Search results for "paralysis"

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

708 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
c HYP051 Hypokalemic Periodic Paralysis 62 7.467
2
c HYP052 Hyperkalemic Periodic Paralysis 46 5.730
3
NRM009 Normokalemic Periodic Paralysis 32 5.380
4
INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 38 4.982
5
P HYP239 Hyperkalemic Periodic Paralysis Type 2 33 4.480
6
AND003 Andersen-Tawil Syndrome 54 4.313
7
FCL012 Facial Paralysis 40 3.999
8
OCL003 Oculomotor Nerve Paralysis 18 3.570
9
c THY054 Thyrotoxic Periodic Paralysis 46 3.553
10
P HYP254 Hypokalemic Periodic Paralysis Type 1 36 3.504
11
KRT022 Keratoderma Palmoplantar Spastic Paralysis 17 3.479
12
TCK002 Tick Paralysis 23 3.411
13
P THY084 Thyrotoxic Periodic Paralysis 1 23 3.231
14
TCK005 Tucker Syndrome 13 3.140
15
BLL003 Bell's Palsy 64 3.049
16
PRN008 Peroneal Nerve Paralysis 17 2.898
17
MBS002 Moebius Syndrome 53 2.873
18
c HYP255 Hypokalemic Periodic Paralysis Type 2 30 2.844
19
c HYP142 Hyperkalemic Periodic Paralysis Type 1 14 2.833
20
PRM028 Paramyotonia Congenita 49 2.625
21
KLM001 Klumpke Paralysis 11 2.551
22
GLS003 Glossopharyngeal Nerve Paralysis 10 2.483
23
VCL002 Vocal Cord Dysfunction Familial 19 2.472
24
FML082 Familial Partial Paralysis 3 2.460
25
P HRD130 Hereditary Congenital Facial Paresis 3 19 2.432
26
LRY043 Laryngeal Abductor Paralysis - Intellectual Disability 12 2.432
27
ISL060 Isolated Hereditary Congenital Facial Paralysis 9 2.432
28
PLM031 Poliomyelitis 54 2.313
29
TDD001 Todd's Paralysis 9 2.180
30
P PRK002 Parkinson's Disease 93 2.018
31
P CRN035 Cranial Nerve Palsy 32 2.018
32
CYC001 Cycloplegia 27 2.018
33
FZL001 Fazio Londe Syndrome 25 2.018
34
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 10 2.018
35
PRL008 Paralytic Ileus 36 2.004
36
PSD001 Pseudobulbar Palsy 31 2.004
37
FML160 Familial Spastic Paralysis 8 2.004
38
LRY021 Laryngeal Adductor Paralysis 6 2.004
39
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 5 2.004
40
LRY023 Laryngeal Abductor Paralysis Mental Retardation 3 2.004
41
SPS003 Spastic Diplegia 38 1.986
42
MBS001 Mobius Syndrome 28 1.986
43
MRK002 Marek Disease 16 1.986
44
c THY083 Thyrotoxic Periodic Paralysis 2 9 1.986
45
VNN001 Venencie Powell Gordon Winkelmann Syndrome 7 1.986
46
PRL020 Paralysis Agitans, Juvenile, of Hunt 2 1.986
47
c SSC005 Susceptibility to Prolonged Paralysis Due to Mivacurium Treatment 2 1.986
48
c SSC006 Susceptibility to Prolonged Paralysis Due to Cisatracurium Treatment 2 1.986
49
c SSC023 Susceptibility to Prolonged Paralysis Due to Pancuronium Treatment 2 1.986
50
P SSC024 Susceptibility to Prolonged Paralysis Due to Rocuronium Treatment 2 1.986
51
c SSC025 Susceptibility to Prolonged Paralysis Due to Satracurium Treatment 2 1.986
52
c SSC026 Susceptibility to Prolonged Paralysis Due to Vecuronium Treatment 2 1.986
53
P PRD017 Periodic Paralyses 28 1.516
54
c OPH004 Ophthalmoplegia 53 1.473
55
P HRN001 Horner's Syndrome 43 1.460
56
c FML159 Familial Periodic Paralyses 9 1.445
57
CNG241 Congenital Laryngeal Palsy 5 1.427
58
GLL022 Guillain-Barre Syndrome 61 1.404
59
TRP002 Tropical Spastic Paraparesis 55 1.404
60
HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 29 1.404
61
ABD002 Abducens Nerve Disease 25 1.404
62
P NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 21 1.404
63
THR010 Third Cranial Nerve Disease 10 1.404
64
RNL007 Renal Tubular Acidosis 57 0.176
65
HYP005 Hypokalemia 50 0.150
66
THY033 Thyrotoxicosis 58 0.145
67
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.137
68
SPS057 Spasticity 38 0.134
69
P LRY019 Laryngitis 65 0.131
70
THR013 Thoracic Outlet Syndrome 52 0.128
71
NRN002 Neuronitis 44 0.128
72
c THY032 Thyroiditis 66 0.125
73
MYT011 Myotonia 44 0.125
74
SYN053 Syndromic Diarrhea 34 0.125
75
P MYP004 Myopathy 62 0.121
76
NRP001 Neuropathy 62 0.121
77
ADN018 Adenoma 66 0.111
78
OTT002 Otitis Media 58 0.111
79
P GRV001 Graves' Disease 51 0.111
80
ANK002 Ankylosing Spondylitis 77 0.104
81
P ANG001 Angelman Syndrome 70 0.104
82
P RSP003 Respiratory Failure 70 0.104
83
ART019 Aortic Valve Stenosis 64 0.104
84
ACN002 Acanthosis Nigricans 63 0.097
85
P MSC003 Muscular Atrophy 54 0.097
86
P ATX010 Ataxia Neuropathy Spectrum 43 0.097
87
P CRV039 Cervicitis 58 0.092
88
ANR040 Aneurysm 46 0.092
89
BNF002 Bone Fracture 45 0.092
90
c BNG076 Benign Exophthalmos Syndrome 22 0.092
91
AND002 Androgen Insensitivity Syndrome 80 0.088
92
c AXN002 Axenfeld-Rieger Syndrome 67 0.088
93
BTL001 Botulism 60 0.088
94
HYP017 Hypophosphatemia 49 0.088
95
c HPT021 Hepatitis 64 0.084
96
c HYP076 Hyperthyroidism 64 0.084
97
P ALT001 Alternating Hemiplegia of Childhood 60 0.084
98
MYC002 Mycobacterium Avium Complex Disease 59 0.084
99
ACS001 Acoustic Neuroma 52 0.084
100
NRM004 Neuroma 46 0.084
101
AND005 Androgen Insensitivity Syndrome, Mild 21 0.084
102
EPL031 Epileptic Hemiplegia 5 0.084
103
P HYP075 Hypertension 87 0.079
104
c MNN013 Meningitis 68 0.079
105
P HRP006 Herpes Simplex 68 0.079
106
c PRG001 Progressive Muscular Atrophy 39 0.079
107
IMM088 Immunodeficiency 36 34 0.079
108
RMS005 Ramsay-Hunt Syndrome 29 0.079
109
P ATX002 Ataxia Telangiectasia 87 0.074
110
MLG056 Malignant Hyperthermia 66 0.074
111
HRP004 Herpes Zoster 58 0.074
112
ART001 Arterial Tortuosity Syndrome 55 0.074
113
CHL069 Cholesteatoma 55 0.074
114
MLK003 Melkersson-Rosenthal Syndrome 51 0.074
115
WST005 West Nile Virus 46 0.074
116
ECT005 Ectropion 43 0.074
117
P MYS003 Myasthenia Gravis 78 0.068
118
LYM017 Lyme Disease 65 0.068
119
MYL001 Myelitis 55 0.068
120
HMP005 Hemiplegia 53 0.068
121
DYS073 Dysphagia 52 0.068
122
MNN014 Mononeuritis 51 0.068
123
PRT026 Parotitis 50 0.068
124
NRT004 Neuritis 49 0.068
125
CNV002 Conversion Disorder 49 0.068
126
LCK001 Locked-in Syndrome 41 0.068
127
PRL013 Paralytic Poliomyelitis 39 0.068
128
TBR010 Tuberculosis 87 0.062
129
P WGN002 Wegener's Granulomatosis 74 0.062
130
P CHR071 Charcot-Marie-Tooth Disease 72 0.062
131
STT002 Status Asthmaticus 64 0.062
132
PTT006 Pituitary Adenoma 62 0.062
133
P PLY019 Polyneuropathy 61 0.062
134
c ATX004 Ataxia 59 0.062
135
P DBT005 Diabetes Insipidus 58 0.062
136
c HYP065 Hyperaldosteronism 58 0.062
137
SNS001 Sensorineural Hearing Loss 57 0.062
138
PTN002 Patent Ductus Arteriosus 57 0.062
139
TTH006 Tooth Disease 56 0.062
140
P NRV007 Nervous System Disease 50 0.062
141
P MSC033 Muscle Disorders 49 0.062
142
CRB009 Cerebritis 39 0.062
143
HYP264 Hypertonia 35 0.062
144
LGP001 Lagophthalmos 32 0.062
145
ERB002 Erb's Palsy 10 0.062
146
P SYS001 Systemic Lupus Erythematosus 88 0.056
147
P MLT020 Multiple Sclerosis 85 0.056
148
P LKM002 Leukemia 77 0.056
149
c LPS004 Lupus Erythematosus 77 0.056
150
P NRC002 Narcolepsy 75 0.056
151
c DBT009 Diabetes Mellitus 74 0.056
152
ART016 Aortic Aneurysm 71 0.056
153
NPH007 Nephrogenic Diabetes Insipidus 70 0.056
154
c HYP086 Hypothyroidism 69 0.056
155
P HPT001 Hepatitis C 67 0.056
156
BRN029 Brain Disease 58 0.056
157
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.056
158
P SYR001 Syringomyelia 56 0.056
159
MNT147 Mental Retardation 52 0.056
160
NRM005 Neuromuscular Disease 51 0.056
161
PRP016 Paraplegia 48 0.056
162
SJG001 Sjogren's Syndrome 48 0.056
163
MDS022 Mediastinitis 46 0.056
164
EPL002 Epilepsy Syndrome 46 0.056
165
SPP008 Suppurative Otitis Media 42 0.056
166
WND001 Wound Botulism 39 0.056
167
MLL002 Miller Fisher Syndrome 38 0.056
168
FTD001 Foot Drop 37 0.056
169
ADS002 Adie Syndrome 35 0.056
170
P LBY004 Labyrinthitis 34 0.056
171
GNC003 Geniculate Herpes Zoster 31 0.056
172
HNM002 Hinman Syndrome 28 0.056
173
ANT054 Anotia 27 0.056
174
PRS053 Parsonage Turner Syndrome 18 0.056
175
MDD008 Middle Ear Adenoma 16 0.056
176
FBR024 Fibrocartilaginous Embolism 14 0.056
177
OLV001 Olivopontocerebellar Atrophy 80 0.048
178
P MLR004 Malaria 75 0.048
179
P HMN010 Hemangioma 71 0.048
180
MLT021 Multiple System Atrophy 71 0.048
181
P NRB001 Neuroblastoma 70 0.048
182
SRC014 Sarcoma 70 0.048
183
PLY017 Polyarteritis Nodosa 69 0.048
184
P AMY004 Amyloidosis 68 0.048
185
c AMY001 Amyotrophic Lateral Sclerosis 67 0.048
186
P TRN020 Turner Syndrome 67 0.048
187
c SPN046 Spinal Muscular Atrophy 66 0.048
188
STT001 Status Epilepticus 66 0.048
189
PHR003 Pharyngitis 66 0.048
190
c ENC004 Encephalitis 66 0.048
191
P ESP024 Esophagitis 64 0.048
192
SPN186 Spinal Cord Injury 62 0.048
193
c MSC005 Muscular Dystrophy 62 0.048
194
P GTR002 Goiter 62 0.048
195
MTR014 Motor Neuron Disease 62 0.048
196
ASP003 Aseptic Meningitis 61 0.048
197
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.048
198
SPN020 Spondylosis 60 0.048
199
P MMP001 Mumps 60 0.048
200
NRL005 Neurilemmoma 58 0.048
201
RBS001 Rabies 57 0.048
202
c THR003 Thoracic Aortic Aneurysm 57 0.048
203
ADR008 Adrenal Adenoma 55 0.048
204
LPT001 Leptospirosis 54 0.048
205
TLR001 Tularemia 54 0.048
206
RLP003 Relapsing Fever 53 0.048
207
BLN003 Blindness 53 0.048
208
P PRP023 Peripheral Neuropathy 52 0.048
209
P FNC004 Fanconi Syndrome 50 0.048
210
TRY002 Troyer Syndrome 50 0.048
211
P MLG090 Malignant Hyperthermia Susceptibility Type 1 48 0.048
212
CRT008 Carotid Artery Dissection 48 0.048
213
P ATN005 Autonomic Dysfunction 47 0.048
214
WST004 West Nile Encephalitis 47 0.048
215
EVN001 Evans' Syndrome 46 0.048
216
c SBC007 Subacute Thyroiditis 46 0.048
217
FSC004 Fasciitis 46 0.048
218
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.048
219
QDR001 Quadriplegia 44 0.048
220
c CHR342 Chiari Malformation 44 0.048
221
SPN185 Spinal Cord Infarction 43 0.048
222
EPD005 Epidural Abscess 43 0.048
223
P SPN091 Spinal Muscular Atrophy with Respiratory Distress 1 42 0.048
224
THY035 Thyroid Adenoma 39 0.048
225
TLS001 Tolosa-Hunt Syndrome 37 0.048
226
TBS001 Tabes Dorsalis 36 0.048
227
c PPL025 Popliteal Pterygium Syndrome 36 0.048
228
CLR007 Colorado Tick Fever 34 0.048
229
c SPS012 Spastic Paraplegia 3a 33 0.048
230
c SPS078 Spastic Paraplegia 7 33 0.048
231
PTR001 Petrositis 29 0.048
232
TFT003 Tufting Enteropathy 28 0.048
233
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.048
234
CVR002 Cavernous Sinus Thrombosis 27 0.048
235
BLB003 Bulbar Polio 22 0.048
236
ABD009 Abducens Palsy 19 0.048
237
PNT023 Pontine Hemorrhage 18 0.048
238
OTP003 Oto-Palatal-Digital Syndrome 17 0.048
239
SKL006 Skull Base Neoplasm 11 0.048
240
P LVR011 Liver Cancer 91 0.039
241
P MLT019 Multiple Myeloma 88 0.039
242
P BRS047 Breast Cancer 86 0.039
243
CDS001 Cadasil 84 0.039
244
P LPR003 Leprosy 78 0.039
245
P PNM007 Pneumonia 78 0.039
246
P BPL003 Bipolar Disorder 77 0.039
247
P FML018 Familial Mediterranean Fever 76 0.039
248
P SRC013 Sarcoidosis 75 0.039
249
P BRD002 Bardet-Biedl Syndrome 73 0.039
250
WLF001 Wolff-Parkinson-White Syndrome 73 0.039
251
P CNG368 Congenital Adrenal Hyperplasia 70 0.039
252
CRB039 Cerebrovascular Disease 69 0.039
253
P GLM007 Glomerulonephritis 69 0.039
254
P CNG401 Congenital Heart Disease 69 0.039
255
P INF038 Influenza 68 0.039
256
MSL001 Measles 68 0.039
257
P LNG044 Long Qt Syndrome 1 68 0.039
258
PLS006 Plasmodium Vivax Malaria 68 0.039
259
SPN038 Spina Bifida 68 0.039
260
TRG002 Trigeminal Neuralgia 67 0.039
261
P FML001 Familial Atrial Fibrillation 67 0.039
262
P HYP117 Hypertriglyceridemia 67 0.039
263
c HML002 Hemolytic Anemia 66 0.039
264
c TXP001 Toxoplasmosis 66 0.039
265
P INS005 Insulin Resistance 65 0.039
266
PRP025 Peripheral Primitive Neuroectodermal Tumor 65 0.039
267
P PRG006 Progressive Supranuclear Palsy 65 0.039
268
c EHL001 Ehlers-Danlos Syndrome 64 0.039
269
c MLG069 Malignant Hypertension 64 0.039
270
BBS001 Babesiosis 64 0.039
271
P ART023 Arthropathy 64 0.039
272
STF001 Stiff-Person Syndrome 64 0.039
273
ART005 Arteriovenous Malformation 63 0.039
274
c PRP029 Porphyria 63 0.039
275
KRN002 Kearns-Sayre Syndrome 63 0.039
276
ARC007 Arachnoid Cysts 62 0.039
277
P ATM010 Autoimmune Hemolytic Anemia 62 0.039
278
GLC003 Glucose Intolerance 62 0.039
279
P PSD020 Pseudohypoaldosteronism Type Ii 61 0.039
280
c PRG013 Paraganglioma 60 0.039
281
CLD007 Cold Agglutinin Disease 59 0.039
282
RHB003 Rhabdomyosarcoma 59 0.039
283
P NRM001 Neuromyelitis Optica 59 0.039
284
YLL002 Yellow Fever 59 0.039
285
NRC020 Neuroectodermal Tumor 59 0.039
286
HDC001 Headache 58 0.039
287
P MYC008 Myocarditis 58 0.039
288
c HRD010 Hereditary Spastic Paraplegia 58 0.039
289
P CNG021 Congenital Toxoplasmosis 57 0.039
290
GST037 Gastroparesis 56 0.039
291
MYL003 Myeloid Sarcoma 56 0.039
292
P CHR095 Chronic Progressive External Ophthalmoplegia 56 0.039
293
P HYP014 Hyperuricemia 56 0.039
294
c TRM003 Tremor 56 0.039
295
JPN002 Japanese Encephalitis 55 0.039
296
NWC001 Newcastle Disease 54 0.039
297
c OST028 Osteochondroma 54 0.039
298
c ACR001 Aicardi-Goutieres Syndrome 54 0.039
299
THY009 Thyroid Lymphoma 54 0.039
300
EHR002 Ehrlichiosis 54 0.039
301
GST045 Gastroenteritis 54 0.039
302
TCK001 Tick-Borne Encephalitis 53 0.039
303
OST011 Osteomalacia 53 0.039
304
PRT029 Parathyroid Adenoma 53 0.039
305
SPT005 Spotted Fever 53 0.039
306
GRW007 Growth Hormone Deficiency 52 0.039
307
P PND001 Pain Disorder 52 0.039
308
STL001 St. Louis Encephalitis 52 0.039
309
RNL011 Renal Osteodystrophy 51 0.039
310
P SZR006 Seizure Disorder 51 0.039
311
c EMR001 Emery-Dreifuss Muscular Dystrophy 51 0.039
312
c EPS003 Episodic Ataxia 51 0.039
313
P MJR001 Major Depressive Disorder 50 0.039
314
P PNM006 Pneumoconiosis 50 0.039
315
P NML001 Nemaline Myopathy 50 0.039
316
OPT009 Optic Neuritis 50 0.039
317
FBR047 Fibromyalgia 50 0.039
318
NPH003 Nephrocalcinosis 49 0.039
319
NSP002 Nasopharyngitis 48 0.039
320
MMB001 Membranoproliferative Glomerulonephritis 48 0.039
321
CNN003 Conn's Syndrome 48 0.039
322
P TRN034 Transverse Myelitis 47 0.039
323
c AML002 Amelogenesis Imperfecta 47 0.039
324
CNT025 Central Pontine Myelinolysis 47 0.039
325
MNN009 Meningoencephalitis 47 0.039
326
MYK002 Myokymia 46 0.039
327
P HMR005 Hemorrhoid 46 0.039
328
PST055 Postural Hypotension 46 0.039
329
KRT012 Keratoderma 46 0.039
330
GYN001 Gynecomastia 46 0.039
331
ILS001 Ileus 45 0.039
332
PRS037 Periostitis 44 0.039
333
ARC002 Arachnoiditis 44 0.039
334
OST006 Osteoblastoma 44 0.039
335
c APH002 Aphasia 44 0.039
336
THY043 Thymic Hyperplasia 43 0.039
337
c HRD086 Hereditary Hypophosphatemic Rickets 42 0.039
338
LCR004 La Crosse Encephalitis 42 0.039
339
c SPS092 Spastic Paraplegia 11 40 0.039
340
TRC023 Trichinosis 40 0.039
341
c NRC009 Narcolepsy 1 39 0.039
342
HYD001 Hydranencephaly 39 0.039
343
P OTT001 Otitis Externa 39 0.039
344
XRP001 Xerophthalmia 38 0.039
345
TRP004 Tropical Sprue 38 0.039
346
RCK002 Rocky Mountain Spotted Fever 36 0.039
347
AXN001 Axonal Neuropathy 36 0.039
348
PRS063 Paresthesia 36 0.039
349
INT042 Internuclear Ophthalmoplegia 34 0.039
350
SPR007 Superior Mesenteric Artery Syndrome 34 0.039
351
PSD029 Pseudocholinesterase Deficiency 34 0.039
352
c FML249 Familial Amyloidosis, Finnish Type 33 0.039
353
SPS016 Spasmodic Dysphonia 33 0.039
354
ENT005 Entropion 33 0.039
355
FCL003 Facial Hemiatrophy 32 0.039
356
BRW001 Brown-Vialetto-Van Laere Syndrome 32 0.039
357
PRS062 Persistent Hyperplastic Primary Vitreous 32 0.039
358
CHL109 Childhood Apraxia of Speech 31 0.039
359
CBB002 Cobb Syndrome 29 0.039
360
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 29 0.039
361
c CHR160 Chiari Malformation Type 2 29 0.039
362
PRR008 Periarteritis Nodosa 28 0.039
363
ECT004 Ecthyma 28 0.039
364
BRW004 Brown-Sequard Syndrome 27 0.039
365
c ACT159 Acute Transverse Myelitis 27 0.039
366
FDB001 Foodborne Botulism 26 0.039
367
VST004 Vestibular Disease 25 0.039
368
TCK004 Tick Infestation 25 0.039
369
STR002 Streptococcal Meningitis 23 0.039
370
GLM016 Glomus Jugulare Tumors 21 0.039
371
PWS001 Powassan Encephalitis 19 0.039
372
MNN005 Meningovascular Neurosyphilis 19 0.039
373
CNT067 Central Cord Syndrome 18 0.039
374
SYR004 Syringobulbia 15 0.039
375
BDR001 Bidirectional Tachycardia 13 0.039
376
UVP001 Uveoparotid Fever 10 0.039
377
SPN015 Spinal Polio 9 0.039
378
BLB001 Bulbospinal Polio 9 0.039
379
MYP026 Myopathy - Thyrotoxic 9 0.039
380
BRC057 Brachial Plexus Birth Injuries 7 0.039
381
WST006 Westphal Disease 5 0.039
382
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.039
383
HMP020 Hemiplegia Alterans 1 0.039
384
P TYP008 Type 1 Diabetes Mellitus 96 0.028
385
P NRF002 Neurofibromatosis 94 0.028
386
P AST005 Asthma 89 0.028
387
P DLT002 Dilated Cardiomyopathy 88 0.028
388
P LFR001 Li-Fraumeni Syndrome 88 0.028
389
GLC006 Galactosemia 86 0.028
390
INF030 Infectious Mononucleosis 84 0.028
391
P GCH001 Gaucher's Disease 84 0.028
392
P TYS001 Tay-Sachs Disease 83 0.028
393
MTC003 Metachromatic Leukodystrophy 83 0.028
394
VNH001 Von Hippel-Lindau Disease 81 0.028
395
P PRC016 Pre-Eclampsia 78 0.028
396
ACT033 Acute Intermittent Porphyria 78 0.028
397
BRK003 Burkitt's Lymphoma 77 0.028
398
P ALX003 Alexander Disease 76 0.028
399
CRH001 Crohn's Disease 76 0.028
400
P OST002 Osteoporosis 76 0.028
401
SKN016 Skin Disease 75 0.028
402
P MYL005 Myelofibrosis 75 0.028
403
21H001 21-Hydroxylase Deficiency 74 0.028
404
CYS008 Cystic Echinococcosis 74 0.028
405
P CLC005 Celiac Disease 73 0.028
406
CFF002 Coffin-Lowry Syndrome 72 0.028
407
HYP458 Hyper Ige Syndrome 72 0.028
408
CCC001 Coccidioidomycosis 72 0.028
409
RLP001 Relapsing Polychondritis 72 0.028
410
PRT036 Peritonitis 72 0.028
411
P ADD001 Addison's Disease 72 0.028
412
ACQ007 Acquired Immunodeficiency Syndrome 71 0.028
413
GTL001 Gitelman Syndrome 70 0.028
414
P MGR002 Migraine 70 0.028
415
SPS077 Sepsis 70 0.028
416
P MYS005 Myositis 70 0.028
417
c HPT016 Hepatitis B 70 0.028
418
DSM004 Desmoid Tumor 69 0.028
419
NRL016 Neural Tube Defects 68 0.028
420
P CMR001 Camurati-Engelmann Disease 68 0.028
421
P BLD042 Bladder Carcinoma 68 0.028
422
P ABD003 Abdominal Aortic Aneurysm 68 0.028
423
P THY023 Thymoma 68 0.028
424
P ATM003 Autoimmune Thyroiditis 67 0.028
425
CHR072 Chordoma 66 0.028
426
GST009 Gastroschisis 66 0.028
427
P MCH002 Machado-Joseph Disease 66 0.028
428
VRG001 Variegate Porphyria 66 0.028
429
P SYS005 Systemic Scleroderma 66 0.028
430
PLM033 Pulmonary Embolism 66 0.028
431
c XRD001 Xeroderma Pigmentosum 66 0.028
432
P OST001 Osteopetrosis 66 0.028
433
P LGH001 Leigh Disease 65 0.028
434
P MLN008 Melanoma 65 0.028
435
ABT001 Abetalipoproteinemia 65 0.028
436
FCT002 Factor Xi Deficiency 65 0.028
437
HYP004 Hypercalcemia 65 0.028
438
STR067 Stroke, Ischemic 65 0.028
439
c SML001 Small Cell Carcinoma 64 0.028
440
MNT001 Mantle Cell Lymphoma 64 0.028
441
FCT003 Factor X Deficiency 64 0.028
442
P OLG002 Oligodendroglioma 64 0.028
443
ISC004 Ischemia 63 0.028
444
P FBR017 Fibrosarcoma 63 0.028
445
CMP002 Campylobacteriosis 63 0.028
446
c INT070 Intestinal Obstruction 63 0.028
447
LRN003 Learning Disability 63 0.028
448
BLR001 Biliary Atresia 63 0.028
449
c KDN018 Kidney Disease 63 0.028
450
P MTR012 Mitral Valve Disease 63 0.028
451
P KRT004 Keratitis 62 0.028
452
P TYR002 Tyrosinemia Type I 62 0.028
453
P CRB042 Cerebellar Ataxia 62 0.028
454
P CNJ013 Conjunctivitis 62 0.028
455
TYP007 Typhoid Fever 62 0.028
456
PTN001 Patent Foramen Ovale 62 0.028
457
GLD001 Goldenhar Syndrome 62 0.028
458
P GLY008 Glycogen Storage Disease Ii 62 0.028
459
P FML043 Familial Idiopathic Basal Ganglia Calcification 61 0.028
460
P SCH018 Schizencephaly 61 0.028
461
c MYL007 Myeloma 61 0.028
462
NRL004 Neuroleptic Malignant Syndrome 61 0.028
463
ALP003 Alpers Syndrome 61 0.028
464
c ALM001 Al Amyloidosis 61 0.028
465
ALP004 Alport Syndrome 61 0.028
466
CHC001 Chickenpox 60 0.028
467
c CHR022 Charcot-Marie-Tooth Disease Type 1 60 0.028
468
c HMP002 Hemophagocytic Lymphohistiocytosis 60 0.028
469
KRT001 Keratoconjunctivitis Sicca 60 0.028
470
CRB021 Cerebral Malaria 60 0.028
471
PMP001 Pemphigus 60 0.028
472
SPH001 Sapho Syndrome 60 0.028
473
MGC001 Megacolon 60 0.028
474
c GLY013 Glycogen Storage Disease 60 0.028
475
c FML023 Familial Hemiplegic Migraine 59 0.028
476
CVR006 Cavernous Hemangioma 59 0.028
477
ANR004 Anuria 59 0.028
478
LYM019 Lymphosarcoma 59 0.028
479
c BRG001 Brugada Syndrome 59 0.028
480
END030 End Stage Renal Failure 58 0.028
481
P VRL012 Viral Meningitis 58 0.028
482
P MYM002 Moyamoya Disease 58 0.028
483
P GNT008 Giant Cell Tumor 58 0.028
484
PRN023 Prion Disease 58 0.028
485
SMT015 Smith Magenis Syndrome 57 0.028
486
ESP020 Esophageal Atresia 57 0.028
487
c WRD001 Waardenburg's Syndrome 57 0.028
488
c CTR002 Cataract 57 0.028
489
P HYP024 Hypoparathyroidism 57 0.028
490
c ACT073 Acute Leukemia 57 0.028
491
c HYP060 Hyperinsulinism 57 0.028
492
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 57 0.028
493
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 56 0.028
494
PLG002 Plague 56 0.028
495
c SPN049 Spinocerebellar Ataxia 56 0.028
496
STR039 Sturge-Weber Syndrome 56 0.028
497
INS008 Insulin-Like Growth Factor I Deficiency 56 0.028
498
BNC003 Bone Cancer 56 0.028
499
c MYT007 Myotonic Dystrophy Type 2 56 0.028
500
CRN012 Craniometaphyseal Dysplasia 55 0.028
501
HMM003 Hemimegalencephaly 55 0.028
502
SLP005 Sleep Disorder 55 0.028
503
P EXP004 Exophthalmos 55 0.028
504
P KLP003 Klippel-Feil Syndrome 55 0.028
505
MDL009 Medullary Sponge Kidney 55 0.028
506
P HYP141 Hyperphenylalaninemia 54 0.028
507
c BRT004 Bartter Disease 54 0.028
508
P BRG005 Brugada Syndrome 1 54 0.028
509
NPH051 Nephritis 54 0.028
510
MLT075 Multifocal Motor Neuropathy 54 0.028
511
LYM022 Lymphangioma 54 0.028
512
MYX004 Myxedema 54 0.028
513
P ENC008 Encephalocele 54 0.028
514
PRN011 Pernicious Anemia 53 0.028
515
c GLY007 Glycogen Storage Disease Iv 53 0.028
516
STS002 Situs Inversus 53 0.028
517
HNT002 Hantavirus Pulmonary Syndrome 53 0.028
518
PRC013 Pericarditis 53 0.028
519
TRN015 Transient Cerebral Ischemia 53 0.028
520
c SPN183 Spontaneous Pneumothorax 52 0.028
521
BRS064 Bursitis 52 0.028
522
c ATR038 Atrial Fibrillation, Familial, 3 52 0.028
523
ANG002 Angiostrongyliasis 52 0.028
524
EXS001 Exostosis 52 0.028
525
c HMP006 Hemiplegic Migraine 51 0.028
526
P CYS016 Cystic Kidney 51 0.028
527
FBR009 Fibrous Dysplasia 51 0.028
528
c CRB126 Cerebral Cavernous Malformation 51 0.028
529
RGD001 Rigid Spine Syndrome 51 0.028
530
CHK001 Chikungunya 51 0.028
531
HRD030 Hereditary Neuralgic Amyotrophy 51 0.028
532
EWN002 Ewing's Family of Tumors 51 0.028
533
HYP006 Hypertensive Heart Disease 50 0.028
534
P APL006 Aplasia Cutis Congenita 50 0.028
535
HJD001 Hajdu-Cheney Syndrome 50 0.028
536
INF058 Inflammatory Myofibroblastic Tumor 50 0.028
537
PNM008 Pneumothorax 50 0.028
538
c ATN004 Autonomic Neuropathy 50 0.028
539
CTS002 Cat-Scratch Disease 50 0.028
540
c OPT004 Optic Atrophy 50 0.028
541
P BNG071 Benign Schwannoma 49 0.028
542
c CNT035 Central Nervous System Disease 49 0.028
543
NRX001 Neuroaxonal Dystrophy 49 0.028
544
PLS016 Plasma Cell Leukemia 49 0.028
545
ASP007 Aspiration Pneumonia 49 0.028
546
TRC040 Tracheoesophageal Fistula 49 0.028
547
MTH009 Mouth Disease 49 0.028
548
PLM010 Pulmonary Edema 49 0.028
549
MTS001 Mutism 49 0.028
550
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 48 0.028
551
LYM021 Lymphadenitis 48 0.028
552
AMB002 Amblyopia 47 0.028
553
SCH016 Schimke Immunoosseous Dysplasia 47 0.028
554
c MLG086 Malignant Hyperthermia Susceptibility 47 0.028
555
MYS001 Myositis Ossificans 47 0.028
556
c DMY001 Demyelinating Polyneuropathy 47 0.028
557
HYP120 Hypoaldosteronism 47 0.028
558
SPN050 Spinocerebellar Degeneration 46 0.028
559
MCP006 Mucoepidermoid Carcinoma 46 0.028
560
TNG009 Tongue Squamous Cell Carcinoma 46 0.028
561
MDD002 Middle Ear Cholesteatoma 46 0.028
562
ACT012 Acute Hemorrhagic Conjunctivitis 46 0.028
563
P NRL007 Neurologic Diseases 45 0.028
564
MGL013 Megalencephaly 45 0.028
565
MYC033 Myoclonus 45 0.028
566
P FCS001 Facioscapulohumeral Muscular Dystrophy 45 0.028
567
ZYG002 Zygomycosis 45 0.028
568
FTT001 Fatty Liver Disease 44 0.028
569
NCR007 Necrotizing Fasciitis 44 0.028
570
RMS001 Rem Sleep Behavior Disorder 43 0.028
571
EST005 Esotropia 43 0.028
572
SRC001 Sarcomatoid Mesothelioma 43 0.028
573
LMB052 Lumbar Disc Herniation 43 0.028
574
HTS001 Hiatus Hernia 43 0.028
575
TTR016 Tetra-Amelia Syndrome 42 0.028
576
P RSM001 Rasmussen Encephalitis 42 0.028
577
CDQ001 Cauda Equina Syndrome 42 0.028
578
SPS019 Spastic Paraparesis 41 0.028
579
HYP265 Hypotonia 41 0.028
580
P MNN007 Meningocele 41 0.028
581
P VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 41 0.028
582
SCT002 Scotoma 40 0.028
583
P BRT034 Bartter Syndrome, Type 2 40 0.028
584
NRG004 Neurogenic Diabetes Insipidus 40 0.028
585
DYG002 Dyggve-Melchior-Clausen Syndrome 40 0.028
586
LRY029 Laryngomalacia 40 0.028
587
c AMY008 Amyotrophic Lateral Sclerosis Type 2 40 0.028
588
END051 Endolymphatic Sac Tumor 39 0.028
589
SPC005 Speech Disorder 39 0.028
590
P FNN001 Finnish Type Amyloidosis 39 0.028
591
VRL011 Viral Infectious Disease 39 0.028
592
HRD025 Hereditary Neuropathy with Liability to Pressure Palsies 39 0.028
593
PLM029 Palmoplantar Keratosis 38 0.028
594
P GLM006 Glomangioma 38 0.028
595
BRN016 Bronchogenic Carcinoma 38 0.028
596
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 37 0.028
597
SML020 Small Patella Syndrome 37 0.028
598
HNS001 Hansen's Disease 37 0.028
599
SCR015 Scarlet Fever 37 0.028
600
LMB010 Lambert Syndrome 37 0.028
601
ODN002 Odontohypophosphatasia 37 0.028
602
IPX001 Ipex Syndrome 37 0.028
603
c SRC025 Sarcoidosis 1 36 0.028
604
PRX020 Proximal Renal Tubular Acidosis with Ocular Abnormalities 35 0.028
605
PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 35 0.028
606
CSL001 Causalgia 35 0.028
607
HYP034 Hypertensive Encephalopathy 35 0.028
608
THM001 Thomsen Disease 35 0.028
609
MRR003 Murray Valley Encephalitis 35 0.028
610
PMP008 Pemphigus Vegetans 35 0.028
611
P AML017 Amelogenesis Imperfecta, Type Ib 34 0.028
612
BLT011 Bilateral Perisylvian Polymicrogyria 34 0.028
613
c SPS091 Spastic Paraplegia 4 34 0.028
614
c CNG112 Congenital Muscular Dystrophy Type 1a 34 0.028
615
ANT018 Anthracosis 33 0.028
616
PNM005 Pneumonic Plague 33 0.028
617
MTC018 Metachondromatosis 33 0.028
618
PST020 Postpoliomyelitis Syndrome 33 0.028
619
HRD088 Hereditary Neuropathies 33 0.028
620
PRX014 Proximal Spinal Muscular Atrophy 32 0.028
621
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.028
622
SPR083 Sporadic Hemiplegic Migraine 32 0.028
623
MYS010 Myostatin-Related Muscle Hypertrophy 32 0.028
624
P CHR454 Chiari Malformation Type 1 31 0.028
625
CRB027 Cerebellar Disease 31 0.028
626
c SPS027 Spastic Paraplegia 17 31 0.028
627
c SPS025 Spastic Paraplegia 15 31 0.028
628
P ATS059 Autosomal Dominant Hyper Ige Syndrome 31 0.028
629
c SCP001 Sc Phocomelia Syndrome 30 0.028
630
VST003 Vestibular Nystagmus 30 0.028
631
P RNL066 Renal Tubular Acidosis, Distal, Ad 30 0.028
632
MNR004 Mounier-Kuhn Syndrome 30 0.028
633
c PHC014 Phocomelia 30 0.028
634
CRV030 Cervical Adenitis 30 0.028
635
BRC010 Brachial Plexus Lesion 30 0.028
636
CRN051 Craniofacial Microsomia 29 0.028
637
LPN001 Louping Ill 29 0.028
638
NRS003 Neurosyphilis 29 0.028
639
FRY001 Frey Syndrome 29 0.028
640
HYP362 Hyperopia 28 0.028
641
c SPS013 Spastic Paraplegia 8 28 0.028
642
FBR028 Fibrosing Mediastinitis 28 0.028
643
c SPS079 Spastic Paraplegia 2 28 0.028
644
MYC014 Mycobacterium Chelonae 28 0.028
645
PRG035 Progressive Supranuclear Palsy Atypical 27 0.028
646
FCL044 Fecal Incontinence 27 0.028
647
AMY005 Amyloid Neuropathy 27 0.028
648
c RNL045 Renal Tubular Acidosis, Distal 27 0.028
649
GNT004 Gnathomiasis 27 0.028
650
ETH009 Ethmoid Sinusitis 26 0.028
651
SNS003 Sensory Peripheral Neuropathy 26 0.028
652
PNT009 Pontine Tegmental Cap Dysplasia 26 0.028
653
ANT013 Anterior Spinal Artery Syndrome 26 0.028
654
RHB020 Rhabdomyosarcoma, Somatic 26 0.028
655
WYB001 Wyburn Mason's Syndrome 26 0.028
656
P CHR097 Chronic Purulent Otitis Media 26 0.028
657
HYP048 Hypotropia 26 0.028
658
EXC003 Excessive Tearing 26 0.028
659
ECH002 Echolalia 25 0.028
660
LTR002 Lateral Sinus Thrombosis 25 0.028
661
FCT022 Factor Xi Deficiency, Autosomal Recessive 25 0.028
662
PRN016 Peroneal Neuropathy 25 0.028
663
c FRT001 Fourth Cranial Nerve Palsy 25 0.028
664
P MYT013 Myotonia Congenita, Dominant 25 0.028
665
CRT009 Critical Illness Polyneuropathy 24 0.028
666
SBS002 Substernal Goiter 23 0.028
667
ATR055 Atrial Septal Aneurysm 23 0.028
668
PRS120 Persistent Idiopathic Facial Pain 23 0.028
669
c SNS011 Sinus Cancer 22 0.028
670
ETH012 Ethylene Glycol Poisoning 22 0.028
671
LRY007 Laryngeal Tuberculosis 22 0.028
672
EXP002 Exposure Keratitis 22 0.028
673
DRS001 Dressler's Syndrome 21 0.028
674
ACT181 Acute Motor Axonal Neuropathy 21 0.028
675
ATL010 Atlantoaxial Subluxation 21 0.028
676
SWL001 Swallowing Disorders 21 0.028
677
PRM041 Primary Cortisol Resistance 21 0.028
678
CNG133 Congenital Varicella Syndrome 21 0.028
679
HYP047 Hypertropia 21 0.028
680
c VRL004 Viral Labyrinthitis 20 0.028
681
c HRD043 Hereditary Congenital Facial Paresis 19 0.028
682
c CNG333 Congenital Horner Syndrome 19 0.028
683
MLN002 Melanomatosis 19 0.028
684
PRP013 Paraphimosis 18 0.028
685
c CNG129 Congenital Torticollis 18 0.028
686
HTR005 Heterochromia Iridis 18 0.028
687
CLV002 Clivus Chordoma 18 0.028
688
CNR001 Coenurosis 17 0.028
689
c CHR094 Chronic Polyneuropathy 17 0.028
690
FHR002 Fahr's Syndrome 16 0.028
691
P INT105 Intellectual Disability Multi-Gene Panels 16 0.028
692
INT095 Internal Carotid Agenesis 15 0.028
693
SPN092 Spinal Shock 15 0.028
694
MNS002 Mini Stroke 15 0.028
695
MLL006 Mollaret Meningitis 14 0.028
696
TRG006 Trigger Thumb 14 0.028
697
c DST048 Distal Hereditary Motor Neuropathy Type 1 13 0.028
698
ATY001 Atypical Depressive Disorder 13 0.028
699
BMF002 Bamforth Syndrome 13 0.028
700
BNP002 Bone Epithelioid Hemangioma 13 0.028
701
SPH008 Sphenoidal Sinus Cancer 13 0.028
702
c CHR161 Chiari Malformation Type 3 13 0.028
703
CNM001 Canomad Syndrome 12 0.028
704
SPR038 Supranuclear Ocular Palsy 12 0.028
705
PRS033 Parasitic Ectoparasitic Infectious Disease 12 0.028
706
INF052 Infantile Scoliosis 10 0.028
707
KNG003 Konigsmark Knox Hussels Syndrome 8 0.028
708
GNT013 Genetic Brain Disorders 5 0.028