Search results for "paralysis"

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

685 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
c HYP051 Hypokalemic Periodic Paralysis 61 7.249
2
c HYP052 Hyperkalemic Periodic Paralysis 44 5.407
3
INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 35 5.019
4
NRM009 Normokalemic Periodic Paralysis 24 4.623
5
AND003 Andersen-Tawil Syndrome 53 4.111
6
FCL012 Facial Paralysis 40 4.025
7
P HYP239 Hyperkalemic Periodic Paralysis Type 2 32 3.805
8
c THY054 Thyrotoxic Periodic Paralysis 46 3.570
9
P HYP254 Hypokalemic Periodic Paralysis Type 1 36 3.545
10
KRT022 Keratoderma Palmoplantar Spastic Paralysis 17 3.520
11
TCK002 Tick Paralysis 24 3.437
12
OCL003 Oculomotor Nerve Paralysis 19 3.315
13
P THY084 Thyrotoxic Periodic Paralysis 1 23 3.269
14
PRN008 Peroneal Nerve Paralysis 17 2.939
15
c HYP255 Hypokalemic Periodic Paralysis Type 2 29 2.877
16
c HYP142 Hyperkalemic Periodic Paralysis Type 1 15 2.866
17
TCK005 Tucker Syndrome 13 2.841
18
BLL003 Bell's Palsy 60 2.715
19
PRM028 Paramyotonia Congenita 48 2.656
20
KLM001 Klumpke Paralysis 11 2.581
21
GLS003 Glossopharyngeal Nerve Paralysis 10 2.512
22
VCL002 Vocal Cord Dysfunction Familial 20 2.501
23
FML082 Familial Partial Paralysis 3 2.489
24
P HRD130 Hereditary Congenital Facial Paresis 3 19 2.460
25
LRY043 Laryngeal Abductor Paralysis - Intellectual Disability 12 2.460
26
ISL060 Isolated Hereditary Congenital Facial Paralysis 9 2.460
27
PLM031 Poliomyelitis 53 2.343
28
TDD001 Todd's Paralysis 9 2.200
29
MBS002 Moebius Syndrome 53 2.089
30
P PRK002 Parkinson's Disease 92 2.042
31
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 9 2.042
32
FML160 Familial Spastic Paralysis 8 2.027
33
LRY021 Laryngeal Adductor Paralysis 6 2.027
34
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 4 2.027
35
LRY023 Laryngeal Abductor Paralysis Mental Retardation 3 2.027
36
c THY083 Thyrotoxic Periodic Paralysis 2 9 2.009
37
VNN001 Venencie Powell Gordon Winkelmann Syndrome 7 2.009
38
PRL020 Paralysis Agitans, Juvenile, of Hunt 2 2.009
39
P PRD017 Periodic Paralyses 28 1.524
40
c OPH004 Ophthalmoplegia 53 1.477
41
P HRN001 Horner's Syndrome 42 1.462
42
c CRN035 Cranial Nerve Palsy 31 1.462
43
CYC001 Cycloplegia 26 1.462
44
FZL001 Fazio Londe Syndrome 20 1.462
45
c FML159 Familial Periodic Paralyses 8 1.462
46
P HYP035 Hypophosphatasia 75 1.444
47
PRL008 Paralytic Ileus 36 1.444
48
PSD001 Pseudobulbar Palsy 29 1.444
49
CNG241 Congenital Laryngeal Palsy 6 1.444
50
GLL022 Guillain-Barre Syndrome 57 1.421
51
TRP002 Tropical Spastic Paraparesis 55 1.421
52
SPS003 Spastic Diplegia 37 1.421
53
HYP143 Hypomyelination and Congenital Cataract 36 1.421
54
MBS001 Mobius Syndrome 28 1.421
55
P HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 26 1.421
56
ABD002 Abducens Nerve Disease 25 1.421
57
c NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 18 1.421
58
MRK002 Marek Disease 17 1.421
59
THR010 Third Cranial Nerve Disease 10 1.421
60
BLN018 Blindness- Scoliosis-Arachnodactyly Syndrome 8 1.421
61
P RNL007 Renal Tubular Acidosis 57 0.180
62
THY033 Thyrotoxicosis 57 0.146
63
HYP005 Hypokalemia 47 0.138
64
P LRY019 Laryngitis 65 0.129
65
c THY032 Thyroiditis 66 0.126
66
c MYP004 Myopathy 62 0.126
67
NRN002 Neuronitis 43 0.126
68
SPS057 Spasticity 37 0.126
69
SYN053 Syndromic Diarrhea 32 0.126
70
NRP001 Neuropathy 61 0.123
71
MYT011 Myotonia 43 0.123
72
THR013 Thoracic Outlet Syndrome 52 0.113
73
ADN018 Adenoma 64 0.109
74
OTT002 Otitis Media 59 0.109
75
ANK002 Ankylosing Spondylitis 74 0.105
76
P ANG001 Angelman Syndrome 70 0.105
77
P RSP003 Respiratory Failure 68 0.105
78
ART019 Aortic Valve Stenosis 64 0.105
79
P GRV001 Graves' Disease 64 0.102
80
ACN002 Acanthosis Nigricans 69 0.098
81
P ATX010 Ataxia Neuropathy Spectrum 41 0.098
82
P MSC003 Muscular Atrophy 53 0.093
83
ANR040 Aneurysm 44 0.093
84
c BNG076 Benign Exophthalmos Syndrome 22 0.093
85
AND002 Androgen Insensitivity Syndrome 80 0.089
86
c AXN002 Axenfeld-Rieger Syndrome 66 0.089
87
BTL001 Botulism 60 0.089
88
HYP017 Hypophosphatemia 48 0.089
89
c HPT021 Hepatitis 64 0.085
90
c HYP076 Hyperthyroidism 62 0.085
91
MYC002 Mycobacterium Avium Complex Disease 58 0.085
92
P CRV039 Cervicitis 57 0.085
93
BNF002 Bone Fracture 45 0.085
94
AND005 Androgen Insensitivity Syndrome, Mild 21 0.085
95
EPL031 Epileptic Hemiplegia 5 0.085
96
P HYP075 Hypertension 85 0.080
97
c MNN013 Meningitis 68 0.080
98
P HRP006 Herpes Simplex 66 0.080
99
ACS001 Acoustic Neuroma 51 0.080
100
NRM004 Neuroma 47 0.080
101
c PRG001 Progressive Muscular Atrophy 38 0.080
102
PSL001 Pasli Disease 27 0.080
103
P ATX002 Ataxia Telangiectasia 86 0.075
104
MLG056 Malignant Hyperthermia 64 0.075
105
HRP004 Herpes Zoster 57 0.075
106
CHL069 Cholesteatoma 54 0.075
107
ART001 Arterial Tortuosity Syndrome 54 0.075
108
ECT005 Ectropion 44 0.075
109
P MYS003 Myasthenia Gravis 78 0.069
110
LYM017 Lyme Disease 64 0.069
111
STT002 Status Asthmaticus 60 0.069
112
HMP005 Hemiplegia 52 0.069
113
DYS073 Dysphagia 51 0.069
114
MNN014 Mononeuritis 51 0.069
115
MLK003 Melkersson-Rosenthal Syndrome 50 0.069
116
PRT026 Parotitis 50 0.069
117
CNV002 Conversion Disorder 49 0.069
118
NRT004 Neuritis 48 0.069
119
LCK001 Locked-in Syndrome 40 0.069
120
PRL013 Paralytic Poliomyelitis 38 0.069
121
RMS005 Ramsay-Hunt Syndrome 30 0.069
122
TBR010 Tuberculosis 83 0.063
123
P WGN002 Wegener's Granulomatosis 71 0.063
124
P CHR071 Charcot-Marie-Tooth Disease 70 0.063
125
PTT006 Pituitary Adenoma 63 0.063
126
P ALT001 Alternating Hemiplegia of Childhood 58 0.063
127
c ATX004 Ataxia 58 0.063
128
c HYP065 Hyperaldosteronism 57 0.063
129
PTN002 Patent Ductus Arteriosus 57 0.063
130
SNS001 Sensorineural Hearing Loss 57 0.063
131
TTH006 Tooth Disease 55 0.063
132
P NRV007 Nervous System Disease 50 0.063
133
WST005 West Nile Virus 42 0.063
134
CRB009 Cerebritis 39 0.063
135
HYP264 Hypertonia 35 0.063
136
LGP001 Lagophthalmos 31 0.063
137
ERB002 Erb's Palsy 10 0.063
138
P AMY001 Amyotrophic Lateral Sclerosis 98 0.056
139
P SYS001 Systemic Lupus Erythematosus 85 0.056
140
c DBT009 Diabetes Mellitus 78 0.056
141
P LKM002 Leukemia 77 0.056
142
c LPS004 Lupus Erythematosus 72 0.056
143
P NRC002 Narcolepsy 71 0.056
144
ART016 Aortic Aneurysm 70 0.056
145
NPH007 Nephrogenic Diabetes Insipidus 70 0.056
146
P MLT020 Multiple Sclerosis 69 0.056
147
c HYP086 Hypothyroidism 69 0.056
148
P HPT001 Hepatitis C 66 0.056
149
P GTR002 Goiter 62 0.056
150
P PLY019 Polyneuropathy 60 0.056
151
P SYR001 Syringomyelia 60 0.056
152
P DBT005 Diabetes Insipidus 57 0.056
153
BRN029 Brain Disease 57 0.056
154
MYL001 Myelitis 54 0.056
155
NRM005 Neuromuscular Disease 51 0.056
156
PRP016 Paraplegia 47 0.056
157
MDS022 Mediastinitis 46 0.056
158
c SBC007 Subacute Thyroiditis 45 0.056
159
SJG001 Sjogren's Syndrome 44 0.056
160
SPP008 Suppurative Otitis Media 41 0.056
161
WND001 Wound Botulism 39 0.056
162
MLL002 Miller Fisher Syndrome 38 0.056
163
FTD001 Foot Drop 37 0.056
164
ADS002 Adie Syndrome 35 0.056
165
GNC003 Geniculate Herpes Zoster 30 0.056
166
HNM002 Hinman Syndrome 27 0.056
167
ANT054 Anotia 27 0.056
168
PRS053 Parsonage Turner Syndrome 18 0.056
169
MDD008 Middle Ear Adenoma 16 0.056
170
FBR024 Fibrocartilaginous Embolism 14 0.056
171
P MLR004 Malaria 75 0.049
172
MLT021 Multiple System Atrophy 70 0.049
173
P NRB001 Neuroblastoma 70 0.049
174
P HMN010 Hemangioma 70 0.049
175
PLY017 Polyarteritis Nodosa 69 0.049
176
P AMY004 Amyloidosis 67 0.049
177
P TRN020 Turner Syndrome 66 0.049
178
STT001 Status Epilepticus 65 0.049
179
c ENC004 Encephalitis 65 0.049
180
PHR003 Pharyngitis 65 0.049
181
P ESP024 Esophagitis 63 0.049
182
SPN186 Spinal Cord Injury 63 0.049
183
c MSC005 Muscular Dystrophy 62 0.049
184
MTR014 Motor Neuron Disease 61 0.049
185
ASP003 Aseptic Meningitis 60 0.049
186
SPN020 Spondylosis 59 0.049
187
NRL005 Neurilemmoma 57 0.049
188
RBS001 Rabies 57 0.049
189
c THR003 Thoracic Aortic Aneurysm 57 0.049
190
ADR008 Adrenal Adenoma 55 0.049
191
LPT001 Leptospirosis 53 0.049
192
TLR001 Tularemia 53 0.049
193
RLP003 Relapsing Fever 53 0.049
194
BLN003 Blindness 52 0.049
195
P PRP023 Peripheral Neuropathy 52 0.049
196
MNT147 Mental Retardation 51 0.049
197
P FNC004 Fanconi Syndrome 49 0.049
198
CRT008 Carotid Artery Dissection 47 0.049
199
WST004 West Nile Encephalitis 46 0.049
200
EVN001 Evans' Syndrome 46 0.049
201
P ATN005 Autonomic Dysfunction 46 0.049
202
P MLG090 Malignant Hyperthermia Susceptibility Type 1 46 0.049
203
EPL002 Epilepsy Syndrome 45 0.049
204
FSC004 Fasciitis 45 0.049
205
QDR001 Quadriplegia 43 0.049
206
SPN185 Spinal Cord Infarction 42 0.049
207
c CHR342 Chiari Malformation 41 0.049
208
THY035 Thyroid Adenoma 39 0.049
209
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.049
210
TLS001 Tolosa-Hunt Syndrome 36 0.049
211
TBS001 Tabes Dorsalis 36 0.049
212
c PPL025 Popliteal Pterygium Syndrome 35 0.049
213
CLR007 Colorado Tick Fever 34 0.049
214
P LBY004 Labyrinthitis 34 0.049
215
PTR001 Petrositis 29 0.049
216
TFT003 Tufting Enteropathy 28 0.049
217
CVR002 Cavernous Sinus Thrombosis 28 0.049
218
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.049
219
BLB003 Bulbar Polio 22 0.049
220
ABD009 Abducens Palsy 18 0.049
221
PNT023 Pontine Hemorrhage 18 0.049
222
OTP003 Oto-Palatal-Digital Syndrome 16 0.049
223
SKL006 Skull Base Neoplasm 11 0.049
224
P BRS047 Breast Cancer 100 0.040
225
CDS001 Cadasil 84 0.040
226
P MLT019 Multiple Myeloma 82 0.040
227
HPT023 Hepatocellular Carcinoma 79 0.040
228
OLV001 Olivopontocerebellar Atrophy 79 0.040
229
P LPR003 Leprosy 77 0.040
230
P PNM007 Pneumonia 76 0.040
231
P BPL003 Bipolar Disorder 75 0.040
232
P FML018 Familial Mediterranean Fever 74 0.040
233
P BRD002 Bardet-Biedl Syndrome 71 0.040
234
WLF001 Wolff-Parkinson-White Syndrome 70 0.040
235
SRC014 Sarcoma 69 0.040
236
c SRC013 Sarcoidosis 68 0.040
237
P GLM007 Glomerulonephritis 68 0.040
238
P INF038 Influenza 68 0.040
239
MSL001 Measles 67 0.040
240
TRG002 Trigeminal Neuralgia 67 0.040
241
SPN038 Spina Bifida 67 0.040
242
P HML002 Hemolytic Anemia 66 0.040
243
P CNG368 Congenital Adrenal Hyperplasia 66 0.040
244
P INS005 Insulin Resistance 66 0.040
245
P HYP117 Hypertriglyceridemia 65 0.040
246
c SPN046 Spinal Muscular Atrophy 65 0.040
247
c TXP001 Toxoplasmosis 65 0.040
248
PLS006 Plasmodium Vivax Malaria 65 0.040
249
CRB039 Cerebrovascular Disease 64 0.040
250
P PRG006 Progressive Supranuclear Palsy 64 0.040
251
c EHL001 Ehlers-Danlos Syndrome 63 0.040
252
c MLG069 Malignant Hypertension 63 0.040
253
STF001 Stiff-Person Syndrome 63 0.040
254
P ART023 Arthropathy 63 0.040
255
P PRP025 Peripheral Primitive Neuroectodermal Tumor 62 0.040
256
P FML001 Familial Atrial Fibrillation 62 0.040
257
ART005 Arteriovenous Malformation 62 0.040
258
ARC007 Arachnoid Cysts 61 0.040
259
c PRP029 Porphyria 61 0.040
260
BBS001 Babesiosis 61 0.040
261
c HRD010 Hereditary Spastic Paraplegia 61 0.040
262
c ATM010 Autoimmune Hemolytic Anemia 60 0.040
263
CLD007 Cold Agglutinin Disease 60 0.040
264
PRM027 Primitive Neuroectodermal Tumor 60 0.040
265
P CNG401 Congenital Heart Disease 58 0.040
266
YLL002 Yellow Fever 58 0.040
267
GLC003 Glucose Intolerance 58 0.040
268
HDC001 Headache 58 0.040
269
P SYP003 Syphilis 57 0.040
270
RHB003 Rhabdomyosarcoma 57 0.040
271
c PSD020 Pseudohypoaldosteronism Type Ii 57 0.040
272
P MYC008 Myocarditis 57 0.040
273
P CNG021 Congenital Toxoplasmosis 57 0.040
274
SCN006 Secondary Syphilis 57 0.040
275
P HYP014 Hyperuricemia 56 0.040
276
c TRM003 Tremor 55 0.040
277
JPN002 Japanese Encephalitis 55 0.040
278
GST037 Gastroparesis 54 0.040
279
c OST028 Osteochondroma 54 0.040
280
NWC001 Newcastle Disease 54 0.040
281
THY009 Thyroid Lymphoma 54 0.040
282
EHR002 Ehrlichiosis 53 0.040
283
c ACR001 Aicardi-Goutieres Syndrome 53 0.040
284
GST045 Gastroenteritis 53 0.040
285
TCK001 Tick-Borne Encephalitis 53 0.040
286
OST011 Osteomalacia 52 0.040
287
ENC006 Encephalomyelitis 52 0.040
288
P PNM006 Pneumoconiosis 52 0.040
289
SPT005 Spotted Fever 52 0.040
290
GRW007 Growth Hormone Deficiency 52 0.040
291
c PRG013 Paraganglioma 51 0.040
292
STL001 St. Louis Encephalitis 51 0.040
293
RNL011 Renal Osteodystrophy 51 0.040
294
P MJR001 Major Depressive Disorder 50 0.040
295
c EMR001 Emery-Dreifuss Muscular Dystrophy 49 0.040
296
OPT009 Optic Neuritis 49 0.040
297
FBR047 Fibromyalgia 49 0.040
298
P NML001 Nemaline Myopathy 49 0.040
299
PRS062 Persistent Hyperplastic Primary Vitreous 48 0.040
300
P PND001 Pain Disorder 48 0.040
301
NPH003 Nephrocalcinosis 48 0.040
302
NSP002 Nasopharyngitis 48 0.040
303
MMB001 Membranoproliferative Glomerulonephritis 47 0.040
304
CNN003 Conn's Syndrome 47 0.040
305
CNT025 Central Pontine Myelinolysis 46 0.040
306
GYN001 Gynecomastia 46 0.040
307
MYK002 Myokymia 46 0.040
308
c AML002 Amelogenesis Imperfecta 46 0.040
309
P HMR005 Hemorrhoid 46 0.040
310
TRY002 Troyer Syndrome 46 0.040
311
PST055 Postural Hypotension 46 0.040
312
KRT012 Keratoderma 45 0.040
313
ARC002 Arachnoiditis 45 0.040
314
c APH002 Aphasia 44 0.040
315
PRS037 Periostitis 44 0.040
316
OST006 Osteoblastoma 44 0.040
317
ILS001 Ileus 44 0.040
318
THY043 Thymic Hyperplasia 43 0.040
319
EPD005 Epidural Abscess 42 0.040
320
LCR004 La Crosse Encephalitis 42 0.040
321
c HRD086 Hereditary Hypophosphatemic Rickets 41 0.040
322
c NRC009 Narcolepsy 1 39 0.040
323
HYD001 Hydranencephaly 38 0.040
324
TRC023 Trichinosis 38 0.040
325
P OTT001 Otitis Externa 38 0.040
326
XRP001 Xerophthalmia 37 0.040
327
RCK002 Rocky Mountain Spotted Fever 36 0.040
328
AXN001 Axonal Neuropathy 36 0.040
329
PRS063 Paresthesia 35 0.040
330
TRP004 Tropical Sprue 35 0.040
331
ENT005 Entropion 34 0.040
332
SPR007 Superior Mesenteric Artery Syndrome 34 0.040
333
SPS016 Spasmodic Dysphonia 33 0.040
334
c FML249 Familial Amyloidosis, Finnish Type 33 0.040
335
FCL003 Facial Hemiatrophy 32 0.040
336
c SPS012 Spastic Paraplegia 3a 32 0.040
337
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 31 0.040
338
CHL109 Childhood Apraxia of Speech 31 0.040
339
BRW001 Brown-Vialetto-Van Laere Syndrome 30 0.040
340
CBB002 Cobb Syndrome 30 0.040
341
c SPS078 Spastic Paraplegia 7 29 0.040
342
c CHR160 Chiari Malformation Type 2 28 0.040
343
BRW004 Brown-Sequard Syndrome 28 0.040
344
PRR008 Periarteritis Nodosa 28 0.040
345
ECT004 Ecthyma 27 0.040
346
VST004 Vestibular Disease 26 0.040
347
FDB001 Foodborne Botulism 26 0.040
348
P HYP078 Hypertrophy of Breast 25 0.040
349
TCK004 Tick Infestation 25 0.040
350
STR002 Streptococcal Meningitis 23 0.040
351
GLM016 Glomus Jugulare Tumors 21 0.040
352
PWS001 Powassan Encephalitis 19 0.040
353
MNN005 Meningovascular Neurosyphilis 19 0.040
354
CNT067 Central Cord Syndrome 18 0.040
355
SYR004 Syringobulbia 16 0.040
356
BDR001 Bidirectional Tachycardia 13 0.040
357
UVP001 Uveoparotid Fever 10 0.040
358
SPN015 Spinal Polio 9 0.040
359
BLB001 Bulbospinal Polio 9 0.040
360
MYP026 Myopathy - Thyrotoxic 9 0.040
361
BRC057 Brachial Plexus Birth Injuries 7 0.040
362
WST006 Westphal Disease 5 0.040
363
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.040
364
HMP020 Hemiplegia Alterans 1 0.040
365
P TYP008 Type 1 Diabetes Mellitus 93 0.028
366
P NRF002 Neurofibromatosis 93 0.028
367
P AST005 Asthma 88 0.028
368
P LFR001 Li-Fraumeni Syndrome 87 0.028
369
MTC003 Metachromatic Leukodystrophy 86 0.028
370
INF030 Infectious Mononucleosis 84 0.028
371
P TYS001 Tay-Sachs Disease 82 0.028
372
P DLT002 Dilated Cardiomyopathy 82 0.028
373
GLC006 Galactosemia 81 0.028
374
VNH001 Von Hippel-Lindau Disease 80 0.028
375
BRK003 Burkitt's Lymphoma 77 0.028
376
P NRL016 Neural Tube Defects 77 0.028
377
ACT033 Acute Intermittent Porphyria 76 0.028
378
P OST002 Osteoporosis 75 0.028
379
SKN016 Skin Disease 75 0.028
380
P CLC005 Celiac Disease 74 0.028
381
PRC016 Pre-Eclampsia 74 0.028
382
CRH001 Crohn's Disease 74 0.028
383
P ALX003 Alexander Disease 73 0.028
384
21H001 21-Hydroxylase Deficiency 73 0.028
385
P MYL005 Myelofibrosis 72 0.028
386
CFF002 Coffin-Lowry Syndrome 72 0.028
387
HYP458 Hyper Ige Syndrome 71 0.028
388
PRT036 Peritonitis 71 0.028
389
SPS077 Sepsis 70 0.028
390
CCC001 Coccidioidomycosis 70 0.028
391
c XRD001 Xeroderma Pigmentosum 70 0.028
392
P MGR002 Migraine 69 0.028
393
P ADD001 Addison's Disease 68 0.028
394
c HPT016 Hepatitis B 68 0.028
395
DSM004 Desmoid Tumor 67 0.028
396
P ABD003 Abdominal Aortic Aneurysm 67 0.028
397
P THY023 Thymoma 66 0.028
398
P LNG044 Long Qt Syndrome 1 66 0.028
399
GST009 Gastroschisis 66 0.028
400
P BLD042 Bladder Carcinoma 66 0.028
401
CHR072 Chordoma 66 0.028
402
MYS005 Myositis 66 0.028
403
P ATM003 Autoimmune Thyroiditis 65 0.028
404
HYP004 Hypercalcemia 65 0.028
405
VRG001 Variegate Porphyria 65 0.028
406
ABT001 Abetalipoproteinemia 64 0.028
407
FCT002 Factor Xi Deficiency 64 0.028
408
MNT001 Mantle Cell Lymphoma 64 0.028
409
GTL001 Gitelman Syndrome 64 0.028
410
P LGH001 Leigh Disease 64 0.028
411
PLM033 Pulmonary Embolism 64 0.028
412
c SML001 Small Cell Carcinoma 64 0.028
413
P OLG002 Oligodendroglioma 64 0.028
414
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.028
415
P CNJ013 Conjunctivitis 63 0.028
416
c INT070 Intestinal Obstruction 63 0.028
417
FCT003 Factor X Deficiency 63 0.028
418
P MLN008 Melanoma 63 0.028
419
ISC004 Ischemia 63 0.028
420
CMP002 Campylobacteriosis 63 0.028
421
P FBR017 Fibrosarcoma 63 0.028
422
LRN003 Learning Disability 62 0.028
423
P KRT004 Keratitis 62 0.028
424
BLR001 Biliary Atresia 62 0.028
425
c KDN018 Kidney Disease 62 0.028
426
P MTR012 Mitral Valve Disease 62 0.028
427
P CRB042 Cerebellar Ataxia 61 0.028
428
PTN001 Patent Foramen Ovale 61 0.028
429
KRN002 Kearns-Sayre Syndrome 61 0.028
430
GLD001 Goldenhar Syndrome 61 0.028
431
P SCH018 Schizencephaly 61 0.028
432
c MYL007 Myeloma 61 0.028
433
ACQ007 Acquired Immunodeficiency Syndrome 61 0.028
434
NRL004 Neuroleptic Malignant Syndrome 60 0.028
435
TYP007 Typhoid Fever 60 0.028
436
PMP001 Pemphigus 60 0.028
437
ALP004 Alport Syndrome 60 0.028
438
KRT001 Keratoconjunctivitis Sicca 60 0.028
439
CHC001 Chickenpox 60 0.028
440
c ALM001 Al Amyloidosis 59 0.028
441
CRB021 Cerebral Malaria 59 0.028
442
MGC001 Megacolon 59 0.028
443
P MMP001 Mumps 59 0.028
444
c GLY013 Glycogen Storage Disease 59 0.028
445
CVR006 Cavernous Hemangioma 58 0.028
446
P MCH002 Machado-Joseph Disease 58 0.028
447
END030 End Stage Renal Failure 58 0.028
448
ANR004 Anuria 57 0.028
449
PRN023 Prion Disease 57 0.028
450
ESP020 Esophageal Atresia 57 0.028
451
P VRL012 Viral Meningitis 57 0.028
452
P GNT008 Giant Cell Tumor 57 0.028
453
P HYP024 Hypoparathyroidism 57 0.028
454
c FML023 Familial Hemiplegic Migraine 57 0.028
455
ANK001 Ankylosis 57 0.028
456
c CTR002 Cataract 57 0.028
457
c ACT073 Acute Leukemia 56 0.028
458
SMT015 Smith Magenis Syndrome 56 0.028
459
P MYM002 Moyamoya Disease 56 0.028
460
PLG002 Plague 56 0.028
461
MYL003 Myeloid Sarcoma 56 0.028
462
c SPN049 Spinocerebellar Ataxia 56 0.028
463
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 55 0.028
464
HMM003 Hemimegalencephaly 55 0.028
465
c HYP060 Hyperinsulinism 55 0.028
466
INS008 Insulin-Like Growth Factor I Deficiency 55 0.028
467
STR039 Sturge-Weber Syndrome 55 0.028
468
c WRD001 Waardenburg's Syndrome 55 0.028
469
P CHR095 Chronic Progressive External Ophthalmoplegia 55 0.028
470
P BRG005 Brugada Syndrome 1 55 0.028
471
MDL009 Medullary Sponge Kidney 55 0.028
472
P EXP004 Exophthalmos 54 0.028
473
P NRM001 Neuromyelitis Optica 54 0.028
474
NPH051 Nephritis 54 0.028
475
SLP005 Sleep Disorder 54 0.028
476
P HYP141 Hyperphenylalaninemia 54 0.028
477
c MYT007 Myotonic Dystrophy Type 2 54 0.028
478
CRN012 Craniometaphyseal Dysplasia 54 0.028
479
LYM019 Lymphosarcoma 54 0.028
480
MYX004 Myxedema 53 0.028
481
P KLP003 Klippel-Feil Syndrome 53 0.028
482
STS002 Situs Inversus 53 0.028
483
HNT002 Hantavirus Pulmonary Syndrome 53 0.028
484
PRC013 Pericarditis 53 0.028
485
PRN011 Pernicious Anemia 53 0.028
486
PRT029 Parathyroid Adenoma 52 0.028
487
ANG002 Angiostrongyliasis 52 0.028
488
c SPN183 Spontaneous Pneumothorax 52 0.028
489
c GLY007 Glycogen Storage Disease Iv 52 0.028
490
c CHR022 Charcot-Marie-Tooth Disease Type 1 52 0.028
491
TRN015 Transient Cerebral Ischemia 52 0.028
492
BRS064 Bursitis 52 0.028
493
c HMP006 Hemiplegic Migraine 51 0.028
494
EXS001 Exostosis 51 0.028
495
P CYS016 Cystic Kidney 51 0.028
496
c BRT004 Bartter Disease 51 0.028
497
ARR001 Arrhythmogenic Right Ventricular Dysplasia 50 0.028
498
RGD001 Rigid Spine Syndrome 50 0.028
499
HRD030 Hereditary Neuralgic Amyotrophy 50 0.028
500
c OPT004 Optic Atrophy 50 0.028
501
FBR009 Fibrous Dysplasia 50 0.028
502
CHK001 Chikungunya 50 0.028
503
c CRB126 Cerebral Cavernous Malformation 50 0.028
504
P INT063 Intellectual Disability 50 0.028
505
HYP006 Hypertensive Heart Disease 50 0.028
506
HJD001 Hajdu-Cheney Syndrome 50 0.028
507
P BNG071 Benign Schwannoma 50 0.028
508
P LCT002 Lactose Intolerance 49 0.028
509
CTS002 Cat-Scratch Disease 49 0.028
510
c ATN004 Autonomic Neuropathy 49 0.028
511
PNM008 Pneumothorax 49 0.028
512
c EPS003 Episodic Ataxia 49 0.028
513
AMB002 Amblyopia 49 0.028
514
c CNT035 Central Nervous System Disease 49 0.028
515
NRX001 Neuroaxonal Dystrophy 49 0.028
516
PLS016 Plasma Cell Leukemia 49 0.028
517
MLT075 Multifocal Motor Neuropathy 49 0.028
518
INF058 Inflammatory Myofibroblastic Tumor 48 0.028
519
ASP007 Aspiration Pneumonia 48 0.028
520
BRN016 Bronchogenic Carcinoma 48 0.028
521
TRC040 Tracheoesophageal Fistula 48 0.028
522
MTS001 Mutism 48 0.028
523
PLM010 Pulmonary Edema 48 0.028
524
P EWN002 Ewing's Family of Tumors 48 0.028
525
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 47 0.028
526
MTH009 Mouth Disease 47 0.028
527
LYM021 Lymphadenitis 47 0.028
528
c MLG086 Malignant Hyperthermia Susceptibility 47 0.028
529
MYS001 Myositis Ossificans 47 0.028
530
P TRN034 Transverse Myelitis 47 0.028
531
c FML043 Familial Idiopathic Basal Ganglia Calcification 46 0.028
532
c DMY001 Demyelinating Polyneuropathy 46 0.028
533
HYP120 Hypoaldosteronism 46 0.028
534
MNN009 Meningoencephalitis 46 0.028
535
SCH016 Schimke Immunoosseous Dysplasia 46 0.028
536
MCP006 Mucoepidermoid Carcinoma 46 0.028
537
c ATR070 Atrial Fibrillation, Familial, 9 45 0.028
538
MDD002 Middle Ear Cholesteatoma 45 0.028
539
MGL013 Megalencephaly 45 0.028
540
P MLT008 Multinodular Goiter 45 0.028
541
MYC033 Myoclonus 45 0.028
542
NRL007 Neurologic Diseases 45 0.028
543
SPN050 Spinocerebellar Degeneration 44 0.028
544
ZYG002 Zygomycosis 44 0.028
545
P FCS001 Facioscapulohumeral Muscular Dystrophy 44 0.028
546
TNG009 Tongue Squamous Cell Carcinoma 44 0.028
547
ACT012 Acute Hemorrhagic Conjunctivitis 44 0.028
548
NCR007 Necrotizing Fasciitis 44 0.028
549
FTT001 Fatty Liver Disease 43 0.028
550
P SZR006 Seizure Disorder 43 0.028
551
CDQ001 Cauda Equina Syndrome 43 0.028
552
RMS001 Rem Sleep Behavior Disorder 42 0.028
553
LMB052 Lumbar Disc Herniation 42 0.028
554
HTS001 Hiatus Hernia 42 0.028
555
ENC017 Encephaloceles 42 0.028
556
TTR016 Tetra-Amelia Syndrome 41 0.028
557
P RSM001 Rasmussen Encephalitis 41 0.028
558
SPS019 Spastic Paraparesis 41 0.028
559
HYP265 Hypotonia 41 0.028
560
EST005 Esotropia 40 0.028
561
SCT002 Scotoma 40 0.028
562
P APL006 Aplasia Cutis Congenita 40 0.028
563
P MNN007 Meningocele 40 0.028
564
DYG002 Dyggve-Melchior-Clausen Syndrome 40 0.028
565
LRY029 Laryngomalacia 40 0.028
566
END051 Endolymphatic Sac Tumor 39 0.028
567
P FNN001 Finnish Type Amyloidosis 38 0.028
568
SPC005 Speech Disorder 38 0.028
569
PLM029 Palmoplantar Keratosis 37 0.028
570
c SPS092 Spastic Paraplegia 11 37 0.028
571
P GLM006 Glomangioma 37 0.028
572
SCR015 Scarlet Fever 37 0.028
573
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 37 0.028
574
P VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 37 0.028
575
IPX001 Ipex Syndrome 37 0.028
576
LMB010 Lambert Syndrome 36 0.028
577
VRL011 Viral Infectious Disease 36 0.028
578
HNS001 Hansen's Disease 36 0.028
579
HRD025 Hereditary Neuropathy with Liability to Pressure Palsies 36 0.028
580
P SRC025 Sarcoidosis 1 36 0.028
581
PRX020 Proximal Renal Tubular Acidosis with Ocular Abnormalities 35 0.028
582
SML020 Small Patella Syndrome 35 0.028
583
P BNC001 Bone Carcinoma 34 0.028
584
c BRT034 Bartter Syndrome, Type 2 34 0.028
585
HYP034 Hypertensive Encephalopathy 34 0.028
586
MRR003 Murray Valley Encephalitis 34 0.028
587
INT042 Internuclear Ophthalmoplegia 34 0.028
588
BLT011 Bilateral Perisylvian Polymicrogyria 34 0.028
589
CSL001 Causalgia 33 0.028
590
c CNG112 Congenital Muscular Dystrophy Type 1a 33 0.028
591
THM001 Thomsen Disease 33 0.028
592
PST020 Postpoliomyelitis Syndrome 33 0.028
593
MTC018 Metachondromatosis 33 0.028
594
PMP008 Pemphigus Vegetans 33 0.028
595
ANT018 Anthracosis 33 0.028
596
PNM005 Pneumonic Plague 32 0.028
597
HRD088 Hereditary Neuropathies 32 0.028
598
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.028
599
PRX014 Proximal Spinal Muscular Atrophy 32 0.028
600
DSR005 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase 31 0.028
601
P CHR454 Chiari Malformation Type 1 31 0.028
602
SPR083 Sporadic Hemiplegic Migraine 30 0.028
603
VST003 Vestibular Nystagmus 30 0.028
604
c SCP001 Sc Phocomelia Syndrome 30 0.028
605
BRC010 Brachial Plexus Lesion 29 0.028
606
c ATS059 Autosomal Dominant Hyper Ige Syndrome 29 0.028
607
CRV030 Cervical Adenitis 29 0.028
608
MNR004 Mounier-Kuhn Syndrome 29 0.028
609
LPN001 Louping Ill 29 0.028
610
PSD029 Pseudocholinesterase Deficiency 29 0.028
611
FBR028 Fibrosing Mediastinitis 29 0.028
612
c PHC014 Phocomelia 28 0.028
613
FRY001 Frey Syndrome 28 0.028
614
HYP362 Hyperopia 28 0.028
615
P AML016 Amelogenesis Imperfecta, Type 1e 28 0.028
616
NRS003 Neurosyphilis 28 0.028
617
MYC014 Mycobacterium Chelonae 27 0.028
618
c ACT159 Acute Transverse Myelitis 27 0.028
619
AMY005 Amyloid Neuropathy 27 0.028
620
CRN051 Craniofacial Microsomia 27 0.028
621
WYB001 Wyburn Mason's Syndrome 27 0.028
622
c RNL045 Renal Tubular Acidosis, Distal 27 0.028
623
GNT004 Gnathomiasis 27 0.028
624
FCL044 Fecal Incontinence 27 0.028
625
RHB020 Rhabdomyosarcoma, Somatic 26 0.028
626
ETH009 Ethmoid Sinusitis 26 0.028
627
ECH002 Echolalia 26 0.028
628
SNS003 Sensory Peripheral Neuropathy 26 0.028
629
P RNL066 Renal Tubular Acidosis, Distal, Ad 26 0.028
630
PNT009 Pontine Tegmental Cap Dysplasia 26 0.028
631
P CHR097 Chronic Purulent Otitis Media 26 0.028
632
HYP048 Hypotropia 25 0.028
633
FCT022 Factor Xi Deficiency, Autosomal Recessive 25 0.028
634
ANT013 Anterior Spinal Artery Syndrome 25 0.028
635
EXC003 Excessive Tearing 25 0.028
636
LTR002 Lateral Sinus Thrombosis 25 0.028
637
P MYT013 Myotonia Congenita, Dominant 25 0.028
638
c FRT001 Fourth Cranial Nerve Palsy 24 0.028
639
PRN016 Peroneal Neuropathy 24 0.028
640
CRT009 Critical Illness Polyneuropathy 24 0.028
641
SBS002 Substernal Goiter 23 0.028
642
MYS010 Myostatin-Related Muscle Hypertrophy 23 0.028
643
ATR055 Atrial Septal Aneurysm 23 0.028
644
ETH012 Ethylene Glycol Poisoning 23 0.028
645
ACT181 Acute Motor Axonal Neuropathy 22 0.028
646
c AMY008 Amyotrophic Lateral Sclerosis Type 2 22 0.028
647
LRY007 Laryngeal Tuberculosis 22 0.028
648
c SNS011 Sinus Cancer 21 0.028
649
SWL001 Swallowing Disorders 21 0.028
650
EXP002 Exposure Keratitis 21 0.028
651
HYP047 Hypertropia 21 0.028
652
c PRM041 Primary Cortisol Resistance 21 0.028
653
CNG133 Congenital Varicella Syndrome 21 0.028
654
c VRL004 Viral Labyrinthitis 19 0.028
655
PRP013 Paraphimosis 19 0.028
656
c HRD043 Hereditary Congenital Facial Paresis 19 0.028
657
c CNG333 Congenital Horner Syndrome 19 0.028
658
CLV002 Clivus Chordoma 18 0.028
659
MLN002 Melanomatosis 18 0.028
660
HTR005 Heterochromia Iridis 18 0.028
661
c CNG129 Congenital Torticollis 18 0.028
662
EMB015 Embryonal Tumor with Multilayered Rosettes 18 0.028
663
DRS001 Dressler's Syndrome 18 0.028
664
CNR001 Coenurosis 17 0.028
665
PRS120 Persistent Idiopathic Facial Pain 17 0.028
666
c CHR094 Chronic Polyneuropathy 16 0.028
667
INT095 Internal Carotid Agenesis 15 0.028
668
SPN092 Spinal Shock 15 0.028
669
MNS002 Mini Stroke 14 0.028
670
MLL006 Mollaret Meningitis 14 0.028
671
TRG006 Trigger Thumb 13 0.028
672
c DST048 Distal Hereditary Motor Neuropathy Type 1 13 0.028
673
ATY001 Atypical Depressive Disorder 13 0.028
674
BMF002 Bamforth Syndrome 13 0.028
675
BNP002 Bone Epithelioid Hemangioma 13 0.028
676
SPH008 Sphenoidal Sinus Cancer 13 0.028
677
SPR038 Supranuclear Ocular Palsy 12 0.028
678
JMP002 Jumping Frenchmen of Maine 12 0.028
679
CNM001 Canomad Syndrome 12 0.028
680
PRS033 Parasitic Ectoparasitic Infectious Disease 12 0.028
681
FHR002 Fahr's Syndrome 11 0.028
682
c CHR161 Chiari Malformation Type 3 11 0.028
683
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 8 0.028
684
KNG003 Konigsmark Knox Hussels Syndrome 8 0.028
685
GNT013 Genetic Brain Disorders 5 0.028