Search results for "paralysis"

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

1085 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
P HYP370 Hypokalemic Periodic Paralysis, Type 1 48 7.662
2
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 42 5.991
3
c INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 35 4.612
4
P AND016 Andersen Syndrome 58 4.581
5
NRM009 Normokalemic Periodic Paralysis 27 4.168
6
FCL012 Facial Paralysis 43 3.858
7
P THY054 Thyrotoxic Periodic Paralysis 39 3.798
8
TCK002 Tick Paralysis 23 3.685
9
PRM028 Paramyotonia Congenita 47 3.326
10
OCL003 Oculomotor Nerve Paralysis 23 3.312
11
c THY083 Thyrotoxic Periodic Paralysis 2 22 3.255
12
c HYP606 Hypokalemic Periodic Paralysis, Type 2 32 3.236
13
c THY084 Thyrotoxic Periodic Paralysis 1 22 2.968
14
KRT022 Keratoderma Palmoplantar Spastic Paralysis 15 2.903
15
BLL003 Bell's Palsy 46 2.701
16
PRN008 Peroneal Nerve Paralysis 26 2.566
17
MBS002 Moebius Syndrome 57 2.541
18
P SPS154 Spastic Paralysis, Infantile Onset Ascending 19 2.518
19
c PRK057 Parkinson Disease, Late-Onset 73 2.501
20
c HYP142 Hyperkalemic Periodic Paralysis Type 1 12 2.501
21
TCK005 Tucker Syndrome 12 2.481
22
PLM031 Poliomyelitis 52 2.306
23
KLM001 Klumpke Paralysis 10 2.133
24
CNG241 Congenital Laryngeal Palsy 7 2.102
25
GLS003 Glossopharyngeal Nerve Paralysis 9 2.080
26
LRY021 Laryngeal Adductor Paralysis 9 2.072
27
FML082 Familial Partial Paralysis 3 2.072
28
VCL002 Vocal Cord Dysfunction Familial 18 2.063
29
CNG302 Congenital Hereditary Facial Paralysis with Variable Hearing Loss 8 2.042
30
c NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 24 2.030
31
VNN001 Venencie Powell Gordon Winkelmann Syndrome 6 2.016
32
TDD001 Todd's Paralysis 6 1.607
33
P CRN035 Cranial Nerve Palsy 33 1.550
34
RMS007 Ramsay Hunt Syndrome 29 1.516
35
c FML159 Familial Periodic Paralyses 8 1.491
36
FZL002 Fazio-Londe Disease 30 1.481
37
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 14 1.481
38
GLL022 Guillain-Barre Syndrome 54 1.471
39
P OPH004 Ophthalmoplegia 43 1.471
40
P HRN001 Horner's Syndrome 36 1.471
41
PRL008 Paralytic Ileus 33 1.471
42
FML160 Familial Spastic Paralysis 6 1.471
43
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 5 1.471
44
LRY023 Laryngeal Abductor Paralysis Mental Retardation 2 1.471
45
c NRP022 Neuropathy, Distal Hereditary Motor, Type Viib 27 1.459
46
CYC001 Cycloplegia 26 1.459
47
LRY043 Laryngeal Abductor Paralysis - Intellectual Disability 10 1.459
48
PRL020 Paralysis Agitans, Juvenile, of Hunt 6 1.459
49
ISL060 Isolated Hereditary Congenital Facial Paralysis 4 1.459
50
TRP002 Tropical Spastic Paraparesis 51 1.444
51
PSD001 Pseudobulbar Palsy 28 1.444
52
P SPS003 Spastic Diplegia 37 1.425
53
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 29 1.425
54
MRK002 Marek Disease 24 1.425
55
ABD002 Abducens Nerve Disease 22 1.425
56
THR010 Third Cranial Nerve Disease 18 1.425
57
BLN017 Balint Syndrome 16 1.425
58
c DST092 Distal Hereditary Motor Neuropathy Type 7 13 1.425
59
RNL007 Renal Tubular Acidosis 46 0.149
60
HYP005 Hypokalemia 39 0.130
61
P MYP004 Myopathy 50 0.128
62
NRN002 Neuronitis 40 0.122
63
SPS057 Spasticity 30 0.113
64
P THY032 Thyroiditis 48 0.104
65
P LRY019 Laryngitis 46 0.104
66
P TRC086 Trichohepatoenteric Syndrome 1 42 0.104
67
P GRV001 Graves' Disease 51 0.099
68
P NRP001 Neuropathy 48 0.099
69
NRM005 Neuromuscular Disease 45 0.099
70
P MSC033 Muscle Disorders 38 0.099
71
P RSP003 Respiratory Failure 58 0.096
72
MYT011 Myotonia 33 0.096
73
THR013 Thoracic Outlet Syndrome 47 0.093
74
OTT002 Otitis Media 57 0.091
75
ADN018 Adenoma 54 0.091
76
P NRL007 Neurologic Diseases 35 0.091
77
ANR002 Aniridia 72 0.088
78
ACN002 Acanthosis Nigricans 53 0.088
79
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.088
80
P ATX010 Ataxia Neuropathy Spectrum 31 0.088
81
c SPN225 Spondyloarthropathy 1 66 0.085
82
P ANG001 Angelman Syndrome 66 0.085
83
c ART101 Aortic Valve Disease 2 46 0.085
84
BTL001 Botulism 50 0.082
85
P MSC003 Muscular Atrophy 45 0.082
86
BNF002 Bone Fracture 39 0.082
87
ANR040 Aneurysm 43 0.078
88
CRB009 Cerebritis 37 0.078
89
CRN031 Cranial Nerve Disease 30 0.078
90
MSC004 Muscle Tissue Disease 23 0.078
91
CRB037 Cerebral Palsy 54 0.075
92
P HYP076 Hyperthyroidism 48 0.075
93
P CRV039 Cervicitis 42 0.075
94
DYS073 Dysphagia 33 0.075
95
AND015 Androgen Insensitivity 65 0.072
96
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.072
97
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.072
98
SPN186 Spinal Cord Injury 55 0.072
99
HNT002 Hantavirus Pulmonary Syndrome 52 0.072
100
ALR002 Al-Raqad Syndrome 23 0.072
101
P PRD017 Periodic Paralyses 22 0.072
102
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.068
103
P HRM001 Hermansky-Pudlak Syndrome 62 0.068
104
c PNC108 Pancreatitis, Hereditary 59 0.068
105
P ALT001 Alternating Hemiplegia of Childhood 52 0.068
106
P NRV007 Nervous System Disease 49 0.068
107
ACS001 Acoustic Neuroma 47 0.068
108
HMP005 Hemiplegia 43 0.068
109
P PTS002 Ptosis 42 0.068
110
NRM004 Neuroma 42 0.068
111
PRP016 Paraplegia 41 0.068
112
HYP017 Hypophosphatemia 39 0.068
113
c PRG001 Progressive Muscular Atrophy 33 0.068
114
LRY017 Laryngeal Disease 19 0.068
115
EPL031 Epileptic Hemiplegia 4 0.068
116
P HPT021 Hepatitis 58 0.064
117
LYM017 Lyme Disease 56 0.064
118
HRP004 Herpes Zoster 54 0.064
119
P MNN013 Meningitis 51 0.064
120
MYC002 Mycobacterium Avium Complex Disease 46 0.064
121
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.064
122
MNN014 Mononeuritis 39 0.064
123
c BNG076 Benign Exophthalmos Syndrome 21 0.064
124
AND005 Androgen Insensitivity Syndrome, Mild 19 0.064
125
VGS001 Vagus Nerve Disease 10 0.064
126
STR067 Stroke, Ischemic 68 0.060
127
P HRP006 Herpes Simplex 60 0.060
128
GTR002 Goiter 47 0.060
129
TTH006 Tooth Disease 47 0.060
130
P PLY019 Polyneuropathy 46 0.060
131
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.060
132
NRT004 Neuritis 43 0.060
133
CHL069 Cholesteatoma 43 0.060
134
P ATX004 Ataxia 43 0.060
135
WST005 West Nile Virus 40 0.060
136
QDR001 Quadriplegia 39 0.060
137
ECT005 Ectropion 38 0.060
138
CNV002 Conversion Disorder 37 0.060
139
PRT026 Parotitis 35 0.060
140
PRL013 Paralytic Poliomyelitis 27 0.060
141
SWL001 Swallowing Disorders 20 0.060
142
CRB039 Cerebrovascular Disease 58 0.055
143
MLG056 Malignant Hyperthermia 56 0.055
144
P SJG001 Sjogren's Syndrome 54 0.055
145
MLK003 Melkersson-Rosenthal Syndrome 53 0.055
146
P HYP086 Hypothyroidism 52 0.055
147
SNS001 Sensorineural Hearing Loss 49 0.055
148
SPN020 Spondylosis 46 0.055
149
STT002 Status Asthmaticus 44 0.055
150
c PND001 Pain Disorder 43 0.055
151
MYL001 Myelitis 39 0.055
152
LCK001 Locked-in Syndrome 37 0.055
153
SPN041 Spinal Cord Disease 33 0.055
154
WND001 Wound Botulism 32 0.055
155
MVM001 Movement Disease 31 0.055
156
HYP264 Hypertonia 30 0.055
157
LGP001 Lagophthalmos 29 0.055
158
c SYS001 Systemic Lupus Erythematosus 90 0.051
159
P ATX030 Ataxia-Telangiectasia 76 0.051
160
TBR010 Tuberculosis 64 0.051
161
P LKM002 Leukemia 61 0.051
162
P MYS003 Myasthenia Gravis 59 0.051
163
P CHR071 Charcot-Marie-Tooth Disease 59 0.051
164
ART001 Arterial Tortuosity Syndrome 59 0.051
165
IMG001 Image Syndrome 56 0.051
166
ART016 Aortic Aneurysm 55 0.051
167
P MSC005 Muscular Dystrophy 52 0.051
168
PTN002 Patent Ductus Arteriosus 46 0.051
169
P HYP065 Hyperaldosteronism 45 0.051
170
PTT006 Pituitary Adenoma 45 0.051
171
MNN009 Meningoencephalitis 40 0.051
172
c SBC007 Subacute Thyroiditis 38 0.051
173
RSP006 Respiratory System Disease 36 0.051
174
FDB001 Foodborne Botulism 33 0.051
175
SPC005 Speech Disorder 31 0.051
176
ERB002 Erb's Palsy 7 0.051
177
P NRC002 Narcolepsy 66 0.045
178
c HPT001 Hepatitis C 64 0.045
179
P LPS004 Lupus Erythematosus 61 0.045
180
P AMY004 Amyloidosis 60 0.045
181
P SPN046 Spinal Muscular Atrophy 58 0.045
182
P PNM007 Pneumonia 56 0.045
183
P EPL002 Epilepsy Syndrome 54 0.045
184
MTR014 Motor Neuron Disease 49 0.045
185
P THR003 Thoracic Aortic Aneurysm 47 0.045
186
P FNC004 Fanconi Syndrome 46 0.045
187
P DBT005 Diabetes Insipidus 46 0.045
188
TRY002 Troyer Syndrome 45 0.045
189
CRD119 Cardiac Arrest 45 0.045
190
P FNC044 Fanconi Anemia, Complementation Group C 44 0.045
191
MTH009 Mouth Disease 44 0.045
192
P EPS003 Episodic Ataxia 44 0.045
193
P NRV006 Nervous System Cancer 44 0.045
194
P SCL018 Scoliosis 44 0.045
195
ARC002 Arachnoiditis 43 0.045
196
SPP008 Suppurative Otitis Media 41 0.045
197
ARC007 Arachnoid Cysts 39 0.045
198
P SYR001 Syringomyelia 39 0.045
199
MLL002 Miller Fisher Syndrome 37 0.045
200
CRT008 Carotid Artery Dissection 34 0.045
201
c SPS078 Spastic Paraplegia 7 34 0.045
202
DPH021 Diaphragm Disease 33 0.045
203
GNC003 Geniculate Herpes Zoster 33 0.045
204
MDS022 Mediastinitis 33 0.045
205
P LBY004 Labyrinthitis 32 0.045
206
SPS004 Spastic Quadriplegia 32 0.045
207
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.045
208
SPN185 Spinal Cord Infarction 29 0.045
209
MST019 Mastoiditis 29 0.045
210
BRW004 Brown-Sequard Syndrome 28 0.045
211
c PLM022 Pulmonary Valve Insufficiency 26 0.045
212
FTD001 Foot Drop 25 0.045
213
FCL011 Facial Nerve Disease 25 0.045
214
MDD008 Middle Ear Adenoma 23 0.045
215
ANT054 Anotia 21 0.045
216
FBR024 Fibrocartilaginous Embolism 13 0.045
217
P NRB001 Neuroblastoma 73 0.039
218
MLR004 Malaria 72 0.039
219
CDS001 Cadasil 70 0.039
220
P CNG401 Congenital Heart Disease 68 0.039
221
c HRD010 Hereditary Spastic Paraplegia 64 0.039
222
MLT021 Multiple System Atrophy 63 0.039
223
GTL001 Gitelman Syndrome 63 0.039
224
PRP083 Porphyria, Acute Intermittent 62 0.039
225
P TRN020 Turner Syndrome 59 0.039
226
SRC014 Sarcoma 57 0.039
227
LPT001 Leptospirosis 55 0.039
228
P ATR011 Atrial Fibrillation 55 0.039
229
P HMN010 Hemangioma 54 0.039
230
MSL001 Measles 52 0.039
231
STT001 Status Epilepticus 51 0.039
232
RBS001 Rabies 51 0.039
233
OLV001 Olivopontocerebellar Atrophy 51 0.039
234
KRT001 Keratoconjunctivitis Sicca 49 0.039
235
P PLY017 Polyarteritis Nodosa 49 0.039
236
P MMP001 Mumps 49 0.039
237
P SZR006 Seizure Disorder 48 0.039
238
P ENC004 Encephalitis 48 0.039
239
c SCN006 Secondary Syphilis 48 0.039
240
P MYC008 Myocarditis 47 0.039
241
SLP005 Sleep Disorder 47 0.039
242
P LTR001 Lateral Sclerosis 46 0.039
243
EVN001 Evans' Syndrome 46 0.039
244
STF001 Stiff-Person Syndrome 46 0.039
245
c CNT033 Central Nervous System Cancer 45 0.039
246
NWC001 Newcastle Disease 45 0.039
247
GST045 Gastroenteritis 45 0.039
248
NRL005 Neurilemmoma 45 0.039
249
VNB005 Van Buchem Disease 44 0.039
250
TLR001 Tularemia 44 0.039
251
ASP003 Aseptic Meningitis 44 0.039
252
ADR008 Adrenal Adenoma 44 0.039
253
P NRN017 Neuronopathy, Distal Hereditary Motor, Type Vi 42 0.039
254
BRN071 Brain Injury 42 0.039
255
P ENC018 Encephalopathy 42 0.039
256
APH002 Aphasia 40 0.039
257
FSC004 Fasciitis 40 0.039
258
P PRP023 Peripheral Neuropathy 40 0.039
259
WST004 West Nile Encephalitis 40 0.039
260
LCR004 La Crosse Encephalitis 39 0.039
261
RLP003 Relapsing Fever 37 0.039
262
ATN005 Autonomic Dysfunction 36 0.039
263
c GRV008 Graves Disease 1 35 0.039
264
P HMR005 Hemorrhoid 35 0.039
265
TBS001 Tabes Dorsalis 34 0.039
266
TLS001 Tolosa-Hunt Syndrome 34 0.039
267
P AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 33 0.039
268
P PRX033 Proximal Renal Tubular Acidosis 33 0.039
269
CLR007 Colorado Tick Fever 32 0.039
270
PRP019 Peripheral Nervous System Disease 31 0.039
271
EPD005 Epidural Abscess 29 0.039
272
CVR002 Cavernous Sinus Thrombosis 28 0.039
273
TFT003 Tufting Enteropathy 27 0.039
274
PTR001 Petrositis 25 0.039
275
RBF003 Riboflavin Transporter Deficiency 23 0.039
276
c NRC009 Narcolepsy 1 23 0.039
277
ABD009 Abducens Palsy 20 0.039
278
BLB003 Bulbar Polio 19 0.039
279
PRS053 Parsonage Turner Syndrome 16 0.039
280
PNT023 Pontine Hemorrhage 16 0.039
281
SKL006 Skull Base Neoplasm 16 0.039
282
MYP026 Myopathy - Thyrotoxic 7 0.039
283
P BRS047 Breast Cancer 100 0.032
284
HPT023 Hepatocellular Carcinoma 90 0.032
285
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.032
286
NRL016 Neural Tube Defects 74 0.032
287
P BRD002 Bardet-Biedl Syndrome 68 0.032
288
BRK010 Burkitt Lymphoma 68 0.032
289
P FML161 Familial Mediterranean Fever, Ar 67 0.032
290
INC002 Inclusion Body Myositis 67 0.032
291
P ALP004 Alport Syndrome 66 0.032
292
INS024 Insulin-Like Growth Factor I 64 0.032
293
P LPR003 Leprosy 63 0.032
294
P KRT004 Keratitis 63 0.032
295
PTR006 Peters Anomaly 63 0.032
296
CNT098 Central Core Disease 60 0.032
297
P EHL033 Ehlers-Danlos Syndrome, Classic Type 60 0.032
298
WLL001 Williams-Beuren Syndrome 59 0.032
299
PRT036 Peritonitis 58 0.032
300
CNG368 Congenital Adrenal Hyperplasia 58 0.032
301
KND001 Kindler Syndrome 56 0.032
302
P HYP117 Hypertriglyceridemia 56 0.032
303
ART005 Arteriovenous Malformation 56 0.032
304
P CRB042 Cerebellar Ataxia 56 0.032
305
c ATM010 Autoimmune Hemolytic Anemia 56 0.032
306
CPR001 Coproporphyria 56 0.032
307
P EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.032
308
HMF006 Hemifacial Microsomia 55 0.032
309
VSC007 Vascular Disease 55 0.032
310
P CMR001 Camurati-Engelmann Disease 54 0.032
311
P MYS005 Myositis 54 0.032
312
P TXP001 Toxoplasmosis 54 0.032
313
CCC001 Coccidioidomycosis 54 0.032
314
P NRM001 Neuromyelitis Optica 54 0.032
315
P RHB017 Rhabdoid Tumor 54 0.032
316
P PRP029 Porphyria 54 0.032
317
EYD002 Eye Disease 54 0.032
318
P ACR001 Aicardi-Goutieres Syndrome 53 0.032
319
P CNG001 Congenital Myasthenic Syndrome 53 0.032
320
PRP025 Peripheral Primitive Neuroectodermal Tumor 52 0.032
321
P HML002 Hemolytic Anemia 52 0.032
322
YLL002 Yellow Fever 52 0.032
323
c CNT035 Central Nervous System Disease 52 0.032
324
END030 End Stage Renal Failure 51 0.032
325
RHB003 Rhabdomyosarcoma 51 0.032
326
TRG002 Trigeminal Neuralgia 51 0.032
327
P EHL001 Ehlers-Danlos Syndrome 51 0.032
328
SCH016 Schimke Immunoosseous Dysplasia 51 0.032
329
P ESP024 Esophagitis 51 0.032
330
BNC003 Bone Cancer 50 0.032
331
PLS006 Plasmodium Vivax Malaria 50 0.032
332
P CNJ013 Conjunctivitis 50 0.032
333
PRN023 Prion Disease 50 0.032
334
P ART023 Arthropathy 50 0.032
335
P ABD003 Abdominal Aortic Aneurysm 50 0.032
336
BBS001 Babesiosis 50 0.032
337
SPT005 Spotted Fever 49 0.032
338
GLC003 Glucose Intolerance 49 0.032
339
P GLM007 Glomerulonephritis 49 0.032
340
c PPL046 Popliteal Pterygium Syndrome 1 48 0.032
341
JPN002 Japanese Encephalitis 48 0.032
342
PHR003 Pharyngitis 48 0.032
343
LYM021 Lymphadenitis 48 0.032
344
BRN004 Brain Edema 47 0.032
345
ISC004 Ischemia 47 0.032
346
P KLP003 Klippel-Feil Syndrome 47 0.032
347
TCK001 Tick-Borne Encephalitis 47 0.032
348
DPH001 Diphtheria 47 0.032
349
c MLG069 Malignant Hypertension 46 0.032
350
P SPR013 Spiradenoma 46 0.032
351
GST037 Gastroparesis 46 0.032
352
P PNM006 Pneumoconiosis 45 0.032
353
P INT070 Intestinal Obstruction 45 0.032
354
PRG097 Paragangliomas 1, with or Without Deafness 45 0.032
355
HYP068 Hyperostosis 45 0.032
356
P INT068 Intestinal Disease 44 0.032
357
P SYP003 Syphilis 44 0.032
358
MMB001 Membranoproliferative Glomerulonephritis 44 0.032
359
P GNT008 Giant Cell Tumor 43 0.032
360
TRC023 Trichinosis 43 0.032
361
P GST049 Gastrointestinal System Cancer 43 0.032
362
EHR002 Ehrlichiosis 43 0.032
363
c CNG021 Congenital Toxoplasmosis 43 0.032
364
OPT009 Optic Neuritis 43 0.032
365
NRC020 Neuroectodermal Tumor 43 0.032
366
P TRM003 Tremor 43 0.032
367
ANK001 Ankylosis 43 0.032
368
OST011 Osteomalacia 42 0.032
369
P OTT001 Otitis Externa 42 0.032
370
HDC001 Headache 42 0.032
371
c CHR095 Chronic Progressive External Ophthalmoplegia 42 0.032
372
MYL003 Myeloid Sarcoma 41 0.032
373
P PRG013 Paraganglioma 41 0.032
374
CNT025 Central Pontine Myelinolysis 41 0.032
375
c AMY008 Amyotrophic Lateral Sclerosis Type 2 41 0.032
376
P MSC007 Muscle Hypertrophy 41 0.032
377
STL001 St. Louis Encephalitis 40 0.032
378
P PRS062 Persistent Hyperplastic Primary Vitreous 40 0.032
379
SPS007 Spastic Cerebral Palsy 40 0.032
380
P OST028 Osteochondroma 40 0.032
381
P TRN034 Transverse Myelitis 40 0.032
382
P PRT029 Parathyroid Adenoma 39 0.032
383
MYH012 Myhre Syndrome 39 0.032
384
NPH003 Nephrocalcinosis 39 0.032
385
RNL011 Renal Osteodystrophy 39 0.032
386
TTR016 Tetra-Amelia Syndrome 38 0.032
387
P ICH004 Ichthyosis 38 0.032
388
NSP002 Nasopharyngitis 38 0.032
389
c HYP293 Hypophosphatasia, Adult 38 0.032
390
PSD029 Pseudocholinesterase Deficiency 38 0.032
391
RCK002 Rocky Mountain Spotted Fever 37 0.032
392
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 37 0.032
393
SPR007 Superior Mesenteric Artery Syndrome 37 0.032
394
P DMY001 Demyelinating Polyneuropathy 36 0.032
395
PPL001 Papillary Adenoma 36 0.032
396
XRP001 Xerophthalmia 36 0.032
397
ANT018 Anthracosis 36 0.032
398
THY009 Thyroid Lymphoma 35 0.032
399
PRP056 Porphyria, Acute Hepatic 35 0.032
400
SPN050 Spinocerebellar Degeneration 35 0.032
401
c MYS064 Myasthenic Syndrome, Congenital, 16 35 0.032
402
P HYP265 Hypotonia 35 0.032
403
P AXN001 Axonal Neuropathy 35 0.032
404
P CHR342 Chiari Malformation 35 0.032
405
SLV003 Salivary Gland Disease 34 0.032
406
ENT001 Enterocele 34 0.032
407
NRP016 Neuropathy, Recurrent, with Pressure Palsies 34 0.032
408
ADS002 Adie Syndrome 34 0.032
409
INT042 Internuclear Ophthalmoplegia 34 0.032
410
HYD001 Hydranencephaly 33 0.032
411
CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 33 0.032
412
ECT004 Ecthyma 33 0.032
413
INT253 Intestinal Benign Neoplasm 33 0.032
414
STR002 Streptococcal Meningitis 33 0.032
415
PRS037 Periostitis 32 0.032
416
VST004 Vestibular Disease 32 0.032
417
CRT009 Critical Illness Polyneuropathy 32 0.032
418
OST006 Osteoblastoma 32 0.032
419
MTC018 Metachondromatosis 32 0.032
420
DVL002 Developmental Disabilities 32 0.032
421
c SPS092 Spastic Paraplegia 11 31 0.032
422
HYP047 Hypertropia 31 0.032
423
SPC010 Speech and Communication Disorders 31 0.032
424
ADJ001 Adjustment Disorder 30 0.032
425
HPT074 Hepatic Adenoma, Somatic 30 0.032
426
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.032
427
ENT005 Entropion 29 0.032
428
FCL003 Facial Hemiatrophy 29 0.032
429
PLY119 Polymicrogyria, Bilateral Perisylvian 29 0.032
430
PST055 Postural Hypotension 29 0.032
431
c PRK027 Parkinson Disease 15, Autosomal Recessive 29 0.032
432
c MLT009 Multiple Cranial Nerve Palsy 28 0.032
433
NRC019 Neurocutaneous Melanosis, Somatic 28 0.032
434
SPS016 Spasmodic Dysphonia 28 0.032
435
MTL002 Metal Metabolism Disorder 28 0.032
436
SPS019 Spastic Paraparesis 27 0.032
437
CHL109 Childhood Apraxia of Speech 27 0.032
438
HNM002 Hinman Syndrome 27 0.032
439
CBB002 Cobb Syndrome 27 0.032
440
PRN016 Peroneal Neuropathy 26 0.032
441
c ACT159 Acute Transverse Myelitis 26 0.032
442
MNN005 Meningovascular Neurosyphilis 25 0.032
443
HNS001 Hansen's Disease 25 0.032
444
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 24 0.032
445
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 24 0.032
446
TCK004 Tick Infestation 24 0.032
447
MTR013 Motor Neuritis 23 0.032
448
PRR008 Periarteritis Nodosa 21 0.032
449
PRS063 Paresthesia 20 0.032
450
c FML249 Familial Amyloidosis, Finnish Type 20 0.032
451
ACT181 Acute Motor Axonal Neuropathy 20 0.032
452
PWS001 Powassan Encephalitis 17 0.032
453
c LTH032 Lethal Congenital Contracture Syndrome 7 17 0.032
454
c LTH030 Lethal Congenital Contracture Syndrome 8 16 0.032
455
ITR001 Iatrogenic Botulism 16 0.032
456
CNT067 Central Cord Syndrome 16 0.032
457
c ADL069 Adult Intestinal Botulism 14 0.032
458
SYR004 Syringobulbia 14 0.032
459
UVP001 Uveoparotid Fever 11 0.032
460
TXN001 Toxin-Mediated Infectious Botulism 11 0.032
461
BLB001 Bulbospinal Polio 8 0.032
462
SPN015 Spinal Polio 7 0.032
463
BRC057 Brachial Plexus Birth Injuries 7 0.032
464
BWM001 Bowman's Membrane Folds or Rupture 7 0.032
465
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.032
466
HMP020 Hemiplegia Alterans 1 0.032
467
P CLR023 Colorectal Cancer 95 0.023
468
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.023
469
P RNL014 Renal Cell Carcinoma 81 0.023
470
P OST012 Osteoarthritis 79 0.023
471
P LFR001 Li-Fraumeni Syndrome 79 0.023
472
P AST005 Asthma 77 0.023
473
HV1006 Hiv-1 77 0.023
474
GLC006 Galactosemia 76 0.023
475
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 0.023
476
P OST002 Osteoporosis 75 0.023
477
P MTC003 Metachromatic Leukodystrophy 72 0.023
478
c FNC027 Fanconi Anemia, Complementation Group a 71 0.023
479
P TYS001 Tay-Sachs Disease 70 0.023
480
P SCL016 Scleroderma 69 0.023
481
MYL009 Myelodysplastic Syndrome 69 0.023
482
c HYP595 Hypertension, Essential 68 0.023
483
P LGH007 Leigh Syndrome 67 0.023
484
CNG034 Congestive Heart Failure 65 0.023
485
P INF038 Influenza 64 0.023
486
P GCH001 Gaucher's Disease 64 0.023
487
P MYL005 Myelofibrosis 64 0.023
488
P OST001 Osteopetrosis 63 0.023
489
BHC002 Behcet's Disease 63 0.023
490
P BPL003 Bipolar Disorder 63 0.023
491
KWS002 Kawasaki Disease 62 0.023
492
P VLC001 Velocardiofacial Syndrome 61 0.023
493
P ALX003 Alexander Disease 61 0.023
494
CHD001 Chediak-Higashi Syndrome 61 0.023
495
SKN016 Skin Disease 61 0.023
496
c GLY008 Glycogen Storage Disease Ii 61 0.023
497
P KDN017 Kidney Cancer 60 0.023
498
P ADD001 Addison's Disease 60 0.023
499
THY028 Thyroid Cancer 60 0.023
500
WLF001 Wolff-Parkinson-White Syndrome 60 0.023
501
MYC006 Mycosis Fungoides 60 0.023
502
MNT001 Mantle Cell Lymphoma 60 0.023
503
c SRC025 Sarcoidosis 1 60 0.023
504
TNG009 Tongue Squamous Cell Carcinoma 60 0.023
505
WGN006 Wegener Granulomatosis 59 0.023
506
c HPT016 Hepatitis B 59 0.023
507
BRN028 Brain Cancer 59 0.023
508
P MCH002 Machado-Joseph Disease 59 0.023
509
CYS010 Cystinosis 59 0.023
510
ALC007 Alcohol Dependence 59 0.023
511
FCL009 Focal Dermal Hypoplasia 58 0.023
512
BLD087 Bladder Cancer, Somatic 58 0.023
513
FCT003 Factor X Deficiency 58 0.023
514
CRB011 Cerebrotendinous Xanthomatosis 58 0.023
515
MCK007 Muckle-Wells Syndrome 58 0.023
516
c MYT021 Myotonic Dystrophy 1 58 0.023
517
P HYP035 Hypophosphatasia 58 0.023
518
TWN003 Townes-Brocks Syndrome 57 0.023
519
P DRM010 Dermatomyositis 57 0.023
520
ABT001 Abetalipoproteinemia 57 0.023
521
c TYR012 Tyrosinemia, Type I 57 0.023
522
c ATM003 Autoimmune Thyroiditis 57 0.023
523
P KDN018 Kidney Disease 57 0.023
524
P WLD002 Waldenstrom Macroglobulinemia 57 0.023
525
PGT001 Paget's Disease of Bone 57 0.023
526
LWS003 Lowe Syndrome 56 0.023
527
BRN024 Bronchitis 56 0.023
528
P RCK004 Rickets 55 0.023
529
RCT015 Reactive Arthritis 55 0.023
530
EWN003 Ewing Sarcoma 55 0.023
531
HJD001 Hajdu-Cheney Syndrome 55 0.023
532
ACQ007 Acquired Immunodeficiency Syndrome 55 0.023
533
P MYM002 Moyamoya Disease 55 0.023
534
PSY004 Psychotic Disorder 55 0.023
535
CHR072 Chordoma 55 0.023
536
P SPN049 Spinocerebellar Ataxia 54 0.023
537
P CFF001 Coffin-Siris Syndrome 54 0.023
538
RBR001 Roberts Syndrome 54 0.023
539
PRP032 Porphyria Variegata 54 0.023
540
DRM006 Dermatitis 54 0.023
541
c MYT020 Myotonic Dystrophy 2 54 0.023
542
MLN008 Melanoma 54 0.023
543
P SCH018 Schizencephaly 54 0.023
544
P WRD001 Waardenburg's Syndrome 53 0.023
545
BRJ001 Borjeson-Forssman-Lehmann Syndrome 53 0.023
546
CHR001 Churg-Strauss Syndrome 53 0.023
547
KRN002 Kearns-Sayre Syndrome 53 0.023
548
PLM033 Pulmonary Embolism 53 0.023
549
P HRD001 Hereditary Multiple Exostoses 53 0.023
550
P CRN012 Craniometaphyseal Dysplasia 53 0.023
551
c LNG044 Long Qt Syndrome 1 53 0.023
552
P HYP097 Hyperekplexia 52 0.023
553
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 52 0.023
554
c SPN301 Spinocerebellar Ataxia 2 52 0.023
555
P GLY010 Glycine Encephalopathy 52 0.023
556
SHG001 Shigellosis 52 0.023
557
RLP001 Relapsing Polychondritis 52 0.023
558
P SPR098 Supranuclear Palsy, Progressive 52 0.023
559
P HYP004 Hypercalcemia 52 0.023
560
P IDP010 Idiopathic Generalized Epilepsy 51 0.023
561
GSG001 Gas Gangrene 51 0.023
562
NTH001 Netherton Syndrome 51 0.023
563
FCS012 Facioscapulohumeral Muscular Dystrophy 1 51 0.023
564
VLV011 Vulvovaginal Candidiasis 51 0.023
565
CYS008 Cystic Echinococcosis 51 0.023
566
ALV002 Alveolar Echinococcosis 50 0.023
567
P CND004 Candidiasis 50 0.023
568
THL016 Thalassemias, Alpha- 50 0.023
569
P FBR017 Fibrosarcoma 50 0.023
570
DSM004 Desmoid Tumor 50 0.023
571
VHW001 Vohwinkel Syndrome 50 0.023
572
MLL005 Miller-Dieker Syndrome 50 0.023
573
c CRB103 Cerebral Cavernous Malformations-1 50 0.023
574
VRL011 Viral Infectious Disease 50 0.023
575
P THY023 Thymoma 50 0.023
576
BRT002 Birt-Hogg-Dube Syndrome 50 0.023
577
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 50 0.023
578
P SML001 Small Cell Carcinoma 49 0.023
579
P SHR029 Short Syndrome 49 0.023
580
P APL006 Aplasia Cutis Congenita 49 0.023
581
c ACT073 Acute Leukemia 49 0.023
582
c LPD037 Lipodystrophy, Familial Partial, 2 49 0.023
583
P MTC069 Mitochondrial Disorders 49 0.023
584
FTT001 Fatty Liver Disease 49 0.023
585
MTC097 Mitochondrial Complex Iv Deficiency 49 0.023
586
CHC001 Chickenpox 49 0.023
587
PNM001 Pneumocystosis 49 0.023
588
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.023
589
P GLY013 Glycogen Storage Disease 49 0.023
590
LMY002 Leiomyoma 49 0.023
591
PTN001 Patent Foramen Ovale 48 0.023
592
c ADL017 Adult T-Cell Leukemia 48 0.023
593
P FNG005 Feingold Syndrome 48 0.023
594
P OLG002 Oligodendroglioma 48 0.023
595
THY022 Thymic Carcinoma 48 0.023
596
NRT001 Neurotic Disorder 48 0.023
597
P MYT002 Myotonic Dystrophy 48 0.023
598
STF002 Stiff Skin Syndrome 48 0.023
599
KRT006 Keratoconjunctivitis 48 0.023
600
P TMT001 Timothy Syndrome 48 0.023
601
WLL006 Wells Syndrome 48 0.023
602
P CTR002 Cataract 48 0.023
603
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 47 0.023
604
OCL001 Ocular Albinism 47 0.023
605
GNG013 Gingivitis 47 0.023
606
LYM019 Lymphosarcoma 47 0.023
607
MFF001 Maffucci Syndrome 47 0.023
608
CHK001 Chikungunya 47 0.023
609
FCT022 Factor Xi Deficiency, Autosomal Recessive 47 0.023
610
BLD044 Bladder Disease 47 0.023
611
LRN003 Learning Disability 47 0.023
612
P STR020 Strabismus 47 0.023
613
RSS002 Roussy-Levy Syndrome 46 0.023
614
ESP020 Esophageal Atresia 46 0.023
615
PLM012 Pulmonary Sarcoidosis 46 0.023
616
YLL001 Yellow Nail Syndrome 46 0.023
617
URB001 Urbach-Wiethe Disease 46 0.023
618
P EMB005 Embryonal Rhabdomyosarcoma 46 0.023
619
P FML035 Familial Hyperlipidemia 46 0.023
620
P LRY016 Laryngeal Carcinoma 46 0.023
621
P ENC008 Encephalocele 46 0.023
622
LYM022 Lymphangioma 46 0.023
623
PRD019 Periodic Fever, Familial 46 0.023
624
SPH001 Sapho Syndrome 46 0.023
625
P MTR012 Mitral Valve Disease 46 0.023
626
OBS006 Obstructive Lung Disease 45 0.023
627
c ALM001 Al Amyloidosis 45 0.023
628
P MST018 Mesothelioma 45 0.023
629
c ACT071 Acute Kidney Failure 45 0.023
630
OCL005 Oculocerebrorenal Syndrome 45 0.023
631
P HYP024 Hypoparathyroidism 45 0.023
632
PMP001 Pemphigus 45 0.023
633
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 45 0.023
634
P HYP014 Hyperuricemia 45 0.023
635
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 45 0.023
636
MGC001 Megacolon 45 0.023
637
P AML002 Amelogenesis Imperfecta 45 0.023
638
PLM010 Pulmonary Edema 45 0.023
639
EXT034 Extrinsic Allergic Alveolitis 44 0.023
640
P GRS003 Griscelli Syndrome 44 0.023
641
P NML001 Nemaline Myopathy 44 0.023
642
PLG002 Plague 44 0.023
643
CTS002 Cat-Scratch Disease 44 0.023
644
c FML023 Familial Hemiplegic Migraine 44 0.023
645
PRN011 Pernicious Anemia 44 0.023
646
WHP001 Whipple Disease 44 0.023
647
MGL013 Megalencephaly 44 0.023
648
P MYT013 Myotonia Congenita, Dominant 44 0.023
649
MST005 Mastitis 44 0.023
650
PRC013 Pericarditis 44 0.023
651
P EXP004 Exophthalmos 44 0.023
652
c OPT055 Optic Atrophy Plus Syndrome 43 0.023
653
MCP006 Mucoepidermoid Carcinoma 43 0.023
654
CYS016 Cystic Kidney 43 0.023
655
TXC002 Toxic Encephalopathy 43 0.023
656
P MMB011 Membranous Nephropathy 43 0.023
657
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 43 0.023
658
TBR006 Tuberculoid Leprosy 43 0.023
659
RCT018 Rectal Neoplasm 43 0.023
660
GST009 Gastroschisis 43 0.023
661
GRN039 Greenberg Skeletal Dysplasia 43 0.023
662
ANR004 Anuria 43 0.023
663
CVR006 Cavernous Hemangioma 43 0.023
664
CLD007 Cold Agglutinin Disease 43 0.023
665
GST050 Gastrointestinal System Disease 43 0.023
666
IPX001 Ipex Syndrome 43 0.023
667
PRR002 Pure Red-Cell Aplasia 43 0.023
668
HYP266 Hypoxia 42 0.023
669
DRY001 Dry Eye Syndrome 42 0.023
670
SLV012 Salivary Gland Adenoid Cystic Carcinoma 42 0.023
671
ADN002 Adenoiditis 42 0.023
672
THY025 Thymus Cancer 42 0.023
673
TPT001 Tauopathy 42 0.023
674
CSL001 Causalgia 42 0.023
675
P SCL009 Sclerosing Cholangitis 42 0.023
676
c VRL012 Viral Meningitis 42 0.023
677
INF058 Inflammatory Myofibroblastic Tumor 42 0.023
678
ART017 Aortic Disease 42 0.023
679
FBR009 Fibrous Dysplasia 42 0.023
680
MCR165 Microphthalmia with Limb Anomalies 42 0.023
681
ADT003 Auditory System Disease 42 0.023
682
P INT030 Intracranial Aneurysm 41 0.023
683
DYS015 Dysentery 41 0.023
684
NNT012 Neonatal Jaundice 41 0.023
685
CHR078 Chorioretinitis 41 0.023
686
PNM008 Pneumothorax 41 0.023
687
MST001 Mast-Cell Sarcoma 41 0.023
688
P EXN002 Exanthem 41 0.023
689
SPN035 Spindle Cell Sarcoma 41 0.023
690
CNN003 Conn's Syndrome 41 0.023
691
INF006 Infant Botulism 41 0.023
692
CLN019 Colonic Disease 41 0.023
693
EWN002 Ewing's Family of Tumors 41 0.023
694
c CHR417 Chronic Graft Versus Host Disease 41 0.023
695
PTT037 Pituitary Tumors 40 0.023
696
CDQ001 Cauda Equina Syndrome 40 0.023
697
IGG001 Iga Glomerulonephritis 40 0.023
698
OBS001 Obstructive Jaundice 40 0.023
699
P MLG086 Malignant Hyperthermia Susceptibility 40 0.023
700
BRN014 Bronchopneumonia 40 0.023
701
MDD002 Middle Ear Cholesteatoma 40 0.023
702
DVR002 Diverticulitis 40 0.023
703
CRT017 Cartilage Disease 40 0.023
704
CRN024 Corneal Disease 40 0.023
705
PRT038 Protein-Energy Malnutrition 40 0.023
706
P TCL004 T-Cell Leukemia 40 0.023
707
HYP006 Hypertensive Heart Disease 40 0.023
708
MDL009 Medullary Sponge Kidney 40 0.023
709
PRT019 Protein-Losing Enteropathy 40 0.023
710
TRC040 Tracheoesophageal Fistula 40 0.023
711
c AMY085 Amyotrophic Lateral Sclerosis 9 40 0.023
712
BRS064 Bursitis 40 0.023
713
DDN006 Duodenitis 40 0.023
714
DNN002 Donnai-Barrow Syndrome 39 0.023
715
c BRG005 Brugada Syndrome 1 39 0.023
716
MRR003 Murray Valley Encephalitis 39 0.023
717
c SHR030 Short Qt Syndrome 39 0.023
718
CD4003 Cd40 Ligand Deficiency 39 0.023
719
PYR011 Pyropoikilocytosis 39 0.023
720
MNT002 Mental Depression 39 0.023
721
EXS001 Exostosis 39 0.023
722
GYN001 Gynecomastia 39 0.023
723
DNT012 Dental Caries 39 0.023
724
P CHR345 Chronic Pain 39 0.023
725
P DND001 Dandy-Walker Syndrome 39 0.023
726
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.023
727
P CHL066 Cholangitis 39 0.023
728
NCR007 Necrotizing Fasciitis 39 0.023
729
c PSD092 Pseudohypoaldosteronism, Type Iie 39 0.023
730
INT017 Intestinal Schistosomiasis 39 0.023
731
ATN004 Autonomic Neuropathy 39 0.023
732
CHR288 Chronic Recurrent Multifocal Osteomyelitis 39 0.023
733
HMM003 Hemimegalencephaly 39 0.023
734
GRW007 Growth Hormone Deficiency 38 0.023
735
P PRM175 Primary Familial Brain Calcification 38 0.023
736
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 38 0.023
737
LMB062 Limb Ischemia 38 0.023
738
EST005 Esotropia 38 0.023
739
HST009 Histiocytoma 38 0.023
740
MLT075 Multifocal Motor Neuropathy 38 0.023
741
HTS001 Hiatus Hernia 38 0.023
742
c AMY090 Amyotrophic Lateral Sclerosis 8 38 0.023
743
HYP458 Hyper Ige Syndrome 38 0.023
744
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 38 0.023
745
NTR003 Natural Killer Cell Leukemia 38 0.023
746
LPD004 Lipoid Nephrosis 38 0.023
747
MYS001 Myositis Ossificans 38 0.023
748
c CNG004 Congenital Epulis 38 0.023
749
CLN045 Colonic Benign Neoplasm 38 0.023
750
ECT026 Ectopic Pregnancy 38 0.023
751
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 38 0.023
752
NCR001 Necrotizing Ulcerative Gingivitis 38 0.023
753
CLL021 Collagenous Colitis 37 0.023
754
CLC001 Calciphylaxis 37 0.023
755
TRN004 Trench Fever 37 0.023
756
GDS001 Good Syndrome 37 0.023
757
c ART120 Arthrogryposis, Distal, Type 3 37 0.023
758
BSL009 Basal Ganglia Calcification 37 0.023
759
c SCP001 Sc Phocomelia Syndrome 37 0.023
760
CHR010 Chorioangioma 37 0.023
761
SCT002 Scotoma 37 0.023
762
P PRX014 Proximal Spinal Muscular Atrophy 37 0.023
763
c OST131 Osteopetrosis, Autosomal Dominant 2 37 0.023
764
SPN040 Spinal Cancer 37 0.023
765
BRN080 Brain Ischemia 37 0.023
766
ASP007 Aspiration Pneumonia 37 0.023
767
ANG002 Angiostrongyliasis 37 0.023
768
c SZR008 Seizures, Benign Neonatal, 1 37 0.023
769
SML020 Small Patella Syndrome 37 0.023
770
ACT012 Acute Hemorrhagic Conjunctivitis 37 0.023
771
TRP004 Tropical Sprue 37 0.023
772
MTB004 Metabolic Acidosis 36 0.023
773
P RSM001 Rasmussen Encephalitis 36 0.023
774
MYP100 Myopathy, X-Linked, with Excessive Autophagy 36 0.023
775
P MNN007 Meningocele 36 0.023
776
SCR015 Scarlet Fever 36 0.023
777
MYX004 Myxedema 36 0.023
778
P INT063 Intellectual Disability 36 0.023
779
UTR043 Uterine Sarcoma 36 0.023
780
PST020 Postpoliomyelitis Syndrome 36 0.023
781
TCL002 T-Cell Large Granular Lymphocyte Leukemia 36 0.023
782
ADN020 Adenosarcoma 36 0.023
783
BRC010 Brachial Plexus Lesion 36 0.023
784
MLY001 Molybdenum Cofactor Deficiency 36 0.023
785
PLM029 Palmoplantar Keratosis 36 0.023
786
NRS003 Neurosyphilis 36 0.023
787
FNC007 Functioning Pituitary Adenoma 36 0.023
788
PNM010 Pneumothorax, Primary Spontaneous 35 0.023
789
VRT003 Vertebrobasilar Insufficiency 35 0.023
790
P MLT008 Multinodular Goiter 35 0.023
791
c PRM022 Primary Syphilis 35 0.023
792
VSC047 Vascular Malformation 35 0.023
793
MRS001 Marasmus 35 0.023
794
P GLM006 Glomangioma 35 0.023
795
P PRM108 Primary Progressive Multiple Sclerosis 35 0.023
796
LRY029 Laryngomalacia 35 0.023
797
AMB002 Amblyopia 35 0.023
798
AVD001 Avoidant Personality Disorder 35 0.023
799
THY030 Thyroid Gland Disease 35 0.023
800
P AMY084 Amyloidosis, Finnish Type 35 0.023
801
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.023
802
c AMY083 Amyotrophic Lateral Sclerosis 11 35 0.023
803
ZYG002 Zygomycosis 35 0.023
804
c SYS043 Systemic Lupus Erythematosus 1 34 0.023
805
P NRX001 Neuroaxonal Dystrophy 34 0.023
806
PRV003 Perivascular Epithelioid Cell Tumor 34 0.023
807
c HRD086 Hereditary Hypophosphatemic Rickets 34 0.023
808
PRM020 Premenstrual Tension 34 0.023
809
c GM2005 Gm2-Gangliosidosis, Ab Variant 34 0.023
810
PTT009 Pituitary Gland Disease 34 0.023
811
DRS001 Dressler's Syndrome 34 0.023
812
RMS001 Rem Sleep Behavior Disorder 34 0.023
813
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 34 0.023
814
PRP021 Peripheral Nervous System Neoplasm 34 0.023
815
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 34 0.023
816
c SPS079 Spastic Paraplegia 2 34 0.023
817
c HRD088 Hereditary Neuropathies 34 0.023
818
P BNG026 Benign Neonatal Seizures 34 0.023
819
UPP004 Upper Respiratory Tract Disease 34 0.023
820
c AMY067 Amyotrophic Lateral Sclerosis 18 34 0.023
821
MTS001 Mutism 34 0.023
822
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 33 0.023
823
MLY006 Molybdenum Cofactor Deficiency a 33 0.023
824
PHY002 Physical Disorder 33 0.023
825
c OST126 Osteopetrosis, Autosomal Recessive 1 33 0.023
826
FTT003 Fatty Acid Oxidation Disorders 33 0.023
827
NTR001 Neutral Lipid Storage Disease 33 0.023
828
THY043 Thymic Hyperplasia 33 0.023
829
c FML156 Familial Hyperaldosteronism 33 0.023
830
c LRY015 Laryngeal Benign Neoplasm 33 0.023
831
CNJ012 Conjunctival Disease 33 0.023
832
SCH003 Schizophreniform Disorder 33 0.023
833
P CHR102 Charcot-Marie-Tooth Neuropathy 33 0.023
834
OLG015 Oligoarticular Juvenile Arthritis 33 0.023
835
CNG041 Congenital Cataracts, Facial Dysmorphism, and Neuropathy 33 0.023
836
GLT018 Glut1 Deficiency Syndrome 1 33 0.023
837
CNT046 Central Nervous System Vasculitis 33 0.023
838
P PLY024 Polymicrogyria 33 0.023
839
ASY002 Asymptomatic Neurosyphilis 33 0.023
840
JPN001 Japanese Spotted Fever 33 0.023
841
DST004 Distal Muscular Dystrophy 32 0.023
842
PNM005 Pneumonic Plague 32 0.023
843
P PLM030 Pleomorphic Rhabdomyosarcoma 32 0.023
844
HYP034 Hypertensive Encephalopathy 32 0.023
845
c ATS282 Autosomal Recessive Malignant Osteopetrosis 32 0.023
846
SPN029 Spondylolysis 32 0.023
847
JXT003 Juxtacortical Osteosarcoma 32 0.023
848
LMB010 Lambert Syndrome 32 0.023
849
VGN020 Vaginal Disease 32 0.023
850
c AMY059 Amyotrophic Lateral Sclerosis 19 32 0.023
851
CRB086 Cerebral Aneurysms 32 0.023
852
RHM009 Rheumatoid Lung Disease 32 0.023
853
SKL002 Skeletal Muscle Neoplasm 32 0.023
854
P GLM044 Glomerular Disease 32 0.023
855
DYS001 Dyskinetic Cerebral Palsy 31 0.023
856
ECH002 Echolalia 31 0.023
857
c PRK045 Parkinson Disease 5 31 0.023
858
SNS003 Sensory Peripheral Neuropathy 31 0.023
859
GNG011 Gingival Disease 31 0.023
860
HRT008 Heart Conduction Disease 31 0.023
861
c ACT053 Acute Thyroiditis 31 0.023
862
SST001 Sost-Related Sclerosing Bone Dysplasia 31 0.023
863
c CRB094 Cerebral Cavernous Malformations 3 31 0.023
864
RTC003 Root Caries 31 0.023
865
TRT003 Tertiary Syphilis 31 0.023
866
P CRB088 Cerebral Atrophy 31 0.023
867
c ACT004 Acute Diarrhea 31 0.023
868
VSL002 Visual Epilepsy 31 0.023
869
EYL005 Eyelid Disease 31 0.023
870
P HYP120 Hypoaldosteronism 31 0.023
871
SKL007 Skeletal Muscle Regeneration 31 0.023
872
PLS016 Plasma Cell Leukemia 30 0.023
873
PLY112 Polyarteritis Nodosa, Childhood-Onset 30 0.023
874
c MYP011 Myopathy Congenital 30 0.023
875
SPN331 Spondyloocular Syndrome 30 0.023
876
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 30 0.023
877
ANT007 Anterior Horn Cell Disease 30 0.023
878
P ATM020 Autoimmune Enteropathy 30 0.023
879
P BNG071 Benign Schwannoma 30 0.023
880
LRG008 Large Granular Lymphocyte Leukemia 30 0.023
881
P CYS007 Cystic Nephroma 30 0.023
882
c CNG020 Congenital Hypogammaglobulinemia 30 0.023
883
c HYP539 Hyperekplexia, Hereditary 1, Autosomal Dominant or Recessive 30 0.023
884
LTR002 Lateral Sinus Thrombosis 30 0.023
885
DFF015 Diffuse Glomerulonephritis 30 0.023
886
ETH009 Ethmoid Sinusitis 30 0.023
887
FCT008 Factitious Disorder 30 0.023
888
HYP048 Hypotropia 30 0.023
889
TRT002 Tertiary Neurosyphilis 30 0.023
890
MTN002 Mite Infestation 30 0.023
891
c AMY062 Amyotrophic Lateral Sclerosis 12 29 0.023
892
SRC001 Sarcomatoid Mesothelioma 29 0.023
893
NZL001 Nezelof Syndrome 29 0.023
894
ENC003 Encephalitozoonosis 29 0.023
895
FRY001 Frey Syndrome 29 0.023
896
VST003 Vestibular Nystagmus 29 0.023
897
MLR010 Melorheostosis with Osteopoikilosis 29 0.023
898
PRN029 Parainfluenza Virus Type 3 29 0.023
899
EXN001 Exanthema Subitum 29 0.023
900
MYC014 Mycobacterium Chelonae 29 0.023
901
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 29 0.023
902
HRP005 Herpetic Whitlow 29 0.023
903
c ACT079 Acute Proliferative Glomerulonephritis 28 0.023
904
c PRG106 Progressive Muscular Dystrophy 28 0.023
905
EXC003 Excessive Tearing 28 0.023
906
PLY010 Polyclonal Hypergammaglobulinemia 28 0.023
907
CRV030 Cervical Adenitis 28 0.023
908
DYG001 Dyggve-Melchior-Clausen Disease 28 0.023
909
ISC005 Ischemic Bone Disease 28 0.023
910
SPP007 Suppression Amblyopia 28 0.023
911
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.023
912
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 28 0.023
913
c SPS027 Spastic Paraplegia 17 28 0.023
914
c OST129 Osteopetrosis, Autosomal Recessive 2 28 0.023
915
FXF001 Fox Fordyce Disease 28 0.023
916
ORT001 Orthostatic Proteinuria 28 0.023
917
RHB022 Rhabdoid Tumors, Somatic 28 0.023
918
P FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 28 0.023
919
NRM006 Neuromuscular Junction Disease 28 0.023
920
PMP008 Pemphigus Vegetans 28 0.023
921
c PRG020 Paragangliomas 3 28 0.023
922
LRY007 Laryngeal Tuberculosis 28 0.023
923
SKL005 Skull Base Meningioma 28 0.023
924
ANT013 Anterior Spinal Artery Syndrome 28 0.023
925
SBS002 Substernal Goiter 27 0.023
926
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 27 0.023
927
c BRG008 Brugada Syndrome 6 27 0.023
928
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 27 0.023
929
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 27 0.023
930
CRN006 Coronary Aneurysm 27 0.023
931
P FRT001 Fourth Cranial Nerve Palsy 27 0.023
932
P RNL066 Renal Tubular Acidosis, Distal, Ad 27 0.023
933
MYT003 Myotonic Disease 27 0.023
934
c SRC023 Sarcoidosis 2 27 0.023
935
c CHR160 Chiari Malformation Type 2 27 0.023
936
TTH007 Tooth Erosion 27 0.023
937
PRM025 Primary Bacterial Infectious Disease 27 0.023
938
c CNG112 Congenital Muscular Dystrophy Type 1a 27 0.023
939
CNR001 Coenurosis 27 0.023
940
CNT009 Central Core Myopathy 27 0.023
941
RNL013 Renal Adenoma 27 0.023
942
MTC005 Mitochondrial Metabolism Disease 26 0.023
943
LPN001 Louping Ill 26 0.023
944
c CLR075 Colorectal Cancer 3 26 0.023
945
SRC008 Sarcomatoid Squamous Cell Skin Carcinoma 26 0.023
946
RNL026 Renal Tubular Acidosis with Deafness 26 0.023
947
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 26 0.023
948
c ATM017 Autoimmune Disease of the Nervous System 26 0.023
949
PRP024 Peripheral Osteosarcoma 26 0.023
950
END034 Endocrine Exophthalmos 26 0.023
951
MTC014 Mitochondrial Dna Deletion Syndromes 26 0.023
952
ABD010 Abdominal Wall Defect 26 0.023
953
CRN033 Cranial Nerve Malignant Neoplasm 26 0.023
954
c SPS025 Spastic Paraplegia 15 26 0.023
955
GNT004 Gnathomiasis 25 0.023
956
c PRG019 Paragangliomas 2 25 0.023
957
PRL014 Paralytic Squint 25 0.023
958
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 0.023
959
CRD016 Cardiac Rupture 25 0.023
960
ISL083 Isolated Cytochrome C Oxidase Deficiency 25 0.023
961
FBR028 Fibrosing Mediastinitis 25 0.023
962
c HYP072 Hypersensitivity Reaction Type Iii Disease 25 0.023
963
CRN051 Craniofacial Microsomia 25 0.023
964
c SPS013 Spastic Paraplegia 8 25 0.023
965
AST003 Asthenopia 25 0.023
966
MYP093 Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset 25 0.023
967
c PSD090 Pseudohypoaldosteronism, Type Iia 25 0.023
968
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 25 0.023
969
GRN004 Granulomatous Amebic Encephalitis 25 0.023
970
c ADL016 Adult Spinal Muscular Atrophy 25 0.023
971
LCR008 Lacrimal Apparatus Disease 25 0.023
972
MNR004 Mounier-Kuhn Syndrome 25 0.023
973
NRG004 Neurogenic Diabetes Insipidus 25 0.023
974
c CHR094 Chronic Polyneuropathy 25 0.023
975
P ANT022 Anterior Cranial Fossa Meningioma 25 0.023
976
INT020 Intravenous Leiomyomatosis 25 0.023
977
PGT009 Paget Disease of Bone 2, Early-Onset 25 0.023
978
CLV002 Clivus Chordoma 25 0.023
979
WYB001 Wyburn Mason's Syndrome 24 0.023
980
NNS003 Non-Secretory Myeloma 24 0.023
981
ATM012 Autoimmune Disease of Blood 24 0.023
982
ATY001 Atypical Depressive Disorder 24 0.023
983
c SPS091 Spastic Paraplegia 4 24 0.023
984
BRC002 Brachial Plexus Neuritis 24 0.023
985
c AMY094 Amyotrophic Lateral Sclerosis 5, Juvenile 24 0.023
986
END051 Endolymphatic Sac Tumor 24 0.023
987
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 24 0.023
988
FNC005 Functional Colonic Disease 24 0.023
989
c MYP081 Myopathy, Myofibrillar, 6 24 0.023
990
ANP019 Anophthalmos with Limb Anomalies 23 0.023
991
BRN036 Brain Stem Infarction 23 0.023
992
RCT017 Rectal Disease 23 0.023
993
c CLR085 Colorectal Cancer 1 23 0.023
994
TNG004 Tongue Disease 23 0.023
995
AMY068 Amyotrophic Lateral Sclerosis 15, with or Without Frontotemporal Dementia 23 0.023
996
CNV003 Conventional Fibrosarcoma 23 0.023
997
MLN002 Melanomatosis 23 0.023
998
BRW009 Brown-Vialetto-Van Laere Syndrome 1 23 0.023
999
c FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 23 0.023
1000
c CHR097 Chronic Purulent Otitis Media 23 0.023
1001
CLL005 Cellular Leiomyoma 23 0.023
1002
LGH012 Leigh Syndrome with Leukodystrophy 23 0.023
1003
c SPS159 Spastic Paraplegia 9b, Autosomal Recessive 23 0.023
1004
c VRL004 Viral Labyrinthitis 22 0.023
1005
c PRM015 Primary Cerebellar Degeneration 22 0.023
1006
c NRC017 Narcolepsy 7 22 0.023
1007
CRB005 Cerebral Arteritis 22 0.023
1008
BNP002 Bone Epithelioid Hemangioma 22 0.023
1009
DYS045 Dysosteosclerosis 22 0.023
1010
SYP001 Syphilitic Meningitis 22 0.023
1011
P INT006 Intestinal Botulism 22 0.023
1012
ENM002 Enamel Erosion 22 0.023
1013
c CLR077 Colorectal Cancer 10 22 0.023
1014
AMY095 Amyotrophic Lateral Sclerosis 6, with or Without Frontotemporal Dementia 22 0.023
1015
VNT001 Ventilation Pneumonitis 22 0.023
1016
GLB003 Globe Disease 22 0.023
1017
OST007 Ostertagiasis 21 0.023
1018
c AMY057 Amyotrophic Lateral Sclerosis 16, Juvenile 21 0.023
1019
CD3003 Cd3gamma Deficiency 21 0.023
1020
c AMY063 Amyotrophic Lateral Sclerosis 20 21 0.023
1021
PRS120 Persistent Idiopathic Facial Pain 21 0.023
1022
PRP013 Paraphimosis 21 0.023
1023
ATR055 Atrial Septal Aneurysm 21 0.023
1024
c SPS037 Spastic Paraplegia 31 21 0.023
1025
HSH001 Hashimoto-Pritzker Syndrome 20 0.023
1026
RDT005 Radiation Induced Cancer 20 0.023
1027
ATL010 Atlantoaxial Subluxation 20 0.023
1028
ETH012 Ethylene Glycol Poisoning 20 0.023
1029
ENC040 Encephalopathy Due to Sulfite Oxidase Deficiency 20 0.023
1030
c TRC078 Trichohepatoenteric Syndrome 2 20 0.023
1031
TTH005 Teeth Hard Tissue Disease 20 0.023
1032
PNT009 Pontine Tegmental Cap Dysplasia 20 0.023
1033
EXP002 Exposure Keratitis 20 0.023
1034
PRS033 Parasitic Ectoparasitic Infectious Disease 19 0.023
1035
c MLT124 Multiple Sclerosis 5 18 0.023
1036
CNG133 Congenital Varicella Syndrome 18 0.023
1037
AMY092 Amyotrophic Lateral Sclerosis 22 with or Without Frontotemoral Dementia 18 0.023
1038
HRT006 Heart Aneurysm 18 0.023
1039
c LKM005 Leukemia, T-Cell, Chronic 18 0.023
1040
ULC003 Ulcerative Blepharitis 18 0.023
1041
c MLT094 Multiple Sclerosis 3 18 0.023
1042
P PHC014 Phocomelia 17 0.023
1043
HRN022 Hearing Loss/deafness 17 0.023
1044
AGL003 Agel Amyloidosis 17 0.023
1045
P INT103 Intrauterine Infections 17 0.023
1046
c CNG129 Congenital Torticollis 17 0.023
1047
CRD009 Cardioencephalomyopathy 17 0.023
1048
FML045 Familial Mosaic Monosomy 7 Syndrome 17 0.023
1049
ACT214 Acetazolamide-Responsive Myotonia 17 0.023
1050
c MRR010 Mirror Movements 2 16 0.023
1051
P SNS011 Sinus Cancer 16 0.023
1052
HTR005 Heterochromia Iridis 16 0.023
1053
c NRN027 Neuronopathy, Distal Hereditary Motor, Type I 16 0.023
1054
DRG016 Drug Induced Dyskinesia