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

717 hits were found for 'paralysis'

# ++ Fam MCID Name MIFTS Score
1
c HYP051 Hypokalemic Periodic Paralysis 53 7.356
2
c HYP052 Hyperkalemic Periodic Paralysis 39 5.498
3
INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 26 5.100
4
NRM009 Normokalemic Periodic Paralysis 22 4.837
5
FCL012 Facial Paralysis 44 4.104
6
P HYP239 Hyperkalemic Periodic Paralysis Type 2 23 4.007
7
AND003 Andersen-Tawil Syndrome 39 3.913
8
c THY054 Thyrotoxic Periodic Paralysis 40 3.731
9
P HYP254 Hypokalemic Periodic Paralysis Type 1 29 3.591
10
KRT022 Keratoderma Palmoplantar Spastic Paralysis 12 3.574
11
TCK002 Tick Paralysis 22 3.485
12
OCL003 Oculomotor Nerve Paralysis 17 3.368
13
P THY084 Thyrotoxic Periodic Paralysis 1 19 3.324
14
c HYP255 Hypokalemic Periodic Paralysis Type 2 19 2.996
15
PRN008 Peroneal Nerve Paralysis 16 2.996
16
c HYP142 Hyperkalemic Periodic Paralysis Type 1 13 2.899
17
TCK005 Tucker Syndrome 10 2.886
18
PRM028 Paramyotonia Congenita 40 2.735
19
KLM001 Klumpke Paralysis 8 2.610
20
VCL002 Vocal Cord Dysfunction Familial 13 2.587
21
GLS003 Glossopharyngeal Nerve Paralysis 6 2.550
22
FML082 Familial Partial Paralysis 1 2.527
23
P HRD130 Hereditary Congenital Facial Paresis 3 15 2.500
24
LRY036 Laryngeal Abductor Paralysis - Intellectual Deficit 9 2.500
25
ISL060 Isolated Hereditary Congenital Facial Paralysis 5 2.500
26
PLM031 Poliomyelitis 51 2.379
27
BLL003 Bell's Palsy 52 2.197
28
P MBS002 Moebius Syndrome 45 2.190
29
TDD001 Todd's Paralysis 7 2.190
30
P PRK002 Parkinson's Disease 86 2.146
31
FML160 Familial Spastic Paralysis 5 2.058
32
LRY021 Laryngeal Adductor Paralysis 4 2.058
33
LRY023 Laryngeal Abductor Paralysis Mental Retardation 0 2.058
34
VNN001 Venencie Powell Gordon Winkelmann Syndrome 4 2.041
35
c THY083 Thyrotoxic Periodic Paralysis 2 3 2.041
36
PRL020 Paralysis Agitans, Juvenile, of Hunt 1 2.041
37
P PRD017 Periodic Paralyses 25 1.553
38
HYP035 Hypophosphatasia 66 1.544
39
HYP143 Hypomyelination and Congenital Cataract 29 1.544
40
c FML159 Familial Periodic Paralyses 9 1.534
41
c OPH004 Ophthalmoplegia 46 1.511
42
P HRN001 Horner's Syndrome 38 1.498
43
PRL008 Paralytic Ileus 37 1.483
44
FZL001 Fazio Londe Syndrome 13 1.483
45
THR010 Third Cranial Nerve Disease 10 1.483
46
c CRN035 Cranial Nerve Palsy 35 1.466
47
PSD001 Pseudobulbar Palsy 28 1.466
48
CYC001 Cycloplegia 25 1.466
49
TRP002 Tropical Spastic Paraparesis 44 1.443
50
SPS003 Spastic Diplegia 36 1.443
51
MRK002 Marek Disease 31 1.443
52
MBS001 Mobius Syndrome 29 1.443
53
P HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 23 1.443
54
ABD002 Abducens Nerve Disease 20 1.443
55
P NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 13 1.443
56
CNG241 Congenital Laryngeal Palsy 3 1.443
57
SDD005 Sudden Cardiac Death Multi-Gene Panels 19 0.238
58
ANK002 Ankylosing Spondylitis 75 0.213
59
c PPL025 Popliteal Pterygium Syndrome 31 0.213
60
THR013 Thoracic Outlet Syndrome 53 0.182
61
RNL007 Renal Tubular Acidosis 57 0.178
62
IDP042 Idiopathic Recurrent Stupor 15 0.178
63
RNL045 Renal Tubular Acidosis, Distal 34 0.172
64
c CHR153 Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant 18 0.170
65
THY033 Thyrotoxicosis 55 0.153
66
c MYT011 Myotonia 41 0.148
67
ATX002 Ataxia Telangiectasia 81 0.146
68
P RSP003 Respiratory Failure 60 0.140
69
HYP005 Hypokalemia 50 0.140
70
ACN002 Acanthosis Nigricans 70 0.129
71
NSY001 N Syndrome 57 0.129
72
c CRD152 Cardiomyopathy, Familial Hypertrophic, 21 15 0.126
73
c LCL006 Localized Scleroderma 64 0.123
74
CHL109 Childhood Apraxia of Speech 19 0.123
75
c MYP004 Myopathy 52 0.120
76
MNN014 Mononeuritis 40 0.120
77
IDP037 Idiopathic Facial Palsy 12 0.120
78
c ERL004 Early Yaws 29 0.117
79
c SPS036 Spastic Paraplegia 3 23 0.117
80
ADN018 Adenoma 67 0.113
81
NRP001 Neuropathy 54 0.113
82
MYC002 Mycobacterium Avium Complex Disease 56 0.110
83
HNM001 Hinman's Syndrome 28 0.107
84
CRK001 Cork-Handlers' Disease 28 0.107
85
OTT002 Otitis Media 54 0.103
86
PRP016 Paraplegia 42 0.103
87
RNL048 Renal Tubular Acidosis, Distal, Type 3 19 0.103
88
WST001 West Syndrome 64 0.099
89
P GRV001 Graves' Disease 63 0.099
90
c SPS012 Spastic Paraplegia 3a 19 0.099
91
WST006 Westphal Disease 7 0.099
92
P ANG001 Angelman Syndrome 67 0.095
93
ART019 Aortic Valve Stenosis 64 0.095
94
c THY032 Thyroiditis 61 0.095
95
P MSC003 Muscular Atrophy 51 0.095
96
EHL006 Ehlers–danlos Syndrome 27 0.095
97
RPD005 Rapidly Involuting Congenital Hemangioma 19 0.095
98
SPS019 Spastic Paraparesis 49 0.091
99
c ATX010 Ataxia Neuropathy Spectrum 33 0.091
100
MLG056 Malignant Hyperthermia 66 0.087
101
CNG368 Congenital Adrenal Hyperplasia 64 0.087
102
BNF002 Bone Fracture 53 0.087
103
GRW007 Growth Hormone Deficiency 52 0.087
104
HYP017 Hypophosphatemia 52 0.087
105
BTL001 Botulism 51 0.087
106
TFT003 Tufting Enteropathy 26 0.087
107
c BNG076 Benign Exophthalmos Syndrome 17 0.087
108
P STR035 Streptococcal Group a Invasive Disease 15 0.087
109
AND002 Androgen Insensitivity Syndrome 75 0.083
110
P INS005 Insulin Resistance 62 0.083
111
c AXN002 Axenfeld-Rieger Syndrome 57 0.083
112
c ATX004 Ataxia 56 0.083
113
SCN006 Secondary Syphilis 53 0.083
114
OST028 Osteochondroma 49 0.083
115
JVN024 Juvenile Hereditary Hemochromatosis 28 0.083
116
RNL066 Renal Tubular Acidosis, Distal, Ad 24 0.083
117
P MYT013 Myotonia Congenita, Dominant 23 0.083
118
c TTL001 Total Internal Ophthalmoplegia 17 0.083
119
c HPT021 Hepatitis 65 0.078
120
21H001 21-Hydroxylase Deficiency 62 0.078
121
ACS001 Acoustic Neuroma 54 0.078
122
P LRY019 Laryngitis 53 0.078
123
P ALV004 Alveolar Rhabdomyosarcoma 51 0.078
124
NRM004 Neuroma 48 0.078
125
MLK003 Melkersson-Rosenthal Syndrome 43 0.078
126
c PRG001 Progressive Muscular Atrophy 34 0.078
127
FCT013 Factor V Leiden Thrombophilia 31 0.078
128
c CNG372 Congenital Generalized Lipodystrophy Type 3 24 0.078
129
AND005 Androgen Insensitivity Syndrome, Mild 19 0.078
130
c HRD043 Hereditary Congenital Facial Paresis 13 0.078
131
EPL031 Epileptic Hemiplegia 5 0.078
132
P AST005 Asthma 86 0.073
133
P MYS003 Myasthenia Gravis 71 0.073
134
NPH007 Nephrogenic Diabetes Insipidus 65 0.073
135
HRP004 Herpes Zoster 60 0.073
136
P HRP006 Herpes Simplex 57 0.073
137
P DBT005 Diabetes Insipidus 56 0.073
138
c HYP076 Hyperthyroidism 55 0.073
139
ART001 Arterial Tortuosity Syndrome 52 0.073
140
CNV002 Conversion Disorder 48 0.073
141
P BRG005 Brugada Syndrome 1 45 0.073
142
SPS057 Spasticity 42 0.073
143
DYS073 Dysphagia 42 0.073
144
SPN015 Spinal Polio 19 0.073
145
P HMP004 Hemophilia B 66 0.067
146
RLP001 Relapsing Polychondritis 66 0.067
147
c MNN013 Meningitis 62 0.067
148
ADR008 Adrenal Adenoma 57 0.067
149
GTL001 Gitelman Syndrome 54 0.067
150
GLL031 Guillain-Barr� Syndrome 54 0.067
151
STT002 Status Asthmaticus 52 0.067
152
CHL069 Cholesteatoma 52 0.067
153
EVN001 Evans' Syndrome 50 0.067
154
WST005 West Nile Virus 46 0.067
155
c MLG086 Malignant Hyperthermia Susceptibility 41 0.067
156
ECT005 Ectropion 39 0.067
157
P MLG090 Malignant Hyperthermia Susceptibility Type 1 34 0.067
158
PRL013 Paralytic Poliomyelitis 27 0.067
159
PRX020 Proximal Renal Tubular Acidosis with Ocular Abnormalities 26 0.067
160
P HYP075 Hypertension 76 0.062
161
P HPT001 Hepatitis C 66 0.062
162
LYM017 Lyme Disease 62 0.062
163
PTN002 Patent Ductus Arteriosus 61 0.062
164
P CHR071 Charcot-Marie-Tooth Disease 61 0.062
165
HYP014 Hyperuricemia 58 0.062
166
PTT006 Pituitary Adenoma 56 0.062
167
SNS001 Sensorineural Hearing Loss 55 0.062
168
P PLY019 Polyneuropathy 54 0.062
169
TTH006 Tooth Disease 54 0.062
170
P DNT039 Dent's Disease 52 0.062
171
c HYP065 Hyperaldosteronism 50 0.062
172
PRP023 Peripheral Neuropathy 46 0.062
173
NRT004 Neuritis 46 0.062
174
PRT026 Parotitis 45 0.062
175
ALT001 Alternating Hemiplegia of Childhood 40 0.062
176
c BRT034 Bartter Syndrome, Type 2 34 0.062
177
HYP264 Hypertonia 34 0.062
178
RMS005 Ramsay-Hunt Syndrome 30 0.062
179
PRM050 Primary Orthostatic Tremor 23 0.062
180
PST048 Postural Orthostatic Tachycardia Syndrome 21 0.062
181
PRS033 Parasitic Ectoparasitic Infectious Disease 9 0.062
182
TBR010 Tuberculosis 82 0.055
183
P MLT020 Multiple Sclerosis 75 0.055
184
BRN024 Bronchitis 71 0.055
185
AGR001 Age Related Macular Degeneration 71 0.055
186
HPT023 Hepatocellular Carcinoma 69 0.055
187
P NRC002 Narcolepsy 67 0.055
188
P INF038 Influenza 63 0.055
189
ART016 Aortic Aneurysm 62 0.055
190
BRN029 Brain Disease 60 0.055
191
c HYP086 Hypothyroidism 59 0.055
192
c HPT003 Hepatitis a 57 0.055
193
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.055
194
P GTR002 Goiter 55 0.055
195
c SBC007 Subacute Thyroiditis 55 0.055
196
SPN020 Spondylosis 53 0.055
197
P SYR001 Syringomyelia 52 0.055
198
MYL001 Myelitis 51 0.055
199
c MNT147 Mental Retardation 51 0.055
200
c TRM003 Tremor 50 0.055
201
LPC002 Lip Cancer 50 0.055
202
SJG001 Sjogren's Syndrome 50 0.055
203
P PND001 Pain Disorder 49 0.055
204
P THR090 Thrombocythemia 1 48 0.055
205
P NRM005 Neuromuscular Disease 48 0.055
206
HMP005 Hemiplegia 47 0.055
207
P AML002 Amelogenesis Imperfecta 47 0.055
208
KRT012 Keratoderma 44 0.055
209
MLL002 Miller Fisher Syndrome 41 0.055
210
ETH009 Ethmoid Sinusitis 40 0.055
211
HYP030 Hypoactive Sexual Desire Disorder 39 0.055
212
SPR007 Superior Mesenteric Artery Syndrome 35 0.055
213
WND001 Wound Botulism 35 0.055
214
LCK001 Locked-in Syndrome 33 0.055
215
TRP004 Tropical Sprue 33 0.055
216
FTD001 Foot Drop 30 0.055
217
HVD003 Hiv/aids 27 0.055
218
BRW004 Brown-Sequard Syndrome 27 0.055
219
LGP001 Lagophthalmos 26 0.055
220
FCL044 Fecal Incontinence 26 0.055
221
NNS006 Non-Suppurative Otitis Media 24 0.055
222
CNG101 Congenital Human Immunodeficiency Virus 24 0.055
223
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.055
224
BLB003 Bulbar Polio 21 0.055
225
P HYP078 Hypertrophy of Breast 20 0.055
226
PRT015 Partial Third-Nerve Palsy 19 0.055
227
PLM108 Pulmonary Interstitial Glycogenosis 18 0.055
228
P AML040 Amelogenesis Imperfecta, Hypoplastic/hypomaturation Type 1e 17 0.055
229
PRS053 Parsonage Turner Syndrome 17 0.055
230
FBR024 Fibrocartilaginous Embolism 12 0.055
231
PRM152 Primary Renal Tubular Acidosis 12 0.055
232
P AMY001 Amyotrophic Lateral Sclerosis 87 0.048
233
P SYS001 Systemic Lupus Erythematosus 83 0.048
234
P TRN020 Turner Syndrome 71 0.048
235
LKM002 Leukemia 70 0.048
236
c DBT009 Diabetes Mellitus 68 0.048
237
P MLR004 Malaria 66 0.048
238
c LPS004 Lupus Erythematosus 65 0.048
239
STT001 Status Epilepticus 64 0.048
240
P MLT021 Multiple System Atrophy 64 0.048
241
SPN186 Spinal Cord Injury 63 0.048
242
GLC003 Glucose Intolerance 62 0.048
243
c ENC004 Encephalitis 56 0.048
244
GYN001 Gynecomastia 56 0.048
245
MTR014 Motor Neuron Disease 56 0.048
246
SLP005 Sleep Disorder 54 0.048
247
c THR003 Thoracic Aortic Aneurysm 54 0.048
248
c MSC005 Muscular Dystrophy 54 0.048
249
YLL002 Yellow Fever 53 0.048
250
P EPL002 Epilepsy Syndrome 52 0.048
251
P MMB001 Membranoproliferative Glomerulonephritis 52 0.048
252
P ATN005 Autonomic Dysfunction 52 0.048
253
P FNC004 Fanconi Syndrome 52 0.048
254
RBS001 Rabies 51 0.048
255
LPT001 Leptospirosis 50 0.048
256
NRN002 Neuronitis 47 0.048
257
AXN001 Axonal Neuropathy 44 0.048
258
THY035 Thyroid Adenoma 44 0.048
259
WST004 West Nile Encephalitis 43 0.048
260
RCR001 Recurrent Corneal Erosion 43 0.048
261
QDR001 Quadriplegia 42 0.048
262
CRT008 Carotid Artery Dissection 41 0.048
263
P CRV039 Cervicitis 41 0.048
264
TLR001 Tularemia 40 0.048
265
RLP003 Relapsing Fever 40 0.048
266
TRY002 Troyer Syndrome 40 0.048
267
CHL079 Children's Interstitial Lung Disease 39 0.048
268
ENT001 Enterocele 39 0.048
269
c CHR455 Chiari Malformations 38 0.048
270
SPN185 Spinal Cord Infarction 37 0.048
271
SPP008 Suppurative Otitis Media 37 0.048
272
LRY029 Laryngomalacia 36 0.048
273
TBS001 Tabes Dorsalis 33 0.048
274
MTR001 Mature Cataract 32 0.048
275
TLS001 Tolosa-Hunt Syndrome 32 0.048
276
ADS002 Adie Syndrome 32 0.048
277
CLR007 Colorado Tick Fever 32 0.048
278
P OTT001 Otitis Externa 31 0.048
279
P VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 31 0.048
280
GNC003 Geniculate Herpes Zoster 31 0.048
281
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 27 0.048
282
ANT054 Anotia 23 0.048
283
MYS010 Myostatin-Related Muscle Hypertrophy 19 0.048
284
c PRM041 Primary Cortisol Resistance 19 0.048
285
OTP003 Oto-Palatal-Digital Syndrome 13 0.048
286
MYP026 Myopathy - Thyrotoxic 11 0.048
287
CRH001 Crohn's Disease 78 0.039
288
P BPL003 Bipolar Disorder 76 0.039
289
OLV001 Olivopontocerebellar Atrophy 70 0.039
290
P PNM007 Pneumonia 67 0.039
291
P LPR003 Leprosy 67 0.039
292
P BRD002 Bardet-Biedl Syndrome 67 0.039
293
P AMY004 Amyloidosis 65 0.039
294
P ART023 Arthropathy 65 0.039
295
SPN038 Spina Bifida 63 0.039
296
P PRG006 Progressive Supranuclear Palsy 63 0.039
297
PLY017 Polyarteritis Nodosa 62 0.039
298
PSY004 Psychotic Disorder 62 0.039
299
HMN010 Hemangioma 62 0.039
300
c SPN046 Spinal Muscular Atrophy 60 0.039
301
P NRB001 Neuroblastoma 60 0.039
302
P GLM007 Glomerulonephritis 60 0.039
303
HML002 Hemolytic Anemia 60 0.039
304
WLF001 Wolff-Parkinson-White Syndrome 60 0.039
305
c HPT015 Hepatitis D 59 0.039
306
c TXP001 Toxoplasmosis 59 0.039
307
HDC001 Headache 58 0.039
308
PHR003 Pharyngitis 57 0.039
309
ANR008 Aneurysm Disease 57 0.039
310
c PRP029 Porphyria 56 0.039
311
OST011 Osteomalacia 56 0.039
312
P MLN008 Melanoma 56 0.039
313
ASP003 Aseptic Meningitis 56 0.039
314
PLS006 Plasmodium Vivax Malaria 56 0.039
315
ATM010 Autoimmune Hemolytic Anemia 55 0.039
316
c EHL001 Ehlers-Danlos Syndrome 55 0.039
317
HRD010 Hereditary Spastic Paraplegia 54 0.039
318
P FML001 Familial Atrial Fibrillation 54 0.039
319
SRC014 Sarcoma 54 0.039
320
c BLN003 Blindness 54 0.039
321
GST037 Gastroparesis 54 0.039
322
BBS001 Babesiosis 54 0.039
323
NWC001 Newcastle Disease 53 0.039
324
HYP003 Hypermethioninemia 52 0.039
325
CLD007 Cold Agglutinin Disease 52 0.039
326
CNN003 Conn's Syndrome 52 0.039
327
NPH003 Nephrocalcinosis 52 0.039
328
FBR047 Fibromyalgia 52 0.039
329
JPN002 Japanese Encephalitis 51 0.039
330
P HYP097 Hyperekplexia 51 0.039
331
SPT005 Spotted Fever 51 0.039
332
P MYC008 Myocarditis 51 0.039
333
P PNM006 Pneumoconiosis 50 0.039
334
TCK001 Tick-Borne Encephalitis 50 0.039
335
ADL002 Adult Syndrome 50 0.039
336
MNN009 Meningoencephalitis 49 0.039
337
P PRT029 Parathyroid Adenoma 49 0.039
338
NRL005 Neurilemmoma 49 0.039
339
P LCT002 Lactose Intolerance 49 0.039
340
c PRG013 Paraganglioma 49 0.039
341
MDS022 Mediastinitis 49 0.039
342
ENC006 Encephalomyelitis 49 0.039
343
P NML001 Nemaline Myopathy 48 0.039
344
P CNG021 Congenital Toxoplasmosis 48 0.039
345
c CTR002 Cataract 48 0.039
346
THY009 Thyroid Lymphoma 48 0.039
347
P LBY004 Labyrinthitis 47 0.039
348
MYC033 Myoclonus 47 0.039
349
P HYP141 Hyperphenylalaninemia 47 0.039
350
ILS001 Ileus 47 0.039
351
GLM008 Glomus Tumor 46 0.039
352
EHR002 Ehrlichiosis 46 0.039
353
AMB002 Amblyopia 46 0.039
354
GST045 Gastroenteritis 46 0.039
355
P CHR095 Chronic Progressive External Ophthalmoplegia 46 0.039
356
c MLT008 Multinodular Goiter 46 0.039
357
c ACR001 Aicardi-Goutieres Syndrome 46 0.039
358
FSC004 Fasciitis 44 0.039
359
c PSD020 Pseudohypoaldosteronism Type Ii 43 0.039
360
HV1006 Hiv-1 42 0.039
361
c OPT004 Optic Atrophy 41 0.039
362
CNT025 Central Pontine Myelinolysis 40 0.039
363
P MYK002 Myokymia 40 0.039
364
EPD005 Epidural Abscess 39 0.039
365
THY043 Thymic Hyperplasia 38 0.039
366
PLM029 Palmoplantar Keratosis 38 0.039
367
P HRD086 Hereditary Hypophosphatemic Rickets 38 0.039
368
STL001 St. Louis Encephalitis 37 0.039
369
RCK002 Rocky Mountain Spotted Fever 37 0.039
370
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.039
371
THM001 Thomsen Disease 37 0.039
372
OP3001 Opa3-Related 3-Methylglutaconic Aciduria 36 0.039
373
c NRC009 Narcolepsy 1 36 0.039
374
HRT015 Heritable Pulmonary Arterial Hypertension 35 0.039
375
VRL011 Viral Infectious Disease 35 0.039
376
EMN001 Emanuel Syndrome 34 0.039
377
P HYD001 Hydranencephaly 34 0.039
378
DYS036 Dysequilibrium Syndrome 32 0.039
379
P HMR005 Hemorrhoid 32 0.039
380
PRS063 Paresthesia 32 0.039
381
ENT005 Entropion 30 0.039
382
c SPN091 Spinal Muscular Atrophy with Respiratory Distress 1 30 0.039
383
P SLP004 Salpingo-Oophoritis 30 0.039
384
P SPS092 Spastic Paraplegia 11 29 0.039
385
LCR004 La Crosse Encephalitis 29 0.039
386
c OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 29 0.039
387
SPS016 Spasmodic Dysphonia 28 0.039
388
BRC010 Brachial Plexus Lesion 28 0.039
389
CVR002 Cavernous Sinus Thrombosis 27 0.039
390
TCK004 Tick Infestation 27 0.039
391
c FML249 Familial Amyloidosis, Finnish Type 27 0.039
392
c HMP017 Hemophilia a, Congenital 26 0.039
393
RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 25 0.039
394
CBB002 Cobb Syndrome 24 0.039
395
STR002 Streptococcal Meningitis 23 0.039
396
LRY017 Laryngeal Disease 22 0.039
397
BRW001 Brown-Vialetto-Van Laere Syndrome 21 0.039
398
FDB001 Foodborne Botulism 19 0.039
399
ACT181 Acute Motor Axonal Neuropathy 19 0.039
400
CNT067 Central Cord Syndrome 17 0.039
401
ABD009 Abducens Palsy 17 0.039
402
PNT023 Pontine Hemorrhage 17 0.039
403
PWS001 Powassan Encephalitis 16 0.039
404
P CHR160 Chiari Malformation Type 2 16 0.039
405
MNN005 Meningovascular Neurosyphilis 16 0.039
406
P ISC010 Isochromosome Yp 14 0.039
407
SYR004 Syringobulbia 14 0.039
408
c MLG042 Malignant Otitis Externa 14 0.039
409
DPH021 Diaphragm Disease 14 0.039
410
SPN092 Spinal Shock 13 0.039
411
FCL011 Facial Nerve Disease 12 0.039
412
ERB002 Erb's Palsy 9 0.039
413
SKL006 Skull Base Neoplasm 8 0.039
414
BLB001 Bulbospinal Polio 8 0.039
415
BRC057 Brachial Plexus Birth Injuries 6 0.039
416
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.039
417
HMP020 Hemiplegia Alterans 1 0.039
418
P BRS047 Breast Cancer 85 0.028
419
CDS001 Cadasil 80 0.028
420
P WSK001 Wiskott-Aldrich Syndrome 76 0.028
421
P MLT019 Multiple Myeloma 76 0.028
422
MTC003 Metachromatic Leukodystrophy 75 0.028
423
P DLT002 Dilated Cardiomyopathy 74 0.028
424
P FML018 Familial Mediterranean Fever 73 0.028
425
P OST002 Osteoporosis 73 0.028
426
P CLC005 Celiac Disease 71 0.028
427
NRL016 Neural Tube Defects 69 0.028
428
ACT074 Acute Lymphocytic Leukemia 69 0.028
429
HYP004 Hypercalcemia 69 0.028
430
STR067 Stroke, Ischemic 69 0.028
431
P MYL005 Myelofibrosis 67 0.028
432
SPS077 Sepsis 67 0.028
433
P WGN002 Wegener's Granulomatosis 67 0.028
434
P ATM003 Autoimmune Thyroiditis 66 0.028
435
ACT033 Acute Intermittent Porphyria 66 0.028
436
INF030 Infectious Mononucleosis 65 0.028
437
P ABD003 Abdominal Aortic Aneurysm 65 0.028
438
c XRD001 Xeroderma Pigmentosum 65 0.028
439
P ALX003 Alexander Disease 64 0.028
440
P THY023 Thymoma 63 0.028
441
DSM004 Desmoid Tumor 63 0.028
442
CCC001 Coccidioidomycosis 63 0.028
443
MNT001 Mantle Cell Lymphoma 63 0.028
444
P HYP117 Hypertriglyceridemia 63 0.028
445
ACT073 Acute Leukemia 62 0.028
446
SML001 Small Cell Carcinoma 62 0.028
447
MSL001 Measles 62 0.028
448
ART005 Arteriovenous Malformation 62 0.028
449
HMP002 Hemophagocytic Lymphohistiocytosis 62 0.028
450
P MGR002 Migraine 61 0.028
451
MYS005 Myositis 61 0.028
452
P BLR001 Biliary Atresia 60 0.028
453
CFF002 Coffin-Lowry Syndrome 60 0.028
454
PMP001 Pemphigus 60 0.028
455
P PRN023 Prion Disease 60 0.028
456
c SRC013 Sarcoidosis 60 0.028
457
PLM033 Pulmonary Embolism 60 0.028
458
TYP007 Typhoid Fever 60 0.028
459
P MCH002 Machado-Joseph Disease 59 0.028
460
TRG002 Trigeminal Neuralgia 59 0.028
461
SQM006 Squamous Cell Carcinoma 58 0.028
462
FTT001 Fatty Liver Disease 58 0.028
463
P TYS001 Tay-Sachs Disease 58 0.028
464
P NRM001 Neuromyelitis Optica 58 0.028
465
CNT009 Central Core Myopathy 58 0.028
466
P MJR001 Major Depressive Disorder 58 0.028
467
CRB021 Cerebral Malaria 58 0.028
468
MLT074 Multiple Endocrine Neoplasia 58 0.028
469
SMT015 Smith Magenis Syndrome 58 0.028
470
GST009 Gastroschisis 58 0.028
471
CRB042 Cerebellar Ataxia 57 0.028
472
ISC004 Ischemia 57 0.028
473
INT051 Intussusception 57 0.028
474
P CMR001 Camurati-Engelmann Disease 57 0.028
475
P HYP024 Hypoparathyroidism 57 0.028
476
CMP002 Campylobacteriosis 56 0.028
477
P LGH001 Leigh Disease 56 0.028
478
P OLG002 Oligodendroglioma 56 0.028
479
STS002 Situs Inversus 56 0.028
480
PTN001 Patent Foramen Ovale 56 0.028
481
KRT004 Keratitis 56 0.028
482
P FBR017 Fibrosarcoma 56 0.028
483
P MMP001 Mumps 56 0.028
484
ALP004 Alport Syndrome 55 0.028
485
c BRG001 Brugada Syndrome 55 0.028
486
CHR072 Chordoma 55 0.028
487
P CNJ013 Conjunctivitis 55 0.028
488
KDS001 Kid Syndrome 55 0.028
489
c HYP060 Hyperinsulinism 55 0.028
490
NPH051 Nephritis 55 0.028
491
TRN015 Transient Cerebral Ischemia 55 0.028
492
STF001 Stiff-Person Syndrome 55 0.028
493
P INT030 Intracranial Aneurysm 55 0.028
494
c SYP003 Syphilis 55 0.028
495
LRN003 Learning Disability 54 0.028
496
ESP020 Esophageal Atresia 54 0.028
497
c WRD001 Waardenburg's Syndrome 54 0.028
498
HNT002 Hantavirus Pulmonary Syndrome 54 0.028
499
KRN002 Kearns-Sayre Syndrome 53 0.028
500
P LNG044 Long Qt Syndrome 1 53 0.028
501
VRG001 Variegate Porphyria 53 0.028
502
c MLG069 Malignant Hypertension 53 0.028
503
c MYL007 Myeloma 53 0.028
504
ANR004 Anuria 53 0.028
505
P MYT006 Myotonic Dystrophy Type 1 53 0.028
506
P MYM002 Moyamoya Disease 52 0.028
507
c KDN018 Kidney Disease 52 0.028
508
c ATN004 Autonomic Neuropathy 52 0.028
509
P GNT008 Giant Cell Tumor 52 0.028
510
c CNT035 Central Nervous System Disease 52 0.028
511
PRN011 Pernicious Anemia 52 0.028
512
P EXP004 Exophthalmos 51 0.028
513
c SPN049 Spinocerebellar Ataxia 51 0.028
514
P ESP024 Esophagitis 51 0.028
515
HYP006 Hypertensive Heart Disease 51 0.028
516
FBR009 Fibrous Dysplasia 51 0.028
517
P PRP025 Peripheral Primitive Neuroectodermal Tumor 51 0.028
518
ANK001 Ankylosis 51 0.028
519
BRN016 Bronchogenic Carcinoma 51 0.028
520
HJD001 Hajdu-Cheney Syndrome 50 0.028
521
LYM021 Lymphadenitis 50 0.028
522
RNL011 Renal Osteodystrophy 50 0.028
523
CYS016 Cystic Kidney 50 0.028
524
HMM003 Hemimegalencephaly 50 0.028
525
c XRD014 Xeroderma Pigmentosum, Group G 50 0.028
526
c EPS003 Episodic Ataxia 50 0.028
527
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 50 0.028
528
PLM010 Pulmonary Edema 50 0.028
529
PRM027 Primitive Neuroectodermal Tumor 50 0.028
530
KRT009 Keratosis 49 0.028
531
PLS016 Plasma Cell Leukemia 49 0.028
532
EXS001 Exostosis 49 0.028
533
c GLY013 Glycogen Storage Disease 49 0.028
534
c XRD019 Xeroderma Pigmentosum, Group C 49 0.028
535
P HRD021 Hereditary Sensory Neuropathy 49 0.028
536
APH002 Aphasia 49 0.028
537
MYX004 Myxedema 49 0.028
538
PRC013 Pericarditis 48 0.028
539
c FML023 Familial Hemiplegic Migraine 48 0.028
540
P KLP003 Klippel-Feil Syndrome 48 0.028
541
PNM008 Pneumothorax 48 0.028
542
RHB003 Rhabdomyosarcoma 48 0.028
543
c MTR012 Mitral Valve Disease 48 0.028
544
c ACT078 Acute Porphyria 48 0.028
545
P BRT004 Bartter Disease 48 0.028
546
CVR006 Cavernous Hemangioma 47 0.028
547
STR039 Sturge-Weber Syndrome 47 0.028
548
P CRB126 Cerebral Cavernous Malformation 47 0.028
549
SYN006 Synovial Sarcoma 47 0.028
550
SCH018 Schizencephaly 47 0.028
551
c GLY007 Glycogen Storage Disease Iv 47 0.028
552
PLG002 Plague 46 0.028
553
MCP006 Mucoepidermoid Carcinoma 46 0.028
554
OPT009 Optic Neuritis 46 0.028
555
c INT070 Intestinal Obstruction 46 0.028
556
P VRL012 Viral Meningitis 46 0.028
557
LMB052 Lumbar Disc Herniation 46 0.028
558
P FCS001 Facioscapulohumeral Muscular Dystrophy 46 0.028
559
NRX001 Neuroaxonal Dystrophy 46 0.028
560
c RSM001 Rasmussen Encephalitis 46 0.028
561
CRN012 Craniometaphyseal Dysplasia 46 0.028
562
c DMY001 Demyelinating Polyneuropathy 45 0.028
563
MDL009 Medullary Sponge Kidney 45 0.028
564
MTH009 Mouth Disease 45 0.028
565
CHK001 Chikungunya 44 0.028
566
PTR001 Petrositis 44 0.028
567
c HMP006 Hemiplegic Migraine 44 0.028
568
TRC040 Tracheoesophageal Fistula 44 0.028
569
c SPN183 Spontaneous Pneumothorax 44 0.028
570
HYP265 Hypotonia 43 0.028
571
TRC023 Trichinosis 43 0.028
572
c HPT073 Hepatitis C Virus 43 0.028
573
ASP007 Aspiration Pneumonia 43 0.028
574
P MLT075 Multifocal Motor Neuropathy 43 0.028
575
ANG002 Angiostrongyliasis 42 0.028
576
PST055 Postural Hypotension 42 0.028
577
HRD030 Hereditary Neuralgic Amyotrophy 42 0.028
578
HYP120 Hypoaldosteronism 42 0.028
579
MYS001 Myositis Ossificans 42 0.028
580
APL006 Aplasia Cutis Congenita 41 0.028
581
SCT002 Scotoma 41 0.028
582
MGL013 Megalencephaly 41 0.028
583
BRS064 Bursitis 41 0.028
584
SPN050 Spinocerebellar Degeneration 41 0.028
585
NRL007 Neurologic Diseases 41 0.028
586
PRS062 Persistent Hyperplastic Primary Vitreous 41 0.028
587
NCR007 Necrotizing Fasciitis 40 0.028
588
RPT002 Ruptured Abdominal Aortic Aneurysm 40 0.028
589
P TRN034 Transverse Myelitis 40 0.028
590
INT052 Intestinal Volvulus 40 0.028
591
SZR006 Seizure Disorder 40 0.028
592
SCH016 Schimke Immunoosseous Dysplasia 40 0.028
593
BNC001 Bone Carcinoma 39 0.028
594
CDQ001 Cauda Equina Syndrome 39 0.028
595
c ATS010 Autosomal Recessive Disease 39 0.028
596
HTS001 Hiatus Hernia 39 0.028
597
P FML043 Familial Idiopathic Basal Ganglia Calcification 38 0.028
598
SPN044 Spinal Cord Ischemia 38 0.028
599
P MNN007 Meningocele 38 0.028
600
SPC005 Speech Disorder 38 0.028
601
NM001 Noma 37 0.028
602
CRB091 Cerebro-Oculo-Facio-Skeletal Syndrome 37 0.028
603
ACT012 Acute Hemorrhagic Conjunctivitis 37 0.028
604
c MYT007 Myotonic Dystrophy Type 2 36 0.028
605
HYP539 Hyperekplexia, Hereditary 1, Autosomal Dominant or Recessive 36 0.028
606
TTR016 Tetra-Amelia Syndrome 36 0.028
607
ENC017 Encephaloceles 36 0.028
608
MRR003 Murray Valley Encephalitis 35 0.028
609
LMB010 Lambert Syndrome 35 0.028
610
OST006 Osteoblastoma 35 0.028
611
PST020 Postpoliomyelitis Syndrome 35 0.028
612
PNM005 Pneumonic Plague 34 0.028
613
SCR015 Scarlet Fever 34 0.028
614
XRP001 Xerophthalmia 34 0.028
615
c HYP324 Hypothyroidism, Autoimmune 34 0.028
616
SNS003 Sensory Peripheral Neuropathy 33 0.028
617
EST005 Esotropia 33 0.028
618
CSL001 Causalgia 33 0.028
619
DYG002 Dyggve-Melchior-Clausen Syndrome 32 0.028
620
AMY005 Amyloid Neuropathy 32 0.028
621
HNS001 Hansen's Disease 32 0.028
622
FCL003 Facial Hemiatrophy 31 0.028
623
HYP362 Hyperopia 31 0.028
624
P GLM006 Glomangioma 31 0.028
625
HYP034 Hypertensive Encephalopathy 30 0.028
626
c SNS011 Sinus Cancer 30 0.028
627
FRY001 Frey Syndrome 29 0.028
628
PMP008 Pemphigus Vegetans 29 0.028
629
ECT004 Ecthyma 29 0.028
630
ANT018 Anthracosis 28 0.028
631
ANT013 Anterior Spinal Artery Syndrome 28 0.028
632
LRN001 Laurence-Moon Syndrome 28 0.028
633
MTC018 Metachondromatosis 27 0.028
634
INT042 Internuclear Ophthalmoplegia 27 0.028
635
PRR008 Periarteritis Nodosa 27 0.028
636
GNT005 Giant Hemangioma 27 0.028
637
PRX014 Proximal Spinal Muscular Atrophy 27 0.028
638
NNT021 Neonatal Meningitis 26 0.028
639
RGD001 Rigid Spine Syndrome 26 0.028
640
c FRT001 Fourth Cranial Nerve Palsy 26 0.028
641
VST004 Vestibular Disease 26 0.028
642
PRT009 Parotid Gland Cancer 25 0.028
643
BLT011 Bilateral Perisylvian Polymicrogyria 25 0.028
644
CRV030 Cervical Adenitis 25 0.028
645
NNP003 Nonepidermolytic Palmoplantar Keratoderma 25 0.028
646
HV1005 Hiv-1 Viremia 25 0.028
647
FBR028 Fibrosing Mediastinitis 25 0.028
648
PSD029 Pseudocholinesterase Deficiency 25 0.028
649
c CNG112 Congenital Muscular Dystrophy Type 1a 24 0.028
650
DSR005 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase 24 0.028
651
NRS003 Neurosyphilis 24 0.028
652
MYC014 Mycobacterium Chelonae 24 0.028
653
c ACT159 Acute Transverse Myelitis 23 0.028
654
c SPS027 Spastic Paraplegia 17 23 0.028
655
WYB001 Wyburn Mason's Syndrome 22 0.028
656
RPT003 Ruptured Aortic Aneurysm 22 0.028
657
VST003 Vestibular Nystagmus 22 0.028
658
DYS013 Dysbaric Osteonecrosis 22 0.028
659
HYP048 Hypotropia 22 0.028
660
LTR002 Lateral Sinus Thrombosis 21 0.028
661
PRN016 Peroneal Neuropathy 21 0.028
662
GNT004 Gnathomiasis 21 0.028
663
EXP002 Exposure Keratitis 21 0.028
664
c SPS079 Spastic Paraplegia 2 21 0.028
665
HYP047 Hypertropia 21 0.028
666
SBS002 Substernal Goiter 21 0.028
667
c ACT067 Acute Conjunctivitis 20 0.028
668
c SPS078 Spastic Paraplegia 7 20 0.028
669
CRT009 Critical Illness Polyneuropathy 20 0.028
670
c SPS091 Spastic Paraplegia 4 20 0.028
671
SWL001 Swallowing Disorders 20 0.028
672
ATR055 Atrial Septal Aneurysm 20 0.028
673
TMP006 Temporomandibular Ankylosis 19 0.028
674
ETH012 Ethylene Glycol Poisoning 19 0.028
675
c CHR454 Chiari Malformation Type 1 19 0.028
676
LRY007 Laryngeal Tuberculosis 19 0.028
677
c CHR094 Chronic Polyneuropathy 18 0.028
678
c KRN003 Kernicterus Due to Isoimmunization 18 0.028
679
c AMY008 Amyotrophic Lateral Sclerosis Type 2 18 0.028
680
CNG133 Congenital Varicella Syndrome 18 0.028
681
LPN001 Louping Ill 18 0.028
682
c SPS013 Spastic Paraplegia 8 18 0.028
683
PRP013 Paraphimosis 17 0.028
684
GLM016 Glomus Jugulare Tumors 17 0.028
685
MLN002 Melanomatosis 17 0.028
686
FCL007 Facial Neuralgia 16 0.028
687
DRS001 Dressler's Syndrome 16 0.028
688
c CNG129 Congenital Torticollis 16 0.028
689
CNR001 Coenurosis 15 0.028
690
INT095 Internal Carotid Agenesis 15 0.028
691
HTR005 Heterochromia Iridis 15 0.028
692
CLV002 Clivus Chordoma 15 0.028
693
MNR004 Mounier-Kuhn Syndrome 14 0.028
694
c DST048 Distal Hereditary Motor Neuropathy Type 1 14 0.028
695
ATY001 Atypical Depressive Disorder 14 0.028
696
c CNG333 Congenital Horner Syndrome 14 0.028
697
MNS002 Mini Stroke 14 0.028
698
c VRL004 Viral Labyrinthitis 14 0.028
699
PNT009 Pontine Tegmental Cap Dysplasia 14 0.028
700
TRG006 Trigger Thumb 13 0.028
701
MTR013 Motor Neuritis 12 0.028
702
MLL006 Mollaret Meningitis 12 0.028
703
FHR002 Fahr's Syndrome 12 0.028
704
BDR001 Bidirectional Tachycardia 11 0.028
705
BMF002 Bamforth Syndrome 11 0.028
706
SPN007 Spinal Cord Oligodendroglioma 11 0.028
707
CHL090 Cholesterol Desmolase-Deficient Congenital Adrenal Hyperplasia 10 0.028
708
c ADL068 Adult-Onset Nemaline Myopathy 10 0.028
709
UVP001 Uveoparotid Fever 9 0.028
710
INF052 Infantile Scoliosis 8 0.028
711
GNT013 Genetic Brain Disorders 8 0.028
712
CNM001 Canomad Syndrome 8 0.028
713
JMP002 Jumping Frenchmen of Maine 7 0.028
714
c CHR161 Chiari Malformation Type 3 6 0.028
715
SYM001 Sympathetic Neurilemmoma 6 0.028
716
c AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 4 0.028
717
KNG003 Konigsmark Knox Hussels Syndrome 4 0.028