Search results for botulinum toxin type a

938 hits were found for botulinum toxin type a

# Family MCID Name MIFTS Score
1
c TYP009 Type 2 Diabetes Mellitus 92 81.837
2
P DBT009 Diabetes Mellitus 67 59.312
3
SPS057 Spasticity 43 58.497
4
c TYP008 Type 1 Diabetes Mellitus 77 54.364
5
P DYS154 Dystonia 64 52.196
6
CRB037 Cerebral Palsy 67 45.815
7
HMN044 Human Immunodeficiency Virus Type 1 76 43.557
8
PRT037 Pertussis 49 43.235
9
CRV043 Cervical Dystonia 45 40.439
10
TTN003 Tetanus 64 38.346
11
P HDC001 Headache 56 37.232
12
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 36.350
13
DPH001 Diphtheria 59 34.927
14
c MGR028 Migraine with or Without Aura 1 64 34.898
15
P BLP003 Blepharospasm 45 32.953
16
STR067 Stroke, Ischemic 79 32.704
17
LWC001 Low Compliance Bladder 44 30.887
18
c BLD140 Blood Group, I System 47 29.466
19
c AMY091 Amyotrophic Lateral Sclerosis 1 88 29.170
20
P TRT019 Torticollis 47 28.916
21
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 28.731
22
DYS073 Dysphagia 53 27.965
23
P HMF004 Hemifacial Spasm 38 27.338
24
HMF011 Hemifacial Spasm, Familial 33 27.301
25
P TRM003 Tremor 50 27.221
26
P HRP006 Herpes Simplex 65 26.837
27
IMM167 Immune Deficiency Disease 77 26.725
28
P NRP001 Neuropathy 59 26.465
29
P STR020 Strabismus 56 26.462
30
P PTS002 Ptosis 52 26.407
31
MCH006 Mechanical Strabismus 40 26.082
32
P ANR048 Aniridia 1 66 25.781
33
c MCP050 Mucopolysaccharidosis, Type Ii 73 25.245
34
CRB039 Cerebrovascular Disease 65 25.176
35
c HYP724 Hyperlipoproteinemia, Type Iii 66 24.845
36
SPN186 Spinal Cord Injury 61 24.106
37
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 23.774
38
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 23.771
39
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 23.722
40
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 23.721
41
c MCR120 Microvascular Complications of Diabetes 7 47 23.700
42
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 23.601
43
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 23.601
44
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 23.601
45
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 23.601
46
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 23.601
47
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 23.585
48
HYP066 Hyperglycemia 60 23.475
49
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 22.923
50
c DYS119 Dystonia 9 54 22.904
51
c HYP836 Hypercholesterolemia, Familial, 1 73 22.686
52
P NRF002 Neurofibromatosis 60 22.484
53
AGN016 Aging 54 22.140
54
ACH005 Achalasia 54 22.123
55
P BRS047 Breast Cancer 97 22.056
56
c MCR113 Microvascular Complications of Diabetes 3 52 21.991
57
P DRR001 Diarrhea 55 21.631
58
TXC005 Toxic Shock Syndrome 62 21.409
59
MSC157 Muscular Dystrophy, Duchenne Type 79 21.399
60
c ATR087 Atrial Standstill 1 74 21.351
61
c PNS012 Paine Syndrome 60 21.339
62
P MVM001 Movement Disease 61 21.245
63
P CNR004 Cone-Rod Dystrophy 2 75 21.077
64
ATM095 Autoimmune Disease 61 21.032
65
P CRG003 Crigler-Najjar Syndrome, Type I 64 20.908
66
OST012 Osteoarthritis 77 20.851
67
c MCR133 Microvascular Complications of Diabetes 4 41 20.786
68
c MCR130 Microvascular Complications of Diabetes 6 41 20.786
69
P PRK039 Parkinsonism 55 20.754
70
P PRP019 Peripheral Nervous System Disease 57 20.734
71
ALL029 Allergic Disease 61 20.704
72
P INT143 Interstitial Cystitis 59 20.648
73
P NRB001 Neuroblastoma 66 20.451
74
48X005 48,xyyy 39 20.160
75
SPS003 Spastic Diplegia 52 19.871
76
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 19.829
77
P HRT032 Heart Disease 84 19.744
78
P MLT020 Multiple Sclerosis 79 19.700
79
P LTR001 Lateral Sclerosis 58 19.697
80
HMP005 Hemiplegia 53 19.400
81
RHB024 Rhabdomyosarcoma 2 65 19.395
82
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 19.375
83
FCL022 Focal Dystonia 41 19.276
84
SPS016 Spasmodic Dysphonia 31 19.275
85
EST005 Esotropia 42 19.234
86
LKC009 Leukocyte Adhesion Deficiency, Type I 70 19.220
87
c MCR115 Microvascular Complications of Diabetes 5 65 19.213
88
P CRN300 Coronary Heart Disease 1 73 19.208
89
MNC001 Monocular Esotropia 30 19.192
90
ISC004 Ischemia 61 19.175
91
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 19.149
92
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 19.093
93
P TRN020 Turner Syndrome 67 19.090
94
P MLT074 Multiple Endocrine Neoplasia 58 19.029
95
P CYS018 Cystitis 59 18.980
96
DPR016 Depression 65 18.844
97
MSC007 Muscle Hypertrophy 64 18.756
98
SCH068 Schwartz-Jampel Syndrome, Type 1 52 18.749
99
HMP009 Haemophilus Influenzae 41 18.513
100
P SZR006 Seizure Disorder 69 18.419
101
P URN019 Urinary Tract Infection 49 18.385
102
CNS004 Constipation 56 18.376
103
END086 End Stage Renal Disease 54 18.353
104
P RHN004 Rhinitis 57 18.180
105
DBT010 Diabetic Neuropathy 54 18.078
106
CYT002 Cytokine Deficiency 43 18.066
107
P PRK057 Parkinson Disease, Late-Onset 79 18.057
108
BLP048 Blepharospasm, Benign Essential 36 18.047
109
P CHR345 Chronic Pain 50 18.038
110
PRS045 Prostatic Hypertrophy 52 18.004
111
P CLR023 Colorectal Cancer 100 17.960
112
c MCL013 Mucolipidosis Iv 64 17.918
113
P PSR002 Psoriasis 63 17.916
114
PST011 Pustulosis of Palm and Sole 52 17.900
115
P MYP004 Myopathy 67 17.841
116
c HYP595 Hypertension, Essential 84 17.763
117
PRS021 Prostatic Adenoma 43 17.744
118
P ALZ034 Alzheimer Disease 87 17.652
119
PRS129 Prostatic Hyperplasia, Benign 48 17.576
120
BCK006 Back Pain 43 17.568
121
P LNG032 Lung Cancer 98 17.546
122
P ATR011 Atrial Fibrillation 66 17.403
123
OCL069 Ocular Motor Apraxia 57 17.368
124
P PHC003 Pheochromocytoma 70 17.278
125
SPS007 Spastic Cerebral Palsy 46 17.241
126
P FNG006 Feingold Syndrome 1 61 17.229
127
NRG002 Neurogenic Bladder 55 17.156
128
c EPS039 Episodic Pain Syndrome, Familial, 1 42 17.142
129
P VSC007 Vascular Disease 62 17.129
130
MNT002 Mental Depression 56 17.047
131
P SPN301 Spinocerebellar Ataxia 2 59 17.012
132
P LYM118 Lymphoma 69 16.888
133
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 16.885
134
P ART022 Arthritis 70 16.884
135
LPD008 Lipid Metabolism Disorder 61 16.837
136
TRG002 Trigeminal Neuralgia 61 16.834
137
GLT035 Glutaric Acidemia I 57 16.726
138
P MSC005 Muscular Dystrophy 66 16.707
139
P PLY019 Polyneuropathy 53 16.688
140
c DYS056 Dystonia 12 63 16.606
141
IMP005 Impotence 52 16.473
142
PRT251 Proteinuria, Chronic Benign 58 16.377
143
ANT039 Antisynthetase Syndrome 55 16.373
144
ADL002 Adult Syndrome 69 16.318
145
SKN016 Skin Disease 62 16.289
146
P LKM002 Leukemia 66 16.193
147
LPP008 Lipoprotein Quantitative Trait Locus 65 16.150
148
RPD005 Rapidly Involuting Congenital Hemangioma 48 16.105
149
c PCH015 Pachyonychia Congenita 1 60 16.052
150
P RSP003 Respiratory Failure 74 16.010
151
P MPL001 Maple Syrup Urine Disease 69 15.997
152
PPL049 Papillon-Lefevre Syndrome 65 15.960
153
INS024 Insulin-Like Growth Factor I 77 15.928
154
c ACT068 Acute Cystitis 61 15.921
155
PRS047 Prostatitis 58 15.834
156
47X002 47,xyy 48 15.647
157
P ALP008 Alopecia 53 15.601
158
c LKM061 Leukemia, Acute Myeloid 83 15.575
159
BRX001 Bruxism 51 15.550
160
MYF002 Myofascial Pain Syndrome 46 15.529
161
FCL012 Facial Paralysis 49 15.498
162
ART140 Arteries, Anomalies of 52 15.493
163
FTT001 Fatty Liver Disease 61 15.491
164
CRH001 Crohn's Disease 80 15.474
165
P DMN002 Dementia 65 15.434
166
DRM006 Dermatitis 62 15.427
167
ANX010 Anxiety 70 15.419
168
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 15.411
169
NNL005 Non-Alcoholic Fatty Liver Disease 63 15.398
170
c HPT003 Hepatitis a 63 15.255
171
CRB009 Cerebritis 43 15.213
172
P LVR013 Liver Disease 68 15.201
173
P RTN008 Retinitis Pigmentosa 79 15.164
174
ALC007 Alcohol Dependence 65 15.134
175
GST045 Gastroenteritis 58 15.128
176
P CRV039 Cervicitis 52 15.071
177
FBR047 Fibromyalgia 58 14.912
178
CMP010 Complex Regional Pain Syndrome 59 14.882
179
P MYC007 Myocardial Infarction 69 14.875
180
P ADN016 Adenocarcinoma 63 14.817
181
P MSC003 Muscular Atrophy 52 14.773
182
P EXN002 Exanthem 58 14.768
183
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 14.765
184
BRN071 Brain Injury 50 14.757
185
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 14.609
186
DWN001 Down Syndrome 70 14.586
187
P GST053 Gastric Cancer 82 14.576
188
GLB002 Glioblastoma 67 14.554
189
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 14.510
190
P ALC033 Alcohol Use Disorder 67 14.499
191
P PRD008 Periodontitis 64 14.494
192
P BCL017 B-Cell Lymphoma 57 14.481
193
RNL114 Renal Cell Carcinoma, Nonpapillary 79 14.451
194
P CHR071 Charcot-Marie-Tooth Disease 64 14.420
195
P EPL164 Epilepsy 70 14.374
196
P MLN008 Melanoma 75 14.369
197
CHR619 Chromosome 2q35 Duplication Syndrome 64 14.192
198
ACQ007 Acquired Immunodeficiency Syndrome 58 14.184
199
P GLM040 Glioma Susceptibility 1 70 14.161
200
P PNC044 Pancreatitis 61 14.139
201
MSC152 Muscular Dystrophy, Becker Type 69 14.127
202
P MCR129 Microvascular Complications of Diabetes 1 68 14.120
203
EXT022 Exotropia 42 14.075
204
DSS032 Disease by Infectious Agent 55 14.053
205
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 14.049
206
BCT022 Bacterial Infectious Disease 56 14.043
207
TRM010 Traumatic Brain Injury 50 14.038
208
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 14.029
209
CNG034 Congestive Heart Failure 69 14.009
210
GLM045 Glioma 62 13.994
211
ALT003 Alternating Exotropia 33 13.947
212
P PRS038 Personality Disorder 65 13.871
213
c ACT071 Acute Kidney Failure 60 13.868
214
EPC002 Epicondylitis 43 13.866
215
c MSC045 Muscular Dystrophy-Dystroglycanopathy , Type a, 3 38 13.845
216
P EYD002 Eye Disease 57 13.805
217
GLL048 Glial Tumor 52 13.787
218
P INF038 Influenza 68 13.782
219
GST037 Gastroparesis 52 13.771
220
LPT014 Leptin Deficiency or Dysfunction 77 13.755
221
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 13.627
222
P SYS005 Systemic Scleroderma 73 13.626
223
ANR040 Aneurysm 60 13.476
224
P MTR014 Motor Neuron Disease 65 13.444
225
P HPT023 Hepatocellular Carcinoma 95 13.406
226
FSC004 Fasciitis 49 13.355
227
c ESS001 Essential Tremor 56 13.350
228
c PLM164 Pulmonary Hypertension, Primary, 1 80 13.331
229
P GLM007 Glomerulonephritis 59 13.309
230
RYN005 Raynaud Phenomenon 45 13.298
231
PRP016 Paraplegia 52 13.291
232
P ENC018 Encephalopathy 62 13.286
233
c DNT047 Dentinogenesis Imperfecta Type 2 35 13.261
234
c BRN108 Branchiootic Syndrome 1 63 13.228
235
NRM005 Neuromuscular Disease 63 13.202
236
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 13.191
237
P PRS040 Prostate Cancer 95 13.166
238
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 13.165
239
CRV035 Cervical Cancer 72 13.153
240
PNG002 Pain Agnosia 51 13.143
241
CLF001 Cleft Lip 54 13.127
242
P CNJ013 Conjunctivitis 66 13.092
243
P DRM053 Dermatitis, Atopic 65 13.075
244
c FNC043 Fanconi Anemia, Complementation Group E 62 12.963
245
BRT054 Brittle Bone Disorder 74 12.952
246
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 12.912
247
P THR014 Thrombocytopenia 66 12.873
248
ORM002 Oromandibular Dystonia 41 12.872
249
P SLP006 Sleep Apnea 69 12.872
250
P PNM007 Pneumonia 64 12.858
251
c EPD030 Epidermolysis Bullosa Simplex, Localized 46 12.817
252
P SPN046 Spinal Muscular Atrophy 62 12.794
253
CYS001 Cystic Fibrosis 77 12.790
254
c SCL052 Scleroderma, Familial Progressive 60 12.785
255
THR024 Thrombosis 56 12.686
256
P OVR042 Ovarian Cancer 88 12.666
257
HYP457 Hypertrophic Scars 42 12.623
259
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 12.569
260
HYP264 Hypertonia 36 12.547
261
ART002 Arts Syndrome 66 12.523
262
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 12.387
263
P ATT013 Attention Deficit-Hyperactivity Disorder 66 12.337
264
BNR002 Bone Resorption Disease 47 12.330
265
P AMY004 Amyloidosis 69 12.315
266
ART016 Aortic Aneurysm 69 12.313
267
P HRS035 Hirschsprung Disease 1 66 12.308
268
P SPP010 Suppressor of Tumorigenicity 3 51 12.299
269
P MYL006 Myeloid Leukemia 60 12.292
270
c PSR017 Psoriasis 2 53 12.239
271
KRT019 Keratitis, Hereditary 66 12.225
272
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 12.221
273
CLT003 Colitis 63 12.176
274
P CLC063 Celiac Disease 1 66 12.116
275
ESP021 Esophageal Cancer 84 12.081
276
CLS016 Clostridium Difficile Colitis 49 12.011
277
DFC004 Deficiency Anemia 74 12.010
278
P MYC033 Myoclonus 46 12.008
279
GLC003 Glucose Intolerance 53 12.008
280
PTH003 Pathologic Nystagmus 52 12.008
281
P MJR001 Major Depressive Disorder 68 12.003
282
NRL016 Neural Tube Defects 81 11.988
283
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 11.971
284
KRT006 Keratoconjunctivitis 53 11.955
285
P MYT002 Myotonic Dystrophy 51 11.951
286
P THY032 Thyroiditis 56 11.908
287
MLT157 Multiple System Atrophy 1 69 11.901
288
CLB002 Clubfoot 51 11.898
289
P PNC035 Pancreatic Cancer 86 11.860
290
PLM129 Pulmonary Disease, Chronic Obstructive 74 11.855
291
ULC004 Ulcerative Colitis 74 11.810
292
MYL020 Myelomeningocele 51 11.801
293
ENT011 Enterocolitis 55 11.774
294
P SCL018 Scoliosis 57 11.773
295
P CLS010 Cluster Headache 42 11.759
296
ADN018 Adenoma 58 11.728
297
P PLM037 Pulmonary Hypertension 69 11.713
298
P ART023 Arthropathy 60 11.635
299
c SML038 Small Cell Cancer of the Lung 69 11.625
300
c ACT027 Acute Pancreatitis 60 11.596
301
P ESP024 Esophagitis 60 11.569
302
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 11.558
303
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 11.508
304
DTR001 Detrusor Sphincter Dyssynergia 37 11.484
305
PST053 Postherpetic Neuralgia 40 11.453
306
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 11.435
307
KLD004 Keloid Disorder 39 11.427
308
P HYP061 Hypertrophic Cardiomyopathy 69 11.423
309
P HYP086 Hypothyroidism 69 11.410
310
P END044 Endometriosis 62 11.393
311
P EPD016 Epidermolysis Bullosa 53 11.393
312
PRT036 Peritonitis 65 11.382
313
P AST005 Asthma 76 11.371
314
LNG099 Lung Disease 62 11.339
315
NRT001 Neurotic Disorder 56 11.323
316
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 11.311
317
c PSR023 Psoriasis 1 52 11.275
318
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 11.269
319
SRC014 Sarcoma 64 11.247
320
P INF037 Inflammatory Bowel Disease 53 11.174
321
P LPR021 Leprosy 3 71 11.174
322
c CNG546 Congenital Muscular Dystrophy-Dystroglycanopathy Type a 31 11.172
323
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 11.165
324
P CTR002 Cataract 59 11.143
325
P MNN013 Meningitis 65 11.099
326
NRF007 Neurofibroma 64 11.079
327
MGS001 Megaesophagus 44 11.074
328
THY029 Thyroid Carcinoma 54 11.068
329
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 11.065
330
P ACN011 Acne 55 11.056
331
P USH001 Usher Syndrome 64 11.056
332
PRP027 Peripheral Vascular Disease 71 11.054
333
P SKN015 Skin Carcinoma 71 11.011
334
P RHM011 Rheumatoid Arthritis 81 10.948
335
PPL022 Papilloma 53 10.939
336
P SRC025 Sarcoidosis 1 70 10.931
337
NRR001 Neuroretinitis 42 10.897
338
c PSR018 Psoriasis 13 40 10.875
339
RTN023 Retinitis 45 10.854
340
END040 Endogenous Depression 54 10.850
341
ALL003 Allergic Rhinitis 66 10.820
342
P EHL001 Ehlers-Danlos Syndrome 57 10.817
343
c DLT002 Dilated Cardiomyopathy 79 10.813
344
SVR004 Severe Combined Immunodeficiency 71 10.812
345
SXL003 Sexual Disorder 49 10.781
346
P NJM001 Nijmegen Breakage Syndrome 75 10.774
347
P LNG064 Lung Cancer Susceptibility 3 70 10.771
348
P ALP009 Alopecia Areata 59 10.756
349
GNG013 Gingivitis 59 10.746
350
P NRV007 Nervous System Disease 66 10.739
351
P SPS133 Spastic Paraplegia 2, X-Linked 50 10.733
352
HYP266 Hypoxia 56 10.729
353
P OST002 Osteoporosis 77 10.722
354
RGD003 Rigid Spine Muscular Dystrophy 1 56 10.705
355
END057 Endometrial Cancer 71 10.645
356
P LKM062 Leukemia, Acute Lymphoblastic 69 10.644
357
SQM006 Squamous Cell Carcinoma 59 10.632
358
P TCD001 Tic Disorder 50 10.625
359
SPN035 Spindle Cell Sarcoma 51 10.609
360
OST159 Osteogenic Sarcoma 66 10.589
361
P CRD119 Cardiac Arrest 68 10.579
362
OST062 Osteoarthritis with Mild Chondrodysplasia 47 10.561
363
ATY005 Atypical Teratoid Rhabdoid Tumor 69 10.516
364
VCC001 Vaccinia 49 10.516
366
PRP030 Purpura 54 10.494
367
P ATX030 Ataxia-Telangiectasia 80 10.457
368
SPS005 Spastic Hemiplegia 40 10.426
369
AGG012 Aggressive Nk-Cell Leukemia 47 10.400
370
P SLP005 Sleep Disorder 62 10.380
371
TLN003 Telangiectasis 51 10.255
372
LBS001 Lubs X-Linked Mental Retardation Syndrome 49 10.245
373
INS001 Insulinoma 59 10.201
374
DYS015 Dysentery 50 10.191
375
SPS019 Spastic Paraparesis 38 10.182
376
INT323 Intraocular Pressure Quantitative Trait Locus 63 10.179
377
P VSC011 Vasculitis 61 10.166
378
P CMP008 Compartment Syndrome 50 10.150
379
c VSC019 Vesicoureteral Reflux 1 56 10.061
380
GST050 Gastrointestinal System Disease 55 10.048
381
ACT098 Acute Erythroid Leukemia 55 10.017
382
P BLD134 Bladder Cancer 79 10.016
383
PLN007 Plantar Fasciitis 35 9.970
384
CNN011 Cenani-Lenz Syndactyly Syndrome 51 9.919
385
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 9.911
386
ATX019 Ataxia with Vitamin E Deficiency 44 9.902
387
BLL003 Bell's Palsy 48 9.897
388
P OVR082 Overgrowth Syndrome 42 9.892
389
P RTN024 Retinoblastoma 72 9.880
390
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 9.879
391
OTT002 Otitis Media 71 9.874
392
THR013 Thoracic Outlet Syndrome 46 9.862
393
TTH006 Tooth Disease 51 9.847
394
c PRC016 Pre-Eclampsia 64 9.826
395
LYM143 Lymphoma, Non-Hodgkin, Familial 79 9.822
396
MLG169 Malignant Astrocytoma 57 9.820
397
P ADL010 Adult Respiratory Distress Syndrome 71 9.815
398
GST092 Gastroesophageal Reflux 60 9.779
399
AND005 Androgen Insensitivity Syndrome, Mild 21 9.755
400
CVD001 Covid-19 58 9.731
401
P NSP012 Nasopharyngeal Carcinoma 60 9.715
402
P BPL003 Bipolar Disorder 56 9.698
403
DBT002 Diabetic Autonomic Neuropathy 40 9.668
404
HRW001 Hair Whorl 35 9.629
405
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 9.582
406
P INF032 Infertility 60 9.575
407
ATN005 Autonomic Dysfunction 45 9.568
408
P CRP001 Carpal Tunnel Syndrome 66 9.555
409
P NTR004 Neutropenia 62 9.541
410
MLR004 Malaria 78 9.483
411
AYM001 Ayme-Gripp Syndrome 57 9.323
412
c LYM145 Lymphatic Malformation 5 48 9.318
413
LYM133 Lymphoma, Hodgkin, Classic 74 9.293
414
STM007 Stomatitis 52 9.261
415
BRN024 Bronchitis 67 9.259
416
GST040 Gastric Adenocarcinoma 66 9.257
417
P GRF003 Graft-Versus-Host Disease 71 9.231
418
CRD223 Cardiac Arrhythmia 63 9.223
419
MTH009 Mouth Disease 57 9.218
420
TYP007 Typhoid Fever 63 9.205
421
CLF027 Cleft Palate, Isolated 64 9.185
422
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 9.184
423
P CRD246 Cardiovascular System Disease 55 9.167
424
P HYD006 Hydrocephalus 63 9.120
425
c PCH010 Pachyonychia Congenita 3 43 9.036
426
P SCH015 Schizophrenia 74 9.035
427
P HNT016 Huntington Disease 73 9.033
428
P HYP265 Hypotonia 42 9.020
429
NRT004 Neuritis 53 9.001
430
KRT001 Keratoconjunctivitis Sicca 49 8.998
431
SVR001 Severe Acute Respiratory Syndrome 68 8.997
432
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 8.981
433
P ATS364 Autism 72 8.896
434
P PMP001 Pemphigus 55 8.887
435
INC021 Incontinentia Pigmenti 63 8.881
436
P BND020 Bone Disease 60 8.874
437
c AMY085 Amyotrophic Lateral Sclerosis 9 35 8.840
438
BHR001 Behr Syndrome 50 8.835
439
c HRD010 Hereditary Spastic Paraplegia 65 8.833
440
CNN005 Connective Tissue Disease 66 8.818
441
P RST001 Restless Legs Syndrome 52 8.814
442
c FML001 Familial Atrial Fibrillation 65 8.766
443
KRT009 Keratosis 52 8.760
444
MYL009 Myelodysplastic Syndrome 67 8.750
445
P UVT001 Uveitis 57 8.738
446
c ACT075 Acute Myocardial Infarction 55 8.733
447
NRM004 Neuroma 49 8.726
448
P GRV001 Graves' Disease 54 8.690
449
c MJR024 Major Affective Disorder 9 40 8.687
450
c MJR022 Major Affective Disorder 8 37 8.687
451
P RCT021 Rectum Cancer 54 8.660
452
c ATS007 Autism Spectrum Disorder 72 8.629
453
INT002 Intermittent Claudication 61 8.608
454
P MCR010 Microcephaly 59 8.586
455
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 8.535
456
RFL001 Reflex Sympathetic Dystrophy 51 8.508
457
c EXD008 Exudative Vitreoretinopathy 1 71 8.500
458
P MMP001 Mumps 56 8.490
459
URT001 Urethritis 52 8.488
460
PTN001 Patent Foramen Ovale 62 8.481
461
P AMY106 Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia 44 8.479
462
HLC007 Helicobacter Pylori Infection 67 8.453
463
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 55 8.446
464
P MGR001 Migraine Without Aura 48 8.407
465
P HYP098 Hypereosinophilic Syndrome 66 8.404
466
TND005 Tendinitis 54 8.399
467
AMB002 Amblyopia 49 8.376
468
3MT013 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome 45 8.374
469
ETN001 Eating Disorder 59 8.372
470
IRN002 Iron Metabolism Disease 56 8.363
471
c SZR022 Seizures, Benign Familial Neonatal, 1 42 8.338
472
IRR002 Irritable Bowel Syndrome 65 8.295
473
RTN017 Retinal Detachment 60 8.257
474
ATR003 Atrophic Rhinitis 39 8.248
475
c LCL006 Localized Scleroderma 64 8.243
476
DRY001 Dry Eye Syndrome 49 8.202
477
P EPD003 Epidermolysis Bullosa Simplex 57 8.192
478
MSL001 Measles 61 8.188
479
c PRM038 Primary Agammaglobulinemia 47 8.188
480
FRN006 Frontotemporal Dementia 68 8.179
481
c PSR028 Psoriasis 7 43 8.169
482
P OPT006 Optic Nerve Disease 57 8.101
483
P SNS001 Sensorineural Hearing Loss 59 8.098
484
DYS192 Dystonia, Dopa-Responsive 56 8.057
485
c GLL024 Gallbladder Disease 1 53 8.008
486
c PSR032 Psoriasis 11 47 7.987
487
SPP007 Suppression Amblyopia 38 7.974
488
c LKM063 Leukemia, Chronic Myeloid 71 7.972
489
P HMP007 Hemophilia 52 7.907
490
P FRG001 Fragile X Syndrome 70 7.898
491
ACH015 Achalasia, Familial Esophageal 42 7.870
492
P SCL057 Scoliosis, Isolated 1 40 7.827
493
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 62 7.819
494
P DST002 Distal Arthrogryposis 63 7.819
495
P KRT007 Keratoconus 50 7.811
496
SCT005 Scott Syndrome 51 7.807
497
MNN043 Meningioma, Familial 79 7.778
498
BNG091 Benign Chronic Pemphigus 56 7.769
499
c DWL002 Dowling-Degos Disease 1 58 7.749
500
TMP019 Temporomandibular Joint Anomaly 28 7.742
501
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 7.720
502
SPN027 Spinal Stenosis 59 7.714
503
HYP080 Hypogonadism 49 7.710
504
BRD001 Brody Myopathy 54 7.693
505
AND014 Androgenic Alopecia 46 7.692
506
P KHL003 Kohlschutter-Tonz Syndrome 57 7.686
507
PPT005 Peptic Ulcer Disease 58 7.658
508
KPS004 Kaposi Sarcoma 76 7.657
509
SNS003 Sensory Peripheral Neuropathy 51 7.617
510
DNT012 Dental Caries 53 7.607
511
P ALP061 Alopecia, Androgenetic, 1 49 7.559
512
PLM010 Pulmonary Edema 54 7.557
513
c PRD040 Periodontitis, Chronic 52 7.537
514
PRP080 Peripheral Artery Disease 54 7.525
515
RYN001 Raynaud Disease 49 7.518
516
MCP033 Mucopolysaccharidoses 44 7.493
517
P THY023 Thymoma 64 7.490
518
P HYP076 Hyperthyroidism 53 7.488
519
P INT068 Intestinal Disease 53 7.412
520
CHL065 Cholangiocarcinoma 58 7.411
521
FCT001 Factor Viii Deficiency 62 7.390
522
SDD001 Sudden Infant Death Syndrome 60 7.387
523
LMY002 Leiomyoma 51 7.330
524
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 7.325
525
GLL008 Gilles De La Tourette Syndrome 64 7.314
526
c THR092 Thrombophilia Due to Thrombin Defect 74 7.313
527
c HMP029 Hemophilia a 69 7.313
528
P SJG008 Sjogren Syndrome 61 7.304
529
ANG054 Angina Pectoris 65 7.297
530
P SML001 Small Cell Carcinoma 52 7.255
531
PST092 Posttransplant Acute Limbic Encephalitis 29 7.254
532
ALB002 Albinism 47 7.253
533
P MYP006 Myopia 55 7.236
534
LGH007 Leigh Syndrome 70 7.234
535
APN008 Apnea, Obstructive Sleep 66 7.231
536
SMT001 Somatization Disorder 50 7.193
537
INT079 Intrahepatic Cholangiocarcinoma 51 7.190
538
DYS011 Dyskinesia of Esophagus 40 7.187
539
FRZ001 Frozen Shoulder 54 7.161
540
c SPN225 Spondyloarthropathy 1 70 7.153
541
P OCL002 Oculocutaneous Albinism 59 7.120
542
P EPD009 Epidermolysis Bullosa Dystrophica 66 7.119
543
VRL011 Viral Infectious Disease 60 7.115
544
P BNG032 Benign Mesothelioma 53 7.108
545
BRS051 Breast Disease 58 7.101
546
PNC129 Pancreatic Adenocarcinoma 65 7.088
547
PHR003 Pharyngitis 57 7.070
548
KRN002 Kearns-Sayre Syndrome 63 7.053
549
DFF003 Diffuse Scleroderma 41 7.015
550
P MGR003 Migraine with Aura 51 7.010
551
VSC002 Vascular Dementia 59 6.992
552
c THY109 Thyroid Cancer, Nonmedullary, 1 55 6.989
553
MYT011 Myotonia 38 6.978
554
APH002 Aphasia 55 6.962
555
PST028 Post-Traumatic Stress Disorder 59 6.938
556
TND004 Tendinopathy 45 6.934
557
P TRC031 Trichorhinophalangeal Syndrome 37 6.911
558
STT001 Status Epilepticus 58 6.901
559
VLV042 Vulvar Vestibulitis Syndrome 37 6.892
560
CHL079 Children's Interstitial Lung Disease 26 6.891
561
P OPN001 Open-Angle Glaucoma 55 6.890
562
FCL049 Focal Hand Dystonia 30 6.865
563
SCL003 Social Phobia 48 6.856
564
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 6.849
565
SWL001 Swallowing Disorders 38 6.826
566
P CRN025 Corneal Dystrophy 49 6.826
567
RBS001 Rabies 58 6.826
568
MCS002 Mucositis 55 6.802
569
PRL023 Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome 48 6.787
570
P RTN016 Retinal Degeneration 52 6.786
571
NRN004 Neuroendocrine Tumor 55 6.714
572
SPL018 Splenomegaly 47 6.701
573
ACT113 Acute Myeloblastic Leukemia with Maturation 46 6.689
574
VRC005 Varicose Veins 59 6.681
575
PRS063 Paresthesia 39 6.676
576
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 6.672
577
DRR014 Darier-White Disease 58 6.658
578
P MLG056 Malignant Hyperthermia 65 6.623
579
BRS064 Bursitis 51 6.572
580
c DNR003 Duane Retraction Syndrome 1 37 6.567
581
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 6.556
582
ACR007 Acromegaly 70 6.533
583
FDL002 Food Allergy 47 6.530
584
SHG001 Shigellosis 61 6.521
585
ATR057 Atrioventricular Block 54 6.512
586
MST022 Masticatory Muscles, Hypertrophy of 19 6.502
587
LYM027 Lymphopenia 56 6.481
588
ESP020 Esophageal Atresia 60 6.450
589
P LCT001 Lactic Acidosis 50 6.441
590
P HMR005 Hemorrhoid 49 6.430
591
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 6.427
592
RSC001 Rosacea 55 6.419
593
LPT006 Leptin Receptor Deficiency 50 6.414
594
ACT011 Acute Contagious Conjunctivitis 42 6.411
595
ALL006 Allergic Asthma 56 6.393
596
RDC002 Radiculopathy 51 6.370
597
c BSL007 Basal Cell Carcinoma 68 6.355
598
PRT013 Portal Hypertension 59 6.311
599
P DYS193 Dystonia 11, Myoclonic 55 6.306
600
TRD006 Tardive Dyskinesia 53 6.267
601
PNC041 Pancreatic Ductal Adenocarcinoma 51 6.233
602
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 6.228
603
FCL014 Focal Epilepsy 53 6.228
604
SYN036 Syncope 44 6.175
605
HYD002 Hydronephrosis 58 6.142
606
PYR010 Peyronie's Disease 50 6.125
607
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 6.123
608
IDP070 Idiopathic Scoliosis 41 6.094
609
ORB013 Orbital Disease 42 6.087
610
RLP002 Relapsing-Remitting Multiple Sclerosis 56 6.072
611
OVR094 Ovarian Epithelial Cancer 39 6.052
613
P SPR120 Supranuclear Palsy, Progressive, 1 69 5.999
614
ING001 Inguinal Hernia 59 5.978
615
P PLV020 Pelvic Organ Prolapse 58 5.955
616
PSR001 Psoriatic Arthritis 61 5.951
617
AVD001 Avoidant Personality Disorder 49 5.935
618
PRM003 Premature Ejaculation 44 5.898
619
HYP458 Hyper Ige Syndrome 60 5.898
620
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 5.873
621
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 50 5.862
622
AST006 Astigmatism 46 5.820
623
P RTT002 Rett Syndrome 79 5.818
624
c ACT073 Acute Leukemia 59 5.811
625
c GLC092 Glaucoma, Primary Open Angle 61 5.791
626
SCH014 Schistosomiasis 56 5.782
627
MCR013 Microphthalmia 60 5.753
628
P TXP001 Toxoplasmosis 60 5.737
629
ALG001 Algoneurodystrophy 37 5.728
630
URN010 Urinary Tract Obstruction 55 5.726
631
MNN028 Mononeuropathy of the Median Nerve, Mild 46 5.700
632
P TRC072 Treacher Collins Syndrome 1 62 5.698
633
ILS001 Ileus 49 5.692
634
ANR007 Anorexia Nervosa 59 5.646
635
ACR041 Acromelic Frontonasal Dysostosis 53 5.646
636
HMC014 Homocysteinemia 52 5.644
637
P EPS003 Episodic Ataxia 59 5.633
638
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 5.626
639
SPT004 Septic Arthritis 58 5.579
640
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 5.578
641
P DYS021 Dysautonomia 38 5.577
642
c DYS151 Dystonia 25 40 5.571
643
P CHR012 Chronic Granulomatous Disease 69 5.557
644
DYS198 Dystonia, Focal, Task-Specific 31 5.544
645
WLS001 Wilson Disease 70 5.533
646
BSL036 Basal Cell Nevus Syndrome 73 5.532
647
THY030 Thyroid Gland Disease 50 5.517
648
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 5.475
649
P CTS001 Cutis Laxa 64 5.456
650
ALP097 Alopecia Universalis Congenita 57 5.449
651
PLM029 Palmoplantar Keratosis 48 5.445
652
CLF004 Cleft Lip/palate 57 5.442
653
STT041 Stuttering 52 5.429
654
P RBL001 Rubella 58 5.426
655
CHR682 Chronic Bilirubin Encephalopathy 37 5.420
656
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 5.416
657
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 43 5.414
658
OBS002 Obsessive-Compulsive Disorder 68 5.384
659
HNT002 Hantavirus Pulmonary Syndrome 55 5.378
660
P FRD001 Friedreich Ataxia 62 5.375
661
PRS120 Persistent Idiopathic Facial Pain 27 5.366
662
TRG001 Trigonitis 36 5.363
663
ANS018 Anismus 29 5.357
664
END072 Endotheliitis 36 5.357
665
ENT004 Enthesopathy 51 5.345
666
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 5.336
667
P BCK002 Beckwith-Wiedemann Syndrome 61 5.334
668
HMG002 Hemoglobinuria 50 5.330
669
ERL001 Early Myoclonic Encephalopathy 63 5.326
670
P URF003 Urofacial Syndrome 1 56 5.301
671
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 5.299
672
c JVN010 Juvenile Rheumatoid Arthritis 66 5.281
673
CMB007 Combined Immunodeficiency 56 5.229
674
CMM005 Common Cold 55 5.213
675
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 5.198
676
NSP002 Nasopharyngitis 45 5.194
677
c RTN041 Retinitis Pigmentosa 11 43 5.184
678
CYN002 Cyanosis, Transient Neonatal 43 5.179
679
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 39 5.167
680
c DNR004 Duane Retraction Syndrome 2 28 5.158
681
MDS022 Mediastinitis 47 5.134
682
ADN011 Adenoid Cystic Carcinoma 68 5.119
683
BLR008 Bilirubin Metabolic Disorder 57 5.102
684
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 5.094
685
BRD004 Borderline Personality Disorder 53 5.081
686
P SPS012 Spastic Paraplegia 3a 32 5.079
687
EXP004 Exophthalmos 50 5.062
688
PSY004 Psychotic Disorder 66 5.060
689
P CHN012 Chondrosarcoma 56 5.057
690
CLN015 Colon Adenocarcinoma 64 5.055
691
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 5.052
692
BNN005 Bunion 31 5.044
693
GRW007 Growth Hormone Deficiency 47 4.980
694
P LCH002 Lichen Planus 55 4.961
695
PRM329 Premature Aging 36 4.952
696
BRN009 Burning Mouth Syndrome 51 4.931
697
CHR100 Chronic Ulcer of Skin 57 4.931
698
BP1002 Bap1 Tumor Predisposition Syndrome 42 4.929
699
SPN020 Spondylosis 46 4.926
700
CHR073 Choreatic Disease 53 4.920
701
APP008 Appendicitis 62 4.919
702
P MCL001 Mucolipidosis 49 4.899
703
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 4.799
704
c DYS163 Dystonia 4, Torsion, Autosomal Dominant 35 4.771
705
P ANT088 Anterior Segment Dysgenesis 53 4.751
706
NRN002 Neuronitis 31 4.742
707
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 4.690
708
c PRS097 Prostate Cancer, Hereditary, 1 38 4.687
709
NRN001 Neuroendocrine Carcinoma 47 4.639
710
DCB001 Decubitus Ulcer 61 4.637
711
NTL003 Notalgia Paresthetica 18 4.619
712
EPD015 Epidemic Typhus 44 4.618
713
P MYT023 Myotonia Congenita 56 4.615
714
BRR014 Barrett Esophagus 66 4.614
715
ANS012 Anus Disease 47 4.613
716
c PNC108 Pancreatitis, Hereditary 68 4.569
717
ALS001 Alstrom Syndrome 65 4.559
718
ABD010 Abdominal Wall Defect 39 4.539
719
PMP006 Pemphigus Vulgaris, Familial 58 4.499
720
ENT001 Enterocele 42 4.493
721
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 4.491
722
P INT070 Intestinal Obstruction 57 4.464
723
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 54 4.442
724
c ATS452 Autosomal Recessive Axonal Hereditary Motor and Sensory Neuropathy 18 4.430
725
c DYS172 Dystonia 27 36 4.415
726
CNG506 Congenital Amyoplasia 27 4.413
727
AMY003 Amyotrophic Neuralgia 41 4.365
728
P MRR011 Mirror Movements 1 51 4.361
729
PTL002 Patellofemoral Pain Syndrome 33 4.345
730
LNG015 Lingual-Facial-Buccal Dyskinesia 47 4.334
731
CLL010 Cellular Ependymoma 58 4.304
732
P HMC002 Homocystinuria 52 4.287
733
P LCR008 Lacrimal Apparatus Disease 39 4.258
734
P NML001 Nemaline Myopathy 49 4.248
735
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 4.218
736
ALV005 Alveolar Soft Part Sarcoma 61 4.208
737
CRY008 Cryopyrin-Associated Periodic Syndrome 48 4.205
738
ESP002 Esophageal Varix 51 4.198
739
IRD001 Iridocyclitis 54 4.183
740
GLM008 Glomus Tumor 48 4.183
741
ANG020 Angiosarcoma 63 4.179
742
c PRS130 Prostate Cancer, Hereditary, 8 32 4.178
743
c PRS136 Prostate Cancer, Hereditary, 6 33 4.178
744
MYF001 Myofibroma 42 4.175
745
c DPH024 Diaphragmatic Hernia, Congenital 64 4.175
747
EXC003 Excessive Tearing 32 4.163
748
OCC008 Occipital Neuralgia 24 4.151
749
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 4.137
750
HST010 Histiocytosis 49 4.132
751
P PYR039 Peyronie Disease 39 4.131
752
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 54 4.119
753
c DYS145 Dystonia 23 33 4.104
754
CLR030 Clear Cell Renal Cell Carcinoma 54 4.042
755
P GLL018 Gallbladder Cancer 53 4.040
756
P BRS044 Breast Adenocarcinoma 58 4.018
757
ERY029 Erythermalgia, Primary 58 4.018
758
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 4.009
759
EPT021 Epithelial Recurrent Erosion Dystrophy 46 4.006
760
ALP048 Alopecia Totalis 31 4.002
761
CRH005 Crohn's Colitis 53 3.969
762
P ACT008 Actinic Keratosis 54 3.959
763
BCT021 Bacterial Sepsis 43 3.932
764
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 3.931
765
P FML018 Familial Mediterranean Fever 73 3.912
766
SDD004 Sudden Arrhythmia Death Syndrome 22 3.907
767
SKN013 Skin Benign Neoplasm 49 3.905
768
HMR023 Hemorrhagic Cystitis 43 3.894
769
SPC005 Speech Disorder 46 3.889
770
SPN041 Spinal Cord Disease 54 3.882
771
c MLT124 Multiple Sclerosis 5 23 3.872
772
EYL005 Eyelid Disease 40 3.871
773
CHR103 Charge Syndrome 65 3.870
774
CRT033 Corticobasal Degeneration 48 3.863
775
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 3.862
776
P WSK001 Wiskott-Aldrich Syndrome 72 3.858
777
LMY003 Leiomyomatosis 43 3.858
778
INT020 Intravenous Leiomyomatosis 36 3.858
779
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 3.829
780
OCL006 Ocular Hypertension 53 3.829
781
P WLF004 Wolfram Syndrome 61 3.828
782
VLV036 Vulvar Disease 47 3.823
783
DRM011 Dermatophytosis 52 3.821
784
MCC013 Mucocutaneous Ulceration, Chronic 39 3.806
785
P EPL198 Epilepsy, Myoclonic Juvenile 61 3.802
786
GLT019 Glut1 Deficiency Syndrome 2 38 3.800
787
P DVL012 Developmental Dysplasia of the Hip 1 45 3.797
788
PLR007 Pleural Empyema 51 3.789
789
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.740
790
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 3.722
791
CST001 Costello Syndrome 68 3.708
792
c RST012 Restless Legs Syndrome 1 33 3.700
793
P DMY001 Demyelinating Polyneuropathy 41 3.699
794
PRG009 Progressive Multifocal Leukoencephalopathy 58 3.697
795
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 3.697
796
P PNC025 Panic Disorder 52 3.669
797
P LRY019 Laryngitis 53 3.665
798
STL007 Steel Syndrome 42 3.644
799
LVT001 Levator Syndrome 19 3.617
800
AMY086 Amyotrophy, Hereditary Neuralgic 45 3.612
801
P PLY018 Polycythemia 56 3.597
802
P DNR001 Duane Retraction Syndrome 53 3.590
803
P OPT009 Optic Neuritis 57 3.580
804
P PRX014 Proximal Spinal Muscular Atrophy 42 3.577
805
IRN001 Iron Deficiency Anemia 58 3.560
806
HND015 Hand Skill, Relative 29 3.559
807
P SPN236 Spina Bifida Cystica 22 3.523
808
BLD044 Bladder Disease 48 3.505
809
OCL011 Ocular Motility Disease 45 3.497
810
NWD001 New Daily-Persistent Headache 19 3.497
811
P ESP035 Esophagitis, Eosinophilic, 1 57 3.489
812
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 3.483
813
PYL006 Pyloric Stenosis 48 3.466
814
FBR011 Fibrodysplasia Ossificans Progressiva 67 3.439
815
P SCL048 Sclerosteosis 58 3.430
816
PNC034 Pancreas Disease 49 3.428
817
SKN023 Skin Tag 41 3.418
818
CCN002 Cocaine Abuse 49 3.418
819
GYN001 Gynecomastia 48 3.415
820
APH001 Aphthous Stomatitis 57 3.411
821
GNR004 Generalized Anxiety Disorder 55 3.399
822
CLB010 Coloboma of Macula 53 3.359
823
P BNC003 Bone Cancer 58 3.359
824
CRN036 Craniopharyngioma 63 3.352
825
P AGN002 Agnosia 53 3.348
826
P MLN069 Melanoma, Uveal 59 3.340
827
INF021 Infant Gynecomastia 30 3.320
828
THR004 Thrombocytosis 52 3.318
829
SPS004 Spastic Quadriplegia 39 3.316
830
c DYS059 Dystonia 16 47 3.313
831
c ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 36 3.308
832
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 3.290
833
PLS007 Plasmodium Falciparum Malaria 52 3.279
834
DRG024 Drug Allergy 40 3.247
835
P ERY008 Erythromelalgia 50 3.246
836
LGG001 Legg-Calve-Perthes Disease 60 3.221
837
CRB011 Cerebrotendinous Xanthomatosis 65 3.207
838
P MTC133 Mitochondrial Myopathy 51 3.196
839
BRS099 Breast Ductal Carcinoma 61 3.177
840
IDP093 Idiopathic Gastroparesis 27 3.156
841
CTS005 Catastrophic Antiphospholipid Syndrome 43 3.155
842
c PNC106 Pancreatic Agenesis 1 51 3.152
843
BLP004 Blepharophimosis 36 3.149
844
INT072 Intestinal Pseudo-Obstruction 60 3.138
845
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 3.125
846
UMB002 Umbilical Hernia 46 3.064
847
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 3.014
848
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 65 3.001
849
SCH018 Schizencephaly 52 2.999
850
PPT001 Peptic Esophagitis 51 2.995
851
LSC001 Lesch-Nyhan Syndrome 62 2.993
852
P MSC002 Muscular Dystrophy-Dystroglycanopathy 37 2.980
853
c DYS146 Dystonia 24 37 2.973
854
CHL152 Childhood Acute Lymphocytic Leukemia 50 2.933
855
c SPS036 Spastic Paraplegia 3 32 2.899
856
CMR002 Coumarin Resistance 60 2.877
857
LNG108 Langerhans Cell Histiocytosis 57 2.872
858
CHP002 Chops Syndrome 47 2.862
859
P PRM018 Primary Hypertrophic Osteoarthropathy 56 2.855
860
GRN037 Granulomatosis with Polyangiitis 67 2.842
861
URN009 Urinary System Disease 47 2.827
862
ART001 Arterial Tortuosity Syndrome 64 2.827
863
ABT001 Abetalipoproteinemia 68 2.820
864
HYD001 Hydranencephaly 43 2.767
865
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 2.750
866
ENP001 Enophthalmos 40 2.726
867
CRD229 Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism 49 2.719
868
GGN004 Gigantomastia 25 2.706
869
NRV004 Nerve Compression Syndrome 47 2.699
870
PCT003 Pectus Excavatum 43 2.686
871
BRW002 Brown's Tendon Sheath Syndrome 28 2.677
872
WTH001 Withdrawal Disorder 47 2.639
873
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 2.574
874
PMP010 Pompholyx 33 2.573
875
P OMP004 Omphalocele 47 2.571
876
FHT001 Fh Tumor Predisposition Syndrome 26 2.522
877
MLD017 Mal De Debarquement Syndrome 33 2.472
878
PLG004 Plagiocephaly 40 2.468
879
TNP001 Tinea Pedis 48 2.446
880
PLY023 Polycystic Liver Disease 62 2.429
881
CHR105 Choreoacanthocytosis 55 2.415
882
CRV040 Cervix Carcinoma 50 2.350
883
CRT008 Carotid Artery Dissection 29 2.345
884
P CND005 Cone Dystrophy 46 2.338
885
KLD003 Keloid Formation 34 2.326
886
P NRM002 Normal Pressure Hydrocephalus 49 2.318
887
GNR027 Generalized Peeling Skin Syndrome 22 2.315
888
LWR018 Lower Urinary Tract Obstruction, Congenital 39 2.263
889
FRS019 Farsightedness 35 2.255
890
CHN065 Choanal Atresia, Posterior 48 2.229
891
EPC005 Epicanthus 36 2.222
892
PRS053 Parsonage Turner Syndrome 22 2.209
893
c CHR095 Chronic Progressive External Ophthalmoplegia 48 2.194
894
BRC002 Brachial Plexus Neuritis 23 2.190
895
TRG003 Trigeminal Nerve Disease 37 2.187
896
PTT041 Pituitary Stalk Interruption Syndrome 54 2.141
897
P MRC003 Mercury Poisoning 48 2.141
898
c CHR056 Chronic Tic Disorder 36 2.091
899
PRN017 Perianal Hematoma 29 2.090
900
LMY001 Leiomyoma Cutis 32 2.089
901
SPN369 Spinal Disease 43 2.028
902
MTC116 Mitochondrial Myopathy, Infantile, Transient 42 2.004
903
RMS001 Rem Sleep Behavior Disorder 47 1.981
904
DYS032 Dystrophinopathies 47 1.953
905
CRB033 Cerebral Degeneration 36 1.925
906
INH017 Inherited Congenital Spastic Tetraplegia 23 1.881
907
PRX097 Paroxysmal Dystonia 32 1.851
908
FWL003 Fowler Urethral Sphincter Dysfunction Syndrome 22 1.837
909
GRM005 Germ Cell Cancer 46 1.814
910
PSY017 Psychogenic Movement Disorders 21 1.811
911
ARG007 Argininemia 59 1.786
912
P SPS008 Spastic Ataxia 41 1.780
913
INT076 Intracranial Sinus Thrombosis 30 1.734
914
P LRY029 Laryngomalacia 47 1.721
915
OPT070 Optic Nerve Hypoplasia, Bilateral 55 1.653
916
c CHR087 Chronic Cystitis 37 1.649
917
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 1.539
918
SPN119 Spondylarthropathy 37 1.513
919
SGC002 Sgce Myoclonus-Dystonia 23 1.469
920
c PRM032 Primary Congenital Glaucoma 40 1.468
921
PCH007 Pouchitis 42 1.463
922
CRP035 Corpus Callosum, Partial Agenesis of, X-Linked 38 1.411
923
PRX086 Paroxysmal Exertion-Induced Dyskinesia 27 1.376
924
WDH003 Woodhouse-Sakati Syndrome 41 1.210
925
ERL030 Early-Onset Generalized Limb-Onset Dystonia 32 1.171
926
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 44 1.168
927
CRB159 Cerebral Visual Impairment 34 1.158
928
BSL008 Basal Ganglia Disease 41 1.102
930
DRG016 Drug Induced Dyskinesia 23 1.030