Search results for blindness

2297 hits were found for blindness

# Family MCID Name MIFTS Score
1
c NGH026 Night Blindness, Congenital Stationary, Type 1a 51 5.727
2
c NGH007 Night Blindness, Congenital Stationary, Type 1b 31 4.694
3
c NGH025 Night Blindness, Congenital Stationary, Type 2a 31 4.694
4
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 45 4.566
5
P CNG010 Congenital Stationary Night Blindness 56 4.359
6
P CLR019 Color Blindness 50 4.132
7
c NGH010 Night Blindness, Congenital Stationary, Autosomal Dominant 2 26 4.061
8
c NGH030 Night Blindness, Congenital Stationary, Type 1f 22 4.055
9
c NGH008 Night Blindness, Congenital Stationary, Autosomal Dominant 3 20 4.041
10
c NGH021 Night Blindness, Congenital Stationary, Autosomal Dominant 1 19 4.033
11
c SPN295 Spinocerebellar Ataxia, Autosomal Recessive 3 30 4.029
12
XLN012 X-Linked Congenital Stationary Night Blindness 26 3.929
13
c NGH029 Night Blindness, Congenital Stationary, Type 1e 32 3.855
14
c NGH028 Night Blindness, Congenital Stationary, Type 1d 22 3.831
15
P NGH001 Night Blindness 51 3.824
16
c NGH027 Night Blindness, Congenital Stationary, Type 1c 23 3.817
17
TRT020 Tritanopia 42 3.562
18
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 20 3.558
19
c HRD015 Hereditary Night Blindness 32 3.338
20
NRR002 Norrie Disease 61 3.328
21
CRT012 Cortical Blindness 34 3.229
22
c NGH024 Night Blindness, Congenital Stationary, Type 1h 19 3.038
23
SZR027 Seizures, Cortical Blindness, and Microcephaly Syndrome 19 3.026
24
c NGH022 Night Blindness, Congenital Stationary, Type 1g 17 3.026
25
BLN006 Blind Loop Syndrome 30 2.892
26
P ACH003 Achromatopsia 57 2.771
27
c OGC001 Oguchi Disease 1 23 2.726
28
c ACH021 Achromatopsia 3 44 2.718
29
RDR002 Rodrigues Blindness 20 2.718
30
P OGC002 Oguchi Disease 2 16 2.709
31
c ATS169 Autosomal Recessive Congenital Stationary Night Blindness 28 2.406
32
RDG001 Red-Green Color Blindness 30 2.379
33
CLR133 Colorblindness, Partial, Protan Series 35 2.348
34
SCT002 Scotoma 42 2.337
35
c LBR004 Leber Congenital Amaurosis 1 41 2.337
36
RTN035 Retinal Cone Dystrophy 3b 28 2.324
37
RTN034 Retinal Cone Dystrophy 3a 25 2.324
38
ONC002 Onchocerciasis 53 2.072
39
KRT002 Keratomalacia 55 2.047
40
c ATS168 Autosomal Dominant Congenital Stationary Night Blindness 29 1.984
41
P LBR001 Leber Congenital Amaurosis 65 1.952
42
MHR001 Mohr-Tranebjaerg Syndrome 39 1.933
43
NGH023 Night Blindness-Skeletal Anomalies-Dysmorphism Syndrome 16 1.933
44
CLR033 Color Vision Deficiency 37 1.927
45
CRT080 Cortical Blindness, Retardation, and Postaxial Polydactyly 15 1.922
46
SCL050 Scoliosis, Arachnodactyly, and Blindness 14 1.922
47
BLC001 Blue Cone Monochromacy 45 1.915
48
c PRS058 Prosopagnosia, Hereditary 20 1.915
49
BLN008 Blind Hypotensive Eye 19 1.915
50
MCR054 Microcephaly Microphthalmos Blindness 3 1.915
51
c EPL123 Epileptic Encephalopathy, Early Infantile, 23 24 1.908
52
BLN007 Blind Hypertensive Eye 5 1.908
53
SLT014 Salt and Pepper Developmental Regression Syndrome 37 1.900
54
CNR037 Cone-Rod Dystrophy and Hearing Loss 23 1.891
55
c DYS121 Dyslexia 1 19 1.891
56
c ACQ002 Acquired Night Blindness 11 1.391
57
ANT040 Anton's Syndrome 12 1.380
58
CRT077 Cortical Blindness-Intellectual Disability-Polydactyly Syndrome 12 1.380
59
AMR003 Amaurosis Fugax 37 1.374
60
CHN047 Chondroectodermal Dysplasia with Night Blindness 16 1.374
61
c ACQ001 Acquired Color Blindness 14 1.374
62
OST144 Osteoporosis-Macrocephaly-Blindness-Joint Hyperlaxity Syndrome 13 1.374
63
PLY155 Polycystic Kidney, Cataract, and Congenital Blindness 11 1.374
64
ECT016 Ectodermal Dysplasia Blindness 3 1.374
65
c ACH020 Achromatopsia 2 40 1.367
66
CLR132 Colorblindness, Partial, Deutan Series 25 1.359
67
BCR005 Bicervical Bicornuate Uterus and Blind Hemivagina 6 1.359
68
c SPS205 Spastic Paraplegia 79, Autosomal Recessive 26 1.349
69
WNS001 Weinstein Kliman Scully Syndrome 5 1.337
70
P HMR011 Hemeralopia, Familial 3 1.337
71
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.200
72
P ART022 Arthritis 77 0.188
73
P SCH015 Schizophrenia 71 0.168
74
ANX010 Anxiety 72 0.155
75
c BLD140 Blood Group, I System 37 0.155
76
ACQ007 Acquired Immunodeficiency Syndrome 65 0.152
77
P DBT009 Diabetes Mellitus 72 0.150
78
P NRV007 Nervous System Disease 75 0.147
79
P ENC018 Encephalopathy 58 0.147
80
RTN023 Retinitis 52 0.144
81
P RHM011 Rheumatoid Arthritis 91 0.141
82
AST005 Asthma 83 0.139
83
P NRP001 Neuropathy 63 0.136
84
PSY004 Psychotic Disorder 72 0.135
85
P HPT021 Hepatitis 75 0.134
86
VRL011 Viral Infectious Disease 64 0.132
87
P ART023 Arthropathy 68 0.130
88
P MLT020 Multiple Sclerosis 85 0.129
89
GST050 Gastrointestinal System Disease 66 0.129
90
JNT002 Joint Disorders 60 0.129
91
SKN027 Skin Conditions 48 0.127
92
SKN016 Skin Disease 68 0.124
93
ATM095 Autoimmune Disease 66 0.124
94
P INT068 Intestinal Disease 65 0.121
95
c CNT035 Central Nervous System Disease 65 0.121
96
AGN016 Aging 65 0.120
97
MNT002 Mental Depression 60 0.119
98
LNG099 Lung Disease 67 0.118
99
RHM027 Rheumatic Disease 62 0.118
100
P CLL015 Collagen Disease 53 0.118
101
GLC008 Glucose Metabolism Disease 38 0.118
102
ENT004 Enthesopathy 38 0.118
103
IMM136 Immune System Disease 57 0.116
104
OST012 Osteoarthritis 88 0.115
105
P DRR001 Diarrhea 60 0.113
106
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.113
107
RSP006 Respiratory System Disease 63 0.112
108
P MJR001 Major Depressive Disorder 70 0.111
109
CRB009 Cerebritis 41 0.111
110
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.110
111
c PNS012 Paine Syndrome 52 0.107
112
P RHN004 Rhinitis 62 0.106
113
HDC001 Headache 55 0.105
114
MNG003 Mungan Syndrome 34 0.105
115
ISC004 Ischemia 66 0.104
116
P CRV039 Cervicitis 49 0.104
117
PRS047 Prostatitis 59 0.103
118
P KDN018 Kidney Disease 69 0.102
119
NRM005 Neuromuscular Disease 60 0.102
120
TRC008 Trachoma 52 0.101
121
URN009 Urinary System Disease 58 0.100
122
SPS003 Spastic Diplegia 55 0.100
123
SCH012 Schizoaffective Disorder 51 0.100
124
CNS004 Constipation 57 0.099
125
DMN002 Dementia 68 0.097
126
P BRS047 Breast Cancer 100 0.094
127
P LVR013 Liver Disease 76 0.094
128
GST045 Gastroenteritis 65 0.094
129
BCK006 Back Pain 46 0.094
130
P EPL164 Epilepsy 70 0.093
131
DRM006 Dermatitis 67 0.093
132
MDD011 Mood Disorder 64 0.093
133
P ALZ034 Alzheimer Disease 95 0.092
134
CNN005 Connective Tissue Disease 65 0.092
135
CMM005 Common Cold 62 0.092
136
PNG002 Pain Agnosia 41 0.092
137
VSC007 Vascular Disease 71 0.091
138
ALL003 Allergic Rhinitis 68 0.091
139
P PSR002 Psoriasis 65 0.091
140
CCN001 Cocaine Dependence 52 0.091
141
SPS057 Spasticity 41 0.091
142
HMN044 Human Immunodeficiency Virus Type 1 71 0.090
143
P ATS364 Autism 70 0.090
144
ART140 Arteries, Anomalies of 51 0.090
145
c BPL002 Bipolar I Disorder 50 0.090
146
P MYC007 Myocardial Infarction 81 0.088
147
P INF032 Infertility 59 0.088
148
PRM003 Premature Ejaculation 47 0.088
149
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.087
150
SLP005 Sleep Disorder 59 0.087
151
P RTN008 Retinitis Pigmentosa 81 0.086
152
P HRT032 Heart Disease 80 0.086
153
P ESP024 Esophagitis 64 0.086
154
P MYP006 Myopia 56 0.086
155
CLN019 Colonic Disease 55 0.086
156
NRT004 Neuritis 55 0.086
157
P CRN018 Coronary Artery Anomaly 69 0.085
158
IRR002 Irritable Bowel Syndrome 63 0.085
159
P DYS154 Dystonia 61 0.085
160
P INF038 Influenza 77 0.083
161
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.083
162
GNG013 Gingivitis 64 0.083
163
CLT003 Colitis 63 0.083
164
PLP001 Pulpitis 50 0.083
165
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.083
166
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.083
167
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.083
168
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.083
169
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.083
170
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.083
171
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.083
172
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.083
173
P MYP004 Myopathy 69 0.082
174
RTN018 Retinal Disease 56 0.082
175
P NRF023 Neurofibromatosis, Type Ii 69 0.081
176
GNR004 Generalized Anxiety Disorder 53 0.081
177
MSC033 Muscle Disorders 53 0.081
178
MYF002 Myofascial Pain Syndrome 44 0.081
179
MVM001 Movement Disease 40 0.081
180
MSC004 Muscle Tissue Disease 39 0.081
181
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.079
182
CNG034 Congestive Heart Failure 74 0.079
183
P CTR002 Cataract 60 0.079
184
STM007 Stomatitis 52 0.079
185
PST053 Postherpetic Neuralgia 44 0.079
186
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.079
187
TNP001 Tinea Pedis 43 0.079
188
MLR004 Malaria 86 0.078
189
P DRM053 Dermatitis, Atopic 68 0.078
190
P PNC044 Pancreatitis 64 0.078
191
DBT010 Diabetic Neuropathy 60 0.077
192
VGN023 Vaginitis 59 0.077
193
END040 Endogenous Depression 53 0.077
194
P LNG032 Lung Cancer 99 0.075
195
c HYP595 Hypertension, Essential 78 0.075
196
ALC007 Alcohol Dependence 65 0.075
197
APH001 Aphthous Stomatitis 64 0.075
198
GST092 Gastroesophageal Reflux 64 0.075
199
MCS002 Mucositis 61 0.075
200
BRN106 Burns 57 0.075
201
PRP019 Peripheral Nervous System Disease 53 0.075
202
CRV043 Cervical Dystonia 45 0.075
203
c CHR089 Chronic Kidney Failure 72 0.074
204
P PNM007 Pneumonia 70 0.074
205
c HPT003 Hepatitis a 63 0.074
206
ANR040 Aneurysm 61 0.074
207
ESP023 Esophageal Disease 58 0.074
208
P ECL001 Eclampsia 57 0.074
209
P CHR345 Chronic Pain 52 0.074
210
BSL008 Basal Ganglia Disease 44 0.074
211
P PRS040 Prostate Cancer 88 0.072
212
P PRK057 Parkinson Disease, Late-Onset 78 0.072
213
P CNJ013 Conjunctivitis 67 0.072
214
P CND004 Candidiasis 61 0.072
215
P SZR006 Seizure Disorder 55 0.072
216
DYS014 Dyspepsia 54 0.072
217
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.072
218
EPC002 Epicondylitis 41 0.072
219
c ACT004 Acute Diarrhea 41 0.072
220
XRP001 Xerophthalmia 35 0.072
221
c ACT075 Acute Myocardial Infarction 64 0.071
222
P EXN002 Exanthem 62 0.071
223
URT039 Urticaria 59 0.071
224
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.071
225
MGR028 Migraine with or Without Aura 1 55 0.071
226
FSC004 Fasciitis 48 0.071
227
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.071
228
c HPT001 Hepatitis C 73 0.069
229
THR024 Thrombosis 61 0.069
230
BRN038 Bronchial Disease 58 0.069
231
c PYR010 Peyronie's Disease 54 0.069
232
c BRN108 Branchiootic Syndrome 1 47 0.069
233
DYS073 Dysphagia 47 0.069
234
DDN006 Duodenitis 46 0.069
235
CYS001 Cystic Fibrosis 85 0.068
236
ULC004 Ulcerative Colitis 80 0.068
237
P MSC005 Muscular Dystrophy 66 0.068
238
P CRN300 Coronary Heart Disease 1 57 0.068
239
KRT009 Keratosis 53 0.068
240
P INF037 Inflammatory Bowel Disease 52 0.068
241
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.068
242
PLN007 Plantar Fasciitis 35 0.068
243
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 33 0.068
244
P CLR023 Colorectal Cancer 98 0.066
245
CRH001 Crohn's Disease 80 0.066
246
P OST002 Osteoporosis 75 0.066
247
P LKM002 Leukemia 75 0.066
248
ISC006 Ischemic Heart Disease 73 0.066
249
P LYM118 Lymphoma 71 0.066
250
P LPS004 Lupus Erythematosus 69 0.066
251
P ART021 Arteriosclerosis 62 0.066
252
P BPL003 Bipolar Disorder 61 0.066
253
GT001 Gout 60 0.066
254
PHR003 Pharyngitis 59 0.066
255
P PLY019 Polyneuropathy 58 0.066
256
DMY004 Demyelinating Disease 58 0.066
257
P RTN016 Retinal Degeneration 56 0.066
258
SWL001 Swallowing Disorders 36 0.066
259
P ANR048 Aniridia 1 68 0.064
260
P TMP003 Temporal Arteritis 67 0.064
261
RSC001 Rosacea 58 0.064
262
P ALP008 Alopecia 56 0.064
263
RST001 Restless Legs Syndrome 54 0.064
264
HPT082 Hepatic Adenomas, Familial 52 0.064
265
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.064
266
ANR038 Anorexia Nervosa 1 21 0.064
267
BLD137 Blood Group--Ahonen 17 0.064
268
LVR012 Liver Cirrhosis 73 0.063
269
c HPT016 Hepatitis B 68 0.063
270
c EXD008 Exudative Vitreoretinopathy 1 65 0.063
271
MTH009 Mouth Disease 64 0.063
272
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.063
273
BCT002 Bacterial Vaginosis 56 0.063
274
NSD001 Nose Disease 51 0.063
275
c LBR014 Leber Congenital Amaurosis 4 48 0.063
276
END072 Endotheliitis 46 0.063
277
P MNN013 Meningitis 71 0.061
278
OBS002 Obsessive-Compulsive Disorder 68 0.061
279
LPD008 Lipid Metabolism Disorder 59 0.061
280
P LCH002 Lichen Planus 58 0.061
281
P ACT008 Actinic Keratosis 56 0.061
282
PST011 Pustulosis of Palm and Sole 47 0.061
283
PRC003 Proctitis 44 0.061
284
DYS011 Dyskinesia of Esophagus 39 0.061
285
BRN024 Bronchitis 67 0.059
286
c PRC016 Pre-Eclampsia 65 0.059
287
P SNS014 Sinusitis 62 0.059
288
HPT019 Hepatic Encephalopathy 59 0.059
289
SPN051 Spondylitis 55 0.059
290
ALL009 Allergic Conjunctivitis 53 0.059
291
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.059
292
ANG054 Angina Pectoris 53 0.059
293
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.059
294
RCT017 Rectal Disease 38 0.059
295
INF009 Inflammatory Spondylopathy 32 0.059
296
c SPN225 Spondyloarthropathy 1 71 0.057
297
P ADN016 Adenocarcinoma 71 0.057
298
CNR004 Cone-Rod Dystrophy 2 69 0.057
299
ADN018 Adenoma 63 0.057
300
FDL002 Food Allergy 55 0.057
301
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.057
302
SBC017 Sebaceous Gland Disease 38 0.057
303
c TRC078 Trichohepatoenteric Syndrome 2 34 0.057
304
MSC157 Muscular Dystrophy, Duchenne Type 74 0.055
305
MLN008 Melanoma 72 0.055
306
CRB037 Cerebral Palsy 70 0.055
307
TRD006 Tardive Dyskinesia 59 0.055
308
SHG001 Shigellosis 57 0.055
309
CHR081 Choroideremia 57 0.055
310
P TRM003 Tremor 54 0.055
311
IMP005 Impotence 54 0.055
312
FND001 Fundus Albipunctatus 54 0.055
313
P VNS003 Venous Insufficiency 53 0.055
314
PTH002 Pathological Gambling 53 0.055
315
PRS045 Prostatic Hypertrophy 51 0.055
316
DRM011 Dermatophytosis 48 0.055
317
P CLS010 Cluster Headache 47 0.055
318
TND004 Tendinopathy 45 0.055
319
c CHR579 Chiari Malformation Type Ii 42 0.055
320
STR067 Stroke, Ischemic 84 0.053
321
c MCL042 Macular Degeneration, Age-Related, 1 79 0.053
322
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.053
323
CRB039 Cerebrovascular Disease 68 0.053
324
TTN003 Tetanus 65 0.053
325
CRP001 Carpal Tunnel Syndrome 64 0.053
326
HYP056 Hypoglycemia 62 0.053
327
GNT003 Genital Herpes 58 0.053
328
BLD044 Bladder Disease 55 0.053
329
ORL013 Oral Lichen Planus 51 0.053
330
HYP025 Hyperphosphatemia 48 0.053
331
RFR003 Refractive Error 45 0.053
332
SXL003 Sexual Disorder 45 0.053
333
P BRN120 Bronchus Cancer 39 0.053
334
c SYS001 Systemic Lupus Erythematosus 86 0.051
335
P ATR011 Atrial Fibrillation 68 0.051
336
c SML038 Small Cell Cancer of the Lung 67 0.051
337
P MCR115 Microvascular Complications of Diabetes 5 66 0.051
338
FTT001 Fatty Liver Disease 62 0.051
339
INT002 Intermittent Claudication 61 0.051
340
DBT062 Diabetic Foot Ulcers 59 0.051
341
PLS007 Plasmodium Falciparum Malaria 59 0.051
342
P CYS018 Cystitis 57 0.051
343
BNF002 Bone Fracture 56 0.051
344
KRT006 Keratoconjunctivitis 56 0.051
345
RDC002 Radiculopathy 55 0.051
346
P HYP014 Hyperuricemia 54 0.051
347
BRN071 Brain Injury 54 0.051
348
ILT001 Ileitis 52 0.051
349
CRP002 Croup 41 0.051
350
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.051
351
MNN028 Mononeuropathy of the Median Nerve, Mild 35 0.051
352
FNC005 Functional Colonic Disease 24 0.051
353
PRT036 Peritonitis 67 0.049
354
PSR001 Psoriatic Arthritis 66 0.049
355
P PLY011 Polycystic Ovary Syndrome 65 0.049
356
HYP066 Hyperglycemia 64 0.049
357
ALC006 Alcoholic Hepatitis 62 0.049
358
PRP030 Purpura 61 0.049
359
TNS005 Tonsillitis 61 0.049
360
PNC034 Pancreas Disease 59 0.049
361
P PNC025 Panic Disorder 57 0.049
362
P THY032 Thyroiditis 56 0.049
363
c INF071 Inflammatory Bowel Disease 1 54 0.049
364
SPN041 Spinal Cord Disease 54 0.049
365
CLL003 Cellulitis 53 0.049
366
LMB062 Limb Ischemia 52 0.049
367
NRM004 Neuroma 51 0.049
368
GYR004 Gyrate Atrophy of Choroid and Retina 51 0.049
369
SYS003 Systolic Heart Failure 44 0.049
370
ESP018 Esophageal Candidiasis 44 0.049
371
CHR078 Chorioretinitis 41 0.049
372
FCL044 Fecal Incontinence 38 0.049
373
P RNG031 Ring Chromosome Y Syndrome 29 0.049
374
CHR066 Chronic Fatigue Syndrome 67 0.047
375
P ENC004 Encephalitis 66 0.047
376
VRC005 Varicose Veins 64 0.047
377
KRT019 Keratitis, Hereditary 62 0.047
378
APH002 Aphasia 58 0.047
379
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.047
380
CRT049 Critical Limb Ischemia 56 0.047
381
AMN001 Amenorrhea 55 0.047
382
HMP005 Hemiplegia 54 0.047
383
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.047
384
P DDN001 Duodenal Ulcer 53 0.047
385
DBT004 Diabetic Polyneuropathy 51 0.047
386
HDN002 Head Injury 48 0.047
387
c CHR431 Chronic Venous Insufficiency 47 0.047
388
c MTR002 Mitral Valve Insufficiency 46 0.047
389
URT001 Urethritis 44 0.047
390
AND014 Androgenic Alopecia 39 0.047
391
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.047
392
PTY002 Pityriasis Versicolor 36 0.047
393
TNC001 Tinea Cruris 33 0.047
394
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.047
395
VSC009 Vascular Skin Disease 10 0.047
396
P PLM037 Pulmonary Hypertension 79 0.044
397
c ATS007 Autism Spectrum Disorder 68 0.044
398
SPN186 Spinal Cord Injury 67 0.044
399
ACR006 Aceruloplasminemia 65 0.044
400
MSL001 Measles 64 0.044
401
P ALP009 Alopecia Areata 64 0.044
402
DPH001 Diphtheria 63 0.044
403
c ACT027 Acute Pancreatitis 61 0.044
404
HYP266 Hypoxia 61 0.044
405
P HMP007 Hemophilia 61 0.044
406
P GLM007 Glomerulonephritis 61 0.044
407
ING001 Inguinal Hernia 59 0.044
408
P STR022 Stargardt Disease 58 0.044
409
CMP010 Complex Regional Pain Syndrome 58 0.044
410
P ACT105 Acute Mountain Sickness 58 0.044
411
GST023 Gastric Ulcer 57 0.044
412
NNL002 Nonalcoholic Steatohepatitis 56 0.044
413
P MSC003 Muscular Atrophy 55 0.044
414
P PRM006 Primary Biliary Cirrhosis 55 0.044
415
OPT009 Optic Neuritis 53 0.044
416
PTT004 Pituitary Apoplexy 47 0.044
417
PRS129 Prostatic Hyperplasia, Benign 47 0.044
418
P BLP003 Blepharospasm 46 0.044
419
P RTN014 Retinal Artery Occlusion 45 0.044
420
URM005 Uremic Pruritus 43 0.044
421
P HYP265 Hypotonia 40 0.044
422
TNC002 Tinea Capitis 40 0.044
423
MLN003 Melancholia 39 0.044
424
ALR002 Al-Raqad Syndrome 30 0.044
425
ORB006 Orbital Cellulitis 29 0.044
426
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.042
427
BHC003 Behcet Syndrome 68 0.042
428
P HYD006 Hydrocephalus 68 0.042
429
OTT002 Otitis Media 67 0.042
430
BRS051 Breast Disease 67 0.042
431
c BSL007 Basal Cell Carcinoma 66 0.042
432
P SLP006 Sleep Apnea 65 0.042
433
P PRS038 Personality Disorder 65 0.042
434
RCT015 Reactive Arthritis 65 0.042
435
P INT143 Interstitial Cystitis 63 0.042
436
CRD119 Cardiac Arrest 63 0.042
437
P UVT001 Uveitis 61 0.042
438
P GST044 Gastritis 61 0.042
439
SPN027 Spinal Stenosis 60 0.042
440
c ESS001 Essential Tremor 58 0.042
441
P LTR001 Lateral Sclerosis 58 0.042
442
P BRN009 Burning Mouth Syndrome 56 0.042
443
P PYL005 Pyelonephritis 56 0.042
444
RTN209 Retinoschisis 1, X-Linked, Juvenile 56 0.042
445
IRN001 Iron Deficiency Anemia 55 0.042
446
P BLM007 Bulimia Nervosa 1 53 0.042
447
STM006 Stomach Disease 52 0.042
448
P CHL066 Cholangitis 52 0.042
449
RDT013 Radiation Proctitis 51 0.042
450
P OPN001 Open-Angle Glaucoma 51 0.042
451
PLL012 Pollen Allergy 48 0.042
452
c ACT042 Acute Pyelonephritis 48 0.042
453
CHR008 Choroiditis 47 0.042
454
MGR001 Migraine Without Aura 47 0.042
455
P DMY001 Demyelinating Polyneuropathy 46 0.042
456
TRC010 Trichotillomania 46 0.042
457
SPS007 Spastic Cerebral Palsy 46 0.042
458
PTY001 Pityriasis Rosea 45 0.042
459
LYM024 Lymphatic System Disease 45 0.042
460
IRN002 Iron Metabolism Disease 45 0.042
461
BRN080 Brain Ischemia 45 0.042
462
c ALP061 Alopecia, Androgenetic, 1 44 0.042
463
ALX001 Alexia 44 0.042
464
SCH003 Schizophreniform Disorder 44 0.042
465
CND005 Cone Dystrophy 42 0.042
466
c BSL024 Basal Cell Carcinoma 1 42 0.042
467
WRN005 Wrinkles 41 0.042
468
MYC033 Myoclonus 40 0.042
469
DRM009 Dermatomycosis 39 0.042
470
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.042
471
MTH047 Methanol Poisoning 32 0.042
472
HYP264 Hypertonia 32 0.042
473
INS024 Insulin-Like Growth Factor I 83 0.039
474
c HPT073 Hepatitis C Virus 73 0.039
475
LSH001 Leishmaniasis 71 0.039
476
P FML011 Familial Adenomatous Polyposis 71 0.039
477
P HRP006 Herpes Simplex 70 0.039
478
PRT037 Pertussis 70 0.039
479
P TBR001 Tuberous Sclerosis 69 0.039
480
P CLC063 Celiac Disease 1 65 0.039
481
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.039
482
P SPN046 Spinal Muscular Atrophy 63 0.039
483
YLL002 Yellow Fever 63 0.039
484
GST033 Gestational Diabetes 62 0.039
485
P HYP086 Hypothyroidism 62 0.039
486
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.039
487
SYN007 Synovitis 61 0.039
488
P HMR003 Hemorrhagic Disease 61 0.039
489
c ACT073 Acute Leukemia 61 0.039
490
HRP004 Herpes Zoster 61 0.039
491
ALL006 Allergic Asthma 60 0.039
492
BRN002 Bronchiolitis 59 0.039
493
c VRL010 Viral Hepatitis 59 0.039
494
PST028 Post-Traumatic Stress Disorder 59 0.039
495
LNN001 Lennox-Gastaut Syndrome 59 0.039
496
P USH001 Usher Syndrome 59 0.039
497
P HYP069 Hyperparathyroidism 58 0.039
498
SML019 Smallpox 57 0.039
499
EPD016 Epidermolysis Bullosa 57 0.039
500
P ANG015 Angioedema 57 0.039
501
ANK001 Ankylosis 56 0.039
502
P MGR003 Migraine with Aura 56 0.039
503
ALS001 Alstrom Syndrome 55 0.039
504
c MCR113 Microvascular Complications of Diabetes 3 55 0.039
505
TTH006 Tooth Disease 54 0.039
506
P TRC086 Trichohepatoenteric Syndrome 1 54 0.039
507
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.039
508
OVR063 Overnutrition 53 0.039
509
GTR002 Goiter 53 0.039
510
OPT006 Optic Nerve Disease 53 0.039
511
HLL004 Hellp Syndrome 53 0.039
512
P SHR001 Short Bowel Syndrome 52 0.039
513
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 51 0.039
514
BRX001 Bruxism 51 0.039
515
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.039
516
SPN119 Spondylarthropathy 46 0.039
517
IMP004 Impetigo 45 0.039
518
CLL021 Collagenous Colitis 43 0.039
519
CRV045 Cervical Intraepithelial Neoplasia 43 0.039
520
DYS009 Dysthymic Disorder 42 0.039
521
SPN369 Spinal Disease 42 0.039
522
c MCR130 Microvascular Complications of Diabetes 6 42 0.039
523
STT004 Steatorrhea 41 0.039
524
SPR005 Superficial Basal Cell Carcinoma 40 0.039
525
TNC003 Tinea Corporis 40 0.039
526
c CNT028 Central Retinal Artery Occlusion 40 0.039
527
ALN001 Aland Island Eye Disease 39 0.039
528
P BLD051 Blood Coagulation Disease 38 0.039
529
PRS063 Paresthesia 36 0.039
530
P PRS013 Prosopagnosia 34 0.039
531
c MCR120 Microvascular Complications of Diabetes 7 34 0.039
532
FND002 Fundus Dystrophy 34 0.039
533
c MCR133 Microvascular Complications of Diabetes 4 32 0.039
534
P KLZ004 Kala-Azar 1 31 0.039
535
c MGR031 Migraine, Familial Hemiplegic, 3 24 0.039
536
BLD163 Blood Group, Dombrock System 23 0.039
537
P HPT023 Hepatocellular Carcinoma 94 0.036
538
c LKM061 Leukemia, Acute Myeloid 81 0.036
539
P MYL005 Myelofibrosis 75 0.036
540
ALP046 Alport Syndrome, X-Linked 74 0.036
541
SQM006 Squamous Cell Carcinoma 74 0.036
542
PHN003 Phenylketonuria 73 0.036
543
PRP027 Peripheral Vascular Disease 71 0.036
544
P TYS001 Tay-Sachs Disease 71 0.036
545
ACR007 Acromegaly 70 0.036
546
P FRG001 Fragile X Syndrome 69 0.036
547
P MYL006 Myeloid Leukemia 69 0.036
548
P CHR071 Charcot-Marie-Tooth Disease 67 0.036
549
APN008 Apnea, Obstructive Sleep 67 0.036
550
P PRD008 Periodontitis 67 0.036
551
VSC011 Vasculitis 66 0.036
552
CTN007 Cutaneous Leishmaniasis 66 0.036
553
SND001 Sandhoff Disease 65 0.036
554
P DRM010 Dermatomyositis 65 0.036
555
CHL123 Chlamydia 64 0.036
556
PRD007 Periodontal Disease 64 0.036
557
P NRC002 Narcolepsy 64 0.036
558
P CMR001 Camurati-Engelmann Disease 62 0.036
559
ETN001 Eating Disorder 61 0.036
560
PPT005 Peptic Ulcer Disease 60 0.036
561
ERY003 Erythema Multiforme 60 0.036
562
END030 End Stage Renal Failure 59 0.036
563
c BCT007 Bacterial Meningitis 59 0.036
564
P INT030 Intracranial Aneurysm 58 0.036
565
P END033 Endocarditis 58 0.036
566
VRN004 Vernal Keratoconjunctivitis 56 0.036
567
PRS042 Prostate Disease 56 0.036
568
HYP060 Hyperinsulinism 56 0.036
569
PLS006 Plasmodium Vivax Malaria 56 0.036
570
GST037 Gastroparesis 56 0.036
571
PRV006 Pervasive Developmental Disorder 56 0.036
572
OST024 Osteoporosis-Pseudoglioma Syndrome 55 0.036
573
PNM001 Pneumocystosis 55 0.036
574
STR020 Strabismus 55 0.036
575
TRM010 Traumatic Brain Injury 54 0.036
576
CND002 Conduct Disorder 54 0.036
577
P CNV004 Canavan Disease 54 0.036
578
HYP080 Hypogonadism 54 0.036
579
THR016 Thrombophlebitis 53 0.036
580
MTN003 Motion Sickness 52 0.036
581
DRY001 Dry Eye Syndrome 51 0.036
582
CCN002 Cocaine Abuse 50 0.036
583
VCC001 Vaccinia 50 0.036
584
GNG011 Gingival Disease 50 0.036
585
HPT014 Hepatorenal Syndrome 49 0.036
586
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.036
587
P LCT002 Lactose Intolerance 48 0.036
588
CRN024 Corneal Disease 47 0.036
589
MLK006 Milk Allergy 46 0.036
590
STT002 Status Asthmaticus 46 0.036
591
ATN004 Autonomic Neuropathy 46 0.036
592
AMB002 Amblyopia 45 0.036
593
CRN031 Cranial Nerve Disease 45 0.036
594
PNN005 Panencephalitis, Subacute Sclerosing 44 0.036
595
TRC003 Trichomoniasis 44 0.036
596
DYS015 Dysentery 43 0.036
597
PCH007 Pouchitis 42 0.036
598
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.036
599
P VSC018 Visceral Steatosis 38 0.036
600
VSM001 Vasomotor Rhinitis 38 0.036
601
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.036
602
BTT001 Bietti Crystalline Corneoretinal Dystrophy 35 0.036
603
PHS001 Phosphorus Metabolism Disease 34 0.036
604
CNT017 Central Nervous System Origin Vertigo 30 0.036
605
ANS006 Anosognosia 27 0.036
606
UVL003 Uveal Diseases 23 0.036
607
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.036
608
ATR076 Atrophic Muscular Disease 6 0.036
609
GST053 Gastric Cancer 84 0.033
610
P OVR042 Ovarian Cancer 82 0.033
611
P RTN024 Retinoblastoma 76 0.033
612
MYL009 Myelodysplastic Syndrome 75 0.033
613
P GRF003 Graft-Versus-Host Disease 72 0.033
614
c JVN010 Juvenile Rheumatoid Arthritis 71 0.033
615
P BCL006 B-Cell Lymphomas 70 0.033
616
P MYC084 Mycobacterium Tuberculosis 1 69 0.033
617
P CRN037 Craniosynostosis 68 0.033
618
P PRD006 Prader-Willi Syndrome 66 0.033
619
P THR014 Thrombocytopenia 65 0.033
620
OVR029 Ovarian Hyperstimulation Syndrome 64 0.033
621
c TBR025 Tuberous Sclerosis 1 63 0.033
622
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.033
623
P PRP029 Porphyria 62 0.033
624
DFC004 Deficiency Anemia 62 0.033
625
SCH014 Schistosomiasis 62 0.033
626
P AGN002 Agnosia 61 0.033
627
P SPN052 Spondyloarthropathy 61 0.033
628
c SCL052 Scleroderma, Familial Progressive 60 0.033
629
PGT001 Paget's Disease of Bone 60 0.033
630
STT001 Status Epilepticus 60 0.033
631
CLR108 Colorectal Adenoma 60 0.033
632
TRG002 Trigeminal Neuralgia 60 0.033
633
CCC001 Coccidioidomycosis 60 0.033
634
RTN017 Retinal Detachment 59 0.033
635
LYM019 Lymphosarcoma 58 0.033
636
P PLY006 Polydactyly 57 0.033
637
P LRY019 Laryngitis 57 0.033
638
AND002 Androgen Insensitivity Syndrome 57 0.033
639
P PMP005 Pemphigus Vulgaris 56 0.033
640
FCL014 Focal Epilepsy 56 0.033
641
P HYP750 Hypertriglyceridemia, Familial 55 0.033
642
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.033
643
P PMP001 Pemphigus 55 0.033
644
PST021 Postpartum Depression 54 0.033
645
P DBT005 Diabetes Insipidus 54 0.033
646
c SVR005 Severe Pre-Eclampsia 53 0.033
647
PRP016 Paraplegia 53 0.033
648
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 53 0.033
649
VLV011 Vulvovaginal Candidiasis 53 0.033
650
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.033
651
PRN021 Paranasal Sinus Disease 51 0.033
652
RFL001 Reflex Sympathetic Dystrophy 51 0.033
653
PPL021 Papilledema 50 0.033
654
BLL003 Bell's Palsy 49 0.033
655
ANV001 Anovulation 48 0.033
656
AGR002 Agoraphobia 47 0.033
657
P HYP263 Hypersomnia 45 0.033
658
EXC002 Exocrine Pancreatic Insufficiency 45 0.033
659
MLL001 Molluscum Contagiosum 43 0.033
660
SHL001 Shoulder Impingement Syndrome 43 0.033
661
CWM001 Cow Milk Allergy 42 0.033
662
CNV002 Conversion Disorder 42 0.033
663
LKP003 Leukoplakia 42 0.033
664
BRS064 Bursitis 42 0.033
665
SPN050 Spinocerebellar Degeneration 41 0.033
666
P HMF004 Hemifacial Spasm 41 0.033
667
c ALC033 Alcohol Use Disorder 40 0.033
668
HYP030 Hypoactive Sexual Desire Disorder 40 0.033
669
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.033
670
CRV002 Cervix Uteri Carcinoma in Situ 40 0.033
671
PPT001 Peptic Esophagitis 40 0.033
672
PST055 Postural Hypotension 40 0.033
673
ALG001 Algoneurodystrophy 39 0.033
674
HYP332 Hypotrichosis, Congenital, with Juvenile Macular Dystrophy 39 0.033
675
P MXL015 Maxillary Sinusitis 39 0.033
676
CPL005 Capillary Disease 38 0.033
677
CHR415 Chronic Venous Leg Ulcers 38 0.033
678
DLT018 Dilution, Pigmentary 37 0.033
679
URT020 Ureterocele 37 0.033
680
c OST126 Osteopetrosis, Autosomal Recessive 1 36 0.033
681
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.033
682
PSD021 Pseudovaginal Perineoscrotal Hypospadias 34 0.033
683
DDN009 Duodenal Obstruction 34 0.033
684
ACR118 Aicar Transformylase/imp Cyclohydrolase Deficiency 31 0.033
685
PTL002 Patellofemoral Pain Syndrome 30 0.033
686
CVR002 Cavernous Sinus Thrombosis 28 0.033
687
PRR001 Periarthritis 27 0.033
688
CNR014 Cone-Rod Dystrophy 16 26 0.033
689
c PMP006 Pemphigus Vulgaris, Familial 26 0.033
690
MLN046 Melanoma-Associated Retinopathy 24 0.033
691
SPH007 Sphenoid Sinusitis 24 0.033
692
HPD002 Hepadnavirus Infection 14 0.033
693
P PNC035 Pancreatic Cancer 89 0.029
694
MYL069 Myeloma, Multiple 86 0.029
695
P FML018 Familial Mediterranean Fever 73 0.029
696
MLD001 Melioidosis 73 0.029
697
P END044 Endometriosis 71 0.029
698
P KRB001 Krabbe Disease 70 0.029
699
c MNN043 Meningioma, Familial 69 0.029
700
P PLM036 Pulmonary Fibrosis 68 0.029
701
LYM017 Lyme Disease 68 0.029
702
SRC014 Sarcoma 68 0.029
703
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.029
704
P NRM001 Neuromyelitis Optica 67 0.029
705
HSH003 Hashimoto Thyroiditis 67 0.029
706
P THL005 Thalassemia 65 0.029
707
DFF005 Diffuse Large B-Cell Lymphoma 64 0.029
708
MSC152 Muscular Dystrophy, Becker Type 64 0.029
709
RBS001 Rabies 63 0.029
710
OST003 Osteonecrosis 63 0.029
711
P MYS005 Myositis 63 0.029
712
MRB003 Morbid Obesity 61 0.029
713
BRN056 Bronchopulmonary Dysplasia 61 0.029
714
P MMP001 Mumps 61 0.029
715
c THR092 Thrombophilia Due to Thrombin Defect 61 0.029
716
P RBL001 Rubella 61 0.029
717
CHL068 Cholestasis 60 0.029
718
P PRT013 Portal Hypertension 59 0.029
719
c HRD002 Hereditary Angioedema 59 0.029
720
JPN002 Japanese Encephalitis 59 0.029
721
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 59 0.029
722
P LPR021 Leprosy 3 59 0.029
723
FLR002 Filariasis 58 0.029
724
HMT018 Hematopoietic Stem Cell Transplantation 58 0.029
725
c GLC092 Glaucoma, Primary Open Angle 58 0.029
726
PLM012 Pulmonary Sarcoidosis 58 0.029
727
GLC003 Glucose Intolerance 58 0.029
728
P MCR010 Microcephaly 57 0.029
729
WST001 West Syndrome 57 0.029
730
ECT006 Ectodermal Dysplasia 57 0.029
731
CYT008 Cytomegalovirus Infection 57 0.029
732
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 57 0.029
733
P STC001 Stickler Syndrome 56 0.029
734
P SCL018 Scoliosis 56 0.029
735
MYM001 Myoma 56 0.029
736
BRN022 Bronchiectasis 55 0.029
737
TBC004 Tobacco Addiction 55 0.029
738
BLR006 Biliary Tract Disease 55 0.029
739
SCK005 Sickle Cell Disease 54 0.029
740
TCD001 Tic Disorder 54 0.029
741
PRP080 Peripheral Artery Disease 54 0.029
742
QDR001 Quadriplegia 54 0.029
743
c ANT034 Anterior Uveitis 53 0.029
744
P CTN003 Cutaneous Lupus Erythematosus 53 0.029
745
INT075 Intracranial Hypertension 53 0.029
746
P PNV001 Panuveitis 52 0.029
747
GRW007 Growth Hormone Deficiency 52 0.029
748
CCC002 Coccidiosis 52 0.029
749
ECT026 Ectopic Pregnancy 52 0.029
750
OCL006 Ocular Hypertension 51 0.029
751
MCL006 Macular Retinal Edema 51 0.029
752
CYT005 Cytomegalovirus Retinitis 51 0.029
753
CHR001 Churg-Strauss Syndrome 51 0.029
754
ATN002 Autonomic Nervous System Disease 51 0.029
755
c STR084 Stargardt Disease 1 51 0.029
756
THY030 Thyroid Gland Disease 51 0.029
757
ATN005 Autonomic Dysfunction 51 0.029
758
P END046 Endometritis 51 0.029
759
STR072 Stromal Keratitis 50 0.029
760
SPP008 Suppurative Otitis Media 50 0.029
761
c PRM108 Primary Progressive Multiple Sclerosis 50 0.029
762
SCL003 Social Phobia 50 0.029
763
P MYM013 Moyamoya Disease 1 50 0.029
764
ANX004 Anoxia 49 0.029
765
DBT006 Diabetic Macular Edema 49 0.029
766
P KRT007 Keratoconus 49 0.029
767
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.029
768
PRM020 Premenstrual Tension 49 0.029
769
EWN002 Ewing's Family of Tumors 49 0.029
770
PNT038 Peanut Allergy 48 0.029
771
ISC002 Ischemic Optic Neuropathy 48 0.029
772
PLC008 Placenta Disease 48 0.029
773
PLY020 Polyradiculoneuropathy 48 0.029
774
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.029
775
P DYS021 Dysautonomia 47 0.029
776
DNG001 Dengue Shock Syndrome 47 0.029
777
P NLD001 Nail Disease 47 0.029
778
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.029
779
c USH021 Usher Syndrome, Type Iid 46 0.029
780
SWN001 Swine Influenza 46 0.029
781
PRD004 Prediabetes Syndrome 46 0.029
782
ENH001 Enhanced S-Cone Syndrome 46 0.029
783
CRY014 Cryptococcal Meningitis 45 0.029
784
MLT075 Multifocal Motor Neuropathy 45 0.029
785
VLV010 Vulvovaginitis 45 0.029
786
ACT058 Active Peptic Ulcer Disease 43 0.029
787
SYM002 Sympathetic Ophthalmia 43 0.029
788
NRN002 Neuronitis 43 0.029
789
CRT008 Carotid Artery Dissection 42 0.029
790
ADS004 Aids Dementia Complex 42 0.029
791
CNN001 Cannabis Dependence 42 0.029
792
c LBR019 Leber Congenital Amaurosis 9 41 0.029
793
BRS090 Breast Reconstruction 41 0.029
794
EGG001 Egg Allergy 41 0.029
795
c MCR263 Microphthalmia, Syndromic 1 41 0.029
796
c RTN058 Retinitis Pigmentosa 3 40 0.029
797
P CHR084 Chromosomal Disease 40 0.029
798
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.029
799
HPT004 Hepatic Coma 40 0.029
800
P SBR004 Seborrheic Dermatitis 40 0.029
801
WHP002 Whiplash 39 0.029
802
OPH002 Ophthalmia Neonatorum 38 0.029
803
c ACT059 Acute Maxillary Sinusitis 38 0.029
804
PRP028 Peripheral Vertigo 37 0.029
805
CHR079 Choroid Disease 37 0.029
806
c LTN004 Late-Onset Retinal Degeneration 37 0.029
807
P GRM010 Germ Cells Tumors 37 0.029
808
IRT001 Iritis 36 0.029
809
VSC008 Vascular Hemostatic Disease 36 0.029
810
LSS001 Loiasis 36 0.029
811
INT003 Intracranial Hypotension 36 0.029
812
TNS014 Tenosynovitis 35 0.029
813
TNN002 Tinea Unguium 35 0.029
814
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.029
815
CYT004 Cytomegalic Inclusion Disease 35 0.029
816
c RTN041 Retinitis Pigmentosa 11 35 0.029
817
P SMK004 Smoking As a Quantitative Trait Locus 3 34 0.029
818
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.029
819
c BLP048 Blepharospasm, Benign Essential 33 0.029
820
GND003 Gonadal Disease 32 0.029
821
MMS001 Momo Syndrome 32 0.029
822
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.029
823
PST036 Posterior Column Ataxia with Retinitis Pigmentosa 31 0.029
824
c NRM008 Neuromyelitis Optica Spectrum Disorder 30 0.029
825
MCP039 Mucoepithelial Dysplasia, Hereditary 30 0.029
826
URN022 Urinary Tract Infections, Recurrent 29 0.029
827
SPN340 Spontaneous Intracranial Hypotension 28 0.029
828
c RTN064 Retinitis Pigmentosa 35 28 0.029
829
TTN001 Tetanus Neonatorum 28 0.029
830
CRY024 Crystal Arthropathies 26 0.029
831
c EXD004 Exudative Vitreoretinopathy 4 25 0.029
832
ULC008 Ulcerative Proctitis 24 0.029
833
ULC005 Ulcer of Lower Limbs 23 0.029
834
MLK001 Milker's Nodule 21 0.029
835
OPH014 Ophthalmomandibulomelic Dysplasia 19 0.029
836
RNL111 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia 18 0.029
837
P RTN200 Retinopathy, Pericentral Pigmentary, Dominant 14 0.029
838
P HYP607 Hypercholesterolemia, Familial 81 0.026
839
c LKM071 Leukemia, Chronic Lymphocytic 75 0.026
840
MRF001 Marfan Syndrome 75 0.026
841
SCK003 Sickle Cell Anemia 73 0.026
842
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.026
843
PLM001 Pulmonary Tuberculosis 72 0.026
844
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.026
845
FBR012 Fabry Disease 72 0.026
846
P RSP003 Respiratory Failure 71 0.026
847
BRC012 Brucellosis 71 0.026
848
DWN001 Down Syndrome 70 0.026
849
c HMP029 Hemophilia a 69 0.026
850
P ADL010 Adult Respiratory Distress Syndrome 67 0.026
851
P SYS005 Systemic Scleroderma 67 0.026
852
NRF007 Neurofibroma 65 0.026
853
CRT072 Creutzfeldt-Jakob Disease 65 0.026
854
INC002 Inclusion Body Myositis 64 0.026
855
HYP020 Hyperprolactinemia 64 0.026
856
HLC007 Helicobacter Pylori Infection 64 0.026
857
P SRC025 Sarcoidosis 1 63 0.026
858
KRT001 Keratoconjunctivitis Sicca 63 0.026
859
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.026
860
RFS006 Refsum Disease, Classic 63 0.026
861
P LYM025 Lymphedema 63 0.026
862
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.026
863
MTR014 Motor Neuron Disease 62 0.026
864
MCR013 Microphthalmia 61 0.026
865
CLF027 Cleft Palate, Isolated 61 0.026
866
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.026
867
P GLM045 Glioma 61 0.026
868
IDP011 Idiopathic Interstitial Pneumonia 60 0.026
869
P NTR004 Neutropenia 60 0.026
870
P PLY014 Polycystic Kidney Disease 60 0.026
871
PRP083 Porphyria, Acute Intermittent 60 0.026
872
P HMR012 Hemorrhagic Fever 60 0.026
873
P FCL005 Focal Segmental Glomerulosclerosis 60 0.026
874
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.026
875
c PRM005 Primary Hyperparathyroidism 59 0.026
876
SNS001 Sensorineural Hearing Loss 59 0.026
877
STR039 Sturge-Weber Syndrome 59 0.026
878
ALL026 Allergic Hypersensitivity Disease 59 0.026
879
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.026
880
TRN015 Transient Cerebral Ischemia 58 0.026
881
SFT003 Soft Tissue Sarcoma 58 0.026
882
LMY002 Leiomyoma 58 0.026
883
P SML001 Small Cell Carcinoma 58 0.026
884
VSC002 Vascular Dementia 58 0.026
885
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.026
886
P THR015 Thrombophilia 58 0.026
887
INT146 Intervertebral Disc Disease 58 0.026
888
TRN018 Transitional Cell Carcinoma 58 0.026
889
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.026
890
IMM158 Immune Suppression 57 0.026
891
P LPD010 Lipodystrophy 57 0.026
892
BRN004 Brain Edema 57 0.026
893
HYP052 Hyperkalemic Periodic Paralysis 57 0.026
894
LBR002 Leber Hereditary Optic Neuropathy 57 0.026
895
CHL014 Cholera 56 0.026
896
PTT009 Pituitary Gland Disease 56 0.026
897
INF034 Infective Endocarditis 56 0.026
898
PLV003 Pelvic Inflammatory Disease 56 0.026
899
DSS009 Disseminated Intravascular Coagulation 56 0.026
900
ESN005 Eosinophilic Gastroenteritis 56 0.026
901
PRM236 Primary Biliary Cholangitis 56 0.026
902
P ESP035 Esophagitis, Eosinophilic, 1 55 0.026
903
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.026
904
TXC002 Toxic Encephalopathy 55 0.026
905
INT007 Intermediate Coronary Syndrome 55 0.026
906
STR008 Strongyloidiasis 54 0.026
907
HDR002 Hidradenitis Suppurativa 54 0.026
908
CLF001 Cleft Lip 54 0.026
909
ESP020 Esophageal Atresia 54 0.026
910
OPT003 Opiate Dependence 54 0.026
911
c ACT071 Acute Kidney Failure 54 0.026
912
c VSC019 Vesicoureteral Reflux 1 54 0.026
913
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.026
914
P SCL009 Sclerosing Cholangitis 53 0.026
915
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 53 0.026
916
CGN006 Cogan Syndrome 53 0.026
917
P EPD003 Epidermolysis Bullosa Simplex 53 0.026
918
DFF035 Diffuse Cutaneous Systemic Sclerosis 53 0.026
919
BRD025 Birdshot Chorioretinopathy 53 0.026
920
ALC009 Alcoholic Liver Cirrhosis 53 0.026
921
c BLM008 Bulimia Nervosa 2 53 0.026
922
P OVR046 Ovarian Cyst 52 0.026
923
CRN030 Coronary Stenosis 52 0.026
924
CRT013 Carotid Stenosis 52 0.026
925
BLD036 Bile Duct Disease 52 0.026
926
PLR008 Pleurisy 52 0.026
927
MYL001 Myelitis 52 0.026
928
c FRS014 Fraser Syndrome 1 51 0.026
929
CLC006 Calcinosis 51 0.026
930
CRY003 Cryptosporidiosis 51 0.026
931
P ATR005 Atrophic Gastritis 51 0.026
932
ORL005 Oral Candidiasis 51 0.026
933
DRG003 Drug Dependence 51 0.026
934
c ERL020 Early-Onset Schizophrenia 51 0.026
935
P OTT001 Otitis Externa 51 0.026
936
P END047 Endophthalmitis 51 0.026
937
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.026
938
SCB001 Scabies 50 0.026
939
HYP043 Hyperandrogenism 50 0.026
940
c RTN162 Retinitis Pigmentosa 2 50 0.026
941
BRD004 Borderline Personality Disorder 50 0.026
942
NDL007 Nodular Goiter 50 0.026
943
THR013 Thoracic Outlet Syndrome 50 0.026
944
ESN011 Eisenmenger Syndrome 49 0.026
945
HMP009 Haemophilus Influenzae 49 0.026
946
MTB004 Metabolic Acidosis 49 0.026
947
PRN009 Paranoid Schizophrenia 49 0.026
948
c MLG069 Malignant Hypertension 49 0.026
949
FBR009 Fibrous Dysplasia 49 0.026
950
CLS016 Clostridium Difficile Colitis 49 0.026
951
BCT004 Bacteriuria 49 0.026
952
FRZ001 Frozen Shoulder 48 0.026
953
DBT008 Diabetic Angiopathy 48 0.026
954
CHC001 Chickenpox 48 0.026
955
MLT006 Multidrug-Resistant Tuberculosis 48 0.026
956
HYP457 Hypertrophic Scars 48 0.026
957
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.026
958
P HYP087 Hypotrichosis 48 0.026
959
P CRN028 Corneal Ulcer 48 0.026
960
c LBR012 Leber Congenital Amaurosis 2 47 0.026
961
HDR003 Hidradenitis 47 0.026
962
DST006 Diastolic Heart Failure 47 0.026
963
ESP002 Esophageal Varix 46 0.026
964
SDD008 Sudden Sensorineural Hearing Loss 46 0.026
965
NRR001 Neuroretinitis 46 0.026
966
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 46 0.026
967
c USH037 Usher Syndrome, Type Iia 45 0.026
968
BLD053 Blood Platelet Disease 45 0.026
969
ALB002 Albinism 45 0.026
970
CHR056 Chronic Tic Disorder 45 0.026
971
ESN004 Eosinophilic Gastritis 44 0.026
972
DFF003 Diffuse Scleroderma 44 0.026
973
IRD001 Iridocyclitis 44 0.026
974
RHY001 Rhyns Syndrome 44 0.026
975
PRS055 Pierson Syndrome 43 0.026
976
BDY001 Body Dysmorphic Disorder 43 0.026
977
IMP006 Impulse Control Disorder 43 0.026
978
PHB001 Phobic Disorder 42 0.026
979
TND005 Tendinitis 42 0.026
980
c RTN043 Retinitis Pigmentosa 13 41 0.026
981
ZKF001 Zika Fever 41 0.026
982
JLL001 Jalili Syndrome 41 0.026
983
c CHR048 Chronic Rhinitis 41 0.026
984
CMM003 Common Wart 41 0.026
985
JJN008 Jejunoileitis 41 0.026
986
MLT001 Multiple Chemical Sensitivity 40 0.026
987
AYM001 Ayme-Gripp Syndrome 40 0.026
988
CHR073 Choreatic Disease 40 0.026
989
KLP001 Kleptomania 40 0.026
990
PRR013 Prurigo Nodularis 39 0.026
991
DLY008 Delayed Sleep Phase Disorder 38 0.026
992
DDN007 Duodenal Disease 38 0.026
993
TRP004 Tropical Sprue 38 0.026
994
c RTN069 Retinitis Pigmentosa 7 38 0.026
995
c BCT006 Bacterial Conjunctivitis 37 0.026
996
PRL047 Prolonged Electroretinal Response Suppression 37 0.026
997
NTL004 Nut Allergy 37 0.026
998
c LKM004 Leukemia, B-Cell, Chronic 37 0.026
999
ORL022 Oral Erosive Lichen 36 0.026
1000
c RTN055 Retinitis Pigmentosa 26 36 0.026
1001
HYD001 Hydranencephaly 36 0.026
1002
BSM002 Bosma Arhinia Microphthalmia Syndrome 35 0.026
1003
URT037 Urethral Stricture 35 0.026
1004
BSL004 Basilar Artery Occlusion 35 0.026
1005
c LBR007 Leber Congenital Amaurosis 12 35 0.026
1006
MLT035 Multifocal Choroiditis 35 0.026
1007
SKN020 Skin Papilloma 34 0.026
1008
SGT001 Sagittal Sinus Thrombosis 34 0.026
1009
LKC003 Leukocyte Disease 34 0.026
1010
c AXN012 Axenfeld-Rieger Syndrome, Type 2 34 0.026
1011
VGN019 Vaginal Discharge 34 0.026
1012
PLS030 Plasminogen Deficiency, Type I 33 0.026
1013
GST039 Gastroduodenitis 33 0.026
1014
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 33 0.026
1015
c RTN131 Retinitis Pigmentosa 27 33 0.026
1016
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.026
1017
DGN003 Degeneration of Macula and Posterior Pole 32 0.026
1018
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.026
1019
VSC012 Vesiculobullous Skin Disease 32 0.026
1020
PDN001 Pudendal Neuralgia 31 0.026
1021
STR019 Steroid-Induced Glaucoma 30 0.026
1022
INT065 Interstitial Keratitis 29 0.026
1023
P PRD017 Periodic Paralyses 29 0.026
1024
ZKV001 Zika Virus Infection 28 0.026
1025
c RTN070 Retinitis Pigmentosa 9 28 0.026
1026
P STR035 Streptococcal Group a Invasive Disease 28 0.026
1027
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.026
1028
c RTN140 Retinitis Pigmentosa 67 26 0.026
1029
SVR058 Severe Early-Childhood-Onset Retinal Dystrophy 25 0.026
1030
HYP213 Hypomelanotic Disorder 25 0.026
1031
CPG001 Capgras Syndrome 25 0.026
1032
MNS002 Mini Stroke 23 0.026
1033
DTR001 Detrusor Sphincter Dyssynergia 23 0.026
1034
BTH002 Bothnia Retinal Dystrophy 22 0.026
1035
NDD001 Nodding Syndrome 22 0.026
1036
CRB087 Cerebral Arteriosclerosis 20 0.026
1037
ERY010 Erythrasma 20 0.026
1038
c NPH069 Nephronophthisis 15 19 0.026
1039
LYM053 Lymphomatous Thyroiditis 19 0.026
1040
c EXD006 Exudative Vitreoretinopathy 5 19 0.026
1041
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 18 0.026
1042
P ACT061 Acute Sphenoidal Sinusitis 15 0.026
1043
AKN001 Akinetopsia 10 0.026
1044
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.021
1045
GLB002 Glioblastoma 74 0.021
1046
P MYS003 Myasthenia Gravis 73 0.021
1047
THY028 Thyroid Cancer 72 0.021
1048
P CRV035 Cervical Cancer 72 0.021
1049
P MTC003 Metachromatic Leukodystrophy 72 0.021
1050
ADR007 Adrenoleukodystrophy 72 0.021
1051
BRN028 Brain Cancer 72 0.021
1052
PTZ001 Peutz-Jeghers Syndrome 70 0.021
1053
ART016 Aortic Aneurysm 70 0.021
1054
P TTR001 Tetralogy of Fallot 70 0.021
1055
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.021
1056
LYM007 Lymphangioleiomyomatosis 68 0.021
1057
BSL036 Basal Cell Nevus Syndrome 67 0.021
1058
TYP007 Typhoid Fever 67 0.021
1059
P LYM026 Lymphoblastic Leukemia 66 0.021
1060
c LCL006 Localized Scleroderma 66 0.021
1061
P TXP001 Toxoplasmosis 65 0.021
1062
P ASP006 Aspergillosis 65 0.021
1063
MLT157 Multiple System Atrophy 1 65 0.021
1064
c CHR417 Chronic Graft Versus Host Disease 65 0.021
1065
SYS004 Systemic Mastocytosis 65 0.021
1066
MCC012 Mccune-Albright Syndrome 65 0.021
1067
GLL008 Gilles De La Tourette Syndrome 64 0.021
1068
P GLL020 Gallbladder Disease 64 0.021
1069
OST017 Osteomyelitis 64 0.021
1070
FCT002 Factor Xi Deficiency 64 0.021
1071
PMS001 Poems Syndrome 64 0.021
1072
BRR014 Barrett Esophagus 64 0.021
1073
c ACT210 Acute Respiratory Distress Syndrome 63 0.021
1074
CRN036 Craniopharyngioma 63 0.021
1075
P PLV020 Pelvic Organ Prolapse 63 0.021
1076
SKN019 Skin Melanoma 63 0.021
1077
P ALC004 Alcohol Abuse 63 0.021
1078
P HRM001 Hermansky-Pudlak Syndrome 62 0.021
1079
CNC002 Cinca Syndrome 62 0.021
1080
PLM033 Pulmonary Embolism 62 0.021
1081
P GRV001 Graves' Disease 62 0.021
1082
LYM021 Lymphadenitis 62 0.021
1083
c MCR129 Microvascular Complications of Diabetes 1 62 0.021
1084
c USH036 Usher Syndrome, Type I 61 0.021
1085
NRV006 Nervous System Cancer 61 0.021
1086
STF001 Stiff-Person Syndrome 61 0.021
1087
TXC005 Toxic Shock Syndrome 61 0.021
1088
LMY014 Leiomyoma, Uterine 61 0.021
1089
BLS001 Blau Syndrome 60 0.021
1090
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 60 0.021
1091
P GST049 Gastrointestinal System Cancer 60 0.021
1092
c CHL119 Cholangitis, Primary Sclerosing 60 0.021
1093
P ANT006 Antiphospholipid Syndrome 59 0.021
1094
P MTR012 Mitral Valve Disease 59 0.021
1095
P PLM034 Pulmonary Emphysema 59 0.021
1096
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.021
1097
ICH054 Ichthyosis, X-Linked 59 0.021
1098
PPL022 Papilloma 58 0.021
1099
P FRD012 Friedreich Ataxia 1 58 0.021
1100
PRT118 Protoporphyria, Erythropoietic 58 0.021
1101
P OVR049 Ovarian Disease 58 0.021
1102
OCL020 Ocular Cicatricial Pemphigoid 58 0.021
1103
ANN002 Anencephaly 57 0.021
1104
P WRD001 Waardenburg's Syndrome 57 0.021
1105
P SBS003 Substance Abuse 57 0.021
1106
P PLY041 Polymyositis 57 0.021
1107
VND007 Van Der Woude Syndrome 1 57 0.021
1108
P PTT006 Pituitary Adenoma 57 0.021
1109
SLC006 Silicosis 57 0.021
1110
PLM010 Pulmonary Edema 57 0.021
1111
NPH009 Nephrolithiasis 57 0.021
1112
NWB001 Newborn Respiratory Distress Syndrome 56 0.021
1113
MTC007 Mitochondrial Complex I Deficiency 56 0.021
1114
HYP730 Hypogonadotropic Hypogonadism 56 0.021
1115
LYS002 Lysosomal Storage Disease 56 0.021
1116
c MYT020 Myotonic Dystrophy 2 56 0.021
1117
BLR001 Biliary Atresia 56 0.021
1118
LYM027 Lymphopenia 56 0.021
1119
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.021
1120
IGR001 Ige Responsiveness, Atopic 56 0.021
1121
RLP001 Relapsing Polychondritis 55 0.021
1122
P INT070 Intestinal Obstruction 55 0.021
1123
P UTR058 Uterine Anomalies 55 0.021