Search results for Inositol

1734 hits were found for Inositol

# Family MCID Name MIFTS Score
1
P PLY011 Polycystic Ovary Syndrome 57 13.607
2
PRT037 Pertussis 49 10.911
3
P BPL003 Bipolar Disorder 56 8.743
4
c MJR022 Major Affective Disorder 8 37 8.741
5
c MJR024 Major Affective Disorder 9 40 8.741
6
GST033 Gestational Diabetes 60 7.057
7
P NRB001 Neuroblastoma 66 6.592
8
P INF032 Infertility 60 6.336
9
HYP043 Hyperandrogenism 47 6.026
10
NRL016 Neural Tube Defects 80 5.703
11
ANV001 Anovulation 46 5.409
12
c TYP009 Type 2 Diabetes Mellitus 91 5.404
13
c EXD008 Exudative Vitreoretinopathy 1 71 5.269
14
PLY105 Polycystic Ovary Syndrome 1 39 5.137
15
P DBT009 Diabetes Mellitus 67 5.038
16
BRN056 Bronchopulmonary Dysplasia 57 4.855
17
CHL014 Cholera 62 4.797
18
ANT039 Antisynthetase Syndrome 55 4.589
19
P MJR007 Major Affective Disorder 1 42 4.406
20
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 4.302
21
DWN001 Down Syndrome 70 4.271
22
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.180
23
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.180
24
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.180
25
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.180
26
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.180
27
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.180
28
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 4.180
29
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.180
30
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.180
31
GLC003 Glucose Intolerance 53 3.963
32
GLM045 Glioma 62 3.901
33
GLL048 Glial Tumor 51 3.852
34
HYP066 Hyperglycemia 60 3.774
35
MNT002 Mental Depression 56 3.762
36
DBT010 Diabetic Neuropathy 54 3.720
37
P GLM040 Glioma Susceptibility 1 70 3.710
38
MLG169 Malignant Astrocytoma 57 3.710
39
P ALZ034 Alzheimer Disease 87 3.700
40
MDD011 Mood Disorder 61 3.697
41
P CLR023 Colorectal Cancer 100 3.359
42
HYP060 Hyperinsulinism 53 3.324
43
48X005 48,xyyy 39 3.241
44
P LNG032 Lung Cancer 98 3.185
45
FTT001 Fatty Liver Disease 61 3.136
46
c SML038 Small Cell Cancer of the Lung 68 3.117
47
AGN016 Aging 53 3.113
48
OBS002 Obsessive-Compulsive Disorder 67 3.086
49
c KNN009 Kenny-Caffey Syndrome, Type 1 35 3.077
50
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.076
51
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 3.076
52
LWC002 Lowe Oculocerebrorenal Syndrome 68 3.015
53
c MJR008 Major Affective Disorder 2 34 2.942
54
ANX010 Anxiety 70 2.896
55
CLT003 Colitis 63 2.896
56
ULC004 Ulcerative Colitis 74 2.896
57
DPR016 Depression 64 2.812
58
P PNC025 Panic Disorder 52 2.780
59
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.740
60
HLX001 Helix Syndrome 47 2.725
61
INS001 Insulinoma 59 2.684
62
OST159 Osteogenic Sarcoma 66 2.662
63
P MLN007 Male Infertility 56 2.626
64
c PRC016 Pre-Eclampsia 64 2.617
65
INS024 Insulin-Like Growth Factor I 77 2.585
66
P PHC003 Pheochromocytoma 70 2.573
67
P MJR001 Major Depressive Disorder 68 2.570
68
ADR040 Adrenal Gland Pheochromocytoma 45 2.569
69
P HNT016 Huntington Disease 73 2.527
70
PPL052 Papillomatosis, Confluent and Reticulated 34 2.495
71
P PRD008 Periodontitis 63 2.485
72
c MJR006 Major Affective Disorder 5 32 2.473
73
c MJR003 Major Affective Disorder 6 32 2.473
74
c MCR133 Microvascular Complications of Diabetes 4 41 2.458
75
c MCR113 Microvascular Complications of Diabetes 3 52 2.458
76
c MCR130 Microvascular Complications of Diabetes 6 41 2.458
77
c MCR120 Microvascular Complications of Diabetes 7 47 2.458
78
TRC010 Trichotillomania 51 2.401
79
c MJR023 Major Affective Disorder 7 33 2.388
80
c MJR004 Major Affective Disorder 4 28 2.388
81
CRH001 Crohn's Disease 80 2.362
82
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 2.354
83
P ATS364 Autism 72 2.342
84
IRN002 Iron Metabolism Disease 56 2.297
85
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.285
86
WHP001 Whipple Disease 45 2.270
87
HYP056 Hypoglycemia 65 2.266
88
CHR178 Chromosomal Triplication 33 2.261
89
ACT098 Acute Erythroid Leukemia 55 2.250
90
GLB002 Glioblastoma 67 2.243
91
c PRD040 Periodontitis, Chronic 52 2.228
92
LNG031 Lung Benign Neoplasm 51 2.227
93
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.207
94
c SPR086 Spermatogenic Failure 3 47 2.183
95
P BCL017 B-Cell Lymphoma 57 2.182
96
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.178
97
OLG022 Oligoasthenoteratozoospermia 36 2.173
98
P ENC018 Encephalopathy 62 2.171
99
c TYP008 Type 1 Diabetes Mellitus 77 2.151
100
P TRN020 Turner Syndrome 67 2.132
101
P CTR002 Cataract 59 2.112
102
ART002 Arts Syndrome 66 2.098
103
HPT019 Hepatic Encephalopathy 59 2.091
104
HPT004 Hepatic Coma 43 2.087
105
P BRS047 Breast Cancer 97 2.039
106
OPS002 Opsismodysplasia 37 2.037
107
P MLG056 Malignant Hyperthermia 65 2.030
108
BNR002 Bone Resorption Disease 47 1.992
109
P ANR048 Aniridia 1 66 1.992
110
PRX085 Preaxial Hallucal Polydactyly 28 1.982
111
P SZR006 Seizure Disorder 69 1.981
112
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.974
113
LPD008 Lipid Metabolism Disorder 61 1.957
114
P HYP086 Hypothyroidism 68 1.951
115
c HYP836 Hypercholesterolemia, Familial, 1 73 1.940
116
END040 Endogenous Depression 54 1.940
117
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 1.933
118
CHL079 Children's Interstitial Lung Disease 25 1.922
119
47X002 47,xyy 47 1.918
120
c ACT027 Acute Pancreatitis 60 1.911
121
c ATS007 Autism Spectrum Disorder 71 1.908
122
HYP266 Hypoxia 56 1.894
123
TTN003 Tetanus 64 1.892
124
CHG001 Chagas Disease 65 1.892
125
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.881
126
P OCY003 Oocyte Maturation Defect 1 46 1.872
127
P GLC113 Galactosemia I 65 1.847
128
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.846
129
PTT037 Pituitary Tumors 44 1.838
130
CYT002 Cytokine Deficiency 43 1.824
131
SLP001 Sleeping Sickness 56 1.796
132
NRL018 Neural Tube Defects, Folate-Sensitive 46 1.793
133
HMG002 Hemoglobinuria 50 1.788
134
SQM006 Squamous Cell Carcinoma 59 1.786
135
ENT011 Enterocolitis 55 1.779
136
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.779
137
FNG004 Fungal Meningitis 46 1.774
138
PRN019 Perinatal Necrotizing Enterocolitis 60 1.774
139
P PLY014 Polycystic Kidney Disease 71 1.773
140
P JBR020 Joubert Syndrome 1 74 1.771
141
P PNC035 Pancreatic Cancer 87 1.770
142
P LTR001 Lateral Sclerosis 57 1.710
143
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 1.709
144
TTH004 Tethered Spinal Cord Syndrome 40 1.709
145
AND005 Androgen Insensitivity Syndrome, Mild 21 1.709
146
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.706
147
P HPT023 Hepatocellular Carcinoma 95 1.700
148
P ACN011 Acne 55 1.695
149
AMN001 Amenorrhea 53 1.695
150
MLD018 Mild Cognitive Impairment 48 1.688
151
P RTN018 Retinal Disease 53 1.684
152
LRN003 Learning Disability 49 1.684
153
HRW001 Hair Whorl 35 1.661
154
OVR029 Ovarian Hyperstimulation Syndrome 63 1.658
155
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.653
156
P VSC007 Vascular Disease 62 1.649
157
c LKM061 Leukemia, Acute Myeloid 83 1.647
158
P CNJ013 Conjunctivitis 66 1.641
159
P THY032 Thyroiditis 56 1.623
160
P OVR049 Ovarian Disease 50 1.618
161
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.614
162
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.610
163
CYS001 Cystic Fibrosis 77 1.603
164
P KLZ004 Kala-Azar 1 41 1.590
165
LSH001 Leishmaniasis 63 1.590
166
CRH005 Crohn's Colitis 53 1.579
167
c INF071 Inflammatory Bowel Disease 1 65 1.579
168
P PRP019 Peripheral Nervous System Disease 57 1.579
169
SVR004 Severe Combined Immunodeficiency 70 1.576
170
c BPL002 Bipolar I Disorder 47 1.573
171
P SCH015 Schizophrenia 74 1.563
172
CHL068 Cholestasis 61 1.553
173
P PNC044 Pancreatitis 61 1.552
174
HSH003 Hashimoto Thyroiditis 60 1.516
175
P MSC005 Muscular Dystrophy 66 1.501
176
CLC006 Calcinosis 47 1.500
177
P PRV006 Pervasive Developmental Disorder 52 1.495
178
ACT011 Acute Contagious Conjunctivitis 41 1.495
179
NTR005 Nutritional Deficiency Disease 60 1.495
180
P RTN024 Retinoblastoma 72 1.490
181
BRN004 Brain Edema 54 1.488
182
P ATX030 Ataxia-Telangiectasia 80 1.462
183
LVR012 Liver Cirrhosis 62 1.462
184
TLN003 Telangiectasis 51 1.462
185
ANN002 Anencephaly 57 1.455
186
c MCR115 Microvascular Complications of Diabetes 5 65 1.452
187
P AGM001 Agammaglobulinemia 67 1.440
188
P SKN015 Skin Carcinoma 71 1.440
189
P FBR017 Fibrosarcoma 55 1.432
190
P KDN018 Kidney Disease 71 1.432
191
STT001 Status Epilepticus 58 1.432
192
P LNG064 Lung Cancer Susceptibility 3 69 1.417
193
ORL015 Oral Squamous Cell Carcinoma 43 1.411
194
P NRP001 Neuropathy 59 1.410
195
P TRM003 Tremor 50 1.409
196
P LKM071 Leukemia, Chronic Lymphocytic 74 1.408
197
NPH009 Nephrolithiasis 54 1.400
198
ADN018 Adenoma 58 1.395
199
P LVR013 Liver Disease 68 1.395
200
ATH013 Atherosclerosis Susceptibility 63 1.379
201
P DNT020 Dent Disease 1 63 1.367
202
P PLY019 Polyneuropathy 52 1.367
203
P ECL001 Eclampsia 52 1.366
204
P CYS018 Cystitis 58 1.361
205
HYP080 Hypogonadism 49 1.359
206
P MYL006 Myeloid Leukemia 60 1.357
207
RHB024 Rhabdomyosarcoma 2 65 1.356
208
c CHL142 Cholestasis, Intrahepatic, of Pregnancy 3 38 1.348
209
P MLN008 Melanoma 75 1.338
210
P HYP730 Hypogonadotropic Hypogonadism 57 1.336
211
PRT251 Proteinuria, Chronic Benign 58 1.330
212
P INF037 Inflammatory Bowel Disease 53 1.328
213
P RSP003 Respiratory Failure 73 1.316
214
CHL065 Cholangiocarcinoma 57 1.316
215
INT079 Intrahepatic Cholangiocarcinoma 51 1.316
216
c ACT134 Acute Liver Failure 57 1.314
217
c PNS012 Paine Syndrome 60 1.312
218
P INT143 Interstitial Cystitis 59 1.312
219
KRT002 Keratomalacia 54 1.312
220
P LKM002 Leukemia 65 1.292
221
DSS008 Disease of Mental Health 74 1.284
222
IMM167 Immune Deficiency Disease 76 1.281
223
BCT022 Bacterial Infectious Disease 55 1.281
224
GST019 Gastrointestinal Stromal Tumor 78 1.277
225
MSC157 Muscular Dystrophy, Duchenne Type 78 1.275
226
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.264
227
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.251
228
MLR004 Malaria 77 1.245
229
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 1.237
230
AGM019 Agammaglobulinemia, X-Linked 71 1.236
231
MNN009 Meningoencephalitis 47 1.236
232
PNM001 Pneumocystosis 60 1.229
233
AGR002 Agoraphobia 45 1.221
234
P BLD134 Bladder Cancer 79 1.216
235
CLN015 Colon Adenocarcinoma 64 1.216
236
P ADL010 Adult Respiratory Distress Syndrome 70 1.216
237
FTL021 Fetal Macrosomia 40 1.216
238
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.214
239
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.206
240
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.206
241
c LKM005 Leukemia, T-Cell, Chronic 33 1.206
242
CND006 Candida Glabrata 29 1.205
243
P MYC084 Mycobacterium Tuberculosis 1 68 1.198
244
KWS002 Kawasaki Disease 65 1.198
245
c PCH010 Pachyonychia Congenita 3 43 1.195
246
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.192
247
PRG017 Paraganglioma and Gastric Stromal Sarcoma 63 1.192
248
c BLD140 Blood Group, I System 47 1.192
249
NNL006 Non-Alcoholic Steatohepatitis 54 1.184
250
P HYP750 Hypertriglyceridemia, Familial 61 1.182
251
c HYP595 Hypertension, Essential 84 1.182
252
P GRV001 Graves' Disease 54 1.182
253
PLY150 Polykaryocytosis Inducer 29 1.165
254
TXC005 Toxic Shock Syndrome 61 1.165
255
CRB004 Cerebral Artery Occlusion 45 1.160
256
ALL014 Allergic Encephalomyelitis 34 1.160
257
P ART021 Arteriosclerosis 53 1.159
258
RCK004 Rickets 64 1.150
259
c SPN101 Spinocerebellar Ataxia 29 58 1.148
260
P CND004 Candidiasis 57 1.147
261
LNG099 Lung Disease 62 1.147
262
INT002 Intermittent Claudication 61 1.139
263
P EPL164 Epilepsy 70 1.138
264
P OVR082 Overgrowth Syndrome 41 1.138
265
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.135
266
TRM010 Traumatic Brain Injury 50 1.134
267
P LKM062 Leukemia, Acute Lymphoblastic 69 1.129
268
DPH001 Diphtheria 59 1.129
269
GLC022 Glucose/galactose Malabsorption 45 1.125
270
P GLM007 Glomerulonephritis 59 1.119
271
PST011 Pustulosis of Palm and Sole 52 1.109
272
P PSR002 Psoriasis 63 1.109
273
DFC004 Deficiency Anemia 74 1.104
274
CLP005 Ciliopathy 40 1.099
275
OLG001 Oligospermia 45 1.098
276
HPT014 Hepatorenal Syndrome 49 1.091
277
ALC007 Alcohol Dependence 65 1.091
278
P MYP004 Myopathy 67 1.091
279
NRT001 Neurotic Disorder 56 1.086
280
NRD004 Neurodegeneration Due to Cerebral Folate Transport Deficiency 33 1.083
281
P APL001 Aplastic Anemia 72 1.078
283
DBT007 Diabetic Cataract 36 1.078
284
NWB001 Newborn Respiratory Distress Syndrome 56 1.078
285
ORL011 Oral Cancer 60 1.078
286
STM007 Stomatitis 52 1.067
287
SMT001 Somatization Disorder 49 1.063
288
P TMP001 Temporal Lobe Epilepsy 49 1.060
289
BRN071 Brain Injury 50 1.060
290
GLL028 Gillespie Syndrome 52 1.031
291
SVR001 Severe Acute Respiratory Syndrome 68 1.031
292
RYN005 Raynaud Phenomenon 45 1.031
293
P OVR042 Ovarian Cancer 88 1.027
294
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.027
295
BRK010 Burkitt Lymphoma 65 1.027
296
HMN044 Human Immunodeficiency Virus Type 1 76 1.027
297
P MCH002 Machado-Joseph Disease 62 1.018
298
ATS010 Autosomal Recessive Disease 42 1.018
299
P END044 Endometriosis 62 1.018
300
ANX004 Anoxia 40 1.018
301
CRY014 Cryptococcal Meningitis 48 1.009
302
c BRN108 Branchiootic Syndrome 1 63 1.005
303
TRT001 Teratocarcinoma 41 1.000
304
P MLT020 Multiple Sclerosis 79 0.993
305
P VSC011 Vasculitis 61 0.991
306
ETN001 Eating Disorder 59 0.991
307
P PLM037 Pulmonary Hypertension 69 0.981
308
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.981
309
PRT013 Portal Hypertension 59 0.981
310
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.980
311
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.980
312
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.979
313
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.979
314
BRS051 Breast Disease 58 0.975
315
P SCK005 Sickle Cell Disease 56 0.975
316
TRY001 Trypanosomiasis 50 0.972
317
BRN028 Brain Cancer 73 0.972
318
PLY012 Polyhydramnios 46 0.972
319
EXN003 Exencephaly 30 0.972
320
ISC004 Ischemia 61 0.961
321
OLV001 Olivopontocerebellar Atrophy 50 0.958
322
LGN006 Legionnaire Disease 52 0.951
323
CRV035 Cervical Cancer 72 0.951
324
HGH043 High Grade Glioma 46 0.951
325
P FML187 Familial Hypertension 34 0.947
326
c SPN290 Spinocerebellar Ataxia 15 42 0.940
327
ALL006 Allergic Asthma 55 0.940
328
P PLY006 Polydactyly 58 0.940
329
P DRM053 Dermatitis, Atopic 65 0.929
330
c ACT071 Acute Kidney Failure 60 0.929
331
IRR002 Irritable Bowel Syndrome 64 0.929
332
ANH002 Anhidrosis 45 0.920
333
P PRN023 Prion Disease 60 0.918
334
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.918
335
P LYM033 Lymphoproliferative Syndrome 59 0.918
336
PLC008 Placenta Disease 48 0.918
337
DSS032 Disease by Infectious Agent 55 0.906
338
THR024 Thrombosis 56 0.906
339
CLR109 Colorectal Adenocarcinoma 50 0.906
340
THY030 Thyroid Gland Disease 50 0.906
341
P ENC004 Encephalitis 61 0.906
342
P MSC003 Muscular Atrophy 52 0.906
343
MNN043 Meningioma, Familial 79 0.903
344
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.903
345
SCR001 Secretory Meningioma 40 0.903
346
INT395 Intracranial Meningioma 47 0.903
347
FND002 Fundus Dystrophy 54 0.898
348
c INH030 Inherited Retinal Disorder 28 0.898
349
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.893
350
GST045 Gastroenteritis 58 0.893
351
P PLM036 Pulmonary Fibrosis 65 0.893
352
PRS045 Prostatic Hypertrophy 53 0.893
353
P FCL005 Focal Segmental Glomerulosclerosis 57 0.893
354
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.880
355
PLM010 Pulmonary Edema 54 0.880
356
P ALP008 Alopecia 53 0.880
357
PRM329 Premature Aging 36 0.880
358
c HNT011 Huntington Disease-Like 3 33 0.880
359
END057 Endometrial Cancer 76 0.872
360
P PTT006 Pituitary Adenoma 55 0.872
361
P PNT019 Pontocerebellar Hypoplasia 45 0.867
362
CRB027 Cerebellar Disease 47 0.867
363
PRS021 Prostatic Adenoma 43 0.867
364
LNG039 Lung Squamous Cell Carcinoma 57 0.867
365
DMY004 Demyelinating Disease 50 0.867
366
MCR013 Microphthalmia 59 0.867
367
AMN003 Amnestic Disorder 53 0.867
368
P PMP001 Pemphigus 54 0.867
369
P FBR031 Febrile Seizures 52 0.867
370
ATM095 Autoimmune Disease 61 0.864
371
P ADN016 Adenocarcinoma 63 0.864
372
P HYP265 Hypotonia 42 0.864
373
THY029 Thyroid Carcinoma 55 0.864
374
c THY107 Thymoma, Familial 42 0.852
375
P THY023 Thymoma 64 0.852
376
CRY005 Cryptococcosis 61 0.852
377
VRC001 Varicocele 48 0.852
378
GLM004 Gliomatosis Cerebri 51 0.852
379
P INF038 Influenza 68 0.852
380
c DLT002 Dilated Cardiomyopathy 79 0.847
381
MYL069 Myeloma, Multiple 76 0.838
382
P ANT006 Antiphospholipid Syndrome 55 0.838
383
ACQ007 Acquired Immunodeficiency Syndrome 58 0.838
384
P HRP006 Herpes Simplex 65 0.838
385
NRX001 Neuroaxonal Dystrophy 38 0.837
386
PMP014 Pemphigoid 48 0.837
387
BLL006 Bullous Pemphigoid 61 0.837
388
MSL001 Measles 61 0.837
389
SPN186 Spinal Cord Injury 60 0.829
390
c SCL052 Scleroderma, Familial Progressive 60 0.820
391
P OLG002 Oligodendroglioma 66 0.820
392
P RHB003 Rhabdomyosarcoma 66 0.820
393
PRN007 Perinephritis 38 0.820
394
P HML002 Hemolytic Anemia 62 0.820
395
WLL004 Wallerian Degeneration 38 0.811
396
LTN004 Late-Onset Retinal Degeneration 59 0.802
397
PRP027 Peripheral Vascular Disease 71 0.802
398
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.802
399
P SLM003 Salmonellosis 54 0.802
400
KRT009 Keratosis 52 0.802
401
ARG004 Argyria 26 0.802
402
P AST005 Asthma 75 0.802
403
c SPN294 Spinocerebellar Ataxia 1 53 0.802
404
c CHR684 Chronic Kidney Disease 73 0.802
405
P DBT005 Diabetes Insipidus 54 0.802
406
STR067 Stroke, Ischemic 79 0.792
407
P MCR010 Microcephaly 59 0.792
408
VSC002 Vascular Dementia 59 0.792
409
P ATR011 Atrial Fibrillation 66 0.782
410
P URT039 Urticaria 57 0.782
411
SKN019 Skin Melanoma 70 0.782
412
P LKD001 Leukodystrophy 58 0.782
413
P SLP006 Sleep Apnea 69 0.771
414
PST028 Post-Traumatic Stress Disorder 58 0.771
415
P HYD006 Hydrocephalus 62 0.771
416
P RTN016 Retinal Degeneration 52 0.771
417
c MGR028 Migraine with or Without Aura 1 63 0.761
418
P GST053 Gastric Cancer 82 0.761
419
PNC129 Pancreatic Adenocarcinoma 64 0.761
420
LWC001 Low Compliance Bladder 44 0.761
421
P DMN002 Dementia 65 0.761
422
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 18 0.761
423
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.760
424
AML001 Amelanotic Melanoma 37 0.760
425
PSY004 Psychotic Disorder 66 0.755
426
P LPR021 Leprosy 3 71 0.749
427
P PRK057 Parkinson Disease, Late-Onset 79 0.749
428
END062 Endometrial Hyperplasia 47 0.749
429
HNS001 Hansen's Disease 32 0.749
430
c ATR087 Atrial Standstill 1 74 0.738
431
VCC001 Vaccinia 49 0.738
432
P LMY004 Leiomyosarcoma 62 0.738
433
PRP016 Paraplegia 52 0.738
434
CNS004 Constipation 56 0.738
435
ATN004 Autonomic Neuropathy 42 0.738
436
PRV004 Periventricular Leukomalacia 52 0.738
437
P ART022 Arthritis 70 0.738
438
SCR011 Scrapie 39 0.738
439
P CNT004 Centronuclear Myopathy 56 0.734
440
CNT061 Conotruncal Heart Malformations 66 0.733
441
CHR710 Chronic Spontaneous Urticaria 45 0.733
442
P NPH005 Nephronophthisis 59 0.733
443
P ACT008 Actinic Keratosis 53 0.733
444
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.726
445
OCL069 Ocular Motor Apraxia 57 0.726
446
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.726
447
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.726
448
DFF005 Diffuse Large B-Cell Lymphoma 55 0.726
449
P CHR071 Charcot-Marie-Tooth Disease 64 0.726
451
CLF027 Cleft Palate, Isolated 64 0.714
452
P BND020 Bone Disease 60 0.714
453
c HRD010 Hereditary Spastic Paraplegia 65 0.714
454
P DRR001 Diarrhea 55 0.714
455
DBT004 Diabetic Polyneuropathy 50 0.714
456
PNF002 Painful Legs and Moving Toes Syndrome 14 0.714
457
P PRC019 Precocious Puberty 48 0.714
458
SRT004 Serotonin Syndrome 54 0.714
459
HND015 Hand Skill, Relative 29 0.701
460
HMC014 Homocysteinemia 52 0.701
461
IMP005 Impotence 52 0.701
462
MYM001 Myoma 54 0.701
463
P GST044 Gastritis 55 0.701
464
GTR002 Goiter 52 0.701
465
HPT022 Hepatoblastoma 54 0.701
466
IGG001 Iga Glomerulonephritis 50 0.698
467
BRR002 Barrett's Adenocarcinoma 37 0.698
468
LWG005 Low-Grade Astrocytoma 38 0.698
469
P MYC007 Myocardial Infarction 69 0.687
470
APN006 Apnea of Prematurity 24 0.687
471
TTH006 Tooth Disease 51 0.687
472
MRP001 Morphine Dependence 41 0.687
473
SYN007 Synovitis 54 0.687
474
PLC002 Plica Syndrome 35 0.687
475
c ACT073 Acute Leukemia 59 0.687
476
ACT084 Acute Stress Disorder 53 0.687
477
GST040 Gastric Adenocarcinoma 66 0.687
478
PRT036 Peritonitis 65 0.687
479
ANR040 Aneurysm 60 0.687
480
PNG002 Pain Agnosia 51 0.673
481
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.673
482
ESP021 Esophageal Cancer 84 0.673
483
P ANP001 Anaplastic Large Cell Lymphoma 59 0.673
484
ACR007 Acromegaly 70 0.673
485
MST004 Mast Cell Neoplasm 41 0.673
486
SCH012 Schizoaffective Disorder 49 0.673
487
P PNM007 Pneumonia 64 0.673
488
EMB004 Embryonal Carcinoma 55 0.673
489
DBT008 Diabetic Angiopathy 47 0.673
490
CRB039 Cerebrovascular Disease 65 0.673
491
P MYC008 Myocarditis 59 0.673
492
DWR001 Dwarfism 44 0.673
493
BLM002 Bulimia Nervosa 56 0.657
494
CLS016 Clostridium Difficile Colitis 49 0.657
495
P OST002 Osteoporosis 76 0.657
496
SCK003 Sickle Cell Anemia 74 0.657
497
P NSP012 Nasopharyngeal Carcinoma 60 0.657
498
c HPT073 Hepatitis C Virus 70 0.657
499
P SPP010 Suppressor of Tumorigenicity 3 50 0.657
500
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.657
501
CRT072 Creutzfeldt-Jakob Disease 67 0.657
502
PMP006 Pemphigus Vulgaris, Familial 57 0.657
503
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.657
504
PRS129 Prostatic Hyperplasia, Benign 48 0.657
505
CRB037 Cerebral Palsy 66 0.657
506
P MVM001 Movement Disease 61 0.657
507
ART016 Aortic Aneurysm 68 0.657
508
EXT007 Extracutaneous Mastocytoma 38 0.657
509
URM002 Uremia 47 0.657
510
DBT002 Diabetic Autonomic Neuropathy 40 0.657
511
CMM004 Common Variable Immunodeficiency 71 0.657
512
GT001 Gout 63 0.657
513
BBS001 Babesiosis 48 0.657
514
CLF001 Cleft Lip 54 0.657
515
CLF056 Cleft Lip with or Without Cleft Palate 43 0.657
516
NRM001 Neuromyelitis Optica 60 0.657
517
CRN285 Corneal Dystrophy, Fleck 48 0.650
518
CHN045 Chondrodysplasia with Joint Dislocations, Gpapp Type 27 0.650
519
c PRM108 Primary Progressive Multiple Sclerosis 51 0.641
520
P GRF003 Graft-Versus-Host Disease 71 0.641
521
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.641
522
CHL123 Chlamydia 58 0.641
523
PMP004 Pemphigus Foliaceus 43 0.641
524
OST015 Osteochondrodysplasia 60 0.641
525
c BSL007 Basal Cell Carcinoma 67 0.641
526
FBR047 Fibromyalgia 57 0.641
527
P TRC031 Trichorhinophalangeal Syndrome 37 0.641
528
P MNC007 Monocytic Leukemia 48 0.641
529
ATN005 Autonomic Dysfunction 45 0.641
530
P CRB059 Cerebellar Degeneration 36 0.641
531
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.623
532
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.623
533
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.623
534
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.623
535
P RTN008 Retinitis Pigmentosa 79 0.623
536
c GRV008 Graves Disease 1 54 0.623
537
P SPN301 Spinocerebellar Ataxia 2 59 0.623
538
MYL031 Myeloproliferative Neoplasm 66 0.623
539
P CNT005 Central Nervous System Lymphoma 51 0.623
540
P BRS053 Breast Fibroadenoma 48 0.623
541
c VRL010 Viral Hepatitis 52 0.623
542
NRR001 Neuroretinitis 42 0.623
543
P SYS005 Systemic Scleroderma 73 0.623
544
P BRS044 Breast Adenocarcinoma 58 0.623
545
ALC006 Alcoholic Hepatitis 61 0.623
546
JPN002 Japanese Encephalitis 61 0.623
547
DYS009 Dysthymic Disorder 51 0.623
548
P NTR004 Neutropenia 62 0.623
549
SCH014 Schistosomiasis 56 0.623
550
RTN023 Retinitis 45 0.623
551
CHR066 Chronic Fatigue Syndrome 59 0.623
552
BNS003 Binswanger's Disease 41 0.623
553
PRM226 Primary Central Nervous System Lymphoma 47 0.623
554
OVR094 Ovarian Epithelial Cancer 39 0.623
555
ADS004 Aids Dementia Complex 39 0.623
556
GLM044 Glomerular Disease 34 0.623
557
P CRD119 Cardiac Arrest 68 0.603
558
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.603
559
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.603
560
MYX004 Myxedema 43 0.603
561
P BRN019 Bernard-Soulier Syndrome 61 0.603
562
CHR100 Chronic Ulcer of Skin 57 0.603
563
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.603
564
BNB002 Bainbridge-Ropers Syndrome 45 0.603
565
P ADL017 Adult T-Cell Leukemia 53 0.603
566
P SNS001 Sensorineural Hearing Loss 60 0.603
567
P HRM001 Hermansky-Pudlak Syndrome 65 0.603
568
CLR030 Clear Cell Renal Cell Carcinoma 53 0.603
569
c HMG004 Hemoglobin D Disease 34 0.603
570
CVD001 Covid-19 59 0.603
571
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 0.603
572
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.603
573
SYS003 Systolic Heart Failure 49 0.603
574
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.599
575
c TBR025 Tuberous Sclerosis 1 84 0.586
576
HYP781 Hypoascorbemia 52 0.583
577
c ART101 Aortic Valve Disease 2 65 0.583
578
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 51 0.580
579
c TYP027 Type 1 Diabetes Mellitus 10 25 0.580
580
ISL122 Isolated Growth Hormone Deficiency, Type Iii, with Agammaglobulinemia 36 0.580
581
MMM006 Mammographic Density 39 0.580
582
P TTR001 Tetralogy of Fallot 69 0.580
583
P MYS005 Myositis 55 0.580
584
INC002 Inclusion Body Myositis 56 0.580
585
c MLG147 Malignant Hyperthermia 1 47 0.580
586
ZKF001 Zika Fever 51 0.580
587
ISL125 Isolated Growth Hormone Deficiency Type Iii 39 0.580
588
ISL003 Isolated Growth Hormone Deficiency 56 0.580
589
CMB007 Combined Immunodeficiency 56 0.580
590
EHR002 Ehrlichiosis 39 0.580
591
HMN047 Human Cytomegalovirus Infection 59 0.580
592
ANP005 Anaplastic Astrocytoma 59 0.580
593
CNT047 Contact Dermatitis 56 0.580
594
VGN023 Vaginitis 56 0.580
595
HMS001 Hemosiderosis 48 0.580
596
ALL010 Allergic Contact Dermatitis 55 0.580
597
ECH003 Echinococcosis 52 0.580
598
PRN009 Paranoid Schizophrenia 49 0.580
599
ILS001 Ileus 49 0.580
600
PTH003 Pathologic Nystagmus 52 0.580
601
P THL005 Thalassemia 56 0.580
602
P RRH023 Rare Hereditary Hemochromatosis 52 0.580
603
LKP003 Leukoplakia 39 0.580
604
CRB090 Cerebral Hypoxia 42 0.580
605
VTR016 Vater/vacterl Association 50 0.566
606
IMM240 Immunodeficiency 14a, Autosomal Dominant 52 0.566
607
c MNT281 Mental Retardation, Autosomal Recessive 59 19 0.553
608
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.553
609
SVN002 Sveinsson Chorioretinal Atrophy 45 0.553
610
P CLC063 Celiac Disease 1 65 0.553
611
FLT006 Floating-Harbor Syndrome 52 0.553
612
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.553
613
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 0.553
614
P RST001 Restless Legs Syndrome 52 0.553
615
HYP025 Hyperphosphatemia 47 0.553
616
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.553
617
P CHN012 Chondrosarcoma 56 0.553
618
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.553
619
MND023 Mend Syndrome 49 0.553
620
c SCH080 Schizophrenia 3 27 0.553
621
OST017 Osteomyelitis 63 0.553
622
TCL003 T Cell Deficiency 44 0.553
623
SBJ001 Subjective Cognitive Decline 29 0.553
624
BRR014 Barrett Esophagus 66 0.553
625
BRN012 Bronchiolitis Obliterans 56 0.553
626
P CHR285 Chronic Myelomonocytic Leukemia 59 0.553
627
HMP001 Hemopericardium 47 0.553
628
P ACH003 Achromatopsia 61 0.553
629
BRN002 Bronchiolitis 57 0.553
630
GLS001 Gliosarcoma 63 0.553
631
PRT018 Portal Vein Thrombosis 50 0.553
632
P PRC012 Pericardial Effusion 50 0.553
633
CHR073 Choreatic Disease 53 0.553
634
CRT013 Carotid Stenosis 51 0.553
635
TNG007 Tongue Carcinoma 55 0.553
636
CYS008 Cystic Echinococcosis 57 0.553
637
CLD011 Cold Urticaria 34 0.553
638
c ACT135 Acute Graft Versus Host Disease 51 0.553
639
P MNN013 Meningitis 65 0.553
640
DRG003 Drug Dependence 46 0.553
641
SFT003 Soft Tissue Sarcoma 43 0.553
642
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.553
643
c CHR417 Chronic Graft Versus Host Disease 55 0.553
644
NNT021 Neonatal Meningitis 22 0.553
645
HRT012 Heart Valve Disease 53 0.548
646
HMM004 Hamamy Syndrome 39 0.518
647
LBR035 Liberfarb Syndrome 28 0.518
648
ATX023 Ataxia, Sensory, 1, Autosomal Dominant 38 0.518
649
c ALZ053 Alzheimer Disease 7 33 0.518
650
c ANM038 Anemia, Autoimmune Hemolytic 63 0.518
651
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.518
652
P FML018 Familial Mediterranean Fever 73 0.518
653
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.518
654
FML037 Female Breast Cancer 51 0.518
655
c DFN253 Deafness, Autosomal Recessive 84a 28 0.518
656
P CRB048 Cerebral Cavernous Malformations 63 0.518
657
c GLL024 Gallbladder Disease 1 53 0.518
658
c LFR007 Li-Fraumeni Syndrome 2 45 0.518
659
P LFR001 Li-Fraumeni Syndrome 73 0.518
660
P CRB045 Cerebellar Hypoplasia 40 0.518
661
HDR002 Hidradenitis Suppurativa 54 0.518
662
HDR003 Hidradenitis 49 0.518
663
P HMR003 Hemorrhagic Disease 59 0.518
664
LNG030 Lung Adenoma 37 0.518
665
CNN005 Connective Tissue Disease 66 0.518
666
DFF016 Diffuse Astrocytoma 48 0.518
667
TCK004 Tick Infestation 29 0.518
668
ADR005 Adrenal Carcinoma 58 0.518
669
P CNG001 Congenital Myasthenic Syndrome 68 0.518
670
VRL004 Viral Labyrinthitis 34 0.518
671
P GLL022 Guillain-Barre Syndrome 59 0.518
672
P KLL001 Kallmann Syndrome 65 0.518
673
PLG002 Plague 58 0.518
674
GSG001 Gas Gangrene 52 0.518
675
P OVR046 Ovarian Cyst 43 0.518
676
P BRN022 Bronchiectasis 59 0.518
677
CGT001 Ciguatera Fish Poisoning 20 0.518
678
MYC013 Mycobacterium Abscessus 42 0.518
679
RNL034 Renal Cell Carcinoma 4 16 0.518
680
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.518
681
CRC006 Carcinoid Syndrome 55 0.518
682
MLG164 Malignant Epithelial Tumor of Ovary 24 0.518
683
P RRT020 Rare Tumor 39 0.518
684
CVR010 Cavernous Malformation 29 0.518
685
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 36 0.518
686
SPN050 Spinocerebellar Degeneration 38 0.518
687
P HYP076 Hyperthyroidism 53 0.469
688
c TYP028 Type 1 Diabetes Mellitus 2 49 0.463
689
HYP784 Hypogonadism, Male 43 0.463
690
c HYP272 Hypercholesterolemia, Familial, 3 46 0.463
691
BWN001 Bowen-Conradi Syndrome 54 0.463
692
CRD220 Cardiac Valvular Defect, Developmental 29 0.463
693
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.463
694
ADL002 Adult Syndrome 69 0.463
695
VTM033 Vitamin K Deficiency Bleeding 49 0.463
696
ATX019 Ataxia with Vitamin E Deficiency 44 0.463
697
END072 Endotheliitis 36 0.463
698
CHR682 Chronic Bilirubin Encephalopathy 37 0.463
699
TCK001 Tick-Borne Encephalitis 58 0.434
700
TRT017 Teratoma, Ovarian 28 0.434
701
GST092 Gastroesophageal Reflux 59 0.434
702
SCH030 Schneckenbecken Dysplasia 43 0.434
703
ANG054 Angina Pectoris 65 0.434
704
P GLY112 Glycosylphosphatidylinositol Biosynthesis Defect 1 35 0.434
705
c HRD202 Hereditary Lymphedema I 54 0.434
706
c PRG106 Progressive Muscular Dystrophy 31 0.434
707
BRN014 Bronchopneumonia 52 0.434
708
ART008 Arteriosclerosis Obliterans 40 0.434
709
ACR014 Acral Lentiginous Melanoma 53 0.434
710
OVR109 Ovarian Germ Cell Teratoma 32 0.434
711
PLM031 Poliomyelitis 62 0.434
712
P TRT010 Teratoma 50 0.434
713
MRS001 Marasmus 41 0.434
714
URL001 Urolithiasis 45 0.434
715
CHL045 Choline Deficiency Disease 39 0.434
716
HYP642 Hypercoagulability Syndrome Due to Glycosylphosphatidylinositol Deficiency 24 0.434
717
LRG008 Large Granular Lymphocyte Leukemia 34 0.434
718
CHR177 Chromophobe Renal Cell Carcinoma 54 0.417
719
EWN003 Ewing Sarcoma 69 0.413
720
P HYP069 Hyperparathyroidism 62 0.386
721
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.377
722
END086 End Stage Renal Disease 54 0.377
723
P CHR345 Chronic Pain 50 0.367
724
MTB004 Metabolic Acidosis 48 0.358
725
P MDL005 Medulloblastoma 75 0.358
726
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.358
727
P FML068 Familial Hypocalciuric Hypercalcemia 55 0.358
728
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.337
729
c WLM018 Wilms Tumor 5 53 0.333
730
CLR108 Colorectal Adenoma 63 0.333
731
P RNL017 Renal Oncocytoma 54 0.333
732
P LYM118 Lymphoma 66 0.327
733
MSC007 Muscle Hypertrophy 64 0.327
734
P FNC004 Fanconi Syndrome 60 0.327
735
c SYS001 Systemic Lupus Erythematosus 85 0.315
736
P PRS040 Prostate Cancer 95 0.315
737
P LPS004 Lupus Erythematosus 61 0.315
738
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.304
739
P ALC033 Alcohol Use Disorder 67 0.304
740
P HPT021 Hepatitis 68 0.304
741
TRN015 Transient Cerebral Ischemia 62 0.304
742
SPN035 Spindle Cell Sarcoma 51 0.304
743
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.304
744
SRC014 Sarcoma 64 0.304
745
P CRB088 Cerebral Atrophy 32 0.304
746
MYL009 Myelodysplastic Syndrome 67 0.292
747
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.292
748
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.292
749
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 0.292
750
P TBR001 Tuberous Sclerosis 69 0.292
751
P HRT032 Heart Disease 84 0.292
752
END041 Endometrial Adenocarcinoma 63 0.292
753
ALL029 Allergic Disease 61 0.292
754
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 45 0.292
755
CRD223 Cardiac Arrhythmia 63 0.280
756
P WSK001 Wiskott-Aldrich Syndrome 72 0.280
757
BCL014 B-Cell Growth Factor 32 0.280
758
P PRK039 Parkinsonism 55 0.280
759
RTN020 Retinal Vascular Disease 45 0.280
760
c HPT016 Hepatitis B 62 0.280
761
ADR022 Adrenomyeloneuropathy 38 0.280
762
ADR007 Adrenoleukodystrophy 73 0.267
764
c LKM063 Leukemia, Chronic Myeloid 70 0.267
765
c HPT001 Hepatitis C 61 0.267
766
P CRD246 Cardiovascular System Disease 55 0.267
767
CHR074 Choriocarcinoma 46 0.267
768
CRT015 Carotid Artery Occlusion 45 0.267
769
P HDC001 Headache 56 0.267
770
P CRN300 Coronary Heart Disease 1 73 0.253
771
RNL077 Renal Fibrosis 46 0.253
772
P FTL001 Fetal Alcohol Syndrome 55 0.253
773
P BNG032 Benign Mesothelioma 53 0.253
774
P ESP024 Esophagitis 60 0.253
775
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.238
776
PRC038 Precocious Puberty, Male-Limited 61 0.238
777
P HYP726 Hypercalcemia, Infantile, 1 58 0.238
778
c WLF013 Wolfram Syndrome 1 60 0.238
779
P MTR014 Motor Neuron Disease 65 0.238
780
NWC001 Newcastle Disease 47 0.238
781
P HYP024 Hypoparathyroidism 55 0.238
782
P THR014 Thrombocytopenia 66 0.238
783
P RHM011 Rheumatoid Arthritis 81 0.223
784
ALX003 Alexander Disease 61 0.223
785
SBC001 Subacute Sclerosing Panencephalitis 53 0.223
786
KPS004 Kaposi Sarcoma 76 0.223
787
MYL005 Myelofibrosis 70 0.223
788
FRN006 Frontotemporal Dementia 68 0.223
789
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 49 0.223
790
INT025 Intermittent Explosive Disorder 39 0.223
791
EMB002 Embryoma 37 0.223
792
P KDN017 Kidney Cancer 60 0.223
793
SNS003 Sensory Peripheral Neuropathy 51 0.223
794
P SBS003 Substance Abuse 54 0.223
795
AZS001 Azoospermia 45 0.223
796
CNN001 Cannabis Dependence 37 0.223
797
SKN016 Skin Disease 63 0.223
798
BRN024 Bronchitis 67 0.223
799
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.223
800
CHR072 Chordoma 56 0.207
801
P CRC039 Coarctation of Aorta 46 0.207
802
CRD132 Cardiac Conduction Defect 59 0.207
803
P FML011 Familial Adenomatous Polyposis 70 0.207
804
P SML001 Small Cell Carcinoma 52 0.207
805
ANR007 Anorexia Nervosa 59 0.207
806
ADR016 Adrenal Cortical Carcinoma 61 0.207
807
FTL006 Fetal Alcohol Spectrum Disorder 43 0.207
808
P ERL057 Early Infantile Epileptic Encephalopathy 61 0.207
809
DNT021 Dent Disease 2 39 0.207
810
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.207
811
CNT105 Central Core Disease of Muscle 59 0.207
812
PCK003 Pick Disease of Brain 70 0.207
813
P HMN036 Hemangiopericytoma, Malignant 56 0.207
814
P FRG001 Fragile X Syndrome 70 0.207
815
P ASP006 Aspergillosis 71 0.207
816
MNT001 Mantle Cell Lymphoma 65 0.207
817
DSS009 Disseminated Intravascular Coagulation 56 0.207
818
LWG006 Low Grade Glioma 41 0.207
819
P WLF004 Wolfram Syndrome 61 0.207
820
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.207
821
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.207
822
NRM005 Neuromuscular Disease 62 0.207
823
P NRM002 Normal Pressure Hydrocephalus 49 0.207
824
ADR004 Adrenal Cortical Adenocarcinoma 38 0.207
825
P NMN002 Niemann-Pick Disease 60 0.207
826
P DVL113 Developmental and Epileptic Encephalopathy 46 0.207
827
P LCT001 Lactic Acidosis 50 0.207
828
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 27 0.207
829
P CHL066 Cholangitis 51 0.207
830
P HYP098 Hypereosinophilic Syndrome 66 0.207
831
HMP009 Haemophilus Influenzae 41 0.207
832
OHT001 Ohtahara Syndrome 39 0.207
833
P AMY004 Amyloidosis 69 0.207
834
HRD223 Hereditary Melanoma 38 0.207
835
BNG091 Benign Chronic Pemphigus 56 0.189
836
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.189
837
GRS011 Gerstmann-Straussler Disease 56 0.189
838
c ERY064 Erythrocytosis, Familial, 6 30 0.189
839
BRT005 Barth Syndrome 55 0.189
840
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.189
841
c CWD006 Cowden Syndrome 1 78 0.189
842
MLT157 Multiple System Atrophy 1 69 0.189
843
IGR001 Ige Responsiveness, Atopic 58 0.189
844
c MST023 Mesothelioma, Malignant 56 0.189
845
P RCT021 Rectum Cancer 54 0.189
846
c ATM011 Autoimmune Hepatitis 62 0.189
847
P GCH001 Gaucher's Disease 69 0.189
848
P LNG028 Long Qt Syndrome 63 0.189
849
THY122 Thyroid Gland Cancer 59 0.189
850
TRC003 Trichomoniasis 53 0.189
851
CHL067 Cholecystitis 59 0.189
852
P BNG030 Benign Ependymoma 51 0.189
853
CLL010 Cellular Ependymoma 58 0.189
854
LYM027 Lymphopenia 56 0.189
855
CRN030 Coronary Stenosis 50 0.189
856
NPH003 Nephrocalcinosis 49 0.189
857
P CWD010 Cowden Syndrome 70 0.189
858
P NRF002 Neurofibromatosis 60 0.189
859
VSC003 Visceral Leishmaniasis 54 0.189
860
BCK006 Back Pain 43 0.189
861
c RNG019 Ring Chromosome 3 19 0.189
862
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 18 0.189
863
MYC014 Mycobacterium Chelonae 29 0.189
864
SPS057 Spasticity 43 0.189
865
P SPN237 Spina Bifida Aperta 19 0.189
866
P PRD021 Periodic Paralysis 42 0.189
867
MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 47 0.169
868
ILT001 Ileitis 49 0.169
869
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.169
870
c NRF024 Neurofibromatosis, Type I 76 0.169
871
c DWL002 Dowling-Degos Disease 1 58 0.169
872
LYM133 Lymphoma, Hodgkin, Classic 69 0.169
873
P KRB001 Krabbe Disease 69 0.169
874
P MRN003 Marinesco-Sjogren Syndrome 51 0.169
875
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.169
876
MSC142 Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability 32 0.169
877
P MYS003 Myasthenia Gravis 67 0.169
878
c NMN015 Niemann-Pick Disease, Type C1 68 0.169
879
SDD001 Sudden Infant Death Syndrome 60 0.169
880
c THY071 Thyroid Dyshormonogenesis 1 31 0.169
881
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.169
882
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.169
883
P TMR010 Tumor Predisposition Syndrome 69 0.169
884
P DNG005 Dengue Virus 55 0.169
885
INV001 Invasive Aspergillosis 48 0.169
886
SLT016 Solitary Fibrous Tumor/hemangiopericytoma 26 0.169
887
P THR015 Thrombophilia 51 0.169
888
CCC002 Coccidiosis 50 0.169
889
URT010 Ureteral Obstruction 44 0.169
890
CRV038 Cervical Squamous Cell Carcinoma 56 0.169
891
P EYD002 Eye Disease 57 0.169
892
CMP010 Complex Regional Pain Syndrome 59 0.169
893
P DYS154 Dystonia 64 0.169
894
CRB033 Cerebral Degeneration 36 0.169
895
ASP004 Asphyxia Neonatorum 50 0.169
896
GST037 Gastroparesis 52 0.169
897
BRC012 Brucellosis 66 0.169
898
LCH001 Leech Infestation 37 0.169
899
P CRN025 Corneal Dystrophy 49 0.169
900
DRM006 Dermatitis 61 0.169
901
PLM001 Pulmonary Tuberculosis 69 0.169
902
P RHN004 Rhinitis 56 0.169
903
PRS042 Prostate Disease 42 0.169
904
PLC005 Placental Insufficiency 55 0.169
905
PRM236 Primary Biliary Cholangitis 62 0.169
906
c PRM005 Primary Hyperparathyroidism 59 0.169
907
PRC002 Paracoccidioidomycosis 53 0.169
908
HST011 Histoplasmosis 54 0.169
909
SCB001 Scabies 49 0.169
910
ACT049 Acute Disseminated Encephalomyelitis 53 0.169
911
OVR059 Ovary Adenocarcinoma 49 0.169
912
TSH001 Tsh Producing Pituitary Tumor 41 0.169
913
LTM002 Luteoma 31 0.169
914
P NRC002 Narcolepsy 55 0.169
915
CNN002 Cannabis Abuse 44 0.169
916
SNL007 Senile Cataract 40 0.169
917
c ACT075 Acute Myocardial Infarction 55 0.169
918
OST012 Osteoarthritis 77 0.169
919
MLT075 Multifocal Motor Neuropathy 46 0.169
920
MLG079 Malignant Pleural Mesothelioma 42 0.169
921
CTN007 Cutaneous Leishmaniasis 61 0.169
922
INT075 Intracranial Hypertension 52 0.169
923
HVY002 Heavy Metal Poisoning 22 0.169
924
MYC015 Mycobacterium Fortuitum 28 0.169
925
INH023 Inherited Cancer-Predisposing Syndrome 53 0.169
926
SPL018 Splenomegaly 47 0.169
927
THR035 Thrombasthenia 48 0.169
928
HDN002 Head Injury 44 0.169
929
WTH001 Withdrawal Disorder 47 0.146
930
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.146
931
c HNT004 Huntington Disease-Like 2 51 0.146
932
P FML023 Familial Hemiplegic Migraine 53 0.146
933
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 0.146
934
VRC005 Varicose Veins 59 0.146
935
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 0.146
936
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.146
937
P RTT002 Rett Syndrome 79 0.146
938
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.146
939
WLS001 Wilson Disease 70 0.146
940
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 39 0.146
941
c CHL119 Cholangitis, Primary Sclerosing 57 0.146
942
CYN002 Cyanosis, Transient Neonatal 43 0.146
943
c SPH014 Spherocytosis, Type 2 38 0.146
945
c PRX094 Paroxysmal Nocturnal Hemoglobinuria 1 30 0.146
946
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 50 0.146
947
c DFN097 Deafness, Autosomal Recessive 1a 49 0.146
948
P MTC003 Metachromatic Leukodystrophy 71 0.146
949
PHN003 Phenylketonuria