Search results for "paralysis"

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

772 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
c HYP051 Hypokalemic Periodic Paralysis 61 7.428
2
c HYP052 Hyperkalemic Periodic Paralysis 45 5.703
3
NRM009 Normokalemic Periodic Paralysis 33 5.371
4
INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 39 4.969
5
P HYP239 Hyperkalemic Periodic Paralysis Type 2 33 4.478
6
AND003 Andersen-Tawil Syndrome 53 4.302
7
FCL012 Facial Paralysis 40 3.948
8
OCL003 Oculomotor Nerve Paralysis 17 3.560
9
c THY054 Thyrotoxic Periodic Paralysis 46 3.519
10
P HYP254 Hypokalemic Periodic Paralysis Type 1 38 3.503
11
KRT022 Keratoderma Palmoplantar Spastic Paralysis 18 3.472
12
TCK002 Tick Paralysis 22 3.383
13
P THY084 Thyrotoxic Periodic Paralysis 1 25 3.229
14
TCK005 Tucker Syndrome 14 3.146
15
BLL003 Bell's Palsy 63 3.036
16
PRN008 Peroneal Nerve Paralysis 17 2.890
17
MBS002 Moebius Syndrome 53 2.866
18
c HYP255 Hypokalemic Periodic Paralysis Type 2 31 2.839
19
c HYP142 Hyperkalemic Periodic Paralysis Type 1 14 2.828
20
PRM028 Paramyotonia Congenita 51 2.614
21
KLM001 Klumpke Paralysis 11 2.543
22
VCL002 Vocal Cord Dysfunction Familial 20 2.477
23
GLS003 Glossopharyngeal Nerve Paralysis 10 2.477
24
FML082 Familial Partial Paralysis 3 2.455
25
P HRD130 Hereditary Congenital Facial Paresis 3 21 2.428
26
LRY043 Laryngeal Abductor Paralysis - Intellectual Disability 13 2.428
27
ISL060 Isolated Hereditary Congenital Facial Paralysis 10 2.428
28
PLM031 Poliomyelitis 53 2.297
29
TDD001 Todd's Paralysis 9 2.169
30
P PRK002 Parkinson's Disease 92 2.014
31
P CRN035 Cranial Nerve Palsy 31 2.014
32
FZL001 Fazio Londe Syndrome 27 2.014
33
CYC001 Cycloplegia 26 2.014
34
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 9 2.014
35
PRL008 Paralytic Ileus 36 2.000
36
PSD001 Pseudobulbar Palsy 30 2.000
37
FML160 Familial Spastic Paralysis 8 2.000
38
LRY021 Laryngeal Adductor Paralysis 8 2.000
39
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 5 2.000
40
LRY023 Laryngeal Abductor Paralysis Mental Retardation 3 2.000
41
SPS003 Spastic Diplegia 37 1.983
42
MBS001 Mobius Syndrome 27 1.983
43
MRK002 Marek Disease 16 1.983
44
c THY083 Thyrotoxic Periodic Paralysis 2 11 1.983
45
VNN001 Venencie Powell Gordon Winkelmann Syndrome 7 1.983
46
c SSC005 Susceptibility to Prolonged Paralysis Due to Mivacurium Treatment 3 1.983
47
c SSC006 Susceptibility to Prolonged Paralysis Due to Cisatracurium Treatment 3 1.983
48
c SSC023 Susceptibility to Prolonged Paralysis Due to Pancuronium Treatment 3 1.983
49
P SSC024 Susceptibility to Prolonged Paralysis Due to Rocuronium Treatment 3 1.983
50
c SSC025 Susceptibility to Prolonged Paralysis Due to Satracurium Treatment 3 1.983
51
c SSC026 Susceptibility to Prolonged Paralysis Due to Vecuronium Treatment 3 1.983
52
PRL020 Paralysis Agitans, Juvenile, of Hunt 2 1.983
53
P PRD017 Periodic Paralyses 28 1.509
54
c OPH004 Ophthalmoplegia 54 1.468
55
P HRN001 Horner's Syndrome 42 1.456
56
c FML159 Familial Periodic Paralyses 10 1.441
57
CNG241 Congenital Laryngeal Palsy 5 1.424
58
GLL022 Guillain-Barre Syndrome 60 1.402
59
TRP002 Tropical Spastic Paraparesis 55 1.402
60
HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 30 1.402
61
ABD002 Abducens Nerve Disease 25 1.402
62
P NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 23 1.402
63
THR010 Third Cranial Nerve Disease 10 1.402
64
RNL007 Renal Tubular Acidosis 56 0.169
65
HYP005 Hypokalemia 49 0.144
66
THY033 Thyrotoxicosis 57 0.139
67
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.131
68
SPS057 Spasticity 37 0.128
69
P LRY019 Laryngitis 64 0.126
70
THR013 Thoracic Outlet Syndrome 52 0.123
71
NRN002 Neuronitis 43 0.123
72
c THY032 Thyroiditis 65 0.120
73
MYT011 Myotonia 43 0.120
74
SYN053 Syndromic Diarrhea 34 0.120
75
P MYP004 Myopathy 61 0.117
76
NRP001 Neuropathy 61 0.117
77
ADN018 Adenoma 65 0.107
78
P GRV001 Graves' Disease 64 0.107
79
OTT002 Otitis Media 58 0.107
80
ANK002 Ankylosing Spondylitis 76 0.100
81
P ANG001 Angelman Syndrome 71 0.100
82
P RSP003 Respiratory Failure 68 0.100
83
ART019 Aortic Valve Stenosis 63 0.100
84
ACN002 Acanthosis Nigricans 64 0.093
85
BTL001 Botulism 60 0.093
86
P MSC003 Muscular Atrophy 53 0.093
87
P ATX010 Ataxia Neuropathy Spectrum 47 0.093
88
P CRV039 Cervicitis 57 0.089
89
ANR040 Aneurysm 45 0.089
90
BNF002 Bone Fracture 45 0.089
91
c BNG076 Benign Exophthalmos Syndrome 22 0.089
92
AND002 Androgen Insensitivity Syndrome 80 0.085
93
c AXN002 Axenfeld-Rieger Syndrome 69 0.085
94
HYP017 Hypophosphatemia 48 0.085
95
c HPT021 Hepatitis 63 0.080
96
c HYP076 Hyperthyroidism 62 0.080
97
P ALT001 Alternating Hemiplegia of Childhood 61 0.080
98
MYC002 Mycobacterium Avium Complex Disease 58 0.080
99
ACS001 Acoustic Neuroma 51 0.080
100
NRM004 Neuroma 45 0.080
101
AND005 Androgen Insensitivity Syndrome, Mild 21 0.080
102
EPL031 Epileptic Hemiplegia 5 0.080
103
P HYP075 Hypertension 85 0.076
104
c MNN013 Meningitis 67 0.076
105
P HRP006 Herpes Simplex 66 0.076
106
c PRG001 Progressive Muscular Atrophy 38 0.076
107
IMM088 Immunodeficiency 36 36 0.076
108
RMS005 Ramsay-Hunt Syndrome 31 0.076
109
P ATX002 Ataxia Telangiectasia 87 0.071
110
MLG056 Malignant Hyperthermia 65 0.071
111
LYM017 Lyme Disease 65 0.071
112
HRP004 Herpes Zoster 57 0.071
113
ART001 Arterial Tortuosity Syndrome 55 0.071
114
CHL069 Cholesteatoma 54 0.071
115
MLK003 Melkersson-Rosenthal Syndrome 51 0.071
116
WST005 West Nile Virus 42 0.071
117
ECT005 Ectropion 42 0.071
118
P MYS003 Myasthenia Gravis 79 0.066
119
P WGN002 Wegener's Granulomatosis 73 0.066
120
MYL001 Myelitis 54 0.066
121
HMP005 Hemiplegia 52 0.066
122
DYS073 Dysphagia 51 0.066
123
MNN014 Mononeuritis 51 0.066
124
PRT026 Parotitis 49 0.066
125
NRT004 Neuritis 49 0.066
126
CNV002 Conversion Disorder 48 0.066
127
LCK001 Locked-in Syndrome 41 0.066
128
WND001 Wound Botulism 40 0.066
129
PRL013 Paralytic Poliomyelitis 38 0.066
130
TBR010 Tuberculosis 85 0.060
131
ACT033 Acute Intermittent Porphyria 78 0.060
132
P CHR071 Charcot-Marie-Tooth Disease 73 0.060
133
STT002 Status Asthmaticus 63 0.060
134
PTT006 Pituitary Adenoma 61 0.060
135
P PLY019 Polyneuropathy 60 0.060
136
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.060
137
c ATX004 Ataxia 58 0.060
138
P DBT005 Diabetes Insipidus 57 0.060
139
PTN002 Patent Ductus Arteriosus 57 0.060
140
c HYP065 Hyperaldosteronism 57 0.060
141
SNS001 Sensorineural Hearing Loss 57 0.060
142
TTH006 Tooth Disease 55 0.060
143
P MSC033 Muscle Disorders 49 0.060
144
P NRV007 Nervous System Disease 49 0.060
145
CRB009 Cerebritis 38 0.060
146
HYP264 Hypertonia 35 0.060
147
LGP001 Lagophthalmos 31 0.060
148
ERB002 Erb's Palsy 10 0.060
149
P SYS001 Systemic Lupus Erythematosus 89 0.054
150
CDS001 Cadasil 84 0.054
151
P MLT020 Multiple Sclerosis 84 0.054
152
P LKM002 Leukemia 76 0.054
153
c LPS004 Lupus Erythematosus 75 0.054
154
P NRC002 Narcolepsy 74 0.054
155
c DBT009 Diabetes Mellitus 73 0.054
156
P NPH007 Nephrogenic Diabetes Insipidus 72 0.054
157
ART016 Aortic Aneurysm 70 0.054
158
c HYP086 Hypothyroidism 68 0.054
159
P HPT001 Hepatitis C 66 0.054
160
BRN029 Brain Disease 57 0.054
161
c MNT147 Mental Retardation 56 0.054
162
P SYR001 Syringomyelia 55 0.054
163
NRM005 Neuromuscular Disease 50 0.054
164
SJG001 Sjogren's Syndrome 47 0.054
165
PRP016 Paraplegia 47 0.054
166
MDS022 Mediastinitis 45 0.054
167
EPL002 Epilepsy Syndrome 45 0.054
168
SPP008 Suppurative Otitis Media 41 0.054
169
MLL002 Miller Fisher Syndrome 38 0.054
170
FTD001 Foot Drop 36 0.054
171
ADS002 Adie Syndrome 35 0.054
172
P LBY004 Labyrinthitis 33 0.054
173
GNC003 Geniculate Herpes Zoster 31 0.054
174
HNM002 Hinman Syndrome 28 0.054
175
ANT054 Anotia 26 0.054
176
FDB001 Foodborne Botulism 26 0.054
177
PRS053 Parsonage Turner Syndrome 18 0.054
178
MDD008 Middle Ear Adenoma 16 0.054
179
FBR024 Fibrocartilaginous Embolism 14 0.054
180
OLV001 Olivopontocerebellar Atrophy 81 0.046
181
P MLR004 Malaria 74 0.046
182
MLT021 Multiple System Atrophy 73 0.046
183
P AMY004 Amyloidosis 73 0.046
184
P HMN010 Hemangioma 70 0.046
185
P NRB001 Neuroblastoma 70 0.046
186
PLY017 Polyarteritis Nodosa 69 0.046
187
SRC014 Sarcoma 68 0.046
188
P TRN020 Turner Syndrome 67 0.046
189
c AMY001 Amyotrophic Lateral Sclerosis 66 0.046
190
c SPN046 Spinal Muscular Atrophy 65 0.046
191
STT001 Status Epilepticus 65 0.046
192
PHR003 Pharyngitis 65 0.046
193
c ENC004 Encephalitis 65 0.046
194
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.046
195
P ESP024 Esophagitis 63 0.046
196
SPN186 Spinal Cord Injury 61 0.046
197
c MSC005 Muscular Dystrophy 61 0.046
198
P GTR002 Goiter 61 0.046
199
MTR014 Motor Neuron Disease 61 0.046
200
ASP003 Aseptic Meningitis 60 0.046
201
SPN020 Spondylosis 59 0.046
202
P MMP001 Mumps 59 0.046
203
RBS001 Rabies 57 0.046
204
NRL005 Neurilemmoma 57 0.046
205
c THR003 Thoracic Aortic Aneurysm 56 0.046
206
ADR008 Adrenal Adenoma 54 0.046
207
TRY002 Troyer Syndrome 53 0.046
208
LPT001 Leptospirosis 53 0.046
209
TLR001 Tularemia 53 0.046
210
RLP003 Relapsing Fever 52 0.046
211
BLN003 Blindness 52 0.046
212
P PRP023 Peripheral Neuropathy 51 0.046
213
P MLG090 Malignant Hyperthermia Susceptibility Type 1 50 0.046
214
P FNC004 Fanconi Syndrome 50 0.046
215
CRT008 Carotid Artery Dissection 47 0.046
216
P ATN005 Autonomic Dysfunction 46 0.046
217
WST004 West Nile Encephalitis 46 0.046
218
EVN001 Evans' Syndrome 45 0.046
219
P SPN091 Spinal Muscular Atrophy with Respiratory Distress 1 45 0.046
220
c SBC007 Subacute Thyroiditis 45 0.046
221
FSC004 Fasciitis 45 0.046
222
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.046
223
QDR001 Quadriplegia 43 0.046
224
c CHR342 Chiari Malformation 43 0.046
225
SPN185 Spinal Cord Infarction 42 0.046
226
EPD005 Epidural Abscess 42 0.046
227
THY035 Thyroid Adenoma 38 0.046
228
TLS001 Tolosa-Hunt Syndrome 36 0.046
229
TBS001 Tabes Dorsalis 36 0.046
230
c PPL025 Popliteal Pterygium Syndrome 35 0.046
231
c SPS012 Spastic Paraplegia 3a 34 0.046
232
c SPS078 Spastic Paraplegia 7 34 0.046
233
CLR007 Colorado Tick Fever 34 0.046
234
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.046
235
PTR001 Petrositis 28 0.046
236
TFT003 Tufting Enteropathy 28 0.046
237
CVR002 Cavernous Sinus Thrombosis 27 0.046
238
BLB003 Bulbar Polio 21 0.046
239
ABD009 Abducens Palsy 21 0.046
240
PNT023 Pontine Hemorrhage 18 0.046
241
OTP003 Oto-Palatal-Digital Syndrome 17 0.046
242
SKL006 Skull Base Neoplasm 11 0.046
243
P LVR011 Liver Cancer 90 0.038
244
P MLT019 Multiple Myeloma 88 0.038
245
P BRS047 Breast Cancer 85 0.038
246
P LPR003 Leprosy 77 0.038
247
P PNM007 Pneumonia 77 0.038
248
P BPL003 Bipolar Disorder 76 0.038
249
P FML018 Familial Mediterranean Fever 75 0.038
250
WLF001 Wolff-Parkinson-White Syndrome 74 0.038
251
P SRC013 Sarcoidosis 73 0.038
252
GTL001 Gitelman Syndrome 73 0.038
253
P BRD002 Bardet-Biedl Syndrome 73 0.038
254
P CNG368 Congenital Adrenal Hyperplasia 72 0.038
255
P CNG401 Congenital Heart Disease 69 0.038
256
CRB039 Cerebrovascular Disease 68 0.038
257
P GLM007 Glomerulonephritis 68 0.038
258
P LNG044 Long Qt Syndrome 1 68 0.038
259
P PRG006 Progressive Supranuclear Palsy 68 0.038
260
P HYP117 Hypertriglyceridemia 67 0.038
261
c PRP029 Porphyria 67 0.038
262
TRG002 Trigeminal Neuralgia 67 0.038
263
P INF038 Influenza 67 0.038
264
MSL001 Measles 67 0.038
265
PLS006 Plasmodium Vivax Malaria 66 0.038
266
SPN038 Spina Bifida 66 0.038
267
STF001 Stiff-Person Syndrome 66 0.038
268
P FML001 Familial Atrial Fibrillation 66 0.038
269
P ATM010 Autoimmune Hemolytic Anemia 66 0.038
270
PRP025 Peripheral Primitive Neuroectodermal Tumor 66 0.038
271
c HML002 Hemolytic Anemia 65 0.038
272
c TXP001 Toxoplasmosis 65 0.038
273
P INS005 Insulin Resistance 64 0.038
274
BBS001 Babesiosis 64 0.038
275
c EHL001 Ehlers-Danlos Syndrome 63 0.038
276
KRN002 Kearns-Sayre Syndrome 63 0.038
277
c MLG069 Malignant Hypertension 63 0.038
278
HRD014 Hereditary Coproporphyria 63 0.038
279
P ART023 Arthropathy 63 0.038
280
c HRD010 Hereditary Spastic Paraplegia 63 0.038
281
ARC007 Arachnoid Cysts 62 0.038
282
ART005 Arteriovenous Malformation 62 0.038
283
P PSD020 Pseudohypoaldosteronism Type Ii 62 0.038
284
GLC003 Glucose Intolerance 61 0.038
285
CLD007 Cold Agglutinin Disease 59 0.038
286
NRC020 Neuroectodermal Tumor 59 0.038
287
c PRG013 Paraganglioma 59 0.038
288
YLL002 Yellow Fever 59 0.038
289
RHB003 Rhabdomyosarcoma 58 0.038
290
P NRM001 Neuromyelitis Optica 58 0.038
291
HDC001 Headache 57 0.038
292
P CNG021 Congenital Toxoplasmosis 57 0.038
293
P MYC008 Myocarditis 57 0.038
294
c CHR095 Chronic Progressive External Ophthalmoplegia 56 0.038
295
GST037 Gastroparesis 55 0.038
296
MYL003 Myeloid Sarcoma 55 0.038
297
P HYP014 Hyperuricemia 55 0.038
298
c TRM003 Tremor 55 0.038
299
JPN002 Japanese Encephalitis 55 0.038
300
P PND001 Pain Disorder 54 0.038
301
NWC001 Newcastle Disease 54 0.038
302
c OST028 Osteochondroma 54 0.038
303
c ACR001 Aicardi-Goutieres Syndrome 54 0.038
304
THY009 Thyroid Lymphoma 53 0.038
305
EHR002 Ehrlichiosis 53 0.038
306
GST045 Gastroenteritis 53 0.038
307
TCK001 Tick-Borne Encephalitis 52 0.038
308
OST011 Osteomalacia 52 0.038
309
PRT029 Parathyroid Adenoma 52 0.038
310
SPT005 Spotted Fever 52 0.038
311
GRW007 Growth Hormone Deficiency 52 0.038
312
STL001 St. Louis Encephalitis 51 0.038
313
RNL011 Renal Osteodystrophy 51 0.038
314
P SZR006 Seizure Disorder 50 0.038
315
P NML001 Nemaline Myopathy 50 0.038
316
c EMR001 Emery-Dreifuss Muscular Dystrophy 50 0.038
317
c EPS003 Episodic Ataxia 50 0.038
318
ACT128 Acute Hepatic Porphyria 50 0.038
319
P MJR001 Major Depressive Disorder 50 0.038
320
P PNM006 Pneumoconiosis 49 0.038
321
OPT009 Optic Neuritis 49 0.038
322
FBR047 Fibromyalgia 49 0.038
323
NPH003 Nephrocalcinosis 48 0.038
324
NSP002 Nasopharyngitis 48 0.038
325
MMB001 Membranoproliferative Glomerulonephritis 47 0.038
326
CNN003 Conn's Syndrome 47 0.038
327
P TRN034 Transverse Myelitis 46 0.038
328
c AML002 Amelogenesis Imperfecta 46 0.038
329
CNT025 Central Pontine Myelinolysis 46 0.038
330
MNN009 Meningoencephalitis 46 0.038
331
MYK002 Myokymia 46 0.038
332
P HMR005 Hemorrhoid 46 0.038
333
PST055 Postural Hypotension 45 0.038
334
KRT012 Keratoderma 45 0.038
335
GYN001 Gynecomastia 45 0.038
336
ARC002 Arachnoiditis 44 0.038
337
ILS001 Ileus 44 0.038
338
PRS037 Periostitis 44 0.038
339
OST006 Osteoblastoma 43 0.038
340
c APH002 Aphasia 43 0.038
341
c HRD086 Hereditary Hypophosphatemic Rickets 43 0.038
342
THY043 Thymic Hyperplasia 42 0.038
343
P OST052 Osteopetrosis Autosomal Recessive 2 42 0.038
344
LCR004 La Crosse Encephalitis 41 0.038
345
c SPS092 Spastic Paraplegia 11 41 0.038
346
RHB022 Rhabdoid Tumors, Somatic 41 0.038
347
c NRC009 Narcolepsy 1 40 0.038
348
TRC023 Trichinosis 39 0.038
349
HYD001 Hydranencephaly 38 0.038
350
P OTT001 Otitis Externa 38 0.038
351
XRP001 Xerophthalmia 37 0.038
352
TRP004 Tropical Sprue 37 0.038
353
RCK002 Rocky Mountain Spotted Fever 36 0.038
354
AXN001 Axonal Neuropathy 36 0.038
355
PRS063 Paresthesia 35 0.038
356
PSD029 Pseudocholinesterase Deficiency 34 0.038
357
INT042 Internuclear Ophthalmoplegia 34 0.038
358
THY025 Thymus Cancer 34 0.038
359
c PRS062 Persistent Hyperplastic Primary Vitreous 34 0.038
360
SPR007 Superior Mesenteric Artery Syndrome 34 0.038
361
MTC018 Metachondromatosis 33 0.038
362
CHL109 Childhood Apraxia of Speech 33 0.038
363
c FML249 Familial Amyloidosis, Finnish Type 33 0.038
364
SPS016 Spasmodic Dysphonia 33 0.038
365
ENT005 Entropion 32 0.038
366
P RNL066 Renal Tubular Acidosis, Distal, Ad 32 0.038
367
FCL003 Facial Hemiatrophy 32 0.038
368
BRW001 Brown-Vialetto-Van Laere Syndrome 32 0.038
369
c CHR160 Chiari Malformation Type 2 32 0.038
370
BRW009 Brown-Vialetto-Van Laere Syndrome 1 32 0.038
371
NRC019 Neurocutaneous Melanosis, Somatic 30 0.038
372
CBB002 Cobb Syndrome 30 0.038
373
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 30 0.038
374
PRR008 Periarteritis Nodosa 28 0.038
375
ECT004 Ecthyma 27 0.038
376
NRP016 Neuropathy, Recurrent, with Pressure Palsies 27 0.038
377
c PRG020 Paragangliomas 3 27 0.038
378
BRW004 Brown-Sequard Syndrome 27 0.038
379
c ACT159 Acute Transverse Myelitis 26 0.038
380
c PRG019 Paragangliomas 2 25 0.038
381
VST004 Vestibular Disease 25 0.038
382
TCK004 Tick Infestation 25 0.038
383
STR002 Streptococcal Meningitis 23 0.038
384
GLM016 Glomus Jugulare Tumors 21 0.038
385
PWS001 Powassan Encephalitis 19 0.038
386
MNN005 Meningovascular Neurosyphilis 19 0.038
387
CNT067 Central Cord Syndrome 18 0.038
388
ITR001 Iatrogenic Botulism 16 0.038
389
c ADL069 Adult Intestinal Botulism 14 0.038
390
SYR004 Syringobulbia 14 0.038
391
PRG097 Paragangliomas 1, with or Without Deafness 14 0.038
392
c NRP022 Neuropathy, Distal Hereditary Motor, Type Viib 13 0.038
393
BDR001 Bidirectional Tachycardia 13 0.038
394
TXN001 Toxin-Mediated Infectious Botulism 11 0.038
395
UVP001 Uveoparotid Fever 10 0.038
396
SPN015 Spinal Polio 9 0.038
397
BLB001 Bulbospinal Polio 9 0.038
398
MYP026 Myopathy - Thyrotoxic 9 0.038
399
BRC057 Brachial Plexus Birth Injuries 7 0.038
400
WST006 Westphal Disease 5 0.038
401
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.038
402
HMP020 Hemiplegia Alterans 1 0.038
403
P TYP008 Type 1 Diabetes Mellitus 95 0.027
404
P NRF002 Neurofibromatosis 94 0.027
405
P LFR001 Li-Fraumeni Syndrome 88 0.027
406
P AST005 Asthma 87 0.027
407
P DLT002 Dilated Cardiomyopathy 87 0.027
408
MTC003 Metachromatic Leukodystrophy 85 0.027
409
GLC006 Galactosemia 85 0.027
410
INF030 Infectious Mononucleosis 84 0.027
411
P GCH001 Gaucher's Disease 83 0.027
412
P TYS001 Tay-Sachs Disease 83 0.027
413
VNH001 Von Hippel-Lindau Disease 81 0.027
414
P PRC016 Pre-Eclampsia 79 0.027
415
BHC002 Behcet's Disease 79 0.027
416
BRK003 Burkitt's Lymphoma 77 0.027
417
PGT001 Paget's Disease of Bone 76 0.027
418
CRB011 Cerebrotendinous Xanthomatosis 76 0.027
419
P OST002 Osteoporosis 76 0.027
420
CHD001 Chediak-Higashi Syndrome 76 0.027
421
P ALX003 Alexander Disease 76 0.027
422
21H001 21-Hydroxylase Deficiency 76 0.027
423
KWS002 Kawasaki Disease 75 0.027
424
CRH001 Crohn's Disease 75 0.027
425
c OST001 Osteopetrosis 75 0.027
426
P CLC005 Celiac Disease 74 0.027
427
SKN016 Skin Disease 74 0.027
428
P MYL005 Myelofibrosis 74 0.027
429
CYS008 Cystic Echinococcosis 73 0.027
430
P ADD001 Addison's Disease 73 0.027
431
CFF002 Coffin-Lowry Syndrome 73 0.027
432
P HYP458 Hyper Ige Syndrome 72 0.027
433
RLP001 Relapsing Polychondritis 72 0.027
434
P MGR002 Migraine 71 0.027
435
P MYS005 Myositis 71 0.027
436
CCC001 Coccidioidomycosis 71 0.027
437
PRT036 Peritonitis 71 0.027
438
ACQ007 Acquired Immunodeficiency Syndrome 70 0.027
439
P MCH002 Machado-Joseph Disease 70 0.027
440
NRL016 Neural Tube Defects 69 0.027
441
SPS077 Sepsis 69 0.027
442
P LGH001 Leigh Disease 69 0.027
443
P CMR001 Camurati-Engelmann Disease 69 0.027
444
c HPT016 Hepatitis B 68 0.027
445
DSM004 Desmoid Tumor 68 0.027
446
ALV002 Alveolar Echinococcosis 68 0.027
447
P THY023 Thymoma 68 0.027
448
P ABD003 Abdominal Aortic Aneurysm 67 0.027
449
P BLD042 Bladder Carcinoma 67 0.027
450
VRG001 Variegate Porphyria 67 0.027
451
MCK007 Muckle-Wells Syndrome 67 0.027
452
P SYS005 Systemic Scleroderma 66 0.027
453
OLL001 Ollier Disease 66 0.027
454
ABT001 Abetalipoproteinemia 66 0.027
455
GST009 Gastroschisis 66 0.027
456
P ATM003 Autoimmune Thyroiditis 66 0.027
457
CHR072 Chordoma 65 0.027
458
FCT003 Factor X Deficiency 65 0.027
459
BLR001 Biliary Atresia 65 0.027
460
PLM033 Pulmonary Embolism 65 0.027
461
c XRD001 Xeroderma Pigmentosum 65 0.027
462
P MLN008 Melanoma 64 0.027
463
STR067 Stroke, Ischemic 64 0.027
464
FCT002 Factor Xi Deficiency 64 0.027
465
HYP004 Hypercalcemia 64 0.027
466
P TYR002 Tyrosinemia Type I 64 0.027
467
MNT001 Mantle Cell Lymphoma 64 0.027
468
c SML001 Small Cell Carcinoma 63 0.027
469
P FBR017 Fibrosarcoma 63 0.027
470
RBR001 Roberts Syndrome 63 0.027
471
P ALP004 Alport Syndrome 63 0.027
472
P KRT004 Keratitis 63 0.027
473
c CHR022 Charcot-Marie-Tooth Disease Type 1 63 0.027
474
P OLG002 Oligodendroglioma 62 0.027
475
ISC004 Ischemia 62 0.027
476
P CRB042 Cerebellar Ataxia 62 0.027
477
CMP002 Campylobacteriosis 62 0.027
478
P FML043 Familial Idiopathic Basal Ganglia Calcification 62 0.027
479
c INT070 Intestinal Obstruction 62 0.027
480
GLD001 Goldenhar Syndrome 62 0.027
481
LRN003 Learning Disability 62 0.027
482
P GLY008 Glycogen Storage Disease Ii 62 0.027
483
ALP003 Alpers Syndrome 62 0.027
484
c KDN018 Kidney Disease 62 0.027
485
TYP007 Typhoid Fever 62 0.027
486
P MTR012 Mitral Valve Disease 62 0.027
487
P SCH018 Schizencephaly 61 0.027
488
P CNJ013 Conjunctivitis 61 0.027
489
PTN001 Patent Foramen Ovale 61 0.027
490
c MYL007 Myeloma 60 0.027
491
NRL004 Neuroleptic Malignant Syndrome 60 0.027
492
c ALM001 Al Amyloidosis 60 0.027
493
SPH001 Sapho Syndrome 60 0.027
494
CHC001 Chickenpox 59 0.027
495
TWN003 Townes-Brocks Syndrome 59 0.027
496
c HMP002 Hemophagocytic Lymphohistiocytosis 59 0.027
497
KRT001 Keratoconjunctivitis Sicca 59 0.027
498
CRB021 Cerebral Malaria 59 0.027
499
PMP001 Pemphigus 59 0.027
500
MGC001 Megacolon 59 0.027
501
NTR001 Neutral Lipid Storage Disease 59 0.027
502
c GLY013 Glycogen Storage Disease 59 0.027
503
c FML023 Familial Hemiplegic Migraine 58 0.027
504
CVR006 Cavernous Hemangioma 58 0.027
505
ANR004 Anuria 58 0.027
506
LYM019 Lymphosarcoma 58 0.027
507
SMT015 Smith Magenis Syndrome 58 0.027
508
c BRG001 Brugada Syndrome 58 0.027
509
END030 End Stage Renal Failure 57 0.027
510
ESP020 Esophageal Atresia 57 0.027
511
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 57 0.027
512
c MYT007 Myotonic Dystrophy Type 2 57 0.027
513
P CRN012 Craniometaphyseal Dysplasia 57 0.027
514
P VRL012 Viral Meningitis 57 0.027
515
P MYM002 Moyamoya Disease 57 0.027
516
P GNT008 Giant Cell Tumor 57 0.027
517
PRN023 Prion Disease 57 0.027
518
c CTR002 Cataract 57 0.027
519
P HYP024 Hypoparathyroidism 57 0.027
520
INS008 Insulin-Like Growth Factor I Deficiency 56 0.027
521
c WRD001 Waardenburg's Syndrome 56 0.027
522
c ACT073 Acute Leukemia 56 0.027
523
c HYP060 Hyperinsulinism 56 0.027
524
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 56 0.027
525
BNC003 Bone Cancer 56 0.027
526
c SPN049 Spinocerebellar Ataxia 56 0.027
527
PLG002 Plague 55 0.027
528
P FNC025 Fanconi Anemia, Complementation Group J 55 0.027
529
P KLP003 Klippel-Feil Syndrome 55 0.027
530
STR039 Sturge-Weber Syndrome 55 0.027
531
P BRG005 Brugada Syndrome 1 55 0.027
532
PRN011 Pernicious Anemia 55 0.027
533
MDL009 Medullary Sponge Kidney 54 0.027
534
HMM003 Hemimegalencephaly 54 0.027
535
SLP005 Sleep Disorder 54 0.027
536
c GLY007 Glycogen Storage Disease Iv 54 0.027
537
P EXP004 Exophthalmos 54 0.027
538
RGD001 Rigid Spine Syndrome 54 0.027
539
P HYP141 Hyperphenylalaninemia 54 0.027
540
c BRT004 Bartter Disease 53 0.027
541
c ATR038 Atrial Fibrillation, Familial, 3 53 0.027
542
NPH051 Nephritis 53 0.027
543
MLT075 Multifocal Motor Neuropathy 53 0.027
544
LYM022 Lymphangioma 53 0.027
545
CHK001 Chikungunya 53 0.027
546
MYX004 Myxedema 53 0.027
547
P ENC008 Encephalocele 53 0.027
548
STS002 Situs Inversus 52 0.027
549
HNT002 Hantavirus Pulmonary Syndrome 52 0.027
550
PRC013 Pericarditis 52 0.027
551
TRN015 Transient Cerebral Ischemia 52 0.027
552
c SPN183 Spontaneous Pneumothorax 52 0.027
553
BRS064 Bursitis 52 0.027
554
HRD030 Hereditary Neuralgic Amyotrophy 51 0.027
555
DGS001 Degos Disease 51 0.027
556
ANG002 Angiostrongyliasis 51 0.027
557
EXS001 Exostosis 51 0.027
558
SST001 Sost-Related Sclerosing Bone Dysplasia 51 0.027
559
HJD001 Hajdu-Cheney Syndrome 51 0.027
560
c HMP006 Hemiplegic Migraine 50 0.027
561
P CYS016 Cystic Kidney 50 0.027
562
FBR009 Fibrous Dysplasia 50 0.027
563
P APL006 Aplasia Cutis Congenita 50 0.027
564
c CRB126 Cerebral Cavernous Malformation 50 0.027
565
EWN002 Ewing's Family of Tumors 50 0.027
566
CHR288 Chronic Recurrent Multifocal Osteomyelitis 50 0.027
567
HYP006 Hypertensive Heart Disease 49 0.027
568
INF058 Inflammatory Myofibroblastic Tumor 49 0.027
569
PNM008 Pneumothorax 49 0.027
570
c ATN004 Autonomic Neuropathy 49 0.027
571
CTS002 Cat-Scratch Disease 49 0.027
572
c OPT004 Optic Atrophy 49 0.027
573
P BNG071 Benign Schwannoma 49 0.027
574
c GRS007 Griscelli Syndrome Type 1 48 0.027
575
SCH016 Schimke Immunoosseous Dysplasia 48 0.027
576
c CNT035 Central Nervous System Disease 48 0.027
577
NRX001 Neuroaxonal Dystrophy 48 0.027
578
PLS016 Plasma Cell Leukemia 48 0.027
579
ASP007 Aspiration Pneumonia 48 0.027
580
TRC040 Tracheoesophageal Fistula 48 0.027
581
MTH009 Mouth Disease 48 0.027
582
PLM010 Pulmonary Edema 48 0.027
583
MTS001 Mutism 48 0.027
584
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 47 0.027
585
LYM021 Lymphadenitis 47 0.027
586
AMB002 Amblyopia 46 0.027
587
c MLG086 Malignant Hyperthermia Susceptibility 46 0.027
588
P FNG005 Feingold Syndrome 46 0.027
589
MYS001 Myositis Ossificans 46 0.027
590
c DMY001 Demyelinating Polyneuropathy 46 0.027
591
HYP120 Hypoaldosteronism 46 0.027
592
SPN050 Spinocerebellar Degeneration 46 0.027
593
MCP006 Mucoepidermoid Carcinoma 45 0.027
594
TNG009 Tongue Squamous Cell Carcinoma 45 0.027
595
MDD002 Middle Ear Cholesteatoma 45 0.027
596
ACT012 Acute Hemorrhagic Conjunctivitis 45 0.027
597
P NRL007 Neurologic Diseases 45 0.027
598
HTS001 Hiatus Hernia 45 0.027
599
MGL013 Megalencephaly 45 0.027
600
MYC033 Myoclonus 44 0.027
601
P FCS001 Facioscapulohumeral Muscular Dystrophy 44 0.027
602
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 44 0.027
603
ZYG002 Zygomycosis 44 0.027
604
P ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 44 0.027
605
FTT001 Fatty Liver Disease 44 0.027
606
c PSD054 Pseudohypoaldosteronism Type Iib 43 0.027
607
P BRT034 Bartter Syndrome, Type 2 43 0.027
608
NCR007 Necrotizing Fasciitis 43 0.027
609
TTR016 Tetra-Amelia Syndrome 43 0.027
610
RMS001 Rem Sleep Behavior Disorder 43 0.027
611
NRG004 Neurogenic Diabetes Insipidus 42 0.027
612
EST005 Esotropia 42 0.027
613
SRC001 Sarcomatoid Mesothelioma 42 0.027
614
LMB052 Lumbar Disc Herniation 42 0.027
615
c AMY008 Amyotrophic Lateral Sclerosis Type 2 42 0.027
616
P RSM001 Rasmussen Encephalitis 41 0.027
617
P VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 41 0.027
618
WHP001 Whipple Disease 41 0.027
619
CDQ001 Cauda Equina Syndrome 41 0.027
620
DYG002 Dyggve-Melchior-Clausen Syndrome 41 0.027
621
P FNN001 Finnish Type Amyloidosis 41 0.027
622
BLT008 Bilateral Frontoparietal Polymicrogyria 41 0.027
623
SPS019 Spastic Paraparesis 40 0.027
624
LRY029 Laryngomalacia 40 0.027
625
HYP265 Hypotonia 40 0.027
626
P LPD015 Lipodystrophy, Familial Partial, Type 2 40 0.027
627
P MNN007 Meningocele 40 0.027
628
HRD025 Hereditary Neuropathy with Liability to Pressure Palsies 40 0.027
629
SCT002 Scotoma 40 0.027
630
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 40 0.027
631
P EXS004 Exostoses, Multiple, Type 1 39 0.027
632
c SRC025 Sarcoidosis 1 39 0.027
633
CYS024 Cystinosis, Ocular Nonnephropathic 39 0.027
634
END051 Endolymphatic Sac Tumor 39 0.027
635
P PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 39 0.027
636
SML020 Small Patella Syndrome 38 0.027
637
SPC005 Speech Disorder 38 0.027
638
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.027
639
VRL011 Viral Infectious Disease 38 0.027
640
PLM029 Palmoplantar Keratosis 38 0.027
641
ODN002 Odontohypophosphatasia 38 0.027
642
LMB010 Lambert Syndrome 38 0.027
643
c SPS091 Spastic Paraplegia 4 37 0.027
644
P GLM006 Glomangioma 37 0.027
645
BRN016 Bronchogenic Carcinoma 37 0.027
646
PRX020 Proximal Renal Tubular Acidosis with Ocular Abnormalities 37 0.027
647
HNS001 Hansen's Disease 37 0.027
648
SCR015 Scarlet Fever 37 0.027
649
INF006 Infant Botulism 37 0.027
650
c CNG112 Congenital Muscular Dystrophy Type 1a 36 0.027
651
IPX001 Ipex Syndrome 36 0.027
652
c SPS025 Spastic Paraplegia 15 36 0.027
653
MCR213 Macroglobulinemia, Waldenstrom, Somatic 35 0.027
654
P AML017 Amelogenesis Imperfecta, Type Ib 35 0.027
655
P CHR454 Chiari Malformation Type 1 35 0.027
656
CSL001 Causalgia 34 0.027
657
HYP034 Hypertensive Encephalopathy 34 0.027
658
THM001 Thomsen Disease 34 0.027
659
c SPS027 Spastic Paraplegia 17 34 0.027
660
MRR003 Murray Valley Encephalitis 34 0.027
661
PMP008 Pemphigus Vegetans 34 0.027
662
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 34 0.027
663
BLT011 Bilateral Perisylvian Polymicrogyria 34 0.027
664
ANT018 Anthracosis 33 0.027
665
c PRX014 Proximal Spinal Muscular Atrophy 32 0.027
666
PNM005 Pneumonic Plague 32 0.027
667
PST020 Postpoliomyelitis Syndrome 32 0.027
668
HRD088 Hereditary Neuropathies 32 0.027
669
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 32 0.027
670
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 31 0.027
671
SPR083 Sporadic Hemiplegic Migraine 31 0.027
672
c SPS013 Spastic Paraplegia 8 31 0.027
673
c ATS059 Autosomal Dominant Hyper Ige Syndrome 31 0.027
674
c OST050 Osteopetrosis Autosomal Dominant Type 2 31 0.027
675
CRB027 Cerebellar Disease 31 0.027
676
MNR004 Mounier-Kuhn Syndrome 31 0.027
677
FRY001 Frey Syndrome 30 0.027
678
c GM2005 Gm2-Gangliosidosis, Ab Variant 30 0.027
679
c SCP001 Sc Phocomelia Syndrome 30 0.027
680
VST003 Vestibular Nystagmus 30 0.027
681
CRN051 Craniofacial Microsomia 30 0.027
682
PNT009 Pontine Tegmental Cap Dysplasia 30 0.027
683
c OST051 Osteopetrosis Autosomal Recessive 1 29 0.027
684
c PHC014 Phocomelia 29 0.027
685
CRV030 Cervical Adenitis 29 0.027
686
c SPS079 Spastic Paraplegia 2 29 0.027
687
BRC010 Brachial Plexus Lesion 29 0.027
688
MLR010 Melorheostosis with Osteopoikilosis 29 0.027
689
PRG035 Progressive Supranuclear Palsy Atypical 29 0.027
690
LPN001 Louping Ill 29 0.027
691
DYS045 Dysosteosclerosis 28 0.027
692
NRS003 Neurosyphilis 28 0.027
693
P PRD019 Periodic Fever, Familial 28 0.027
694
HYP362 Hyperopia 28 0.027
695
c RNL045 Renal Tubular Acidosis, Distal 28 0.027
696
FBR028 Fibrosing Mediastinitis 28 0.027
697
FCT022 Factor Xi Deficiency, Autosomal Recessive 27 0.027
698
MYC014 Mycobacterium Chelonae 27 0.027
699
P LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 27 0.027
700
FCL044 Fecal Incontinence 27 0.027
701
AMY005 Amyloid Neuropathy 27 0.027
702
RHB020 Rhabdomyosarcoma, Somatic 27 0.027
703
WYB001 Wyburn Mason's Syndrome 26 0.027
704
GNT004 Gnathomiasis 26 0.027
705
P MYT013 Myotonia Congenita, Dominant 26 0.027
706
ETH009 Ethmoid Sinusitis 26 0.027
707
SNS003 Sensory Peripheral Neuropathy 26 0.027
708
GLT018 Glut1 Deficiency Syndrome 1 26 0.027
709
ANT013 Anterior Spinal Artery Syndrome 26 0.027
710
P CHR097 Chronic Purulent Otitis Media 25 0.027
711
HYP048 Hypotropia 25 0.027
712
EXC003 Excessive Tearing 25 0.027
713
ECH002 Echolalia 25 0.027
714
MYS010 Myostatin-Related Muscle Hypertrophy 25 0.027
715
LTR002 Lateral Sinus Thrombosis 25 0.027
716
P INT006 Intestinal Botulism 25 0.027
717
PRN016 Peroneal Neuropathy 24 0.027
718
c FRT001 Fourth Cranial Nerve Palsy 24 0.027
719
CRT009 Critical Illness Polyneuropathy 24 0.027
720
HSH001 Hashimoto-Pritzker Syndrome 23 0.027
721
SBS002 Substernal Goiter 22 0.027
722
ATR055 Atrial Septal Aneurysm 22 0.027
723
PRS120 Persistent Idiopathic Facial Pain 22 0.027
724
c SNS011 Sinus Cancer 22 0.027
725
ETH012 Ethylene Glycol Poisoning 22 0.027
726
ERL024 Early-Onset Myopathy, Areflexia, Respiratory Distress and Dysphagia 22 0.027
727
LRY007 Laryngeal Tuberculosis 21 0.027
728
EXP002 Exposure Keratitis 21 0.027
729
DRS001 Dressler's Syndrome 21 0.027
730
ACT181 Acute Motor Axonal Neuropathy 21 0.027
731
ATL010 Atlantoaxial Subluxation 21 0.027
732
SWL001 Swallowing Disorders 21 0.027
733
c CNG333 Congenital Horner Syndrome 21 0.027
734
PRM041 Primary Cortisol Resistance 21 0.027
735
CNG133 Congenital Varicella Syndrome 21 0.027
736
HYP047 Hypertropia 20 0.027
737
c CRB094 Cerebral Cavernous Malformations 3 20 0.027
738
c VRL004 Viral Labyrinthitis 19 0.027
739
c HRD043 Hereditary Congenital Facial Paresis 19 0.027
740
MLN002 Melanomatosis 19 0.027
741
DND013 Dandy-Walker Malformation with Postaxial Polydactyly 19 0.027
742
P SPN115 Spinocerebellar Ataxia X-Linked Type 3 19 0.027
743
PRP013 Paraphimosis 18 0.027
744
c CNG129 Congenital Torticollis 18 0.027
745
HTR005 Heterochromia Iridis 17 0.027
746
CLV002 Clivus Chordoma 17 0.027
747
CNR001 Coenurosis 17 0.027
748
c MYP081 Myopathy, Myofibrillar, 6 17 0.027
749
c CHR094 Chronic Polyneuropathy 16 0.027
750
FHR002 Fahr's Syndrome 16 0.027
751
c DST048 Distal Hereditary Motor Neuropathy Type 1 16 0.027
752
P INT105 Intellectual Disability Multi-Gene Panels 16 0.027
753
INT095 Internal Carotid Agenesis 15 0.027
754
SPN092 Spinal Shock 15 0.027
755
FCL035 Facial Dysmorphism - Macrocephaly - Myopia - Dandy-Walker Malformation 15 0.027
756
INH013 Inhalational Botulism 15 0.027
757
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 15 0.027
758
MNS002 Mini Stroke 14 0.027
759
MLL006 Mollaret Meningitis 14 0.027
760
TRG006 Trigger Thumb 13 0.027
761
ATY001 Atypical Depressive Disorder 13 0.027
762
BMF002 Bamforth Syndrome 13 0.027
763
BNP002 Bone Epithelioid Hemangioma 13 0.027
764
DFN229 Deafness - Ear Malformation - Facial Palsy 13 0.027
765
SPH008 Sphenoidal Sinus Cancer 13 0.027
766
c CHR161 Chiari Malformation Type 3 12 0.027
767
CNM001 Canomad Syndrome 12 0.027
768
SPR038 Supranuclear Ocular Palsy 12 0.027
769
PRS033 Parasitic Ectoparasitic Infectious Disease 12 0.027
770
INF052 Infantile Scoliosis 10 0.027
771
KNG003 Konigsmark Knox Hussels Syndrome 8 0.027
772
GNT013 Genetic Brain Disorders 5 0.027