 Acute Retrobulbar Neuritis 24 5.845
96
SML006 Small Intestine Leiomyoma 26 5.845
97
c CHR018 Chronic Salpingo-Oophoritis 21 5.845
98
GRN006 Granulomatous Angiitis 34 5.845
99
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 61 5.845
100
ACT032 Acute Hemorrhagic Leukoencephalitis 33 5.845
101
PLY021 Polyradiculopathy 32 5.845
102
SLP002 Salpingitis Isthmica Nodosa 25 5.845
103
RTV008 Rete Ovarii Benign Neoplasm 22 5.845
104
CPP004 Copper Deficiency Myelopathy 28 5.845
105
P CHR342 Chiari Malformation 41 5.845
106
RTV004 Rete Ovarii Adenoma 22 5.845
107
PTR002 Petroclival Meningioma 25 5.845
108
PLY004 Polyp of Corpus Uteri 28 5.845
109
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.270
110
P OST002 Osteoporosis 77 2.861
111
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.861
112
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.861
113
BNR002 Bone Resorption Disease 47 2.722
114
P ADN016 Adenocarcinoma 63 2.379
115
PRT037 Pertussis 49 2.349
116
DWN001 Down Syndrome 70 2.263
117
CYT002 Cytokine Deficiency 43 2.135
118
c SYS001 Systemic Lupus Erythematosus 86 2.130
119
BRR014 Barrett Esophagus 66 2.095
120
P LPS004 Lupus Erythematosus 61 2.048
121
P ESP024 Esophagitis 60 2.020
122
CHL014 Cholera 62 1.907
123
P TRM003 Tremor 50 1.837
124
SPN186 Spinal Cord Injury 61 1.833
125
PRP016 Paraplegia 52 1.819
126
P RCT021 Rectum Cancer 54 1.774
127
P PRS040 Prostate Cancer 95 1.773
128
P DRR001 Diarrhea 55 1.728
129
MNC002 Munchausen by Proxy 29 1.716
130
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.702
131
P HYP098 Hypereosinophilic Syndrome 66 1.669
132
P BRS047 Breast Cancer 97 1.640
133
GST040 Gastric Adenocarcinoma 66 1.607
134
ARG004 Argyria 26 1.593
135
c HYP595 Hypertension, Essential 84 1.579
136
VCC001 Vaccinia 49 1.549
137
GLM045 Glioma 62 1.549
138
GLL048 Glial Tumor 52 1.533
139
c HPT073 Hepatitis C Virus 71 1.518
140
ESP021 Esophageal Cancer 84 1.511
141
WLL004 Wallerian Degeneration 38 1.510
142
P LKD001 Leukodystrophy 58 1.492
143
HMN044 Human Immunodeficiency Virus Type 1 76 1.492
144
P SPP010 Suppressor of Tumorigenicity 3 51 1.480
145
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.468
146
P HRP006 Herpes Simplex 65 1.468
147
SVR004 Severe Combined Immunodeficiency 71 1.443
148
P OVR042 Ovarian Cancer 88 1.432
149
HYP266 Hypoxia 56 1.417
150
MCR004 Macroglobulinemia 48 1.390
151
KRT019 Keratitis, Hereditary 66 1.381
152
BCK006 Back Pain 43 1.363
153
AND005 Androgen Insensitivity Syndrome, Mild 21 1.359
154
CRB037 Cerebral Palsy 67 1.354
155
47X002 47,xyy 48 1.343
156
P HPT023 Hepatocellular Carcinoma 95 1.320
157
PLY150 Polykaryocytosis Inducer 29 1.320
158
P UVT001 Uveitis 57 1.295
159
P ALZ034 Alzheimer Disease 87 1.250
160
PRT036 Peritonitis 65 1.250
161
ACN019 Acanthamoeba Keratitis 30 1.230
162
FCT008 Factitious Disorder 34 1.201
163
IRD001 Iridocyclitis 54 1.188
164
P MYL006 Myeloid Leukemia 60 1.174
165
CMB007 Combined Immunodeficiency 56 1.164
166
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.159
167
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 1.147
168
IGG001 Iga Glomerulonephritis 50 1.147
169
P LKM002 Leukemia 66 1.141
170
P NRB001 Neuroblastoma 66 1.140
171
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.117
172
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.111
173
GST045 Gastroenteritis 58 1.111
174
P URT039 Urticaria 57 1.111
175
ESN005 Eosinophilic Gastroenteritis 55 1.080
176
IRN008 Iron Overload in Africa 51 1.030
177
RJS001 Ruijs-Aalfs Syndrome 47 1.030
178
HPT079 Hepatoid Adenocarcinoma 39 1.030
179
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 1.030
180
ADL096 Adult Hepatocellular Carcinoma 60 1.030
181
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 1.030
182
PDT042 Pediatric Hepatocellular Carcinoma 50 1.030
183
PTY007 Pityriasis Rotunda 26 1.030
184
FBR086 Fibrolamellar Carcinoma 59 1.030
185
HPT011 Hepatocellular Clear Cell Carcinoma 45 1.030
186
c LKM061 Leukemia, Acute Myeloid 83 1.014
187
DYS073 Dysphagia 53 1.001
188
ANG054 Angina Pectoris 65 0.992
189
P LCH002 Lichen Planus 55 0.992
190
ORL013 Oral Lichen Planus 45 0.992
191
P HNT016 Huntington Disease 73 0.982
192
P MST009 Mastocytosis 64 0.982
193
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.972
194
P MSC003 Muscular Atrophy 52 0.972
195
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.961
196
P MYC084 Mycobacterium Tuberculosis 1 68 0.961
197
SCH014 Schistosomiasis 56 0.961
198
P PNC044 Pancreatitis 61 0.950
199
P NPH012 Nephrotic Syndrome 62 0.950
200
P PRD008 Periodontitis 64 0.950
201
P PRC019 Precocious Puberty 49 0.916
202
LNG031 Lung Benign Neoplasm 51 0.903
203
THY029 Thyroid Carcinoma 54 0.903
204
ILS001 Ileus 49 0.893
205
EPD015 Epidemic Typhus 44 0.891
206
BRS099 Breast Ductal Carcinoma 61 0.891
207
SCR008 Scrub Typhus 57 0.891
208
CRH001 Crohn's Disease 80 0.891
209
PLY100 Polyploidy 36 0.891
210
P INS002 in Situ Carcinoma 53 0.877
211
CRB004 Cerebral Artery Occlusion 46 0.872
212
P RHN004 Rhinitis 57 0.867
213
OTT002 Otitis Media 71 0.863
214
HLX001 Helix Syndrome 47 0.854
215
P PLV020 Pelvic Organ Prolapse 58 0.848
216
P MCH002 Machado-Joseph Disease 63 0.848
217
OVR094 Ovarian Epithelial Cancer 39 0.848
218
AMB007 Amoebic Keratitis 19 0.848
219
MST024 Mastocytosis, Cutaneous 66 0.832
220
P FBR017 Fibrosarcoma 55 0.832
221
c FML015 Familial Nephrotic Syndrome 47 0.832
222
ISC004 Ischemia 61 0.831
223
P ENC018 Encephalopathy 62 0.803
225
MSL001 Measles 61 0.784
226
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.779
227
c ART115 Aortic Valve Disease 1 72 0.775
228
GLL008 Gilles De La Tourette Syndrome 64 0.775
229
MYL031 Myeloproliferative Neoplasm 66 0.775
230
PSY004 Psychotic Disorder 66 0.775
231
c NMN015 Niemann-Pick Disease, Type C1 68 0.775
232
ALL003 Allergic Rhinitis 66 0.769
233
P DRM053 Dermatitis, Atopic 65 0.748
234
48X005 48,xyyy 39 0.743
235
c ATM089 Autoimmune Neuropathy 28 0.724
236
END057 Endometrial Cancer 71 0.724
237
GLM012 Glomuvenous Malformations 37 0.724
238
8P2002 8p23.1 Duplication Syndrome 22 0.724
239
ALL029 Allergic Disease 61 0.712
240
P PNC035 Pancreatic Cancer 86 0.700
241
DRM006 Dermatitis 62 0.695
242
P KBK002 Kabuki Syndrome 1 66 0.688
243
c SPN294 Spinocerebellar Ataxia 1 53 0.688
244
LKD025 Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 48 0.688
245
SPR004 Supravalvular Aortic Stenosis 57 0.688
246
P CRN037 Craniosynostosis 67 0.688
247
CHL035 Cholinergic Urticaria 29 0.688
248
SYN005 Synostosis 43 0.688
249
THY123 Thyroid Gland Follicular Carcinoma 53 0.688
250
ATS309 Autosomal Dominant Leukodystrophy with Autonomic Disease 27 0.688
251
P MYT002 Myotonic Dystrophy 51 0.688
252
P ANR048 Aniridia 1 66 0.686
253
c CHR064 Chronic Monocytic Leukemia 36 0.686
254
c PNS012 Paine Syndrome 60 0.673
255
c DRR009 Diarrhea 6 46 0.673
256
P HYP726 Hypercalcemia, Infantile, 1 58 0.673
257
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.673
258
P ENC004 Encephalitis 61 0.673
259
INS024 Insulin-Like Growth Factor I 77 0.667
260
CLL010 Cellular Ependymoma 58 0.628
261
PRT251 Proteinuria, Chronic Benign 58 0.613
262
BCT022 Bacterial Infectious Disease 56 0.607
263
P ESP035 Esophagitis, Eosinophilic, 1 57 0.607
264
CRB039 Cerebrovascular Disease 65 0.607
265
TXC005 Toxic Shock Syndrome 62 0.607
266
OST022 Osteopathia Striata with Cranial Sclerosis 54 0.600
267
CRB159 Cerebral Visual Impairment 34 0.600
268
P BCL017 B-Cell Lymphoma 57 0.594
269
LNG039 Lung Squamous Cell Carcinoma 57 0.591
270
P SLP006 Sleep Apnea 69 0.574
271
PPL052 Papillomatosis, Confluent and Reticulated 34 0.574
272
P GLM040 Glioma Susceptibility 1 70 0.574
273
P LKM062 Leukemia, Acute Lymphoblastic 69 0.561
274
ATN005 Autonomic Dysfunction 45 0.561
275
MLG169 Malignant Astrocytoma 57 0.554
276
RBS001 Rabies 58 0.540
277
P THY032 Thyroiditis 56 0.540
278
PRT058 Pure Autonomic Failure 58 0.540
279
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.533
280
P CLR023 Colorectal Cancer 100 0.533
281
P LTR001 Lateral Sclerosis 58 0.533
282
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.518
283
DBT010 Diabetic Neuropathy 54 0.511
284
P AST005 Asthma 76 0.503
285
HGH043 High Grade Glioma 46 0.503
286
DFF005 Diffuse Large B-Cell Lymphoma 55 0.496
287
P OPN001 Open-Angle Glaucoma 55 0.496
288
P LYM118 Lymphoma 69 0.496
289
c MJR024 Major Affective Disorder 9 40 0.496
290
c MJR022 Major Affective Disorder 8 37 0.496
291
IGR001 Ige Responsiveness, Atopic 59 0.496
292
P BPL003 Bipolar Disorder 56 0.496
293
HDN002 Head Injury 44 0.496
294
c PRC016 Pre-Eclampsia 64 0.488
295
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.488
296
P CNJ013 Conjunctivitis 66 0.488
297
P GLM007 Glomerulonephritis 59 0.488
298
CYS001 Cystic Fibrosis 77 0.480
299
c ATS007 Autism Spectrum Disorder 72 0.480
300
PNG002 Pain Agnosia 51 0.480
301
c HPT016 Hepatitis B 62 0.480
302
SYN036 Syncope 44 0.480
303
VLV047 Volvulus of Midgut 55 0.472
304
CHG001 Chagas Disease 65 0.472
305
c ATM075 Autoimmune Encephalitis 39 0.472
306
HMP009 Haemophilus Influenzae 41 0.472
307
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.464
308
c ACT249 Acute Asthma 40 0.464
309
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.464
310
P DBT009 Diabetes Mellitus 67 0.464
311
P MNN013 Meningitis 65 0.464
312
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.455
313
c GLC092 Glaucoma, Primary Open Angle 61 0.455
314
GLB002 Glioblastoma 67 0.447
315
PLM001 Pulmonary Tuberculosis 69 0.447
316
P DMN002 Dementia 65 0.447
317
P RNV001 Renovascular Hypertension 49 0.447
318
P RTN024 Retinoblastoma 72 0.438
319
c LKM063 Leukemia, Chronic Myeloid 71 0.438
320
MDD018 Middle East Respiratory Syndrome 44 0.438
321
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.438
322
END086 End Stage Renal Disease 54 0.438
323
P MSC005 Muscular Dystrophy 66 0.438
324
P HYP086 Hypothyroidism 69 0.429
325
c ACT071 Acute Kidney Failure 60 0.429
326
c CHR684 Chronic Kidney Disease 74 0.429
327
c MCR133 Microvascular Complications of Diabetes 4 41 0.420
328
P RHM011 Rheumatoid Arthritis 81 0.420
329
ADR040 Adrenal Gland Pheochromocytoma 45 0.420
330
P PHC003 Pheochromocytoma 70 0.420
331
c MCR113 Microvascular Complications of Diabetes 3 52 0.420
332
c MCR130 Microvascular Complications of Diabetes 6 41 0.420
333
c MCR120 Microvascular Complications of Diabetes 7 47 0.420
334
P VSC007 Vascular Disease 62 0.420
335
ATN004 Autonomic Neuropathy 42 0.420
336
ONC002 Onchocerciasis 50 0.420
337
PHN003 Phenylketonuria 76 0.420
338
P KDN018 Kidney Disease 72 0.420
339
P RBL001 Rubella 58 0.420
340
AMB001 Amebiasis 56 0.420
341
OCL069 Ocular Motor Apraxia 57 0.411
342
CHL123 Chlamydia 58 0.411
343
LYM017 Lyme Disease 63 0.411
344
ADS004 Aids Dementia Complex 40 0.411
345
P LPR021 Leprosy 3 71 0.401
346
P URN019 Urinary Tract Infection 49 0.401
347
IRN002 Iron Metabolism Disease 56 0.401
348
HNS001 Hansen's Disease 32 0.401
349
P LKM071 Leukemia, Chronic Lymphocytic 74 0.392
350
P INF032 Infertility 60 0.392
351
ALL006 Allergic Asthma 56 0.392
352
GST092 Gastroesophageal Reflux 60 0.382
353
P FML011 Familial Adenomatous Polyposis 71 0.382
354
MNT002 Mental Depression 56 0.382
355
P SYP003 Syphilis 59 0.382
356
MNN043 Meningioma, Familial 79 0.382
357
SPS019 Spastic Paraparesis 38 0.382
358
LNG099 Lung Disease 62 0.382
359
DVR002 Diverticulitis 46 0.382
360
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.382
361
c LKM005 Leukemia, T-Cell, Chronic 33 0.382
362
P PLY014 Polycystic Kidney Disease 71 0.372
363
INT395 Intracranial Meningioma 48 0.372
364
c HYP836 Hypercholesterolemia, Familial, 1 73 0.372
365
P MCR010 Microcephaly 59 0.372
366
P NTR004 Neutropenia 62 0.372
367
P CRN300 Coronary Heart Disease 1 73 0.372
368
SCR001 Secretory Meningioma 40 0.372
369
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.372
370
c BCT007 Bacterial Meningitis 55 0.372
371
PST092 Posttransplant Acute Limbic Encephalitis 29 0.372
372
c TYP009 Type 2 Diabetes Mellitus 92 0.361
373
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.361
374
DSS032 Disease by Infectious Agent 55 0.361
375
c TYP008 Type 1 Diabetes Mellitus 77 0.361
376
P HYP750 Hypertriglyceridemia, Familial 62 0.361
377
c SML038 Small Cell Cancer of the Lung 69 0.361
378
P HYP069 Hyperparathyroidism 62 0.361
379
DPH001 Diphtheria 59 0.361
380
MSC157 Muscular Dystrophy, Duchenne Type 79 0.361
381
LPR001 Lepromatous Leprosy 49 0.361
382
PST054 Postinfectious Encephalomyelitis 15 0.361
383
P FTL001 Fetal Alcohol Syndrome 55 0.350
384
P RHB003 Rhabdomyosarcoma 66 0.350
385
P CTR002 Cataract 59 0.350
386
VRL011 Viral Infectious Disease 60 0.350
387
P ART022 Arthritis 70 0.350
388
NRF007 Neurofibroma 64 0.350
389
P INF037 Inflammatory Bowel Disease 53 0.339
390
P PRK039 Parkinsonism 55 0.339
392
P KLZ004 Kala-Azar 1 41 0.339
393
P MJR001 Major Depressive Disorder 68 0.339
394
c SCL052 Scleroderma, Familial Progressive 60 0.339
395
ADN018 Adenoma 58 0.339
396
BRN024 Bronchitis 67 0.339
397
CNN005 Connective Tissue Disease 66 0.339
398
P DMY001 Demyelinating Polyneuropathy 41 0.339
399
SKN016 Skin Disease 62 0.339
400
TRP002 Tropical Spastic Paraparesis 48 0.339
401
CRB090 Cerebral Hypoxia 42 0.339
402
c CNG216 Congenital Hydrocephalus 50 0.339
403
LSH001 Leishmaniasis 63 0.339
404
c ACT075 Acute Myocardial Infarction 55 0.339
405
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.328
406
ANX010 Anxiety 70 0.328
407
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.328
408
P PLM037 Pulmonary Hypertension 69 0.328
409
PMP014 Pemphigoid 49 0.328
410
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.328
411
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.328
412
P MYC007 Myocardial Infarction 69 0.328
413
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.328
414
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.328
415
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.328
416
c EXD008 Exudative Vitreoretinopathy 1 71 0.328
417
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.328
418
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.328
419
MLT113 Multicentric Castleman Disease 47 0.328
420
CLT003 Colitis 63 0.328
421
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.328
422
LVR012 Liver Cirrhosis 62 0.328
423
PPL022 Papilloma 53 0.328
424
P LVR013 Liver Disease 68 0.328
425
P ART021 Arteriosclerosis 53 0.328
426
VSC003 Visceral Leishmaniasis 54 0.328
427
P MYP004 Myopathy 67 0.328
428
SCR011 Scrapie 39 0.328
429
KRT006 Keratoconjunctivitis 53 0.328
430
P MNN019 Mannosidosis, Beta a, Lysosomal 49 0.316
431
RCK004 Rickets 65 0.316
432
MTB004 Metabolic Acidosis 48 0.316
433
C1Q001 C1q Deficiency 39 0.316
434
P EPL164 Epilepsy 70 0.316
435
P MLN007 Male Infertility 56 0.316
436
LST001 Listeriosis 59 0.316
437
P PLM036 Pulmonary Fibrosis 65 0.316
438
P CHR012 Chronic Granulomatous Disease 69 0.316
439
BLR008 Bilirubin Metabolic Disorder 57 0.316
440
TRN015 Transient Cerebral Ischemia 62 0.316
441
P THY023 Thymoma 64 0.316
442
c THY107 Thymoma, Familial 42 0.316
443
P VSC011 Vasculitis 61 0.316
444
P INF038 Influenza 68 0.316
445
P HYP076 Hyperthyroidism 53 0.316
446
c RTN046 Retinitis Pigmentosa 17 37 0.303
447
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.303
448
P PLY041 Polymyositis 59 0.303
449
ALC007 Alcohol Dependence 65 0.303
450
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.303
451
P CLC063 Celiac Disease 1 66 0.303
452
P MMB011 Membranous Nephropathy 50 0.303
453
PRP027 Peripheral Vascular Disease 71 0.303
454
c HPT001 Hepatitis C 61 0.303
455
P MLN008 Melanoma 75 0.303
456
P ECL001 Eclampsia 52 0.303
457
c PRM005 Primary Hyperparathyroidism 59 0.303
458
P NRM002 Normal Pressure Hydrocephalus 49 0.303
459
P MTR014 Motor Neuron Disease 65 0.303
460
ATP013 Atopic Keratoconjunctivitis 41 0.303
461
ART140 Arteries, Anomalies of 52 0.291
462
P ATX030 Ataxia-Telangiectasia 80 0.291
463
ATS010 Autosomal Recessive Disease 42 0.291
464
MNN032 Meningococcal Meningitis 52 0.291
465
LTX001 Latex Allergy 41 0.291
466
HYP017 Hypophosphatemia 49 0.291
467
MLR004 Malaria 78 0.291
468
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.291
469
c ACT068 Acute Cystitis 61 0.291
470
BRN004 Brain Edema 54 0.291
471
P PRN023 Prion Disease 60 0.291
472
PST028 Post-Traumatic Stress Disorder 59 0.291
473
TLN003 Telangiectasis 51 0.291
474
c DLT002 Dilated Cardiomyopathy 79 0.291
475
HYP066 Hyperglycemia 60 0.291
476
DPR016 Depression 65 0.291
477
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.291
478
c BRN108 Branchiootic Syndrome 1 63 0.277
479
TBL029 Tubulin, Beta 28 0.277
480
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.277
481
WST005 West Nile Virus 55 0.277
482
P GRF003 Graft-Versus-Host Disease 71 0.277
483
P MMP001 Mumps 56 0.277
484
c ATR087 Atrial Standstill 1 74 0.277
485
c SPN225 Spondyloarthropathy 1 70 0.277
486
ATH013 Atherosclerosis Susceptibility 63 0.277
487
P LNG032 Lung Cancer 98 0.277
488
P CRD119 Cardiac Arrest 68 0.277
489
CHL147 Chlamydia Pneumonia 47 0.277
491
NRL016 Neural Tube Defects 81 0.277
492
c PRG020 Paragangliomas 3 39 0.277
493
P SJG008 Sjogren Syndrome 61 0.277
494
INT030 Intracranial Aneurysm 55 0.277
495
P ALC033 Alcohol Use Disorder 67 0.277
496
MST005 Mastitis 52 0.277
497
CRT013 Carotid Stenosis 51 0.277
498
c ACT027 Acute Pancreatitis 60 0.277
499
BRN002 Bronchiolitis 57 0.277
500
SPN051 Spondylitis 51 0.277
501
MCN007 Meconium Aspiration Syndrome 53 0.277
502
KRT008 Keratopathy 46 0.277
503
IMP005 Impotence 52 0.277
504
P CRN025 Corneal Dystrophy 49 0.277
505
PPT001 Peptic Esophagitis 51 0.277
506
ALL009 Allergic Conjunctivitis 51 0.277
507
INF009 Inflammatory Spondylopathy 30 0.277
508
INT010 Intracranial Embolism 48 0.277
509
LYS002 Lysosomal Storage Disease 51 0.277
510
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.277
511
RST023 Resting Heart Rate, Variation in 40 0.277
512
ADR007 Adrenoleukodystrophy 74 0.277
513
MST020 Mast Cell Activation Syndrome 27 0.277
514
TBR011 Tuberculous Meningitis 48 0.277
515
ACT162 Acute Sensory Ataxic Neuropathy 24 0.277
516
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.277
517
AVN001 Avian Influenza 61 0.277
518
BLL006 Bullous Pemphigoid 61 0.277
519
ADR022 Adrenomyeloneuropathy 39 0.277
520
CHC001 Chickenpox 56 0.277
521
P ALP008 Alopecia 53 0.277
522
P RNG032 Ring Chromosome 39 0.277
523
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.277
524
LYM133 Lymphoma, Hodgkin, Classic 74 0.263
525
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.263
526
c PRD040 Periodontitis, Chronic 52 0.263
527
CYS005 Cysticercosis 60 0.263
528
P ATR011 Atrial Fibrillation 66 0.263
529
ANG002 Angiostrongyliasis 45 0.263
530
MYL057 Myelopathy, Htlv-1-Associated 39 0.263
531
CLF027 Cleft Palate, Isolated 64 0.263
532
P LNG064 Lung Cancer Susceptibility 3 70 0.263
533
P FRG001 Fragile X Syndrome 70 0.263
534
MLD001 Melioidosis 67 0.263
535
HRW001 Hair Whorl 35 0.263
536
BRC012 Brucellosis 66 0.263
537
STT001 Status Epilepticus 58 0.263
538
PRN009 Paranoid Schizophrenia 49 0.263
539
P SPN046 Spinal Muscular Atrophy 62 0.263
540
CLN003 Clonorchiasis 42 0.263
541
LPD008 Lipid Metabolism Disorder 61 0.263
542
P ANT006 Antiphospholipid Syndrome 55 0.263
543
P HYP040 Hypospadias 51 0.263
544
P HPT021 Hepatitis 68 0.263
545
FCL012 Facial Paralysis 49 0.263
546
JPN002 Japanese Encephalitis 61 0.263
547
CRN036 Craniopharyngioma 63 0.263
548
P PTN014 Patent Ductus Arteriosus 1 59 0.263
549
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.263
550
VRN004 Vernal Keratoconjunctivitis 47 0.263
551
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.263
552
PLM033 Pulmonary Embolism 58 0.263
553
ORL011 Oral Cancer 60 0.263
554
P BLD134 Bladder Cancer 79 0.248
555
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.248
556
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.248
557
P MYS005 Myositis 56 0.248
558
IMM003 Immunoglobulin Alpha Deficiency 44 0.248
559
P SLM003 Salmonellosis 54 0.248
560
P RSP003 Respiratory Failure 74 0.248
561
LCH016 Lichen Sclerosus Et Atrophicus 41 0.248
562
c VRL010 Viral Hepatitis 52 0.248
563
c CHR708 Chronic Urticaria 42 0.248
564
THR024 Thrombosis 56 0.248
565
BLL003 Bell's Palsy 48 0.248
566
P SBS003 Substance Abuse 54 0.248
567
P ESN008 Eosinophilic Pneumonia 50 0.248
568
CCC001 Coccidioidomycosis 58 0.248
569
P PLY011 Polycystic Ovary Syndrome 57 0.248
570
HYP008 Hypertensive Retinopathy 39 0.248
571
PNT038 Peanut Allergy 46 0.248
572
MDD011 Mood Disorder 62 0.248
573
ANP005 Anaplastic Astrocytoma 59 0.248
574
SDD001 Sudden Infant Death Syndrome 60 0.248
575
PRP030 Purpura 54 0.248
576
P CHL066 Cholangitis 51 0.248
577
PRS129 Prostatic Hyperplasia, Benign 48 0.232
578
P RTN008 Retinitis Pigmentosa 79 0.232
579
MYL009 Myelodysplastic Syndrome 67 0.232
580
MSC007 Muscle Hypertrophy 64 0.232
581
P DNG005 Dengue Virus 55 0.232
582
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.232
583
LPP008 Lipoprotein Quantitative Trait Locus 65 0.232
584
c SPH014 Spherocytosis, Type 2 38 0.232
585
NRR001 Neuroretinitis 42 0.232
586
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.232
587
THY111 Thyroid Carcinoma, Familial Medullary 67 0.232
588
ING001 Inguinal Hernia 59 0.232
589
P PRN026 Porencephaly 54 0.232
590
PLL012 Pollen Allergy 44 0.232
591
P TRM004 Trimethylaminuria 45 0.232
592
c SPH013 Spherocytosis, Type 1 41 0.232
593
c INF084 Inflammatory Bowel Disease 26 18 0.232
594
P BND020 Bone Disease 60 0.232
595
ATR057 Atrioventricular Block 54 0.232
596
DFC004 Deficiency Anemia 74 0.232
597
P TBR001 Tuberous Sclerosis 69 0.232
598
PRS021 Prostatic Adenoma 43 0.232
599
ACT084 Acute Stress Disorder 53 0.232
600
PLM031 Poliomyelitis 62 0.232
601
PRS045 Prostatic Hypertrophy 52 0.232
602
ENT004 Enthesopathy 51 0.232
603
c ATM011 Autoimmune Hepatitis 62 0.232
604
HYP014 Hyperuricemia 51 0.232
605
TST015 Testicular Disease 42 0.232
606
CHR073 Choreatic Disease 53 0.232
607
SQM002 Squamous Cell Papilloma 45 0.232
608
P RTN022 Retinal Vein Occlusion 54 0.232
609
RFT001 Rift Valley Fever 50 0.232
610
PRM236 Primary Biliary Cholangitis 62 0.232
611
FLR002 Filariasis 55 0.232
612
CCT002 Cicatricial Pemphigoid 53 0.232
613
NPH010 Nephrosclerosis 50 0.232
614
CLL003 Cellulitis 53 0.232
615
MCL006 Macular Retinal Edema 56 0.232
616
RTN023 Retinitis 45 0.232
617
PPL018 Papillary Adenocarcinoma 44 0.232
618
THY125 Thyroid Gland Medullary Carcinoma 48 0.232
619
KRN002 Kearns-Sayre Syndrome 63 0.232
620
c RNG013 Ring Chromosome 18 23 0.232
622
PRM209 Primary Trimethylaminuria 19 0.232
623
INT075 Intracranial Hypertension 52 0.232
624
PTH003 Pathologic Nystagmus 52 0.232
625
BLR005 Biliary Papillomatosis 27 0.232
626
NRT001 Neurotic Disorder 56 0.232
627
WLL006 Wells Syndrome 49 0.232
628
CCN002 Cocaine Abuse 49 0.232
629
INT040 Intrinsic Asthma 36 0.232
630
STT002 Status Asthmaticus 49 0.232
631
OLG006 Oligoastrocytoma 35 0.232
632
PLM035 Pulmonary Eosinophilia 49 0.232
633
P SCK005 Sickle Cell Disease 56 0.232
634
PRT107 Proton-Pump Inhibitor-Responsive Esophageal Eosinophilia 14 0.232
635
CLS049 Classic Phenylketonuria 42 0.232
636
P MPL001 Maple Syrup Urine Disease 69 0.215
637
FRN006 Frontotemporal Dementia 68 0.215
638
MLD018 Mild Cognitive Impairment 48 0.215
639
c CHR711 Chronic Asthma 41 0.215
640
APN008 Apnea, Obstructive Sleep 66 0.215
641
BRK010 Burkitt Lymphoma 66 0.215
642
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.215
643
MYL020 Myelomeningocele 51 0.215
644
HYP114 Hypertensive Nephropathy 35 0.215
645
PSR001 Psoriatic Arthritis 61 0.215
646
CRT072 Creutzfeldt-Jakob Disease 67 0.215
647
c DPH024 Diaphragmatic Hernia, Congenital 64 0.215
648
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.215
649
c HRD202 Hereditary Lymphedema I 55 0.215
650
SVR001 Severe Acute Respiratory Syndrome 68 0.215
651
P PRL003 Proliferative Glomerulonephritis 43 0.215
652
FBR047 Fibromyalgia 58 0.215
653
P PLC011 Pilocytic Astrocytoma 55 0.215
654
AMN003 Amnestic Disorder 54 0.215
655
c HPT015 Hepatitis D 49 0.215
656
NRN004 Neuroendocrine Tumor 55 0.215
657
P OBS001 Obstructive Jaundice 49 0.215
658
GST033 Gestational Diabetes 61 0.215
659
MTH009 Mouth Disease 57 0.215
660
PLX004 Plexopathy 29 0.215
661
P MLT074 Multiple Endocrine Neoplasia 58 0.215
662
P TRT010 Teratoma 50 0.215
663
MDS022 Mediastinitis 47 0.215
664
P CHR345 Chronic Pain 50 0.215
665
RDC002 Radiculopathy 51 0.215
666
P GST044 Gastritis 55 0.215
667
P DYS021 Dysautonomia 38 0.215
668
P SZR006 Seizure Disorder 69 0.215
669
STM007 Stomatitis 52 0.215
670
ULC004 Ulcerative Colitis 74 0.215
671
GST050 Gastrointestinal System Disease 55 0.215
672
P NRF002 Neurofibromatosis 60 0.215
673
NSS002 Neisseria Meningitidis Infection 47 0.215
674
P FML187 Familial Hypertension 34 0.215
675
BNG077 Benign Idiopathic Neonatal Seizures 22 0.215
676
P TMR010 Tumor Predisposition Syndrome 69 0.196
677
P PRG092 Pregnancy Loss, Recurrent 1 42 0.196
678
EXR010 Exercise-Induced Bronchoconstriction 34 0.196
679
P SNS001 Sensorineural Hearing Loss 59 0.196
680
P MYF003 Myofibrillar Myopathy 50 0.196
681
ASY002 Asymptomatic Neurosyphilis 41 0.196
682
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.196
683
LMB010 Lambert Syndrome 30 0.196
684
RTN017 Retinal Detachment 60 0.196
685
LMB062 Limb Ischemia 55 0.196
686
GRN004 Granulomatous Amebic Encephalitis 30 0.196
687
P FLL037 Follicular Lymphoma 73 0.196
688
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 46 0.196
689
P TTR001 Tetralogy of Fallot 69 0.196
690
NRM004 Neuroma 49 0.196
691
P BNC003 Bone Cancer 58 0.196
692
HYP060 Hyperinsulinism 53 0.196
693
P ANG015 Angioedema 56 0.196
694
TBS001 Tabes Dorsalis 30 0.196
695
OST017 Osteomyelitis 63 0.196
696
PHY002 Physical Disorder 41 0.196
697
LMY002 Leiomyoma 51 0.196
698
BRN026 Branch Retinal Artery Occlusion 41 0.196
699
GT001 Gout 63 0.196
700
P END044 Endometriosis 62 0.196
701
CNG034 Congestive Heart Failure 69 0.196
702
ACR007 Acromegaly 70 0.196
703
P AGM001 Agammaglobulinemia 67 0.196
704
P GCH001 Gaucher's Disease 69 0.196
705
TYP007 Typhoid Fever 63 0.196
706
P CRD246 Cardiovascular System Disease 55 0.196
707
ASP003 Aseptic Meningitis 51 0.196
708
SLV003 Salivary Gland Disease 39 0.196
709
PLC005 Placental Insufficiency 56 0.196
710
P PTT006 Pituitary Adenoma 55 0.196
711
c SCN007 Secondary Hyperparathyroidism 51 0.196
712
RTN003 Retinal Ischemia 48 0.196
713
STN013 Stenotrophomonas Maltophilia Infection 26 0.196
714
MNN041 Mannose-Binding Lectin Protein Deficiency 12 0.196
715
NRS003 Neurosyphilis 45 0.196
716
P CRN028 Corneal Ulcer 47 0.196
717
P RTN014 Retinal Artery Occlusion 47 0.196
718
NNT008 Neonatal Abstinence Syndrome 40 0.196
719
FSC004 Fasciitis 49 0.196
720
SPN011 Spongiotic Dermatitis 31 0.196
721
TNS014 Tenosynovitis 45 0.196
722
WHP002 Whiplash 35 0.196
723
BRN056 Bronchopulmonary Dysplasia 57 0.196
724
CL1007 Col1a1/2 Osteogenesis Imperfecta 25 0.196
725
TRC023 Trichinosis 53 0.196
726
DWR001 Dwarfism 45 0.196
727
P SRC025 Sarcoidosis 1 70 0.175
728
SCH076 Schnyder Corneal Dystrophy 46 0.175
729
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.175
730
P PSD087 Pseudoxanthoma Elasticum 66 0.175
731
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.175
732
HMC014 Homocysteinemia 52 0.175
733
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.175
734
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.175
735
P ADL017 Adult T-Cell Leukemia 54 0.175
736
FTL006 Fetal Alcohol Spectrum Disorder 43 0.175
737
CHR005 Chorioamnionitis 50 0.175
738
HMN001 Human Monocytic Ehrlichiosis 29 0.175
739
GLC003 Glucose Intolerance 53 0.175
740
INT067 Interstitial Nephritis 47 0.175
741
URL001 Urolithiasis 45 0.175
742
ART004 Aortic Atherosclerosis 46 0.175
743
P RNL015 Renal Hypertension 45 0.175
744
P MDL005 Medulloblastoma 75 0.175
745
OBS002 Obsessive-Compulsive Disorder 68 0.175
746
P HMN036 Hemangiopericytoma, Malignant 57 0.175
747
P NJM001 Nijmegen Breakage Syndrome 75 0.175
748
FBR089 Fibrosclerosis, Multifocal 35 0.175
749
P EXN002 Exanthem 58 0.175
750
CLL021 Collagenous Colitis 41 0.175
751
PRP080 Peripheral Artery Disease 54 0.175
752
SWN001 Swine Influenza 45 0.175
753
IFP003 Ifap Syndrome 2 42 0.175
754
SPP012 Suppressor of Tumorigenicity 11 19 0.175
755
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 0.175
756
P HRM021 Hair Morphology 2 20 0.175
757
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.175
758
CRD132 Cardiac Conduction Defect 59 0.175
759
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.175
760
c RTN147 Retinitis Pigmentosa 48 30 0.175
761
CHL065 Cholangiocarcinoma 58 0.175
762
HPT004 Hepatic Coma 43 0.175
763
P HML001 Hemolytic-Uremic Syndrome 52 0.175
764
CRD223 Cardiac Arrhythmia 63 0.175
765
DGR001 Digeorge Syndrome 62 0.175
766
CLC006 Calcinosis 47 0.175
767
P ECT005 Ectropion 41 0.175
768
ACT098 Acute Erythroid Leukemia 55 0.175
769
DTR001 Detrusor Sphincter Dyssynergia 37 0.175
770
DYS015 Dysentery 50 0.175
771
P STR001 Striatonigral Degeneration 37 0.175
772
INT079 Intrahepatic Cholangiocarcinoma 51 0.175
773
PPL019 Papillary Conjunctivitis 32 0.175
774
RTN020 Retinal Vascular Disease 45 0.175
775
CCT001 Cicatricial Ectropion 23 0.175
776
SQM006 Squamous Cell Carcinoma 59 0.175
777
END021 Endomyocardial Fibrosis 56 0.175
778
BLN009 Balanoposthitis 30 0.175
779
HPT019 Hepatic Encephalopathy 59 0.175
780
c ACT036 Acute Cholangitis 35 0.175
781
P SCL009 Sclerosing Cholangitis 46 0.175
782
PYR004 Pyuria 36 0.175
783
P GND004 Gonadal Dysgenesis 46 0.175
784
DMP001 Dumping Syndrome 43 0.175
785
P PNV001 Panuveitis 48 0.175
786
EHR002 Ehrlichiosis 39 0.175
787
P ADL010 Adult Respiratory Distress Syndrome 71 0.175
788
P TRN020 Turner Syndrome 67 0.175
789
BCT002 Bacterial Vaginosis 53 0.175
790
CNJ012 Conjunctival Disease 44 0.175
791
GNT006 Giant Papillary Conjunctivitis 34 0.175
792
c GM1007 Gm1 Gangliosidosis 65 0.175
793
CHR001 Churg-Strauss Syndrome 61 0.175
794
CD4008 Cd4/cd8 T-Cell Ratio 19 0.175
795
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.175
796
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.175
797
c MYP072 Myopathy, Myofibrillar, 1 55 0.175
798
P MYC008 Myocarditis 59 0.175
799
P CRB088 Cerebral Atrophy 33 0.175
800
CRN030 Coronary Stenosis 50 0.175
801
FBR016 Fibrosclerosis of Breast 26 0.175
802
NNT024 Neonatal Stroke 31 0.175
803
ANX004 Anoxia 40 0.175
804
SPS057 Spasticity 43 0.175
805
P PNM007 Pneumonia 64 0.175
806
RTR011 Retroperitoneal Fibrosis 47 0.175
807
CHR178 Chromosomal Triplication 34 0.175
808
ALL012 Allergic Angiitis 24 0.175
809
P CRB059 Cerebellar Degeneration 36 0.175
810
BNS003 Binswanger's Disease 41 0.175
811
P RTN016 Retinal Degeneration 52 0.175
812
CHR066 Chronic Fatigue Syndrome 60 0.175
813
HRN003 Heroin Dependence 44 0.175
814
IRR002 Irritable Bowel Syndrome 65 0.175
815
ETN001 Eating Disorder 59 0.175
816
P GNG009 Gangliosidosis 44 0.175
817
LSS003 Lassa Fever 49 0.175
818
OCL006 Ocular Hypertension 53 0.175
819
RRS010 Rare Soft Tissue Tumor 18 0.175
820
LWG005 Low-Grade Astrocytoma 38 0.175
821
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.175
822
INH023 Inherited Cancer-Predisposing Syndrome 53 0.175
823
c ACT134 Acute Liver Failure 57 0.175
824
P OVR082 Overgrowth Syndrome 42 0.175
825
c RTN162 Retinitis Pigmentosa 2 45 0.152
826
HLC007 Helicobacter Pylori Infection 67 0.152
827
MYL069 Myeloma, Multiple 77 0.152
828
EKR001 Eukaryotic Translation Elongation Factor 1 Alpha-1-Like 14 10 0.152
829
PLY001 Polycythemia Vera 69 0.152
830
MYL005 Myelofibrosis 70 0.152
831
ARL004 Aural Atresia, Congenital 32 0.152
832
c ATM099 Autoimmune Uveitis 44 0.152
833
LG4001 Lig4 Syndrome 55 0.152
834
P RST001 Restless Legs Syndrome 52 0.152
835
OCC016 Occupational Asthma 33 0.152
836
MCR013 Microphthalmia 60 0.152
837
ART074 Aortic Dissection 53 0.152
838
MLN079 Melanoma in Congenital Melanocytic Nevus 37 0.152
839
MRF001 Marfan Syndrome 76 0.152
840
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.152
841
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.152
842
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.152
843
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.152
844
INT303 Intracranial Hypertension, Idiopathic 56 0.152
845
MTH071 Methane Production 25 0.152
846
RNL077 Renal Fibrosis 46 0.152
847
VTM002 Vitamin B12 Deficiency 48 0.152
848
P XNT004 Xanthinuria 37 0.152
849
PHY008 Physical Urticaria 33 0.152
850
PNC005 Penicilliosis 30 0.152
851
c SHR030 Short Qt Syndrome 44 0.152
852
NTM002 Nut Midline Carcinoma 43 0.152
853
CNN010 Connective Tissue Benign Neoplasm 44 0.152
854
c NMN014 Niemann-Pick Disease, Type C2 49 0.152
855
OCL020 Ocular Cicatricial Pemphigoid 52 0.152
856
c RTN152 Retinitis Pigmentosa 66 34 0.152
857
P WSK001 Wiskott-Aldrich Syndrome 72 0.152
858
c SCK009 Seckel Syndrome 1 48 0.152
859
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.152
860
BLS001 Blau Syndrome 68 0.152
861
c SCH079 Schizophrenia 1 44 0.152
862
WLL001 Williams-Beuren Syndrome 60 0.152
863
NPH003 Nephrocalcinosis 49 0.152
864
P SCK004 Seckel Syndrome 58 0.152
865
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.152
866
CMM005 Common Cold 55 0.152
867
c INH020 Inherited Metabolic Disorder 47 0.152
868
LYM027 Lymphopenia 56 0.152
869
NTR005 Nutritional Deficiency Disease 60 0.152
870
RCT015 Reactive Arthritis 60 0.152
871
P ART018 Aortic Valve Insufficiency 52 0.152
872
P LMY004 Leiomyosarcoma 62 0.152
873
LND001 Landau-Kleffner Syndrome 50 0.152
874
c MLG084 Malignant Fibrous Histiocytoma 62 0.152
875
SNS003 Sensory Peripheral Neuropathy 51 0.152
876
MGL001 Megaloblastic Anemia 59 0.152
877
CHL012 Childhood Disintegrative Disease 44 0.152
878
SHG001 Shigellosis 61 0.152
879
GST023 Gastric Ulcer 52 0.152
880
ESN006 Eosinophilic Meningitis 36 0.152
881
c MLG069 Malignant Hypertension 46 0.152
882
HMP001 Hemopericardium 47 0.152
883
P PRC012 Pericardial Effusion 50 0.152
884
MSN004 Mesenchymal Cell Neoplasm 42 0.152
885
P SKN015 Skin Carcinoma 71 0.152
886
P TMP001 Temporal Lobe Epilepsy 49 0.152
887
PPL001 Papillary Adenoma 44 0.152
888
INC021 Incontinentia Pigmenti 63 0.152
889
P ORT004 Orthostatic Intolerance 62 0.152
890
OST159 Osteogenic Sarcoma 66 0.152
891
CRB086 Cerebral Aneurysms 40 0.152
892
HRT012 Heart Valve Disease 53 0.152
893
P SYS005 Systemic Scleroderma 73 0.152
894
GST010 Gestational Trophoblastic Neoplasm 52 0.152
895
P BCT020 Bacteremia 2 43 0.152
896
P FBR003 Fibrous Histiocytoma 43 0.152
897
CRT033 Corticobasal Degeneration 48 0.152
898
SFT003 Soft Tissue Sarcoma 57 0.152
899
OPD006 Opioid Addiction 48 0.152
900
c HRD142 Hereditary Xanthinuria 43 0.152
901
P HYP265 Hypotonia 42 0.152
902
P PLY018 Polycythemia 56 0.152
903
MTS001 Mutism 44 0.152
904
DDN004 Duodenogastric Reflux 31 0.152
905
CLF001 Cleft Lip 54 0.152
906
HYP005 Hypokalemia 55 0.152
907
P LNG035 Lung Large Cell Carcinoma 53 0.152
908
MXD026 Mixed Glioma 45 0.152
909
P SLP005 Sleep Disorder 62 0.152
910
P MNC007 Monocytic Leukemia 48 0.152
911
SPN050 Spinocerebellar Degeneration 39 0.152
912
ATM077 Autoimmune Gastrointestinal Dysmotility 16 0.152
913
ANP009 Anaplastic Oligodendroglioma 41 0.152
914
DRM008 Dermatographia 26 0.152
915
ANT024 Anthrax Disease 58 0.152
916
KMR001 Kimura Disease 41 0.152
917
GGN002 Gigantism 33 0.152
918
GRW007 Growth Hormone Deficiency 47 0.152
919
c ACT135 Acute Graft Versus Host Disease 51 0.152
920
ESN022 Eosinophilic Colitis 24 0.152
921
TXC020 Toxic Oil Syndrome 32 0.152
922
SLR005 Solar Urticaria 29 0.152
923
PRM163 Primary Mediastinal Large B-Cell Lymphoma 40 0.152
924
PRM329 Premature Aging 36 0.152
925
c FML294 Familial Short Qt Syndrome 44 0.152
926
ARC023 Arcus Corneae 36 0.124
927
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.124
928
SPN405 Spondyloepiphyseal Dysplasia Tarda, X-Linked 47 0.124
929
P PRR016 Pierre Robin Syndrome 50 0.124
930
CFF002 Coffin-Lowry Syndrome 59 0.124
931
WRN001 Werner Syndrome 69 0.124
932
MNT146 Mental Retardation, X-Linked, Syndromic, Martin-Probst Type 32 0.124
933
ABT001 Abetalipoproteinemia 68 0.124
934
CRV035 Cervical Cancer 72 0.124
935
CHR081 Choroideremia 58 0.124
936
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.124
937
CMP007 Complement Component 5 Deficiency 44 0.124
938
c RTN061 Retinitis Pigmentosa 32 32 0.124
939
GLT039 Glutathione Peroxidase Deficiency 33 0.124
940
HYP529 Hyperuricemic Nephropathy, Familial Juvenile, 3 16 0.124
941
CHK001 Chikungunya 60 0.124
942
HMN002 Human Granulocytic Anaplasmosis 31 0.124
943
HMN047 Human Cytomegalovirus Infection 59 0.124
944
P WLF004 Wolfram Syndrome 61 0.124
945
PLM005 Pleomorphic Lipoma 40 0.124
946
P CRB045 Cerebellar Hypoplasia 40 0.124
947
MCS002 Mucositis 55 0.124
948
INT072 Intestinal Pseudo-Obstruction 60 0.124
949
P ERY036 Erythema Nodosum 49 0.124
950
SLP001 Sleeping Sickness 56 0.124
951
c MGR028 Migraine with or Without Aura 1 64 0.124
952
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.124
953
HYP784 Hypogonadism, Male 43 0.124
954
RYN001 Raynaud Disease 49 0.124
955
c ACH020 Achromatopsia 2 49 0.124
956
CRN264 Craniosynostosis with Fibular Aplasia 29 0.124
957
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.124
958
MLL018 Miller-Dieker Lissencephaly Syndrome 53 0.124
959