Search results for Vitamin D3

1141 hits were found for Vitamin D3

# Family MCID Name MIFTS Score
1
c VTM029 Vitamin D Hydroxylation-Deficient Rickets, Type 1b 24 6.228
2
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 38 6.209
3
RCK004 Rickets 68 1.329
4
P HYP069 Hyperparathyroidism 63 0.493
5
P OST002 Osteoporosis 74 0.469
6
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.448
7
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.448
8
KRT002 Keratomalacia 47 0.448
9
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.426
10
c SCN007 Secondary Hyperparathyroidism 51 0.400
11
BNR002 Bone Resorption Disease 48 0.398
12
P KDN018 Kidney Disease 72 0.389
13
OST011 Osteomalacia 52 0.362
14
VTM002 Vitamin B12 Deficiency 48 0.351
15
P BND020 Bone Disease 59 0.349
16
c CHR684 Chronic Kidney Disease 70 0.336
17
ATM095 Autoimmune Disease 62 0.331
18
P CLR023 Colorectal Cancer 99 0.308
19
OST159 Osteogenic Sarcoma 66 0.297
20
VTM033 Vitamin K Deficiency Bleeding 48 0.287
21
P PSR002 Psoriasis 62 0.281
22
PST011 Pustulosis of Palm and Sole 52 0.275
23
P LVR013 Liver Disease 68 0.265
24
P BRS047 Breast Cancer 97 0.254
25
P PRS040 Prostate Cancer 97 0.252
26
DFC004 Deficiency Anemia 70 0.250
27
P MLT020 Multiple Sclerosis 72 0.237
28
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.236
29
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.234
30
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.234
31
P DBT009 Diabetes Mellitus 64 0.232
32
END086 End Stage Renal Disease 51 0.226
33
P INF037 Inflammatory Bowel Disease 54 0.222
34
c PRC016 Pre-Eclampsia 63 0.222
35
SKN016 Skin Disease 63 0.212
36
CYT002 Cytokine Deficiency 42 0.211
37
P SKN015 Skin Carcinoma 66 0.210
38
RNL011 Renal Osteodystrophy 50 0.209
39
P HYP024 Hypoparathyroidism 56 0.208
40
IRN002 Iron Metabolism Disease 57 0.207
41
DRM006 Dermatitis 61 0.206
42
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.206
43
P CRD246 Cardiovascular System Disease 57 0.205
44
48X005 48,xyyy 39 0.205
45
P LKM002 Leukemia 68 0.204
46
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.204
47
HMC014 Homocysteinemia 53 0.204
48
HYP781 Hypoascorbemia 51 0.204
49
CRH001 Crohn's Disease 74 0.202
50
AST005 Asthma 76 0.202
51
NTR005 Nutritional Deficiency Disease 62 0.202
52
HYP017 Hypophosphatemia 50 0.201
53
CYS001 Cystic Fibrosis 81 0.201
54
FTT001 Fatty Liver Disease 61 0.200
55
P MYL006 Myeloid Leukemia 60 0.198
56
HYP025 Hyperphosphatemia 48 0.196
57
P PLY011 Polycystic Ovary Syndrome 56 0.195
58
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.192
59
LVR012 Liver Cirrhosis 62 0.190
60
c PRM005 Primary Hyperparathyroidism 58 0.190
61
c SYS001 Systemic Lupus Erythematosus 86 0.188
62
ATH013 Atherosclerosis Susceptibility 65 0.186
63
P ALP008 Alopecia 54 0.182
64
P HRT032 Heart Disease 75 0.182
65
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.181
66
P DRR001 Diarrhea 55 0.181
67
PLM001 Pulmonary Tuberculosis 69 0.181
68
P DRM053 Dermatitis, Atopic 66 0.179
69
P VSC007 Vascular Disease 63 0.179
70
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.179
71
c HYP595 Hypertension, Essential 84 0.178
72
P SCH015 Schizophrenia 74 0.178
73
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.178
74
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.177
75
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.177
76
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.177
77
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.177
78
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.177
79
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.177
80
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.177
81
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.177
82
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.177
83
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.177
84
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.177
85
GST033 Gestational Diabetes 61 0.176
86
ADN018 Adenoma 59 0.176
87
P LPS004 Lupus Erythematosus 61 0.176
88
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.176
89
LPD008 Lipid Metabolism Disorder 62 0.175
90
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.175
91
P NRP001 Neuropathy 56 0.174
92
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.173
93
c MCR120 Microvascular Complications of Diabetes 7 47 0.173
94
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.172
95
P CRN300 Coronary Heart Disease 1 63 0.171
96
c MCR113 Microvascular Complications of Diabetes 3 52 0.171
97
ATX019 Ataxia with Vitamin E Deficiency 42 0.171
98
P PRD008 Periodontitis 64 0.169
99
PRT037 Pertussis 65 0.169
100
c MCR130 Microvascular Complications of Diabetes 6 41 0.168
101
c MCR133 Microvascular Complications of Diabetes 4 41 0.168
102
P ATR011 Atrial Fibrillation 66 0.167
103
P ALZ034 Alzheimer Disease 88 0.164
104
P HPT023 Hepatocellular Carcinoma 100 0.164
105
ALL014 Allergic Encephalomyelitis 38 0.163
106
ALC007 Alcohol Dependence 66 0.163
107
URM002 Uremia 49 0.162
108
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.161
109
HYP066 Hyperglycemia 61 0.160
110
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.160
111
ULC004 Ulcerative Colitis 73 0.158
112
CNG034 Congestive Heart Failure 69 0.158
113
P RTN024 Retinoblastoma 73 0.158
114
c FML008 Familial Retinoblastoma 53 0.158
115
NPH009 Nephrolithiasis 55 0.157
116
P MYP004 Myopathy 70 0.156
117
LPP008 Lipoprotein Quantitative Trait Locus 62 0.156
118
MYL009 Myelodysplastic Syndrome 70 0.156
119
P ADN016 Adenocarcinoma 64 0.156
120
CRB039 Cerebrovascular Disease 67 0.154
121
DPR016 Depression 63 0.154
122
P SRC025 Sarcoidosis 1 70 0.153
123
P ECL001 Eclampsia 50 0.153
124
CLT003 Colitis 62 0.151
125
LNG099 Lung Disease 60 0.151
126
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.150
127
STR067 Stroke, Ischemic 81 0.150
128
P ATS364 Autism 70 0.150
129
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.150
130
c LKM061 Leukemia, Acute Myeloid 84 0.150
131
AGN016 Aging 56 0.149
132
c HYP057 Hypervitaminosis D 42 0.149
133
P HYP086 Hypothyroidism 69 0.149
134
OST012 Osteoarthritis 78 0.148
135
P OVR042 Ovarian Cancer 88 0.148
136
ISC004 Ischemia 58 0.148
137
P GST053 Gastric Cancer 83 0.147
138
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.147
139
MSL001 Measles 62 0.147
140
c RHB024 Rhabdomyosarcoma 2 67 0.146
141
P PRK057 Parkinson Disease, Late-Onset 78 0.145
142
P HYP726 Hypercalcemia, Infantile, 1 58 0.145
143
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.145
144
THY029 Thyroid Carcinoma 59 0.145
145
P PNC035 Pancreatic Cancer 84 0.145
146
ART140 Arteries, Anomalies of 52 0.144
147
GLC003 Glucose Intolerance 54 0.144
148
c PCH010 Pachyonychia Congenita 3 44 0.144
149
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.144
150
P MLN008 Melanoma 69 0.143
151
CHL079 Children's Interstitial Lung Disease 26 0.143
152
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.143
153
ALL026 Allergic Hypersensitivity Disease 62 0.142
154
P RHM011 Rheumatoid Arthritis 80 0.142
155
P RHN004 Rhinitis 57 0.142
156
TQP001 Taqi Polymorphism 32 0.142
157
c NRF023 Neurofibromatosis, Type Ii 80 0.141
158
P PRP019 Peripheral Nervous System Disease 58 0.141
159
NRL016 Neural Tube Defects 82 0.141
160
c DBT099 Diabetes Mellitus, Type I 65 0.140
161
P LYM118 Lymphoma 68 0.139
162
MNT002 Mental Depression 58 0.138
163
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.137
164
P NRB001 Neuroblastoma 72 0.137
165
P TRN020 Turner Syndrome 67 0.137
166
TRD006 Tardive Dyskinesia 54 0.137
167
ACT119 Acute Promyelocytic Leukemia 63 0.137
168
P LNG032 Lung Cancer 98 0.136
169
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.136
170
HMN044 Human Immunodeficiency Virus Type 1 71 0.136
171
P ART021 Arteriosclerosis 54 0.135
172
c ATS007 Autism Spectrum Disorder 67 0.135
173
P MYC084 Mycobacterium Tuberculosis 1 68 0.135
174
P PNM007 Pneumonia 68 0.134
175
DWN001 Down Syndrome 70 0.134
176
CLR108 Colorectal Adenoma 64 0.133
177
c HYP836 Hypercholesterolemia, Familial, 1 73 0.133
178
P SCK005 Sickle Cell Disease 50 0.132
179
P THL005 Thalassemia 60 0.132
180
NNL006 Non-Alcoholic Steatohepatitis 54 0.132
181
P HYP076 Hyperthyroidism 55 0.132
182
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.132
183
ALL003 Allergic Rhinitis 67 0.131
184
P INF032 Infertility 57 0.130
185
P SZR006 Seizure Disorder 56 0.130
186
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.129
187
47X002 47,xyy 49 0.129
188
P ART022 Arthritis 69 0.129
189
KRT009 Keratosis 51 0.128
190
P MCR115 Microvascular Complications of Diabetes 5 66 0.128
191
P MYC007 Myocardial Infarction 70 0.128
192
P BLD134 Bladder Cancer 79 0.127
193
KRT001 Keratoconjunctivitis Sicca 49 0.127
195
CHL068 Cholestasis 61 0.127
196
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.127
197
CMM005 Common Cold 57 0.125
198
NPH003 Nephrocalcinosis 51 0.123
199
P GST044 Gastritis 56 0.122
200
VSL002 Visual Epilepsy 59 0.122
201
c INF071 Inflammatory Bowel Disease 1 67 0.122
202
P DMN002 Dementia 66 0.120
203
P CTR002 Cataract 60 0.120
204
ATS010 Autosomal Recessive Disease 48 0.120
205
P BCL017 B-Cell Lymphoma 58 0.120
206
IMM167 Immune Deficiency Disease 78 0.119
207
P CLC063 Celiac Disease 1 66 0.119
208
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.119
209
P PRM006 Primary Biliary Cirrhosis 62 0.119
210
ACQ007 Acquired Immunodeficiency Syndrome 60 0.119
211
HLX001 Helix Syndrome 47 0.119
212
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.118
213
P RCT021 Rectum Cancer 52 0.118
214
c HPT001 Hepatitis C 62 0.118
215
CRH005 Crohn's Colitis 53 0.118
216
INS024 Insulin-Like Growth Factor I 79 0.117
217
c PRM038 Primary Agammaglobulinemia 44 0.117
218
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.117
219
MYL005 Myelofibrosis 70 0.116
220
ATM052 Autoimmune Disease 1 37 0.116
221
P GLM045 Glioma 63 0.116
222
ANX010 Anxiety 73 0.116
223
TXC005 Toxic Shock Syndrome 62 0.116
224
P HPT021 Hepatitis 67 0.116
225
ADL002 Adult Syndrome 70 0.115
226
P CHR345 Chronic Pain 44 0.115
227
GLL048 Glial Tumor 45 0.115
228
LPT014 Leptin Deficiency or Dysfunction 74 0.115
229
LMY002 Leiomyoma 52 0.115
230
P MJR001 Major Depressive Disorder 68 0.113
231
P HYP058 Hypervitaminosis a 48 0.113
232
PLC008 Placenta Disease 50 0.113
233
P END044 Endometriosis 63 0.113
234
SQM006 Squamous Cell Carcinoma 60 0.113
235
P LKM062 Leukemia, Acute Lymphoblastic 69 0.112
236
P THY032 Thyroiditis 52 0.112
237
P CNR004 Cone-Rod Dystrophy 2 73 0.111
238
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.111
239
CLC006 Calcinosis 48 0.111
240
THR024 Thrombosis 57 0.111
241
P HYP733 Hypercalciuria, Absorptive, 2 45 0.111
242
P RSP003 Respiratory Failure 74 0.110
243
PRP027 Peripheral Vascular Disease 71 0.110
244
SCK003 Sickle Cell Anemia 74 0.109
245
MDD011 Mood Disorder 62 0.109
246
SPN186 Spinal Cord Injury 60 0.108
247
P TRM003 Tremor 54 0.108
248
CVD001 Covid-19 44 0.107
249
IRN001 Iron Deficiency Anemia 59 0.106
250
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.106
251
HMS001 Hemosiderosis 54 0.106
252
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.105
253
c MGR028 Migraine with or Without Aura 1 67 0.105
254
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.105
255
CLN015 Colon Adenocarcinoma 65 0.105
256
P MSC005 Muscular Dystrophy 66 0.105
257
P PSD015 Pseudohypoparathyroidism 56 0.105
258
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.105
259
c THR092 Thrombophilia Due to Thrombin Defect 73 0.104
260
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.104
261
HYP081 Hypolipoproteinemia 51 0.104
262
c PRS136 Prostate Cancer, Hereditary, 6 33 0.103
263
P NTR004 Neutropenia 63 0.103
264
c PRS130 Prostate Cancer, Hereditary, 8 32 0.103
265
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.103
266
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.103
267
c ACT071 Acute Kidney Failure 60 0.102
268
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.102
269
MYF001 Myofibroma 45 0.102
270
HYP060 Hyperinsulinism 54 0.101
271
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.101
272
c HPT073 Hepatitis C Virus 72 0.101
273
P URT039 Urticaria 58 0.101
274
P RST001 Restless Legs Syndrome 54 0.101
275
PSY004 Psychotic Disorder 67 0.101
276
ESP021 Esophageal Cancer 90 0.100
277
P BPL003 Bipolar Disorder 56 0.100
278
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.100
279
BCT022 Bacterial Infectious Disease 56 0.100
280
P NPH012 Nephrotic Syndrome 60 0.100
281
c ACT073 Acute Leukemia 58 0.100
282
URL001 Urolithiasis 45 0.099
283
BNN003 Bone Inflammation Disease 48 0.099
284
P INF038 Influenza 68 0.099
285
P LTR001 Lateral Sclerosis 54 0.099
286
P RRH023 Rare Hereditary Hemochromatosis 41 0.099
287
P INT068 Intestinal Disease 53 0.099
288
c HPT016 Hepatitis B 59 0.099
289
GST050 Gastrointestinal System Disease 56 0.098
290
P HML002 Hemolytic Anemia 63 0.098
291
MTB004 Metabolic Acidosis 50 0.098
292
c MJR024 Major Affective Disorder 9 41 0.098
293
c MJR022 Major Affective Disorder 8 38 0.098
294
P HDC001 Headache 57 0.098
295
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.097
296
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.097
297
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.097
298
P SYS005 Systemic Scleroderma 68 0.097
299
DNT012 Dental Caries 53 0.097
300
CHL014 Cholera 59 0.097
301
HYP266 Hypoxia 57 0.097
302
P GRV001 Graves' Disease 55 0.096
303
PRT036 Peritonitis 64 0.096
304
BRN056 Bronchopulmonary Dysplasia 57 0.096
305
LYM133 Lymphoma, Hodgkin, Classic 69 0.095
306
PNC001 Pancytopenia 54 0.095
307
MMM001 Mammary Paget's Disease 53 0.095
308
OST004 Osteitis Fibrosa 41 0.095
309
PRS045 Prostatic Hypertrophy 53 0.094
310
FDL002 Food Allergy 51 0.094
311
CNT047 Contact Dermatitis 58 0.094
312
P ENC018 Encephalopathy 61 0.094
313
P GLM007 Glomerulonephritis 57 0.094
314
P SHR001 Short Bowel Syndrome 53 0.094
315
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.094
316
IGR001 Ige Responsiveness, Atopic 59 0.094
317
c SVR001 Severe Acute Respiratory Syndrome 62 0.093
318
c ATR087 Atrial Standstill 1 75 0.093
319
FBR047 Fibromyalgia 58 0.093
320
P MVM001 Movement Disease 63 0.093
321
c DRR009 Diarrhea 6 46 0.093
322
MYL069 Myeloma, Multiple 85 0.093
323
P SBS003 Substance Abuse 55 0.093
324
MST005 Mastitis 53 0.092
325
c BSL007 Basal Cell Carcinoma 68 0.092
326
c FML001 Familial Atrial Fibrillation 65 0.092
327
END040 Endogenous Depression 55 0.092
328
PRD004 Prediabetes Syndrome 47 0.092
329
c PRD040 Periodontitis, Chronic 53 0.092
330
c FNC043 Fanconi Anemia, Complementation Group E 62 0.091
331
ENT011 Enterocolitis 51 0.091
332
SKN019 Skin Melanoma 68 0.091
333
LYM019 Lymphosarcoma 46 0.090
334
P SLP005 Sleep Disorder 59 0.090
335
c ACT075 Acute Myocardial Infarction 57 0.090
336
GTR002 Goiter 53 0.090
337
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.090
338
PRP030 Purpura 54 0.090
339
EYD002 Eye Disease 58 0.090
340
ALL006 Allergic Asthma 56 0.089
341
P PRC031 Preeclampsia/eclampsia 1 38 0.089
342
DFF005 Diffuse Large B-Cell Lymphoma 55 0.089
343
STM007 Stomatitis 50 0.089
344
P HYP750 Hypertriglyceridemia, Familial 62 0.089
345
DMY004 Demyelinating Disease 52 0.089
346
HYP043 Hyperandrogenism 48 0.088
347
P PNC044 Pancreatitis 61 0.088
348
P ALC033 Alcohol Use Disorder 58 0.088
349
c PSR023 Psoriasis 1 52 0.088
350
P THR014 Thrombocytopenia 67 0.088
351
P EXN002 Exanthem 57 0.088
352
PLM033 Pulmonary Embolism 59 0.088
353
IRR002 Irritable Bowel Syndrome 65 0.088
354
HYP080 Hypogonadism 50 0.088
355
P EPL164 Epilepsy 71 0.087
356
P GRF003 Graft-Versus-Host Disease 72 0.087
357
TTN003 Tetanus 65 0.087
358
P LKM071 Leukemia, Chronic Lymphocytic 79 0.087
359
c HPT003 Hepatitis a 62 0.087
360
PPT005 Peptic Ulcer Disease 59 0.087
361
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.087
362
P MSC003 Muscular Atrophy 52 0.087
363
c PLY105 Polycystic Ovary Syndrome 1 38 0.087
364
HLC007 Helicobacter Pylori Infection 59 0.086
365
PGM030 Pigmentation Anomaly of the Skin 26 0.086
366
c SCL052 Scleroderma, Familial Progressive 61 0.086
367
GLB015 Glioblastoma Multiforme 75 0.086
368
49X006 49, Xxxxy Syndrome 41 0.085
369
END057 Endometrial Cancer 74 0.085
370
PST092 Posttransplant Acute Limbic Encephalitis 29 0.085
371
PRS129 Prostatic Hyperplasia, Benign 49 0.085
372
P MLN007 Male Infertility 55 0.085
373
c PNS012 Paine Syndrome 61 0.084
374
P ADL010 Adult Respiratory Distress Syndrome 65 0.084
375
LMY014 Leiomyoma, Uterine 56 0.084
376
c MCR129 Microvascular Complications of Diabetes 1 66 0.084
377
PRN019 Perinatal Necrotizing Enterocolitis 59 0.084
378
PRS021 Prostatic Adenoma 51 0.084
379
P KDN017 Kidney Cancer 60 0.084
380
P INS002 in Situ Carcinoma 53 0.084
381
P PLM036 Pulmonary Fibrosis 65 0.084
382
c PSR017 Psoriasis 2 53 0.084
383
ANG054 Angina Pectoris 66 0.083
384
c PSR032 Psoriasis 11 47 0.083
385
c PSR028 Psoriasis 7 42 0.083
386
c PSR018 Psoriasis 13 41 0.083
387
THY030 Thyroid Gland Disease 52 0.083
388
P HYP098 Hypereosinophilic Syndrome 67 0.083
389
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.083
390
SPR126 Superior Semicircular Canal Dehiscence 40 0.082
391
c HMG029 Hemoglobin Se Disease 39 0.082
392
DSS008 Disease of Mental Health 58 0.082
393
SRC014 Sarcoma 65 0.082
394
c BTT014 Beta-Thalassemia 74 0.082
395
KHL003 Kohlschutter-Tonz Syndrome 65 0.082
396
BRN002 Bronchiolitis 59 0.082
397
CRB037 Cerebral Palsy 69 0.081
398
CNS004 Constipation 58 0.081
399
P OST001 Osteopetrosis 70 0.081
400
SPL018 Splenomegaly 48 0.081
401
NRT001 Neurotic Disorder 53 0.081
402
c SYS043 Systemic Lupus Erythematosus 1 38 0.081
403
c SPN225 Spondyloarthropathy 1 73 0.081
404
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.081
405
ORL011 Oral Cancer 60 0.081
406
GNG013 Gingivitis 59 0.081
407
HYP005 Hypokalemia 55 0.081
408
NRT004 Neuritis 52 0.081
409
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.080
410
BRN024 Bronchitis 68 0.080
411
DBT010 Diabetic Neuropathy 54 0.080
412
PRM020 Premenstrual Tension 40 0.080
413
MSC007 Muscle Hypertrophy 64 0.079
414
PPL022 Papilloma 54 0.079
415
NWB001 Newborn Respiratory Distress Syndrome 58 0.079
416
c FML035 Familial Hyperlipidemia 55 0.079
417
P MNC007 Monocytic Leukemia 53 0.079
418
MCS002 Mucositis 56 0.079
419
ERY051 Erythroleukemia, Familial 56 0.078
420
P LCH002 Lichen Planus 53 0.078
421
P HRP006 Herpes Simplex 65 0.078
422
ANV001 Anovulation 47 0.078
423
CNN005 Connective Tissue Disease 68 0.078
424
P ICH004 Ichthyosis 54 0.078
425
TRP009 Triple X Syndrome 42 0.078
426
c MCR112 Microvascular Complications of Diabetes 2 41 0.078
427
c SML038 Small Cell Cancer of the Lung 65 0.078
428
MLR004 Malaria 81 0.078
429
P OVR082 Overgrowth Syndrome 50 0.078
430
SVR004 Severe Combined Immunodeficiency 73 0.077
431
P MJR007 Major Affective Disorder 1 43 0.077
432
BLR001 Biliary Atresia 50 0.077
433
PRP080 Peripheral Artery Disease 53 0.077
434
P OCL013 Oculodentodigital Dysplasia 69 0.077
435
HYP056 Hypoglycemia 66 0.077
436
P FBR017 Fibrosarcoma 56 0.076
437
VRL011 Viral Infectious Disease 61 0.076
438
ANR007 Anorexia Nervosa 63 0.076
439
P BRS044 Breast Adenocarcinoma 59 0.076
440
c ALP101 Alpha-Thalassemia 62 0.076
441
AMN001 Amenorrhea 54 0.076
442
CHR066 Chronic Fatigue Syndrome 61 0.076
443
SQM002 Squamous Cell Papilloma 46 0.075
444
RFR010 Refractory Anemia 48 0.075
445
PNG002 Pain Agnosia 51 0.075
446
c VRL010 Viral Hepatitis 52 0.075
447
SPN051 Spondylitis 51 0.075
448
HNS001 Hansen's Disease 34 0.075
449
INF009 Inflammatory Spondylopathy 31 0.075
450
P LPR021 Leprosy 3 69 0.074
451
CHY002 Chylomicron Retention Disease 65 0.074
452
c SVR005 Severe Pre-Eclampsia 50 0.074
453
CLN045 Colonic Benign Neoplasm 46 0.074
454
BCK006 Back Pain 42 0.074
455
DPH001 Diphtheria 60 0.073
456
HYP636 Hypocalcemic Vitamin D-Dependent Rickets 39 0.073
457
SCH012 Schizoaffective Disorder 50 0.073
458
SBC016 Subacute Delirium 44 0.073
459
P VSC018 Visceral Steatosis 33 0.073
460
c ACT027 Acute Pancreatitis 60 0.073
461
P ALP009 Alopecia Areata 60 0.073
462
BRN071 Brain Injury 49 0.072
463
DRG003 Drug Dependence 47 0.072
464
CMR002 Coumarin Resistance 56 0.072
465
ACT017 Acute Chest Syndrome 51 0.071
466
HSH003 Hashimoto Thyroiditis 62 0.071
467
BRN028 Brain Cancer 74 0.071
468
c HMC039 Hemochromatosis, Type 1 74 0.071
469
OST003 Osteonecrosis 61 0.071
470
P DYS154 Dystonia 65 0.070
471
ORL015 Oral Squamous Cell Carcinoma 43 0.070
472
MMM006 Mammographic Density 41 0.070
473
P NRV007 Nervous System Disease 66 0.070
474
BCT002 Bacterial Vaginosis 53 0.070
475
P HYD006 Hydrocephalus 66 0.070
476
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.070
477
P HYP265 Hypotonia 43 0.070
478
ACR007 Acromegaly 71 0.070
479
P NRF002 Neurofibromatosis 56 0.070
480
SPN035 Spindle Cell Sarcoma 53 0.070
481
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.070
482
HYP014 Hyperuricemia 52 0.070
483
OTT002 Otitis Media 72 0.070
484
HRW001 Hair Whorl 36 0.070
485
GT001 Gout 64 0.069
486
GLS018 Glass Syndrome 57 0.069
487
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.069
488
PNC129 Pancreatic Adenocarcinoma 68 0.069
489
GST045 Gastroenteritis 59 0.069
490
CHR178 Chromosomal Triplication 35 0.069
491
P ART023 Arthropathy 62 0.068
492
P VSC011 Vasculitis 62 0.068
493
P ESP024 Esophagitis 62 0.068
494
P FLL037 Follicular Lymphoma 67 0.068
495
c GRV008 Graves Disease 1 56 0.068
496
TBC004 Tobacco Addiction 64 0.068
497
GLS007 Glossitis 47 0.068
498
IDP085 Idiopathic Infantile Hypercalcemia 28 0.067
499
P RTN018 Retinal Disease 53 0.067
500
ILS001 Ileus 51 0.067
501
P SJG008 Sjogren Syndrome 61 0.067
502
BRR014 Barrett Esophagus 65 0.066
503
BRS051 Breast Disease 58 0.066
504
NRM005 Neuromuscular Disease 64 0.066
505
P OPT009 Optic Neuritis 57 0.066
506
EXC002 Exocrine Pancreatic Insufficiency 42 0.066
507
c ACT135 Acute Graft Versus Host Disease 52 0.066
508
CCN002 Cocaine Abuse 49 0.066
509
OCL069 Ocular Motor Apraxia 51 0.066
510
SNS003 Sensory Peripheral Neuropathy 54 0.065
511
GRW007 Growth Hormone Deficiency 46 0.065
512
PRT013 Portal Hypertension 59 0.065
513
KRT013 Keratolytic Winter Erythema 46 0.065
514
c DRM054 Dermatitis, Atopic, 2 44 0.065
515
RDN001 Reading Disorder 40 0.065
516
P RNL007 Renal Tubular Acidosis 51 0.065
517
CYT018 Cytochrome P450 2d6 Variant 27 0.065
518
CLR109 Colorectal Adenocarcinoma 51 0.065
519
CRN030 Coronary Stenosis 50 0.064
520
IMP005 Impotence 52 0.064
521
P LNG064 Lung Cancer Susceptibility 3 78 0.064
522
CCN001 Cocaine Dependence 48 0.063
523
CHL065 Cholangiocarcinoma 68 0.063
524
INT079 Intrahepatic Cholangiocarcinoma 51 0.063
525
PRS063 Paresthesia 41 0.063
527
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.063
528
HPT022 Hepatoblastoma 56 0.063
529
RSC001 Rosacea 54 0.062
530
P SCL018 Scoliosis 60 0.062
531
PST021 Postpartum Depression 50 0.062
532
PPL052 Papillomatosis, Confluent and Reticulated 33 0.062
533
PSR001 Psoriatic Arthritis 61 0.062
534
BRN004 Brain Edema 56 0.062
535
P APL001 Aplastic Anemia 74 0.062
536
SBS004 Substance Dependence 48 0.061
537
PLY150 Polykaryocytosis Inducer 31 0.061
538
P CNJ013 Conjunctivitis 65 0.061
539
PPL001 Papillary Adenoma 44 0.061
540
BNG018 Benign Paroxysmal Positional Nystagmus 37 0.061
541
P SPP010 Suppressor of Tumorigenicity 3 51 0.061
542
TRN018 Transitional Cell Carcinoma 56 0.061
543
OVR094 Ovarian Epithelial Cancer 38 0.061
544
c LKM063 Leukemia, Chronic Myeloid 72 0.060
545
c PNC108 Pancreatitis, Hereditary 70 0.060
546
TLN003 Telangiectasis 52 0.060
547
TRM010 Traumatic Brain Injury 51 0.060
548
c INH020 Inherited Metabolic Disorder 47 0.060
549
GST040 Gastric Adenocarcinoma 70 0.060
550
RTC005 Reticulosarcoma 47 0.060
551
BRT054 Brittle Bone Disorder 72 0.060
552
ORL013 Oral Lichen Planus 45 0.060
553
c CHR682 Chronic Bilirubin Encephalopathy 39 0.060
554
OST017 Osteomyelitis 64 0.060
555
WLL001 Williams-Beuren Syndrome 60 0.060
556
P BRN022 Bronchiectasis 59 0.060
557
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.060
558
SCH003 Schizophreniform Disorder 56 0.060
559
OST016 Osteochondrosis 53 0.060
560
TXC002 Toxic Encephalopathy 53 0.060
561
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.059
562
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.059
563
CRB004 Cerebral Artery Occlusion 45 0.059
564
P OCY003 Oocyte Maturation Defect 1 45 0.059
565
c SRC023 Sarcoidosis 2 43 0.059
566
KWS002 Kawasaki Disease 65 0.059
567
DRY001 Dry Eye Syndrome 47 0.058
568
ATN005 Autonomic Dysfunction 46 0.058
569
P DNG005 Dengue Virus 59 0.058
570
P ANG015 Angioedema 57 0.058
571
SYN007 Synovitis 54 0.058
572
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.058
573
PLC002 Plica Syndrome 36 0.058
574
ANR040 Aneurysm 59 0.058
575
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.058
576
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.058
577
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.058
578
P PTY003 Pityriasis Rubra Pilaris 58 0.058
579
PRM329 Premature Aging 35 0.058
580
P GLM040 Glioma Susceptibility 1 81 0.057
581
HYP020 Hyperprolactinemia 64 0.057
582
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.057
583
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.057
584
P MNN013 Meningitis 66 0.057
585
DSS009 Disseminated Intravascular Coagulation 57 0.057
586
P DDN001 Duodenal Ulcer 52 0.057
587
BCK003 Background Diabetic Retinopathy 46 0.057
588
P PMP001 Pemphigus 54 0.057
589
c OVR114 Ovarian Cancer 1 38 0.057
590
c MJR008 Major Affective Disorder 2 35 0.057
591
RSP007 Respiratory Distress Syndrome, Infant 30 0.057
592
c ATM011 Autoimmune Hepatitis 63 0.057
593
P LCT002 Lactose Intolerance 53 0.056
594
CHP002 Chops Syndrome 44 0.056
595
P FML011 Familial Adenomatous Polyposis 72 0.056
596
URT010 Ureteral Obstruction 45 0.056
597
P ASP006 Aspergillosis 69 0.056
598
P PRS038 Personality Disorder 65 0.056
599
MYF002 Myofascial Pain Syndrome 42 0.056
600
GST023 Gastric Ulcer 53 0.056
601
CHG001 Chagas Disease 66 0.056
602
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.055
603
c JVN010 Juvenile Rheumatoid Arthritis 64 0.055
604
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.055
606
NRF007 Neurofibroma 64 0.055
607
RSP006 Respiratory System Disease 50 0.055
608
P TCD001 Tic Disorder 53 0.055
609
P ACT008 Actinic Keratosis 53 0.055
610
P FNC004 Fanconi Syndrome 50 0.055
611
SXL003 Sexual Disorder 47 0.055
612
P PRG092 Pregnancy Loss, Recurrent 1 40 0.055
613
P CRD119 Cardiac Arrest 67 0.054
614
c JVN061 Juvenile Arthritis 60 0.054
615
ETN001 Eating Disorder 60 0.054
616
LNG031 Lung Benign Neoplasm 51 0.054
617
P OBS001 Obstructive Jaundice 50 0.054
618
c CNT035 Central Nervous System Disease 52 0.054
619
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.054
620
c INF145 Infantile Liver Failure Syndrome 1 50 0.054
621
MNT001 Mantle Cell Lymphoma 69 0.054
622
BRC012 Brucellosis 64 0.054
623
LSH001 Leishmaniasis 63 0.054
624
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.054
625
IDP073 Idiopathic Hypercalciuria 43 0.054
626
P KLZ004 Kala-Azar 1 41 0.054
627
c DSR027 Disorders of Vitamin D Metabolism 12 0.054
628
P VNW001 Von Willebrand's Disease 65 0.053
629
KPS004 Kaposi Sarcoma 75 0.053
630
SKN005 Skin Atrophy 43 0.053
631
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.053
632
c ART101 Aortic Valve Disease 2 65 0.053
633
P MYC008 Myocarditis 59 0.053
634
IDP070 Idiopathic Scoliosis 42 0.053
635
FCT007 Factor Vii Deficiency 67 0.053
636
PLM010 Pulmonary Edema 54 0.053
637
P AGG001 Aggressive Periodontitis 50 0.053
638
CHR074 Choriocarcinoma 47 0.053
639
P FNC034 Fanconi Renotubular Syndrome 2 40 0.053
640
TRP008 Tropical Calcific Pancreatitis 46 0.053
641
C1N001 C1 Inhibitor Deficiency 39 0.053
642
BRK010 Burkitt Lymphoma 67 0.052
643
c LKM005 Leukemia, T-Cell, Chronic 34 0.052
644
CRD132 Cardiac Conduction Defect 58 0.052
645
RTN020 Retinal Vascular Disease 46 0.052
646
GST020 Gastric Antral Vascular Ectasia 41 0.052
647
LYM040 Lymphoblastic Lymphoma 54 0.052
648
HLL004 Hellp Syndrome 54 0.052
649
c HYP272 Hypercholesterolemia, Familial, 3 44 0.052
650
LWC001 Low Compliance Bladder 43 0.052
651
HYP344 Hyperthyroidism, Familial Gestational 39 0.052
652
c MJR023 Major Affective Disorder 7 33 0.052
653
c MJR003 Major Affective Disorder 6 33 0.052
654
c MJR006 Major Affective Disorder 5 33 0.052
655
c MJR004 Major Affective Disorder 4 28 0.052
656
P CHR012 Chronic Granulomatous Disease 67 0.052
657
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.052
658
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.052
659
CRT017 Cartilage Disease 54 0.052
660
DYS073 Dysphagia 50 0.052
661
P SCL057 Scoliosis, Isolated 1 41 0.052
662
VTM030 Vitamin D-Dependent Rickets, Type 2b, with Normal Vitamin D Receptor 16 0.052
663
BRS099 Breast Ductal Carcinoma 62 0.052
664
PDT035 Pediatric Systemic Lupus Erythematosus 46 0.052
665
P MMP001 Mumps 58 0.051
666
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.051
667
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.051
668
FLL027 Fallopian Tube Carcinoma 67 0.051
669
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.051
670
P AMY004 Amyloidosis 70 0.051
671
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.051
672
P PSD087 Pseudoxanthoma Elasticum 65 0.051
673
KRT006 Keratoconjunctivitis 53 0.051
674
CLC001 Calciphylaxis 51 0.051
675
c ESS001 Essential Tremor 56 0.051
676
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.050
677
P RBL001 Rubella 59 0.050
678
c XNT010 Xanthinuria, Type I 53 0.050
679
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.050
680
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.050
681
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.050
682
PRM003 Premature Ejaculation 44 0.050
683
ANX004 Anoxia 40 0.050
684
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.050
685
SYS071 Systemic Autoimmune Disease 37 0.050
686
PLY068 Polysubstance Abuse 43 0.050
687
THY111 Thyroid Carcinoma, Familial Medullary 67 0.050
688
KRT071 Keratosis, Seborrheic 58 0.050
689
P SCL048 Sclerosteosis 55 0.050
690
THY125 Thyroid Gland Medullary Carcinoma 50 0.050
691
OBS002 Obsessive-Compulsive Disorder 68 0.050
692
PPL049 Papillon-Lefevre Syndrome 65 0.050
693
P MCR010 Microcephaly 59 0.050
694
P SYP003 Syphilis 58 0.050
695
PRS047 Prostatitis 56 0.050
696
DBT002 Diabetic Autonomic Neuropathy 41 0.050
697
GLC008 Glucose Metabolism Disease 40 0.050
698
c LCL006 Localized Scleroderma 62 0.050
699
INS001 Insulinoma 60 0.050
700
P HYP730 Hypogonadotropic Hypogonadism 52 0.050
701
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.050
702
MYL031 Myeloproliferative Neoplasm 66 0.049
703
PST028 Post-Traumatic Stress Disorder 58 0.049
704
MCR013 Microphthalmia 57 0.049
705
c BSL024 Basal Cell Carcinoma 1 56 0.049
706
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.049
707
SPS003 Spastic Diplegia 51 0.049
708
HPT004 Hepatic Coma 45 0.049
709
c RST012 Restless Legs Syndrome 1 34 0.049
710
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.049
711
DNG002 Dengue Hemorrhagic Fever 60 0.049
712
P CHR285 Chronic Myelomonocytic Leukemia 60 0.049
713
DCT002 Ductal Carcinoma in Situ 59 0.049
714
ANS011 Anus Cancer 56 0.049
715
c OST164 Osteoporosis, Juvenile 53 0.049
716
VCC001 Vaccinia 49 0.049
717
P VTR007 Vitreoretinopathy 46 0.049
718
c FML021 Familial Hypercholesterolemia 66 0.048
719
HPT019 Hepatic Encephalopathy 60 0.048
720
P PGT001 Paget's Disease of Bone 58 0.048
721
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.048
722
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.048
723
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.048
724
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.048
725
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.048
726
PMP006 Pemphigus Vulgaris, Familial 57 0.048
727
SFT003 Soft Tissue Sarcoma 56 0.048
728
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.048
729
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.048
730
ACT084 Acute Stress Disorder 47 0.048
731
VRC005 Varicose Veins 60 0.048
732
AYM001 Ayme-Gripp Syndrome 57 0.048
733
PRP036 Peripheral T-Cell Lymphoma 53 0.048
734
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.048
735
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.048
736
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.048
737
HMP009 Haemophilus Influenzae 43 0.048
738
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.048
739
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.048
740
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.047
741
c LKM070 Leukemia, Acute Monocytic 57 0.047
742
AMN003 Amnestic Disorder 54 0.047
743
c CNG027 Congenital Hemolytic Anemia 50 0.047
744
P MYS003 Myasthenia Gravis 68 0.047
745
c DNG003 Dengue Disease 59 0.047
746
P LRY044 Larynx Cancer 55 0.047
747
P PHT010 Photoparoxysmal Response 1 42 0.047
748
P RHB003 Rhabdomyosarcoma 63 0.047
749
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.047
750
PLY100 Polyploidy 40 0.047
751
INV005 Inverted Follicular Keratosis 32 0.047
752
P ATX030 Ataxia-Telangiectasia 82 0.047
753
MSC157 Muscular Dystrophy, Duchenne Type 72 0.047
754
CHC001 Chickenpox 60 0.047
755
c MCL013 Mucolipidosis Iv 66 0.046
756
PLG002 Plague 63 0.046
757
IDP011 Idiopathic Interstitial Pneumonia 59 0.046
758
P LYM033 Lymphoproliferative Syndrome 59 0.046
759
EMB004 Embryonal Carcinoma 56 0.046
760
c HYP243 Hyperparathyroidism 1 51 0.046
761
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.046
762
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.046
763
BNM001 Bone Marrow Cancer 43 0.046
764
HYP784 Hypogonadism, Male 40 0.046
765
P PHC003 Pheochromocytoma 71 0.046
766
P THY023 Thymoma 65 0.046
767
MGK001 Megakaryocytic Leukemia 64 0.046
768
CRC021 Carcinosarcoma 62 0.046
769
c THY107 Thymoma, Familial 52 0.046
770
PTH002 Pathological Gambling 49 0.046
771
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.046
772
c ART115 Aortic Valve Disease 1 75 0.046
773
P HNT016 Huntington Disease 72 0.046
774
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.046
775
P CYS018 Cystitis 59 0.046
776
BWN001 Bowen-Conradi Syndrome 52 0.046
777
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.046
778
RNL077 Renal Fibrosis 47 0.046
779
SPS057 Spasticity 45 0.046
780
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.046
781
GLL008 Gilles De La Tourette Syndrome 66 0.045
782
CNN003 Conn's Syndrome 79 0.045
783
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.045
784
SPP011 Suppression of Tumorigenicity 12 59 0.045
785
CLN019 Colonic Disease 47 0.045
786
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.045
787
FTL073 Fetal Anticonvulsant Syndrome 26 0.045
788
ADR007 Adrenoleukodystrophy 75 0.045
789
MYC006 Mycosis Fungoides 66 0.045
790
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.045
791
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.045
792
ACD008 Acid-Labile Subunit Deficiency 54 0.045
793
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.045
794
ACR041 Acromelic Frontonasal Dysostosis 52 0.045
795
IGG001 Iga Glomerulonephritis 48 0.045
796
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.045
797
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.045
798
OPT003 Opiate Dependence 50 0.045
799
ADR040 Adrenal Gland Pheochromocytoma 46 0.045
800
BLD131 Bladder Urothelial Carcinoma 62 0.044
801
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.044
802
PLS009 Plasma Cell Neoplasm 51 0.044
803
LPT006 Leptin Receptor Deficiency 48 0.044
804
RST023 Resting Heart Rate, Variation in 41 0.044
805
ADR022 Adrenomyeloneuropathy 38 0.044
806
HRP008 Herpes Simiae 25 0.044
807
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.044
808
c HYP292 Hypophosphatasia, Infantile 57 0.044
809
OLG003 Oligohydramnios 51 0.044
810
PLY012 Polyhydramnios 46 0.044
811
PRT035 Peritoneum Cancer 44 0.044
812
GLM044 Glomerular Disease 37 0.044
813
c CHR064 Chronic Monocytic Leukemia 33 0.044
814
TNG007 Tongue Carcinoma 51 0.043
815
AGR002 Agoraphobia 45 0.043
816
c JVN025 Juvenile Primary Osteoporosis 22 0.043
817
HMT002 Hematologic Cancer 62 0.043
818
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.043
819
c CHR417 Chronic Graft Versus Host Disease 57 0.043
820
SPN041 Spinal Cord Disease 56 0.043
821
HMP005 Hemiplegia 55 0.043
822
P CTN003 Cutaneous Lupus Erythematosus 53 0.043
823
SKN013 Skin Benign Neoplasm 51 0.043
824
OST115 Osteonecrosis of the Jaw 40 0.043
825
c NRF024 Neurofibromatosis, Type I 77 0.043
826
THY122 Thyroid Gland Cancer 57 0.043
827
ANG005 Anogenital Venereal Wart 55 0.043
828
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.043
829
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.043
830
ACT011 Acute Contagious Conjunctivitis 40 0.043
831
FML039 Female Reproductive System Disease 39 0.043
832
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.043
833
UTR054 Uterine Hypoplasia 25 0.043
834
P GCH001 Gaucher's Disease 63 0.042
835
NRM001 Neuromyelitis Optica 61 0.042
836
CHR100 Chronic Ulcer of Skin 55 0.042
837
MLT006 Multidrug-Resistant Tuberculosis 48 0.042
838
MCR018 Microcytic Anemia 47 0.042
839
KHN001 Kuhnt-Junius Degeneration 47 0.042
840
PLL012 Pollen Allergy 46 0.042
841
FLL008 Folliculitis 46 0.042
842
CRP002 Croup 44 0.042
843
ONC003 Oncogenic Osteomalacia 42 0.042
844
KLD004 Keloid Disorder 40 0.042
845
PTT037 Pituitary Tumors 44 0.041
846
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.041
847
IRR003 Irritant Dermatitis 49 0.041
848
c BCT013 Bacterial Pneumonia 48 0.041
849
P MLT008 Multinodular Goiter 42 0.041
850
c INF089 Inflammatory Bowel Disease 6 32 0.041
851
OVR029 Ovarian Hyperstimulation Syndrome 64 0.041
852
P FCL005 Focal Segmental Glomerulosclerosis 57 0.041
853
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.041
854
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.041
855
P SML001 Small Cell Carcinoma 52 0.041
856
P AST007 Astrocytoma 51 0.041
857
P CMP008 Compartment Syndrome 49 0.041
858
P CTN015 Cutaneous T Cell Lymphoma 49 0.041
859
NSS002 Neisseria Meningitidis Infection 47 0.041
860
SYN036 Syncope 45 0.041
861
CYN002 Cyanosis, Transient Neonatal 45 0.041
862
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.041
863
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.041
864
BSL036 Basal Cell Nevus Syndrome 73 0.040
865
P ORT004 Orthostatic Intolerance 62 0.040
866
INT066 Interstitial Lung Disease 60 0.040
867
CYS010 Cystinosis 59 0.040
868
PNN001 Panniculitis 51 0.040
869
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.040
870
WGN007 Wagner Vitreoretinopathy 38 0.040
871
WGN003 Wagner Syndrome 36 0.040
872
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.040
873
ADN011 Adenoid Cystic Carcinoma 70 0.040
874
P TBR001 Tuberous Sclerosis 70 0.040
875
c WLM018 Wilms Tumor 5 61 0.040
876
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.040
877
CRY005 Cryptococcosis 58 0.040
878
c BNG091 Benign Chronic Pemphigus 58 0.040
879
PLM012 Pulmonary Sarcoidosis 53 0.040
880
PNM005 Pneumonic Plague 51 0.040
881
P MDL005 Medulloblastoma 77 0.039
882
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.039
883
P INT070 Intestinal Obstruction 58 0.039
884
ANL018 Analbuminemia 54 0.039
885
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.039
886
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.039
887
MCN017 Meconium Ileus 52 0.039
888
DFF036 Differentiated Thyroid Carcinoma 52 0.039
889
NTR018 Neutrophilia, Hereditary 52 0.039
890
WTH001 Withdrawal Disorder 48 0.039
891
MNN020 Meningococcal Infection 46 0.039
892
FCL012 Facial Paralysis 46 0.039
893
CNT017 Central Nervous System Origin Vertigo 45 0.039
894
ATY042 Atypical Chronic Myeloid Leukemia 49 0.038
895
HYP114 Hypertensive Nephropathy 36 0.038
897
OPD001 Opioid Abuse 46 0.038
898
c GCH015 Gaucher Disease, Type I 70 0.038
899
c PRM196 Premature Ovarian Failure 1 67 0.038
900
LNG039 Lung Squamous Cell Carcinoma 66 0.038
901
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.038
902
END041 Endometrial Adenocarcinoma 63 0.038
903
P INT143 Interstitial Cystitis 61 0.038
904
SPR004 Supravalvular Aortic Stenosis 58 0.038
905
CLL003 Cellulitis 54 0.038
906
CLR030 Clear Cell Renal Cell Carcinoma 53 0.038
907
c FLL041 Follicular Lymphoma 1 49 0.038
908
EXS001 Exostosis 46 0.038
909
PRT019 Protein-Losing Enteropathy 45 0.038
910
CRD118 Cardiovascular Cancer 41 0.038
911
ACT088 Acute Insulin Response 41 0.038
912
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 0.038
913
CRN027 Corneal Neovascularization 47 0.037
914
P ADL017 Adult T-Cell Leukemia 56 0.036
915
NRM004 Neuroma 51 0.036
916
TRT001 Teratocarcinoma 45 0.036
917
FBR019 Fibromatosis 41 0.036
918
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.036
919
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.036
920
GRN037 Granulomatosis with Polyangiitis 65 0.036
921
c CHL140 Chilblain Lupus 1 58 0.036
922
SPT004 Septic Arthritis 58 0.036
923
MYL001 Myelitis 51 0.036
924
ALL009 Allergic Conjunctivitis 50 0.036
925
SPN369 Spinal Disease 43 0.036
926
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.036
927
FNT004 Fainting 30 0.036
928
c FNC027 Fanconi Anemia, Complementation Group a 81 0.035
929
GST019 Gastrointestinal Stromal Tumor 78 0.035
930
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.035
931
P LKD001 Leukodystrophy 59 0.035
932
P ANP001 Anaplastic Large Cell Lymphoma 58 0.035
933
P BNC003 Bone Cancer 58 0.035
934
HMT008 Hematuria, Benign Familial 56 0.035
935
GST037 Gastroparesis 54 0.035
936
c HRD202 Hereditary Lymphedema I 50 0.035
937
ECT026 Ectopic Pregnancy 50 0.035
938
P MYT002 Myotonic Dystrophy 49 0.035
939
BLD053 Blood Platelet Disease 49 0.035
940
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.035
941
ANC002 Anca-Associated Vasculitis 41 0.035
942
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.035
943
c SCH080 Schizophrenia 3 32 0.035
944
c PRS080 Prostate Cancer, Hereditary, 7 22 0.035
945
P PTT006 Pituitary Adenoma 55 0.034
946
AVD001 Avoidant Personality Disorder 51 0.034
947
MLT113 Multicentric Castleman Disease 47 0.034
948
SKN020 Skin Papilloma 39 0.034
949
RCT009 Rectosigmoid Cancer 37 0.034
950
HRY003 Hairy Cell Leukemia 55 0.034
951
HYL004 Hyaline Fibromatosis Syndrome 67 0.033
952
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.033
953
CHR001 Churg-Strauss Syndrome 61 0.033
954
DNN002 Donnai-Barrow Syndrome 56 0.033
955
MCR088 Microscopic Polyangiitis 51 0.033
956
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.033
957
P MMB011 Membranous Nephropathy 50 0.033
958
CHL122 Cholesteatoma of Middle Ear 50 0.033
959
ADR038 Adermatoglyphia 49 0.033
960
ERY004 Erysipelas 49 0.033
961
GYN001 Gynecomastia 49 0.033
962
c DSB006 Desbuquois Dysplasia 1 48 0.033
963
CLS016 Clostridium Difficile Colitis 48 0.033
964
FBR009 Fibrous Dysplasia 48 0.033
965
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.033
966
EXT033 Extrapulmonary Tuberculosis 46 0.033
967
CRB016 Carbuncle 43 0.033
968
PRM013 Premature Menopause 41 0.033
969
P HYP263 Hypersomnia 41 0.033
970
HYP001 Hypochromic Microcytic Anemia 38 0.033
971
INF021 Infant Gynecomastia 31 0.033
972
c ALL027 Allergic Bronchopulmonary Aspergillosis, Familial 30 0.033
973
PRN035 Perniosis 28 0.033
974
PRX085 Preaxial Hallucal Polydactyly 28 0.033
975
ARG004 Argyria 27 0.033
976
c RNG015 Ring Chromosome 2 26 0.033
977
ACT162 Acute Sensory Ataxic Neuropathy 26 0.033
978
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.033
979
c BSL011 Basal Cell Carcinoma, Multiple 25 0.033
980
ALL012 Allergic Angiitis 24 0.033
981
c HYP311 Hyperparathyroidism 3 23 0.033
982
GLS013 Glossodynia 18 0.033
983
P DNT020 Dent Disease 1 62 0.032
984
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 51 0.032
985
NDL001 Nodular Malignant Melanoma 44 0.032
986
P FML187 Familial Hypertension 37 0.032
987
SMT004 Smith-Lemli-Opitz Syndrome 70 0.032
988
RTN017 Retinal Detachment 61 0.032
989
P TXP001 Toxoplasmosis 60 0.032
990
SLP001 Sleeping Sickness 54 0.032
991
HYP741 Hyperparathyroidism 2 with Jaw Tumors 53 0.032
992
c BRS049 Breast Carcinoma in Situ 51 0.032
993
P TMP001 Temporal Lobe Epilepsy 50 0.032
994
LPR001 Lepromatous Leprosy 50 0.032
995
P IGN003 Iga Nephropathy 1 49 0.032
996
MCN001 Mucinous Adenocarcinoma 49 0.032
997
HYP006 Hypertensive Heart Disease 49 0.032
998
IMP004 Impetigo 49 0.032
999
INT067 Interstitial Nephritis 48 0.032
1000
LPD004 Lipoid Nephrosis 46 0.032
1001
CHD004 Chudley-Mccullough Syndrome 46 0.032
1002
OBS003 Obsessive-Compulsive Personality Disorder 46 0.032
1003
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.032
1004
P END084 Endocrine System Disease 45 0.032
1006
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.032
1007
CLN044 Colon Adenoma 44 0.032
1008
P HYP121 Hypoalphalipoproteinemia 43 0.032
1009
MCR019 Microglandular Adenosis 43 0.032
1010
P HRD018 Hair Disease 43 0.032
1011
ADS004 Aids Dementia Complex 40 0.032
1012
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.032
1013
VSD001 Vas Deferens, Congenital Bilateral Aplasia of, X-Linked 28 0.032
1014
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.032
1015
FCL009 Focal Dermal Hypoplasia 66 0.030
1016
P GLC113 Galactosemia I 64 0.030
1017
P LMY004 Leiomyosarcoma 63 0.030
1018
CTN007 Cutaneous Leishmaniasis 62 0.030
1019
SZR001 Sezary's Disease 60 0.030
1020
c SVR003 Severe Congenital Neutropenia 59 0.030
1021
LYM021 Lymphadenitis 57 0.030
1022
EPD002 Epidermolytic Hyperkeratosis 56 0.030
1023
PLS016 Plasma Cell Leukemia 53 0.030
1024
OCL006 Ocular Hypertension 53 0.030
1025
STT002 Status Asthmaticus 50 0.030
1026
P ART018 Aortic Valve Insufficiency 49 0.030
1027
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.030
1028
MSN004 Mesenchymal Cell Neoplasm 41 0.030
1029
JWD001 Jawad Syndrome 40 0.030
1030
MLN079 Melanoma in Congenital Melanocytic Nevus 39 0.030
1031
THR017 Thoracoabdominal Syndrome 39 0.030
1032
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.030
1033
TYM001 Tympanosclerosis 38 0.030
1034
PRR013 Prurigo Nodularis 36 0.030
1035
PDT025 Pediatric Multiple Sclerosis 36 0.030
1036
P MDL008 Medullary Cystic Kidney Disease 1 34 0.030
1037
c CNG562 Congenital Hypogonadotropic Hypogonadism 34 0.030
1038
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 30 0.030
1039
P VRT013 Vertigo, Benign Recurrent 29 0.030
1040
CLN002 Colon Mucinous Adenocarcinoma 28 0.030
1041
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.030
1043
c VNW005 Von Willebrand Disease, Type 1 48 0.029
1044
LNT001 Linitis Plastica 32 0.029
1045
ARG006 Aregenerative Anemia 27 0.029
1046
P KRB001 Krabbe Disease 69 0.028
1047
P ART005 Arteriovenous Malformation 65 0.028
1048
P LPS002 Liposarcoma 65 0.028
1049
DSM004 Desmoid Tumor 64 0.028
1050
c OPT053 Optic Atrophy 1 63 0.028
1051
BLM002 Bulimia Nervosa 57 0.028
1052
NRL004 Neuroleptic Malignant Syndrome 56 0.028
1053
INT030 Intracranial Aneurysm 56 0.028
1054
P SLM003 Salmonellosis 55 0.028
1055
OVR059 Ovary Adenocarcinoma 53 0.028
1056
MRG003 Marginal Zone B-Cell Lymphoma 52 0.028
1057
ACT200 Acute Monoblastic Leukemia 52 0.028
1058
c INF023 Inflammatory Breast Carcinoma 50 0.028
1059
ADR016 Adrenal Cortical Carcinoma 48 0.028
1060
SPH010 Sphingolipidosis 47 0.028
1061
GNR003 Generalized Atherosclerosis 46 0.028
1062
IMP006 Impulse Control Disorder 45 0.028
1063
RTC009 Reticulum Cell Sarcoma 43 0.028
1064
c CNG023 Congenital Fibrosarcoma 42 0.028
1065
P 8P1002 8p11 Myeloproliferative Syndrome 39 0.028
1066
ADR004 Adrenal Cortical Adenocarcinoma 39 0.028
1067
TTH008 Tooth Resorption 37 0.028
1068
SML011 Smoldering Myeloma 33 0.028
1069
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.028
1070
BRT055 Breath-Holding Spells 30 0.028
1071
LYM007 Lymphangioleiomyomatosis 69 0.026
1072
STH001 Saethre-Chotzen Syndrome 67 0.026
1073
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.026
1074
THY022 Thymic Carcinoma 57 0.026
1075
c DMN023