Search results for blindness

3144 hits were found for blindness

# Family MCID Name MIFTS Score
1
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 4.923
2
c NGH014 Night Blindness, Congenital Stationary , 1b, Autosomal Recessive 30 4.567
3
c NGH008 Night Blindness, Congenital Stationary, Autosomal Dominant 3 21 4.355
4
c NGH010 Night Blindness, Congenital Stationary, Autosomal Dominant 2 23 4.352
5
c NGH021 Night Blindness, Congenital Stationary, Autosomal Dominant 1 22 4.151
6
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 4.084
7
P XLN012 X-Linked Congenital Stationary Night Blindness 29 4.039
8
c NGH013 Night Blindness, Congenital Stationary , 1f, Autosomal Recessive 21 3.952
9
P CNG010 Congenital Stationary Night Blindness 53 3.744
10
P CLR019 Color Blindness 46 3.742
11
c NGH018 Night Blindness, Congenital Stationary , 1e, Autosomal Recessive 27 3.737
12
c NGH017 Night Blindness, Congenital Stationary , 1d, Autosomal Recessive 22 3.737
13
c NGH016 Night Blindness, Congenital Stationary , 1c, Autosomal Recessive 25 3.729
14
c NGH020 Night Blindness, Congenital Stationary , 2a, X-Linked 23 3.723
15
P NGH001 Night Blindness 48 3.375
16
NRR002 Norrie Disease 60 3.237
17
c HRD015 Hereditary Night Blindness 36 3.228
18
CRT012 Cortical Blindness 35 3.058
19
P ACH003 Achromatopsia 55 2.960
20
c NGH022 Night Blindness, Congenital Stationary, Type 1g 17 2.947
21
BLN006 Blind Loop Syndrome 28 2.790
22
RDG001 Red-Green Color Blindness 30 2.658
23
RDR002 Rodrigues Blindness 15 2.644
24
CLR064 Colorblindness, Tritan 32 2.633
25
BLC005 Blue Color Blindness 29 2.633
26
c SPN295 Spinocerebellar Ataxia, Autosomal Recessive 3 24 2.624
27
c CNG169 Congenital Stationary Night Blindness, Type 2b 14 2.624
28
c ACH036 Achromatopsia-3 41 2.613
29
c ATS169 Autosomal Recessive Congenital Stationary Night Blindness 25 2.336
30
P OGC003 Oguchi Disease-1 17 2.293
31
c CNG484 Congenital Stationary Night Blindness 1h 12 2.293
32
RDC001 Red Color Blindness 30 2.289
33
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 16 2.289
34
SCT002 Scotoma 40 2.275
35
MHR001 Mohr-Tranebjaerg Syndrome 41 2.269
36
RTN084 Retinal Cone Dystrophy 3 26 2.269
37
ONC002 Onchocerciasis 49 1.972
38
KRT002 Keratomalacia 52 1.949
39
c ATS168 Autosomal Dominant Congenital Stationary Night Blindness 28 1.923
40
P LBR001 Leber Congenital Amaurosis 61 1.885
41
c OGC004 Oguchi Disease-2 18 1.881
42
CLR033 Color Vision Deficiency 29 1.877
43
NGH002 Night Blindness Skeletal Anomalies Unusual Facies 3 1.872
44
BLN008 Blind Hypotensive Eye 14 1.867
45
MCR054 Microcephaly Microphthalmos Blindness 2 1.867
46
BLC001 Blue Cone Monochromacy 40 1.862
47
CRT080 Cortical Blindness, Retardation, and Postaxial Polydactyly 12 1.862
48
BLN007 Blind Hypertensive Eye 11 1.862
49
SCL050 Scoliosis, Arachnodactyly, and Blindness 7 1.862
50
AMS002 Amish Infantile Epilepsy Syndrome 35 1.855
51
c EPL123 Epileptic Encephalopathy, Early Infantile, 23 25 1.855
52
RTN035 Retinal Cone Dystrophy 3b 24 1.855
53
RDG002 Red-Green Color Vision Defects 21 1.855
54
c ACQ002 Acquired Night Blindness 11 1.350
55
ANT040 Anton's Syndrome 19 1.346
56
AMR003 Amaurosis Fugax 38 1.336
57
c ACQ001 Acquired Color Blindness 12 1.336
58
CHN047 Chondroectodermal Dysplasia with Night Blindness 12 1.336
59
OST144 Osteoporosis-Macrocephaly-Blindness-Joint Hyperlaxity Syndrome 9 1.336
60
ECT016 Ectodermal Dysplasia Blindness 3 1.336
61
NGH023 Night Blindness-Skeletal Anomalies-Dysmorphism Syndrome 10 1.330
62
CRT031 Cortical Blindness Mental Retardation Polydactyly 2 1.330
63
CLR063 Colorblindness, Deutan 31 1.324
64
CLR062 Colorblindness, Protan 24 1.324
65
BCR005 Bicervical Bicornuate Uterus and Blind Hemivagina 5 1.324
66
c CCN004 Cacna1f-Related X-Linked Congenital Stationary Night Blindness 5 1.324
67
c NYX001 Nyx-Related X-Linked Congenital Stationary Night Blindness 5 1.324
68
PRG127 Progressive Microcephaly-Seizures-Cortical Blindness-Developmental Delay Syndrome 4 1.324
69
c LBR004 Leber Congenital Amaurosis 1 44 1.316
70
c ACH034 Achromatopsia-2 39 1.316
71
NRD013 Neurodegeneration with Optic Atrophy, Childhood Onset 19 1.316
72
c DYS121 Dyslexia 1 23 1.306
73
DVL017 Developmental Prosopagnosia 19 1.306
74
WNS001 Weinstein Kliman Scully Syndrome 3 1.306
75
P HMR011 Hemeralopia, Familial 3 1.306
76
P ART022 Arthritis 75 0.142
77
P SCH015 Schizophrenia 77 0.133
78
RTN023 Retinitis 50 0.116
79
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.116
80
PRM097 Primary Immunodeficiency Disease 60 0.114
81
P RHM011 Rheumatoid Arthritis 89 0.112
82
P HPT021 Hepatitis 69 0.108
83
c PND001 Pain Disorder 54 0.106
84
P ENC018 Encephalopathy 59 0.104
85
P AST005 Asthma 82 0.103
86
P NRP001 Neuropathy 59 0.103
87
END040 Endogenous Depression 53 0.099
88
ANX002 Anxiety Disorder 67 0.099
89
DSS008 Disease of Mental Health 52 0.098
90
GNR004 Generalized Anxiety Disorder 51 0.098
91
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.098
92
ACQ007 Acquired Immunodeficiency Syndrome 60 0.097
93
SKN016 Skin Disease 66 0.096
94
SXL003 Sexual Disorder 42 0.096
95
DRG001 Drug Psychosis 38 0.093
96
P OST012 Osteoarthritis 83 0.091
97
P NRV007 Nervous System Disease 71 0.090
98
GST050 Gastrointestinal System Disease 56 0.090
99
SKN027 Skin Conditions 43 0.089
100
NTR005 Nutritional Deficiency Disease 36 0.089
101
CRB009 Cerebritis 39 0.089
102
P DRR001 Diarrhea 60 0.088
103
SLP005 Sleep Disorder 53 0.088
104
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.087
105
P INT068 Intestinal Disease 60 0.087
106
ATP002 Atopy 66 0.085
107
P RHN004 Rhinitis 60 0.085
108
NRM005 Neuromuscular Disease 56 0.085
109
PRP019 Peripheral Nervous System Disease 55 0.085
110
P CLL015 Collagen Disease 50 0.085
111
c CNT035 Central Nervous System Disease 60 0.084
112
RHM027 Rheumatic Disease 58 0.084
113
P CHR345 Chronic Pain 50 0.084
114
PRS047 Prostatitis 56 0.084
115
P CRV039 Cervicitis 45 0.084
116
P OBS005 Obesity 92 0.083
117
HDC001 Headache 54 0.083
118
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.083
119
ALN001 Aland Island Eye Disease 45 0.083
120
ATM054 Autoimmune Disease 3 15 0.083
121
P ART023 Arthropathy 64 0.082
122
MDD011 Mood Disorder 61 0.082
123
MDY003 Mody, Type Ii 36 0.082
124
JNT002 Joint Disorders 55 0.081
125
TRC008 Trachoma 47 0.081
126
MTH009 Mouth Disease 61 0.080
127
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.079
128
ACN011 Acne 62 0.079
129
MNT002 Mental Depression 53 0.079
130
BCK006 Back Pain 43 0.079
131
GLC008 Glucose Metabolism Disease 42 0.079
132
ATM053 Autoimmune Disease 2 16 0.079
133
ADM013 Adamantinoma of Long Bones 57 0.078
134
KDS001 Kid Syndrome 53 0.078
135
c AST037 Asthma 1 28 0.078
136
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.078
137
APH001 Aphthous Stomatitis 62 0.077
138
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.077
139
CHL071 Child Syndrome 58 0.077
140
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.077
141
PSY004 Psychotic Disorder 67 0.076
142
P EPL164 Epilepsy 66 0.076
143
DMN002 Dementia 65 0.076
144
CNS004 Constipation 57 0.076
145
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.076
146
GST045 Gastroenteritis 59 0.075
147
RSP006 Respiratory System Disease 58 0.075
148
ALL026 Allergic Hypersensitivity Disease 52 0.075
149
c AST039 Asthma 2 28 0.075
150
ATM052 Autoimmune Disease 1 25 0.075
151
P MYP004 Myopathy 67 0.074
152
DRM006 Dermatitis 66 0.074
153
ALL003 Allergic Rhinitis 63 0.074
154
EYD002 Eye Disease 61 0.074
155
P MSC033 Muscle Disorders 52 0.074
156
MVM001 Movement Disease 49 0.074
157
ATN002 Autonomic Nervous System Disease 48 0.074
158
c BPL002 Bipolar I Disorder 47 0.074
159
WTH001 Withdrawal Disorder 37 0.074
160
OPT006 Optic Nerve Disease 52 0.073
161
IMM136 Immune System Disease 51 0.073
162
URN009 Urinary System Disease 50 0.073
163
CSY001 C Syndrome 50 0.073
164
CCN001 Cocaine Dependence 49 0.073
165
SPS057 Spasticity 42 0.073
166
HV1006 Hiv-1 80 0.072
167
LNG099 Lung Disease 64 0.072
168
CMM005 Common Cold 59 0.072
169
C3D001 C3 Deficiency 53 0.072
170
ADL002 Adult Syndrome 52 0.072
171
CLN019 Colonic Disease 51 0.072
172
FST001 Foster-Kennedy Syndrome 31 0.072
173
P PSR002 Psoriasis 61 0.071
174
P SPS003 Spastic Diplegia 52 0.071
175
P URF003 Urofacial Syndrome 1 50 0.071
176
PRM003 Premature Ejaculation 45 0.071
177
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.071
178
P RTN008 Retinitis Pigmentosa 80 0.070
179
P KDN018 Kidney Disease 66 0.070
180
P DYS154 Dystonia 65 0.070
181
ISC004 Ischemia 61 0.070
182
P ESP024 Esophagitis 61 0.070
183
P BRS047 Breast Cancer 100 0.069
184
CNN005 Connective Tissue Disease 62 0.069
185
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.068
186
P SZR006 Seizure Disorder 56 0.068
187
RTN018 Retinal Disease 53 0.068
188
P MYC007 Myocardial Infarction 79 0.067
189
P LVR013 Liver Disease 75 0.067
190
PRP027 Peripheral Vascular Disease 68 0.067
191
P INF032 Infertility 59 0.067
192
VRL011 Viral Infectious Disease 55 0.067
193
ART111 Artery Disease 55 0.067
194
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.067
195
P HRT032 Heart Disease 75 0.065
196
P INF038 Influenza 72 0.065
197
GNG013 Gingivitis 61 0.064
198
TNP001 Tinea Pedis 40 0.064
199
MYF002 Myofascial Pain Syndrome 39 0.064
200
CNG034 Congestive Heart Failure 72 0.063
201
P ATP001 Atopic Dermatitis 62 0.063
202
CLT003 Colitis 60 0.063
203
IRR002 Irritable Bowel Syndrome 58 0.063
204
DBT010 Diabetic Neuropathy 55 0.063
205
PST053 Postherpetic Neuralgia 40 0.063
206
SPN369 Spinal Disease 39 0.063
207
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.063
208
c HPT001 Hepatitis C 68 0.062
209
ATS001 Autistic Disorder 63 0.062
210
ALC007 Alcohol Dependence 63 0.062
211
ESP023 Esophageal Disease 54 0.062
212
BRN038 Bronchial Disease 51 0.062
213
STM007 Stomatitis 50 0.062
214
CRV043 Cervical Dystonia 44 0.062
215
PHY002 Physical Disorder 43 0.062
216
MLR007 Male Reproductive System Disease 34 0.062
217
P ALZ034 Alzheimer Disease 92 0.061
218
MLR004 Malaria 83 0.061
219
STR067 Stroke, Ischemic 75 0.061
220
P PNC044 Pancreatitis 61 0.061
221
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.061
222
c HPT003 Hepatitis a 59 0.061
223
LPD008 Lipid Metabolism Disorder 58 0.061
224
P MYP006 Myopia 56 0.061
225
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.061
226
VGN023 Vaginitis 42 0.061
227
PRM025 Primary Bacterial Infectious Disease 41 0.061
228
P CRN211 Coronary Artery Disease 74 0.060
229
P PNM007 Pneumonia 68 0.060
230
P INF037 Inflammatory Bowel Disease 63 0.060
231
WST001 West Syndrome 57 0.060
232
NSD001 Nose Disease 48 0.060
233
PLP001 Pulpitis 47 0.060
234
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.060
235
P CRN178 Coronary Heart Disease 6 21 0.060
236
ATM055 Autoimmune Disease 4 15 0.060
237
P PRS040 Prostate Cancer 90 0.059
238
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.059
239
P CNJ013 Conjunctivitis 64 0.059
240
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.059
241
GST092 Gastroesophageal Reflux 62 0.059
242
c ACT075 Acute Myocardial Infarction 60 0.059
243
P CTR002 Cataract 58 0.059
244
CTS003 Coats Disease 57 0.059
245
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.059
246
BRN106 Burns 52 0.059
247
STM006 Stomach Disease 50 0.059
248
c ACT004 Acute Diarrhea 39 0.059
249
MSC004 Muscle Tissue Disease 34 0.059
250
GLB003 Globe Disease 32 0.059
251
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.059
252
P PRK057 Parkinson Disease, Late-Onset 70 0.057
253
c HYP595 Hypertension, Essential 69 0.057
254
c HPT016 Hepatitis B 64 0.057
255
CND002 Conduct Disorder 54 0.057
256
P ECL001 Eclampsia 54 0.057
257
AYM001 Ayme-Gripp Syndrome 41 0.057
258
BSL008 Basal Ganglia Disease 40 0.057
259
CD4004 Cd4 Deficiency 14 0.057
260
P CLR023 Colorectal Cancer 97 0.056
261
P LNG032 Lung Cancer 95 0.056
262
P CND004 Candidiasis 57 0.056
263
P EXN002 Exanthem 57 0.056
264
URT039 Urticaria 57 0.056
265
EXF001 Exfoliation Syndrome 57 0.056
266
PHR003 Pharyngitis 56 0.056
267
PYR010 Peyronie's Disease 53 0.056
268
DYS014 Dyspepsia 50 0.056
269
c DWL002 Dowling-Degos Disease 1 49 0.056
270
FSC004 Fasciitis 48 0.056
271
PRP021 Peripheral Nervous System Neoplasm 46 0.056
272
P PLN008 Peeling Skin Syndrome 45 0.056
273
DDN006 Duodenitis 42 0.056
274
EPC002 Epicondylitis 39 0.056
275
IMP003 Impaired Renal Function Disease 34 0.056
276
CYS001 Cystic Fibrosis 83 0.055
277
CRH001 Crohn's Disease 75 0.055
278
PCK002 Pick Disease 68 0.055
279
VSC007 Vascular Disease 67 0.055
280
P MSC005 Muscular Dystrophy 65 0.055
281
P BPL003 Bipolar Disorder 62 0.055
282
ETH011 Ethylmalonic Encephalopathy 56 0.055
283
MCS002 Mucositis 55 0.055
284
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.055
285
SWL001 Swallowing Disorders 33 0.055
286
c INF078 Inflammatory Bowel Disease 2 31 0.055
287
c TRC078 Trichohepatoenteric Syndrome 2 29 0.055
288
c CRN174 Coronary Heart Disease 2 20 0.055
289
P LKM002 Leukemia 71 0.053
290
P LYM118 Lymphoma 69 0.053
291
OBS002 Obsessive-Compulsive Disorder 66 0.053
292
P OST002 Osteoporosis 64 0.053
293
P NRV006 Nervous System Cancer 60 0.053
294
WLL006 Wells Syndrome 59 0.053
295
KRT009 Keratosis 52 0.053
296
LPD004 Lipoid Nephrosis 48 0.053
297
DYS073 Dysphagia 48 0.053
298
GDS001 Good Syndrome 44 0.053
299
RCT017 Rectal Disease 40 0.053
300
XRP001 Xerophthalmia 33 0.053
301
LVR012 Liver Cirrhosis 67 0.052
302
c CHR089 Chronic Kidney Failure 66 0.052
303
ALP008 Alopecia 57 0.052
304
THR024 Thrombosis 57 0.052
305
P PLY019 Polyneuropathy 56 0.052
306
RST001 Restless Legs Syndrome 54 0.052
307
c INF071 Inflammatory Bowel Disease 1 51 0.052
308
INC022 Inclusion-Cell Disease 46 0.052
309
ACR041 Acromelic Frontonasal Dysostosis 45 0.052
310
BRT030 Birth Defects 43 0.052
311
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.052
312
PLN007 Plantar Fasciitis 31 0.052
313
c ATM007 Autoimmune Disease of Central Nervous System 25 0.052
314
c MJR007 Major Affective Disorder 1 24 0.052
315
ATM059 Autoimmune Disease 6 22 0.052
316
c MJR008 Major Affective Disorder 2 19 0.052
317
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.051
318
ALL006 Allergic Asthma 58 0.051
319
ART021 Arteriosclerosis 58 0.051
320
ANR040 Aneurysm 57 0.051
321
FDL002 Food Allergy 53 0.051
322
P ATX004 Ataxia 53 0.051
323
RSC001 Rosacea 52 0.051
324
c PRK031 Parkinson Disease 1 51 0.051
325
BLD044 Bladder Disease 51 0.051
326
SPN041 Spinal Cord Disease 51 0.051
327
FML039 Female Reproductive System Disease 48 0.051
328
END072 Endotheliitis 42 0.051
329
GST078 Gastrointestinal Allergy 40 0.051
330
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.051
331
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.051
332
ULC004 Ulcerative Colitis 76 0.049
333
P LPS004 Lupus Erythematosus 64 0.049
334
DFC004 Deficiency Anemia 64 0.049
335
c VRL010 Viral Hepatitis 60 0.049
336
P GT001 Gout 58 0.049
337
HPT019 Hepatic Encephalopathy 56 0.049
338
FCL014 Focal Epilepsy 55 0.049
339
P MCR129 Microvascular Complications of Diabetes 1 54 0.049
340
DMY004 Demyelinating Disease 53 0.049
341
ACT008 Actinic Keratosis 51 0.049
342
MGR028 Migraine with or Without Aura 1 47 0.049
343
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.049
344
PRC003 Proctitis 41 0.049
345
c PSR017 Psoriasis 2 37 0.049
346
ALR002 Al-Raqad Syndrome 36 0.049
347
TYP027 Type 1 Diabetes Mellitus 10 27 0.049
348
c CRN214 Coronary Heart Disease 5 22 0.049
349
c CRN172 Coronary Heart Disease 3 19 0.049
350
DCH001 Duchenne Muscular Dystrophy 79 0.048
351
P MNN013 Meningitis 67 0.048
352
CRB037 Cerebral Palsy 66 0.048
353
ATH003 Atherosclerosis 65 0.048
354
P SNS014 Sinusitis 60 0.048
355
GST023 Gastric Ulcer 56 0.048
356
P RTN016 Retinal Degeneration 54 0.048
357
SBS003 Substance Abuse 54 0.048
358
P LCH002 Lichen Planus 53 0.048
359
BCT002 Bacterial Vaginosis 52 0.048
360
PTH002 Pathological Gambling 51 0.048
361
ALL009 Allergic Conjunctivitis 51 0.048
362
c HMG001 Hemoglobin C Disease 47 0.048
363
BLD053 Blood Platelet Disease 46 0.048
364
SNS023 Sensory System Cancer 43 0.048
365
RPR002 Reproductive System Disease 41 0.048
366
c PLN018 Peeling Skin Syndrome 2 40 0.048
367
ADJ001 Adjustment Disorder 38 0.048
368
c CNT068 Central Pain Syndrome 29 0.048
369
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.048
370
BRN024 Bronchitis 64 0.046
371
HYP056 Hypoglycemia 61 0.046
372
P TMP003 Temporal Arteritis 60 0.046
373
P GST049 Gastrointestinal System Cancer 60 0.046
374
ADN018 Adenoma 58 0.046
375
PNC034 Pancreas Disease 58 0.046
376
P INT143 Interstitial Cystitis 57 0.046
377
P VNS003 Venous Insufficiency 54 0.046
378
IMP005 Impotence 51 0.046
379
P MSC003 Muscular Atrophy 50 0.046
380
DRG003 Drug Dependence 50 0.046
381
HPT074 Hepatic Adenoma, Somatic 50 0.046
382
ANG054 Angina Pectoris 50 0.046
383
VND001 Vein Disease 47 0.046
384
INT253 Intestinal Benign Neoplasm 47 0.046
385
SKN023 Skin Tag 44 0.046
386
c INF086 Inflammatory Bowel Disease 3 38 0.046
387
BLD054 Blood Protein Disease 37 0.046
388
ATM014 Autoimmune Disease of Endocrine System 36 0.046
389
DYS011 Dyskinesia of Esophagus 28 0.046
390
FNC005 Functional Colonic Disease 27 0.046
391
HNM002 Hinman Syndrome 25 0.046
392
c RNL016 Renal Infectious Disease 20 0.046
393
VSC009 Vascular Skin Disease 19 0.046
394
c PRC016 Pre-Eclampsia 56 0.045
395
P TRM003 Tremor 54 0.045
396
TTH006 Tooth Disease 52 0.045
397
BRN071 Brain Injury 52 0.045
398
SPN051 Spondylitis 51 0.045
399
P DDN001 Duodenal Ulcer 50 0.045
400
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.045
401
HYP025 Hyperphosphatemia 47 0.045
402
DRM011 Dermatophytosis 46 0.045
403
PRD011 Proud Syndrome 42 0.045
404
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.045
405
HYP030 Hypoactive Sexual Desire Disorder 39 0.045
406
BNS002 Bone Structure Disease 37 0.045
407
SBC017 Sebaceous Gland Disease 34 0.045
408
c OST147 Osteoarthritis 1 30 0.045
409
P ADN016 Adenocarcinoma 69 0.043
410
CRB039 Cerebrovascular Disease 63 0.043
411
TTN003 Tetanus 61 0.043
412
ETN001 Eating Disorder 58 0.043
413
SHG001 Shigellosis 54 0.043
414
GNT003 Genital Herpes 53 0.043
415
OLV001 Olivopontocerebellar Atrophy 53 0.043
416
MYC002 Mycobacterium Avium Complex Disease 52 0.043
417
DBT062 Diabetic Foot Ulcers 51 0.043
418
TRD006 Tardive Dyskinesia 49 0.043
419
TCL003 T Cell Deficiency 45 0.043
420
PRS045 Prostatic Hypertrophy 45 0.043
421
CLS010 Cluster Headache 44 0.043
422
RFR003 Refractive Error 43 0.043
423
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.043
424
LKC003 Leukocyte Disease 43 0.043
425
ADT003 Auditory System Disease 40 0.043
426
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.043
427
c PNC106 Pancreatic Agenesis 1 37 0.043
428
c MLT094 Multiple Sclerosis 3 24 0.043
429
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.043
430
c CRN175 Coronary Heart Disease 4 19 0.043
431
P RSP003 Respiratory Failure 71 0.041
432
ISC006 Ischemic Heart Disease 68 0.041
433
P PLR004 Pleuropulmonary Blastoma 65 0.041
434
P PLY011 Polycystic Ovary Syndrome 65 0.041
435
MLN008 Melanoma 62 0.041
436
HYP066 Hyperglycemia 61 0.041
437
ALC006 Alcoholic Hepatitis 59 0.041
438
FTT001 Fatty Liver Disease 59 0.041
439
P SHR029 Short Syndrome 58 0.041
440
TNS005 Tonsillitis 57 0.041
441
ORL011 Oral Cancer 56 0.041
442
PLS007 Plasmodium Falciparum Malaria 55 0.041
443
CHR081 Choroideremia 54 0.041
444
NWC001 Newcastle Disease 54 0.041
445
BNF002 Bone Fracture 50 0.041
446
c INH020 Inherited Metabolic Disorder 49 0.041
447
LMB062 Limb Ischemia 48 0.041
448
P FML035 Familial Hyperlipidemia 48 0.041
449
ORL013 Oral Lichen Planus 47 0.041
450
HDN002 Head Injury 45 0.041
451
ACD009 Acid-Labile Subunit, Deficiency of 45 0.041
452
SYS003 Systolic Heart Failure 43 0.041
453
TND004 Tendinopathy 42 0.041
454
ESP018 Esophageal Candidiasis 41 0.041
455
c INF087 Inflammatory Bowel Disease 4 40 0.041
456
c CHR579 Chiari Malformation Type Ii 37 0.041
457
CRP002 Croup 37 0.041
458
RDN001 Reading Disorder 34 0.041
459
ANG049 Angioedema Induced by Ace Inhibitors 34 0.041
460
CVT001 Cavitary Optic Disc Anomalies 31 0.041
461
c INF088 Inflammatory Bowel Disease 5 31 0.041
462
WSC001 Wisconsin Syndrome 14 0.041
463
c SYS001 Systemic Lupus Erythematosus 86 0.040
464
P HNT016 Huntington Disease 80 0.040
465
KRT004 Keratitis 71 0.040
466
TBR010 Tuberculosis 70 0.040
467
P ATR011 Atrial Fibrillation 66 0.040
468
CNR002 Cone-Rod Dystrophy 64 0.040
469
HMT002 Hematologic Cancer 64 0.040
470
PSR001 Psoriatic Arthritis 64 0.040
471
RCT015 Reactive Arthritis 63 0.040
472
PRT036 Peritonitis 63 0.040
473
P ORL007 Oral Cavity Cancer 59 0.040
474
INT002 Intermittent Claudication 56 0.040
475
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.040
476
RCT018 Rectal Neoplasm 54 0.040
477
P THY032 Thyroiditis 54 0.040
478
P CYS018 Cystitis 52 0.040
479
KRT006 Keratoconjunctivitis 52 0.040
480
P PRM006 Primary Biliary Cirrhosis 51 0.040
481
CRT049 Critical Limb Ischemia 51 0.040
482
CLL003 Cellulitis 51 0.040
483
NNL002 Nonalcoholic Steatohepatitis 50 0.040
484
MLK006 Milk Allergy 47 0.040
485
GNG011 Gingival Disease 46 0.040
486
P CRN035 Cranial Nerve Palsy 46 0.040
487
SNS003 Sensory Peripheral Neuropathy 45 0.040
488
P BRN120 Bronchus Cancer 44 0.040
489
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.040
490
BRN080 Brain Ischemia 41 0.040
491
URT001 Urethritis 41 0.040
492
BND014 Bone Development Disease 40 0.040
493
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.040
494
ATM012 Autoimmune Disease of Blood 35 0.040
495
FCL044 Fecal Incontinence 35 0.040
496
c PLN017 Peeling Skin Syndrome 1 34 0.040
497
ACR002 Acrocapitofemoral Dysplasia 33 0.040
498
c PLN021 Peeling Skin Syndrome 3 29 0.040
499
c CLR079 Colorectal Cancer 2 29 0.040
500
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 24 0.040
501
FCL001 Facial Dermatosis 23 0.040
502
P GNR027 Generalized Peeling Skin Syndrome 19 0.040
503
c CRN173 Coronary Heart Disease 8 18 0.040
504
c MLT093 Multiple Sclerosis 2 18 0.040
505
c HPT073 Hepatitis C Virus 73 0.038
506
P PLM036 Pulmonary Fibrosis 71 0.038
507
KWS002 Kawasaki Disease 70 0.038
508
CHR066 Chronic Fatigue Syndrome 64 0.038
509
P CRB042 Cerebellar Ataxia 63 0.038
510
P ENC004 Encephalitis 63 0.038
511
SPN186 Spinal Cord Injury 63 0.038
512
P IDP010 Idiopathic Generalized Epilepsy 61 0.038
513
P HYP117 Hypertriglyceridemia 61 0.038
514
MSL001 Measles 61 0.038
515
P PNC025 Panic Disorder 60 0.038
516
ING001 Inguinal Hernia 58 0.038
517
P HMP007 Hemophilia 57 0.038
518
P FND001 Fundus Albipunctatus 55 0.038
519
DBT004 Diabetic Polyneuropathy 52 0.038
520
P HYP014 Hyperuricemia 50 0.038
521
AMN001 Amenorrhea 50 0.038
522
c ACT068 Acute Cystitis 50 0.038
523
CCN002 Cocaine Abuse 48 0.038
524
c CLR085 Colorectal Cancer 1 45 0.038
525
SPS007 Spastic Cerebral Palsy 44 0.038
526
c CHR431 Chronic Venous Insufficiency 44 0.038
527
ACT058 Active Peptic Ulcer Disease 43 0.038
528
P BLP003 Blepharospasm 43 0.038
529
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.038
530
CWM001 Cow Milk Allergy 40 0.038
531
CRN031 Cranial Nerve Disease 40 0.038
532
CHR078 Chorioretinitis 40 0.038
533
SPC003 Specific Developmental Disorder 38 0.038
534
PRP080 Peripheral Artery Disease 37 0.038
535
NSY001 N Syndrome 36 0.038
536
MLN003 Melancholia 34 0.038
537
P XLN007 X-Linked Disease 34 0.038
538
TNC001 Tinea Cruris 31 0.038
539
EYD001 Eye Degenerative Disease 30 0.038
540
VSL004 Visual Cortex Disease 28 0.038
541
c PRK022 Parkinson Disease 12 21 0.038
542
IMM142 Immunodeficiency 50 20 0.038
543
GLC077 Glucocorticoid Therapy, Response to 16 0.038
544
c MJR004 Major Affective Disorder 4 16 0.038
545
P HPT023 Hepatocellular Carcinoma 92 0.036
546
GST053 Gastric Cancer 78 0.036
547
P ATS007 Autism Spectrum Disorder 65 0.036
548
P ALP009 Alopecia Areata 62 0.036
549
P SLP006 Sleep Apnea 61 0.036
550
DPH001 Diphtheria 59 0.036
551
P ALC004 Alcohol Abuse 59 0.036
552
P GLM007 Glomerulonephritis 59 0.036
553
SYN007 Synovitis 58 0.036
554
GST033 Gestational Diabetes 57 0.036
555
HYP266 Hypoxia 56 0.036
556
P STR022 Stargardt Disease 56 0.036
557
END030 End Stage Renal Failure 55 0.036
558
APH002 Aphasia 54 0.036
559
CMP010 Complex Regional Pain Syndrome 54 0.036
560
P ACT105 Acute Mountain Sickness 52 0.036
561
ATR060 Atrial Standstill, Digenic 51 0.036
562
HMP005 Hemiplegia 51 0.036
563
RDC002 Radiculopathy 50 0.036
564
OVR063 Overnutrition 50 0.036
565
BCL002 B Cell Deficiency 49 0.036
566
SBS004 Substance Dependence 47 0.036
567
CRB085 Cerebral Hemorrhage 46 0.036
568
PTT004 Pituitary Apoplexy 46 0.036
569
PLL012 Pollen Allergy 44 0.036
570
CRD118 Cardiovascular Cancer 44 0.036
571
c PRM023 Pre-Malignant Neoplasm 41 0.036
572
CNV002 Conversion Disorder 41 0.036
573
PRS036 Parasitic Protozoa Infectious Disease 41 0.036
574
ENT001 Enterocele 40 0.036
575
TNC002 Tinea Capitis 40 0.036
576
ADR009 Adrenal Cortex Disease 39 0.036
577
c PRK030 Parkinson Disease 4 38 0.036
578
SXD001 Sex Differentiation Disease 38 0.036
579
P OCY001 Oocyte Maturation Defect 38 0.036
580
IMM065 Immunodeficiency 10 36 0.036
581
c INF089 Inflammatory Bowel Disease 6 34 0.036
582
PTY002 Pityriasis Versicolor 31 0.036
583
VSC008 Vascular Hemostatic Disease 30 0.036
584
c CLR075 Colorectal Cancer 3 28 0.036
585
c SCH051 Schizophrenia 4 28 0.036
586
ORB006 Orbital Cellulitis 26 0.036
587
IMM071 Immunodeficiency 12 26 0.036
588
c CRN177 Coronary Heart Disease 7 20 0.036
589
c MJR003 Major Affective Disorder 6 15 0.036
590
INS024 Insulin-Like Growth Factor I 75 0.034
591
BRN028 Brain Cancer 70 0.034
592
P CLC005 Celiac Disease 68 0.034
593
c BSL007 Basal Cell Carcinoma 65 0.034
594
P SPN046 Spinal Muscular Atrophy 65 0.034
595
P PRS038 Personality Disorder 62 0.034
596
BRS051 Breast Disease 61 0.034
597
PRD007 Periodontal Disease 60 0.034
598
RBR001 Roberts Syndrome 60 0.034
599
c ESS001 Essential Tremor 59 0.034
600
PRP030 Purpura 58 0.034
601
P GST044 Gastritis 56 0.034
602
MLN007 Male Infertility 55 0.034
603
SPN027 Spinal Stenosis 55 0.034
604
c BCT007 Bacterial Meningitis 54 0.034
605
P BRN009 Burning Mouth Syndrome 54 0.034
606
P LTR001 Lateral Sclerosis 53 0.034
607
P USH001 Usher Syndrome 53 0.034
608
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.034
609
c HPT015 Hepatitis D 52 0.034
610
P MGR003 Migraine with Aura 52 0.034
611
NRT004 Neuritis 52 0.034
612
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.034
613
SRT004 Serotonin Syndrome 49 0.034
614
LRN003 Learning Disability 49 0.034
615
PRN021 Paranasal Sinus Disease 49 0.034
616
NRM004 Neuroma 48 0.034
617
P TRC086 Trichohepatoenteric Syndrome 1 48 0.034
618
BRD001 Brody Myopathy 47 0.034
619
GLT021 Glutaricaciduria, Type I 46 0.034
620
P RTN014 Retinal Artery Occlusion 44 0.034
621
P SKN013 Skin Benign Neoplasm 43 0.034
622
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.034
623
BHR001 Behr Syndrome 42 0.034
624
P BLD051 Blood Coagulation Disease 42 0.034
625
PTY001 Pityriasis Rosea 42 0.034
626
MYC033 Myoclonus 42 0.034
627
RDT013 Radiation Proctitis 42 0.034
628
c PRG106 Progressive Muscular Dystrophy 40 0.034
629
ALX001 Alexia 40 0.034
630
TRC010 Trichotillomania 40 0.034
631
HYP264 Hypertonia 39 0.034
632
MNR003 Mineral Metabolism Disease 38 0.034
633
c CNG031 Congenital Nervous System Abnormality 37 0.034
634
TTR016 Tetra-Amelia Syndrome 36 0.034
635
DRM009 Dermatomycosis 35 0.034
636
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.034
637
DDN007 Duodenal Disease 33 0.034
638
MDY006 Mody, Type Iv 30 0.034
639
MTH047 Methanol Poisoning 30 0.034
640
IMM068 Immunodeficiency 8 30 0.034
641
c SCH056 Schizophrenia 15 23 0.034
642
c INF091 Inflammatory Bowel Disease 8 22 0.034
643
c SCH064 Schizophrenia 10 19 0.034
644
c CRN176 Coronary Heart Disease 9 18 0.034
645
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.034
646
PRT056 Protein R Deficiency 10 0.034
647
P PLM037 Pulmonary Hypertension 79 0.032
648
P OVR042 Ovarian Cancer 76 0.032
649
SQM006 Squamous Cell Carcinoma 70 0.032
650
P CHR071 Charcot-Marie-Tooth Disease 67 0.032
651
OTT002 Otitis Media 66 0.032
652
P HYD006 Hydrocephalus 66 0.032
653
OBS061 Obstructive Sleep Apnea 66 0.032
654
LSH001 Leishmaniasis 66 0.032
655
ACR007 Acromegaly 66 0.032
656
P HRP006 Herpes Simplex 65 0.032
657
CNT098 Central Core Disease 65 0.032
658
PRT037 Pertussis 64 0.032
659
P HYP086 Hypothyroidism 64 0.032
660
P PRD008 Periodontitis 63 0.032
661
CRD119 Cardiac Arrest 61 0.032
662
c ACT073 Acute Leukemia 60 0.032
663
OCL009 Ocular Cancer 59 0.032
664
MRB003 Morbid Obesity 58 0.032
665
c FML001 Familial Atrial Fibrillation 58 0.032
666
P HYP060 Hyperinsulinism 58 0.032
667
P UVT001 Uveitis 58 0.032
668
YLL002 Yellow Fever 58 0.032
669
P HYP069 Hyperparathyroidism 58 0.032
670
PST028 Post-Traumatic Stress Disorder 57 0.032
671
c ACT027 Acute Pancreatitis 57 0.032
672
BRN002 Bronchiolitis 56 0.032
673
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.032
674
GTR002 Goiter 52 0.032
675
BLM002 Bulimia Nervosa 52 0.032
676
TRM010 Traumatic Brain Injury 52 0.032
677
P ANG015 Angioedema 52 0.032
678
P PYL005 Pyelonephritis 52 0.032
679
PRS042 Prostate Disease 52 0.032
680
IRN001 Iron Deficiency Anemia 52 0.032
681
ART002 Arts Syndrome 51 0.032
682
DRG011 Drug Addiction 51 0.032
683
PNM001 Pneumocystosis 50 0.032
684
OPT009 Optic Neuritis 50 0.032
685
HLL004 Hellp Syndrome 50 0.032
686
P OPN001 Open-Angle Glaucoma 49 0.032
687
P SHR001 Short Bowel Syndrome 49 0.032
688
BCT015 Bacteremia 48 0.032
689
MSS002 Mass Syndrome 48 0.032
690
FND002 Fundus Dystrophy 46 0.032
691
LCT002 Lactose Intolerance 46 0.032
692
ATN004 Autonomic Neuropathy 45 0.032
693
c ACT042 Acute Pyelonephritis 45 0.032
694
CHR008 Choroiditis 44 0.032
695
P DMY001 Demyelinating Polyneuropathy 43 0.032
696
IMP004 Impetigo 42 0.032
697
GYR003 Gyrate Atrophy of Choroid and Retina with or Without Ornithinemia 42 0.032
698
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.032
699
OPP002 Opportunistic Mycosis 41 0.032
700
STT004 Steatorrhea 40 0.032
701
SCH003 Schizophreniform Disorder 40 0.032
702
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.032
703
ATN003 Autonomic Nervous System Neoplasm 40 0.032
704
URM005 Uremic Pruritus 39 0.032
705
CLL021 Collagenous Colitis 39 0.032
706
NSL022 Nasal Cavity Disease 38 0.032
707
CRV045 Cervical Intraepithelial Neoplasia 38 0.032
708
PRP028 Peripheral Vertigo 38 0.032
709
TNC003 Tinea Corporis 38 0.032
710
DYS009 Dysthymic Disorder 37 0.032
711
PRS063 Paresthesia 36 0.032
712
c DRM035 Dermatitis, Atopic 2 36 0.032
713
c DYS119 Dystonia 9 36 0.032
714
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.032
715
SPR005 Superficial Basal Cell Carcinoma 34 0.032
716
PLC008 Placenta Disease 33 0.032
717
c ALZ012 Alzheimer Disease 12 32 0.032
718
PRS013 Prosopagnosia 31 0.032
719
MDY005 Mody, Type I 30 0.032
720
IMM066 Immunodeficiency 9 30 0.032
721
MRG013 Mirage Syndrome 29 0.032
722
IMM076 Immunodeficiency 24 27 0.032
723
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 26 0.032
724
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.032
725
SBC016 Subacute Delirium 24 0.032
726
SPC022 Specific Antibody Deficiency 18 0.032
727
ATR076 Atrophic Muscular Disease 15 0.032
728
c BCT003 Bacterial Exanthem 11 0.032
729
P HYP607 Hypercholesterolemia, Familial 76 0.029
730
PHN003 Phenylketonuria 72 0.029
731
SCK003 Sickle Cell Anemia 71 0.029
732
TST021 Testicular Germ Cell Tumor 69 0.029
733
P CRD011 Cardiomyopathy 68 0.029
734
P FML011 Familial Adenomatous Polyposis 68 0.029
735
P MYL005 Myelofibrosis 67 0.029
736
P MYL006 Myeloid Leukemia 66 0.029
737
DWN001 Down Syndrome 66 0.029
738
CTN007 Cutaneous Leishmaniasis 62 0.029
739
P NRC002 Narcolepsy 62 0.029
740
P ANR007 Anorexia Nervosa 61 0.029
741
BHC003 Behcet Syndrome 60 0.029
742
P CLR108 Colorectal Adenoma 60 0.029
743
SPT004 Septic Arthritis 60 0.029
744
PGT001 Paget's Disease of Bone 59 0.029
745
PPT005 Peptic Ulcer Disease 58 0.029
746
DMN031 Dementia, Lewy Body 58 0.029
747
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.029
748
CHY002 Chylomicron Retention Disease 57 0.029
749
LNN001 Lennox-Gastaut Syndrome 57 0.029
750
EPD016 Epidermolysis Bullosa 57 0.029
751
HRP004 Herpes Zoster 56 0.029
752
P LYM033 Lymphoproliferative Syndrome 56 0.029
753
P PLY006 Polydactyly 56 0.029
754
GLC003 Glucose Intolerance 55 0.029
755
PLM012 Pulmonary Sarcoidosis 54 0.029
756
c HPT007 Hepatitis E 54 0.029
757
P END033 Endocarditis 54 0.029
758
P INT030 Intracranial Aneurysm 54 0.029
759
P LRY019 Laryngitis 54 0.029
760
SML019 Smallpox 54 0.029
761
P MTC069 Mitochondrial Disorders 53 0.029
762
HYP080 Hypogonadism 53 0.029
763
THR016 Thrombophlebitis 53 0.029
764
ALS001 Alstrom Syndrome 53 0.029
765
PRV006 Pervasive Developmental Disorder 53 0.029
766
LYM024 Lymphatic System Disease 52 0.029
767
FML038 Female Reproductive Organ Cancer 50 0.029
768
BRX001 Bruxism 49 0.029
769
PST021 Postpartum Depression 49 0.029
770
c SVR005 Severe Pre-Eclampsia 49 0.029
771
ATN005 Autonomic Dysfunction 49 0.029
772
ORL005 Oral Candidiasis 48 0.029
773
P RNL015 Renal Hypertension 48 0.029
774
LYM116 Lymph Node Disease 47 0.029
775
PLM102 Palmoplantar Keratoderma, Epidermolytic 47 0.029
776
PPL021 Papilledema 47 0.029
777
UPP004 Upper Respiratory Tract Disease 46 0.029
778
CRB025 Carbohydrate Metabolic Disorder 46 0.029
779
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.029
780
HPT014 Hepatorenal Syndrome 46 0.029
781
VCC001 Vaccinia 46 0.029
782
c CLL013 Cell Type Cancer 46 0.029
783
P PRM108 Primary Progressive Multiple Sclerosis 46 0.029
784
AMB002 Amblyopia 46 0.029
785
c MCR113 Microvascular Complications of Diabetes 3 45 0.029
786
CCN007 Cocoon Syndrome 45 0.029
787
CRB033 Cerebral Degeneration 44 0.029
788
BNN003 Bone Inflammation Disease 44 0.029
789
CRN024 Corneal Disease 44 0.029
790
STT002 Status Asthmaticus 42 0.029
791
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.029
792
c VRL005 Viral Pneumonia 42 0.029
793
P CHL066 Cholangitis 42 0.029
794
VGN020 Vaginal Disease 41 0.029
795
SPC010 Speech and Communication Disorders 41 0.029
796
TRC003 Trichomoniasis 41 0.029
797
ACT084 Acute Stress Disorder 40 0.029
798
DYS015 Dysentery 40 0.029
799
P HYP263 Hypersomnia 40 0.029
800
HYP540 Hypertension, Diastolic 39 0.029
801
PCH007 Pouchitis 38 0.029
802
P HYP265 Hypotonia 38 0.029
803
ABD010 Abdominal Wall Defect 38 0.029
804
PHS001 Phosphorus Metabolism Disease 38 0.029
805
P UTR038 Uterine Disease 37 0.029
806
BNR001 Bone Remodeling Disease 37 0.029
807
CHR415 Chronic Venous Leg Ulcers 37 0.029
808
WRN005 Wrinkles 37 0.029
809
c CNT028 Central Retinal Artery Occlusion 37 0.029
810
GRM001 Germ Cell and Embryonal Cancer 36 0.029
811
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.029
812
IMM078 Immunodeficiency 21 35 0.029
813
VSM001 Vasomotor Rhinitis 34 0.029
814
ALL007 Allergic Urticaria 31 0.029
815
c DRR009 Diarrhea 6 29 0.029
816
LPD027 Lip Disease 28 0.029
817
IMM090 Immunodeficiency 27a, Mycobacteriosis, Ar 26 0.029
818
ANS006 Anosognosia 25 0.029
819
c ADL096 Adult Hepatocellular Carcinoma 24 0.029
820
OPP001 Opportunistic Bacterial Infectious Disease 21 0.029
821
c INF073 Inflammatory Bowel Disease 12 21 0.029
822
UVL003 Uveal Diseases 18 0.029
823
c MLT095 Multiple Sclerosis 4 16 0.029
824
c MJR006 Major Affective Disorder 5 15 0.029
825
P PNC035 Pancreatic Cancer 87 0.027
826
MYL009 Myelodysplastic Syndrome 73 0.027
827
P TYS001 Tay-Sachs Disease 71 0.027
828
P FRG001 Fragile X Syndrome 69 0.027
829
P TBR001 Tuberous Sclerosis 67 0.027
830
INC002 Inclusion Body Myositis 66 0.027
831
P CRN037 Craniosynostosis 66 0.027
832
P BCL006 B-Cell Lymphomas 65 0.027
833
P KDN017 Kidney Cancer 65 0.027
834
P ALX003 Alexander Disease 63 0.027
835
VSC011 Vasculitis 62 0.027
836
P DRM010 Dermatomyositis 62 0.027
837
c SRC025 Sarcoidosis 1 61 0.027
838
OVR029 Ovarian Hyperstimulation Syndrome 61 0.027
839
INT146 Intervertebral Disc Disease 60 0.027
840
P PRT013 Portal Hypertension 60 0.027
841
CHL123 Chlamydia 60 0.027
842
STT001 Status Epilepticus 59 0.027
843
P PRP029 Porphyria 59 0.027
844
BNC003 Bone Cancer 58 0.027
845
ART017 Aortic Disease 57 0.027
846
TRG002 Trigeminal Neuralgia 57 0.027
847
P AGN002 Agnosia 57 0.027
848
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 57 0.027
849
c ACT210 Acute Respiratory Distress Syndrome 57 0.027
850
P HMR003 Hemorrhagic Disease 57 0.027
851
P MST009 Mastocytosis 56 0.027
852
RBS001 Rabies 56 0.027
853
P OVR049 Ovarian Disease 56 0.027
854
CCC001 Coccidioidomycosis 55 0.027
855
P LPD010 Lipodystrophy 55 0.027
856
ERY003 Erythema Multiforme 55 0.027
857
EXT034 Extrinsic Allergic Alveolitis 54 0.027
858
P NLD001 Nail Disease 54 0.027
859
GST037 Gastroparesis 54 0.027
860
P DBT005 Diabetes Insipidus 53 0.027
861
PLS006 Plasmodium Vivax Malaria 53 0.027
862
LYM019 Lymphosarcoma 53 0.027
863
CYT008 Cytomegalovirus Infection 52 0.027
864
ANK001 Ankylosis 51 0.027
865
P STR020 Strabismus 51 0.027
866
VRN004 Vernal Keratoconjunctivitis 51 0.027
867
CCC002 Coccidiosis 51 0.027
868
CRN030 Coronary Stenosis 51 0.027
869
GRW007 Growth Hormone Deficiency 50 0.027
870
OPT003 Opiate Dependence 50 0.027
871
DRY001 Dry Eye Syndrome 50 0.027
872
P PNV001 Panuveitis 50 0.027
873
END035 Endocrine Gland Cancer 49 0.027
874
MSC072 Muscle Cancer 49 0.027
875
PRP016 Paraplegia 49 0.027
876
c ACT071 Acute Kidney Failure 49 0.027
877
c INF067 Inflammatory Bowel Disease 10 49 0.027
878
P INT063 Intellectual Disability 49 0.027
879
c RTN162 Retinitis Pigmentosa 2 48 0.027
880
MTN003 Motion Sickness 48 0.027
881
BLL003 Bell's Palsy 48 0.027
882
c ANT034 Anterior Uveitis 48 0.027
883
MTC056 Mitochondrial Dna Depletion Syndrome 4a 48 0.027
884
RFL001 Reflex Sympathetic Dystrophy 48 0.027
885
SLP001 Sleeping Sickness 48 0.027
886
HRT007 Heart Cancer 46 0.027
887
ADR038 Adermatoglyphia 46 0.027
888
SCL003 Social Phobia 46 0.027
889
PNT038 Peanut Allergy 44 0.027
890
c MTR002 Mitral Valve Insufficiency 44 0.027
891
c RTN172 Retinitis Pigmentosa 1 43 0.027
892
MLR006 Male Reproductive Organ Cancer 43 0.027
893
EXC002 Exocrine Pancreatic Insufficiency 43 0.027
894
c RTN087 Retinal Degeneration, Late-Onset, Autosomal Dominant 43 0.027
895
SPN119 Spondylarthropathy 42 0.027
896
SHL001 Shoulder Impingement Syndrome 42 0.027
897
GST071 Gastrointestinal Carcinoma 42 0.027
898
MLL001 Molluscum Contagiosum 42 0.027
899
FCT008 Factitious Disorder 41 0.027
900
EGG001 Egg Allergy 41 0.027
901
END038 Endocrine Pancreas Disease 41 0.027
902
BRS064 Bursitis 39 0.027
903
GND003 Gonadal Disease 39 0.027
904
P HMF004 Hemifacial Spasm 39 0.027
905
LKP003 Leukoplakia 38 0.027
906
P MXL015 Maxillary Sinusitis 38 0.027
907
c ACT059 Acute Maxillary Sinusitis 37 0.027
908
FNC002 Functional Diarrhea 37 0.027
909
VSC018 Visceral Steatosis 37 0.027
910
HRD016 Hereditary Retinal Dystrophy 36 0.027
911
OPH002 Ophthalmia Neonatorum 36 0.027
912
SPN050 Spinocerebellar Degeneration 36 0.027
913
PPT001 Peptic Esophagitis 35 0.027
914
PNL013 Penile Disease 34 0.027
915
BTT001 Bietti Crystalline Corneoretinal Dystrophy 34 0.027
916
c BRN108 Branchiootic Syndrome 1 34 0.027
917
MDY004 Mody, Type Iii 34 0.027
918
TNS014 Tenosynovitis 33 0.027
919
LYM023 Lymphatic System Cancer 33 0.027
920
DDN009 Duodenal Obstruction 32 0.027
921
P HRT017 Heart Tumor 32 0.027
922
IMM102 Immunodeficiency 14 31 0.027
923
CYT002 Cytokine Deficiency 30 0.027
924
VTM003 Vitamin Metabolic Disorder 30 0.027
925
CVR002 Cavernous Sinus Thrombosis 28 0.027
926
PRR001 Periarthritis 27 0.027
927
IMM077 Immunodeficiency 20 27 0.027
928
IMM062 Immunodeficiency 11 26 0.027
929
SPH007 Sphenoid Sinusitis 25 0.027
930
IMM025 Immunoglobulin a Deficiency 2 24 0.027
931
CNT067 Central Cord Syndrome 23 0.027
932
HPD002 Hepadnavirus Infection 22 0.027
933
MND006 Mondor Disease 21 0.027
934
c ADL079 Adult Heart Tumor 16 0.027
935
c SCH061 Schizophrenia 16 16 0.027
936
NVD002 Nevada Syndrome 14 0.027
937
ORL014 Oral Pharyngeal Disorders 11 0.027
938
P MDL005 Medulloblastoma 77 0.024
939
P RTN024 Retinoblastoma 74 0.024
940
MRF001 Marfan Syndrome 73 0.024
941
c MCL042 Macular Degeneration, Age-Related, 1 73 0.024
942
MLT021 Multiple System Atrophy 70 0.024
943
BCK001 Becker Muscular Dystrophy 69 0.024
944
P LPR003 Leprosy 69 0.024
945
PLM001 Pulmonary Tuberculosis 67 0.024
946
MLD001 Melioidosis 67 0.024
947
P END044 Endometriosis 66 0.024
948
EWN003 Ewing Sarcoma 66 0.024
949
P THL005 Thalassemia 64 0.024
950
P THR014 Thrombocytopenia 64 0.024
951
c HMP029 Hemophilia a 63 0.024
952
LYM017 Lyme Disease 63 0.024
953
P RFS001 Refsum Disease 63 0.024
954
P ADD001 Addison's Disease 62 0.024
955
P PRD006 Prader-Willi Syndrome 62 0.024
956
HSH003 Hashimoto Thyroiditis 62 0.024
957
P MYM002 Moyamoya Disease 61 0.024
958
P SYS005 Systemic Scleroderma 61 0.024
959
P MCP010 Mucopolysaccharidosis 60 0.024
960
TXC005 Toxic Shock Syndrome 60 0.024
961
P GRV001 Graves' Disease 59 0.024
962
INT066 Interstitial Lung Disease 59 0.024
963
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.024
964
DFF005 Diffuse Large B-Cell Lymphoma 59 0.024
965
P RTN025 Retinoschisis 58 0.024
966
MTR014 Motor Neuron Disease 58 0.024
967
P CMR001 Camurati-Engelmann Disease 58 0.024
968
P MMP001 Mumps 58 0.024
969
FCT006 Factor V Deficiency 57 0.024
970
P RBL001 Rubella 57 0.024
971
P MYS005 Myositis 57 0.024
972
SNS001 Sensorineural Hearing Loss 57 0.024
973
P INT070 Intestinal Obstruction 57 0.024
974
STR026 Star Syndrome 57 0.024
975
RTN017 Retinal Detachment 56 0.024
976
c HRD002 Hereditary Angioedema 55 0.024
977
P SCL018 Scoliosis 55 0.024
978
JPN002 Japanese Encephalitis 55 0.024
979
P STC001 Stickler Syndrome 55 0.024
980
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.024
981
P CNV004 Canavan Disease 54 0.024
982
FLR002 Filariasis 54 0.024
983
OST024 Osteoporosis-Pseudoglioma Syndrome 54 0.024
984
FRB001 Farber Lipogranulomatosis 53 0.024
985
BLR006 Biliary Tract Disease 52 0.024
986
QDR001 Quadriplegia 52 0.024
987
ECT006 Ectodermal Dysplasia 52 0.024
988
PRT011 Protein C Deficiency 52 0.024
989
TXC002 Toxic Encephalopathy 51 0.024
990
CHC001 Chickenpox 51 0.024
991
P PMP005 Pemphigus Vulgaris 51 0.024
992
P HRD018 Hair Disease 51 0.024
993
SCK005 Sickle Cell Disease 51 0.024
994
BRN022 Bronchiectasis 50 0.024
995
PMP001 Pemphigus 50 0.024
996
VTR013 Vitreoretinopathy, Neovascular Inflammatory 50 0.024
997
INT075 Intracranial Hypertension 50 0.024
998
ALC009 Alcoholic Liver Cirrhosis 49 0.024
999
CHR001 Churg-Strauss Syndrome 49 0.024
1000
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.024
1001
ECT026 Ectopic Pregnancy 48 0.024
1002
c PRK059 Parkinson Disease 8 48 0.024
1003
ADR012 Adrenal Gland Disease 48 0.024
1004
PST062 Pustulosis Palmaris Et Plantaris 48 0.024
1005
TCD001 Tic Disorder 48 0.024
1006
THY030 Thyroid Gland Disease 48 0.024
1007
BRN056 Bronchopulmonary Dysplasia 48 0.024
1008
BLD036 Bile Duct Disease 48 0.024
1009
P CTN003 Cutaneous Lupus Erythematosus 48 0.024
1010
CYT005 Cytomegalovirus Retinitis 47 0.024
1011
DBT006 Diabetic Macular Edema 47 0.024
1012
STR072 Stromal Keratitis 46 0.024
1013
P GNR032 Generalized Dystonia 45 0.024
1014
CRT017 Cartilage Disease 45 0.024
1015
PLY020 Polyradiculoneuropathy 45 0.024
1016
VSC047 Vascular Malformation 45 0.024
1017
OST003 Osteonecrosis 45 0.024
1018
HYP457 Hypertrophic Scars 45 0.024
1019
ANV001 Anovulation 44 0.024
1020
AGR002 Agoraphobia 44 0.024
1021
SWN001 Swine Influenza 44 0.024
1022
c CNT015 Central Sleep Apnea 44 0.024
1023
PRM020 Premenstrual Tension 44 0.024
1024
DNG001 Dengue Shock Syndrome 43 0.024
1025
c OPT053 Optic Atrophy 1 43 0.024
1026
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 42 0.024
1027
NRR001 Neuroretinitis 42 0.024
1028
BLR008 Bilirubin Metabolic Disorder 42 0.024
1029
VNT011 Ventricular Fibrillation, Familial, 1 41 0.024
1030
IRN002 Iron Metabolism Disease 41 0.024
1031
CRT008 Carotid Artery Dissection 41 0.024
1032
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.024
1033
HMT018 Hematopoietic Stem Cell Transplantation 41 0.024
1034
MLT075 Multifocal Motor Neuropathy 41 0.024
1035
DFF003 Diffuse Scleroderma 41 0.024
1036
c PRK045 Parkinson Disease 5 40 0.024
1037
CNN002 Cannabis Abuse 40 0.024
1038
LSS001 Loiasis 40 0.024
1039
SYM002 Sympathetic Ophthalmia 40 0.024
1040
c CHR096 Chronic Pulmonary Heart Disease 40 0.024
1041
IMP006 Impulse Control Disorder 40 0.024
1042
LYM020 Lymph Node Cancer 39 0.024
1043
SPN040 Spinal Cancer 39 0.024
1044
TNG004 Tongue Disease 39 0.024
1045
ADS004 Aids Dementia Complex 39 0.024
1046
c ADL001 Adult Lymphoma 39 0.024
1047
HPT004 Hepatic Coma 39 0.024
1048
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.024
1049
BRS090 Breast Reconstruction 38 0.024
1050
c CHR048 Chronic Rhinitis 38 0.024
1051
P FML187 Familial Hypertension 38 0.024
1052
ABR009 Abruzzo-Erickson Syndrome 38 0.024
1053
c PRK025 Parkinson Disease 10 38 0.024
1054
P ACQ009 Acquired Metabolic Disease 38 0.024
1055
c OST112 Osteoarthritis-5 38 0.024
1056
TMP012 Temple Syndrome 38 0.024
1057
CNN001 Cannabis Dependence 38 0.024
1058
P CRN276 Corneal Endothelial Dystrophy 37 0.024
1059
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 37 0.024
1060
PTL002 Patellofemoral Pain Syndrome 36 0.024
1061
BSL004 Basilar Artery Occlusion 36 0.024
1062
PST055 Postural Hypotension 36 0.024
1063
MTC005 Mitochondrial Metabolism Disease 36 0.024
1064
WHP002 Whiplash 36 0.024
1065
c ALZ032 Alzheimer Disease 18 35 0.024
1066
SGT001 Sagittal Sinus Thrombosis 35 0.024
1067
INT003 Intracranial Hypotension 34 0.024
1068
PRP026 Peripheral Retinal Degeneration 34 0.024
1069
IRT001 Iritis 34 0.024
1070
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.024
1071
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 34 0.024
1072
HYP332 Hypotrichosis, Congenital, with Juvenile Macular Dystrophy 34 0.024
1073
c OST126 Osteopetrosis, Autosomal Recessive 1 34 0.024
1074
c CRD187 Cardiomyopathy, Dilated, 3b 33 0.024
1075
TNN002 Tinea Unguium 33 0.024
1076
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.024
1077
ATY001 Atypical Depressive Disorder 32 0.024
1078
DSS010 Dissociative Disorder 32 0.024
1079
P CHR084 Chromosomal Disease 32 0.024
1080
URT020 Ureterocele 32 0.024
1081
GST039 Gastroduodenitis 31 0.024
1082
VSL002 Visual Epilepsy 31 0.024
1083
CYT004 Cytomegalic Inclusion Disease 31 0.024
1084
c CLR087 Colorectal Cancer 12 30 0.024
1085
CMP006 Complex Partial Epilepsy 30 0.024
1086
CHL035 Cholinergic Urticaria 29 0.024
1087
c CLR077 Colorectal Cancer 10 29 0.024
1088
IMM081 Immunodeficiency 19 29 0.024
1089
PSD021 Pseudovaginal Perineoscrotal Hypospadias 28 0.024
1090
c MYC058 Myocardial Infarction 2 28 0.024
1091
IMM063 Immunodeficiency 15 26 0.024
1092
SPN340 Spontaneous Intracranial Hypotension 26 0.024
1093
CNR014 Cone-Rod Dystrophy 16 26 0.024
1094
c BLP015 Blepharospasm, Primary Benign 26 0.024
1095
ACR021 Aica-Ribosiduria Due to Atic Deficiency 26 0.024
1096
HRN022 Hearing Loss/deafness 26 0.024
1097
MLK001 Milker's Nodule 26 0.024
1098
TTN001 Tetanus Neonatorum 25 0.024
1099
CNT017 Central Nervous System Origin Vertigo 24 0.024
1100
MSC012 Muscular Dystrophy, Duchenne and Becker Type 22 0.024
1101
ULC008 Ulcerative Proctitis 22 0.024
1102
CRB087 Cerebral Arteriosclerosis 21 0.024
1103
BNR002 Bone Resorption Disease 21 0.024
1104
c SYS046 Systemic Lupus Erythematosus 3 21 0.024
1105
c INF079 Inflammatory Bowel Disease 20 21 0.024
1106
ULC005 Ulcer of Lower Limbs 20 0.024
1107
SCL001 Scalp Dermatosis 18 0.024
1108
ATN001 Autonomic Peripheral Neuropathy 17 0.024
1109
AND005 Androgen Insensitivity Syndrome, Mild 16 0.024
1110
c FTT007 Fatty Liver Disease, Nonalcoholic 2 16 0.024
1111
LGD001 Leg Dermatosis 16 0.024
1112
BRN069 Brain and Spinal Tumors 12 0.024
1113
HRD059 Hereditary Peripheral Nervous Disorder 11 0.024
1114
MNT045 Montefiore Syndrome 10 0.024
1115
P RNL014 Renal Cell Carcinoma 82 0.021
1116
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.021
1117
c CHR090 Chronic Lymphocytic Leukemia 76 0.021
1118
WLS001 Wilson Disease 72 0.021
1119
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.021
1120
ADR007 Adrenoleukodystrophy 72 0.021
1121
THY028 Thyroid Cancer 69 0.021
1122
FBR012 Fabry Disease 69 0.021
1123