Search results for "paralysis"

The MalaCard for "paralysis" has been retired.
Searching MalaCards for entries containing "paralysis"

1212 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
P HYP370 Hypokalemic Periodic Paralysis, Type 1 49 7.087
2
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 45 6.652
3
P AND016 Andersen Syndrome 58 4.670
4
NRM009 Normokalemic Periodic Paralysis 26 4.061
5
c INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 28 4.041
6
FCL012 Facial Paralysis 50 3.776
7
c THY083 Thyrotoxic Periodic Paralysis 2 19 3.748
8
P THY054 Thyrotoxic Periodic Paralysis 47 3.712
9
TCK002 Tick Paralysis 28 3.592
10
c HYP606 Hypokalemic Periodic Paralysis, Type 2 31 3.459
11
P SPS154 Spastic Paralysis, Infantile Onset Ascending 22 3.453
12
FML036 Familial Periodic Paralysis 39 3.274
13
PRM028 Paramyotonia Congenita 49 3.244
14
OCL003 Oculomotor Nerve Paralysis 27 3.236
15
LRY047 Laryngeal Abductor Paralysis 23 3.227
16
c THY084 Thyrotoxic Periodic Paralysis 1 19 2.894
17
BLL003 Bell's Palsy 46 2.632
18
PRN008 Peroneal Nerve Paralysis 22 2.506
19
MBS002 Moebius Syndrome 44 2.489
20
KRT022 Keratoderma Palmoplantar Spastic Paralysis 7 2.483
21
P PRK057 Parkinson Disease, Late-Onset 72 2.454
22
CNG485 Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome 8 2.437
23
PLM031 Poliomyelitis 59 2.251
24
P CRN035 Cranial Nerve Palsy 43 2.092
25
KLM001 Klumpke Paralysis 9 2.065
26
GLS003 Glossopharyngeal Nerve Paralysis 8 2.032
27
LRY021 Laryngeal Adductor Paralysis 10 2.025
28
FML082 Familial Partial Paralysis 10 2.025
29
c HYP142 Hyperkalemic Periodic Paralysis Type 1 14 2.007
30
VCL007 Vocal Cord Paralysis and Ptosis 11 2.007
31
PSD001 Pseudobulbar Palsy 34 1.997
32
GNC003 Geniculate Herpes Zoster 32 1.997
33
CNG241 Congenital Laryngeal Palsy 6 1.997
34
c NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 23 1.986
35
KRT067 Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy 14 1.986
36
TCK005 Tucker Syndrome 13 1.986
37
TDD001 Todd's Paralysis 11 1.572
38
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 14 1.447
39
FML160 Familial Spastic Paralysis 10 1.447
40
P HRN001 Horner's Syndrome 44 1.437
41
PRL008 Paralytic Ileus 39 1.437
42
c FML159 Familial Periodic Paralyses 15 1.437
43
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 4 1.437
44
LRY023 Laryngeal Abductor Paralysis Mental Retardation 2 1.437
45
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 36 1.426
46
CYC001 Cycloplegia 31 1.426
47
c NRP022 Neuropathy, Distal Hereditary Motor, Type Viib 25 1.426
48
PRL020 Paralysis Agitans, Juvenile, of Hunt 6 1.426
49
KRN002 Kearns-Sayre Syndrome 59 1.412
50
TRP002 Tropical Spastic Paraparesis 57 1.412
51
GLL022 Guillain-Barre Syndrome 56 1.412
52
P SPS003 Spastic Diplegia 53 1.412
53
MRK002 Marek Disease 35 1.395
54
THR010 Third Cranial Nerve Disease 28 1.395
55
PRT015 Partial Third-Nerve Palsy 27 1.395
56
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 24 1.395
57
ABD002 Abducens Nerve Disease 22 1.395
58
BLN017 Balint Syndrome 19 1.395
59
c AND007 Andersen Syndrome Type 1 15 1.395
60
c FCL030 Facial Paresis, Hereditary Congenital, 1 13 1.395
61
c DST092 Distal Hereditary Motor Neuropathy Type 7 11 1.395
62
RNL007 Renal Tubular Acidosis 50 0.142
63
P LRY019 Laryngitis 55 0.123
64
HYP005 Hypokalemia 51 0.121
65
P MYP004 Myopathy 67 0.112
66
P NRV007 Nervous System Disease 71 0.110
67
SPS057 Spasticity 42 0.103
68
P GRV001 Graves' Disease 61 0.101
69
P THY032 Thyroiditis 54 0.097
70
P NRP001 Neuropathy 60 0.094
71
MYT011 Myotonia 40 0.092
72
P RSP003 Respiratory Failure 70 0.087
73
ADN018 Adenoma 59 0.087
74
NRM005 Neuromuscular Disease 57 0.087
75
OTT002 Otitis Media 66 0.084
76
BNF002 Bone Fracture 47 0.084
77
NRN002 Neuronitis 42 0.079
78
CRN031 Cranial Nerve Disease 40 0.079
79
ANR040 Aneurysm 57 0.076
80
P MSC033 Muscle Disorders 52 0.076
81
P PTS002 Ptosis 56 0.073
82
P HYP076 Hyperthyroidism 56 0.073
83
P MSC003 Muscular Atrophy 51 0.073
84
PRP016 Paraplegia 49 0.073
85
FDB001 Foodborne Botulism 45 0.073
86
P CRV039 Cervicitis 44 0.070
87
LYM017 Lyme Disease 63 0.067
88
ACS001 Acoustic Neuroma 57 0.067
89
MVM001 Movement Disease 54 0.067
90
P ALT001 Alternating Hemiplegia of Childhood 52 0.067
91
DYS073 Dysphagia 49 0.067
92
NRM004 Neuroma 48 0.067
93
ALR002 Al-Raqad Syndrome 36 0.067
94
P HRP006 Herpes Simplex 65 0.063
95
CRB037 Cerebral Palsy 54 0.063
96
HYP017 Hypophosphatemia 42 0.063
97
LRY017 Laryngeal Disease 37 0.063
98
EPL031 Epileptic Hemiplegia 4 0.063
99
P HPT021 Hepatitis 70 0.060
100
P LYM118 Lymphoma 70 0.060
101
P EPL164 Epilepsy 66 0.060
102
P MNN013 Meningitis 65 0.060
103
MTH009 Mouth Disease 63 0.060
104
SPN186 Spinal Cord Injury 62 0.060
105
HRP004 Herpes Zoster 56 0.060
106
HMP005 Hemiplegia 54 0.060
107
TTH006 Tooth Disease 52 0.060
108
CHL069 Cholesteatoma 51 0.060
109
AYM001 Ayme-Gripp Syndrome 45 0.060
110
c PRG001 Progressive Muscular Atrophy 40 0.060
111
CRB009 Cerebritis 38 0.060
112
LCK001 Locked-in Syndrome 38 0.060
113
WND001 Wound Botulism 32 0.060
114
LGP001 Lagophthalmos 29 0.060
115
P PRD017 Periodic Paralyses 27 0.060
116
VGS001 Vagus Nerve Disease 20 0.060
117
AND005 Androgen Insensitivity Syndrome, Mild 16 0.060
118
P MYS003 Myasthenia Gravis 65 0.056
119
P PLY019 Polyneuropathy 54 0.056
120
P ATX004 Ataxia 53 0.056
121
WST005 West Nile Virus 53 0.056
122
P SJG001 Sjogren's Syndrome 53 0.056
123
QDR001 Quadriplegia 52 0.056
124
NRT004 Neuritis 52 0.056
125
ECT005 Ectropion 40 0.056
126
MSC004 Muscle Tissue Disease 36 0.056
127
SWL001 Swallowing Disorders 34 0.056
128
PRL013 Paralytic Poliomyelitis 28 0.056
129
STR067 Stroke, Ischemic 77 0.052
130
MLT021 Multiple System Atrophy 71 0.052
131
P PNM007 Pneumonia 66 0.052
132
P CHR071 Charcot-Marie-Tooth Disease 66 0.052
133
P HYP086 Hypothyroidism 65 0.052
134
P HYP065 Hyperaldosteronism 51 0.052
135
MLK003 Melkersson-Rosenthal Syndrome 50 0.052
136
SPN041 Spinal Cord Disease 48 0.052
137
MYL001 Myelitis 48 0.052
138
STT002 Status Asthmaticus 43 0.052
139
SPC005 Speech Disorder 43 0.052
140
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.052
141
PRT026 Parotitis 42 0.052
142
CNV002 Conversion Disorder 42 0.052
143
SPN369 Spinal Disease 41 0.052
144
FCL011 Facial Nerve Disease 38 0.052
145
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.052
146
GNC005 Geniculate Ganglionitis 31 0.052
147
c SYS001 Systemic Lupus Erythematosus 87 0.047
148
P HRT032 Heart Disease 76 0.047
149
P LKM002 Leukemia 70 0.047
150
TBR010 Tuberculosis 69 0.047
151
ART016 Aortic Aneurysm 67 0.047
152
CRD119 Cardiac Arrest 63 0.047
153
MLG056 Malignant Hyperthermia 57 0.047
154
PRP083 Porphyria, Acute Intermittent 55 0.047
155
PTT006 Pituitary Adenoma 55 0.047
156
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.047
157
GTR002 Goiter 54 0.047
158
P PTN002 Patent Ductus Arteriosus 52 0.047
159
c SBC007 Subacute Thyroiditis 39 0.047
160
MST019 Mastoiditis 33 0.047
161
FTD001 Foot Drop 32 0.047
162
TXN001 Toxin-Mediated Infectious Botulism 9 0.047
163
ERB002 Erb's Palsy 6 0.047
164
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.042
165
c HPT001 Hepatitis C 68 0.042
166
P MSC005 Muscular Dystrophy 64 0.042
167
P AMY004 Amyloidosis 64 0.042
168
P SPN046 Spinal Muscular Atrophy 63 0.042
169
P LPS004 Lupus Erythematosus 63 0.042
170
P NRV006 Nervous System Cancer 62 0.042
171
RSP006 Respiratory System Disease 62 0.042
172
c CNT035 Central Nervous System Disease 59 0.042
173
P ENC018 Encephalopathy 59 0.042
174
MTR014 Motor Neuron Disease 59 0.042
175
P THR003 Thoracic Aortic Aneurysm 57 0.042
176
SNS001 Sensorineural Hearing Loss 57 0.042
177
CPR001 Coproporphyria 55 0.042
178
P DBT005 Diabetes Insipidus 53 0.042
179
THY025 Thymus Cancer 51 0.042
180
P SYR001 Syringomyelia 47 0.042
181
SPP008 Suppurative Otitis Media 45 0.042
182
MNN009 Meningoencephalitis 45 0.042
183
DPH021 Diaphragm Disease 45 0.042
184
ATN005 Autonomic Dysfunction 45 0.042
185
MLL002 Miller Fisher Syndrome 43 0.042
186
TLR001 Tularemia 42 0.042
187
CRT008 Carotid Artery Dissection 41 0.042
188
P LBY004 Labyrinthitis 40 0.042
189
c PLM022 Pulmonary Valve Insufficiency 38 0.042
190
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.042
191
ARC007 Arachnoid Cysts 38 0.042
192
ARC002 Arachnoiditis 38 0.042
193
SPN185 Spinal Cord Infarction 36 0.042
194
NRP016 Neuropathy, Recurrent, with Pressure Palsies 30 0.042
195
FZL002 Fazio-Londe Disease 24 0.042
196
MDD008 Middle Ear Adenoma 20 0.042
197
ITR001 Iatrogenic Botulism 12 0.042
198
c ADL069 Adult Intestinal Botulism 12 0.042
199
HPT023 Hepatocellular Carcinoma 91 0.037
200
MLR004 Malaria 79 0.037
201
P NRB001 Neuroblastoma 69 0.037
202
SRC014 Sarcoma 66 0.037
203
P ATR011 Atrial Fibrillation 64 0.037
204
P TRN020 Turner Syndrome 64 0.037
205
LPT001 Leptospirosis 63 0.037
206
P NRC002 Narcolepsy 62 0.037
207
P ENC004 Encephalitis 61 0.037
208
P INT068 Intestinal Disease 61 0.037
209
GTL001 Gitelman Syndrome 60 0.037
210
P HMN010 Hemangioma 60 0.037
211
GST045 Gastroenteritis 60 0.037
212
STT001 Status Epilepticus 59 0.037
213
PHR003 Pharyngitis 58 0.037
214
P MMP001 Mumps 56 0.037
215
SPT005 Spotted Fever 56 0.037
216
P SCL018 Scoliosis 56 0.037
217
P INT070 Intestinal Obstruction 56 0.037
218
P MYS005 Myositis 56 0.037
219
RBS001 Rabies 56 0.037
220
P PRP019 Peripheral Nervous System Disease 54 0.037
221
MCN017 Meconium Ileus 54 0.037
222
P MYC008 Myocarditis 54 0.037
223
P STR020 Strabismus 53 0.037
224
BRN071 Brain Injury 52 0.037
225
ASP003 Aseptic Meningitis 51 0.037
226
NRL005 Neurilemmoma 51 0.037
227
VNB005 Van Buchem Disease 50 0.037
228
P OTT001 Otitis Externa 47 0.037
229
c MLG069 Malignant Hypertension 47 0.037
230
PRT029 Parathyroid Adenoma 47 0.037
231
RLP003 Relapsing Fever 46 0.037
232
ASP007 Aspiration Pneumonia 46 0.037
233
SPC010 Speech and Communication Disorders 46 0.037
234
ADR008 Adrenal Adenoma 46 0.037
235
FSC004 Fasciitis 46 0.037
236
c GRV008 Graves Disease 1 45 0.037
237
CNT025 Central Pontine Myelinolysis 42 0.037
238
EYL005 Eyelid Disease 42 0.037
239
P CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 41 0.037
240
MDS022 Mediastinitis 41 0.037
241
EXT056 External Ear Disease 41 0.037
242
HYP068 Hyperostosis 40 0.037
243
NRC019 Neurocutaneous Melanosis, Somatic 39 0.037
244
WST004 West Nile Encephalitis 39 0.037
245
P NRN017 Neuronopathy, Distal Hereditary Motor, Type Vi 36 0.037
246
CLR007 Colorado Tick Fever 35 0.037
247
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 34 0.037
248
P PRX033 Proximal Renal Tubular Acidosis 33 0.037
249
BRW004 Brown-Sequard Syndrome 32 0.037
250
EPD005 Epidural Abscess 32 0.037
251
TBS001 Tabes Dorsalis 32 0.037
252
c NRC009 Narcolepsy 1 29 0.037
253
CVR002 Cavernous Sinus Thrombosis 28 0.037
254
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 27 0.037
255
SKL006 Skull Base Neoplasm 25 0.037
256
PTR001 Petrositis 24 0.037
257
PNT023 Pontine Hemorrhage 20 0.037
258
PRS053 Parsonage Turner Syndrome 18 0.037
259
ABD009 Abducens Palsy 18 0.037
260
BLB003 Bulbar Polio 17 0.037
261
INH013 Inhalational Botulism 12 0.037
262
FBR024 Fibrocartilaginous Embolism 11 0.037
263
P BRS047 Breast Cancer 100 0.030
264
NRL016 Neural Tube Defects 76 0.030
265
INS024 Insulin-Like Growth Factor I 74 0.030
266
HDG012 Hodgkin Lymphoma 73 0.030
267
c FNC027 Fanconi Anemia, Complementation Group a 73 0.030
268
BRN028 Brain Cancer 70 0.030
269
KRT004 Keratitis 70 0.030
270
KWS002 Kawasaki Disease 70 0.030
271
P ADN016 Adenocarcinoma 69 0.030
272
CNR002 Cone-Rod Dystrophy 68 0.030
273
P LPR003 Leprosy 68 0.030
274
P KDN017 Kidney Cancer 67 0.030
275
c LNG044 Long Qt Syndrome 1 67 0.030
276
VSC007 Vascular Disease 67 0.030
277
CNT098 Central Core Disease 66 0.030
278
c GCH015 Gaucher Disease, Type I 66 0.030
279
P HYP117 Hypertriglyceridemia 65 0.030
280
P CNJ013 Conjunctivitis 65 0.030
281
c HRD010 Hereditary Spastic Paraplegia 65 0.030
282
ART005 Arteriovenous Malformation 65 0.030
283
c HMP029 Hemophilia a 64 0.030
284
P CRB042 Cerebellar Ataxia 64 0.030
285
P ART023 Arthropathy 63 0.030
286
GLN010 Glanzmann Thrombasthenia 63 0.030
287
EYD002 Eye Disease 63 0.030
288
P SPN301 Spinocerebellar Ataxia 2 63 0.030
289
P BRD002 Bardet-Biedl Syndrome 62 0.030
290
P WLD002 Waldenstrom Macroglobulinemia 62 0.030
291
PRT036 Peritonitis 62 0.030
292
FCT003 Factor X Deficiency 62 0.030
293
WGN006 Wegener Granulomatosis 62 0.030
294
MCK007 Muckle-Wells Syndrome 61 0.030
295
WLL001 Williams-Beuren Syndrome 61 0.030
296
VNW001 Von Willebrand's Disease 61 0.030
297
BHC003 Behcet Syndrome 61 0.030
298
MSL001 Measles 61 0.030
299
P HML002 Hemolytic Anemia 60 0.030
300
P TXP001 Toxoplasmosis 60 0.030
301
P LYM026 Lymphoblastic Leukemia 60 0.030
302
c ATM010 Autoimmune Hemolytic Anemia 60 0.030
303
PLM033 Pulmonary Embolism 59 0.030
304
P CMR001 Camurati-Engelmann Disease 59 0.030
305
ETH011 Ethylmalonic Encephalopathy 59 0.030
306
P THR015 Thrombophilia 59 0.030
307
P MTR012 Mitral Valve Disease 59 0.030
308
ISC004 Ischemia 59 0.030
309
P NRM001 Neuromyelitis Optica 59 0.030
310
RHB003 Rhabdomyosarcoma 58 0.030
311
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 0.030
312
PRG097 Paragangliomas 1, with or Without Deafness 58 0.030
313
P PRP029 Porphyria 58 0.030
314
P HMR003 Hemorrhagic Disease 57 0.030
315
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.030
316
YLL002 Yellow Fever 57 0.030
317
P SZR006 Seizure Disorder 57 0.030
318
TRG002 Trigeminal Neuralgia 56 0.030
319
c THR092 Thrombophilia Due to Thrombin Defect 56 0.030
320
PLM010 Pulmonary Edema 56 0.030
321
FCT022 Factor Xi Deficiency, Autosomal Recessive 56 0.030
322
P HMP007 Hemophilia 56 0.030
323
P GRS014 Griscelli Syndrome, Type 2 55 0.030
324
c PND001 Pain Disorder 55 0.030
325
P PLY017 Polyarteritis Nodosa 55 0.030
326
GLC003 Glucose Intolerance 55 0.030
327
RCT018 Rectal Neoplasm 55 0.030
328
GST050 Gastrointestinal System Disease 54 0.030
329
HDC001 Headache 54 0.030
330
NWC001 Newcastle Disease 54 0.030
331
JPN002 Japanese Encephalitis 54 0.030
332
HMF006 Hemifacial Microsomia 54 0.030
333
GST037 Gastroparesis 53 0.030
334
P CNG001 Congenital Myasthenic Syndrome 53 0.030
335
APH002 Aphasia 53 0.030
336
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.030
337
SLP005 Sleep Disorder 53 0.030
338
P SYP003 Syphilis 53 0.030
339
PLS006 Plasmodium Vivax Malaria 53 0.030
340
ATR060 Atrial Standstill, Digenic 53 0.030
341
TWN003 Townes-Brocks Syndrome 53 0.030
342
END030 End Stage Renal Failure 52 0.030
343
ANK001 Ankylosis 52 0.030
344
CYS010 Cystinosis 51 0.030
345
c LPD037 Lipodystrophy, Familial Partial, 2 51 0.030
346
P PNM006 Pneumoconiosis 51 0.030
347
OPT006 Optic Nerve Disease 51 0.030
348
ADT003 Auditory System Disease 51 0.030
349
HPT074 Hepatic Adenoma, Somatic 51 0.030
350
CLN019 Colonic Disease 50 0.030
351
PRD019 Periodic Fever, Familial 50 0.030
352
INT253 Intestinal Benign Neoplasm 50 0.030
353
VNW005 Von Willebrand Disease, Type 1 50 0.030
354
HYP006 Hypertensive Heart Disease 50 0.030
355
TCK001 Tick-Borne Encephalitis 49 0.030
356
RLP001 Relapsing Polychondritis 49 0.030
357
SPN020 Spondylosis 49 0.030
358
THR013 Thoracic Outlet Syndrome 49 0.030
359
c INH020 Inherited Metabolic Disorder 49 0.030
360
OST011 Osteomalacia 48 0.030
361
RHB001 Rhabdoid Cancer 48 0.030
362
P CMP008 Compartment Syndrome 48 0.030
363
P TRN034 Transverse Myelitis 48 0.030
364
HMR002 Hemarthrosis 48 0.030
365
MYL003 Myeloid Sarcoma 48 0.030
366
UPP004 Upper Respiratory Tract Disease 48 0.030
367
P HMR005 Hemorrhoid 48 0.030
368
OPT009 Optic Neuritis 48 0.030
369
WHP001 Whipple Disease 48 0.030
370
P OST028 Osteochondroma 48 0.030
371
PPL046 Popliteal Pterygium Syndrome 1 47 0.030
372
MCP006 Mucoepidermoid Carcinoma 47 0.030
373
VST004 Vestibular Disease 47 0.030
374
THY009 Thyroid Lymphoma 47 0.030
375
RNL011 Renal Osteodystrophy 47 0.030
376
INF006 Infant Botulism 47 0.030
377
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.030
378
P NML001 Nemaline Myopathy 46 0.030
379
c CNG021 Congenital Toxoplasmosis 46 0.030
380
BLD053 Blood Platelet Disease 46 0.030
381
NPH003 Nephrocalcinosis 46 0.030
382
P KLP003 Klippel-Feil Syndrome 46 0.030
383
P AFB001 Afibrinogenemia 46 0.030
384
HML015 Hemolytic Anemia Due to Triosephosphate Isomerase Deficiency 46 0.030
385
STL001 St. Louis Encephalitis 46 0.030
386
P BLD051 Blood Coagulation Disease 45 0.030
387
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.030
388
HMM003 Hemimegalencephaly 45 0.030
389
BBS001 Babesiosis 45 0.030
390
SPH001 Sapho Syndrome 44 0.030
391
CRN024 Corneal Disease 44 0.030
392
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.030
393
c PRK045 Parkinson Disease 5 44 0.030
394
P DMY001 Demyelinating Polyneuropathy 43 0.030
395
P ABD003 Abdominal Aortic Aneurysm 43 0.030
396
c SHR030 Short Qt Syndrome 43 0.030
397
VNT011 Ventricular Fibrillation, Familial, 1 43 0.030
398
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 43 0.030
399
TRC023 Trichinosis 43 0.030
400
c HRD104 Hereditary Multiple Osteochondromas 43 0.030
401
RCK002 Rocky Mountain Spotted Fever 43 0.030
402
c ACT159 Acute Transverse Myelitis 42 0.030
403
LCR004 La Crosse Encephalitis 42 0.030
404
ANT018 Anthracosis 42 0.030
405
c FML191 Familial Long Qt Syndrome 41 0.030
406
NSP002 Nasopharyngitis 41 0.030
407
c SCN006 Secondary Syphilis 41 0.030
408
EHR002 Ehrlichiosis 41 0.030
409
TNG004 Tongue Disease 41 0.030
410
PSD029 Pseudocholinesterase Deficiency 40 0.030
411
MLT145 Multiple Enchondromatosis, Maffucci Type 40 0.030
412
c OST131 Osteopetrosis, Autosomal Dominant 2 40 0.030
413
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.030
414
SPR007 Superior Mesenteric Artery Syndrome 39 0.030
415
P HYP265 Hypotonia 39 0.030
416
c INH004 Inherited Blood Coagulation Disease 39 0.030
417
CRT009 Critical Illness Polyneuropathy 39 0.030
418
RCT017 Rectal Disease 39 0.030
419
ADJ001 Adjustment Disorder 38 0.030
420
EXC003 Excessive Tearing 38 0.030
421
STR002 Streptococcal Meningitis 38 0.030
422
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.030
423
MYX004 Myxedema 38 0.030
424
P AXN001 Axonal Neuropathy 38 0.030
425
MTL002 Metal Metabolism Disorder 38 0.030
426
PRP056 Porphyria, Acute Hepatic 37 0.030
427
P CHR342 Chiari Malformation 37 0.030
428
P PRS062 Persistent Hyperplastic Primary Vitreous 37 0.030
429
PST055 Postural Hypotension 37 0.030
430
P HYP120 Hypoaldosteronism 37 0.030
431
c BRN108 Branchiootic Syndrome 1 36 0.030
432
INT042 Internuclear Ophthalmoplegia 36 0.030
433
ACQ017 Acquired Von Willebrand Syndrome 36 0.030
434
MYH012 Myhre Syndrome 35 0.030
435
GLB003 Globe Disease 35 0.030
436
XRP001 Xerophthalmia 35 0.030
437
ECT004 Ecthyma 35 0.030
438
c ATS282 Autosomal Recessive Malignant Osteopetrosis 35 0.030
439
CRB029 Cerebellopontine Angle Tumor 35 0.030
440
FST001 Foster-Kennedy Syndrome 34 0.030
441
c SPS078 Spastic Paraplegia 7 34 0.030
442
FNT004 Fainting 33 0.030
443
TLS001 Tolosa-Hunt Syndrome 33 0.030
444
ENT005 Entropion 32 0.030
445
THY043 Thymic Hyperplasia 32 0.030
446
c PRG019 Paragangliomas 2 32 0.030
447
OST006 Osteoblastoma 31 0.030
448
c PRG020 Paragangliomas 3 31 0.030
449
c MLT009 Multiple Cranial Nerve Palsy 31 0.030
450
CBB002 Cobb Syndrome 30 0.030
451
TYP015 Type 2b Von Willebrand Disease 30 0.030
452
P ATR081 Atrial Standstill 30 0.030
453
PRS037 Periostitis 30 0.030
454
P MLD013 Mild Hemophilia a 30 0.030
455
TCK004 Tick Infestation 29 0.030
456
PLY119 Polymicrogyria, Bilateral Perisylvian 29 0.030
457
MTC018 Metachondromatosis 29 0.030
458
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 29 0.030
459
SPS016 Spasmodic Dysphonia 28 0.030
460
c JVN024 Juvenile Hereditary Hemochromatosis 28 0.030
461
P ATX010 Ataxia Neuropathy Spectrum 28 0.030
462
RHB022 Rhabdoid Tumors, Somatic 28 0.030
463
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 26 0.030
464
END051 Endolymphatic Sac Tumor 25 0.030
465
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 24 0.030
466
CNT067 Central Cord Syndrome 24 0.030
467
MNN005 Meningovascular Neurosyphilis 24 0.030
468
PRS120 Persistent Idiopathic Facial Pain 21 0.030
469
ACT181 Acute Motor Axonal Neuropathy 19 0.030
470
P INT006 Intestinal Botulism 19 0.030
471
TYP017 Type 2n Von Willebrand Disease 18 0.030
472
PRL006 Paralytic Lagophthalmos 18 0.030
473
TYP016 Type 2m Von Willebrand Disease 17 0.030
474
PWS001 Powassan Encephalitis 16 0.030
475
c LTH032 Lethal Congenital Contracture Syndrome 7 15 0.030
476
c LTH030 Lethal Congenital Contracture Syndrome 8 15 0.030
477
SPN015 Spinal Polio 14 0.030
478
SYR004 Syringobulbia 13 0.030
479
UVP001 Uveoparotid Fever 11 0.030
480
MYP026 Myopathy - Thyrotoxic 8 0.030
481
BLB001 Bulbospinal Polio 7 0.030
482
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.030
483
HMP020 Hemiplegia Alterans 1 0.030
484
P CLR023 Colorectal Cancer 97 0.021
485
P AST005 Asthma 82 0.021
486
P MLT019 Multiple Myeloma 80 0.021
487
GST053 Gastric Cancer 77 0.021
488
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.021
489
c DLT002 Dilated Cardiomyopathy 75 0.021
490
P INF038 Influenza 74 0.021
491
P NRF019 Neurofibromatosis, Type 2 73 0.021
492
CNG034 Congestive Heart Failure 71 0.021
493
P TYS001 Tay-Sachs Disease 71 0.021
494
P MTC003 Metachromatic Leukodystrophy 71 0.021
495
PTZ001 Peutz-Jeghers Syndrome 70 0.021
496
MNT001 Mantle Cell Lymphoma 70 0.021
497
ANX002 Anxiety Disorder 69 0.021
498
PRP027 Peripheral Vascular Disease 69 0.021
499
P ALP004 Alport Syndrome 68 0.021
500
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.021
501
P CWD006 Cowden Syndrome 1 68 0.021
502
THY028 Thyroid Cancer 68 0.021
503
P MYL005 Myelofibrosis 67 0.021
504
P CRD011 Cardiomyopathy 67 0.021
505
PSY004 Psychotic Disorder 67 0.021
506
OBS002 Obsessive-Compulsive Disorder 66 0.021
507
c BSL007 Basal Cell Carcinoma 64 0.021
508
P OST002 Osteoporosis 64 0.021
509
c HPT016 Hepatitis B 64 0.021
510
P ALX003 Alexander Disease 64 0.021
511
CHR066 Chronic Fatigue Syndrome 64 0.021
512
CHD001 Chediak-Higashi Syndrome 64 0.021
513
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.021
514
ACN011 Acne 63 0.021
515
P ANR007 Anorexia Nervosa 63 0.021
516
INC002 Inclusion Body Myositis 63 0.021
517
c HMP004 Hemophilia B 62 0.021
518
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.021
519
DNG002 Dengue Hemorrhagic Fever 62 0.021
520
P MCH002 Machado-Joseph Disease 62 0.021
521
P ESP024 Esophagitis 62 0.021
522
P ADD001 Addison's Disease 62 0.021
523
P BPL003 Bipolar Disorder 62 0.021
524
P OST001 Osteopetrosis 62 0.021
525
FCT007 Factor Vii Deficiency 62 0.021
526
c ACT073 Acute Leukemia 62 0.021
527
OCL009 Ocular Cancer 62 0.021
528
GST092 Gastroesophageal Reflux 61 0.021
529
MDD011 Mood Disorder 61 0.021
530
P SDD001 Sudden Infant Death Syndrome 61 0.021
531
P PRS038 Personality Disorder 61 0.021
532
c GLY008 Glycogen Storage Disease Ii 61 0.021
533
P IDP010 Idiopathic Generalized Epilepsy 61 0.021
534
c ACT075 Acute Myocardial Infarction 60 0.021
535
P MYM002 Moyamoya Disease 60 0.021
536
ISB001 Isobutyryl-Coa Dehydrogenase Deficiency 60 0.021
537
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.021
538
P TMP003 Temporal Arteritis 60 0.021
539
P GST049 Gastrointestinal System Cancer 60 0.021
540
CRB011 Cerebrotendinous Xanthomatosis 60 0.021
541
LDD001 Ladd Syndrome 60 0.021
542
P HYP055 Hypoplastic Left Heart Syndrome 60 0.021
543
P PNC025 Panic Disorder 60 0.021
544
FCT006 Factor V Deficiency 60 0.021
545
SPT004 Septic Arthritis 59 0.021
546
P LRY044 Larynx Cancer 59 0.021
547
MSM014 Mismatch Repair Cancer Syndrome 59 0.021
548
RBR001 Roberts Syndrome 59 0.021
549
CHL123 Chlamydia 59 0.021
550
CHR072 Chordoma 59 0.021
551
P MSC007 Muscle Hypertrophy 59 0.021
552
ADM013 Adamantinoma of Long Bones 59 0.021
553
P BRG001 Brugada Syndrome 59 0.021
554
c FML001 Familial Atrial Fibrillation 59 0.021
555
PRP030 Purpura 59 0.021
556
HJD001 Hajdu-Cheney Syndrome 58 0.021
557
P ANT006 Antiphospholipid Syndrome 58 0.021
558
P SYS005 Systemic Scleroderma 58 0.021
559
c ATM011 Autoimmune Hepatitis 58 0.021
560
DPH001 Diphtheria 58 0.021
561
P GST044 Gastritis 58 0.021
562
ART017 Aortic Disease 58 0.021
563
LYM021 Lymphadenitis 58 0.021
564
P GLM045 Glioma 58 0.021
565
P CTR002 Cataract 57 0.021
566
P PRC031 Preeclampsia/eclampsia 1 57 0.021
567
PST028 Post-Traumatic Stress Disorder 57 0.021
568
P EXN002 Exanthem 57 0.021
569
ABL002 Ablepharon-Macrostomia Syndrome 57 0.021
570
CNS004 Constipation 57 0.021
571
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.021
572
P SML001 Small Cell Carcinoma 57 0.021
573
WLF001 Wolff-Parkinson-White Syndrome 57 0.021
574
P EPS003 Episodic Ataxia 56 0.021
575
WLL006 Wells Syndrome 56 0.021
576
P GLM007 Glomerulonephritis 56 0.021
577
STF001 Stiff-Person Syndrome 56 0.021
578
CND002 Conduct Disorder 56 0.021
579
P TMT001 Timothy Syndrome 56 0.021
580
P FBR017 Fibrosarcoma 56 0.021
581
TRN015 Transient Cerebral Ischemia 56 0.021
582
P BDD001 Budd-Chiari Syndrome 56 0.021
583
URN010 Urinary Tract Obstruction 56 0.021
584
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.021
585
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.021
586
HYP266 Hypoxia 55 0.021
587
CHN016 Cohen Syndrome 55 0.021
588
c TYR012 Tyrosinemia, Type I 55 0.021
589
c ART101 Aortic Valve Disease 2 55 0.021
590
c FML023 Familial Hemiplegic Migraine 55 0.021
591
CCC001 Coccidioidomycosis 55 0.021
592
DSS008 Disease of Mental Health 55 0.021
593
c MYT020 Myotonic Dystrophy 2 55 0.021
594
PPL022 Papilloma 55 0.021
595
P OLG002 Oligodendroglioma 55 0.021
596
P HMR012 Hemorrhagic Fever 55 0.021
597
SCR008 Scrub Typhus 54 0.021
598
MNT002 Mental Depression 54 0.021
599
P HYP620 Hypoprothrombinemia 54 0.021
600
PTN001 Patent Foramen Ovale 54 0.021
601
LYM022 Lymphangioma 54 0.021
602
P TRM003 Tremor 54 0.021
603
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.021
604
TRN018 Transitional Cell Carcinoma 54 0.021
605
P EXP004 Exophthalmos 54 0.021
606
P INT030 Intracranial Aneurysm 54 0.021
607
c AFB002 Afibrinogenemia, Congenital 54 0.021
608
CHR177 Chromophobe Renal Cell Carcinoma 53 0.021
609
URN009 Urinary System Disease 53 0.021
610
P THY023 Thymoma 53 0.021
611
P INT063 Intellectual Disability 53 0.021
612
ADL002 Adult Syndrome 53 0.021
613
STF002 Stiff Skin Syndrome 53 0.021
614
ALL026 Allergic Hypersensitivity Disease 53 0.021
615
INT075 Intracranial Hypertension 53 0.021
616
P JRV003 Jervell and Lange-Nielsen Syndrome 52 0.021
617
THR016 Thrombophlebitis 52 0.021
618
PRT014 Protein S Deficiency 52 0.021
619
KRT006 Keratoconjunctivitis 52 0.021
620
P HYP083 Hypopituitarism 52 0.021
621
CYS039 Cystic Kidney Disease 52 0.021
622
P CRV031 Cervical Adenocarcinoma 52 0.021
623
PRP032 Porphyria Variegata 52 0.021
624
PNM008 Pneumothorax 52 0.021
625
P LTR001 Lateral Sclerosis 52 0.021
626
PLR022 Pleural Disease 52 0.021
627
P HYP024 Hypoparathyroidism 52 0.021
628
APP015 Apparent Mineralocorticoid Excess 52 0.021
629
VND001 Vein Disease 52 0.021
630
NSD001 Nose Disease 52 0.021
631
PRC013 Pericarditis 52 0.021
632
ALV002 Alveolar Echinococcosis 51 0.021
633
PRT058 Pure Autonomic Failure 51 0.021
634
BLR001 Biliary Atresia 51 0.021
635
TXC002 Toxic Encephalopathy 51 0.021
636
DRY001 Dry Eye Syndrome 51 0.021
637
BRT002 Birt-Hogg-Dube Syndrome 51 0.021
638
GNR004 Generalized Anxiety Disorder 51 0.021
639
NNT012 Neonatal Jaundice 51 0.021
640
THY030 Thyroid Gland Disease 51 0.021
641
DSM004 Desmoid Tumor 51 0.021
642
MGL013 Megalencephaly 51 0.021
643
ADN009 Adenosquamous Carcinoma 51 0.021
644
PRT011 Protein C Deficiency 51 0.021
645
DSS009 Disseminated Intravascular Coagulation 51 0.021
646
ANG054 Angina Pectoris 51 0.021
647
BRX001 Bruxism 51 0.021
648
MSC072 Muscle Cancer 51 0.021
649
HNT002 Hantavirus Pulmonary Syndrome 51 0.021
650
BRN004 Brain Edema 51 0.021
651
BLD044 Bladder Disease 51 0.021
652
PTH002 Pathological Gambling 51 0.021
653
P DRR001 Diarrhea 51 0.021
654
FCT004 Factor Xii Deficiency 51 0.021
655
P SCH018 Schizencephaly 51 0.021
656
c VRL012 Viral Meningitis 50 0.021
657
PTT048 Pituitary Adenoma, Prolactin-Secreting 50 0.021
658
c CNG464 Congenital Myopathy 50 0.021
659
SCT005 Scott Syndrome 50 0.021
660
P HYP014 Hyperuricemia 50 0.021
661
c ACT071 Acute Kidney Failure 50 0.021
662
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.021
663
CHK001 Chikungunya 50 0.021
664
PRP021 Peripheral Nervous System Neoplasm 50 0.021
665
MGC001 Megacolon 50 0.021
666
BRN082 Bernard-Soulier Syndrome, Type C 50 0.021
667
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.021
668
CYS008 Cystic Echinococcosis 50 0.021
669
PST095 Post-Thrombotic Syndrome 50 0.021
670
STR081 Stormorken Syndrome 50 0.021
671
CHN055 Chanarin-Dorfman Syndrome 49 0.021
672
CLF001 Cleft Lip 49 0.021
673
PMP001 Pemphigus 49 0.021
674
SRT004 Serotonin Syndrome 49 0.021
675
PST021 Postpartum Depression 49 0.021
676
ESP020 Esophageal Atresia 49 0.021
677
ATR057 Atrioventricular Block 49 0.021
678
P GNT008 Giant Cell Tumor 49 0.021
679
HLL004 Hellp Syndrome 49 0.021
680
BRK001 Brooke-Spiegler Syndrome 49 0.021
681
PLG002 Plague 49 0.021
682
P CHR345 Chronic Pain 49 0.021
683
GYN001 Gynecomastia 49 0.021
684
c CRB103 Cerebral Cavernous Malformations-1 49 0.021
685
PRT018 Portal Vein Thrombosis 49 0.021
686
GRW007 Growth Hormone Deficiency 48 0.021
687
LMB062 Limb Ischemia 48 0.021
688
MTB004 Metabolic Acidosis 48 0.021
689
PTT009 Pituitary Gland Disease 48 0.021
690
APR001 Apraxia 48 0.021
691
c CLL013 Cell Type Cancer 48 0.021
692
RPP001 Rapp-Hodgkin Syndrome 48 0.021
693
P OPN001 Open-Angle Glaucoma 48 0.021
694
P APL006 Aplasia Cutis Congenita 48 0.021
695
LYM008 Lymphangiosarcoma 48 0.021
696
CRN017 Coronary Thrombosis 48 0.021
697
SPR010 Sporotrichosis 48 0.021
698
SPL012 Splenic Disease 47 0.021
699
P RNL015 Renal Hypertension 47 0.021
700
DVR002 Diverticulitis 47 0.021
701
SYN036 Syncope 47 0.021
702
PLC007 Placental Abruption 47 0.021
703
P RNV001 Renovascular Hypertension 47 0.021
704
PRN009 Paranoid Schizophrenia 47 0.021
705
c BPL002 Bipolar I Disorder 47 0.021
706
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.021
707
MLT113 Multicentric Castleman Disease 47 0.021
708
P PRN026 Porencephaly 47 0.021
709
P CRN012 Craniometaphyseal Dysplasia 47 0.021
710
CNJ012 Conjunctival Disease 46 0.021
711
BRD004 Borderline Personality Disorder 46 0.021
712
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.021
713
c GLC062 Glaucoma 1, Open Angle, E 46 0.021
714
c INT072 Intestinal Pseudo-Obstruction 46 0.021
715
VLV011 Vulvovaginal Candidiasis 46 0.021
716
ACR041 Acromelic Frontonasal Dysostosis 46 0.021
717
HPT014 Hepatorenal Syndrome 46 0.021
718
SDD007 Sudden Cardiac Death 46 0.021
719
PLR006 Pleural Cancer 46 0.021
720
PRN011 Pernicious Anemia 46 0.021
721
ACT058 Active Peptic Ulcer Disease 46 0.021
722
c ERL020 Early-Onset Schizophrenia 46 0.021
723
CRT017 Cartilage Disease 46 0.021
724
CVR006 Cavernous Hemangioma 46 0.021
725
ANR004 Anuria 46 0.021
726
CYS014 Cystadenocarcinoma 46 0.021
727
DST006 Diastolic Heart Failure 46 0.021
728
PRM003 Premature Ejaculation 46 0.021
729
SNS023 Sensory System Cancer 46 0.021
730
SKN023 Skin Tag 46 0.021
731
c SVR056 Severe Hemophilia a 46 0.021
732
AMB002 Amblyopia 46 0.021
733
IDP033 Idiopathic Edema 45 0.021
734
ALN001 Aland Island Eye Disease 45 0.021
735
MTR003 Mitral Valve Stenosis 45 0.021
736
CTS002 Cat-Scratch Disease 45 0.021
737
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 45 0.021
738
BNC003 Bone Cancer 45 0.021
739
P MLG086 Malignant Hyperthermia Susceptibility 45 0.021
740
VSC047 Vascular Malformation 45 0.021
741
MMB001 Membranoproliferative Glomerulonephritis 45 0.021
742
c CHR095 Chronic Progressive External Ophthalmoplegia 45 0.021
743
PTT037 Pituitary Tumors 45 0.021
744
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 45 0.021
745
GDS001 Good Syndrome 45 0.021
746
NCR007 Necrotizing Fasciitis 45 0.021
747
RNL097 Renal Artery Disease 45 0.021
748
SPS007 Spastic Cerebral Palsy 45 0.021
749
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.021
750
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 44 0.021
751
P PNB001 Pineoblastoma 44 0.021
752
c PRK027 Parkinson Disease 15, Autosomal Recessive 44 0.021
753
c MTR002 Mitral Valve Insufficiency 44 0.021
754
PHY002 Physical Disorder 44 0.021
755
PTT008 Pituitary Carcinoma 44 0.021
756
BRN107 Branchiootorenal Syndrome 1, with or Without Cataracts 44 0.021
757
FBR009 Fibrous Dysplasia 44 0.021
758
ATN004 Autonomic Neuropathy 44 0.021
759
DDN006 Duodenitis 44 0.021
760
ANS011 Anus Cancer 44 0.021
761
c HMG003 Hemoglobin E Disease 44 0.021
762
CRD001 Cardiac Tamponade 44 0.021
763
PRD002 Periodic Limb Movement Disorder 44 0.021
764
DND001 Dandy-Walker Syndrome 44 0.021
765
c CNT015 Central Sleep Apnea 44 0.021
766
EXS001 Exostosis 44 0.021
767
OPP004 Oppositional Defiant Disorder 43 0.021
768
CRT015 Carotid Artery Occlusion 43 0.021
769
AGR002 Agoraphobia 43 0.021
770
SPN040 Spinal Cancer 43 0.021
771
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.021
772
P AML002 Amelogenesis Imperfecta 43 0.021
773
P RTN014 Retinal Artery Occlusion 43 0.021
774
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.021
775
HRT008 Heart Conduction Disease 43 0.021
776
MTC056 Mitochondrial Dna Depletion Syndrome 4a 43 0.021
777
SYS003 Systolic Heart Failure 43 0.021
778
PRM025 Primary Bacterial Infectious Disease 43 0.021
779
P FNG005 Feingold Syndrome 43 0.021
780
BRT030 Birth Defects 43 0.021
781
CRB006 Cribriform Carcinoma 43 0.021
782
TRN003 Transverse Colon Cancer 43 0.021
783
FCT008 Factitious Disorder 43 0.021
784
GST009 Gastroschisis 43 0.021
785
P MYP087 Myopathy, Tubular Aggregate, 1 43 0.021
786
SPN032 Spindle Cell Carcinoma 43 0.021
787
ART031 Aortic Coarctation 42 0.021
788
PRD011 Proud Syndrome 42 0.021
789
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.021
790
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 42 0.021
791
P CRB088 Cerebral Atrophy 42 0.021
792
PLM029 Palmoplantar Keratosis 42 0.021
793
c LNG098 Long Qt Syndrome 14 42 0.021
794
c LNG096 Long Qt Syndrome 15 42 0.021
795
TRY002 Troyer Syndrome 42 0.021
796
c BRG005 Brugada Syndrome 1 42 0.021
797
c CLR085 Colorectal Cancer 1 42 0.021
798
P MYT013 Myotonia Congenita, Dominant 42 0.021
799
P PRP034 Purpura Fulminans 42 0.021
800
CDQ001 Cauda Equina Syndrome 42 0.021
801
c ACQ014 Acquired Hemophilia 42 0.021
802
BRN045 Brunner Syndrome 42 0.021
803
FCT005 Factor Xiii Deficiency 42 0.021
804
HDR006 Hidradenocarcinoma 42 0.021
805
THR035 Thrombasthenia 42 0.021
806
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.021
807
PLS016 Plasma Cell Leukemia 42 0.021
808
P ART018 Aortic Valve Insufficiency 42 0.021
809
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 41 0.021
810
c HRD088 Hereditary Neuropathies 41 0.021
811
BRS064 Bursitis 41 0.021
812
P DYS026 Dysfibrinogenemia 41 0.021
813
PRP028 Peripheral Vertigo 41 0.021
814
P ADV001 Advanced Sleep Phase Syndrome 41 0.021
815
EST005 Esotropia 41 0.021
816
MLT075 Multifocal Motor Neuropathy 41 0.021
817
CTS005 Catastrophic Antiphospholipid Syndrome 41 0.021
818
CHR222 Chromosome 1p36 Deletion Syndrome 41 0.021
819
TRC040 Tracheoesophageal Fistula 41 0.021
820
TBR008 Tuberculous Peritonitis 41 0.021
821
SKL003 Skeletal Muscle Cancer 41 0.021
822
PRP009 Peripartum Cardiomyopathy 41 0.021
823
NRS003 Neurosyphilis 41 0.021
824
c AMY085 Amyotrophic Lateral Sclerosis 9 41 0.021
825
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 41 0.021
826
FNC007 Functioning Pituitary Adenoma 41 0.021
827
THY049 Thyroid Cancer, Anaplastic 41 0.021
828
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 41 0.021
829
MYS001 Myositis Ossificans 41 0.021
830
c PRG106 Progressive Muscular Dystrophy 41 0.021
831
MLT008 Multinodular Goiter 41 0.021
832
ENT001 Enterocele 41 0.021
833
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 41 0.021
834
NSL006 Nasal Cavity Squamous Cell Carcinoma 41 0.021
835
WTH001 Withdrawal Disorder 41 0.021
836
BRN080 Brain Ischemia 41 0.021
837
SCR001 Secretory Meningioma 41 0.021
838
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 40 0.021
839
MLY001 Molybdenum Cofactor Deficiency 40 0.021
840
LCR008 Lacrimal Apparatus Disease 40 0.021
841
ISC015 Ischemic Colitis 40 0.021
842
MDL009 Medullary Sponge Kidney 40 0.021
843
SPN029 Spondylolysis 40 0.021
844
SWT002 Sweat Gland Cancer 40 0.021
845
c MLG053 Malignant Ovarian Brenner Tumor 40 0.021
846
P HYP263 Hypersomnia 40 0.021
847
NNF007 Non-Functioning Pituitary Adenoma 40 0.021
848
APP009 Appendix Adenocarcinoma 40 0.021
849
BLD032 Bile Duct Adenocarcinoma 40 0.021
850
KDN015 Kidney Angiomyolipoma 40 0.021
851
HYP264 Hypertonia 40 0.021
852
RMS001 Rem Sleep Behavior Disorder 40 0.021
853
BRN003 Branchiooculofacial Syndrome 40 0.021
854
MNN017 Mononeuropathy 40 0.021
855
KRN001 Korean Hemorrhagic Fever 40 0.021
856
c AMY090 Amyotrophic Lateral Sclerosis 8 40 0.021
857
P OVR010 Ovarian Brenner Tumor 39 0.021
858
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 39 0.021
859
CRB086 Cerebral Aneurysms 39 0.021
860
FBR086 Fibrolamellar Carcinoma 39 0.021
861
SCT002 Scotoma 39 0.021
862
SCR015 Scarlet Fever 39 0.021
863
P BRN042 Branchiootic Syndrome 39 0.021
864
ANG002 Angiostrongyliasis 39 0.021
865
c ACQ042 Acquired Hemophilia a 39 0.021
866
PST020 Postpoliomyelitis Syndrome 39 0.021
867
ATS009 Autosomal Genetic Disease 39 0.021
868
ACT012 Acute Hemorrhagic Conjunctivitis 39 0.021
869
MRR003 Murray Valley Encephalitis 39 0.021
870
P NRX001 Neuroaxonal Dystrophy 39 0.021
871
ATY002 Atypical Choroid Plexus Papilloma 39 0.021
872
c AMY067 Amyotrophic Lateral Sclerosis 18 39 0.021
873
HYP034 Hypertensive Encephalopathy 38 0.021
874
OVR054 Ovarian Mucinous Neoplasm 38 0.021
875
P ORF002 Orofacial Cleft 38 0.021
876
CLR005 Clear Cell Chondrosarcoma 38 0.021
877
ABD010 Abdominal Wall Defect 38 0.021
878
DLY005 Delayed Sleep Phase Syndrome 38 0.021
879
TRC025 Tracheal Cancer 38 0.021
880
HTS001 Hiatus Hernia 38 0.021
881
PNM005 Pneumonic Plague 38 0.021
882
CCM001 Cecum Adenocarcinoma 38 0.021
883
ISC005 Ischemic Bone Disease 38 0.021
884
KLP001 Kleptomania 38 0.021
885
NRM006 Neuromuscular Junction Disease 38 0.021
886
c CHR579 Chiari Malformation Type Ii 38 0.021
887
SPN033 Spontaneous Ocular Nystagmus 38 0.021
888
PHB001 Phobic Disorder 38 0.021
889
c CHR098 Chronic Pyelonephritis 38 0.021
890
NDL005 Nodular Medulloblastoma 38 0.021
891
DYS009 Dysthymic Disorder 38 0.021
892
OTM001 Otomycosis 37 0.021
893
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.021
894
DVL001 Developmental Coordination Disorder 37 0.021
895
OST115 Osteonecrosis of the Jaw 37 0.021
896
FRY001 Frey Syndrome 37 0.021
897
CVR010 Cavernous Malformation 37 0.021
898
VNT001 Ventilation Pneumonitis 37 0.021
899
c DYS119 Dystonia 9 37 0.021
900
c KDN016 Kidney Benign Neoplasm 37 0.021
901
ALX002 Alexithymia 37 0.021
902
c FML156 Familial Hyperaldosteronism 37 0.021
903
NTV001 Native American Myopathy 37 0.021
904
SPN050 Spinocerebellar Degeneration 37 0.021
905
LCH001 Leech Infestation 37 0.021
906
VRT001 Vertebral Artery Occlusion 37 0.021
907
PRC010 Pericardial Mesothelioma 37 0.021
908
PRC005 Pericardial Tuberculosis 37 0.021
909
BRS063 Breast Squamous Cell Carcinoma 37 0.021
910
P MNN007 Meningocele 36 0.021
911
PRX014 Proximal Spinal Muscular Atrophy 36 0.021
912
c AMY083 Amyotrophic Lateral Sclerosis 11 36 0.021
913
CSL001 Causalgia 36 0.021
914
TRP004 Tropical Sprue 36 0.021
915
SML020 Small Patella Syndrome 36 0.021
916
c PSD092 Pseudohypoaldosteronism, Type Iie 36 0.021
917
VTM001 Vitamin K Deficiency Hemorrhagic Disease 36 0.021
918
OVR059 Ovary Adenocarcinoma 36 0.021
919
c AMY059 Amyotrophic Lateral Sclerosis 19 36 0.021
920
OVR017 Ovarian Cystic Teratoma 36 0.021
921
CRV026 Cervical Clear Cell Adenocarcinoma 36 0.021
922
ALC003 Alcoholic Psychosis 36 0.021
923
TSH001 Tsh Producing Pituitary Tumor 36 0.021
924
ADN015 Adenoid Basal Cell Carcinoma 36 0.021
925
BRS062 Breast Secretory Carcinoma 36 0.021
926
c CNG413 Congenital Short Bowel Syndrome 36 0.021
927
LPD027 Lip Disease 36 0.021
928
FML005 Female Reproductive Endometrioid Cancer 36 0.021
929
LTR003 Lateral Medullary Syndrome 35 0.021
930
MLG012 Malignant Epithelial Mesothelioma 35 0.021
931
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 35 0.021
932
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.021
933
LMB010 Lambert Syndrome 35 0.021
934
PNC002 Pancreatic Mucinous Cystadenoma 35 0.021
935
P EXT032 Extraosseous Osteosarcoma 35 0.021
936
SNT005 Sinoatrial Node Disease 35 0.021
937
CCN007 Cocoon Syndrome 35 0.021
938
BRN036 Brain Stem Infarction 35 0.021
939
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 35 0.021
940
ATY001 Atypical Depressive Disorder 35 0.021
941
BRC010 Brachial Plexus Lesion 35 0.021
942
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.021
943
BLT003 Blue Toe Syndrome 35 0.021
944
c SCP001 Sc Phocomelia Syndrome 35 0.021
945
FMR003 Femoral Neuropathy 34 0.021
946
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.021
947
P GLM006 Glomangioma 34 0.021
948
MSN003 Mesenteric Vascular Occlusion 34 0.021
949
c URT035 Urethral Benign Neoplasm 34 0.021
950
NCR003 Necrotizing Sialometaplasia 34 0.021
951
c GM2005 Gm2-Gangliosidosis, Ab Variant 34 0.021
952
ADP007 Adie Pupil 34 0.021
953
FRN014 Fournier Gangrene 34 0.021
954
GLT018 Glut1 Deficiency Syndrome 1 34 0.021
955
CRD016 Cardiac Rupture 34 0.021
956
PGT003 Paget Disease, Extramammary 34 0.021
957
c PRG021 Paragangliomas 4 34 0.021
958
MYT003 Myotonic Disease 34 0.021
959
HMC014 Homocysteinemia 34 0.021
960
WST003 West Nile Fever 34 0.021
961
ODN006 Odontoma 34 0.021
962
SPS019 Spastic Paraparesis 34 0.021
963
HYD001 Hydranencephaly 34 0.021
964
c SRC023 Sarcoidosis 2 33 0.021
965
OVR021 Ovarian Lymphoma 33 0.021
966
PRN016 Peroneal Neuropathy 33 0.021
967
SGT001 Sagittal Sinus Thrombosis 33 0.021
968
DRS001 Dressler's Syndrome 33 0.021
969
INT004 Intraneural Perineurioma 33 0.021
970
BLR005 Biliary Papillomatosis 33 0.021
971
PRS004 Prostate Squamous Cell Carcinoma 33 0.021
972
c OST126 Osteopetrosis, Autosomal Recessive 1 33 0.021
973
VST003 Vestibular Nystagmus 33 0.021
974
MLN002 Melanomatosis 33 0.021
975
OST022 Osteopathia Striata with Cranial Sclerosis 33 0.021
976
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.021
977
LCR001 Lacrimal Duct Obstruction 33 0.021
978
END034 Endocrine Exophthalmos 33 0.021
979
GNT005 Giant Hemangioma 33 0.021
980
c ACT037 Acute Dacryocystitis 33 0.021
981
c MLG036 Malignant Spiradenoma 33 0.021
982
OXY002 Oxyphilic Adenoma 32 0.021
983
QLT001 Qualitative Platelet Defect 32 0.021
984
RNL013 Renal Adenoma 32 0.021
985
VLL006 Villous Adenoma 32 0.021
986
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.021
987
VSC004 Vasculogenic Impotence 32 0.021
988
c SVR057 Severe Hemophilia B 32 0.021
989
FCT016 Factor V and Factor Viii, Combined Deficiency of 32 0.021
990
c PTS008 Ptosis, Congenital 32 0.021
991
CRN006 Coronary Aneurysm 32 0.021
992
c MYS064 Myasthenic Syndrome, Congenital, 16 32 0.021
993
WRT003 Warthin Tumor 32 0.021
994
PNC018 Pancreatic Serous Cystadenoma 32 0.021
995
MRN001 Marantic Endocarditis 32 0.021
996
AMY095 Amyotrophic Lateral Sclerosis 6, with or Without Frontotemporal Dementia 32 0.021
997
AMY005 Amyloid Neuropathy 32 0.021
998
CLV002 Clivus Chordoma 32 0.021
999
PSY003 Psychosexual Disorder 32 0.021
1000
ART110 Arteritic Anterior Ischemic Optic Neuropathy 32 0.021
1001
CTN009 Cutaneous Adenocystic Carcinoma 32 0.021
1002
HMF009 Hemifacial Hyperplasia 32 0.021
1003
MYC014 Mycobacterium Chelonae 32 0.021
1004
BLD019 Bile Duct Cystadenocarcinoma 32 0.021
1005
c CRB094 Cerebral Cavernous Malformations 3 32 0.021
1006
c HRD020 Hereditary Renal Cell Carcinoma 32 0.021
1007
c TRC078 Trichohepatoenteric Syndrome 2 31 0.021
1008
PRL042 Proliferating Trichilemmal Cyst 31 0.021
1009
BLD005 Bile Duct Mucoepidermoid Carcinoma 31 0.021
1010
c CLR077 Colorectal Cancer 10 31 0.021
1011
LVD002 Livedoid Vasculopathy 31 0.021
1012
CRN033 Cranial Nerve Malignant Neoplasm 31 0.021
1013
INT050 Intestinal Impaction 31 0.021
1014
c AMY062 Amyotrophic Lateral Sclerosis 12 31 0.021
1015
CRV030 Cervical Adenitis 31 0.021
1016
ANL012 Anal Gland Adenocarcinoma 31 0.021
1017
c SPS079 Spastic Paraplegia 2 31 0.021
1018
c DRR009 Diarrhea 6 31 0.021
1019
ADN008 Adenosquamous Pancreas Carcinoma 31 0.021
1020
PRS002 Prostate Lymphoma 31 0.021
1021
P ATX024 Ataxia-Oculomotor Apraxia 3 31 0.021
1022
c CLR079 Colorectal Cancer 2 31 0.021
1023
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.021
1024
CRB132 Cerebral Sinovenous Thrombosis 31 0.021
1025
P FRT001 Fourth Cranial Nerve Palsy 31 0.021
1026
SRC001 Sarcomatoid Mesothelioma 31 0.021
1027
PRC014 Pericardium Cancer 30 0.021
1028
XNT002 Xanthogranulomatous Cholecystitis 30 0.021
1029
c AMY057 Amyotrophic Lateral Sclerosis 16, Juvenile 30 0.021
1030
MYL057 Myelopathy, Htlv-1-Associated 30 0.021
1031
MBM001 Meibomian Cyst 30 0.021
1032
GST017 Gastric Tubular Adenocarcinoma 30 0.021
1033
URT016 Urethral Diverticulum 30 0.021
1034
c CHR094 Chronic Polyneuropathy 30 0.021
1035
CHR077 Chorioretinal Scar 30 0.021
1036
RNL104 Renal Hypodysplasia 30 0.021
1037
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 30 0.021
1038
c CLR075 Colorectal Cancer 3 30 0.021
1039
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.021
1040
c ACT053 Acute Thyroiditis 30 0.021
1041
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.021
1042
LRY007 Laryngeal Tuberculosis 29 0.021
1043
SRC011 Sarcocystosis 29 0.021
1044
HNS001 Hansen's Disease 29 0.021
1045
NPH006 Nephrogenic Adenofibroma 29 0.021
1046
NNS003 Non-Secretory Myeloma 29 0.021
1047
ANT013 Anterior Spinal Artery Syndrome 29 0.021
1048
JJN007 Jejunal Adenocarcinoma 29 0.021
1049
P DCR004 Dacryocystitis 29 0.021
1050
LVR006 Liver Lymphoma 29 0.021
1051
THY024 Thymus Adenocarcinoma 29 0.021
1052
MLG141 Malignant Atrophic Papulosis 29 0.021
1053
c AMY063 Amyotrophic Lateral Sclerosis 20 28 0.021
1054
CYS003 Cystitis Cystica 28 0.021
1055
HYP047 Hypertropia 28 0.021
1056
LPD007 Lipoadenoma 28 0.021
1057
HYP048 Hypotropia 28 0.021