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

739 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
c HYP051 Hypokalemic Periodic Paralysis 56 7.335
2
c HYP052 Hyperkalemic Periodic Paralysis 41 5.479
3
INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 31 5.096
4
NRM009 Normokalemic Periodic Paralysis 20 4.706
5
FCL012 Facial Paralysis 49 4.080
6
P HYP239 Hyperkalemic Periodic Paralysis Type 2 34 3.976
7
AND003 Andersen-Tawil Syndrome 43 3.906
8
P HYP254 Hypokalemic Periodic Paralysis Type 1 35 3.593
9
KRT022 Keratoderma Palmoplantar Spastic Paralysis 16 3.569
10
TCK002 Tick Paralysis 23 3.472
11
OCL003 Oculomotor Nerve Paralysis 18 3.361
12
P THY084 Thyrotoxic Periodic Paralysis 1 21 3.311
13
c THY054 Thyrotoxic Periodic Paralysis 31 3.028
14
c HYP255 Hypokalemic Periodic Paralysis Type 2 26 2.991
15
PRN008 Peroneal Nerve Paralysis 18 2.991
16
c HYP142 Hyperkalemic Periodic Paralysis Type 1 12 2.907
17
TCK005 Tucker Syndrome 13 2.882
18
PRM028 Paramyotonia Congenita 41 2.626
19
KLM001 Klumpke Paralysis 9 2.605
20
VCL002 Vocal Cord Dysfunction Familial 19 2.590
21
GLS003 Glossopharyngeal Nerve Paralysis 7 2.546
22
FML082 Familial Partial Paralysis 2 2.523
23
P HRD130 Hereditary Congenital Facial Paresis 3 22 2.496
24
LRY036 Laryngeal Abductor Paralysis - Intellectual Deficit 12 2.496
25
ISL060 Isolated Hereditary Congenital Facial Paralysis 9 2.496
26
PLM031 Poliomyelitis 58 2.359
27
BLL003 Bell's Palsy 56 2.300
28
P MBS002 Moebius Syndrome 42 2.221
29
P PRK002 Parkinson's Disease 92 2.141
30
TDD001 Todd's Paralysis 4 2.141
31
LRY023 Laryngeal Abductor Paralysis Mental Retardation 1 2.055
32
c THY083 Thyrotoxic Periodic Paralysis 2 8 2.038
33
FML160 Familial Spastic Paralysis 6 2.038
34
LRY021 Laryngeal Adductor Paralysis 4 2.038
35
VNN001 Venencie Powell Gordon Winkelmann Syndrome 4 2.038
36
PRL020 Paralysis Agitans, Juvenile, of Hunt 1 2.038
37
P PRD017 Periodic Paralyses 20 1.540
38
P HYP035 Hypophosphatasia 73 1.530
39
HYP143 Hypomyelination and Congenital Cataract 41 1.530
40
c FML159 Familial Periodic Paralyses 7 1.530
41
c OPH004 Ophthalmoplegia 52 1.520
42
P HRN001 Horner's Syndrome 40 1.495
43
ABD002 Abducens Nerve Disease 23 1.495
44
c CRN035 Cranial Nerve Palsy 41 1.481
45
FZL001 Fazio Londe Syndrome 16 1.481
46
THR010 Third Cranial Nerve Disease 12 1.481
47
PRL008 Paralytic Ileus 39 1.464
48
PSD001 Pseudobulbar Palsy 29 1.464
49
CYC001 Cycloplegia 28 1.464
50
CNG241 Congenital Laryngeal Palsy 7 1.464
51
TRP002 Tropical Spastic Paraparesis 67 1.441
52
SPS003 Spastic Diplegia 36 1.441
53
P HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 32 1.441
54
MRK002 Marek Disease 31 1.441
55
MBS001 Mobius Syndrome 30 1.441
56
P NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 18 1.441
57
SDD005 Sudden Cardiac Death Multi-Gene Panels 21 0.235
58
ANK002 Ankylosing Spondylitis 75 0.210
59
c PPL025 Popliteal Pterygium Syndrome 24 0.210
60
THR013 Thoracic Outlet Syndrome 54 0.186
61
IDP042 Idiopathic Recurrent Stupor 15 0.175
62
P RNL007 Renal Tubular Acidosis 58 0.173
63
CHR153 Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant 23 0.167
64
THY033 Thyrotoxicosis 58 0.146
65
P RSP003 Respiratory Failure 70 0.138
66
P LRY019 Laryngitis 62 0.138
67
HYP005 Hypokalemia 50 0.138
68
P ATX002 Ataxia Telangiectasia 93 0.133
69
ACN002 Acanthosis Nigricans 73 0.127
70
P MYP004 Myopathy 58 0.127
71
c CRD152 Cardiomyopathy, Familial Hypertrophic, 21 17 0.124
72
c LCL006 Localized Scleroderma 68 0.121
73
c THY032 Thyroiditis 67 0.121
74
c RNL045 Renal Tubular Acidosis, Distal 23 0.121
75
NRP001 Neuropathy 61 0.115
76
MYC002 Mycobacterium Avium Complex Disease 57 0.115
77
SYN053 Syndromic Diarrhea 42 0.115
78
ERL004 Early Yaws 33 0.115
79
c SPS036 Spastic Paraplegia 3 23 0.115
80
ADN018 Adenoma 67 0.112
81
MNN014 Mononeuritis 48 0.108
82
HNM002 Hinman Syndrome 24 0.108
83
NRN002 Neuronitis 64 0.105
84
OTT002 Otitis Media 60 0.105
85
P MSC003 Muscular Atrophy 52 0.105
86
P SRC025 Sarcoidosis 1 32 0.105
87
CRK001 Cork-Handlers' Disease 32 0.105
88
MYT011 Myotonia 29 0.105
89
WST001 West Syndrome 64 0.101
90
PRP016 Paraplegia 48 0.101
91
WST006 Westphal Disease 4 0.101
92
P HYP117 Hypertriglyceridemia 54 0.098
93
P BNG071 Benign Schwannoma 34 0.098
94
c SPS012 Spastic Paraplegia 3a 25 0.098
95
P ANG001 Angelman Syndrome 70 0.094
96
ART019 Aortic Valve Stenosis 68 0.094
97
P GRV001 Graves' Disease 63 0.094
98
BNF002 Bone Fracture 55 0.094
99
FCT013 Factor V Leiden Thrombophilia 35 0.094
100
RPD005 Rapidly Involuting Congenital Hemangioma 16 0.094
101
P CRV039 Cervicitis 52 0.090
102
P ATX010 Ataxia Neuropathy Spectrum 44 0.090
103
SPS019 Spastic Paraparesis 35 0.090
104
c BNG076 Benign Exophthalmos Syndrome 21 0.090
105
MLG056 Malignant Hyperthermia 65 0.086
106
BTL001 Botulism 55 0.086
107
LYM019 Lymphosarcoma 54 0.086
108
MLK003 Melkersson-Rosenthal Syndrome 48 0.086
109
ARC007 Arachnoid Cysts 45 0.086
110
PRS062 Persistent Hyperplastic Primary Vitreous 36 0.086
111
PST055 Postural Hypotension 33 0.086
112
CHL109 Childhood Apraxia of Speech 24 0.086
113
c PRG018 Paragangliomas 1 23 0.086
114
TFT003 Tufting Enteropathy 21 0.086
115
P STR035 Streptococcal Group a Invasive Disease 14 0.086
116
AND002 Androgen Insensitivity Syndrome 88 0.081
117
P HMP004 Hemophilia B 80 0.081
118
c HYP076 Hyperthyroidism 61 0.081
119
c AXN002 Axenfeld-Rieger Syndrome 60 0.081
120
SCN006 Secondary Syphilis 55 0.081
121
HYP017 Hypophosphatemia 53 0.081
122
OST006 Osteoblastoma 41 0.081
123
SPP008 Suppurative Otitis Media 40 0.081
124
GRW007 Growth Hormone Deficiency 39 0.081
125
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.081
126
P RNL066 Renal Tubular Acidosis, Distal, Ad 28 0.081
127
P MYT013 Myotonia Congenita, Dominant 25 0.081
128
AND005 Androgen Insensitivity Syndrome, Mild 18 0.081
129
c TTL001 Total Internal Ophthalmoplegia 17 0.081
130
P HYP075 Hypertension 86 0.077
131
c HPT021 Hepatitis 75 0.077
132
c MNN013 Meningitis 71 0.077
133
P HRP006 Herpes Simplex 63 0.077
134
HRP004 Herpes Zoster 61 0.077
135
ACS001 Acoustic Neuroma 60 0.077
136
CHL069 Cholesteatoma 58 0.077
137
P ALT001 Alternating Hemiplegia of Childhood 55 0.077
138
NRM004 Neuroma 55 0.077
139
P ALV004 Alveolar Rhabdomyosarcoma 51 0.077
140
OST028 Osteochondroma 37 0.077
141
c PRG001 Progressive Muscular Atrophy 36 0.077
142
c HRD043 Hereditary Congenital Facial Paresis 12 0.077
143
GLM016 Glomus Jugulare Tumors 12 0.077
144
P MYS003 Myasthenia Gravis 79 0.072
145
P BRG005 Brugada Syndrome 1 53 0.072
146
CNV002 Conversion Disorder 50 0.072
147
ECT005 Ectropion 45 0.072
148
FCT022 Factor Xi Deficiency, Autosomal Recessive 29 0.072
149
P RNL048 Renal Tubular Acidosis, Distal, Type 3 20 0.072
150
SPN015 Spinal Polio 15 0.072
151
EPL031 Epileptic Hemiplegia 3 0.072
152
HPT023 Hepatocellular Carcinoma 89 0.066
153
RLP001 Relapsing Polychondritis 69 0.066
154
LYM017 Lyme Disease 67 0.066
155
PHR003 Pharyngitis 62 0.066
156
ART001 Arterial Tortuosity Syndrome 62 0.066
157
c MLG069 Malignant Hypertension 60 0.066
158
STT002 Status Asthmaticus 57 0.066
159
EVN001 Evans' Syndrome 54 0.066
160
P THR090 Thrombocythemia 1 54 0.066
161
FSC004 Fasciitis 50 0.066
162
P MLG090 Malignant Hyperthermia Susceptibility Type 1 47 0.066
163
PRT026 Parotitis 46 0.066
164
c MLG086 Malignant Hyperthermia Susceptibility 44 0.066
165
c ALM001 Al Amyloidosis 44 0.066
166
ENT001 Enterocele 42 0.066
167
LCK001 Locked-in Syndrome 39 0.066
168
c ATX004 Ataxia 38 0.066
169
PRX020 Proximal Renal Tubular Acidosis with Ocular Abnormalities 36 0.066
170
MYK002 Myokymia 32 0.066
171
PRL013 Paralytic Poliomyelitis 31 0.066
172
CVR002 Cavernous Sinus Thrombosis 29 0.066
173
VST004 Vestibular Disease 28 0.066
174
DYS073 Dysphagia 28 0.066
175
GRF006 Grfoma 26 0.066
176
GRW022 Growth Retardation-Mild Developmental Delay-Chronic Hepatitis Syndrome 18 0.066
177
P AMY001 Amyotrophic Lateral Sclerosis 100 0.061
178
TBR010 Tuberculosis 84 0.061
179
P LKM002 Leukemia 79 0.061
180
NPH007 Nephrogenic Diabetes Insipidus 77 0.061
181
P WGN002 Wegener's Granulomatosis 75 0.061
182
c CHR071 Charcot-Marie-Tooth Disease 69 0.061
183
PTN002 Patent Ductus Arteriosus 65 0.061
184
P PLY019 Polyneuropathy 64 0.061
185
P DNT039 Dent's Disease 64 0.061
186
TRG002 Trigeminal Neuralgia 63 0.061
187
HYP014 Hyperuricemia 61 0.061
188
STF001 Stiff-Person Syndrome 60 0.061
189
c HYP065 Hyperaldosteronism 59 0.061
190
P DBT005 Diabetes Insipidus 57 0.061
191
SNS001 Sensorineural Hearing Loss 56 0.061
192
MDS022 Mediastinitis 56 0.061
193
CRB009 Cerebritis 56 0.061
194
TTH006 Tooth Disease 55 0.061
195
LPC002 Lip Cancer 55 0.061
196
P LBY004 Labyrinthitis 53 0.061
197
PRP023 Peripheral Neuropathy 53 0.061
198
NRT004 Neuritis 51 0.061
199
c PRG013 Paraganglioma 49 0.061
200
P BRT034 Bartter Syndrome, Type 2 42 0.061
201
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 36 0.061
202
LGP001 Lagophthalmos 31 0.061
203
SPS057 Spasticity 29 0.061
204
ZYG002 Zygomycosis 28 0.061
205
HNS001 Hansen's Disease 22 0.061
206
PRM050 Primary Orthostatic Tremor 19 0.061
207
PST048 Postural Orthostatic Tachycardia Syndrome 13 0.061
208
PRR008 Periarteritis Nodosa 13 0.061
209
PRS033 Parasitic Ectoparasitic Infectious Disease 10 0.061
210
P SYS001 Systemic Lupus Erythematosus 87 0.054
211
21H001 21-Hydroxylase Deficiency 87 0.054
212
AGR001 Age Related Macular Degeneration 83 0.054
213
P MLT020 Multiple Sclerosis 82 0.054
214
P LPR003 Leprosy 78 0.054
215
BRN024 Bronchitis 76 0.054
216
P NRC002 Narcolepsy 75 0.054
217
PRC016 Pre-Eclampsia 75 0.054
218
c LPS004 Lupus Erythematosus 73 0.054
219
P INF038 Influenza 69 0.054
220
P HMN010 Hemangioma 68 0.054
221
c HYP086 Hypothyroidism 68 0.054
222
PTT006 Pituitary Adenoma 64 0.054
223
c SPN046 Spinal Muscular Atrophy 63 0.054
224
ART016 Aortic Aneurysm 62 0.054
225
BRN029 Brain Disease 62 0.054
226
P GTR002 Goiter 61 0.054
227
SQM006 Squamous Cell Carcinoma 61 0.054
228
c SBC007 Subacute Thyroiditis 58 0.054
229
RNL011 Renal Osteodystrophy 56 0.054
230
P SYR001 Syringomyelia 55 0.054
231
NRM005 Neuromuscular Disease 55 0.054
232
HMP005 Hemiplegia 54 0.054
233
SPN020 Spondylosis 54 0.054
234
GST045 Gastroenteritis 53 0.054
235
MYL001 Myelitis 52 0.054
236
SJG001 Sjogren's Syndrome 52 0.054
237
ANK001 Ankylosis 50 0.054
238
c ACR001 Aicardi-Goutieres Syndrome 49 0.054
239
TRC023 Trichinosis 48 0.054
240
c AML002 Amelogenesis Imperfecta 47 0.054
241
MLL002 Miller Fisher Syndrome 45 0.054
242
NRP002 Neuroepithelioma 41 0.054
243
WND001 Wound Botulism 40 0.054
244
HYP030 Hypoactive Sexual Desire Disorder 39 0.054
245
SPR007 Superior Mesenteric Artery Syndrome 36 0.054
246
TRP004 Tropical Sprue 35 0.054
247
GNC003 Geniculate Herpes Zoster 34 0.054
248
ADS002 Adie Syndrome 33 0.054
249
c ICH041 Ichthyosis, Autosomal Recessive 4b 31 0.054
250
HVD003 Hiv/aids 29 0.054
251
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.054
252
BRW004 Brown-Sequard Syndrome 28 0.054
253
RHB020 Rhabdomyosarcoma, Somatic 27 0.054
254
P HYP078 Hypertrophy of Breast 26 0.054
255
FCL044 Fecal Incontinence 26 0.054
256
PRT015 Partial Third-Nerve Palsy 26 0.054
257
NNS006 Non-Suppurative Otitis Media 26 0.054
258
HYP264 Hypertonia 23 0.054
259
AML040 Amelogenesis Imperfecta, Hypoplastic/hypomaturation Type 1e 22 0.054
260
HRL001 Harlequin Type Ichthyosis 22 0.054
261
CNG101 Congenital Human Immunodeficiency Virus 20 0.054
262
MDD008 Middle Ear Adenoma 16 0.054
263
PLM108 Pulmonary Interstitial Glycogenosis 14 0.054
264
P NRF002 Neurofibromatosis 100 0.047
265
VNH001 Von Hippel-Lindau Disease 89 0.047
266
c DBT009 Diabetes Mellitus 80 0.047
267
P TRN020 Turner Syndrome 77 0.047
268
MLT021 Multiple System Atrophy 76 0.047
269
P MLR004 Malaria 73 0.047
270
P NRB001 Neuroblastoma 71 0.047
271
PLY017 Polyarteritis Nodosa 68 0.047
272
P HPT001 Hepatitis C 66 0.047
273
P AMY004 Amyloidosis 65 0.047
274
c SML001 Small Cell Carcinoma 64 0.047
275
c ENC004 Encephalitis 64 0.047
276
MTR014 Motor Neuron Disease 63 0.047
277
ART005 Arteriovenous Malformation 63 0.047
278
ACQ007 Acquired Immunodeficiency Syndrome 63 0.047
279
PMP001 Pemphigus 63 0.047
280
SRC014 Sarcoma 63 0.047
281
c MSC005 Muscular Dystrophy 62 0.047
282
P NRV007 Nervous System Disease 61 0.047
283
c HPT003 Hepatitis a 60 0.047
284
P MMP001 Mumps 59 0.047
285
ASP003 Aseptic Meningitis 58 0.047
286
YLL002 Yellow Fever 57 0.047
287
EPL002 Epilepsy Syndrome 57 0.047
288
SLP005 Sleep Disorder 57 0.047
289
GYN001 Gynecomastia 57 0.047
290
RBS001 Rabies 56 0.047
291
c THR003 Thoracic Aortic Aneurysm 56 0.047
292
LPT001 Leptospirosis 55 0.047
293
NRL005 Neurilemmoma 55 0.047
294
RHB003 Rhabdomyosarcoma 54 0.047
295
MYL003 Myeloid Sarcoma 54 0.047
296
MMB001 Membranoproliferative Glomerulonephritis 53 0.047
297
OPT009 Optic Neuritis 53 0.047
298
P FNC004 Fanconi Syndrome 53 0.047
299
PTR001 Petrositis 51 0.047
300
PRS037 Periostitis 51 0.047
301
MDD002 Middle Ear Cholesteatoma 51 0.047
302
RLP003 Relapsing Fever 49 0.047
303
ARS002 Arsacs 49 0.047
304
WST004 West Nile Encephalitis 47 0.047
305
CHL079 Children's Interstitial Lung Disease 46 0.047
306
AXN001 Axonal Neuropathy 45 0.047
307
RCR001 Recurrent Corneal Erosion 44 0.047
308
ETH009 Ethmoid Sinusitis 44 0.047
309
TLR001 Tularemia 44 0.047
310
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.047
311
QDR001 Quadriplegia 43 0.047
312
CRT008 Carotid Artery Dissection 42 0.047
313
P BNC001 Bone Carcinoma 41 0.047
314
TRY002 Troyer Syndrome 38 0.047
315
INF058 Inflammatory Myofibroblastic Tumor 37 0.047
316
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 37 0.047
317
c RSM001 Rasmussen Encephalitis 37 0.047
318
VRL011 Viral Infectious Disease 37 0.047
319
c TRM003 Tremor 36 0.047
320
P VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 36 0.047
321
P EWN002 Ewing's Family of Tumors 36 0.047
322
CLR007 Colorado Tick Fever 36 0.047
323
TBS001 Tabes Dorsalis 35 0.047
324
TLS001 Tolosa-Hunt Syndrome 35 0.047
325
MNT147 Mental Retardation 35 0.047
326
MTR001 Mature Cataract 34 0.047
327
ENT005 Entropion 34 0.047
328
KRT012 Keratoderma 31 0.047
329
LRY029 Laryngomalacia 30 0.047
330
ECT004 Ecthyma 30 0.047
331
c CHR342 Chiari Malformation 29 0.047
332
TCK004 Tick Infestation 27 0.047
333
c CNG372 Congenital Stationary Night Blindness, Type 1f 22 0.047
334
RMS005 Ramsay-Hunt Syndrome 21 0.047
335
c HMP017 Hemophilia a, Congenital 21 0.047
336
FTD001 Foot Drop 21 0.047
337
BLB003 Bulbar Polio 21 0.047
338
c PRM041 Primary Cortisol Resistance 13 0.047
339
OTP003 Oto-Palatal-Digital Syndrome 13 0.047
340
SKL006 Skull Base Neoplasm 10 0.047
341
P BRS047 Breast Cancer 105 0.038
342
CDS001 Cadasil 92 0.038
343
P MLT019 Multiple Myeloma 89 0.038
344
P WSK001 Wiskott-Aldrich Syndrome 87 0.038
345
CRH001 Crohn's Disease 83 0.038
346
P BPL003 Bipolar Disorder 80 0.038
347
P PNM007 Pneumonia 79 0.038
348
OLV001 Olivopontocerebellar Atrophy 77 0.038
349
P ACT074 Acute Lymphocytic Leukemia 77 0.038
350
P FML018 Familial Mediterranean Fever 74 0.038
351
P BLD042 Bladder Carcinoma 73 0.038
352
ABT001 Abetalipoproteinemia 73 0.038
353
P BRD002 Bardet-Biedl Syndrome 71 0.038
354
SPN038 Spina Bifida 70 0.038
355
P PRG006 Progressive Supranuclear Palsy 70 0.038
356
PSY004 Psychotic Disorder 69 0.038
357
c SRC013 Sarcoidosis 69 0.038
358
P HML002 Hemolytic Anemia 68 0.038
359
MSL001 Measles 66 0.038
360
STT001 Status Epilepticus 66 0.038
361
P GLM007 Glomerulonephritis 66 0.038
362
KRT004 Keratitis 66 0.038
363
P ART023 Arthropathy 66 0.038
364
WLF001 Wolff-Parkinson-White Syndrome 65 0.038
365
HYP458 Hyper Ige Syndrome 65 0.038
366
c PRP029 Porphyria 64 0.038
367
P PRP025 Peripheral Primitive Neuroectodermal Tumor 63 0.038
368
GLL022 Guillain-Barre Syndrome 63 0.038
369
PLS006 Plasmodium Vivax Malaria 62 0.038
370
c TXP001 Toxoplasmosis 62 0.038
371
ADR008 Adrenal Adenoma 62 0.038
372
HYP003 Hypermethioninemia 60 0.038
373
P ESP024 Esophagitis 60 0.038
374
P PNM006 Pneumoconiosis 59 0.038
375
PRM027 Primitive Neuroectodermal Tumor 59 0.038
376
HRD010 Hereditary Spastic Paraplegia 59 0.038
377
BBS001 Babesiosis 58 0.038
378
OST011 Osteomalacia 57 0.038
379
c ATM010 Autoimmune Hemolytic Anemia 57 0.038
380
HNT002 Hantavirus Pulmonary Syndrome 57 0.038
381
ANR008 Aneurysm Disease 57 0.038
382
P FML001 Familial Atrial Fibrillation 57 0.038
383
GST037 Gastroparesis 57 0.038
384
ARC002 Arachnoiditis 57 0.038
385
P MYC008 Myocarditis 56 0.038
386
PRT029 Parathyroid Adenoma 56 0.038
387
P SYP003 Syphilis 56 0.038
388
GLM008 Glomus Tumor 56 0.038
389
JPN002 Japanese Encephalitis 55 0.038
390
ATX019 Ataxia with Vitamin E Deficiency 55 0.038
391
c PSD020 Pseudohypoaldosteronism Type Ii 55 0.038
392
SPT005 Spotted Fever 55 0.038
393
ENC006 Encephalomyelitis 55 0.038
394
TCK001 Tick-Borne Encephalitis 55 0.038
395
NWC001 Newcastle Disease 54 0.038
396
P CNG021 Congenital Toxoplasmosis 54 0.038
397
THY009 Thyroid Lymphoma 54 0.038
398
FBR009 Fibrous Dysplasia 54 0.038
399
EHR002 Ehrlichiosis 54 0.038
400
CHC001 Chickenpox 54 0.038
401
NPH003 Nephrocalcinosis 53 0.038
402
c CTR002 Cataract 53 0.038
403
c EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.038
404
ADL002 Adult Syndrome 52 0.038
405
SPN186 Spinal Cord Injury 52 0.038
406
P HYP097 Hyperekplexia 52 0.038
407
CTS002 Cat-Scratch Disease 51 0.038
408
MNN009 Meningoencephalitis 50 0.038
409
P CHR095 Chronic Progressive External Ophthalmoplegia 50 0.038
410
P PND001 Pain Disorder 49 0.038
411
NSP002 Nasopharyngitis 49 0.038
412
P HYP141 Hyperphenylalaninemia 49 0.038
413
P NML001 Nemaline Myopathy 49 0.038
414
MCP006 Mucoepidermoid Carcinoma 48 0.038
415
CRN012 Craniometaphyseal Dysplasia 47 0.038
416
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 47 0.038
417
P MLT008 Multinodular Goiter 47 0.038
418
STL001 St. Louis Encephalitis 46 0.038
419
AMB002 Amblyopia 46 0.038
420
c OPT004 Optic Atrophy 46 0.038
421
CNT025 Central Pontine Myelinolysis 42 0.038
422
HV1006 Hiv-1 42 0.038
423
SPN091 Spinal Muscular Atrophy with Respiratory Distress 1 41 0.038
424
LCR004 La Crosse Encephalitis 40 0.038
425
P HMR005 Hemorrhoid 39 0.038
426
RCK002 Rocky Mountain Spotted Fever 39 0.038
427
EPD005 Epidural Abscess 39 0.038
428
PLM029 Palmoplantar Keratosis 39 0.038
429
IPX001 Ipex Syndrome 39 0.038
430
P OTT001 Otitis Externa 39 0.038
431
c BLN003 Blindness 37 0.038
432
HYD001 Hydranencephaly 37 0.038
433
c NRC009 Narcolepsy 1 36 0.038
434
c SPS092 Spastic Paraplegia 11 35 0.038
435
XRP001 Xerophthalmia 35 0.038
436
THM001 Thomsen Disease 35 0.038
437
MYC033 Myoclonus 33 0.038
438
FRY001 Frey Syndrome 32 0.038
439
INS008 Insulin-Like Growth Factor I Deficiency 32 0.038
440
FCL003 Facial Hemiatrophy 32 0.038
441
P SLP004 Salpingo-Oophoritis 31 0.038
442
BRW001 Brown-Vialetto-Van Laere Syndrome 31 0.038
443
SML020 Small Patella Syndrome 30 0.038
444
SPN248 Spondyloepimetaphyseal Dysplasia, Sponastrime Type 29 0.038
445
DYS036 Dysequilibrium Syndrome 28 0.038
446
BRC010 Brachial Plexus Lesion 28 0.038
447
PLS008 Plasmodium Malariae Malaria 28 0.038
448
LRY017 Laryngeal Disease 27 0.038
449
c FML249 Familial Amyloidosis, Finnish Type 27 0.038
450
CRN051 Craniofacial Microsomia 26 0.038
451
STR002 Streptococcal Meningitis 25 0.038
452
EXP002 Exposure Keratitis 24 0.038
453
FDB001 Foodborne Botulism 24 0.038
454
PRS063 Paresthesia 22 0.038
455
P KRN003 Kernicterus Due to Isoimmunization 21 0.038
456
c CHR160 Chiari Malformation Type 2 20 0.038
457
MYS010 Myostatin-Related Muscle Hypertrophy 20 0.038
458
MDD006 Middle Ear Cholesterol Granuloma 18 0.038
459
PWS001 Powassan Encephalitis 17 0.038
460
FCL011 Facial Nerve Disease 17 0.038
461
MNN005 Meningovascular Neurosyphilis 17 0.038
462
DPH021 Diaphragm Disease 16 0.038
463
P ISC010 Isochromosome Yp 14 0.038
464
UVP001 Uveoparotid Fever 10 0.038
465
IDP037 Idiopathic Facial Palsy 9 0.038
466
BLB001 Bulbospinal Polio 7 0.038
467
PNT023 Pontine Hemorrhage 6 0.038
468
BRC057 Brachial Plexus Birth Injuries 3 0.038
469
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.038
470
HMP020 Hemiplegia Alterans 1 0.038
471
GLC006 Galactosemia 93 0.027
472
P LFR001 Li-Fraumeni Syndrome 93 0.027
473
P AST005 Asthma 88 0.027
474
MTC003 Metachromatic Leukodystrophy 87 0.027
475
P TYS001 Tay-Sachs Disease 82 0.027
476
P DLT002 Dilated Cardiomyopathy 82 0.027
477
PRT036 Peritonitis 78 0.027
478
INF030 Infectious Mononucleosis 78 0.027
479
ACT033 Acute Intermittent Porphyria 78 0.027
480
BRK003 Burkitt's Lymphoma 78 0.027
481
P OST002 Osteoporosis 77 0.027
482
P MYL005 Myelofibrosis 75 0.027
483
ADD001 Addison's Disease 75 0.027
484
P ALX003 Alexander Disease 74 0.027
485
STR067 Stroke, Ischemic 74 0.027
486
P CLC005 Celiac Disease 73 0.027
487
P CNG026 Congenital Heart Defect 73 0.027
488
PRN023 Prion Disease 71 0.027
489
P ABD003 Abdominal Aortic Aneurysm 71 0.027
490
P MGR002 Migraine 71 0.027
491
CFF002 Coffin-Lowry Syndrome 70 0.027
492
CNT009 Central Core Myopathy 70 0.027
493
P ATM003 Autoimmune Thyroiditis 70 0.027
494
ALP004 Alport Syndrome 69 0.027
495
P TYP020 Type 1 Diabetes 69 0.027
496
HYP004 Hypercalcemia 69 0.027
497
CCC001 Coccidioidomycosis 68 0.027
498
PLM033 Pulmonary Embolism 68 0.027
499
DBT010 Diabetic Neuropathy 68 0.027
500
GTL001 Gitelman Syndrome 67 0.027
501
MYS005 Myositis 67 0.027
502
P LGH001 Leigh Disease 67 0.027
503
MNT001 Mantle Cell Lymphoma 67 0.027
504
P NRL016 Neural Tube Defects 67 0.027
505
P MYT006 Myotonic Dystrophy Type 1 67 0.027
506
BLR001 Biliary Atresia 67 0.027
507
CHR072 Chordoma 67 0.027
508
c XRD001 Xeroderma Pigmentosum 67 0.027
509
P OLG002 Oligodendroglioma 67 0.027
510
P THY023 Thymoma 66 0.027
511
P FBR017 Fibrosarcoma 66 0.027
512
CRB042 Cerebellar Ataxia 66 0.027
513
P CNG368 Congenital Adrenal Hyperplasia 66 0.027
514
P LNG044 Long Qt Syndrome 1 66 0.027
515
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.027
516
P CMR001 Camurati-Engelmann Disease 65 0.027
517
GLD001 Goldenhar Syndrome 65 0.027
518
VRG001 Variegate Porphyria 65 0.027
519
c HPT016 Hepatitis B 65 0.027
520
P MLN008 Melanoma 65 0.027
521
FCT003 Factor X Deficiency 64 0.027
522
ISC004 Ischemia 64 0.027
523
P NRM001 Neuromyelitis Optica 64 0.027
524
c GLY007 Glycogen Storage Disease Iv 64 0.027
525
GST009 Gastroschisis 63 0.027
526
P MCH002 Machado-Joseph Disease 63 0.027
527
TYP007 Typhoid Fever 63 0.027
528
GLC003 Glucose Intolerance 63 0.027
529
c ACT073 Acute Leukemia 62 0.027
530
SMT015 Smith Magenis Syndrome 62 0.027
531
FCT002 Factor Xi Deficiency 62 0.027
532
FTT001 Fatty Liver Disease 61 0.027
533
P CNJ013 Conjunctivitis 61 0.027
534
P GNT008 Giant Cell Tumor 60 0.027
535
PTN001 Patent Foramen Ovale 60 0.027
536
c CNT035 Central Nervous System Disease 60 0.027
537
CRB021 Cerebral Malaria 59 0.027
538
c MYL007 Myeloma 59 0.027
539
KRN002 Kearns-Sayre Syndrome 59 0.027
540
ARR001 Arrhythmogenic Right Ventricular Dysplasia 59 0.027
541
CMP002 Campylobacteriosis 59 0.027
542
P MJR001 Major Depressive Disorder 58 0.027
543
LYM021 Lymphadenitis 58 0.027
544
P HRD021 Hereditary Sensory Neuropathy 58 0.027
545
LRN003 Learning Disability 58 0.027
546
c KDN018 Kidney Disease 58 0.027
547
P HYP024 Hypoparathyroidism 58 0.027
548
HJD001 Hajdu-Cheney Syndrome 57 0.027
549
PRC013 Pericarditis 57 0.027
550
c CYS016 Cystic Kidney 56 0.027
551
P INT030 Intracranial Aneurysm 56 0.027
552
c BRG001 Brugada Syndrome 56 0.027
553
ESP020 Esophageal Atresia 56 0.027
554
P MYM002 Moyamoya Disease 56 0.027
555
HYP006 Hypertensive Heart Disease 56 0.027
556
STS002 Situs Inversus 56 0.027
557
PLG002 Plague 56 0.027
558
c HYP060 Hyperinsulinism 56 0.027
559
P MTR012 Mitral Valve Disease 56 0.027
560
PNM008 Pneumothorax 55 0.027
561
TRN015 Transient Cerebral Ischemia 55 0.027
562
c GLY013 Glycogen Storage Disease 55 0.027
563
NSY001 N Syndrome 55 0.027
564
ANR004 Anuria 55 0.027
565
BRN016 Bronchogenic Carcinoma 55 0.027
566
c EPS003 Episodic Ataxia 55 0.027
567
KRT001 Keratoconjunctivitis Sicca 54 0.027
568
c ATN004 Autonomic Neuropathy 54 0.027
569
CVR006 Cavernous Hemangioma 54 0.027
570
EXS001 Exostosis 54 0.027
571
c INT070 Intestinal Obstruction 54 0.027
572
P VRL012 Viral Meningitis 54 0.027
573
KRT009 Keratosis 53 0.027
574
c WRD001 Waardenburg's Syndrome 53 0.027
575
c DMY001 Demyelinating Polyneuropathy 53 0.027
576
PRN011 Pernicious Anemia 52 0.027
577
END030 End Stage Renal Failure 52 0.027
578
P EXP004 Exophthalmos 51 0.027
579
SYN006 Synovial Sarcoma 51 0.027
580
ART002 Arts Syndrome 51 0.027
581
c FML023 Familial Hemiplegic Migraine 51 0.027
582
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 51 0.027
583
c SPN049 Spinocerebellar Ataxia 51 0.027
584
HRD030 Hereditary Neuralgic Amyotrophy 51 0.027
585
CNN003 Conn's Syndrome 50 0.027
586
MTH009 Mouth Disease 50 0.027
587
ANG002 Angiostrongyliasis 50 0.027
588
MYX004 Myxedema 50 0.027
589
PLM010 Pulmonary Edema 50 0.027
590
SCH016 Schimke Immunoosseous Dysplasia 49 0.027
591
P KLP003 Klippel-Feil Syndrome 49 0.027
592
c APH002 Aphasia 49 0.027
593
P SPN087 Spinal Muscular Atrophy 1 49 0.027
594
c BRT004 Bartter Disease 49 0.027
595
DBT002 Diabetic Autonomic Neuropathy 48 0.027
596
c ACT078 Acute Porphyria 48 0.027
597
c MYT007 Myotonic Dystrophy Type 2 48 0.027
598
CHK001 Chikungunya 48 0.027
599
NRX001 Neuroaxonal Dystrophy 48 0.027
600
P FCS001 Facioscapulohumeral Muscular Dystrophy 47 0.027
601
CLD007 Cold Agglutinin Disease 47 0.027
602
P FNN001 Finnish Type Amyloidosis 46 0.027
603
BRS064 Bursitis 45 0.027
604
HMM003 Hemimegalencephaly 45 0.027
605
ASP007 Aspiration Pneumonia 45 0.027
606
c CHR022 Charcot-Marie-Tooth Disease Type 1 45 0.027
607
c JVN006 Juvenile Spinal Muscular Atrophy 44 0.027
608
NRL007 Neurologic Diseases 44 0.027
609
RPT002 Ruptured Abdominal Aortic Aneurysm 44 0.027
610
c MLT074 Multiple Endocrine Neoplasia 43 0.027
611
HND002 Hand, Foot and Mouth Disease 43 0.027
612
HDC001 Headache 43 0.027
613
SPN050 Spinocerebellar Degeneration 43 0.027
614
TTR016 Tetra-Amelia Syndrome 43 0.027
615
MYS001 Myositis Ossificans 43 0.027
616
SCT002 Scotoma 42 0.027
617
HTS001 Hiatus Hernia 42 0.027
618
NCR007 Necrotizing Fasciitis 41 0.027
619
SPN044 Spinal Cord Ischemia 40 0.027
620
RMS001 Rem Sleep Behavior Disorder 40 0.027
621
CDQ001 Cauda Equina Syndrome 40 0.027
622
P ATN005 Autonomic Dysfunction 39 0.027
623
ACT012 Acute Hemorrhagic Conjunctivitis 39 0.027
624
PST020 Postpoliomyelitis Syndrome 39 0.027
625
c CRB126 Cerebral Cavernous Malformation 39 0.027
626
c ATS010 Autosomal Recessive Disease 39 0.027
627
c ADL016 Adult Spinal Muscular Atrophy 39 0.027
628
P SCH018 Schizencephaly 38 0.027
629
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 38 0.027
630
FBR047 Fibromyalgia 38 0.027
631
SPC005 Speech Disorder 38 0.027
632
MRR003 Murray Valley Encephalitis 37 0.027
633
P MNN007 Meningocele 37 0.027
634
STR039 Sturge-Weber Syndrome 37 0.027
635
PNM005 Pneumonic Plague 37 0.027
636
EMN001 Emanuel Syndrome 36 0.027
637
P GLM006 Glomangioma 36 0.027
638
c SPS091 Spastic Paraplegia 4 36 0.027
639
CSL001 Causalgia 36 0.027
640
c FML043 Familial Idiopathic Basal Ganglia Calcification 36 0.027
641
EST005 Esotropia 36 0.027
642
SCR015 Scarlet Fever 36 0.027
643
HRD025 Hereditary Neuropathy with Liability to Pressure Palsies 36 0.027
644
HRD086 Hereditary Hypophosphatemic Rickets 36 0.027
645
SNS003 Sensory Peripheral Neuropathy 35 0.027
646
MGL013 Megalencephaly 34 0.027
647
c CNG112 Congenital Muscular Dystrophy Type 1a 33 0.027
648
SLL001 Sialolithiasis 33 0.027
649
THY035 Thyroid Adenoma 32 0.027
650
HYP034 Hypertensive Encephalopathy 32 0.027
651
LRN001 Laurence-Moon Syndrome 32 0.027
652
DYG002 Dyggve-Melchior-Clausen Syndrome 31 0.027
653
ANT018 Anthracosis 31 0.027
654
NNP003 Nonepidermolytic Palmoplantar Keratoderma 31 0.027
655
c HMP006 Hemiplegic Migraine 31 0.027
656
HYP265 Hypotonia 30 0.027
657
c FRT001 Fourth Cranial Nerve Palsy 30 0.027
658
SPN185 Spinal Cord Infarction 30 0.027
659
CRV030 Cervical Adenitis 29 0.027
660
LPN001 Louping Ill 29 0.027
661
INT042 Internuclear Ophthalmoplegia 29 0.027
662
PRT009 Parotid Gland Cancer 29 0.027
663
THY043 Thymic Hyperplasia 28 0.027
664
ANT013 Anterior Spinal Artery Syndrome 28 0.027
665
c SPS027 Spastic Paraplegia 17 28 0.027
666
GNT005 Giant Hemangioma 28 0.027
667
END051 Endolymphatic Sac Tumor 27 0.027
668
EXC003 Excessive Tearing 27 0.027
669
BLT011 Bilateral Perisylvian Polymicrogyria 27 0.027
670
VST003 Vestibular Nystagmus 27 0.027
671
RPT003 Ruptured Aortic Aneurysm 27 0.027
672
ENC017 Encephaloceles 26 0.027
673
c SCP001 Sc Phocomelia Syndrome 26 0.027
674
MTC018 Metachondromatosis 26 0.027
675
WYB001 Wyburn Mason's Syndrome 26 0.027
676
HYP048 Hypotropia 25 0.027
677
HV1005 Hiv-1 Viremia 25 0.027
678
c SPS013 Spastic Paraplegia 8 25 0.027
679
PRN016 Peroneal Neuropathy 24 0.027
680
c SPS078 Spastic Paraplegia 7 24 0.027
681
CBB002 Cobb Syndrome 24 0.027
682
P CHR097 Chronic Purulent Otitis Media 24 0.027
683
PMP008 Pemphigus Vegetans 24 0.027
684
DYS013 Dysbaric Osteonecrosis 23 0.027
685
LTR002 Lateral Sinus Thrombosis 23 0.027
686
c ACT067 Acute Conjunctivitis 23 0.027
687
c CHR094 Chronic Polyneuropathy 23 0.027
688
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 23 0.027
689
P CHR454 Chiari Malformation Type 1 23 0.027
690
GNT004 Gnathomiasis 23 0.027
691
HYP047 Hypertropia 22 0.027
692
SBS002 Substernal Goiter 22 0.027
693
CRT009 Critical Illness Polyneuropathy 21 0.027
694
LRY007 Laryngeal Tuberculosis 21 0.027
695
PNT009 Pontine Tegmental Cap Dysplasia 21 0.027
696
SPR083 Sporadic Hemiplegic Migraine 20 0.027
697
c AMY008 Amyotrophic Lateral Sclerosis Type 2 20 0.027
698
PRP013 Paraphimosis 19 0.027
699
ANT054 Anotia 19 0.027
700
FCL007 Facial Neuralgia 18 0.027
701
c SPS079 Spastic Paraplegia 2 18 0.027
702
CLV002 Clivus Chordoma 18 0.027
703
P ACT001 Acute Tympanitis 18 0.027
704
c SPS025 Spastic Paraplegia 15 17 0.027
705
DRS001 Dressler's Syndrome 17 0.027
706
MLN002 Melanomatosis 17 0.027
707
CNR001 Coenurosis 16 0.027
708
ATY001 Atypical Depressive Disorder 16 0.027
709
c VRL004 Viral Labyrinthitis 16 0.027
710
EMB015 Embryonal Tumor with Multilayered Rosettes 15 0.027
711
MTR013 Motor Neuritis 15 0.027
712
ACT181 Acute Motor Axonal Neuropathy 14 0.027
713
c DST048 Distal Hereditary Motor Neuropathy Type 1 14 0.027
714
NNT025 Neonatal Systemic Lupus Erythematosus 14 0.027
715
SPN007 Spinal Cord Oligodendroglioma 14 0.027
716
c CNG333 Congenital Horner Syndrome 14 0.027
717
BNP002 Bone Epithelioid Hemangioma 13 0.027
718
SPN196 Spinal Muscular Atrophy, Lower Extremity, Autosomal Dominant 13 0.027
719
CHL090 Cholesterol Desmolase-Deficient Congenital Adrenal Hyperplasia 13 0.027
720
INT095 Internal Carotid Agenesis 13 0.027
721
CNM001 Canomad Syndrome 12 0.027
722
ETH012 Ethylene Glycol Poisoning 11 0.027
723
SPH008 Sphenoidal Sinus Cancer 11 0.027
724
SPR038 Supranuclear Ocular Palsy 11 0.027
725
MYC014 Mycobacterium Chelonae 11 0.027
726
PRS053 Parsonage Turner Syndrome 10 0.027
727
ABD009 Abducens Palsy 10 0.027
728
GNT013 Genetic Brain Disorders 10 0.027
729
MNS002 Mini Stroke 9 0.027
730
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 8 0.027
731
KNG003 Konigsmark Knox Hussels Syndrome 8 0.027
732
SYM001 Sympathetic Neurilemmoma 8 0.027
733
MLL006 Mollaret Meningitis 7 0.027
734
MYP026 Myopathy - Thyrotoxic 7 0.027
735
JMP002 Jumping Frenchmen of Maine 7 0.027
736
FBR024 Fibrocartilaginous Embolism 7 0.027
737
c CHR161 Chiari Malformation Type 3 6 0.027
738
FHR002 Fahr's Syndrome 6 0.027
739
SPN092 Spinal Shock 5 0.027