Search results for "paralysis"

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

716 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
P HYP370 Hypokalemic Periodic Paralysis, Type 1 46 7.030
2
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 30 6.079
3
c INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 37 4.886
4
NRM009 Normokalemic Periodic Paralysis 33 4.701
5
P AND016 Andersen Syndrome 61 4.640
6
P THY054 Thyrotoxic Periodic Paralysis 50 4.511
7
FCL012 Facial Paralysis 38 4.058
8
OCL003 Oculomotor Nerve Paralysis 17 3.653
9
VNN001 Venencie Powell Gordon Winkelmann Syndrome 18 3.536
10
TCK002 Tick Paralysis 22 3.480
11
MBS002 Moebius Syndrome 57 3.277
12
c HYP606 Hypokalemic Periodic Paralysis, Type 2 31 3.250
13
TCK005 Tucker Syndrome 13 3.230
14
BLL003 Bell's Palsy 63 3.122
15
PRN008 Peroneal Nerve Paralysis 16 2.973
16
c THY084 Thyrotoxic Periodic Paralysis 1 19 2.958
17
P SPS154 Spastic Paralysis, Infantile Onset Ascending 17 2.903
18
c HYP142 Hyperkalemic Periodic Paralysis Type 1 12 2.891
19
PRM028 Paramyotonia Congenita 52 2.670
20
KLM001 Klumpke Paralysis 11 2.609
21
GLS003 Glossopharyngeal Nerve Paralysis 9 2.543
22
KRT022 Keratoderma Palmoplantar Spastic Paralysis 6 2.543
23
FML082 Familial Partial Paralysis 3 2.520
24
LRY021 Laryngeal Adductor Paralysis 10 2.507
25
c THY083 Thyrotoxic Periodic Paralysis 2 14 2.493
26
CNG302 Congenital Hereditary Facial Paralysis with Variable Hearing Loss 9 2.493
27
PLM031 Poliomyelitis 52 2.372
28
TDD001 Todd's Paralysis 7 2.219
29
VCL002 Vocal Cord Dysfunction Familial 20 2.092
30
c PRK057 Parkinson Disease, Late-Onset 70 2.067
31
P CRN035 Cranial Nerve Palsy 31 2.067
32
CYC001 Cycloplegia 25 2.067
33
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 10 2.067
34
PRL008 Paralytic Ileus 35 2.053
35
PSD001 Pseudobulbar Palsy 29 2.053
36
FML160 Familial Spastic Paralysis 7 2.053
37
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 6 2.053
38
LRY023 Laryngeal Abductor Paralysis Mental Retardation 3 2.053
39
P SPS003 Spastic Diplegia 40 2.035
40
MRK002 Marek Disease 19 2.035
41
LRY043 Laryngeal Abductor Paralysis - Intellectual Disability 12 2.035
42
PRL020 Paralysis Agitans, Juvenile, of Hunt 6 2.035
43
ISL060 Isolated Hereditary Congenital Facial Paralysis 5 2.035
44
P PRD017 Periodic Paralyses 27 1.529
45
P OPH004 Ophthalmoplegia 54 1.494
46
P HRN001 Horner's Syndrome 42 1.494
47
FZL002 Fazio-Londe Disease 28 1.479
48
c FML159 Familial Periodic Paralyses 10 1.479
49
CNG241 Congenital Laryngeal Palsy 6 1.462
50
GLL022 Guillain-Barre Syndrome 60 1.439
51
TRP002 Tropical Spastic Paraparesis 53 1.439
52
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 29 1.439
53
ABD002 Abducens Nerve Disease 24 1.439
54
c DST092 Distal Hereditary Motor Neuropathy Type 7 16 1.439
55
THR010 Third Cranial Nerve Disease 9 1.439
56
RNL007 Renal Tubular Acidosis 56 0.172
57
HYP005 Hypokalemia 48 0.146
58
THY033 Thyrotoxicosis 57 0.138
59
SPS057 Spasticity 37 0.130
60
P LRY019 Laryngitis 63 0.124
61
P THY032 Thyroiditis 65 0.121
62
P NRP001 Neuropathy 60 0.118
63
P TRC086 Trichohepatoenteric Syndrome 1 45 0.115
64
MYT011 Myotonia 43 0.115
65
NRN002 Neuronitis 42 0.115
66
P MYP004 Myopathy 61 0.112
67
GRV001 Graves' Disease 63 0.109
68
OTT002 Otitis Media 58 0.109
69
THR013 Thoracic Outlet Syndrome 52 0.109
70
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 42 0.109
71
ADN018 Adenoma 64 0.105
72
P RSP003 Respiratory Failure 68 0.094
73
ACN002 Acanthosis Nigricans 63 0.094
74
BTL001 Botulism 59 0.094
75
P ATX010 Ataxia Neuropathy Spectrum 29 0.094
76
P ANG001 Angelman Syndrome 76 0.090
77
P CRV039 Cervicitis 56 0.090
78
c SPN225 Spondyloarthropathy 1 52 0.090
79
P MSC003 Muscular Atrophy 51 0.090
80
ANR040 Aneurysm 45 0.090
81
BNF002 Bone Fracture 45 0.090
82
c ART101 Aortic Valve Disease 2 37 0.090
83
P HYP076 Hyperthyroidism 62 0.081
84
P ALT001 Alternating Hemiplegia of Childhood 61 0.081
85
ACS001 Acoustic Neuroma 50 0.081
86
HYP017 Hypophosphatemia 47 0.081
87
NRM004 Neuroma 46 0.081
88
P PTS002 Ptosis 44 0.081
89
EPL031 Epileptic Hemiplegia 5 0.081
90
AND015 Androgen Insensitivity 78 0.077
91
P MNN013 Meningitis 67 0.077
92
P HRP006 Herpes Simplex 66 0.077
93
LYM017 Lyme Disease 65 0.077
94
P HPT021 Hepatitis 63 0.077
95
MYC002 Mycobacterium Avium Complex Disease 59 0.077
96
P AXN010 Axenfeld-Rieger Syndrome, Type 3 57 0.077
97
c PRG001 Progressive Muscular Atrophy 36 0.077
98
c BNG076 Benign Exophthalmos Syndrome 21 0.077
99
AND005 Androgen Insensitivity Syndrome, Mild 19 0.077
100
HRP004 Herpes Zoster 56 0.072
101
CHL069 Cholesteatoma 52 0.072
102
MNN014 Mononeuritis 49 0.072
103
CNV002 Conversion Disorder 48 0.072
104
WST005 West Nile Virus 47 0.072
105
GTR002 Goiter 61 0.066
106
STT002 Status Asthmaticus 60 0.066
107
P ATX004 Ataxia 58 0.066
108
MYL001 Myelitis 53 0.066
109
MLK003 Melkersson-Rosenthal Syndrome 51 0.066
110
PRT026 Parotitis 48 0.066
111
NRT004 Neuritis 48 0.066
112
ECT005 Ectropion 42 0.066
113
LCK001 Locked-in Syndrome 41 0.066
114
WND001 Wound Botulism 40 0.066
115
PRL013 Paralytic Poliomyelitis 37 0.066
116
PSL001 Pasli Disease 35 0.066
117
LGP001 Lagophthalmos 30 0.066
118
P ATX030 Ataxia-Telangiectasia 86 0.061
119
TBR010 Tuberculosis 84 0.061
120
c AMY091 Amyotrophic Lateral Sclerosis 1 81 0.061
121
P MYS003 Myasthenia Gravis 72 0.061
122
MLG056 Malignant Hyperthermia 69 0.061
123
P CHR071 Charcot-Marie-Tooth Disease 69 0.061
124
P PLY019 Polyneuropathy 60 0.061
125
PTN002 Patent Ductus Arteriosus 57 0.061
126
ART001 Arterial Tortuosity Syndrome 56 0.061
127
SNS001 Sensorineural Hearing Loss 55 0.061
128
TTH006 Tooth Disease 53 0.061
129
DYS073 Dysphagia 51 0.061
130
P MSC033 Muscle Disorders 48 0.061
131
PRP016 Paraplegia 46 0.061
132
CRB009 Cerebritis 37 0.061
133
ERB002 Erb's Palsy 10 0.061
134
c SYS001 Systemic Lupus Erythematosus 92 0.054
135
P NRC002 Narcolepsy 78 0.054
136
P LPS004 Lupus Erythematosus 76 0.054
137
P LKM002 Leukemia 76 0.054
138
PRP083 Porphyria, Acute Intermittent 73 0.054
139
ART016 Aortic Aneurysm 71 0.054
140
P HYP086 Hypothyroidism 68 0.054
141
c HPT001 Hepatitis C 65 0.054
142
PTT006 Pituitary Adenoma 60 0.054
143
P DBT005 Diabetes Insipidus 57 0.054
144
P SYR001 Syringomyelia 57 0.054
145
ARC007 Arachnoid Cysts 57 0.054
146
P HYP065 Hyperaldosteronism 57 0.054
147
BRN029 Brain Disease 56 0.054
148
HMP005 Hemiplegia 51 0.054
149
P SCL018 Scoliosis 51 0.054
150
NRM005 Neuromuscular Disease 50 0.054
151
P NRV007 Nervous System Disease 49 0.054
152
P SJG001 Sjogren's Syndrome 46 0.054
153
CRT008 Carotid Artery Dissection 46 0.054
154
MDS022 Mediastinitis 45 0.054
155
MNN009 Meningoencephalitis 45 0.054
156
c SBC007 Subacute Thyroiditis 44 0.054
157
ARC002 Arachnoiditis 43 0.054
158
QDR001 Quadriplegia 42 0.054
159
SPP008 Suppurative Otitis Media 40 0.054
160
MLL002 Miller Fisher Syndrome 37 0.054
161
FTD001 Foot Drop 36 0.054
162
P LBY004 Labyrinthitis 33 0.054
163
GNC003 Geniculate Herpes Zoster 31 0.054
164
FDB001 Foodborne Botulism 26 0.054
165
ANT054 Anotia 24 0.054
166
MDD008 Middle Ear Adenoma 15 0.054
167
FBR024 Fibrocartilaginous Embolism 14 0.054
168
MLR004 Malaria 84 0.047
169
CDS001 Cadasil 81 0.047
170
MLT021 Multiple System Atrophy 80 0.047
171
P PNM007 Pneumonia 76 0.047
172
P AMY004 Amyloidosis 73 0.047
173
P NRB001 Neuroblastoma 72 0.047
174
P HMN010 Hemangioma 69 0.047
175
PLY017 Polyarteritis Nodosa 69 0.047
176
SRC014 Sarcoma 68 0.047
177
OLV001 Olivopontocerebellar Atrophy 67 0.047
178
P TRN020 Turner Syndrome 67 0.047
179
P SPN046 Spinal Muscular Atrophy 66 0.047
180
P ENC004 Encephalitis 64 0.047
181
STT001 Status Epilepticus 64 0.047
182
SPN186 Spinal Cord Injury 62 0.047
183
P ATR011 Atrial Fibrillation 62 0.047
184
P MSC005 Muscular Dystrophy 62 0.047
185
MTR014 Motor Neuron Disease 61 0.047
186
ASP003 Aseptic Meningitis 60 0.047
187
P MMP001 Mumps 58 0.047
188
SPN020 Spondylosis 58 0.047
189
P THR003 Thoracic Aortic Aneurysm 58 0.047
190
NRL005 Neurilemmoma 58 0.047
191
RBS001 Rabies 57 0.047
192
P MNT147 Mental Retardation 56 0.047
193
ADR008 Adrenal Adenoma 55 0.047
194
P BLN003 Blindness 54 0.047
195
TRY002 Troyer Syndrome 54 0.047
196
LPT001 Leptospirosis 52 0.047
197
TLR001 Tularemia 52 0.047
198
P FNC004 Fanconi Syndrome 51 0.047
199
RLP003 Relapsing Fever 48 0.047
200
WST004 West Nile Encephalitis 46 0.047
201
P EPL002 Epilepsy Syndrome 46 0.047
202
ATN005 Autonomic Dysfunction 45 0.047
203
FSC004 Fasciitis 45 0.047
204
P NRN017 Neuronopathy, Distal Hereditary Motor, Type Vi 44 0.047
205
SPN185 Spinal Cord Infarction 42 0.047
206
P PRX033 Proximal Renal Tubular Acidosis 42 0.047
207
PPL046 Popliteal Pterygium Syndrome 1 42 0.047
208
EPD005 Epidural Abscess 41 0.047
209
PRG097 Paragangliomas 1, with or Without Deafness 40 0.047
210
BRW001 Brown-Vialetto-Van Laere Syndrome 37 0.047
211
P FML249 Familial Amyloidosis, Finnish Type 36 0.047
212
TLS001 Tolosa-Hunt Syndrome 36 0.047
213
HYP264 Hypertonia 35 0.047
214
c SPS078 Spastic Paraplegia 7 35 0.047
215
P SPS012 Spastic Paraplegia 3a 35 0.047
216
TBS001 Tabes Dorsalis 35 0.047
217
CLR007 Colorado Tick Fever 34 0.047
218
TFT003 Tufting Enteropathy 31 0.047
219
UND005 Undifferentiated Pleomorphic Sarcoma 30 0.047
220
PTR001 Petrositis 27 0.047
221
CVR002 Cavernous Sinus Thrombosis 26 0.047
222
PRS053 Parsonage Turner Syndrome 22 0.047
223
BLB003 Bulbar Polio 20 0.047
224
ABD009 Abducens Palsy 20 0.047
225
PNT023 Pontine Hemorrhage 18 0.047
226
SKL006 Skull Base Neoplasm 10 0.047
227
P BRS047 Breast Cancer 91 0.038
228
P DBT085 Diabetes Mellitus, Insulin-Dependent 85 0.038
229
P LPR003 Leprosy 81 0.038
230
NRL016 Neural Tube Defects 79 0.038
231
P BRD002 Bardet-Biedl Syndrome 75 0.038
232
P CNG368 Congenital Adrenal Hyperplasia 74 0.038
233
GTL001 Gitelman Syndrome 73 0.038
234
P HYP117 Hypertriglyceridemia 71 0.038
235
PRT036 Peritonitis 71 0.038
236
P CNG401 Congenital Heart Disease 70 0.038
237
STR067 Stroke, Ischemic 69 0.038
238
MSL001 Measles 67 0.038
239
PLS006 Plasmodium Vivax Malaria 66 0.038
240
CRB039 Cerebrovascular Disease 66 0.038
241
c ATM010 Autoimmune Hemolytic Anemia 66 0.038
242
P PRP029 Porphyria 66 0.038
243
INS024 Insulin-Like Growth Factor I 65 0.038
244
PHR003 Pharyngitis 65 0.038
245
P TXP001 Toxoplasmosis 65 0.038
246
P HML002 Hemolytic Anemia 65 0.038
247
c LNG044 Long Qt Syndrome 1 64 0.038
248
P EHL001 Ehlers-Danlos Syndrome 64 0.038
249
TRG002 Trigeminal Neuralgia 63 0.038
250
BBS001 Babesiosis 63 0.038
251
CPR001 Coproporphyria 63 0.038
252
c HRD010 Hereditary Spastic Paraplegia 62 0.038
253
P KLP003 Klippel-Feil Syndrome 62 0.038
254
c MLG069 Malignant Hypertension 62 0.038
255
P ACR001 Aicardi-Goutieres Syndrome 62 0.038
256
P ESP024 Esophagitis 62 0.038
257
P ART023 Arthropathy 62 0.038
258
ART005 Arteriovenous Malformation 61 0.038
259
STF001 Stiff-Person Syndrome 60 0.038
260
P NRM001 Neuromyelitis Optica 59 0.038
261
GLC003 Glucose Intolerance 59 0.038
262
RHB003 Rhabdomyosarcoma 59 0.038
263
NRC020 Neuroectodermal Tumor 58 0.038
264
P SZR006 Seizure Disorder 58 0.038
265
P EMR001 Emery-Dreifuss Muscular Dystrophy 58 0.038
266
YLL002 Yellow Fever 58 0.038
267
c SCN006 Secondary Syphilis 58 0.038
268
HDC001 Headache 57 0.038
269
c CNG021 Congenital Toxoplasmosis 57 0.038
270
HMF006 Hemifacial Microsomia 57 0.038
271
P MYC008 Myocarditis 56 0.038
272
P NML001 Nemaline Myopathy 56 0.038
273
PRP025 Peripheral Primitive Neuroectodermal Tumor 56 0.038
274
P SYP003 Syphilis 56 0.038
275
P TRM003 Tremor 56 0.038
276
c CHR095 Chronic Progressive External Ophthalmoplegia 55 0.038
277
MYL003 Myeloid Sarcoma 55 0.038
278
GST037 Gastroparesis 55 0.038
279
JPN002 Japanese Encephalitis 54 0.038
280
P OST028 Osteochondroma 54 0.038
281
P PRG013 Paraganglioma 54 0.038
282
THY009 Thyroid Lymphoma 54 0.038
283
P PRT029 Parathyroid Adenoma 53 0.038
284
NWC001 Newcastle Disease 53 0.038
285
SCH016 Schimke Immunoosseous Dysplasia 53 0.038
286
EHR002 Ehrlichiosis 52 0.038
287
TCK001 Tick-Borne Encephalitis 52 0.038
288
P EPS003 Episodic Ataxia 52 0.038
289
GST045 Gastroenteritis 52 0.038
290
SPT005 Spotted Fever 52 0.038
291
OST011 Osteomalacia 51 0.038
292
PRP023 Peripheral Neuropathy 51 0.038
293
STL001 St. Louis Encephalitis 50 0.038
294
RNL011 Renal Osteodystrophy 49 0.038
295
P PNM006 Pneumoconiosis 49 0.038
296
OPT009 Optic Neuritis 49 0.038
297
NPH003 Nephrocalcinosis 48 0.038
298
P TRN034 Transverse Myelitis 47 0.038
299
P HMR005 Hemorrhoid 47 0.038
300
NSP002 Nasopharyngitis 46 0.038
301
EVN001 Evans' Syndrome 45 0.038
302
KRT012 Keratoderma 45 0.038
303
CNT025 Central Pontine Myelinolysis 45 0.038
304
P PRS062 Persistent Hyperplastic Primary Vitreous 45 0.038
305
PST055 Postural Hypotension 44 0.038
306
ILS001 Ileus 44 0.038
307
PRS037 Periostitis 44 0.038
308
OST006 Osteoblastoma 44 0.038
309
P CHR342 Chiari Malformation 43 0.038
310
TTR016 Tetra-Amelia Syndrome 42 0.038
311
MYH012 Myhre Syndrome 42 0.038
312
LCR004 La Crosse Encephalitis 41 0.038
313
APH002 Aphasia 41 0.038
314
c AMY008 Amyotrophic Lateral Sclerosis Type 2 40 0.038
315
TRC023 Trichinosis 39 0.038
316
THY035 Thyroid Adenoma 38 0.038
317
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.038
318
HYD001 Hydranencephaly 38 0.038
319
P AXN001 Axonal Neuropathy 37 0.038
320
P OTT001 Otitis Externa 37 0.038
321
PSD029 Pseudocholinesterase Deficiency 37 0.038
322
c SPS092 Spastic Paraplegia 11 36 0.038
323
XRP001 Xerophthalmia 36 0.038
324
NRP016 Neuropathy, Recurrent, with Pressure Palsies 36 0.038
325
RCK002 Rocky Mountain Spotted Fever 36 0.038
326
MTC018 Metachondromatosis 35 0.038
327
ADS002 Adie Syndrome 34 0.038
328
NRC019 Neurocutaneous Melanosis, Somatic 34 0.038
329
SPS016 Spasmodic Dysphonia 33 0.038
330
INT042 Internuclear Ophthalmoplegia 32 0.038
331
ENT005 Entropion 31 0.038
332
c CHR160 Chiari Malformation Type 2 31 0.038
333
CBB002 Cobb Syndrome 30 0.038
334
FCL003 Facial Hemiatrophy 30 0.038
335
HNM002 Hinman Syndrome 29 0.038
336
PLY119 Polymicrogyria, Bilateral Perisylvian 29 0.038
337
PRP056 Porphyria, Acute Hepatic 28 0.038
338
c PRG020 Paragangliomas 3 28 0.038
339
c ACT159 Acute Transverse Myelitis 27 0.038
340
PRR008 Periarteritis Nodosa 27 0.038
341
BRW004 Brown-Sequard Syndrome 26 0.038
342
ECT004 Ecthyma 26 0.038
343
c PRG019 Paragangliomas 2 25 0.038
344
TCK004 Tick Infestation 25 0.038
345
VST004 Vestibular Disease 24 0.038
346
c SPS042 Spastic Paraplegia 9 23 0.038
347
STR002 Streptococcal Meningitis 22 0.038
348
c NRP022 Neuropathy, Distal Hereditary Motor, Type Viib 20 0.038
349
PWS001 Powassan Encephalitis 18 0.038
350
MNN005 Meningovascular Neurosyphilis 18 0.038
351
CNT067 Central Cord Syndrome 18 0.038
352
ITR001 Iatrogenic Botulism 17 0.038
353
c NRC009 Narcolepsy 1 17 0.038
354
OTP003 Oto-Palatal-Digital Syndrome 17 0.038
355
SYR004 Syringobulbia 15 0.038
356
c ADL069 Adult Intestinal Botulism 15 0.038
357
TXN001 Toxin-Mediated Infectious Botulism 12 0.038
358
MYP026 Myopathy - Thyrotoxic 8 0.038
359
SPN015 Spinal Polio 8 0.038
360
BLB001 Bulbospinal Polio 8 0.038
361
BRC057 Brachial Plexus Birth Injuries 7 0.038
362
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.038
363
HMP020 Hemiplegia Alterans 1 0.038
364
HPT023 Hepatocellular Carcinoma 100 0.027
365
P AST005 Asthma 91 0.027
366
P LFR001 Li-Fraumeni Syndrome 90 0.027
367
P MTC003 Metachromatic Leukodystrophy 87 0.027
368
P DLT002 Dilated Cardiomyopathy 86 0.027
369
GLC006 Galactosemia 85 0.027
370
c MLT019 Multiple Myeloma 85 0.027
371
P TYS001 Tay-Sachs Disease 84 0.027
372
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.027
373
P OST002 Osteoporosis 81 0.027
374
P GCH001 Gaucher's Disease 80 0.027
375
P NRF002 Neurofibromatosis 79 0.027
376
HV1006 Hiv-1 79 0.027
377
BHC002 Behcet's Disease 79 0.027
378
P MYL005 Myelofibrosis 78 0.027
379
c FNC027 Fanconi Anemia, Complementation Group a 78 0.027
380
P ALX003 Alexander Disease 76 0.027
381
CHD001 Chediak-Higashi Syndrome 76 0.027
382
CRB011 Cerebrotendinous Xanthomatosis 76 0.027
383
KWS002 Kawasaki Disease 75 0.027
384
P BPL003 Bipolar Disorder 75 0.027
385
WLF001 Wolff-Parkinson-White Syndrome 74 0.027
386
P OST001 Osteopetrosis 74 0.027
387
P HYP035 Hypophosphatasia 74 0.027
388
CYS008 Cystic Echinococcosis 73 0.027
389
ADD001 Addison's Disease 73 0.027
390
ABT001 Abetalipoproteinemia 72 0.027
391
RLP001 Relapsing Polychondritis 72 0.027
392
MCK007 Muckle-Wells Syndrome 72 0.027
393
P SCL016 Scleroderma 72 0.027
394
P MYS005 Myositis 71 0.027
395
CCC001 Coccidioidomycosis 71 0.027
396
CNT098 Central Core Disease 70 0.027
397
PGT005 Paget Disease of Bone 70 0.027
398
P MCH002 Machado-Joseph Disease 70 0.027
399
P CMR001 Camurati-Engelmann Disease 69 0.027
400
P ALP004 Alport Syndrome 69 0.027
401
KRT004 Keratitis 69 0.027
402
ALC007 Alcohol Dependence 68 0.027
403
c HPT016 Hepatitis B 68 0.027
404
P INF038 Influenza 68 0.027
405
P GLM007 Glomerulonephritis 67 0.027
406
P ABD003 Abdominal Aortic Aneurysm 67 0.027
407
c PRC016 Pre-Eclampsia 67 0.027
408
c NRF019 Neurofibromatosis, Type 2 67 0.027
409
ALV002 Alveolar Echinococcosis 67 0.027
410
FCT003 Factor X Deficiency 67 0.027
411
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 67 0.027
412
BRK010 Burkitt Lymphoma 67 0.027
413
WLL001 Williams-Beuren Syndrome 66 0.027
414
P THY023 Thymoma 66 0.027
415
PLM033 Pulmonary Embolism 66 0.027
416
P HYP004 Hypercalcemia 66 0.027
417
TWN003 Townes-Brocks Syndrome 66 0.027
418
P WRD001 Waardenburg's Syndrome 65 0.027
419
c FML001 Familial Atrial Fibrillation 65 0.027
420
CYS010 Cystinosis 65 0.027
421
c ALM001 Al Amyloidosis 65 0.027
422
P KDN018 Kidney Disease 64 0.027
423
c ATM003 Autoimmune Thyroiditis 64 0.027
424
P BRG001 Brugada Syndrome 64 0.027
425
GST009 Gastroschisis 64 0.027
426
P SCH018 Schizencephaly 64 0.027
427
c TYR012 Tyrosinemia, Type I 63 0.027
428
c SML001 Small Cell Carcinoma 63 0.027
429
MNT001 Mantle Cell Lymphoma 63 0.027
430
P CRB042 Cerebellar Ataxia 63 0.027
431
RBR001 Roberts Syndrome 63 0.027
432
MLN008 Melanoma 63 0.027
433
WLD002 Waldenstrom Macroglobulinemia 63 0.027
434
P RHB017 Rhabdoid Tumor 62 0.027
435
P OLG002 Oligodendroglioma 62 0.027
436
c GLY008 Glycogen Storage Disease Ii 62 0.027
437
P HMP002 Hemophagocytic Lymphohistiocytosis 62 0.027
438
P CNG001 Congenital Myasthenic Syndrome 62 0.027
439
CHR072 Chordoma 62 0.027
440
c HYP595 Hypertension, Essential 62 0.027
441
WGN006 Wegener Granulomatosis 61 0.027
442
LRN003 Learning Disability 61 0.027
443
P CNJ013 Conjunctivitis 61 0.027
444
P INT070 Intestinal Obstruction 61 0.027
445
KRN002 Kearns-Sayre Syndrome 60 0.027
446
P MTR012 Mitral Valve Disease 60 0.027
447
PTN001 Patent Foramen Ovale 60 0.027
448
CLD007 Cold Agglutinin Disease 60 0.027
449
NRL004 Neuroleptic Malignant Syndrome 60 0.027
450
SPH001 Sapho Syndrome 60 0.027
451
P FBR017 Fibrosarcoma 60 0.027
452
P FML043 Familial Idiopathic Basal Ganglia Calcification 60 0.027
453
P HYP141 Hyperphenylalaninemia 59 0.027
454
P MYL007 Myeloma 59 0.027
455
P MYM002 Moyamoya Disease 59 0.027
456
CHC001 Chickenpox 59 0.027
457
MGC001 Megacolon 59 0.027
458
PMP001 Pemphigus 59 0.027
459
BLR001 Biliary Atresia 58 0.027
460
KRT001 Keratoconjunctivitis Sicca 58 0.027
461
P CTR002 Cataract 58 0.027
462
P MST018 Mesothelioma 58 0.027
463
BLD087 Bladder Cancer, Somatic 57 0.027
464
CVR006 Cavernous Hemangioma 57 0.027
465
LYM019 Lymphosarcoma 57 0.027
466
BNC003 Bone Cancer 57 0.027
467
ANR004 Anuria 57 0.027
468
END030 End Stage Renal Failure 57 0.027
469
HMM003 Hemimegalencephaly 57 0.027
470
P CRN012 Craniometaphyseal Dysplasia 57 0.027
471
THY022 Thymic Carcinoma 57 0.027
472
PRN023 Prion Disease 56 0.027
473
HYP458 Hyper Ige Syndrome 56 0.027
474
HYP024 Hypoparathyroidism 56 0.027
475
P ENC008 Encephalocele 56 0.027
476
c FML023 Familial Hemiplegic Migraine 55 0.027
477
c MLT024 Multiple Endocrine Neoplasia Iia 55 0.027
478
P FML161 Familial Mediterranean Fever, Ar 55 0.027
479
ANK001 Ankylosis 55 0.027
480
c VRL012 Viral Meningitis 55 0.027
481
P DND001 Dandy-Walker Syndrome 55 0.027
482
P SPN049 Spinocerebellar Ataxia 55 0.027
483
MDL009 Medullary Sponge Kidney 55 0.027
484
c ACT073 Acute Leukemia 55 0.027
485
P GNT008 Giant Cell Tumor 55 0.027
486
MLT075 Multifocal Motor Neuropathy 54 0.027
487
P HYP014 Hyperuricemia 54 0.027
488
PLG002 Plague 54 0.027
489
P EXP004 Exophthalmos 54 0.027
490
SLP005 Sleep Disorder 54 0.027
491
FBR009 Fibrous Dysplasia 54 0.027
492
LYM022 Lymphangioma 54 0.027
493
PRN011 Pernicious Anemia 53 0.027
494
STS002 Situs Inversus 53 0.027
495
c PND001 Pain Disorder 53 0.027
496
ESP020 Esophageal Atresia 53 0.027
497
VNB005 Van Buchem Disease 53 0.027
498
HNT002 Hantavirus Pulmonary Syndrome 52 0.027
499
P GRS003 Griscelli Syndrome 52 0.027
500
P AML002 Amelogenesis Imperfecta 52 0.027
501
BSL009 Basal Ganglia Calcification 52 0.027
502
PRC013 Pericarditis 52 0.027
503
MYX004 Myxedema 52 0.027
504
GRW007 Growth Hormone Deficiency 52 0.027
505
P SPN183 Spontaneous Pneumothorax 52 0.027
506
ACQ007 Acquired Immunodeficiency Syndrome 51 0.027
507
ANG002 Angiostrongyliasis 51 0.027
508
TRN015 Transient Cerebral Ischemia 51 0.027
509
DGS001 Degos Disease 51 0.027
510
TRC040 Tracheoesophageal Fistula 51 0.027
511
CYS016 Cystic Kidney 51 0.027
512
BRS064 Bursitis 50 0.027
513
PRP032 Porphyria Variegata 50 0.027
514
EWN002 Ewing's Family of Tumors 50 0.027
515
EXS001 Exostosis 50 0.027
516
P NRX001 Neuroaxonal Dystrophy 50 0.027
517
MTH009 Mouth Disease 49 0.027
518
HYP006 Hypertensive Heart Disease 49 0.027
519
P APL006 Aplasia Cutis Congenita 49 0.027
520
CHR288 Chronic Recurrent Multifocal Osteomyelitis 49 0.027
521
P BNG071 Benign Schwannoma 49 0.027
522
FBR047 Fibromyalgia 49 0.027
523
INF058 Inflammatory Myofibroblastic Tumor 49 0.027
524
CTS002 Cat-Scratch Disease 49 0.027
525
PNM008 Pneumothorax 48 0.027
526
c CRB103 Cerebral Cavernous Malformations-1 48 0.027
527
PLS016 Plasma Cell Leukemia 48 0.027
528
MMB001 Membranoproliferative Glomerulonephritis 48 0.027
529
P HYP120 Hypoaldosteronism 48 0.027
530
HJD001 Hajdu-Cheney Syndrome 48 0.027
531
SLV012 Salivary Gland Adenoid Cystic Carcinoma 48 0.027
532
ATN004 Autonomic Neuropathy 48 0.027
533
MLR003 Melorheostosis 48 0.027
534
c PSD092 Pseudohypoaldosteronism, Type Iie 48 0.027
535
P HYP345 Hyper-Ige Recurrent Infection Syndrome 48 0.027
536
ASP007 Aspiration Pneumonia 47 0.027
537
CHK001 Chikungunya 47 0.027
538
MFF001 Maffucci Syndrome 47 0.027
539
PLM010 Pulmonary Edema 47 0.027
540
P MLG086 Malignant Hyperthermia Susceptibility 47 0.027
541
P FNG005 Feingold Syndrome 47 0.027
542
CNN003 Conn's Syndrome 46 0.027
543
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 46 0.027
544
P MLT008 Multinodular Goiter 46 0.027
545
MTS001 Mutism 46 0.027
546
AMB002 Amblyopia 46 0.027
547
P DMY001 Demyelinating Polyneuropathy 46 0.027
548
LYM021 Lymphadenitis 45 0.027
549
MYS001 Myositis Ossificans 45 0.027
550
FTT001 Fatty Liver Disease 45 0.027
551
TNG009 Tongue Squamous Cell Carcinoma 45 0.027
552
MCP006 Mucoepidermoid Carcinoma 45 0.027
553
FCT022 Factor Xi Deficiency, Autosomal Recessive 44 0.027
554
MDD002 Middle Ear Cholesteatoma 44 0.027
555
ACT012 Acute Hemorrhagic Conjunctivitis 44 0.027
556
ZYG002 Zygomycosis 44 0.027
557
SPN050 Spinocerebellar Degeneration 44 0.027
558
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 44 0.027
559
c OPT055 Optic Atrophy Plus Syndrome 44 0.027
560
c HRD086 Hereditary Hypophosphatemic Rickets 44 0.027
561
NCR007 Necrotizing Fasciitis 44 0.027
562
HTS001 Hiatus Hernia 43 0.027
563
c SRC025 Sarcoidosis 1 43 0.027
564
NTR001 Neutral Lipid Storage Disease 43 0.027
565
GYN001 Gynecomastia 43 0.027
566
ATY005 Atypical Teratoid Rhabdoid Tumor 43 0.027
567
WHP001 Whipple Disease 43 0.027
568
RSS002 Roussy-Levy Syndrome 43 0.027
569
THY043 Thymic Hyperplasia 42 0.027
570
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 42 0.027
571
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 42 0.027
572
c LPD037 Lipodystrophy, Familial Partial, 2 42 0.027
573
MTC056 Mitochondrial Dna Depletion Syndrome 4a 42 0.027
574
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 41 0.027
575
c OST137 Osteopetrosis, Autosomal Recessive 4 41 0.027
576
SRC001 Sarcomatoid Mesothelioma 41 0.027
577
EST005 Esotropia 41 0.027
578
P RSM001 Rasmussen Encephalitis 41 0.027
579
P RNL066 Renal Tubular Acidosis, Distal, Ad 41 0.027
580
ADR043 Adrenal Hyperplasia, Congenital, Due to 11-Beta-Hydroxylase Deficiency 41 0.027
581
P HYP265 Hypotonia 41 0.027
582
RMS001 Rem Sleep Behavior Disorder 41 0.027
583
SPS019 Spastic Paraparesis 41 0.027
584
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 40 0.027
585
CDQ001 Cauda Equina Syndrome 40 0.027
586
P PRC031 Preeclampsia/eclampsia 1 40 0.027
587
ESN020 Eosinophilic Granulomatosis with Polyangiitis 40 0.027
588
c EXS004 Exostoses, Multiple, Type 1 40 0.027
589
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 40 0.027
590
P MNN007 Meningocele 40 0.027
591
LRY029 Laryngomalacia 40 0.027
592
SCT002 Scotoma 39 0.027
593
c SPS079 Spastic Paraplegia 2 39 0.027
594
END051 Endolymphatic Sac Tumor 39 0.027
595
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 38 0.027
596
c SCP001 Sc Phocomelia Syndrome 38 0.027
597
PLM029 Palmoplantar Keratosis 38 0.027
598
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 37 0.027
599
SPC005 Speech Disorder 37 0.027
600
P NRV006 Nervous System Cancer 37 0.027
601
BRN016 Bronchogenic Carcinoma 37 0.027
602
INF006 Infant Botulism 37 0.027
603
HNS001 Hansen's Disease 37 0.027
604
LMB010 Lambert Syndrome 37 0.027
605
TRP004 Tropical Sprue 36 0.027
606
IPX001 Ipex Syndrome 36 0.027
607
SCR015 Scarlet Fever 36 0.027
608
P GLM006 Glomangioma 36 0.027
609
c CNT033 Central Nervous System Cancer 36 0.027
610
VRL011 Viral Infectious Disease 35 0.027
611
PLM074 Pulmonary Function 35 0.027
612
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 35 0.027
613
CSL001 Causalgia 34 0.027
614
PMP008 Pemphigus Vegetans 34 0.027
615
c HRD088 Hereditary Neuropathies 34 0.027
616
MRR003 Murray Valley Encephalitis 34 0.027
617
PST020 Postpoliomyelitis Syndrome 33 0.027
618
HYP034 Hypertensive Encephalopathy 33 0.027
619
SPR007 Superior Mesenteric Artery Syndrome 33 0.027
620
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.027
621
ANT018 Anthracosis 33 0.027
622
c GM2005 Gm2-Gangliosidosis, Ab Variant 32 0.027
623
PNM005 Pneumonic Plague 31 0.027
624
c OST131 Osteopetrosis, Autosomal Dominant 2 31 0.027
625
CNG133 Congenital Varicella Syndrome 31 0.027
626
NRG004 Neurogenic Diabetes Insipidus 30 0.027
627
c OST126 Osteopetrosis, Autosomal Recessive 1 30 0.027
628
c SPS027 Spastic Paraplegia 17 30 0.027
629
CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 30 0.027
630
P PHC014 Phocomelia 30 0.027
631
MNR004 Mounier-Kuhn Syndrome 30 0.027
632
c CNG112 Congenital Muscular Dystrophy Type 1a 29 0.027
633
FRY001 Frey Syndrome 29 0.027
634
VST003 Vestibular Nystagmus 29 0.027
635
BRC010 Brachial Plexus Lesion 29 0.027
636
c SPS025 Spastic Paraplegia 15 29 0.027
637
DYG001 Dyggve-Melchior-Clausen Disease 29 0.027
638
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 29 0.027
639
NRS003 Neurosyphilis 28 0.027
640
CRV030 Cervical Adenitis 28 0.027
641
CRN051 Craniofacial Microsomia 28 0.027
642
THY025 Thymus Cancer 28 0.027
643
FBR028 Fibrosing Mediastinitis 28 0.027
644
HYP362 Hyperopia 28 0.027
645
LPN001 Louping Ill 28 0.027
646
WYB001 Wyburn Mason's Syndrome 27 0.027
647
MYC014 Mycobacterium Chelonae 27 0.027
648
AMY005 Amyloid Neuropathy 27 0.027
649
c OST129 Osteopetrosis, Autosomal Recessive 2 27 0.027
650
c SYS043 Systemic Lupus Erythematosus 1 26 0.027
651
c SPS013 Spastic Paraplegia 8 26 0.027
652
c CRB094 Cerebral Cavernous Malformations 3 26 0.027
653
GNT004 Gnathomiasis 26 0.027
654
SNS003 Sensory Peripheral Neuropathy 25 0.027
655
c SPS091 Spastic Paraplegia 4 25 0.027
656
P INT006 Intestinal Botulism 25 0.027
657
ANT013 Anterior Spinal Artery Syndrome 25 0.027
658
c PSD090 Pseudohypoaldosteronism, Type Iia 25 0.027
659
c CHR097 Chronic Purulent Otitis Media 24 0.027
660
P FRT001 Fourth Cranial Nerve Palsy 24 0.027
661
ECH002 Echolalia 24 0.027
662
LTR002 Lateral Sinus Thrombosis 24 0.027
663
EXC003 Excessive Tearing 24 0.027
664
HSH001 Hashimoto-Pritzker Syndrome 24 0.027
665
HYP048 Hypotropia 24 0.027
666
TMR013 Tumor Necrosis Factor Receptor 1 Associated Periodic Syndrome 24 0.027
667
MYP093 Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset 23 0.027
668
PRS120 Persistent Idiopathic Facial Pain 23 0.027
669
ATR055 Atrial Septal Aneurysm 23 0.027
670
CRT009 Critical Illness Polyneuropathy 23 0.027
671
ETH012 Ethylene Glycol Poisoning 22 0.027
672
PRN016 Peroneal Neuropathy 22 0.027
673
ACT181 Acute Motor Axonal Neuropathy 22 0.027
674
ATL010 Atlantoaxial Subluxation 22 0.027
675
SBS002 Substernal Goiter 22 0.027
676
PNT009 Pontine Tegmental Cap Dysplasia 22 0.027
677
GLT018 Glut1 Deficiency Syndrome 1 21 0.027
678
c MYP081 Myopathy, Myofibrillar, 6 21 0.027
679
DRS001 Dressler's Syndrome 21 0.027
680
EXP002 Exposure Keratitis 21 0.027
681
SWL001 Swallowing Disorders 21 0.027
682
LRY007 Laryngeal Tuberculosis 20 0.027
683
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 20 0.027
684
c NRF011 Neurofibromatosis Type 3a 20 0.027
685
MYC001 Myoclonic Cerebellar Dyssynergia 20 0.027
686
P SNS011 Sinus Cancer 20 0.027
687
HYP047 Hypertropia 19 0.027
688
ACT214 Acetazolamide-Responsive Myotonia 19 0.027
689
c VRL004 Viral Labyrinthitis 19 0.027
690
HTR005 Heterochromia Iridis 18 0.027
691
BRW009 Brown-Vialetto-Van Laere Syndrome 1 18 0.027
692
c CNG129 Congenital Torticollis 18 0.027
693
MLN002 Melanomatosis 18 0.027
694
c NRN027 Neuronopathy, Distal Hereditary Motor, Type I 18 0.027
695
PRP013 Paraphimosis 17 0.027
696
BMF002 Bamforth Syndrome 17 0.027
697
INT095 Internal Carotid Agenesis 17 0.027
698
P INT105 Intellectual Disability Multi-Gene Panels 17 0.027
699
CLV002 Clivus Chordoma 16 0.027
700
CNR001 Coenurosis 16 0.027
701
c CHR094 Chronic Polyneuropathy 15 0.027
702
MLL006 Mollaret Meningitis 15 0.027
703
INH013 Inhalational Botulism 15 0.027
704
SPN092 Spinal Shock 15 0.027
705
MNS002 Mini Stroke 14 0.027
706
TRG006 Trigger Thumb 13 0.027
707
CNM001 Canomad Syndrome 12 0.027
708
BDR001 Bidirectional Tachycardia 12 0.027
709
SPH008 Sphenoidal Sinus Cancer 12 0.027
710
ATY001 Atypical Depressive Disorder 12 0.027
711
BNP002 Bone Epithelioid Hemangioma 11 0.027
712
PRS033 Parasitic Ectoparasitic Infectious Disease 11 0.027
713
c INF052 Infantile Scoliosis 10 0.027
714
SPR038 Supranuclear Ocular Palsy 10 0.027
715
KNG003 Konigsmark Knox Hussels Syndrome 9 0.027
716
WST006 Westphal Disease 4 0.027