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 41 7.180
2
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 26 6.086
3
c INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 32 4.677
4
P AND016 Andersen Syndrome 54 4.640
5
P THY054 Thyrotoxic Periodic Paralysis 43 4.241
6
NRM009 Normokalemic Periodic Paralysis 24 4.234
7
FCL012 Facial Paralysis 35 3.688
8
VNN001 Venencie Powell Gordon Winkelmann Syndrome 16 3.525
9
TCK002 Tick Paralysis 19 3.111
10
OCL003 Oculomotor Nerve Paralysis 15 3.030
11
c HYP606 Hypokalemic Periodic Paralysis, Type 2 27 2.933
12
TCK005 Tucker Syndrome 11 2.891
13
BLL003 Bell's Palsy 54 2.746
14
PRN008 Peroneal Nerve Paralysis 13 2.609
15
MBS002 Moebius Syndrome 51 2.562
16
P SPS154 Spastic Paralysis, Infantile Onset Ascending 15 2.542
17
c HYP142 Hyperkalemic Periodic Paralysis Type 1 10 2.532
18
PLM031 Poliomyelitis 45 2.372
19
PRM028 Paramyotonia Congenita 45 2.225
20
KLM001 Klumpke Paralysis 10 2.176
21
c THY084 Thyrotoxic Periodic Paralysis 1 15 2.147
22
GLS003 Glossopharyngeal Nerve Paralysis 8 2.112
23
KRT022 Keratoderma Palmoplantar Spastic Paralysis 5 2.112
24
VCL002 Vocal Cord Dysfunction Familial 18 2.092
25
FML082 Familial Partial Paralysis 3 2.092
26
LRY021 Laryngeal Adductor Paralysis 9 2.080
27
c PRK057 Parkinson Disease, Late-Onset 63 2.067
28
c THY083 Thyrotoxic Periodic Paralysis 2 11 2.067
29
CNG302 Congenital Hereditary Facial Paralysis with Variable Hearing Loss 8 2.067
30
TDD001 Todd's Paralysis 6 1.651
31
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 9 1.506
32
P OPH004 Ophthalmoplegia 47 1.494
33
P HRN001 Horner's Syndrome 36 1.494
34
FML160 Familial Spastic Paralysis 6 1.494
35
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 4 1.494
36
LRY023 Laryngeal Abductor Paralysis Mental Retardation 2 1.494
37
P CRN035 Cranial Nerve Palsy 26 1.479
38
FZL002 Fazio-Londe Disease 25 1.479
39
CYC001 Cycloplegia 21 1.479
40
LRY043 Laryngeal Abductor Paralysis - Intellectual Disability 10 1.479
41
c FML159 Familial Periodic Paralyses 8 1.479
42
PRL020 Paralysis Agitans, Juvenile, of Hunt 6 1.479
43
ISL060 Isolated Hereditary Congenital Facial Paralysis 4 1.479
44
PRL008 Paralytic Ileus 30 1.462
45
PSD001 Pseudobulbar Palsy 24 1.462
46
CNG241 Congenital Laryngeal Palsy 5 1.462
47
GLL022 Guillain-Barre Syndrome 50 1.439
48
TRP002 Tropical Spastic Paraparesis 46 1.439
49
P SPS003 Spastic Diplegia 34 1.439
50
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 25 1.439
51
ABD002 Abducens Nerve Disease 21 1.439
52
MRK002 Marek Disease 17 1.439
53
c DST092 Distal Hereditary Motor Neuropathy Type 7 14 1.439
54
BLN017 Balint Syndrome 14 1.439
55
THR010 Third Cranial Nerve Disease 8 1.439
56
RNL007 Renal Tubular Acidosis 48 0.172
57
HYP005 Hypokalemia 42 0.146
58
THY033 Thyrotoxicosis 49 0.138
59
SPS057 Spasticity 32 0.130
60
P LRY019 Laryngitis 56 0.124
61
P THY032 Thyroiditis 56 0.121
62
P NRP001 Neuropathy 52 0.118
63
P TRC086 Trichohepatoenteric Syndrome 1 39 0.115
64
MYT011 Myotonia 37 0.115
65
NRN002 Neuronitis 36 0.115
66
P MYP004 Myopathy 53 0.112
67
OTT002 Otitis Media 56 0.109
68
GRV001 Graves' Disease 54 0.109
69
THR013 Thoracic Outlet Syndrome 45 0.109
70
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.109
71
ADN018 Adenoma 55 0.105
72
P RSP003 Respiratory Failure 62 0.094
73
ACN002 Acanthosis Nigricans 55 0.094
74
BTL001 Botulism 52 0.094
75
P ATX010 Ataxia Neuropathy Spectrum 29 0.094
76
P ANG001 Angelman Syndrome 66 0.090
77
P CRV039 Cervicitis 49 0.090
78
c SPN225 Spondyloarthropathy 1 48 0.090
79
P MSC003 Muscular Atrophy 44 0.090
80
BNF002 Bone Fracture 39 0.090
81
ANR040 Aneurysm 35 0.090
82
c ART101 Aortic Valve Disease 2 32 0.090
83
P HYP076 Hyperthyroidism 54 0.081
84
P ALT001 Alternating Hemiplegia of Childhood 54 0.081
85
ACS001 Acoustic Neuroma 43 0.081
86
HYP017 Hypophosphatemia 42 0.081
87
NRM004 Neuroma 39 0.081
88
P PTS002 Ptosis 39 0.081
89
EPL031 Epileptic Hemiplegia 4 0.081
90
AND015 Androgen Insensitivity 69 0.077
91
P HRP006 Herpes Simplex 63 0.077
92
P MNN013 Meningitis 58 0.077
93
LYM017 Lyme Disease 56 0.077
94
P HPT021 Hepatitis 55 0.077
95
MYC002 Mycobacterium Avium Complex Disease 51 0.077
96
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.077
97
c PRG001 Progressive Muscular Atrophy 31 0.077
98
c BNG076 Benign Exophthalmos Syndrome 19 0.077
99
AND005 Androgen Insensitivity Syndrome, Mild 17 0.077
100
HRP004 Herpes Zoster 49 0.072
101
CHL069 Cholesteatoma 45 0.072
102
MNN014 Mononeuritis 43 0.072
103
CNV002 Conversion Disorder 42 0.072
104
WST005 West Nile Virus 40 0.072
105
GTR002 Goiter 53 0.066
106
STT002 Status Asthmaticus 52 0.066
107
P ATX004 Ataxia 50 0.066
108
MYL001 Myelitis 46 0.066
109
MLK003 Melkersson-Rosenthal Syndrome 44 0.066
110
PRT026 Parotitis 43 0.066
111
NRT004 Neuritis 40 0.066
112
ECT005 Ectropion 36 0.066
113
LCK001 Locked-in Syndrome 35 0.066
114
WND001 Wound Botulism 32 0.066
115
PRL013 Paralytic Poliomyelitis 32 0.066
116
PSL001 Pasli Disease 30 0.066
117
LGP001 Lagophthalmos 26 0.066
118
P PRD017 Periodic Paralyses 22 0.066
119
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.061
120
P ATX030 Ataxia-Telangiectasia 76 0.061
121
TBR010 Tuberculosis 73 0.061
122
P MYS003 Myasthenia Gravis 64 0.061
123
MLG056 Malignant Hyperthermia 62 0.061
124
P CHR071 Charcot-Marie-Tooth Disease 60 0.061
125
P PLY019 Polyneuropathy 52 0.061
126
PTN002 Patent Ductus Arteriosus 49 0.061
127
ART001 Arterial Tortuosity Syndrome 48 0.061
128
SNS001 Sensorineural Hearing Loss 48 0.061
129
TTH006 Tooth Disease 46 0.061
130
DYS073 Dysphagia 45 0.061
131
P MSC033 Muscle Disorders 43 0.061
132
PRP016 Paraplegia 40 0.061
133
CRB009 Cerebritis 33 0.061
134
ERB002 Erb's Palsy 8 0.061
135
c SYS001 Systemic Lupus Erythematosus 91 0.054
136
PRP083 Porphyria, Acute Intermittent 67 0.054
137
P LPS004 Lupus Erythematosus 67 0.054
138
P NRC002 Narcolepsy 67 0.054
139
P LKM002 Leukemia 66 0.054
140
ART016 Aortic Aneurysm 62 0.054
141
P HYP086 Hypothyroidism 59 0.054
142
c HPT001 Hepatitis C 57 0.054
143
P DBT005 Diabetes Insipidus 53 0.054
144
PTT006 Pituitary Adenoma 52 0.054
145
P SYR001 Syringomyelia 49 0.054
146
ARC007 Arachnoid Cysts 49 0.054
147
P HYP065 Hyperaldosteronism 49 0.054
148
BRN029 Brain Disease 49 0.054
149
P SCL018 Scoliosis 45 0.054
150
HMP005 Hemiplegia 44 0.054
151
NRM005 Neuromuscular Disease 43 0.054
152
P NRV007 Nervous System Disease 42 0.054
153
P SJG001 Sjogren's Syndrome 42 0.054
154
CRT008 Carotid Artery Dissection 40 0.054
155
MDS022 Mediastinitis 39 0.054
156
ARC002 Arachnoiditis 39 0.054
157
MNN009 Meningoencephalitis 39 0.054
158
c SBC007 Subacute Thyroiditis 38 0.054
159
QDR001 Quadriplegia 37 0.054
160
SPP008 Suppurative Otitis Media 34 0.054
161
MLL002 Miller Fisher Syndrome 31 0.054
162
FTD001 Foot Drop 31 0.054
163
P LBY004 Labyrinthitis 29 0.054
164
GNC003 Geniculate Herpes Zoster 27 0.054
165
FDB001 Foodborne Botulism 22 0.054
166
ANT054 Anotia 21 0.054
167
FBR024 Fibrocartilaginous Embolism 12 0.054
168
MDD008 Middle Ear Adenoma 12 0.054
169
MLR004 Malaria 81 0.047
170
CDS001 Cadasil 73 0.047
171
MLT021 Multiple System Atrophy 70 0.047
172
P NRB001 Neuroblastoma 68 0.047
173
P PNM007 Pneumonia 64 0.047
174
P AMY004 Amyloidosis 63 0.047
175
P ATR011 Atrial Fibrillation 62 0.047
176
SRC014 Sarcoma 61 0.047
177
P HMN010 Hemangioma 60 0.047
178
PLY017 Polyarteritis Nodosa 60 0.047
179
P TRN020 Turner Syndrome 58 0.047
180
OLV001 Olivopontocerebellar Atrophy 58 0.047
181
P SPN046 Spinal Muscular Atrophy 57 0.047
182
P ENC004 Encephalitis 56 0.047
183
STT001 Status Epilepticus 56 0.047
184
SPN186 Spinal Cord Injury 54 0.047
185
P MSC005 Muscular Dystrophy 54 0.047
186
MTR014 Motor Neuron Disease 53 0.047
187
ASP003 Aseptic Meningitis 52 0.047
188
SPN020 Spondylosis 51 0.047
189
P MMP001 Mumps 51 0.047
190
P THR003 Thoracic Aortic Aneurysm 50 0.047
191
NRL005 Neurilemmoma 50 0.047
192
RBS001 Rabies 50 0.047
193
ADR008 Adrenal Adenoma 48 0.047
194
P BLN003 Blindness 47 0.047
195
TRY002 Troyer Syndrome 47 0.047
196
P MNT147 Mental Retardation 46 0.047
197
LPT001 Leptospirosis 46 0.047
198
TLR001 Tularemia 45 0.047
199
P EPS003 Episodic Ataxia 45 0.047
200
P FNC004 Fanconi Syndrome 44 0.047
201
P EPL002 Epilepsy Syndrome 44 0.047
202
RLP003 Relapsing Fever 42 0.047
203
WST004 West Nile Encephalitis 41 0.047
204
ATN005 Autonomic Dysfunction 39 0.047
205
FSC004 Fasciitis 39 0.047
206
P NRN017 Neuronopathy, Distal Hereditary Motor, Type Vi 38 0.047
207
P PRX033 Proximal Renal Tubular Acidosis 38 0.047
208
SPN185 Spinal Cord Infarction 36 0.047
209
PPL046 Popliteal Pterygium Syndrome 1 36 0.047
210
EPD005 Epidural Abscess 35 0.047
211
PRG097 Paragangliomas 1, with or Without Deafness 34 0.047
212
BRW001 Brown-Vialetto-Van Laere Syndrome 31 0.047
213
TLS001 Tolosa-Hunt Syndrome 31 0.047
214
c FML249 Familial Amyloidosis, Finnish Type 31 0.047
215
HYP264 Hypertonia 30 0.047
216
c SPS078 Spastic Paraplegia 7 30 0.047
217
P SPS012 Spastic Paraplegia 3a 30 0.047
218
TBS001 Tabes Dorsalis 30 0.047
219
CLR007 Colorado Tick Fever 29 0.047
220
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.047
221
TFT003 Tufting Enteropathy 26 0.047
222
PTR001 Petrositis 24 0.047
223
CVR002 Cavernous Sinus Thrombosis 23 0.047
224
PRS053 Parsonage Turner Syndrome 19 0.047
225
BLB003 Bulbar Polio 18 0.047
226
ABD009 Abducens Palsy 18 0.047
227
PNT023 Pontine Hemorrhage 16 0.047
228
SKL006 Skull Base Neoplasm 9 0.047
229
P BRS047 Breast Cancer 90 0.038
230
P DBT085 Diabetes Mellitus, Insulin-Dependent 83 0.038
231
NRL016 Neural Tube Defects 78 0.038
232
P LPR003 Leprosy 71 0.038
233
P CNG368 Congenital Adrenal Hyperplasia 66 0.038
234
STR067 Stroke, Ischemic 65 0.038
235
P BRD002 Bardet-Biedl Syndrome 65 0.038
236
GTL001 Gitelman Syndrome 64 0.038
237
P CNG401 Congenital Heart Disease 62 0.038
238
c HRD010 Hereditary Spastic Paraplegia 62 0.038
239
P HYP117 Hypertriglyceridemia 61 0.038
240
PRT036 Peritonitis 61 0.038
241
CRB039 Cerebrovascular Disease 59 0.038
242
MSL001 Measles 58 0.038
243
INS024 Insulin-Like Growth Factor I 58 0.038
244
c ATM010 Autoimmune Hemolytic Anemia 57 0.038
245
PLS006 Plasmodium Vivax Malaria 57 0.038
246
P PRP029 Porphyria 57 0.038
247
PHR003 Pharyngitis 56 0.038
248
P TXP001 Toxoplasmosis 56 0.038
249
P HML002 Hemolytic Anemia 56 0.038
250
TRG002 Trigeminal Neuralgia 56 0.038
251
P SZR006 Seizure Disorder 56 0.038
252
CPR001 Coproporphyria 56 0.038
253
P EHL001 Ehlers-Danlos Syndrome 56 0.038
254
BBS001 Babesiosis 54 0.038
255
P ESP024 Esophagitis 54 0.038
256
P KLP003 Klippel-Feil Syndrome 54 0.038
257
c MLG069 Malignant Hypertension 54 0.038
258
P ACR001 Aicardi-Goutieres Syndrome 54 0.038
259
P ART023 Arthropathy 54 0.038
260
ART005 Arteriovenous Malformation 53 0.038
261
STF001 Stiff-Person Syndrome 52 0.038
262
P NRM001 Neuromyelitis Optica 52 0.038
263
c SCN006 Secondary Syphilis 51 0.038
264
NRC020 Neuroectodermal Tumor 51 0.038
265
P EMR001 Emery-Dreifuss Muscular Dystrophy 51 0.038
266
HMF006 Hemifacial Microsomia 50 0.038
267
YLL002 Yellow Fever 50 0.038
268
GLC003 Glucose Intolerance 50 0.038
269
PRP025 Peripheral Primitive Neuroectodermal Tumor 50 0.038
270
HDC001 Headache 50 0.038
271
P MYC008 Myocarditis 50 0.038
272
c CNG021 Congenital Toxoplasmosis 50 0.038
273
RHB003 Rhabdomyosarcoma 49 0.038
274
P NML001 Nemaline Myopathy 49 0.038
275
P SYP003 Syphilis 48 0.038
276
P TRM003 Tremor 48 0.038
277
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.038
278
MYL003 Myeloid Sarcoma 48 0.038
279
P OST028 Osteochondroma 47 0.038
280
JPN002 Japanese Encephalitis 46 0.038
281
THY009 Thyroid Lymphoma 46 0.038
282
P PRG013 Paraganglioma 46 0.038
283
P PRT029 Parathyroid Adenoma 46 0.038
284
GST037 Gastroparesis 46 0.038
285
SCH016 Schimke Immunoosseous Dysplasia 46 0.038
286
NWC001 Newcastle Disease 46 0.038
287
EHR002 Ehrlichiosis 45 0.038
288
TCK001 Tick-Borne Encephalitis 45 0.038
289
GST045 Gastroenteritis 45 0.038
290
SPT005 Spotted Fever 45 0.038
291
OST011 Osteomalacia 45 0.038
292
PRP023 Peripheral Neuropathy 44 0.038
293
STL001 St. Louis Encephalitis 43 0.038
294
RNL011 Renal Osteodystrophy 43 0.038
295
P PNM006 Pneumoconiosis 43 0.038
296
OPT009 Optic Neuritis 42 0.038
297
NPH003 Nephrocalcinosis 41 0.038
298
P TRN034 Transverse Myelitis 41 0.038
299
P HMR005 Hemorrhoid 41 0.038
300
NSP002 Nasopharyngitis 40 0.038
301
EVN001 Evans' Syndrome 39 0.038
302
KRT012 Keratoderma 39 0.038
303
CNT025 Central Pontine Myelinolysis 39 0.038
304
P PRS062 Persistent Hyperplastic Primary Vitreous 39 0.038
305
ILS001 Ileus 38 0.038
306
PRS037 Periostitis 38 0.038
307
OST006 Osteoblastoma 38 0.038
308
PST055 Postural Hypotension 37 0.038
309
P CHR342 Chiari Malformation 37 0.038
310
TTR016 Tetra-Amelia Syndrome 36 0.038
311
MYH012 Myhre Syndrome 36 0.038
312
P OTT001 Otitis Externa 35 0.038
313
LCR004 La Crosse Encephalitis 35 0.038
314
APH002 Aphasia 35 0.038
315
c AMY008 Amyotrophic Lateral Sclerosis Type 2 34 0.038
316
TRC023 Trichinosis 33 0.038
317
THY035 Thyroid Adenoma 33 0.038
318
HYD001 Hydranencephaly 33 0.038
319
P AXN001 Axonal Neuropathy 32 0.038
320
PSD029 Pseudocholinesterase Deficiency 31 0.038
321
NRP016 Neuropathy, Recurrent, with Pressure Palsies 31 0.038
322
c SPS092 Spastic Paraplegia 11 31 0.038
323
XRP001 Xerophthalmia 31 0.038
324
RCK002 Rocky Mountain Spotted Fever 31 0.038
325
ADS002 Adie Syndrome 30 0.038
326
MTC018 Metachondromatosis 30 0.038
327
NRC019 Neurocutaneous Melanosis, Somatic 29 0.038
328
SPS016 Spasmodic Dysphonia 29 0.038
329
INT042 Internuclear Ophthalmoplegia 28 0.038
330
ENT005 Entropion 27 0.038
331
c CHR160 Chiari Malformation Type 2 26 0.038
332
CBB002 Cobb Syndrome 26 0.038
333
HNM002 Hinman Syndrome 26 0.038
334
PLY119 Polymicrogyria, Bilateral Perisylvian 26 0.038
335
FCL003 Facial Hemiatrophy 25 0.038
336
c JVN024 Juvenile Hereditary Hemochromatosis 25 0.038
337
PRP056 Porphyria, Acute Hepatic 25 0.038
338
c PRG020 Paragangliomas 3 24 0.038
339
c ACT159 Acute Transverse Myelitis 23 0.038
340
PRR008 Periarteritis Nodosa 23 0.038
341
ECT004 Ecthyma 22 0.038
342
BRW004 Brown-Sequard Syndrome 22 0.038
343
c PRG019 Paragangliomas 2 22 0.038
344
TCK004 Tick Infestation 21 0.038
345
VST004 Vestibular Disease 21 0.038
346
c SPS042 Spastic Paraplegia 9 21 0.038
347
STR002 Streptococcal Meningitis 19 0.038
348
c NRP022 Neuropathy, Distal Hereditary Motor, Type Viib 17 0.038
349
PWS001 Powassan Encephalitis 16 0.038
350
MNN005 Meningovascular Neurosyphilis 16 0.038
351
CNT067 Central Cord Syndrome 16 0.038
352
ITR001 Iatrogenic Botulism 15 0.038
353
OTP003 Oto-Palatal-Digital Syndrome 14 0.038
354
SYR004 Syringobulbia 14 0.038
355
c NRC009 Narcolepsy 1 14 0.038
356
c ADL069 Adult Intestinal Botulism 13 0.038
357
TXN001 Toxin-Mediated Infectious Botulism 11 0.038
358
MYP026 Myopathy - Thyrotoxic 7 0.038
359
BLB001 Bulbospinal Polio 7 0.038
360
SPN015 Spinal Polio 6 0.038
361
BRC057 Brachial Plexus Birth Injuries 6 0.038
362
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.038
363
HMP020 Hemiplegia Alterans 1 0.038
364
HPT023 Hepatocellular Carcinoma 95 0.027
365
P AST005 Asthma 84 0.027
366
HV1006 Hiv-1 83 0.027
367
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 82 0.027
368
P LFR001 Li-Fraumeni Syndrome 81 0.027
369
P DLT002 Dilated Cardiomyopathy 77 0.027
370
P MTC003 Metachromatic Leukodystrophy 76 0.027
371
P SCL016 Scleroderma 76 0.027
372
c MLT019 Multiple Myeloma 75 0.027
373
GLC006 Galactosemia 75 0.027
374
P TYS001 Tay-Sachs Disease 73 0.027
375
P OST002 Osteoporosis 71 0.027
376
P GCH001 Gaucher's Disease 70 0.027
377
P NRF002 Neurofibromatosis 69 0.027
378
c FNC027 Fanconi Anemia, Complementation Group a 68 0.027
379
P MYL005 Myelofibrosis 68 0.027
380
BHC002 Behcet's Disease 68 0.027
381
P INF038 Influenza 67 0.027
382
P ALX003 Alexander Disease 66 0.027
383
c HYP595 Hypertension, Essential 66 0.027
384
CHD001 Chediak-Higashi Syndrome 66 0.027
385
CRB011 Cerebrotendinous Xanthomatosis 66 0.027
386
KWS002 Kawasaki Disease 66 0.027
387
WLF001 Wolff-Parkinson-White Syndrome 65 0.027
388
ADD001 Addison's Disease 65 0.027
389
PGT005 Paget Disease of Bone 65 0.027
390
P OST001 Osteopetrosis 65 0.027
391
P BPL003 Bipolar Disorder 65 0.027
392
CYS008 Cystic Echinococcosis 64 0.027
393
P HYP035 Hypophosphatasia 64 0.027
394
ABT001 Abetalipoproteinemia 63 0.027
395
BRK010 Burkitt Lymphoma 63 0.027
396
CCC001 Coccidioidomycosis 63 0.027
397
RLP001 Relapsing Polychondritis 63 0.027
398
P MYS005 Myositis 63 0.027
399
MCK007 Muckle-Wells Syndrome 62 0.027
400
CNT098 Central Core Disease 62 0.027
401
P MCH002 Machado-Joseph Disease 61 0.027
402
c HPT016 Hepatitis B 60 0.027
403
ALC007 Alcohol Dependence 60 0.027
404
P CMR001 Camurati-Engelmann Disease 60 0.027
405
P ALP004 Alport Syndrome 60 0.027
406
KRT004 Keratitis 60 0.027
407
ALV002 Alveolar Echinococcosis 60 0.027
408
c NRF019 Neurofibromatosis, Type 2 59 0.027
409
P GLM007 Glomerulonephritis 59 0.027
410
FCT003 Factor X Deficiency 58 0.027
411
P ABD003 Abdominal Aortic Aneurysm 58 0.027
412
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 0.027
413
c PRC016 Pre-Eclampsia 58 0.027
414
WLL001 Williams-Beuren Syndrome 58 0.027
415
c FML001 Familial Atrial Fibrillation 58 0.027
416
c ATM003 Autoimmune Thyroiditis 58 0.027
417
P THY023 Thymoma 57 0.027
418
P HYP004 Hypercalcemia 57 0.027
419
c SML001 Small Cell Carcinoma 57 0.027
420
P KDN018 Kidney Disease 57 0.027
421
P WRD001 Waardenburg's Syndrome 57 0.027
422
TWN003 Townes-Brocks Syndrome 57 0.027
423
WGN006 Wegener Granulomatosis 57 0.027
424
CYS010 Cystinosis 57 0.027
425
PLM033 Pulmonary Embolism 56 0.027
426
END030 End Stage Renal Failure 56 0.027
427
c ALM001 Al Amyloidosis 56 0.027
428
c TYR012 Tyrosinemia, Type I 56 0.027
429
WLD002 Waldenstrom Macroglobulinemia 56 0.027
430
P BRG001 Brugada Syndrome 56 0.027
431
GST009 Gastroschisis 55 0.027
432
P SCH018 Schizencephaly 55 0.027
433
MNT001 Mantle Cell Lymphoma 55 0.027
434
MLN008 Melanoma 55 0.027
435
c LNG044 Long Qt Syndrome 1 55 0.027
436
P OLG002 Oligodendroglioma 55 0.027
437
BLD087 Bladder Cancer, Somatic 55 0.027
438
P CRB042 Cerebellar Ataxia 54 0.027
439
P RHB017 Rhabdoid Tumor 54 0.027
440
c GLY008 Glycogen Storage Disease Ii 54 0.027
441
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.027
442
CHR072 Chordoma 54 0.027
443
P MYL007 Myeloma 53 0.027
444
RBR001 Roberts Syndrome 53 0.027
445
LRN003 Learning Disability 53 0.027
446
P INT070 Intestinal Obstruction 53 0.027
447
P CNJ013 Conjunctivitis 53 0.027
448
P SPN049 Spinocerebellar Ataxia 53 0.027
449
P CNG001 Congenital Myasthenic Syndrome 53 0.027
450
KRN002 Kearns-Sayre Syndrome 52 0.027
451
P MTR012 Mitral Valve Disease 52 0.027
452
CLD007 Cold Agglutinin Disease 52 0.027
453
NRL004 Neuroleptic Malignant Syndrome 52 0.027
454
P FBR017 Fibrosarcoma 52 0.027
455
SPH001 Sapho Syndrome 52 0.027
456
KRT001 Keratoconjunctivitis Sicca 52 0.027
457
P FML043 Familial Idiopathic Basal Ganglia Calcification 52 0.027
458
PTN001 Patent Foramen Ovale 52 0.027
459
P HYP141 Hyperphenylalaninemia 51 0.027
460
P FML161 Familial Mediterranean Fever, Ar 51 0.027
461
P MYM002 Moyamoya Disease 51 0.027
462
P MST018 Mesothelioma 51 0.027
463
CHC001 Chickenpox 51 0.027
464
PMP001 Pemphigus 51 0.027
465
MLT075 Multifocal Motor Neuropathy 51 0.027
466
MGC001 Megacolon 51 0.027
467
BLR001 Biliary Atresia 51 0.027
468
BNC003 Bone Cancer 50 0.027
469
LYM019 Lymphosarcoma 50 0.027
470
P CTR002 Cataract 50 0.027
471
CVR006 Cavernous Hemangioma 50 0.027
472
THY022 Thymic Carcinoma 50 0.027
473
P CRN012 Craniometaphyseal Dysplasia 49 0.027
474
HMM003 Hemimegalencephaly 49 0.027
475
c MLT024 Multiple Endocrine Neoplasia Iia 49 0.027
476
PRN023 Prion Disease 49 0.027
477
P ENC008 Encephalocele 49 0.027
478
ANR004 Anuria 48 0.027
479
HYP024 Hypoparathyroidism 48 0.027
480
c FML023 Familial Hemiplegic Migraine 48 0.027
481
ANK001 Ankylosis 48 0.027
482
c ACT073 Acute Leukemia 48 0.027
483
P DND001 Dandy-Walker Syndrome 48 0.027
484
MDL009 Medullary Sponge Kidney 48 0.027
485
SLP005 Sleep Disorder 48 0.027
486
P GNT008 Giant Cell Tumor 47 0.027
487
P HYP014 Hyperuricemia 47 0.027
488
TNG009 Tongue Squamous Cell Carcinoma 47 0.027
489
HYP458 Hyper Ige Syndrome 47 0.027
490
PLG002 Plague 47 0.027
491
P EXP004 Exophthalmos 47 0.027
492
FBR009 Fibrous Dysplasia 47 0.027
493
VNB005 Van Buchem Disease 47 0.027
494
LYM022 Lymphangioma 46 0.027
495
EWN002 Ewing's Family of Tumors 46 0.027
496
PRN011 Pernicious Anemia 46 0.027
497
STS002 Situs Inversus 46 0.027
498
BSL009 Basal Ganglia Calcification 46 0.027
499
c PND001 Pain Disorder 46 0.027
500
ESP020 Esophageal Atresia 46 0.027
501
c VRL012 Viral Meningitis 46 0.027
502
GRW007 Growth Hormone Deficiency 46 0.027
503
HNT002 Hantavirus Pulmonary Syndrome 46 0.027
504
ACQ007 Acquired Immunodeficiency Syndrome 46 0.027
505
P GRS003 Griscelli Syndrome 45 0.027
506
P AML002 Amelogenesis Imperfecta 45 0.027
507
PRC013 Pericarditis 45 0.027
508
MYX004 Myxedema 45 0.027
509
P SPN183 Spontaneous Pneumothorax 45 0.027
510
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 45 0.027
511
ANG002 Angiostrongyliasis 44 0.027
512
c SRC025 Sarcoidosis 1 44 0.027
513
PRP032 Porphyria Variegata 44 0.027
514
CYS016 Cystic Kidney 44 0.027
515
DGS001 Degos Disease 44 0.027
516
BRS064 Bursitis 44 0.027
517
TRN015 Transient Cerebral Ischemia 44 0.027
518
TRC040 Tracheoesophageal Fistula 44 0.027
519
P MLG086 Malignant Hyperthermia Susceptibility 43 0.027
520
EXS001 Exostosis 43 0.027
521
P NRX001 Neuroaxonal Dystrophy 43 0.027
522
PNM008 Pneumothorax 43 0.027
523
MTH009 Mouth Disease 43 0.027
524
HYP006 Hypertensive Heart Disease 43 0.027
525
CHR288 Chronic Recurrent Multifocal Osteomyelitis 42 0.027
526
P BNG071 Benign Schwannoma 42 0.027
527
ADR043 Adrenal Hyperplasia, Congenital, Due to 11-Beta-Hydroxylase Deficiency 42 0.027
528
FBR047 Fibromyalgia 42 0.027
529
P APL006 Aplasia Cutis Congenita 42 0.027
530
INF058 Inflammatory Myofibroblastic Tumor 42 0.027
531
CTS002 Cat-Scratch Disease 42 0.027
532
SLV012 Salivary Gland Adenoid Cystic Carcinoma 42 0.027
533
P HYP345 Hyper-Ige Recurrent Infection Syndrome 42 0.027
534
c CRB103 Cerebral Cavernous Malformations-1 42 0.027
535
PLS016 Plasma Cell Leukemia 42 0.027
536
MMB001 Membranoproliferative Glomerulonephritis 42 0.027
537
P HYP120 Hypoaldosteronism 42 0.027
538
HJD001 Hajdu-Cheney Syndrome 42 0.027
539
MFF001 Maffucci Syndrome 42 0.027
540
ATN004 Autonomic Neuropathy 41 0.027
541
MLR003 Melorheostosis 41 0.027
542
ASP007 Aspiration Pneumonia 41 0.027
543
CHK001 Chikungunya 41 0.027
544
PLM010 Pulmonary Edema 41 0.027
545
P FNG005 Feingold Syndrome 40 0.027
546
c OPT055 Optic Atrophy Plus Syndrome 40 0.027
547
CNN003 Conn's Syndrome 40 0.027
548
P MLT008 Multinodular Goiter 40 0.027
549
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.027
550
MTS001 Mutism 40 0.027
551
AMB002 Amblyopia 39 0.027
552
P DMY001 Demyelinating Polyneuropathy 39 0.027
553
LYM021 Lymphadenitis 39 0.027
554
MYS001 Myositis Ossificans 39 0.027
555
FTT001 Fatty Liver Disease 39 0.027
556
c HRD086 Hereditary Hypophosphatemic Rickets 39 0.027
557
ZYG002 Zygomycosis 39 0.027
558
MCP006 Mucoepidermoid Carcinoma 39 0.027
559
FCT022 Factor Xi Deficiency, Autosomal Recessive 38 0.027
560
MDD002 Middle Ear Cholesteatoma 38 0.027
561
RSS002 Roussy-Levy Syndrome 38 0.027
562
P PRC031 Preeclampsia/eclampsia 1 38 0.027
563
NCR007 Necrotizing Fasciitis 38 0.027
564
HTS001 Hiatus Hernia 38 0.027
565
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 37 0.027
566
c LPD037 Lipodystrophy, Familial Partial, 2 37 0.027
567
SPN050 Spinocerebellar Degeneration 37 0.027
568
GYN001 Gynecomastia 37 0.027
569
MTC056 Mitochondrial Dna Depletion Syndrome 4a 37 0.027
570
ATY005 Atypical Teratoid Rhabdoid Tumor 37 0.027
571
WHP001 Whipple Disease 37 0.027
572
ACT012 Acute Hemorrhagic Conjunctivitis 37 0.027
573
THY043 Thymic Hyperplasia 36 0.027
574
c OST137 Osteopetrosis, Autosomal Recessive 4 36 0.027
575
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 36 0.027
576
P RSM001 Rasmussen Encephalitis 36 0.027
577
P RNL066 Renal Tubular Acidosis, Distal, Ad 35 0.027
578
NTR001 Neutral Lipid Storage Disease 35 0.027
579
SRC001 Sarcomatoid Mesothelioma 35 0.027
580
RMS001 Rem Sleep Behavior Disorder 35 0.027
581
SPS019 Spastic Paraparesis 35 0.027
582
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 35 0.027
583
CDQ001 Cauda Equina Syndrome 35 0.027
584
ESN020 Eosinophilic Granulomatosis with Polyangiitis 35 0.027
585
c EXS004 Exostoses, Multiple, Type 1 35 0.027
586
P MNN007 Meningocele 34 0.027
587
P HYP265 Hypotonia 34 0.027
588
LRY029 Laryngomalacia 34 0.027
589
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 34 0.027
590
EST005 Esotropia 34 0.027
591
SCT002 Scotoma 34 0.027
592
c SPS079 Spastic Paraplegia 2 33 0.027
593
END051 Endolymphatic Sac Tumor 33 0.027
594
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 33 0.027
595
c SCP001 Sc Phocomelia Syndrome 33 0.027
596
PLM029 Palmoplantar Keratosis 33 0.027
597
P NRV006 Nervous System Cancer 32 0.027
598
LMB010 Lambert Syndrome 32 0.027
599
SPC005 Speech Disorder 32 0.027
600
BRN016 Bronchogenic Carcinoma 32 0.027
601
IPX001 Ipex Syndrome 32 0.027
602
INF006 Infant Botulism 31 0.027
603
VRL011 Viral Infectious Disease 31 0.027
604
HNS001 Hansen's Disease 31 0.027
605
SCR015 Scarlet Fever 31 0.027
606
P GLM006 Glomangioma 31 0.027
607
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 31 0.027
608
TRP004 Tropical Sprue 30 0.027
609
c CNT033 Central Nervous System Cancer 30 0.027
610
PLM074 Pulmonary Function 30 0.027
611
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 30 0.027
612
c SYS043 Systemic Lupus Erythematosus 1 30 0.027
613
PMP008 Pemphigus Vegetans 29 0.027
614
c HRD088 Hereditary Neuropathies 29 0.027
615
PST020 Postpoliomyelitis Syndrome 29 0.027
616
CSL001 Causalgia 29 0.027
617
MRR003 Murray Valley Encephalitis 29 0.027
618
HYP034 Hypertensive Encephalopathy 29 0.027
619
SPR007 Superior Mesenteric Artery Syndrome 28 0.027
620
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 28 0.027
621
ANT018 Anthracosis 28 0.027
622
c OST131 Osteopetrosis, Autosomal Dominant 2 27 0.027
623
CNG133 Congenital Varicella Syndrome 27 0.027
624
PNM005 Pneumonic Plague 27 0.027
625
c GM2005 Gm2-Gangliosidosis, Ab Variant 27 0.027
626
c OST126 Osteopetrosis, Autosomal Recessive 1 27 0.027
627
CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 27 0.027
628
MNR004 Mounier-Kuhn Syndrome 26 0.027
629
c SPS027 Spastic Paraplegia 17 26 0.027
630
P PHC014 Phocomelia 25 0.027
631
NRG004 Neurogenic Diabetes Insipidus 25 0.027
632
DYG001 Dyggve-Melchior-Clausen Disease 25 0.027
633
THY025 Thymus Cancer 25 0.027
634
NRS003 Neurosyphilis 25 0.027
635
c CNG112 Congenital Muscular Dystrophy Type 1a 25 0.027
636
FRY001 Frey Syndrome 25 0.027
637
VST003 Vestibular Nystagmus 25 0.027
638
FBR028 Fibrosing Mediastinitis 25 0.027
639
c SPS025 Spastic Paraplegia 15 24 0.027
640
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 24 0.027
641
BRC010 Brachial Plexus Lesion 24 0.027
642
WYB001 Wyburn Mason's Syndrome 24 0.027
643
CRV030 Cervical Adenitis 24 0.027
644
CRN051 Craniofacial Microsomia 24 0.027
645
c OST129 Osteopetrosis, Autosomal Recessive 2 24 0.027
646
HYP362 Hyperopia 24 0.027
647
LPN001 Louping Ill 23 0.027
648
MYC014 Mycobacterium Chelonae 23 0.027
649
AMY005 Amyloid Neuropathy 23 0.027
650
c SPS013 Spastic Paraplegia 8 22 0.027
651
c CRB094 Cerebral Cavernous Malformations 3 22 0.027
652
GNT004 Gnathomiasis 22 0.027
653
c NRF011 Neurofibromatosis Type 3a 21 0.027
654
SNS003 Sensory Peripheral Neuropathy 21 0.027
655
ECH002 Echolalia 21 0.027
656
LTR002 Lateral Sinus Thrombosis 21 0.027
657
c SPS091 Spastic Paraplegia 4 21 0.027
658
P INT006 Intestinal Botulism 21 0.027
659
ANT013 Anterior Spinal Artery Syndrome 21 0.027
660
c PSD090 Pseudohypoaldosteronism, Type Iia 21 0.027
661
TMR013 Tumor Necrosis Factor Receptor 1 Associated Periodic Syndrome 21 0.027
662
c CHR097 Chronic Purulent Otitis Media 21 0.027
663
MYP093 Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset 20 0.027
664
PRS120 Persistent Idiopathic Facial Pain 20 0.027
665
P FRT001 Fourth Cranial Nerve Palsy 20 0.027
666
ATR055 Atrial Septal Aneurysm 20 0.027
667
HSH001 Hashimoto-Pritzker Syndrome 20 0.027
668
HYP048 Hypotropia 20 0.027
669
EXC003 Excessive Tearing 20 0.027
670
ACT181 Acute Motor Axonal Neuropathy 20 0.027
671
CRT009 Critical Illness Polyneuropathy 19 0.027
672
ETH012 Ethylene Glycol Poisoning 19 0.027
673
PRN016 Peroneal Neuropathy 19 0.027
674
ATL010 Atlantoaxial Subluxation 19 0.027
675
SBS002 Substernal Goiter 19 0.027
676
PNT009 Pontine Tegmental Cap Dysplasia 18 0.027
677
DRS001 Dressler's Syndrome 18 0.027
678
SWL001 Swallowing Disorders 18 0.027
679
c VRL004 Viral Labyrinthitis 18 0.027
680
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 18 0.027
681
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 18 0.027
682
c MYP081 Myopathy, Myofibrillar, 6 18 0.027
683
MYC001 Myoclonic Cerebellar Dyssynergia 18 0.027
684
EXP002 Exposure Keratitis 17 0.027
685
LRY007 Laryngeal Tuberculosis 17 0.027
686
ACT214 Acetazolamide-Responsive Myotonia 17 0.027
687
GLT018 Glut1 Deficiency Syndrome 1 17 0.027
688
c CNG129 Congenital Torticollis 16 0.027
689
HYP047 Hypertropia 16 0.027
690
HTR005 Heterochromia Iridis 16 0.027
691
c NRN027 Neuronopathy, Distal Hereditary Motor, Type I 16 0.027
692
P SNS011 Sinus Cancer 15 0.027
693
P INT105 Intellectual Disability Multi-Gene Panels 15 0.027
694
PRP013 Paraphimosis 15 0.027
695
BRW009 Brown-Vialetto-Van Laere Syndrome 1 15 0.027
696
MLN002 Melanomatosis 15 0.027
697
BMF002 Bamforth Syndrome 15 0.027
698
INT095 Internal Carotid Agenesis 15 0.027
699
CLV002 Clivus Chordoma 14 0.027
700
CNR001 Coenurosis 14 0.027
701
MLL006 Mollaret Meningitis 13 0.027
702
INH013 Inhalational Botulism 13 0.027
703
SPN092 Spinal Shock 13 0.027
704
MNS002 Mini Stroke 13 0.027
705
c CHR094 Chronic Polyneuropathy 13 0.027
706
TRG006 Trigger Thumb 12 0.027
707
CNM001 Canomad Syndrome 11 0.027
708
SPH008 Sphenoidal Sinus Cancer 11 0.027
709
BDR001 Bidirectional Tachycardia 11 0.027
710
ATY001 Atypical Depressive Disorder 10 0.027
711
BNP002 Bone Epithelioid Hemangioma 10 0.027
712
PRS033 Parasitic Ectoparasitic Infectious Disease 9 0.027
713
SPR038 Supranuclear Ocular Palsy 9 0.027
714
c INF052 Infantile Scoliosis 9 0.027
715
KNG003 Konigsmark Knox Hussels Syndrome 7 0.027
716
WST006 Westphal Disease 4 0.027