Search results for "paralysis"

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

1267 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
P HYP370 Hypokalemic Periodic Paralysis, Type 1 51 7.135
2
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 46 6.694
3
P AND016 Andersen Syndrome 58 4.696
4
NRM009 Normokalemic Periodic Paralysis 27 4.096
5
c INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 33 4.074
6
FCL012 Facial Paralysis 50 3.777
7
c THY083 Thyrotoxic Periodic Paralysis 2 19 3.771
8
P THY054 Thyrotoxic Periodic Paralysis 48 3.720
9
TCK002 Tick Paralysis 23 3.605
10
c HYP606 Hypokalemic Periodic Paralysis, Type 2 31 3.476
11
P SPS154 Spastic Paralysis, Infantile Onset Ascending 22 3.476
12
FML036 Familial Periodic Paralysis 39 3.289
13
PRM028 Paramyotonia Congenita 48 3.263
14
OCL003 Oculomotor Nerve Paralysis 27 3.255
15
LRY047 Laryngeal Abductor Paralysis 22 3.246
16
c THY084 Thyrotoxic Periodic Paralysis 1 21 2.911
17
BLL003 Bell's Palsy 48 2.662
18
PRN008 Peroneal Nerve Paralysis 22 2.521
19
MBS002 Moebius Syndrome 47 2.504
20
KRT022 Keratoderma Palmoplantar Spastic Paralysis 7 2.498
21
CNG490 Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome 8 2.453
22
PLM031 Poliomyelitis 60 2.264
23
P CRN035 Cranial Nerve Palsy 46 2.108
24
KLM001 Klumpke Paralysis 9 2.093
25
CNG241 Congenital Laryngeal Palsy 7 2.065
26
GLS003 Glossopharyngeal Nerve Paralysis 9 2.045
27
LRY021 Laryngeal Adductor Paralysis 10 2.037
28
FML082 Familial Partial Paralysis 8 2.037
29
GNC003 Geniculate Herpes Zoster 32 2.029
30
c HYP142 Hyperkalemic Periodic Paralysis Type 1 14 2.020
31
VCL007 Vocal Cord Paralysis and Ptosis 10 2.020
32
P PRK057 Parkinson Disease, Late-Onset 70 2.010
33
PSD001 Pseudobulbar Palsy 33 1.999
34
c NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 24 1.999
35
KRT067 Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy 13 1.999
36
TCK005 Tucker Syndrome 11 1.999
37
TDD001 Todd's Paralysis 10 1.578
38
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 13 1.456
39
FML160 Familial Spastic Paralysis 10 1.456
40
P HRN001 Horner's Syndrome 42 1.446
41
c FML159 Familial Periodic Paralyses 15 1.446
42
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 4 1.446
43
LRY023 Laryngeal Abductor Paralysis Mental Retardation 2 1.446
44
GLL022 Guillain-Barre Syndrome 56 1.435
45
P SPS003 Spastic Diplegia 52 1.435
46
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 36 1.435
47
CYC001 Cycloplegia 27 1.435
48
c NRP022 Neuropathy, Distal Hereditary Motor, Type Viib 25 1.435
49
PRL020 Paralysis Agitans, Juvenile, of Hunt 6 1.435
50
KRN002 Kearns-Sayre Syndrome 61 1.421
51
TRP002 Tropical Spastic Paraparesis 55 1.404
52
MRK002 Marek Disease 33 1.404
53
PRT015 Partial Third-Nerve Palsy 26 1.404
54
THR010 Third Cranial Nerve Disease 26 1.404
55
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 25 1.404
56
ABD002 Abducens Nerve Disease 23 1.404
57
c AND007 Andersen Syndrome Type 1 17 1.404
58
BLN017 Balint Syndrome 14 1.404
59
c FCL030 Facial Paresis, Hereditary Congenital, 1 13 1.404
60
c DST092 Distal Hereditary Motor Neuropathy Type 7 12 1.404
61
RNL007 Renal Tubular Acidosis 50 0.139
62
P LRY019 Laryngitis 54 0.123
63
HYP005 Hypokalemia 51 0.119
64
P MYP004 Myopathy 67 0.110
65
P NRV007 Nervous System Disease 71 0.106
66
P GRV001 Graves' Disease 59 0.102
67
SPS057 Spasticity 42 0.102
68
P THY032 Thyroiditis 54 0.097
69
P NRP001 Neuropathy 59 0.093
70
MYT011 Myotonia 36 0.090
71
P RSP003 Respiratory Failure 71 0.088
72
OTT002 Otitis Media 66 0.086
73
ADN018 Adenoma 58 0.086
74
NRM005 Neuromuscular Disease 56 0.086
75
BNF002 Bone Fracture 50 0.083
76
CRN031 Cranial Nerve Disease 40 0.080
77
NRN002 Neuronitis 41 0.078
78
ANR040 Aneurysm 57 0.075
79
P HYP076 Hyperthyroidism 55 0.075
80
P MSC003 Muscular Atrophy 50 0.075
81
P MSC033 Muscle Disorders 52 0.072
82
P PTS002 Ptosis 51 0.072
83
FDB001 Foodborne Botulism 45 0.069
84
P CRV039 Cervicitis 45 0.069
85
ALR002 Al-Raqad Syndrome 36 0.069
86
CRB037 Cerebral Palsy 66 0.066
87
LYM017 Lyme Disease 63 0.066
88
ACS001 Acoustic Neuroma 58 0.066
89
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.066
90
P ALT001 Alternating Hemiplegia of Childhood 50 0.066
91
DYS073 Dysphagia 48 0.066
92
NRM004 Neuroma 48 0.066
93
P HRP006 Herpes Simplex 65 0.062
94
MVM001 Movement Disease 49 0.062
95
HYP017 Hypophosphatemia 43 0.062
96
LRY017 Laryngeal Disease 34 0.062
97
AND005 Androgen Insensitivity Syndrome, Mild 16 0.062
98
EPL031 Epileptic Hemiplegia 4 0.062
99
P LYM118 Lymphoma 69 0.059
100
P HPT021 Hepatitis 69 0.059
101
P MNN013 Meningitis 67 0.059
102
P MYS003 Myasthenia Gravis 67 0.059
103
P EPL164 Epilepsy 66 0.059
104
SPN186 Spinal Cord Injury 63 0.059
105
MTH009 Mouth Disease 61 0.059
106
HRP004 Herpes Zoster 56 0.059
107
TTH006 Tooth Disease 52 0.059
108
PRP016 Paraplegia 49 0.059
109
CHL069 Cholesteatoma 49 0.059
110
AYM001 Ayme-Gripp Syndrome 41 0.059
111
CRB009 Cerebritis 39 0.059
112
c PRG001 Progressive Muscular Atrophy 39 0.059
113
MSC004 Muscle Tissue Disease 34 0.059
114
WND001 Wound Botulism 31 0.059
115
LGP001 Lagophthalmos 27 0.059
116
VGS001 Vagus Nerve Disease 18 0.059
117
STR067 Stroke, Ischemic 75 0.055
118
MLT021 Multiple System Atrophy 70 0.055
119
P PNM007 Pneumonia 68 0.055
120
P CHR071 Charcot-Marie-Tooth Disease 67 0.055
121
P HYP086 Hypothyroidism 64 0.055
122
CRB039 Cerebrovascular Disease 63 0.055
123
P PLY019 Polyneuropathy 56 0.055
124
WST005 West Nile Virus 53 0.055
125
P ATX004 Ataxia 53 0.055
126
NRT004 Neuritis 52 0.055
127
MYL001 Myelitis 51 0.055
128
HMP005 Hemiplegia 51 0.055
129
P SJG001 Sjogren's Syndrome 50 0.055
130
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.055
131
CNV002 Conversion Disorder 41 0.055
132
ECT005 Ectropion 39 0.055
133
LCK001 Locked-in Syndrome 38 0.055
134
FCL011 Facial Nerve Disease 36 0.055
135
SWL001 Swallowing Disorders 33 0.055
136
PRL013 Paralytic Poliomyelitis 28 0.055
137
GNC005 Geniculate Ganglionitis 27 0.055
138
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.051
139
P NRC002 Narcolepsy 62 0.051
140
RSP006 Respiratory System Disease 58 0.051
141
GTR002 Goiter 52 0.051
142
QDR001 Quadriplegia 52 0.051
143
SPN041 Spinal Cord Disease 51 0.051
144
P FNC004 Fanconi Syndrome 49 0.051
145
MLL002 Miller Fisher Syndrome 43 0.051
146
PRT026 Parotitis 42 0.051
147
STT002 Status Asthmaticus 42 0.051
148
ARC002 Arachnoiditis 41 0.051
149
MLK003 Melkersson-Rosenthal Syndrome 41 0.051
150
SPC005 Speech Disorder 41 0.051
151
c SBC007 Subacute Thyroiditis 40 0.051
152
SPN369 Spinal Disease 39 0.051
153
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.051
154
P PRD017 Periodic Paralyses 27 0.051
155
P HRT032 Heart Disease 75 0.046
156
P LKM002 Leukemia 71 0.046
157
TBR010 Tuberculosis 70 0.046
158
ART016 Aortic Aneurysm 69 0.046
159
CRD119 Cardiac Arrest 61 0.046
160
SNS001 Sensorineural Hearing Loss 57 0.046
161
PTT006 Pituitary Adenoma 56 0.046
162
PRP083 Porphyria, Acute Intermittent 54 0.046
163
P PTN002 Patent Ductus Arteriosus 52 0.046
164
P HYP065 Hyperaldosteronism 50 0.046
165
ATN005 Autonomic Dysfunction 49 0.046
166
MNN009 Meningoencephalitis 47 0.046
167
NRP016 Neuropathy, Recurrent, with Pressure Palsies 38 0.046
168
c PLM022 Pulmonary Valve Insufficiency 34 0.046
169
FTD001 Foot Drop 33 0.046
170
MST019 Mastoiditis 32 0.046
171
MDD008 Middle Ear Adenoma 20 0.046
172
TXN001 Toxin-Mediated Infectious Botulism 9 0.046
173
ERB002 Erb's Palsy 6 0.046
174
c SYS001 Systemic Lupus Erythematosus 86 0.041
175
c HPT001 Hepatitis C 68 0.041
176
P MSC005 Muscular Dystrophy 65 0.041
177
P TRN020 Turner Syndrome 65 0.041
178
P AMY004 Amyloidosis 65 0.041
179
P SPN046 Spinal Muscular Atrophy 65 0.041
180
P LPS004 Lupus Erythematosus 64 0.041
181
LPT001 Leptospirosis 62 0.041
182
c CNT035 Central Nervous System Disease 60 0.041
183
P HMN010 Hemangioma 59 0.041
184
GST045 Gastroenteritis 59 0.041
185
P ENC018 Encephalopathy 59 0.041
186
MTR014 Motor Neuron Disease 58 0.041
187
MLG056 Malignant Hyperthermia 58 0.041
188
P THR003 Thoracic Aortic Aneurysm 57 0.041
189
THR024 Thrombosis 57 0.041
190
PHR003 Pharyngitis 56 0.041
191
P FNC043 Fanconi Anemia, Complementation Group E 55 0.041
192
CPR001 Coproporphyria 53 0.041
193
P DBT005 Diabetes Insipidus 53 0.041
194
ASP003 Aseptic Meningitis 51 0.041
195
P TRN034 Transverse Myelitis 49 0.041
196
FSC004 Fasciitis 48 0.041
197
P SYR001 Syringomyelia 47 0.041
198
SPP008 Suppurative Otitis Media 45 0.041
199
c GRV008 Graves Disease 1 44 0.041
200
CRT008 Carotid Artery Dissection 41 0.041
201
DPH021 Diaphragm Disease 41 0.041
202
CNT025 Central Pontine Myelinolysis 41 0.041
203
MDS022 Mediastinitis 41 0.041
204
P LBY004 Labyrinthitis 40 0.041
205
TLR001 Tularemia 39 0.041
206
WST004 West Nile Encephalitis 39 0.041
207
ARC007 Arachnoid Cysts 39 0.041
208
P NRN017 Neuronopathy, Distal Hereditary Motor, Type Vi 35 0.041
209
SPN185 Spinal Cord Infarction 34 0.041
210
BRW004 Brown-Sequard Syndrome 29 0.041
211
FZL002 Fazio-Londe Disease 24 0.041
212
ITR001 Iatrogenic Botulism 13 0.041
213
FBR024 Fibrocartilaginous Embolism 12 0.041
214
INH013 Inhalational Botulism 12 0.041
215
c ADL069 Adult Intestinal Botulism 12 0.041
216
P HPT023 Hepatocellular Carcinoma 92 0.036
217
MLR004 Malaria 83 0.036
218
KRT004 Keratitis 71 0.036
219
P NRB001 Neuroblastoma 70 0.036
220
VSC007 Vascular Disease 67 0.036
221
P ATR011 Atrial Fibrillation 66 0.036
222
SRC014 Sarcoma 66 0.036
223
P CNJ013 Conjunctivitis 64 0.036
224
P ENC004 Encephalitis 63 0.036
225
PRT036 Peritonitis 63 0.036
226
ISC004 Ischemia 61 0.036
227
GTL001 Gitelman Syndrome 61 0.036
228
EYD002 Eye Disease 61 0.036
229
c ATM010 Autoimmune Hemolytic Anemia 61 0.036
230
P INT068 Intestinal Disease 60 0.036
231
P NRV006 Nervous System Cancer 60 0.036
232
STT001 Status Epilepticus 59 0.036
233
P MMP001 Mumps 58 0.036
234
P MYS005 Myositis 57 0.036
235
P INT070 Intestinal Obstruction 57 0.036
236
RBS001 Rabies 56 0.036
237
PRP019 Peripheral Nervous System Disease 55 0.036
238
P SCL018 Scoliosis 55 0.036
239
P PRG013 Paraganglioma 54 0.036
240
P MYC008 Myocarditis 54 0.036
241
MCN017 Meconium Ileus 54 0.036
242
PRG097 Paragangliomas 1, with or Without Deafness 54 0.036
243
OLV001 Olivopontocerebellar Atrophy 53 0.036
244
PLS006 Plasmodium Vivax Malaria 53 0.036
245
BRN071 Brain Injury 52 0.036
246
ATR060 Atrial Standstill, Digenic 51 0.036
247
P PNM006 Pneumoconiosis 51 0.036
248
NRL005 Neurilemmoma 51 0.036
249
THY025 Thymus Cancer 50 0.036
250
HPT074 Hepatic Adenoma, Somatic 50 0.036
251
VNB005 Van Buchem Disease 49 0.036
252
PRT029 Parathyroid Adenoma 48 0.036
253
ADR008 Adrenal Adenoma 47 0.036
254
ASP007 Aspiration Pneumonia 47 0.036
255
RLP003 Relapsing Fever 45 0.036
256
HMM003 Hemimegalencephaly 45 0.036
257
CRN024 Corneal Disease 44 0.036
258
c ACT159 Acute Transverse Myelitis 42 0.036
259
LCR004 La Crosse Encephalitis 42 0.036
260
SPC010 Speech and Communication Disorders 41 0.036
261
ADT003 Auditory System Disease 40 0.036
262
HYP068 Hyperostosis 40 0.036
263
NRC019 Neurocutaneous Melanosis, Somatic 39 0.036
264
P HYP265 Hypotonia 38 0.036
265
PRL008 Paralytic Ileus 37 0.036
266
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 36 0.036
267
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.036
268
MYX004 Myxedema 35 0.036
269
P PRX033 Proximal Renal Tubular Acidosis 35 0.036
270
TLS001 Tolosa-Hunt Syndrome 33 0.036
271
EPD005 Epidural Abscess 33 0.036
272
TBS001 Tabes Dorsalis 32 0.036
273
CLR007 Colorado Tick Fever 29 0.036
274
c NRC009 Narcolepsy 1 29 0.036
275
CVR002 Cavernous Sinus Thrombosis 28 0.036
276
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 28 0.036
277
PTR001 Petrositis 24 0.036
278
CNT067 Central Cord Syndrome 23 0.036
279
SKL006 Skull Base Neoplasm 21 0.036
280
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.036
281
PNT023 Pontine Hemorrhage 21 0.036
282
ABD009 Abducens Palsy 19 0.036
283
PRS053 Parsonage Turner Syndrome 19 0.036
284
BLB003 Bulbar Polio 16 0.036
285
P BRS047 Breast Cancer 100 0.029
286
HDG012 Hodgkin Lymphoma 77 0.029
287
NRL016 Neural Tube Defects 76 0.029
288
INS024 Insulin-Like Growth Factor I 75 0.029
289
ADR007 Adrenoleukodystrophy 72 0.029
290
c FNC027 Fanconi Anemia, Complementation Group a 71 0.029
291
KWS002 Kawasaki Disease 70 0.029
292
BRN028 Brain Cancer 70 0.029
293
SQM006 Squamous Cell Carcinoma 70 0.029
294
P ADN016 Adenocarcinoma 69 0.029
295
P LPR003 Leprosy 69 0.029
296
c HRD010 Hereditary Spastic Paraplegia 67 0.029
297
ART005 Arteriovenous Malformation 66 0.029
298
P KDN017 Kidney Cancer 65 0.029
299
CNR002 Cone-Rod Dystrophy 64 0.029
300
P ART023 Arthropathy 64 0.029
301
P CRB042 Cerebellar Ataxia 63 0.029
302
P BRD002 Bardet-Biedl Syndrome 63 0.029
303
WGN006 Wegener Granulomatosis 63 0.029
304
P HML002 Hemolytic Anemia 62 0.029
305
GST092 Gastroesophageal Reflux 62 0.029
306
P GCH001 Gaucher's Disease 62 0.029
307
P LYM026 Lymphoblastic Leukemia 62 0.029
308
c LNG044 Long Qt Syndrome 1 62 0.029
309
CNG368 Congenital Adrenal Hyperplasia 62 0.029
310
P TXP001 Toxoplasmosis 61 0.029
311
P ESP024 Esophagitis 61 0.029
312
P HYP117 Hypertriglyceridemia 61 0.029
313
MCK007 Muckle-Wells Syndrome 61 0.029
314
MSL001 Measles 61 0.029
315
P MYM002 Moyamoya Disease 61 0.029
316
P NRM001 Neuromyelitis Optica 60 0.029
317
PLM033 Pulmonary Embolism 60 0.029
318
BHC003 Behcet Syndrome 60 0.029
319
WLL001 Williams-Beuren Syndrome 60 0.029
320
CHL123 Chlamydia 60 0.029
321
P OCL013 Oculodentodigital Dysplasia 59 0.029
322
P PRP029 Porphyria 59 0.029
323
WLL006 Wells Syndrome 59 0.029
324
P CMR001 Camurati-Engelmann Disease 58 0.029
325
YLL002 Yellow Fever 58 0.029
326
P WLD002 Waldenstrom Macroglobulinemia 58 0.029
327
KND001 Kindler Syndrome 57 0.029
328
RHB003 Rhabdomyosarcoma 57 0.029
329
TRG002 Trigeminal Neuralgia 57 0.029
330
c CWD006 Cowden Syndrome 1 57 0.029
331
P EPS003 Episodic Ataxia 57 0.029
332
ETH011 Ethylmalonic Encephalopathy 56 0.029
333
P SZR006 Seizure Disorder 56 0.029
334
P SML001 Small Cell Carcinoma 56 0.029
335
GST050 Gastrointestinal System Disease 56 0.029
336
CCC001 Coccidioidomycosis 55 0.029
337
GLC003 Glucose Intolerance 55 0.029
338
JPN002 Japanese Encephalitis 55 0.029
339
P TMT001 Timothy Syndrome 55 0.029
340
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 0.029
341
END030 End Stage Renal Failure 55 0.029
342
HMF006 Hemifacial Microsomia 55 0.029
343
P CNG001 Congenital Myasthenic Syndrome 55 0.029
344
HDC001 Headache 54 0.029
345
c PND001 Pain Disorder 54 0.029
346
APH002 Aphasia 54 0.029
347
CHN016 Cohen Syndrome 54 0.029
348
GST037 Gastroparesis 54 0.029
349
PLM010 Pulmonary Edema 54 0.029
350
NWC001 Newcastle Disease 54 0.029
351
CHK001 Chikungunya 54 0.029
352
CYS005 Cysticercosis 54 0.029
353
TWN003 Townes-Brocks Syndrome 53 0.029
354
SPT005 Spotted Fever 53 0.029
355
P SYP003 Syphilis 53 0.029
356
CYS010 Cystinosis 53 0.029
357
BRN004 Brain Edema 52 0.029
358
P SCH018 Schizencephaly 52 0.029
359
c LPD037 Lipodystrophy, Familial Partial, 2 52 0.029
360
P ICH004 Ichthyosis 52 0.029
361
OPT006 Optic Nerve Disease 52 0.029
362
MYC002 Mycobacterium Avium Complex Disease 52 0.029
363
PRC013 Pericarditis 51 0.029
364
ANK001 Ankylosis 51 0.029
365
P GRS003 Griscelli Syndrome 51 0.029
366
P PLY017 Polyarteritis Nodosa 51 0.029
367
c VRL012 Viral Meningitis 50 0.029
368
RLP001 Relapsing Polychondritis 50 0.029
369
TCK001 Tick-Borne Encephalitis 50 0.029
370
NNT012 Neonatal Jaundice 50 0.029
371
RHB001 Rhabdoid Cancer 50 0.029
372
THR013 Thoracic Outlet Syndrome 50 0.029
373
OPT009 Optic Neuritis 50 0.029
374
OST011 Osteomalacia 49 0.029
375
WHP001 Whipple Disease 49 0.029
376
c INH020 Inherited Metabolic Disorder 49 0.029
377
LMB062 Limb Ischemia 48 0.029
378
MYL003 Myeloid Sarcoma 48 0.029
379
ATN002 Autonomic Nervous System Disease 48 0.029
380
NPH003 Nephrocalcinosis 48 0.029
381
THY030 Thyroid Gland Disease 48 0.029
382
c CNG021 Congenital Toxoplasmosis 48 0.029
383
SPN020 Spondylosis 48 0.029
384
P CTN003 Cutaneous Lupus Erythematosus 48 0.029
385
P OST028 Osteochondroma 47 0.029
386
P HMR005 Hemorrhoid 47 0.029
387
P OTT001 Otitis Externa 47 0.029
388
P MYT023 Myotonia Congenita 47 0.029
389
INT253 Intestinal Benign Neoplasm 47 0.029
390
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 47 0.029
391
c MLG069 Malignant Hypertension 47 0.029
392
P NML001 Nemaline Myopathy 47 0.029
393
THY009 Thyroid Lymphoma 47 0.029
394
UPP004 Upper Respiratory Tract Disease 46 0.029
395
INF006 Infant Botulism 46 0.029
396
SPH001 Sapho Syndrome 46 0.029
397
P KLP003 Klippel-Feil Syndrome 46 0.029
398
STL001 St. Louis Encephalitis 46 0.029
399
NCR007 Necrotizing Fasciitis 46 0.029
400
BBS001 Babesiosis 46 0.029
401
PTT004 Pituitary Apoplexy 46 0.029
402
HML015 Hemolytic Anemia Due to Triosephosphate Isomerase Deficiency 46 0.029
403
ATN004 Autonomic Neuropathy 45 0.029
404
P ABD003 Abdominal Aortic Aneurysm 45 0.029
405
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.029
406
RNL011 Renal Osteodystrophy 45 0.029
407
VST004 Vestibular Disease 44 0.029
408
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.029
409
DND001 Dandy-Walker Syndrome 44 0.029
410
P PNB001 Pineoblastoma 44 0.029
411
PRN011 Pernicious Anemia 44 0.029
412
P DMY001 Demyelinating Polyneuropathy 43 0.029
413
c HRD104 Hereditary Multiple Osteochondromas 43 0.029
414
PLM029 Palmoplantar Keratosis 43 0.029
415
P RSM001 Rasmussen Encephalitis 43 0.029
416
TRC023 Trichinosis 42 0.029
417
THY049 Thyroid Cancer, Anaplastic 42 0.029
418
ANT018 Anthracosis 42 0.029
419
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.029
420
SPR007 Superior Mesenteric Artery Syndrome 41 0.029
421
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.029
422
CHR222 Chromosome 1p36 Deletion Syndrome 41 0.029
423
BRN080 Brain Ischemia 41 0.029
424
CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 41 0.029
425
c SCN006 Secondary Syphilis 41 0.029
426
c OST131 Osteopetrosis, Autosomal Dominant 2 41 0.029
427
MLT008 Multinodular Goiter 41 0.029
428
NSP002 Nasopharyngitis 40 0.029
429
MLT145 Multiple Enchondromatosis, Maffucci Type 40 0.029
430
ENT001 Enterocele 40 0.029
431
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.029
432
PSD029 Pseudocholinesterase Deficiency 40 0.029
433
RCT017 Rectal Disease 40 0.029
434
CRT009 Critical Illness Polyneuropathy 40 0.029
435
SPN040 Spinal Cancer 39 0.029
436
TNG004 Tongue Disease 39 0.029
437
RCK002 Rocky Mountain Spotted Fever 39 0.029
438
ESN020 Eosinophilic Granulomatosis with Polyangiitis 39 0.029
439
EYL005 Eyelid Disease 39 0.029
440
P PRS062 Persistent Hyperplastic Primary Vitreous 38 0.029
441
c PSD092 Pseudohypoaldosteronism, Type Iie 38 0.029
442
STR002 Streptococcal Meningitis 38 0.029
443
MYH012 Myhre Syndrome 38 0.029
444
EHR002 Ehrlichiosis 38 0.029
445
ADJ001 Adjustment Disorder 38 0.029
446
P CHR342 Chiari Malformation 38 0.029
447
P AXN001 Axonal Neuropathy 38 0.029
448
LCR008 Lacrimal Apparatus Disease 37 0.029
449
PRP056 Porphyria, Acute Hepatic 37 0.029
450
INT042 Internuclear Ophthalmoplegia 37 0.029
451
EXT056 External Ear Disease 36 0.029
452
PST055 Postural Hypotension 36 0.029
453
EXC003 Excessive Tearing 36 0.029
454
MTL002 Metal Metabolism Disorder 35 0.029
455
VNT001 Ventilation Pneumonitis 35 0.029
456
c ATS282 Autosomal Recessive Malignant Osteopetrosis 35 0.029
457
HYD001 Hydranencephaly 35 0.029
458
ECT004 Ecthyma 35 0.029
459
c BRN108 Branchiootic Syndrome 1 34 0.029
460
XRP001 Xerophthalmia 33 0.029
461
c MLT009 Multiple Cranial Nerve Palsy 33 0.029
462
CRB029 Cerebellopontine Angle Tumor 33 0.029
463
GLB003 Globe Disease 32 0.029
464
THY043 Thymic Hyperplasia 32 0.029
465
OST006 Osteoblastoma 31 0.029
466
FST001 Foster-Kennedy Syndrome 31 0.029
467
HYP193 Hypocomplementemic Urticarial Vasculitis 31 0.029
468
P ATX010 Ataxia Neuropathy Spectrum 30 0.029
469
PRS037 Periostitis 30 0.029
470
CBB002 Cobb Syndrome 30 0.029
471
HNS001 Hansen's Disease 30 0.029
472
PLY119 Polymicrogyria, Bilateral Perisylvian 30 0.029
473
ENT005 Entropion 30 0.029
474
FCL003 Facial Hemiatrophy 30 0.029
475
SPS016 Spasmodic Dysphonia 29 0.029
476
c JVN024 Juvenile Hereditary Hemochromatosis 29 0.029
477
TCK004 Tick Infestation 28 0.029
478
CRN033 Cranial Nerve Malignant Neoplasm 28 0.029
479
LPD027 Lip Disease 28 0.029
480
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 26 0.029
481
c SPS092 Spastic Paraplegia 11 25 0.029
482
HSH002 Hashimoto's Encephalitis 25 0.029
483
HNM002 Hinman Syndrome 25 0.029
484
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 24 0.029
485
MNN005 Meningovascular Neurosyphilis 24 0.029
486
RBF003 Riboflavin Transporter Deficiency 22 0.029
487
PRS120 Persistent Idiopathic Facial Pain 21 0.029
488
P INT006 Intestinal Botulism 19 0.029
489
ACT181 Acute Motor Axonal Neuropathy 19 0.029
490
c FML249 Familial Amyloidosis, Finnish Type 19 0.029
491
c LTH032 Lethal Congenital Contracture Syndrome 7 17 0.029
492
PRL006 Paralytic Lagophthalmos 16 0.029
493
c LTH030 Lethal Congenital Contracture Syndrome 8 16 0.029
494
PWS001 Powassan Encephalitis 15 0.029
495
GLM046 Glomus Vagale Tumor 15 0.029
496
FML325 Familial Cervical Artery Dissection 14 0.029
497
SYR004 Syringobulbia 13 0.029
498
SPN015 Spinal Polio 13 0.029
499
UVP001 Uveoparotid Fever 10 0.029
500
MBS006 Moebius Syndrome-Axonal Neuropathy-Hypogonadotropic Hypogonadism Syndrome 10 0.029
501
MYP026 Myopathy - Thyrotoxic 7 0.029
502
BLB001 Bulbospinal Polio 6 0.029
503
HMP020 Hemiplegia Alterans 1 0.029
504
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.029
505
P CLR023 Colorectal Cancer 97 0.021
506
P MLT019 Multiple Myeloma 83 0.021
507
P AST005 Asthma 82 0.021
508
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.021
509
GST053 Gastric Cancer 78 0.021
510
c DLT002 Dilated Cardiomyopathy 76 0.021
511
ULC004 Ulcerative Colitis 76 0.021
512
P ART022 Arthritis 75 0.021
513
P CRN211 Coronary Artery Disease 74 0.021
514
MNT001 Mantle Cell Lymphoma 72 0.021
515
P INF038 Influenza 72 0.021
516
P PHC003 Pheochromocytoma 71 0.021
517
TTR001 Tetralogy of Fallot 71 0.021
518
P TYS001 Tay-Sachs Disease 71 0.021
519
PTZ001 Peutz-Jeghers Syndrome 71 0.021
520
P MTC003 Metachromatic Leukodystrophy 70 0.021
521
THY028 Thyroid Cancer 69 0.021
522
P ALP004 Alport Syndrome 69 0.021
523
PRP027 Peripheral Vascular Disease 69 0.021
524
P CRD011 Cardiomyopathy 68 0.021
525
ISC006 Ischemic Heart Disease 68 0.021
526
P MYL005 Myelofibrosis 67 0.021
527
CHG001 Chagas Disease 67 0.021
528
MLD001 Melioidosis 67 0.021
529
P END044 Endometriosis 66 0.021
530
P KDN018 Kidney Disease 66 0.021
531
SKN016 Skin Disease 66 0.021
532
INC002 Inclusion Body Myositis 66 0.021
533
BRC012 Brucellosis 66 0.021
534
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.021
535
P NMN002 Niemann-Pick Disease 65 0.021
536
CNT098 Central Core Disease 65 0.021
537
c HPT016 Hepatitis B 65 0.021
538
P LNG028 Long Qt Syndrome 64 0.021
539
CHD001 Chediak-Higashi Syndrome 64 0.021
540
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.021
541
CHR066 Chronic Fatigue Syndrome 64 0.021
542
P OST002 Osteoporosis 64 0.021
543
P INF037 Inflammatory Bowel Disease 63 0.021
544
P PRD008 Periodontitis 63 0.021
545
P ALX003 Alexander Disease 63 0.021
546
P MCH002 Machado-Joseph Disease 63 0.021
547
P OST001 Osteopetrosis 63 0.021
548
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.021
549
MLN008 Melanoma 62 0.021
550
P ADD001 Addison's Disease 62 0.021
551
P BPL003 Bipolar Disorder 62 0.021
552
APH001 Aphthous Stomatitis 62 0.021
553
c NRF019 Neurofibromatosis, Type 2 62 0.021
554
HSH003 Hashimoto Thyroiditis 62 0.021
555
c MCP003 Mucopolysaccharidosis Vii 62 0.021
556
FCT003 Factor X Deficiency 61 0.021
557
GNG013 Gingivitis 61 0.021
558
CNT047 Contact Dermatitis 61 0.021
559
P SLP006 Sleep Apnea 61 0.021
560
OST017 Osteomyelitis 61 0.021
561
P SDD001 Sudden Infant Death Syndrome 61 0.021
562
P IDP010 Idiopathic Generalized Epilepsy 61 0.021
563
CRB011 Cerebrotendinous Xanthomatosis 61 0.021
564
P ADL010 Adult Respiratory Distress Syndrome 61 0.021
565
TYP007 Typhoid Fever 61 0.021
566
P SYS005 Systemic Scleroderma 61 0.021
567
CHR072 Chordoma 61 0.021
568
ADR016 Adrenal Cortical Carcinoma 61 0.021
569
c ACT075 Acute Myocardial Infarction 60 0.021
570
INT146 Intervertebral Disc Disease 60 0.021
571
P TMP003 Temporal Arteritis 60 0.021
572
ACQ007 Acquired Immunodeficiency Syndrome 60 0.021
573
c CNG006 Congenital Hypothyroidism 60 0.021
574
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.021
575
CLT003 Colitis 60 0.021
576
TXC005 Toxic Shock Syndrome 60 0.021
577
APP008 Appendicitis 60 0.021
578
P GLM045 Glioma 60 0.021
579
P GST049 Gastrointestinal System Cancer 60 0.021
580
PRD007 Periodontal Disease 60 0.021
581
c ACT073 Acute Leukemia 60 0.021
582
P DRR001 Diarrhea 60 0.021
583
RBR001 Roberts Syndrome 60 0.021
584
P BRG001 Brugada Syndrome 59 0.021
585
KRT001 Keratoconjunctivitis Sicca 59 0.021
586
ALC006 Alcoholic Hepatitis 59 0.021
587
OCL009 Ocular Cancer 59 0.021
588
HJD001 Hajdu-Cheney Syndrome 59 0.021
589
c GLY008 Glycogen Storage Disease Ii 59 0.021
590
DPH001 Diphtheria 59 0.021
591
INT066 Interstitial Lung Disease 59 0.021
592
P GLM007 Glomerulonephritis 59 0.021
593
ADL030 Adult-Onset Still's Disease 59 0.021
594
c FML001 Familial Atrial Fibrillation 58 0.021
595
P CTR002 Cataract 58 0.021
596
P MCR010 Microcephaly 58 0.021
597
RHM027 Rheumatic Disease 58 0.021
598
PPT005 Peptic Ulcer Disease 58 0.021
599
P MTR012 Mitral Valve Disease 58 0.021
600
LYM021 Lymphadenitis 58 0.021
601
BRN012 Bronchiolitis Obliterans 58 0.021
602
P MSC007 Muscle Hypertrophy 58 0.021
603
P THY102 Thyroid Cancer, Nonmedullary, 2 58 0.021
604
BNC003 Bone Cancer 58 0.021
605
SYN007 Synovitis 58 0.021
606
c LNG047 Long Qt Syndrome 2 57 0.021
607
P LRY044 Larynx Cancer 57 0.021
608
MSM014 Mismatch Repair Cancer Syndrome 57 0.021
609
ABL002 Ablepharon-Macrostomia Syndrome 57 0.021
610
ART017 Aortic Disease 57 0.021
611
P EXN002 Exanthem 57 0.021
612
CNS004 Constipation 57 0.021
613
P THY023 Thymoma 57 0.021
614
c ACT210 Acute Respiratory Distress Syndrome 57 0.021
615
ALL010 Allergic Contact Dermatitis 57 0.021
616
P INT143 Interstitial Cystitis 57 0.021
617
TNS005 Tonsillitis 57 0.021
618
P FBR017 Fibrosarcoma 56 0.021
619
HYP266 Hypoxia 56 0.021
620
INT002 Intermittent Claudication 56 0.021
621
TRN015 Transient Cerebral Ischemia 56 0.021
622
P OLG002 Oligodendroglioma 56 0.021
623
WLF001 Wolff-Parkinson-White Syndrome 56 0.021
624
P GST044 Gastritis 56 0.021
625
NRN004 Neuroendocrine Tumor 56 0.021
626
DSM004 Desmoid Tumor 56 0.021
627
GST023 Gastric Ulcer 56 0.021
628
P SPN301 Spinocerebellar Ataxia 2 56 0.021
629
STF001 Stiff-Person Syndrome 56 0.021
630
PRS047 Prostatitis 56 0.021
631
JNT002 Joint Disorders 55 0.021
632
P PND002 Pendred Syndrome 55 0.021
633
PTN001 Patent Foramen Ovale 55 0.021
634
THR004 Thrombocytosis 55 0.021
635
P CDS001 Cadasil 55 0.021
636
c TYR012 Tyrosinemia, Type I 55 0.021
637
P WRD001 Waardenburg's Syndrome 55 0.021
638
SCR008 Scrub Typhus 55 0.021
639
P MNC007 Monocytic Leukemia 55 0.021
640
EXT034 Extrinsic Allergic Alveolitis 55 0.021
641
P TRM003 Tremor 54 0.021
642
P HYP083 Hypopituitarism 54 0.021
643
RCT018 Rectal Neoplasm 54 0.021
644
c BCT007 Bacterial Meningitis 54 0.021
645
c VRL007 Viral Encephalitis 54 0.021
646
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 54 0.021
647
LYM022 Lymphangioma 54 0.021
648
CMP010 Complex Regional Pain Syndrome 54 0.021
649
P INT030 Intracranial Aneurysm 54 0.021
650
P BRN009 Burning Mouth Syndrome 54 0.021
651
SML033 Small Cell Cancer of the Lung, Somatic 54 0.021
652
P VNS003 Venous Insufficiency 54 0.021
653
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.021
654
KDS001 Kid Syndrome 53 0.021
655
SLC006 Silicosis 53 0.021
656
GNT003 Genital Herpes 53 0.021
657
SLP005 Sleep Disorder 53 0.021
658
P LTR001 Lateral Sclerosis 53 0.021
659
P HYP024 Hypoparathyroidism 53 0.021
660
P EXP004 Exophthalmos 53 0.021
661
PNM008 Pneumothorax 53 0.021
662
STF002 Stiff Skin Syndrome 53 0.021
663
PTT048 Pituitary Adenoma, Prolactin-Secreting 53 0.021
664
DSS008 Disease of Mental Health 52 0.021
665
LYS002 Lysosomal Storage Disease 52 0.021
666
KRT006 Keratoconjunctivitis 52 0.021
667
TRM010 Traumatic Brain Injury 52 0.021
668
PRT058 Pure Autonomic Failure 52 0.021
669
CYT008 Cytomegalovirus Infection 52 0.021
670
P PYL005 Pyelonephritis 52 0.021
671
MRK001 Merkel Cell Carcinoma 52 0.021
672
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 52 0.021
673
PMS001 Poems Syndrome 52 0.021
674
BCT002 Bacterial Vaginosis 52 0.021
675
ALL026 Allergic Hypersensitivity Disease 52 0.021
676
P APL006 Aplasia Cutis Congenita 52 0.021
677
MGL013 Megalencephaly 52 0.021
678
CRH005 Crohn's Colitis 52 0.021
679
MCN007 Meconium Aspiration Syndrome 52 0.021
680
ATY005 Atypical Teratoid Rhabdoid Tumor 52 0.021
681
CRC006 Carcinoid Syndrome 52 0.021
682
BLR001 Biliary Atresia 52 0.021
683
BRT002 Birt-Hogg-Dube Syndrome 52 0.021
684
CYS039 Cystic Kidney Disease 52 0.021
685
BLD044 Bladder Disease 51 0.021
686
TXC002 Toxic Encephalopathy 51 0.021
687
P STR020 Strabismus 51 0.021
688
CHC001 Chickenpox 51 0.021
689
SLV012 Salivary Gland Adenoid Cystic Carcinoma 51 0.021
690
c CHR417 Chronic Graft Versus Host Disease 51 0.021
691
c LRG001 Large Cell Carcinoma 51 0.021
692
c LNG050 Long Qt Syndrome 5 51 0.021
693
P PRC031 Preeclampsia/eclampsia 1 51 0.021
694
c FML023 Familial Hemiplegic Migraine 51 0.021
695
APR001 Apraxia 51 0.021
696
MST005 Mastitis 51 0.021
697
TRY001 Trypanosomiasis 51 0.021
698
CLN019 Colonic Disease 51 0.021
699
CCC002 Coccidiosis 51 0.021
700
PRC012 Pericardial Effusion 51 0.021
701
PLG002 Plague 51 0.021
702
SCH002 Schnitzler Syndrome 51 0.021
703
STM006 Stomach Disease 50 0.021
704
c ART115 Aortic Valve Disease 1 50 0.021
705
P HYP014 Hyperuricemia 50 0.021
706
GRW007 Growth Hormone Deficiency 50 0.021
707
P LFT003 Left Ventricular Noncompaction 50 0.021
708
c CRB103 Cerebral Cavernous Malformations-1 50 0.021
709
P DDN001 Duodenal Ulcer 50 0.021
710
CLF001 Cleft Lip 50 0.021
711
ESP020 Esophageal Atresia 50 0.021
712
PMP001 Pemphigus 50 0.021
713
P CHR345 Chronic Pain 50 0.021
714
c ACT068 Acute Cystitis 50 0.021
715
P AGG001 Aggressive Periodontitis 50 0.021
716
c KNN009 Kenny-Caffey Syndrome, Type 1 50 0.021
717
PRP032 Porphyria Variegata 50 0.021
718
DRY001 Dry Eye Syndrome 50 0.021
719
P PNV001 Panuveitis 50 0.021
720
PNM001 Pneumocystosis 50 0.021
721
GNG004 Ganglioglioma 50 0.021
722
P SCK002 Sick Sinus Syndrome 50 0.021
723
HYP006 Hypertensive Heart Disease 50 0.021
724
STR081 Stormorken Syndrome 49 0.021
725
END035 Endocrine Gland Cancer 49 0.021
726
c LNG051 Long Qt Syndrome 6 49 0.021
727
P GNT008 Giant Cell Tumor 49 0.021
728
MSC072 Muscle Cancer 49 0.021
729
ATR057 Atrioventricular Block 49 0.021
730
c DYS166 Dysautonomia, Familial 49 0.021
731
PRD019 Periodic Fever, Familial 49 0.021
732
c ACT071 Acute Kidney Failure 49 0.021
733
ACT049 Acute Disseminated Encephalomyelitis 49 0.021
734
c INF067 Inflammatory Bowel Disease 10 49 0.021
735
URB001 Urbach-Wiethe Disease 49 0.021
736
PLM032 Pulmonary Blastoma 49 0.021
737
INN002 Inner Ear Disease 49 0.021
738
P INT063 Intellectual Disability 49 0.021
739
CHR001 Churg-Strauss Syndrome 49 0.021
740
c LNG092 Long Qt Syndrome-3 49 0.021
741
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 0.021
742
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.021
743
MCP006 Mucoepidermoid Carcinoma 48 0.021
744
OBS001 Obstructive Jaundice 48 0.021
745
BRL010 Buruli Ulcer 48 0.021
746
NSD001 Nose Disease 48 0.021
747
c ATS308 Autosomal Dominant Cerebellar Ataxia 48 0.021
748
MTB004 Metabolic Acidosis 48 0.021
749
MTC056 Mitochondrial Dna Depletion Syndrome 4a 48 0.021
750
P ENC008 Encephalocele 48 0.021
751
CCN002 Cocaine Abuse 48 0.021
752
CHR005 Chorioamnionitis 48 0.021
753
P PRN026 Porencephaly 48 0.021
754
FML039 Female Reproductive System Disease 48 0.021
755
GYN001 Gynecomastia 48 0.021
756
ERY021 Erythrokeratodermia Variabilis Et Progressiva 47 0.021
757
PTT009 Pituitary Gland Disease 47 0.021
758
GST009 Gastroschisis 47 0.021
759
SDD007 Sudden Cardiac Death 47 0.021
760
SYN036 Syncope 47 0.021
761
DSM007 Desmoplastic Small Round Cell Tumor 47 0.021
762
ELS001 Eales Disease 47 0.021
763
GNG002 Ganglioneuroma 47 0.021
764
SLV003 Salivary Gland Disease 47 0.021
765
PLP001 Pulpitis 47 0.021
766
MCC002 Mucocutaneous Leishmaniasis 47 0.021
767
c INT072 Intestinal Pseudo-Obstruction 46 0.021
768
GNG011 Gingival Disease 46 0.021
769
PRP021 Peripheral Nervous System Neoplasm 46 0.021
770
NDL007 Nodular Goiter 46 0.021
771
HYD005 Hydrocele 46 0.021
772
MLT006 Multidrug-Resistant Tuberculosis 46 0.021
773
c PRK027 Parkinson Disease 15, Autosomal Recessive 46 0.021
774
MMB001 Membranoproliferative Glomerulonephritis 46 0.021
775
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.021
776
CNT046 Central Nervous System Vasculitis 46 0.021
777
CTS002 Cat-Scratch Disease 46 0.021
778
P HRD021 Hereditary Sensory Neuropathy 46 0.021
779
CD4003 Cd40 Ligand Deficiency 46 0.021
780
CVR006 Cavernous Hemangioma 46 0.021
781
PRT082 Preterm Premature Rupture of the Membranes 46 0.021
782
CYS008 Cystic Echinococcosis 46 0.021
783
P CRN012 Craniometaphyseal Dysplasia 46 0.021
784
STS002 Situs Inversus 46 0.021
785
AMB002 Amblyopia 46 0.021
786
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 46 0.021
787
ANR004 Anuria 45 0.021
788
ACR041 Acromelic Frontonasal Dysostosis 45 0.021
789
BRN014 Bronchopneumonia 45 0.021
790
ECT078 Ectodermal Dysplasia 2, Clouston Type 45 0.021
791
P PRM175 Primary Familial Brain Calcification 45 0.021
792
CRT017 Cartilage Disease 45 0.021
793
BCT004 Bacteriuria 45 0.021
794
c CLR085 Colorectal Cancer 1 45 0.021
795
PTT037 Pituitary Tumors 45 0.021
796
VSC047 Vascular Malformation 45 0.021
797
DVR002 Diverticulitis 45 0.021
798
P END047 Endophthalmitis 45 0.021
799
c ACT042 Acute Pyelonephritis 45 0.021
800
PTT008 Pituitary Carcinoma 45 0.021
801
c LNG056 Long Qt Syndrome 12 45 0.021
802
CCN007 Cocoon Syndrome 45 0.021
803
c RTN160 Retinitis Pigmentosa 60 45 0.021
804
CWP001 Cowpox 45 0.021
805
P ATR005 Atrophic Gastritis 45 0.021
806
FBR009 Fibrous Dysplasia 45 0.021
807
ALN001 Aland Island Eye Disease 45 0.021
808
TRC040 Tracheoesophageal Fistula 45 0.021
809
P AML002 Amelogenesis Imperfecta 45 0.021
810
c HRT021 Heart Block, Progressive, Type Ia 44 0.021
811
c SHR030 Short Qt Syndrome 44 0.021
812
GDS001 Good Syndrome 44 0.021
813
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.021
814
CHR008 Choroiditis 44 0.021
815
CNJ012 Conjunctival Disease 44 0.021
816
TRY002 Troyer Syndrome 44 0.021
817
RGH001 Right Bundle Branch Block 44 0.021
818
CRD001 Cardiac Tamponade 44 0.021
819
SPS007 Spastic Cerebral Palsy 44 0.021
820
c LNG057 Long Qt Syndrome 13 44 0.021
821
c LNG053 Long Qt Syndrome 9 44 0.021
822
OLF005 Olfactory Neuroblastoma 44 0.021
823
P DYS021 Dysautonomia 44 0.021
824
c CHR431 Chronic Venous Insufficiency 44 0.021
825
SYS003 Systolic Heart Failure 43 0.021
826
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.021
827
DNG001 Dengue Shock Syndrome 43 0.021
828
PHY002 Physical Disorder 43 0.021
829
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 43 0.021
830
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 43 0.021
831
BSL009 Basal Ganglia Calcification 43 0.021
832
BRT030 Birth Defects 43 0.021
833
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.021
834
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.021
835
SNS023 Sensory System Cancer 43 0.021
836
c PRG126 Progressive Familial Heart Block 43 0.021
837
P PLM040 Pulmonary Valve Disease 43 0.021
838
P CRB088 Cerebral Atrophy 43 0.021
839
c ART120 Arthrogryposis, Distal, Type 3 42 0.021
840
c NNS007 Nonsyndromic Deafness 42 0.021
841
P FNG005 Feingold Syndrome 42 0.021
842
c FML191 Familial Long Qt Syndrome 42 0.021
843
PLS016 Plasma Cell Leukemia 42 0.021
844
PRN019 Perinatal Necrotizing Enterocolitis 42 0.021
845
BMF001 Bamforth-Lazarus Syndrome 42 0.021
846
DDN006 Duodenitis 42 0.021
847
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.021
848
HRT008 Heart Conduction Disease 42 0.021
849
PLM020 Pleomorphic Xanthoastrocytoma 42 0.021
850
RHM014 Rheumatoid Vasculitis 42 0.021
851
PLM039 Pulmonary Neuroendocrine Tumor 42 0.021
852
SBP004 Subependymoma 42 0.021
853
FLL031 Follicular Adenoma 42 0.021
854
c SML034 Small Cell Neuroendocrine Carcinoma 42 0.021
855
DBT002 Diabetic Autonomic Neuropathy 42 0.021
856
EXS001 Exostosis 42 0.021
857
BNS003 Binswanger's Disease 42 0.021
858
PRD011 Proud Syndrome 42 0.021
859
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 42 0.021
860
P CRN026 Corneal Edema 42 0.021
861
ACT200 Acute Monoblastic Leukemia 42 0.021
862
c LNG031 Lung Benign Neoplasm 41 0.021
863
VNT011 Ventricular Fibrillation, Familial, 1 41 0.021
864
MDL009 Medullary Sponge Kidney 41 0.021
865
FCT008 Factitious Disorder 41 0.021
866
VHW001 Vohwinkel Syndrome 41 0.021
867
EST005 Esotropia 41 0.021
868
PRM025 Primary Bacterial Infectious Disease 41 0.021
869
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.021
870
VGN020 Vaginal Disease 41 0.021
871
BRB001 Beriberi 41 0.021
872
NRS003 Neurosyphilis 41 0.021
873
PRM013 Premature Menopause 41 0.021
874
SCL017 Sclerosing Hemangioma 41 0.021
875
P LRG014 Large Cell Neuroendocrine Carcinoma 41 0.021
876
OPP002 Opportunistic Mycosis 41 0.021
877
BSL006 Basaloid Squamous Cell Carcinoma 41 0.021
878
CNT019 Central Neurocytoma 41 0.021
879
ESN004 Eosinophilic Gastritis 41 0.021
880
CDQ001 Cauda Equina Syndrome 41 0.021
881
c AMY090 Amyotrophic Lateral Sclerosis 8 41 0.021
882
FNC007 Functioning Pituitary Adenoma 41 0.021
883
SPS019 Spastic Paraparesis 41 0.021
884
P CPL003 Capillary Leak Syndrome 41 0.021
885
NNF007 Non-Functioning Pituitary Adenoma 41 0.021
886
RMS001 Rem Sleep Behavior Disorder 41 0.021
887
c AMY067 Amyotrophic Lateral Sclerosis 18 41 0.021
888
MLT075 Multifocal Motor Neuropathy 41 0.021
889
TNS007 Taeniasis 41 0.021
890
KDN015 Kidney Angiomyolipoma 41 0.021
891
c AMY085 Amyotrophic Lateral Sclerosis 9 41 0.021
892
c PRG106 Progressive Muscular Dystrophy 40 0.021
893
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.021
894
URT026 Ureter Cancer 40 0.021
895
c PRK045 Parkinson Disease 5 40 0.021
896
c MCL046 Mucolipidosis Iii Alpha/beta 40 0.021
897
c CRB094 Cerebral Cavernous Malformations 3 40 0.021
898
CRC014 Carcinoid Tumors, Intestinal 40 0.021
899
OST022 Osteopathia Striata with Cranial Sclerosis 40 0.021
900
HRT012 Heart Valve Disease 40 0.021
901
HTS001 Hiatus Hernia 40 0.021
902
c DFN097 Deafness, Autosomal Recessive 1a 40 0.021
903
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.021
904
STR077 Streptococcal Toxic-Shock Syndrome 40 0.021
905
SCT002 Scotoma 40 0.021
906
CYS009 Cystadenoma 40 0.021
907
MNN017 Mononeuropathy 40 0.021
908
BRT001 Bart-Pumphrey Syndrome 40 0.021
909
c HRD088 Hereditary Neuropathies 40 0.021
910
P SPS133 Spastic Paraplegia 2, X-Linked 40 0.021
911
LSB001 Louse-Borne Relapsing Fever 40 0.021
912
ANG002 Angiostrongyliasis 39 0.021
913
BRS064 Bursitis 39 0.021
914
CRB086 Cerebral Aneurysms 39 0.021
915
HYP264 Hypertonia 39 0.021
916
PNC056 Pineocytoma 39 0.021
917
BTN002 Boutonneuse Fever 39 0.021
918
SKL003 Skeletal Muscle Cancer 39 0.021
919
SPN029 Spondylolysis 39 0.021
920
c PRM225 Primary Thrombocytopenia 39 0.021
921
CHR466 Chronic Thromboembolic Pulmonary Hypertension 39 0.021
922
PLM018 Pulmonary Sclerosing Hemangioma 39 0.021
923
MRR003 Murray Valley Encephalitis 39 0.021
924
URM005 Uremic Pruritus 39 0.021
925
DNT008 Denture Stomatitis 39 0.021
926
MDN005 Mednik Syndrome 39 0.021
927
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 38 0.021
928
ABD010 Abdominal Wall Defect 38 0.021
929
GNT006 Giant Papillary Conjunctivitis 38 0.021
930
RHM009 Rheumatoid Lung Disease 38 0.021
931
SCR015 Scarlet Fever 38 0.021
932
P NRX001 Neuroaxonal Dystrophy 38 0.021
933
HYP034 Hypertensive Encephalopathy 38 0.021
934
PST020 Postpoliomyelitis Syndrome 38 0.021
935
NCR001 Necrotizing Ulcerative Gingivitis 38 0.021
936
MLY001 Molybdenum Cofactor Deficiency 38 0.021
937
IMM015 Immune Defect Due to Absence of Thymus 38 0.021
938
MYP002 Myoepithelial Carcinoma 38 0.021
939
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.021
940
GRN022 Granulosa Cell Tumor of the Ovary 38 0.021
941
c AMY083 Amyotrophic Lateral Sclerosis 11 37 0.021
942
MYS001 Myositis Ossificans 37 0.021
943
CVR010 Cavernous Malformation 37 0.021
944
c CHR579 Chiari Malformation Type Ii 37 0.021
945
WTH001 Withdrawal Disorder 37 0.021
946
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 37 0.021
947
EXT035 Extrinsic Cardiomyopathy 37 0.021
948
ACT012 Acute Hemorrhagic Conjunctivitis 37 0.021
949
SHW001 Shwartzman Phenomenon 37 0.021
950
HYP189 Hypoadrenalism 37 0.021
951
GNR003 Generalized Atherosclerosis 37 0.021
952
P ATR081 Atrial Standstill 37 0.021
953
HYP343 Hypothryoidism, Congenital, Nongoitrous 4 37 0.021
954
PNM005 Pneumonic Plague 37 0.021
955
GST028 Gastric Squamous Cell Carcinoma 37 0.021
956
PNC038 Pancreatic Cystadenocarcinoma 37 0.021
957
STC004 Stachybotrys Chartarum 37 0.021
958
TSH001 Tsh Producing Pituitary Tumor 37 0.021
959
ART006 Arthus Reaction 37 0.021
960
PRC001 Pericoronitis 37 0.021
961
SML031 Small Cell Carcinoma of the Bladder 37 0.021
962
c DFN190 Deafness, Autosomal Dominant 2a 37 0.021
963
c FML156 Familial Hyperaldosteronism 37 0.021
964
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.021
965
FNS001 Funisitis 37 0.021
966
PLM038 Pulmonary Large Cell Neuroendocrine Carcinoma 37 0.021
967
PRM026 Primary Systemic Mycosis 37 0.021
968
P HYP120 Hypoaldosteronism 36 0.021
969
CNG069 Congenital Cytomegalovirus 36 0.021
970
FML005 Female Reproductive Endometrioid Cancer 36 0.021
971
OPS001 Opisthorchiasis 36 0.021
972
P ADT004 Auditory Neuropathy 36 0.021
973
ASY002 Asymptomatic Neurosyphilis 36 0.021
974
ISC005 Ischemic Bone Disease 36 0.021
975
c CNG413 Congenital Short Bowel Syndrome 36 0.021
976
ETH004 Euthyroid Sick Syndrome 36 0.021
977
LTR003 Lateral Medullary Syndrome 36 0.021
978
c AMY059 Amyotrophic Lateral Sclerosis 19 36 0.021
979
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 36 0.021
980
P MNN007 Meningocele 36 0.021
981
NDL005 Nodular Medulloblastoma 36 0.021
982
PRX014 Proximal Spinal Muscular Atrophy 36 0.021
983
c DFN143 Deafness, Autosomal Recessive 16 36 0.021
984
OST008 Osteosclerotic Myeloma 36 0.021
985
SML020 Small Patella Syndrome 36 0.021
986
BRC010 Brachial Plexus Lesion 36 0.021
987
SNT005 Sinoatrial Node Disease 36 0.021
988
DVL001 Developmental Coordination Disorder 36 0.021
989
SPN050 Spinocerebellar Degeneration 36 0.021
990
BRT043 Bartonellosis 36 0.021
991
MRN002 Mooren's Ulcer 36 0.021
992
LMB010 Lambert Syndrome 36 0.021
993
c DYS119 Dystonia 9 36 0.021
994
END028 Endemic Goiter 35 0.021
995
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.021
996
ACL001 Acalculous Cholecystitis 35 0.021
997
NRM006 Neuromuscular Junction Disease 35 0.021
998
RCR001 Recurrent Corneal Erosion 35 0.021
999
c SCP001 Sc Phocomelia Syndrome 35 0.021
1000
c KDN016 Kidney Benign Neoplasm 35 0.021
1001
BLT003 Blue Toe Syndrome 35 0.021
1002
NNF001 Non-Functioning Pancreatic Endocrine Tumor 35 0.021
1003
PPL019 Papillary Conjunctivitis 35 0.021
1004
ACT060 Acute Vascular Insufficiency of Intestine 35 0.021
1005
LKS001 Leukostasis 35 0.021
1006
GST015 Gastric Small Cell Carcinoma 35 0.021
1007
PLM011 Plummer's Disease 35 0.021
1008
MLN002 Melanomatosis 35 0.021
1009
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 35 0.021
1010
NNT010 Nontoxic Goiter 35 0.021
1011
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 35 0.021
1012
PLY024 Polymicrogyria 35 0.021
1013
PRM004 Primary Amebic Meningoencephalitis 35 0.021
1014
PPT001 Peptic Esophagitis 35 0.021
1015
P GLM006 Glomangioma 35 0.021
1016
FRY001 Frey Syndrome 35 0.021
1017
TRP004 Tropical Sprue 35 0.021
1018
WST003 West Nile Fever 34 0.021
1019
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.021
1020
ADP007 Adie Pupil 34 0.021
1021
c GM2005 Gm2-Gangliosidosis, Ab Variant 34 0.021
1022
BRS032 Breast Papillary Carcinoma 34 0.021
1023
SLC005 Selective Iga Deficiency Disease 34 0.021
1024
CSL001 Causalgia 34 0.021
1025
c DFN103 Deafness, Autosomal Recessive 1b 34 0.021
1026
c CNG020 Congenital Hypogammaglobulinemia 34 0.021
1027
c OST129 Osteopetrosis, Autosomal Recessive 2 34 0.021
1028
c DFN114 Deafness, Autosomal Recessive 67 34 0.021
1029
PNC027 Pancreatic Gastrinoma 34 0.021
1030
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 34 0.021
1031
CRD016 Cardiac Rupture 34 0.021
1032
c OST126 Osteopetrosis, Autosomal Recessive 1 34 0.021
1033
NNT019 Neonatal Hypothyroidism 34 0.021
1034
CHN056 Chondrosarcoma, Extraskeletal Myxoid 34 0.021
1035
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 0.021
1036
c MYS064 Myasthenic Syndrome, Congenital, 16 33 0.021
1037
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.021
1038
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.021
1039
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.021
1040
BGS001 Bagassosis 33 0.021
1041
GLT018 Glut1 Deficiency Syndrome 1 33 0.021
1042
LYM004 Lymphoid Interstitial Pneumonia 33 0.021
1043
LYM045 Lymphocytic Vasculitis 33 0.021
1044
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 33 0.021
1045
c SRC023 Sarcoidosis 2 33 0.021
1046
DRS001 Dressler's Syndrome 33 0.021
1047
HRS011 Horseshoe Kidney 33 0.021
1048
PRN016 Peroneal Neuropathy 33 0.021
1049
OXY002 Oxyphilic Adenoma 33 0.021
1050
AMY005 Amyloid Neuropathy 33 0.021
1051
CRB022 Cerebellar Liponeurocytoma 33 0.021
1052
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.021
1053
ANT013 Anterior Spinal Artery Syndrome 33 0.021
1054
c NRP014 Neuropathy, Hereditary Sensory, with Spastic Paraplegia 32 0.021
1055
PLY010 Polyclonal Hypergammaglobulinemia 32 0.021
1056
CRN006 Coronary Aneurysm 32 0.021
1057