Search results for "vitamin d"

1241 hits were found for "vitamin d"

# Family MCID Name MIFTS Score
1
VTM027 Vitamin D-Dependent Rickets, Type 2a 53 13.191
2
RCK004 Rickets 65 10.792
3
HYP609 Hypophosphatemic Rickets, X-Linked Dominant 60 9.552
4
c VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 33 8.772
5
VTM029 Vitamin D Hydroxylation-Deficient Rickets, Type 1b 24 8.240
6
HYP636 Hypocalcemic Vitamin D-Dependent Rickets 28 6.797
7
VTM030 Vitamin D-Dependent Rickets, Type 2b, with Normal Vitamin D Receptor 15 5.578
8
HRD086 Hereditary Hypophosphatemic Rickets 44 4.708
9
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 48 3.887
10
EPD026 Epidermal Nevus Vitamin D Resistant Rickets 4 2.792
11
c HYP788 Hypophosphatemic Rickets, Autosomal Recessive, 1 21 2.765
12
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 41 2.749
13
IDP085 Idiopathic Infantile Hypercalcemia 30 2.749
14
OST002 Osteoporosis 74 0.451
15
HYP069 Hyperparathyroidism 59 0.445
16
DBT009 Diabetes Mellitus 67 0.403
17
KDN018 Kidney Disease 68 0.376
18
BND020 Bone Disease 61 0.356
19
PRS040 Prostate Cancer 94 0.333
20
BRS047 Breast Cancer 100 0.314
21
DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.313
22
MLT020 Multiple Sclerosis 75 0.295
23
SCN001 Secondary Hyperparathyroidism of Renal Origin 52 0.280
24
AST005 Asthma 82 0.279
25
LVR013 Liver Disease 75 0.271
26
OST011 Osteomalacia 52 0.271
27
ART022 Arthritis 77 0.270
28
CLR023 Colorectal Cancer 99 0.265
29
BNF002 Bone Fracture 46 0.262
30
c PRM005 Primary Hyperparathyroidism 60 0.261
31
HPT021 Hepatitis 75 0.257
32
ATM095 Autoimmune Disease 65 0.256
33
c CHR089 Chronic Kidney Failure 73 0.250
34
URN009 Urinary System Disease 49 0.249
35
PLY011 Polycystic Ovary Syndrome 64 0.246
36
INF037 Inflammatory Bowel Disease 54 0.236
37
HRT032 Heart Disease 73 0.235
38
LPS004 Lupus Erythematosus 69 0.226
39
LNG099 Lung Disease 67 0.225
40
RHM011 Rheumatoid Arthritis 82 0.217
41
HYP060 Hyperinsulinism 55 0.217
42
c HPT001 Hepatitis C 70 0.214
43
ALP008 Alopecia 55 0.214
44
AGN016 Aging 62 0.209
45
c SYS001 Systemic Lupus Erythematosus 88 0.205
46
VRL011 Viral Infectious Disease 72 0.202
47
DRM006 Dermatitis 68 0.202
48
DPR016 Depression 73 0.197
49
PRD008 Periodontitis 66 0.197
50
SKN016 Skin Disease 64 0.197
51
GST033 Gestational Diabetes 62 0.197
52
INT068 Intestinal Disease 60 0.197
53
c PRC016 Pre-Eclampsia 60 0.197
54
c PLY105 Polycystic Ovary Syndrome 1 45 0.197
55
SKN027 Skin Conditions 46 0.195
56
INF038 Influenza 76 0.194
57
PSR002 Psoriasis 66 0.190
58
CRH001 Crohn\'s Disease 77 0.188
59
GST050 Gastrointestinal System Disease 63 0.188
60
PLM001 Pulmonary Tuberculosis 73 0.186
61
MLN008 Melanoma 63 0.186
62
CNG034 Congestive Heart Failure 68 0.185
63
IMM136 Immune System Disease 49 0.185
64
DRM053 Dermatitis, Atopic 71 0.181
65
ADN018 Adenoma 64 0.181
66
FTT001 Fatty Liver Disease 66 0.179
67
ACQ007 Acquired Immunodeficiency Syndrome 63 0.175
68
PRT030 Parathyroid Gland Disease 47 0.175
69
NPH009 Nephrolithiasis 57 0.173
70
OST012 Osteoarthritis 81 0.171
71
THY032 Thyroiditis 53 0.171
72
RSP006 Respiratory System Disease 56 0.167
73
BRN038 Bronchial Disease 55 0.165
74
DBT085 Diabetes Mellitus, Insulin-Dependent 72 0.163
75
MYP004 Myopathy 63 0.163
76
NNL004 Nonalcoholic Fatty Liver Disease 55 0.163
77
CYS001 Cystic Fibrosis 83 0.161
78
c HPT073 Hepatitis C Virus 67 0.161
79
BRS051 Breast Disease 63 0.161
80
MNT002 Mental Depression 62 0.159
81
HYP017 Hypophosphatemia 48 0.159
82
LKM002 Leukemia 72 0.157
83
CLT003 Colitis 64 0.157
84
RHM027 Rheumatic Disease 61 0.157
85
INF032 Infertility 58 0.157
86
VSC007 Vascular Disease 68 0.154
87
ECL001 Eclampsia 57 0.154
88
CNN005 Connective Tissue Disease 64 0.152
89
CLR108 Colorectal Adenoma 61 0.152
90
BCT022 Bacterial Infectious Disease 60 0.152
91
GLC003 Glucose Intolerance 58 0.152
92
MYC007 Myocardial Infarction 77 0.150
93
c HPT003 Hepatitis a 67 0.150
94
OST097 Osteoporotic Fracture 44 0.150
95
OVR042 Ovarian Cancer 83 0.148
96
ADN016 Adenocarcinoma 70 0.145
97
PSY004 Psychotic Disorder 72 0.143
98
PNM007 Pneumonia 71 0.143
99
LYM118 Lymphoma 70 0.143
100
LNG032 Lung Cancer 99 0.141
101
ULC004 Ulcerative Colitis 80 0.141
102
ISC006 Ischemic Heart Disease 67 0.141
103
NRP001 Neuropathy 62 0.141
104
GST045 Gastroenteritis 62 0.141
105
END030 End Stage Renal Failure 59 0.141
106
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.138
107
RNL011 Renal Osteodystrophy 49 0.138
108
SCH015 Schizophrenia 70 0.136
109
ALP009 Alopecia Areata 64 0.136
110
PRM236 Primary Biliary Cholangitis 62 0.136
111
MSC033 Muscle Disorders 50 0.136
112
PRD007 Periodontal Disease 65 0.133
113
c LRG017 Large Intestine Cancer 59 0.133
114
CLN019 Colonic Disease 57 0.133
115
PRM006 Primary Biliary Cirrhosis 53 0.133
116
c HYP057 Hypervitaminosis D 40 0.133
117
c INF071 Inflammatory Bowel Disease 1 53 0.130
118
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 62 0.128
119
GRV001 Graves\' Disease 61 0.128
120
OVR049 Ovarian Disease 58 0.128
121
SCK005 Sickle Cell Disease 57 0.128
122
c BLR024 Biliary Cirrhosis, Primary, 1 38 0.128
123
PNC035 Pancreatic Cancer 82 0.125
124
EPL164 Epilepsy 73 0.125
125
ATS364 Autism 69 0.125
126
DMY004 Demyelinating Disease 57 0.125
127
HYP024 Hypoparathyroidism 54 0.125
128
TRC086 Trichohepatoenteric Syndrome 1 51 0.125
129
MSC190 Muscular Disease 51 0.125
130
MSC004 Muscle Tissue Disease 27 0.125
131
ALZ034 Alzheimer Disease 86 0.122
132
LVR012 Liver Cirrhosis 66 0.122
133
ISC004 Ischemia 66 0.122
134
ART140 Arteries, Anomalies of 65 0.122
135
RHN004 Rhinitis 62 0.122
136
c MCR113 Microvascular Complications of Diabetes 3 57 0.122
137
FDL002 Food Allergy 56 0.122
138
NNL002 Nonalcoholic Steatohepatitis 53 0.122
139
PSD015 Pseudohypoparathyroidism 50 0.122
140
c MCR120 Microvascular Complications of Diabetes 7 44 0.122
141
c MCR130 Microvascular Complications of Diabetes 6 43 0.122
142
c MCR133 Microvascular Complications of Diabetes 4 43 0.122
143
CRN018 Coronary Artery Anomaly 75 0.120
144
MDD011 Mood Disorder 62 0.120
145
EXN002 Exanthem 56 0.120
146
c HPT016 Hepatitis B 70 0.117
147
ART023 Arthropathy 64 0.117
148
HYP066 Hyperglycemia 64 0.117
149
JNT002 Joint Disorders 58 0.117
150
OVR046 Ovarian Cyst 53 0.117
151
NPH003 Nephrocalcinosis 51 0.117
152
PRD004 Prediabetes Syndrome 48 0.117
153
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 47 0.117
154
c BDY007 Body Mass Index Quantitative Trait Locus 1 47 0.117
155
CLL015 Collagen Disease 46 0.117
156
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 44 0.117
157
c PRC031 Preeclampsia/eclampsia 1 34 0.117
158
URT039 Urticaria 61 0.114
159
ART021 Arteriosclerosis 57 0.114
160
SPS003 Spastic Diplegia 54 0.114
161
BNR002 Bone Resorption Disease 53 0.114
162
IRR002 Irritable Bowel Syndrome 50 0.114
163
c ATM017 Autoimmune Disease of the Nervous System 49 0.114
164
CLC006 Calcinosis 48 0.114
165
ALL003 Allergic Rhinitis 70 0.111
166
PRP019 Peripheral Nervous System Disease 62 0.111
167
NPH012 Nephrotic Syndrome 59 0.111
168
PRS129 Prostatic Hyperplasia, Benign 51 0.111
169
PRS042 Prostate Disease 42 0.111
170
ANX010 Anxiety 72 0.108
171
NRV007 Nervous System Disease 69 0.108
172
LPD008 Lipid Metabolism Disorder 64 0.108
173
SKN019 Skin Melanoma 63 0.108
174
BRN002 Bronchiolitis 62 0.108
175
RLP002 Relapsing-Remitting Multiple Sclerosis 58 0.108
176
DRR001 Diarrhea 57 0.108
177
HYP080 Hypogonadism 52 0.108
178
RCT017 Rectal Disease 40 0.108
179
c TRC078 Trichohepatoenteric Syndrome 2 22 0.108
180
THL005 Thalassemia 65 0.104
181
END044 Endometriosis 65 0.104
182
HYP086 Hypothyroidism 63 0.104
183
LYM031 Lymphocytic Leukemia 61 0.104
184
DMN002 Dementia 68 0.101
185
ATT013 Attention Deficit-Hyperactivity Disorder 67 0.101
186
SPN186 Spinal Cord Injury 65 0.101
187
RNL114 Renal Cell Carcinoma, Nonpapillary 62 0.101
188
c CRN300 Coronary Heart Disease 1 59 0.101
189
c PRD040 Periodontitis, Chronic 59 0.101
190
NRM005 Neuromuscular Disease 58 0.101
191
PNC034 Pancreas Disease 56 0.101
192
MSC003 Muscular Atrophy 55 0.101
193
URM002 Uremia 52 0.101
194
DNT012 Dental Caries 51 0.101
195
OVR063 Overnutrition 48 0.101
196
HPT023 Hepatocellular Carcinoma 98 0.098
197
c SPN225 Spondyloarthropathy 1 75 0.098
198
FML018 Familial Mediterranean Fever 72 0.098
199
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 68 0.098
200
FBR047 Fibromyalgia 61 0.098
201
HDC001 Headache 61 0.098
202
HMT018 Hematopoietic Stem Cell Transplantation 58 0.098
203
SCL018 Scoliosis 58 0.098
204
DGN001 Degenerative Disc Disease 52 0.098
205
MMM006 Mammographic Density 47 0.098
206
ATM052 Autoimmune Disease 1 46 0.098
207
GLC086 Glucocorticoid-Induced Osteoporosis 46 0.098
208
TQP001 Taqi Polymorphism 30 0.098
209
CLC063 Celiac Disease 1 74 0.094
210
MYL006 Myeloid Leukemia 67 0.094
211
DFC004 Deficiency Anemia 66 0.094
212
c CNT035 Central Nervous System Disease 62 0.094
213
MTH009 Mouth Disease 61 0.094
214
MYP006 Myopia 58 0.094
215
BCT002 Bacterial Vaginosis 55 0.094
216
SPN051 Spondylitis 54 0.094
217
RNL007 Renal Tubular Acidosis 52 0.094
218
IDP070 Idiopathic Scoliosis 39 0.094
219
INS024 Insulin-Like Growth Factor I 76 0.090
220
HMN044 Human Immunodeficiency Virus Type 1 74 0.090
221
THY028 Thyroid Cancer 71 0.090
222
SLP006 Sleep Apnea 70 0.090
223
MYL005 Myelofibrosis 69 0.090
224
c ATS007 Autism Spectrum Disorder 64 0.090
225
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 63 0.090
226
LYM019 Lymphosarcoma 56 0.090
227
PST021 Postpartum Depression 55 0.090
228
RST001 Restless Legs Syndrome 54 0.090
229
HYP025 Hyperphosphatemia 49 0.090
230
ALL014 Allergic Encephalomyelitis 42 0.090
231
c HYP595 Hypertension, Essential 78 0.087
232
c SML038 Small Cell Cancer of the Lung 72 0.087
233
GRF003 Graft-Versus-Host Disease 72 0.087
234
SRC014 Sarcoma 70 0.087
235
ANR007 Anorexia Nervosa 68 0.087
236
CRB039 Cerebrovascular Disease 67 0.087
237
BRN024 Bronchitis 67 0.087
238
BRN056 Bronchopulmonary Dysplasia 60 0.087
239
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.087
240
DBT010 Diabetic Neuropathy 58 0.087
241
NRT004 Neuritis 55 0.087
242
OPT009 Optic Neuritis 53 0.087
243
THY030 Thyroid Gland Disease 43 0.087
244
c CHR579 Chiari Malformation Type Ii 42 0.087
245
VSC018 Visceral Steatosis 29 0.087
246
SCK003 Sickle Cell Anemia 72 0.083
247
c JVN010 Juvenile Rheumatoid Arthritis 72 0.083
248
PRP027 Peripheral Vascular Disease 71 0.083
249
BLD134 Bladder Cancer 70 0.083
250
OTT002 Otitis Media 68 0.083
251
HSH003 Hashimoto Thyroiditis 65 0.083
252
THR024 Thrombosis 63 0.083
253
LTR001 Lateral Sclerosis 60 0.083
254
CHL068 Cholestasis 60 0.083
255
SQM006 Squamous Cell Carcinoma 59 0.083
256
AGG001 Aggressive Periodontitis 56 0.083
257
BRN106 Burns 55 0.083
258
GRW007 Growth Hormone Deficiency 52 0.083
259
PRM020 Premenstrual Tension 51 0.083
260
PRT029 Parathyroid Adenoma 51 0.083
261
SCL057 Scoliosis, Isolated 1 42 0.083
262
HYP064 Hypogonadotropism 39 0.083
263
c LKM071 Leukemia, Chronic Lymphocytic 77 0.078
264
MCR115 Microvascular Complications of Diabetes 5 70 0.078
265
APN008 Apnea, Obstructive Sleep 68 0.078
266
LKM062 Leukemia, Acute Lymphoblastic 68 0.078
267
NVS017 Nevus, Epidermal 68 0.078
268
c SCL052 Scleroderma, Familial Progressive 68 0.078
269
c ATM011 Autoimmune Hepatitis 61 0.078
270
PGT001 Paget\'s Disease of Bone 61 0.078
271
UVT001 Uveitis 61 0.078
272
c VRL010 Viral Hepatitis 60 0.078
273
SZR006 Seizure Disorder 58 0.078
274
c GLC092 Glaucoma, Primary Open Angle 58 0.078
275
LMY002 Leiomyoma 57 0.078
276
IMP005 Impotence 57 0.078
277
c ACT075 Acute Myocardial Infarction 56 0.078
278
LMY014 Leiomyoma, Uterine 56 0.078
279
OPN001 Open-Angle Glaucoma 53 0.078
280
DBT005 Diabetes Insipidus 52 0.078
281
BNG018 Benign Paroxysmal Positional Nystagmus 39 0.078
282
NRR001 Neuroretinitis 39 0.078
283
c LKM004 Leukemia, B-Cell, Chronic 37 0.078
284
VRT013 Vertigo, Benign Recurrent 37 0.078
285
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 34 0.078
286
HML018 Homologous Wasting Disease 24 0.078
287
GST053 Gastric Cancer 79 0.074
288
DLT002 Dilated Cardiomyopathy 74 0.074
289
MNN013 Meningitis 71 0.074
290
PRT036 Peritonitis 66 0.074
291
OST003 Osteonecrosis 66 0.074
292
SNS014 Sinusitis 63 0.074
293
c ACT210 Acute Respiratory Distress Syndrome 62 0.074
294
PHR003 Pharyngitis 57 0.074
295
SLP005 Sleep Disorder 57 0.074
296
HYP076 Hyperthyroidism 56 0.074
297
RTN018 Retinal Disease 56 0.074
298
c SVR005 Severe Pre-Eclampsia 56 0.074
299
IRN001 Iron Deficiency Anemia 55 0.074
300
HMG005 Hemoglobinopathy 52 0.074
301
CTN003 Cutaneous Lupus Erythematosus 52 0.074
302
SPN041 Spinal Cord Disease 52 0.074
303
SPR004 Supravalvular Aortic Stenosis 51 0.074
304
IDP073 Idiopathic Hypercalciuria 49 0.074
305
NSD001 Nose Disease 47 0.074
306
URN022 Urinary Tract Infections, Recurrent 28 0.074
307
c AMY091 Amyotrophic Lateral Sclerosis 1 91 0.069
308
c LKM061 Leukemia, Acute Myeloid 83 0.069
309
BRN028 Brain Cancer 74 0.069
310
RSP003 Respiratory Failure 72 0.069
311
CRP001 Carpal Tunnel Syndrome 71 0.069
312
SYS005 Systemic Scleroderma 69 0.069
313
TRN020 Turner Syndrome 69 0.069
314
ASP006 Aspergillosis 66 0.069
315
THR014 Thrombocytopenia 64 0.069
316
MYS005 Myositis 64 0.069
317
PNC044 Pancreatitis 63 0.069
318
INT146 Intervertebral Disc Disease 62 0.069
319
IGR001 Ige Responsiveness, Atopic 62 0.069
320
HYP266 Hypoxia 62 0.069
321
BPL003 Bipolar Disorder 60 0.069
322
ANT006 Antiphospholipid Syndrome 60 0.069
323
IRN002 Iron Metabolism Disease 60 0.069
324
NTR005 Nutritional Deficiency Disease 58 0.069
325
CNS004 Constipation 57 0.069
326
c ACT068 Acute Cystitis 56 0.069
327
CMR001 Camurati-Engelmann Disease 56 0.069
328
DRY001 Dry Eye Syndrome 53 0.069
329
GNR004 Generalized Anxiety Disorder 53 0.069
330
c PSR017 Psoriasis 2 52 0.069
331
FNC004 Fanconi Syndrome 50 0.069
332
FSH001 Fish-Eye Disease 50 0.069
333
c PSR028 Psoriasis 7 46 0.069
334
c PSR032 Psoriasis 11 46 0.069
335
MNN028 Mononeuropathy of the Median Nerve, Mild 45 0.069
336
c PSR018 Psoriasis 13 45 0.069
337
OVR094 Ovarian Epithelial Cancer 39 0.069
338
PRS063 Paresthesia 39 0.069
339
AMN006 Aminoaciduria 38 0.069
340
ATX010 Ataxia Neuropathy Spectrum 32 0.069
341
LRG015 Large Intestine Adenoma 10 0.069
343
NRF023 Neurofibromatosis, Type Ii 75 0.064
344
GLB002 Glioblastoma 74 0.064
345
c BTT014 Beta-Thalassemia 71 0.064
346
OBS002 Obsessive-Compulsive Disorder 69 0.064
347
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.064
348
ATH013 Atherosclerosis Susceptibility 66 0.064
349
c CHR417 Chronic Graft Versus Host Disease 66 0.064
350
c BSL007 Basal Cell Carcinoma 65 0.064
351
GCH001 Gaucher\'s Disease 64 0.064
352
CRD119 Cardiac Arrest 64 0.064
353
CNJ013 Conjunctivitis 63 0.064
354
c ACT074 Acute Lymphocytic Leukemia 63 0.064
355
GNG013 Gingivitis 62 0.064
356
ADL010 Adult Respiratory Distress Syndrome 62 0.064
357
ANG054 Angina Pectoris 62 0.064
358
GT001 Gout 60 0.064
359
HYP035 Hypophosphatasia 59 0.064
360
KDN017 Kidney Cancer 59 0.064
361
IGG001 Iga Glomerulonephritis 58 0.064
362
NRN004 Neuroendocrine Tumor 56 0.064
363
NWB001 Newborn Respiratory Distress Syndrome 55 0.064
364
VSC002 Vascular Dementia 55 0.064
365
HYP726 Hypercalcemia, Infantile, 1 55 0.064
366
OCL006 Ocular Hypertension 55 0.064
367
BRN071 Brain Injury 54 0.064
368
KRT009 Keratosis 54 0.064
369
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.064
370
SHR001 Short Bowel Syndrome 53 0.064
371
STM007 Stomatitis 52 0.064
372
c ACT071 Acute Kidney Failure 51 0.064
373
HYP043 Hyperandrogenism 50 0.064
374
PST011 Pustulosis of Palm and Sole 49 0.064
375
SXL003 Sexual Disorder 49 0.064
376
LCT002 Lactose Intolerance 48 0.064
377
OST115 Osteonecrosis of the Jaw 44 0.064
378
RSP007 Respiratory Distress Syndrome, Infant 35 0.064
379
c PSD104 Pseudohypoparathyroidism, Type Ii 33 0.064
380
ART153 Arthrochalasia Ehlers-Danlos Syndrome 24 0.064
381
MYL069 Myeloma, Multiple 85 0.058
382
SRC025 Sarcoidosis 1 76 0.058
383
LYM133 Lymphoma, Hodgkin, Classic 75 0.058
384
MYS003 Myasthenia Gravis 74 0.058
385
NRB001 Neuroblastoma 73 0.058
386
LYM143 Lymphoma, Non-Hodgkin, Familial 73 0.058
387
MYC006 Mycosis Fungoides 73 0.058
388
RTN024 Retinoblastoma 72 0.058
389
CRB037 Cerebral Palsy 71 0.058
390
FLL037 Follicular Lymphoma 71 0.058
391
ART016 Aortic Aneurysm 70 0.058
392
BRT054 Brittle Bone Disorder 70 0.058
393
BSL036 Basal Cell Nevus Syndrome 69 0.058
394
PSR001 Psoriatic Arthritis 67 0.058
395
CHR066 Chronic Fatigue Syndrome 67 0.058
396
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 67 0.058
397
NRM001 Neuromyelitis Optica 66 0.058
398
MJR001 Major Depressive Disorder 66 0.058
399
ACN002 Acanthosis Nigricans 66 0.058
400
THR100 Thrombocytopenic Purpura, Autoimmune 65 0.058
401
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.058
402
APH001 Aphthous Stomatitis 64 0.058
403
DNG005 Dengue Virus 64 0.058
404
HYP056 Hypoglycemia 63 0.058
405
GLB015 Glioblastoma Multiforme 63 0.058
406
OST001 Osteopetrosis 62 0.058
407
CRB011 Cerebrotendinous Xanthomatosis 62 0.058
408
MRB003 Morbid Obesity 61 0.058
409
GST044 Gastritis 60 0.058
410
OPT006 Optic Nerve Disease 60 0.058
411
CLL003 Cellulitis 59 0.058
412
ORL011 Oral Cancer 59 0.058
413
HMR012 Hemorrhagic Fever 57 0.058
414
CLN015 Colon Adenocarcinoma 57 0.058
415
ALL008 Allergic Bronchopulmonary Aspergillosis 56 0.058
416
BRN022 Bronchiectasis 56 0.058
417
ICH004 Ichthyosis 56 0.058
418
NRV006 Nervous System Cancer 56 0.058
419
THR013 Thoracic Outlet Syndrome 55 0.058
420
THR015 Thrombophilia 55 0.058
421
PRP080 Peripheral Artery Disease 54 0.058
422
ACT008 Actinic Keratosis 54 0.058
423
CLC001 Calciphylaxis 53 0.058
424
PRV006 Pervasive Developmental Disorder 53 0.058
425
PRC019 Precocious Puberty 52 0.058
426
CRN030 Coronary Stenosis 51 0.058
427
MLK006 Milk Allergy 48 0.058
428
PRN021 Paranasal Sinus Disease 47 0.058
429
c PNC128 Pain - Chronic 46 0.058
430
LYM067 Lymphoid Leukemia 43 0.058
431
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.058
432
c MYS011 Myasthenia Gravis Congenital 36 0.058
433
CRN031 Cranial Nerve Disease 36 0.058
434
FCL044 Fecal Incontinence 36 0.058
435
c NRM008 Neuromyelitis Optica Spectrum Disorder 33 0.058
436
HRW001 Hair Whorl 23 0.058
437
HRP008 Herpes Simiae 4 0.058
438
STR067 Stroke, Ischemic 85 0.052
439
ESP021 Esophageal Cancer 83 0.052
440
KPS004 Kaposi Sarcoma 76 0.052
441
ACR007 Acromegaly 71 0.052
442
MYL009 Myelodysplastic Syndrome 70 0.052
443
LPR021 Leprosy 3 70 0.052
444
c HMP029 Hemophilia a 70 0.052
445
BRR014 Barrett Esophagus 70 0.052
446
ATR011 Atrial Fibrillation 69 0.052
447
c PRM196 Premature Ovarian Failure 1 69 0.052
448
END057 Endometrial Cancer 68 0.052
449
HYP802 Hypocalcemia, Autosomal Dominant 1 67 0.052
450
MSC005 Muscular Dystrophy 66 0.052
451
BRC012 Brucellosis 66 0.052
452
c LKM056 Leukemia, Chronic Lymphocytic 2 66 0.052
453
OST159 Osteogenic Sarcoma 66 0.052
454
BCL006 B-Cell Lymphomas 65 0.052
455
ANR048 Aniridia 1 65 0.052
456
HLC007 Helicobacter Pylori Infection 65 0.052
457
HYP020 Hyperprolactinemia 64 0.052
458
NRF007 Neurofibroma 64 0.052
459
FLL027 Fallopian Tube Carcinoma 63 0.052
460
WLL001 Williams-Beuren Syndrome 63 0.052
461
c CHL119 Cholangitis, Primary Sclerosing 63 0.052
462
CMM005 Common Cold 63 0.052
463
HRP004 Herpes Zoster 61 0.052
464
SPN027 Spinal Stenosis 61 0.052
465
HMP007 Hemophilia 61 0.052
466
TNS005 Tonsillitis 61 0.052
467
RSC001 Rosacea 60 0.052
468
CYT008 Cytomegalovirus Infection 60 0.052
469
c INS002 in Situ Carcinoma 59 0.052
470
MTR014 Motor Neuron Disease 59 0.052
471
ANG015 Angioedema 57 0.052
472
PRN019 Perinatal Necrotizing Enterocolitis 57 0.052
473
VGN023 Vaginitis 57 0.052
474
GLM045 Glioma 55 0.052
475
CYS010 Cystinosis 55 0.052
476
PMP001 Pemphigus 55 0.052
477
TRM003 Tremor 55 0.052
478
SCH012 Schizoaffective Disorder 54 0.052
479
WVR001 Weaver Syndrome 54 0.052
480
RTN022 Retinal Vein Occlusion 54 0.052
481
HRT012 Heart Valve Disease 54 0.052
482
KRT006 Keratoconjunctivitis 54 0.052
483
ENT011 Enterocolitis 53 0.052
484
PRT038 Protein-Energy Malnutrition 52 0.052
485
MLN007 Male Infertility 52 0.052
486
DFF036 Differentiated Thyroid Carcinoma 51 0.052
487
OBS082 Obstructive Nephropathy 51 0.052
488
INT303 Intracranial Hypertension, Idiopathic 50 0.052
489
IDP024 Idiopathic Inflammatory Myopathy 50 0.052
490
c CNT016 Central Retinal Vein Occlusion 50 0.052
491
PRS021 Prostatic Adenoma 49 0.052
492
c MTR002 Mitral Valve Insufficiency 48 0.052
493
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 46 0.052
494
FTL021 Fetal Macrosomia 46 0.052
495
GNG011 Gingival Disease 46 0.052
496
HYP087 Hypotrichosis 46 0.052
497
SYS003 Systolic Heart Failure 46 0.052
498
CRV045 Cervical Intraepithelial Neoplasia 45 0.052
499
RFR003 Refractive Error 44 0.052
500
BSL008 Basal Ganglia Disease 43 0.052
501
SPN369 Spinal Disease 42 0.052
502
HYP784 Hypogonadism, Male 42 0.052
503
CLN044 Colon Adenoma 39 0.052
504
MYF001 Myofibroma 39 0.052
505
CHR084 Chromosomal Disease 34 0.052
506
ACT232 Acute Necrotizing Encephalopathy 33 0.052
507
PHT003 Phototoxic Dermatitis 32 0.052
508
HNS001 Hansen\'s Disease 32 0.052
509
UND007 Undifferentiated Connective Tissue Disease 30 0.052
510
RNL115 Renal Tubular Acidosis, Proximal 29 0.052
511
DRM009 Dermatomycosis 29 0.052
512
LYM053 Lymphomatous Thyroiditis 25 0.052
513
BLD137 Blood Group--Ahonen 24 0.052
514
UTR054 Uterine Hypoplasia 24 0.052
515
MLR004 Malaria 85 0.045
516
NRL016 Neural Tube Defects 79 0.045
517
LNG064 Lung Cancer Susceptibility 3 79 0.045
518
BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.045
519
PRK057 Parkinson Disease, Late-Onset 76 0.045
520
APL001 Aplastic Anemia 74 0.045
521
FML011 Familial Adenomatous Polyposis 72 0.045
522
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.045
523
c MGR028 Migraine with or Without Aura 1 69 0.045
524
c NRF024 Neurofibromatosis, Type I 68 0.045
525
PNC033 Pancreas Adenocarcinoma 66 0.045
526
MSC157 Muscular Dystrophy, Duchenne Type 66 0.045
527
VSC011 Vasculitis 66 0.045
528
DNG002 Dengue Hemorrhagic Fever 65 0.045
529
TTN003 Tetanus 65 0.045
530
GST092 Gastroesophageal Reflux 65 0.045
531
c ART138 Aortic Aneurysm, Familial Abdominal, 1 65 0.045
532
PLY014 Polycystic Kidney Disease 63 0.045
533
GLM040 Glioma Susceptibility 1 62 0.045
534
ESP024 Esophagitis 62 0.045
535
TRN018 Transitional Cell Carcinoma 62 0.045
536
c ACT073 Acute Leukemia 61 0.045
537
c ACT027 Acute Pancreatitis 61 0.045
538
CRH005 Crohn\'s Colitis 61 0.045
539
BRN012 Bronchiolitis Obliterans 60 0.045
540
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.045
541
c PRT132 Protoporphyria, Erythropoietic, 1 60 0.045
542
INT099 Intrahepatic Cholestasis of Pregnancy 60 0.045
543
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.045
544
c BCT007 Bacterial Meningitis 58 0.045
545
BRN004 Brain Edema 58 0.045
546
LCH002 Lichen Planus 58 0.045
547
PLM010 Pulmonary Edema 58 0.045
548
PMP005 Pemphigus Vulgaris 58 0.045
549
GST049 Gastrointestinal System Cancer 58 0.045
550
HYP730 Hypogonadotropic Hypogonadism 58 0.045
551
c ACT135 Acute Graft Versus Host Disease 57 0.045
552
c OST164 Osteoporosis, Juvenile 57 0.045
553
DBT062 Diabetic Foot Ulcers 57 0.045
554
DCT002 Ductal Carcinoma in Situ 57 0.045
555
SFT003 Soft Tissue Sarcoma 56 0.045
556
PRS047 Prostatitis 56 0.045
557
HMR003 Hemorrhagic Disease 56 0.045
558
c BCT013 Bacterial Pneumonia 55 0.045
559
PPL022 Papilloma 55 0.045
560
PTT009 Pituitary Gland Disease 55 0.045
561
TBR011 Tuberculous Meningitis 55 0.045
562
c PYR010 Peyronie\'s Disease 54 0.045
563
c ANT034 Anterior Uveitis 54 0.045
564
CHR005 Chorioamnionitis 54 0.045
565
ALB001 Albright\'s Hereditary Osteodystrophy 53 0.045
566
PNM001 Pneumocystosis 53 0.045
567
ECT026 Ectopic Pregnancy 53 0.045
568
c PSD066 Pseudohypoparathyroidism, Type Ib 53 0.045
569
BRT004 Bartter Disease 53 0.045
570
ALC009 Alcoholic Liver Cirrhosis 53 0.045
571
GTR002 Goiter 53 0.045
572
c CNT075 Central Precocious Puberty 53 0.045
573
WDH003 Woodhouse-Sakati Syndrome 52 0.045
574
EST001 Estrogen-Receptor Positive Breast Cancer 52 0.045
575
CYS036 Cystinosis, Nephropathic 52 0.045
576
HMS001 Hemosiderosis 52 0.045
577
CHL066 Cholangitis 51 0.045
578
ORL013 Oral Lichen Planus 51 0.045
579
CHL061 Childhood Leukemia 51 0.045
580
LPD004 Lipoid Nephrosis 51 0.045
581
RNL077 Renal Fibrosis 50 0.045
582
TTH006 Tooth Disease 49 0.045
583
CHR074 Choriocarcinoma 49 0.045
584
ART084 Arteriovenous Fistula 48 0.045
585
FML068 Familial Hypocalciuric Hypercalcemia 48 0.045
586
MLT006 Multidrug-Resistant Tuberculosis 48 0.045
587
INT007 Intermediate Coronary Syndrome 47 0.045
588
PYR039 Peyronie Disease 47 0.045
589
CHC001 Chickenpox 47 0.045
590
HYP085 Hypothalamic Disease 47 0.045
591
PNN001 Panniculitis 47 0.045
592
HRD018 Hair Disease 46 0.045
593
PLY012 Polyhydramnios 46 0.045
594
STT002 Status Asthmaticus 46 0.045
595
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.045
596
CRN024 Corneal Disease 44 0.045
597
CNJ012 Conjunctival Disease 44 0.045
598
OST004 Osteitis Fibrosa 42 0.045
599
c BDY019 Body Mass Index Quantitative Trait Locus 18 42 0.045
600
c RTN162 Retinitis Pigmentosa 2 42 0.045
601
VGN020 Vaginal Disease 42 0.045
602
c BDY020 Body Mass Index Quantitative Trait Locus 19 41 0.045
603
AND014 Androgenic Alopecia 41 0.045
604
c CRN278 Craniosynostosis 1 41 0.045
605
c PMP006 Pemphigus Vulgaris, Familial 41 0.045
606
MYF002 Myofascial Pain Syndrome 41 0.045
607
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.045
608
EXC002 Exocrine Pancreatic Insufficiency 40 0.045
609
c BDY011 Body Mass Index Quantitative Trait Locus 10 40 0.045
610
HYP070 Hyperpituitarism 38 0.045
611
c BSL011 Basal Cell Carcinoma, Multiple 37 0.045
612
DGS002 Degos \'en Cocarde\' Erythrokeratoderma 36 0.045
613
HYD003 Hydrarthrosis 34 0.045
614
SLT009 Solitary Bone Cyst 34 0.045
615
PNL013 Penile Disease 33 0.045
616
STT009 Sutton Disease 2 32 0.045
617
FXF002 Fox-Fordyce Disease 30 0.045
618
c PRS080 Prostate Cancer, Hereditary, 7 28 0.045
619
PRX010 Paroxysmal Ventricular Fibrillation 25 0.045
620
c BLC018 Bile Acid Synthesis Defect, Congenital, 6 21 0.045
621
GLC025 Galactorrhoea-Hyperprolactinaemia 16 0.045
622
RTT002 Rett Syndrome 84 0.037
623
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 77 0.037
624
CRV035 Cervical Cancer 76 0.037
625
c LKM063 Leukemia, Chronic Myeloid 74 0.037
626
PHN003 Phenylketonuria 73 0.037
627
ADR007 Adrenoleukodystrophy 72 0.037
628
KWS002 Kawasaki Disease 72 0.037
629
DWN001 Down Syndrome 72 0.037
630
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.037
631
SMT004 Smith-Lemli-Opitz Syndrome 69 0.037
632
ALC004 Alcohol Abuse 69 0.037
633
TMP003 Temporal Arteritis 69 0.037
634
AMY004 Amyloidosis 68 0.037
635
c JVN004 Juvenile Myelomonocytic Leukemia 68 0.037
636
GRN037 Granulomatosis with Polyangiitis 68 0.037
637
ORT004 Orthostatic Intolerance 68 0.037
638
LYM007 Lymphangioleiomyomatosis 68 0.037
639
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 67 0.037
640
ANG001 Angelman Syndrome 67 0.037
641
c HMP004 Hemophilia B 66 0.037
642
MCC012 Mccune-Albright Syndrome 66 0.037
643
c DNG003 Dengue Disease 66 0.037
644
DRM010 Dermatomyositis 66 0.037
645
DSS008 Disease of Mental Health 65 0.037
646
ART005 Arteriovenous Malformation 65 0.037
647
NSP012 Nasopharyngeal Carcinoma 65 0.037
648
CHR285 Chronic Myelomonocytic Leukemia 65 0.037
649
BLL006 Bullous Pemphigoid 65 0.037
650
OVR029 Ovarian Hyperstimulation Syndrome 65 0.037
651
ETN001 Eating Disorder 64 0.037
652
c FML346 Familial Adenomatous Polyposis 1 64 0.037
653
CHL065 Cholangiocarcinoma 64 0.037
654
MSC007 Muscle Hypertrophy 64 0.037
655
INT002 Intermittent Claudication 63 0.037
656
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.037
657
CNT047 Contact Dermatitis 63 0.037
658
c LCL006 Localized Scleroderma 63 0.037
659
HML002 Hemolytic Anemia 63 0.037
660
PLM033 Pulmonary Embolism 63 0.037
661
c CNG006 Congenital Hypothyroidism 63 0.037
662
PRD006 Prader-Willi Syndrome 63 0.037
663
PPT005 Peptic Ulcer Disease 62 0.037
664
RHM001 Rheumatic Fever 62 0.037
665
HMT002 Hematologic Cancer 62 0.037
666
MYL031 Myeloproliferative Neoplasm 62 0.037
667
ENC018 Encephalopathy 62 0.037
668
ORL007 Oral Cavity Cancer 61 0.037
669
ALL006 Allergic Asthma 61 0.037
670
KRT001 Keratoconjunctivitis Sicca 60 0.037
671
GLM007 Glomerulonephritis 60 0.037
672
NTR004 Neutropenia 60 0.037
673
TRD006 Tardive Dyskinesia 60 0.037
674
FCL005 Focal Segmental Glomerulosclerosis 60 0.037
675
HMN014 Human Immunodeficiency Virus Infectious Disease 60 0.037
676
ESP035 Esophagitis, Eosinophilic, 1 60 0.037
677
ANP001 Anaplastic Large Cell Lymphoma 60 0.037
678
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 59 0.037
679
ALL010 Allergic Contact Dermatitis 59 0.037
680
RCT018 Rectal Neoplasm 59 0.037
681
c PRM126 Primary Peritoneal Carcinoma 59 0.037
682
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.037
683
SJG008 Sjogren Syndrome 59 0.037
684
NRC002 Narcolepsy 59 0.037
685
HMR039 Hemorrhage, Intracerebral 59 0.037
686
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.037
687
BNC003 Bone Cancer 58 0.037
688
MMB011 Membranous Nephropathy 58 0.037
689
PLY041 Polymyositis 58 0.037
690
MRG003 Marginal Zone B-Cell Lymphoma 57 0.037
691
SML001 Small Cell Carcinoma 57 0.037
692
EXF001 Exfoliation Syndrome 57 0.037
693
LKD001 Leukodystrophy 57 0.037
694
c MCP004 Mucopolysaccharidosis Iv 57 0.037
695
PRP036 Peripheral T-Cell Lymphoma 57 0.037
696
KRT002 Keratomalacia 56 0.037
697
VRN004 Vernal Keratoconjunctivitis 56 0.037
698
DFF005 Diffuse Large B-Cell Lymphoma 56 0.037
699
c PSD108 Pseudohypoparathyroidism, Type Ia 56 0.037
700
EPD002 Epidermolytic Hyperkeratosis 56 0.037
701
c BRS049 Breast Carcinoma in Situ 56 0.037
702
CRY007 Cryoglobulinemia, Familial Mixed 56 0.037
703
HND002 Hand, Foot and Mouth Disease 56 0.037
704
TRM010 Traumatic Brain Injury 56 0.037
705
TCD001 Tic Disorder 55 0.037
706
CTN015 Cutaneous T Cell Lymphoma 55 0.037
707
FCT001 Factor Viii Deficiency 55 0.037
708
HYP005 Hypokalemia 55 0.037
709
CRD223 Cardiac Arrhythmia 55 0.037
710
LRY019 Laryngitis 54 0.037
711
SCL009 Sclerosing Cholangitis 54 0.037
712
TST014 Testicular Cancer 54 0.037
713
PLS025 Plasmablastic Lymphoma 54 0.037
714
ESP023 Esophageal Disease 53 0.037
715
OTS001 Otosclerosis 53 0.037
716
INT070 Intestinal Obstruction 53 0.037
717
TXC002 Toxic Encephalopathy 53 0.037
718
OLG003 Oligohydramnios 53 0.037
719
RTN016 Retinal Degeneration 53 0.037
720
PNC041 Pancreatic Ductal Adenocarcinoma 53 0.037
721
OST016 Osteochondrosis 52 0.037
722
NNT012 Neonatal Jaundice 52 0.037
723
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 52 0.037
724
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.037
725
HLL004 Hellp Syndrome 51 0.037
726
DYS073 Dysphagia 51 0.037
727
MYT002 Myotonic Dystrophy 51 0.037
728
ISL003 Isolated Growth Hormone Deficiency 51 0.037
729
PLC007 Placental Abruption 51 0.037
730
PLL012 Pollen Allergy 51 0.037
731
PSD014 Pseudopseudohypoparathyroidism 51 0.037
732
INN002 Inner Ear Disease 51 0.037
733
OST015 Osteochondrodysplasia 50 0.037
734
ACT017 Acute Chest Syndrome 50 0.037
735
CHL004 Cholelithiasis 50 0.037
736
CRY004 Cryoglobulinemia 50 0.037
737
HYP006 Hypertensive Heart Disease 50 0.037
738
RCR004 Recurrent Respiratory Papillomatosis 50 0.037
739
GND004 Gonadal Dysgenesis 50 0.037
740
c SPR009 Sporadic Breast Cancer 50 0.037
741
AST007 Astrocytoma 49 0.037
742
CRV040 Cervix Carcinoma 49 0.037
743
ATN002 Autonomic Nervous System Disease 49 0.037
744
PRP021 Peripheral Nervous System Neoplasm 49 0.037
745
PLS009 Plasma Cell Neoplasm 49 0.037
746
UTR043 Uterine Sarcoma 49 0.037
747
PRP056 Porphyria, Acute Hepatic 48 0.037
748
RTC009 Reticulum Cell Sarcoma 48 0.037
750
VTM002 Vitamin B12 Deficiency 48 0.037
751
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.037
752
RTC005 Reticulosarcoma 48 0.037
753
c WLM011 Wilms Tumor 6 48 0.037
754
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 47 0.037
755
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.037
756
SYN036 Syncope 47 0.037
757
c BSL024 Basal Cell Carcinoma 1 47 0.037
758
ADR012 Adrenal Gland Disease 47 0.037
759
RTR008 Root Resorption 47 0.037
760
SKN022 Skin Squamous Cell Carcinoma 46 0.037
761
ATN004 Autonomic Neuropathy 46 0.037
762
PST048 Postural Orthostatic Tachycardia Syndrome 46 0.037
763
ANC002 Anca-Associated Vasculitis 46 0.037
764
VTM001 Vitamin K Deficiency Hemorrhagic Disease 46 0.037
765
RNL045 Renal Tubular Acidosis, Distal 45 0.037
766
DYS021 Dysautonomia 45 0.037
767
CRB085 Cerebral Hemorrhage 45 0.037
768
PRM013 Premature Menopause 44 0.037
769
DBT008 Diabetic Angiopathy 44 0.037
770
INT071 Intestinal Perforation 43 0.037
771
DYS018 Dysostosis 43 0.037
772
SKL017 Skeletal Dysplasias 43 0.037
773
VST004 Vestibular Disease 43 0.037
774
CRP002 Croup 42 0.037
775
PRT035 Peritoneum Cancer 42 0.037
776
PTY001 Pityriasis Rosea 42 0.037
778
HYP189 Hypoadrenalism 41 0.037
779
NNT019 Neonatal Hypothyroidism 41 0.037
780
HYP265 Hypotonia 41 0.037
781
ADR022 Adrenomyeloneuropathy 41 0.037
782
DFF003 Diffuse Scleroderma 41 0.037
783
LCR008 Lacrimal Apparatus Disease 41 0.037
784
PRG002 Progesterone-Receptor Positive Breast Cancer 41 0.037
785
GRN007 Granuloma Annulare 40 0.037
786
STT004 Steatorrhea 40 0.037
787
NDL024 Nodal Marginal Zone Lymphoma 40 0.037
788
IGN003 Iga Nephropathy 1 40 0.037
789
OLG001 Oligospermia 40 0.037
790
ENT008 Enteropathy-Associated T-Cell Lymphoma 39 0.037
791
BLN001 Blount\'s Disease 39 0.037
792
INT038 Interdigitating Dendritic Cell Sarcoma 39 0.037
793
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.037
794
SKN023 Skin Tag 39 0.037
795
ACR062 Acroosteolysis 38 0.037
796
SYN012 Synpolydactyly 38 0.037
797
SBC024 Subcutaneous Panniculitis-Like T-Cell Lymphoma 38 0.037
798
CRB088 Cerebral Atrophy 38 0.037
799
ALC005 Alcoholic Pancreatitis 38 0.037
800
LTH001 Lethal Midline Granuloma 38 0.037
801
ADR010 Adrenal Cortical Hypofunction 37 0.037
802
SLP010 Slipped Capital Femoral Epiphysis 37 0.037
803
c PLM022 Pulmonary Valve Insufficiency 37 0.037
804
CRV030 Cervical Adenitis 36 0.037
805
CRV069 Cervix Disease 36 0.037
806
OLG022 Oligoasthenoteratozoospermia 36 0.037
807
PRX077 Peroxisomal Biogenesis Disorders 36 0.037
808
SBC017 Sebaceous Gland Disease 36 0.037
809
VSC008 Vascular Hemostatic Disease 35 0.037
810
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 35 0.037
811
ATS411 Autosomal Dominant Epidermolytic Ichthyosis 35 0.037
812
LBY004 Labyrinthitis 35 0.037
813
GNG006 Gingival Hypertrophy 34 0.037
814
CYT004 Cytomegalic Inclusion Disease 34 0.037
815
HYP111 Hyperprolinemia 34 0.037
816
SWL001 Swallowing Disorders 34 0.037
817
FNT004 Fainting 34 0.037
818
CHL013 Cholecystolithiasis 34 0.037
819
OST006 Osteoblastoma 34 0.037
820
CLC008 Colchicine Resistance 34 0.037
821
TTH008 Tooth Resorption 33 0.037
822
STR103 Streptococcus Pneumonia 33 0.037
823
END014 Endemic Typhus 33 0.037
824
BNN005 Bunion 33 0.037
825
MYL074 Myelodysplastic Syndrome with Excess Blasts 32 0.037
826
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 30 0.037
827
LCH004 Lichen Disease 30 0.037
828
c ACT072 Acute Laryngitis 30 0.037
829
MRQ003 Morquio Syndrome 30 0.037
831
LRY004 Laryngotracheitis 29 0.037
832
FLL029 Fallopian Tube Disease 29 0.037
833
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 28 0.037
834
c SYN084 Synpolydactyly 1 28 0.037
835
NPH056 Nephrolithiasis/osteoporosis, Hypophosphatemic, 1 28 0.037
836
MYT026 Myotonia Atrophica 28 0.037
837
c ICH014 Ichthyosis Lamellar 1 25 0.037
838
c DMN022 Diamond-Blackfan Anemia 9 25 0.037
839
RFR007 Refractory Anemia with Excess Blasts in Transformation 25 0.037
840
UTR037 Uterine Corpus Sarcoma 24 0.037
841
c DMN024 Diamond-Blackfan Anemia 7 23 0.037
842
PLY179 Polyomavirus-Associated Nephropathy 22 0.037
843
NKJ001 Nakajo Syndrome 21 0.037
844
c HYP369 Hypophosphatemic Rickets, Autosomal Recessive, 2 21 0.037
845
NRD050 Neurodevelopmental Disorder with Brain, Liver, and Lung Abnormalities 21 0.037
846
CRC034 Carcinoma Showing Thymus-Like Differentiation 19 0.037
847
LPN002 Lip and Oral Cavity Cancer 18 0.037
848
c WSK002 Wiskott-Aldrich Syndrome 2 18 0.037
849
SCL001 Scalp Dermatosis 17 0.037
850
ATX030 Ataxia-Telangiectasia 84 0.026
851
RTN008 Retinitis Pigmentosa 79 0.026
852
PFF001 Pfeiffer Syndrome 78 0.026
853
PLM037 Pulmonary Hypertension 77 0.026
854
WSK001 Wiskott-Aldrich Syndrome 76 0.026
855
c HMC039 Hemochromatosis, Type 1 74 0.026
856
ALP046 Alport Syndrome, X-Linked 74 0.026
857
MYC084 Mycobacterium Tuberculosis 1 74 0.026
858
MLT157 Multiple System Atrophy 1 74 0.026
859
HNT016 Huntington Disease 73 0.026
860
c TBR025 Tuberous Sclerosis 1 72 0.026
861
FBR012 Fabry Disease 72 0.026
862
EWN003 Ewing Sarcoma 72 0.026
863
c EXD008 Exudative Vitreoretinopathy 1 72 0.026
864
CMM004 Common Variable Immunodeficiency 71 0.026
865
RNL065 Renal Cell Carcinoma, Papillary, 1 71 0.026
866
LSH001 Leishmaniasis 71 0.026
867
c MYT021 Myotonic Dystrophy 1 70 0.026
868
THY111 Thyroid Carcinoma, Familial Medullary 70 0.026
869
SVR004 Severe Combined Immunodeficiency 69 0.026
870
TBR001 Tuberous Sclerosis 69 0.026
871
PSD087 Pseudoxanthoma Elasticum 68 0.026
872
PRT037 Pertussis 68 0.026
873
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 68 0.026
874
ALC007 Alcohol Dependence 68 0.026
875
FRN006 Frontotemporal Dementia 67 0.026
876
SZR001 Sezary\'s Disease 67 0.026
877
DMN031 Dementia, Lewy Body 67 0.026
878
c ATR087 Atrial Standstill 1 67 0.026
879
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 66 0.026
880
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 66 0.026
881
GLC006 Galactosemia 66 0.026
882
CHL123 Chlamydia 66 0.026
883
SPN046 Spinal Muscular Atrophy 66 0.026
884
HYP098 Hypereosinophilic Syndrome 65 0.026
885
AND002 Androgen Insensitivity Syndrome 65 0.026
886
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.026
887
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.026
888
MSL001 Measles 65 0.026
889
c DPH024 Diaphragmatic Hernia, Congenital 65 0.026
890
c ART101 Aortic Valve Disease 2 65 0.026
891
OST017 Osteomyelitis 64 0.026
892
PCK003 Pick Disease of Brain 64 0.026
893
CRN037 Craniosynostosis 64 0.026
894
MGK001 Megakaryocytic Leukemia 64 0.026
895
ANP031 Anaplastic Thyroid Cancer 64 0.026
896
PRP083 Porphyria, Acute Intermittent 64 0.026
897
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 63 0.026
898
CRB048 Cerebral Cavernous Malformations 63 0.026
899
c OVR114 Ovarian Cancer 1 62 0.026
900
BLD131 Bladder Urothelial Carcinoma 62 0.026
901
SVR066 Severe Combined Immunodeficiency, X-Linked 62 0.026
902
DGR001 Digeorge Syndrome 62 0.026
903
EHL001 Ehlers-Danlos Syndrome 61 0.026
904
SCH014 Schistosomiasis 61 0.026
905
PRP029 Porphyria 61 0.026
906
HRD008 Hereditary Hemorrhagic Telangiectasia 61 0.026
907
PRP030 Purpura 61 0.026
908
c GCH015 Gaucher Disease, Type I 61 0.026
909
ECT006 Ectodermal Dysplasia 61 0.026
910
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 61 0.026
911
SYN007 Synovitis 61 0.026
912
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 60 0.026
913
ACT119 Acute Promyelocytic Leukemia 60 0.026
914
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.026
915
CND004 Candidiasis 60 0.026
916
SPP011 Suppression of Tumorigenicity 12 60 0.026
917
APH002 Aphasia 60 0.026
918
MRK001 Merkel Cell Carcinoma 60 0.026
919
STT001 Status Epilepticus 60 0.026
920
ART001 Arterial Tortuosity Syndrome 60 0.026
921
MTR004 Maturity-Onset Diabetes of the Young 60 0.026
922
c GRV008 Graves Disease 1 60 0.026
923
NTH001 Netherton Syndrome 59 0.026
924
MCS002 Mucositis 59 0.026
925
CHL028 Childhood Type Dermatomyositis 59 0.026
926
GST037 Gastroparesis 59 0.026
927
BLD062 Bile Duct Cancer 59 0.026
928
OST009 Osteochondritis Dissecans 59 0.026
929
INT030 Intracranial Aneurysm 59 0.026
930
LNG039 Lung Squamous Cell Carcinoma 59 0.026
931
EXT034 Extrinsic Allergic Alveolitis 58 0.026
932
CTR002 Cataract 58 0.026
933
ERY003 Erythema Multiforme 58 0.026
934
PLM012 Pulmonary Sarcoidosis 58 0.026
935
c ESS001 Essential Tremor 58 0.026
936
MNC007 Monocytic Leukemia 58 0.026
937
CYS018 Cystitis 58 0.026
938
PLY019 Polyneuropathy 58 0.026
939
CHR619 Chromosome 2q35 Duplication Syndrome 58 0.026
940
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 57 0.026
941
LYM040 Lymphoblastic Lymphoma 57 0.026
942
c LKM070 Leukemia, Acute Monocytic 57 0.026
943
c INF023 Inflammatory Breast Carcinoma 57 0.026
944
RHB003 Rhabdomyosarcoma 57 0.026
945
TMP001 Temporal Lobe Epilepsy 57 0.026
946
EPD016 Epidermolysis Bullosa 57 0.026
947
PRT082 Preterm Premature Rupture of the Membranes 57 0.026
948
BRS099 Breast Ductal Carcinoma 57 0.026
949
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 57 0.026
950
BLR001 Biliary Atresia 57 0.026
951
AXN002 Axenfeld-Rieger Syndrome 56 0.026
952
PLC008 Placenta Disease 56 0.026
953
AMN001 Amenorrhea 56 0.026
954
c HYD046 Hydatidiform Mole, Recurrent, 1 56 0.026
955
HMP005 Hemiplegia 56 0.026
956
HDR002 Hidradenitis Suppurativa 56 0.026
957
SPN052 Spondyloarthropathy 56 0.026
958
HYP014 Hyperuricemia 56 0.026
959
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.026
960
BLR008 Bilirubin Metabolic Disorder 55 0.026
961
TRP002 Tropical Spastic Paraparesis 55 0.026
962
LMB006 Limb-Girdle Muscular Dystrophy 55 0.026
963
OPT003 Opiate Dependence 55 0.026
964
CHY002 Chylomicron Retention Disease 55 0.026
965
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.026
966
c MYT020 Myotonic Dystrophy 2 55 0.026
967
MNR012 Meniere Disease 55 0.026
968
c OST163 Osteopetrosis, Autosomal Recessive 3 55 0.026
969
PLV003 Pelvic Inflammatory Disease 55 0.026
970
LPR001 Lepromatous Leprosy 55 0.026
971
MMM001 Mammary Paget\'s Disease 55 0.026
972
DNN002 Donnai-Barrow Syndrome 55 0.026
973
ALP061 Alopecia, Androgenetic, 1 55 0.026
974
LYS002 Lysosomal Storage Disease 55 0.026
975
CHR177 Chromophobe Renal Cell Carcinoma 55 0.026
976
SCK002 Sick Sinus Syndrome 54 0.026
977
RHM028 Rheumatic Heart Disease 54 0.026
978
CLR109 Colorectal Adenocarcinoma 54 0.026
979
DRM007 Dermatitis Herpetiformis 54 0.026
980
HYP614 Hyperlipidemia, Familial Combined 54 0.026
981
APR001 Apraxia 54 0.026
982
PRP016 Paraplegia 54 0.026
983
VNS003 Venous Insufficiency 54 0.026
984
GST027 Gastric Lymphoma 54 0.026
985
INT079 Intrahepatic Cholangiocarcinoma 54 0.026
986
ESN008 Eosinophilic Pneumonia 54 0.026
987
RTN020 Retinal Vascular Disease 54 0.026
988
MNC006 Monoclonal Gammopathy of Uncertain Significance 53 0.026
989
EMB005 Embryonal Rhabdomyosarcoma 53 0.026
990
RDC002 Radiculopathy 53 0.026
991
c INH020 Inherited Metabolic Disorder 53 0.026
992
NRL018 Neural Tube Defects, Folate-Sensitive 53 0.026
993
CRY005 Cryptococcosis 53 0.026
994
FML037 Female Breast Cancer 53 0.026
995
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 53 0.026
996
c OST131 Osteopetrosis, Autosomal Dominant 2 53 0.026
997
PLY017 Polyarteritis Nodosa 52 0.026
998
ESN005 Eosinophilic Gastroenteritis 52 0.026
999
PRR002 Pure Red-Cell Aplasia 52 0.026
1000
ALL009 Allergic Conjunctivitis 52 0.026
1001
ARM001 Aromatase Deficiency 52 0.026
1002
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.026
1003
LRN003 Learning Disability 52 0.026
1004
CYS014 Cystadenocarcinoma 52 0.026
1005
c INV001 Invasive Aspergillosis 52 0.026
1006
GRM005 Germ Cell Cancer 52 0.026
1007
OCC006 Occipital Horn Syndrome 52 0.026
1008
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 52 0.026
1009
ATY042 Atypical Chronic Myeloid Leukemia 51 0.026
1010
BLD044 Bladder Disease 51 0.026
1011
PNC001 Pancytopenia 51 0.026
1012
ATR005 Atrophic Gastritis 51 0.026
1013
XNT003 Xanthomatosis 51 0.026
1014
PPL002 Papillary Carcinoma 51 0.026
1015
EXP004 Exophthalmos 51 0.026
1016
MCN001 Mucinous Adenocarcinoma 51 0.026
1017
BNG036 Bone Giant Cell Tumor 51 0.026
1018
HPT082 Hepatic Adenomas, Familial 51 0.026
1019
TRP008 Tropical Calcific Pancreatitis 51 0.026
1020
SMN008 Semantic Dementia 51 0.026
1021
SPN020 Spondylosis 51 0.026
1022
c BNG091 Benign Chronic Pemphigus 51 0.026
1023
SCL015 Scleritis 51 0.026
1024
CRD137 Cardiogenic Shock 51 0.026
1025
c SPN393 Spinal Muscular Atrophy, Type I 50 0.026
1026
HMP009 Haemophilus Influenzae 50 0.026
1027
PNT038 Peanut Allergy 50 0.026
1028
FBR009 Fibrous Dysplasia 50 0.026
1029
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 50 0.026
1030
HYP068 Hyperostosis 50 0.026
1031
ICH054 Ichthyosis, X-Linked 50 0.026
1032
ORL005 Oral Candidiasis 50 0.026
1033
RNL015 Renal Hypertension 50 0.026
1034
SYR001 Syringomyelia 49 0.026
1035
CLR030 Clear Cell Renal Cell Carcinoma 49 0.026
1036
KRT007 Keratoconus 49 0.026
1037
GNT008 Giant Cell Tumor 49 0.026
1038
TBR006 Tuberculoid Leprosy 49 0.026
1039
ACN001 Acinar Cell Carcinoma 49 0.026
1040
NGH001 Night Blindness 49 0.026
1041
HMR002 Hemarthrosis 49 0.026
1042
SPN119 Spondylarthropathy 49 0.026
1043
MTB004 Metabolic Acidosis 49 0.026
1044
CTS002 Cat-Scratch Disease 49 0.026
1045
KLD001 Keloids 49 0.026
1046
ECZ002 Eczema Herpeticum 49 0.026
1047
ANR004 Anuria 49 0.026
1048
LPD009 Lipid Storage Disease 49 0.026
1049
MNN009 Meningoencephalitis 49 0.026
1050
ACT088 Acute Insulin Response 48 0.026
1051
HYP781 Hypoascorbemia 48 0.026
1052
MGR001 Migraine Without Aura 48 0.026
1053
MLR002 Miliary Tuberculosis 48 0.026
1054
RNL017 Renal Oncocytoma 48 0.026
1055
SYN005 Synostosis 48 0.026
1056
ACT098 Acute Erythroid Leukemia 48 0.026
1057
c PNC106 Pancreatic Agenesis 1 48 0.026
1058
HDN002 Head Injury 48 0.026
1059
ACT200 Acute Monoblastic Leukemia 48 0.026
1060
PRK001 Porokeratosis 48 0.026
1061
PRS045 Prostatic Hypertrophy 48 0.026
1062
HYP058 Hypervitaminosis a 48 0.026
1063
CRN017 Coronary Thrombosis 48 0.026
1064
RTN023 Retinitis 48 0.026
1065
ASP030 Aspirin Resistance 47 0.026
1066
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 47 0.026
1067
HYP457 Hypertrophic Scars 47 0.026
1068
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.026
1069
DNT011 Dentinogenesis Imperfecta 47 0.026
1070
GYN001 Gynecomastia 47 0.026
1071
HDR003 Hidradenitis 47 0.026
1072
ATS010 Autosomal Recessive Disease 47 0.026
1073
MCR191 Microscopic Colitis 47 0.026
1074
LMN006 Luminal Breast Carcinoma 47 0.026
1075
ALB002 Albinism 47 0.026
1076
c OST129 Osteopetrosis, Autosomal Recessive 2 47 0.026
1077
PRM003 Premature Ejaculation 47 0.026
1078
DNG001 Dengue Shock Syndrome 47 0.026
1079
PTT041 Pituitary Stalk Interruption Syndrome 47 0.026
1080
CLS010 Cluster Headache 46 0.026
1081
CHR031 Chromoblastomycosis 46 0.026
1082
GRN017 Granulocytopenia 46 0.026
1083
ONC003 Oncogenic Osteomalacia 46 0.026
1084
DVR002 Diverticulitis 46 0.026
1085
END011 Endometriosis of Ovary 46 0.026
1086
ORL015 Oral Squamous Cell Carcinoma 46 0.026
1087
IMP004 Impetigo 46 0.026
1088
GST010 Gestational Trophoblastic Neoplasm 46 0.026
1089
CHR342 Chiari Malformation 46 0.026
1090
PRS115 Prosthetic Joint Infection 46 0.026
1091
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.026
1092
OSS001 Ossifying Fibroma 46 0.026
1093
GLL017 Gallbladder Adenocarcinoma 45 0.026
1094
DCB001 Decubitus Ulcer 45 0.026
1095
DWR001 Dwarfism 45 0.026
1096
BLS002 Blastomycosis 45 0.026
1097
GNG008 Ganglioneuroblastoma 44 0.026
1098
SPC005 Speech Disorder 44 0.026
1099
GNG003 Gingival Recession 44 0.026
1100
TCL003 T Cell Deficiency 44 0.026
1101
CDQ001 Cauda Equina Syndrome 44 0.026
1102
PSD086 Pseudoarthrosis 44 0.026
1103
c HMC010 Hemochromatosis, Type 3 44 0.026
1104
KRT008 Keratopathy 44 0.026
1105
c MLG079 Malignant Pleural Mesothelioma 44 0.026
1106
c OST136 Osteopetrosis, Autosomal Recessive 7 44 0.026
1107
PRC003 Proctitis 44 0.026
1108
HYP263 Hypersomnia 44 0.026
1109
ADP007 Adie Pupil 43 0.026
1110
SPH010 Sphingolipidosis