Search results for paralysis

1012 hits were found for paralysis

# Family MCID Name MIFTS Score
1
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 8.022
2
HYP052 Hyperkalemic Periodic Paralysis 57 6.965
3
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 4.946
4
FCL012 Facial Paralysis 50 4.239
5
NRM009 Normokalemic Periodic Paralysis 32 4.103
6
P THY054 Thyrotoxic Periodic Paralysis 54 4.093
7
TCK002 Tick Paralysis 22 3.952
8
FML036 Familial Periodic Paralysis 41 3.899
9
c THY083 Thyrotoxic Periodic Paralysis 2 28 3.666
10
PRM057 Paramyotonia Congenita of Von Eulenburg 39 3.566
11
c INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 29 3.539
12
P SPS225 Spastic Paralysis, Infantile-Onset Ascending 31 3.497
13
c THY084 Thyrotoxic Periodic Paralysis 1 29 3.390
14
OCL003 Oculomotor Nerve Paralysis 27 3.255
15
c HYP606 Hypokalemic Periodic Paralysis, Type 2 30 3.203
16
BLL003 Bell's Palsy 49 2.684
17
LRY047 Laryngeal Abductor Paralysis 24 2.560
18
PRN008 Peroneal Nerve Paralysis 23 2.528
19
MBS002 Moebius Syndrome 53 2.502
20
KRT022 Keratoderma Palmoplantar Spastic Paralysis 15 2.496
21
c THY119 Thyrotoxic Periodic Paralysis 3 10 2.473
22
P PRK057 Parkinson Disease, Late-Onset 78 2.445
23
P NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 26 2.445
24
CNG490 Congenital Hereditary Facial Paralysis-Variable Hearing Loss Syndrome 8 2.445
25
PLM031 Poliomyelitis 64 2.296
26
KLM001 Klumpke Paralysis 11 2.098
27
CNG241 Congenital Laryngeal Palsy 7 2.051
28
GLS003 Glossopharyngeal Nerve Paralysis 8 2.043
29
c NRN040 Neuronopathy, Distal Hereditary Motor, Type Viib 26 2.026
30
LRY021 Laryngeal Adductor Paralysis 15 2.026
31
VCL007 Vocal Cord Paralysis and Ptosis 15 2.026
32
FML082 Familial Partial Paralysis 3 2.026
33
P CRN035 Cranial Nerve Palsy 42 2.005
34
PRL020 Paralysis Agitans, Juvenile, of Hunt 12 2.005
35
PSD001 Pseudobulbar Palsy 35 1.992
36
KRT067 Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy 17 1.992
37
TCK005 Tucker Syndrome 6 1.992
38
TDD001 Todd's Paralysis 6 1.603
39
THR010 Third Cranial Nerve Disease 26 1.560
40
MYC078 Myoclonus and Ataxia 30 1.492
41
GNC003 Geniculate Herpes Zoster 37 1.475
42
MYT030 Myotonia, Potassium-Aggravated 39 1.456
43
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 14 1.456
44
FML160 Familial Spastic Paralysis 6 1.456
45
LRY045 Laryngeal Abductor Paralysis-Intellectual Disability Syndrome 6 1.456
46
P GLL022 Guillain-Barre Syndrome 61 1.445
47
P HRN001 Horner's Syndrome 45 1.445
48
LRY052 Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy 11 1.445
49
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 4 1.445
50
KRN002 Kearns-Sayre Syndrome 59 1.432
51
SPS003 Spastic Diplegia 55 1.432
52
CYC001 Cycloplegia 29 1.432
53
c FML159 Familial Periodic Paralyses 10 1.432
54
SPN389 Spinocerebellar Atrophy with Pupillary Paralysis 6 1.432
55
c DST092 Distal Hereditary Motor Neuropathy Type 7 11 1.417
56
TRP002 Tropical Spastic Paraparesis 58 1.398
57
ABD002 Abducens Nerve Disease 28 1.398
58
MRK002 Marek Disease 28 1.398
59
HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 27 1.398
60
PRT015 Partial Third-Nerve Palsy 21 1.398
61
c FCL030 Facial Paresis, Hereditary Congenital, 1 19 1.398
62
BLN017 Balint Syndrome 16 1.398
63
P RNL007 Renal Tubular Acidosis 51 0.160
64
P LRY019 Laryngitis 57 0.140
65
HYP005 Hypokalemia 53 0.132
66
P NRV007 Nervous System Disease 75 0.130
67
c GRV008 Graves Disease 1 52 0.124
68
P MYP004 Myopathy 69 0.121
69
P GRV001 Graves' Disease 62 0.117
70
P THY032 Thyroiditis 56 0.117
71
SPS057 Spasticity 41 0.114
72
P RNL045 Renal Tubular Acidosis, Distal 42 0.110
73
MYT011 Myotonia 41 0.110
74
P RSP003 Respiratory Failure 71 0.107
75
P NRP001 Neuropathy 63 0.107
76
P ANR048 Aniridia 1 68 0.099
77
ADN018 Adenoma 63 0.099
78
CRN031 Cranial Nerve Disease 45 0.099
79
ANR038 Anorexia Nervosa 1 21 0.099
80
BLD137 Blood Group--Ahonen 17 0.099
81
OTT002 Otitis Media 67 0.096
82
BNF002 Bone Fracture 56 0.096
83
P HYP076 Hyperthyroidism 56 0.090
84
NRN002 Neuronitis 43 0.087
85
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.087
86
ANR040 Aneurysm 61 0.084
87
P PRD017 Periodic Paralyses 29 0.084
88
P MYS003 Myasthenia Gravis 73 0.081
89
P MSC003 Muscular Atrophy 55 0.081
90
P PTS002 Ptosis 50 0.081
91
P CRV039 Cervicitis 49 0.081
92
ALR002 Al-Raqad Syndrome 30 0.081
93
MSC033 Muscle Disorders 53 0.077
94
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.077
95
c BLD140 Blood Group, I System 37 0.077
96
LYM017 Lyme Disease 68 0.074
97
c CNT035 Central Nervous System Disease 65 0.074
98
MTH009 Mouth Disease 64 0.074
99
ACS001 Acoustic Neuroma 60 0.074
100
NRM004 Neuroma 51 0.074
101
FDB001 Foodborne Botulism 46 0.074
102
HYP017 Hypophosphatemia 45 0.074
103
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 42 0.074
104
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.074
105
P HPT021 Hepatitis 75 0.070
106
P HRP006 Herpes Simplex 70 0.070
107
P EPL164 Epilepsy 70 0.070
108
AGN016 Aging 65 0.070
109
HRP004 Herpes Zoster 61 0.070
110
NRM005 Neuromuscular Disease 60 0.070
111
CRD223 Cardiac Arrhythmia 52 0.070
112
MYL001 Myelitis 52 0.070
113
P ALT001 Alternating Hemiplegia of Childhood 48 0.070
114
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.070
115
FCL011 Facial Nerve Disease 35 0.070
116
EPL031 Epileptic Hemiplegia 4 0.070
117
ALP046 Alport Syndrome, X-Linked 74 0.066
118
P MNN013 Meningitis 71 0.066
119
P LYM118 Lymphoma 71 0.066
120
SPN186 Spinal Cord Injury 67 0.066
121
P MLG056 Malignant Hyperthermia 60 0.066
122
PRP083 Porphyria, Acute Intermittent 60 0.066
123
P PLY019 Polyneuropathy 58 0.066
124
P ENC018 Encephalopathy 58 0.066
125
HMP005 Hemiplegia 54 0.066
126
PRP016 Paraplegia 53 0.066
127
P CHL069 Cholesteatoma 52 0.066
128
DYS073 Dysphagia 47 0.066
129
c PRG001 Progressive Muscular Atrophy 41 0.066
130
CRB009 Cerebritis 41 0.066
131
LRY017 Laryngeal Disease 38 0.066
132
WND001 Wound Botulism 31 0.066
133
LGP001 Lagophthalmos 29 0.066
134
VGS001 Vagus Nerve Disease 16 0.066
135
P CHR071 Charcot-Marie-Tooth Disease 67 0.062
136
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.062
137
WST005 West Nile Virus 58 0.062
138
P SJG008 Sjogren Syndrome 58 0.062
139
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 57 0.062
140
NRT004 Neuritis 55 0.062
141
P FNC004 Fanconi Syndrome 54 0.062
142
c BRN108 Branchiootic Syndrome 1 47 0.062
143
ECT005 Ectropion 47 0.062
144
LCK001 Locked-in Syndrome 47 0.062
145
CNT025 Central Pontine Myelinolysis 45 0.062
146
CNV002 Conversion Disorder 42 0.062
147
c PLM022 Pulmonary Valve Insufficiency 38 0.062
148
PRL013 Paralytic Poliomyelitis 28 0.062
149
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.057
150
P MLT020 Multiple Sclerosis 85 0.057
151
P PNM007 Pneumonia 70 0.057
152
CRB039 Cerebrovascular Disease 68 0.057
153
MLT157 Multiple System Atrophy 1 65 0.057
154
P NRC002 Narcolepsy 64 0.057
155
P HYP086 Hypothyroidism 62 0.057
156
TTH006 Tooth Disease 54 0.057
157
QDR001 Quadriplegia 54 0.057
158
HPT082 Hepatic Adenomas, Familial 52 0.057
159
P FNC043 Fanconi Anemia, Complementation Group E 52 0.057
160
STT002 Status Asthmaticus 46 0.057
161
ARC002 Arachnoiditis 45 0.057
162
P PRT026 Parotitis 45 0.057
163
MLL002 Miller Fisher Syndrome 44 0.057
164
MLK003 Melkersson-Rosenthal Syndrome 42 0.057
165
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.057
166
MSC004 Muscle Tissue Disease 39 0.057
167
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.057
168
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.057
169
c MYS011 Myasthenia Gravis Congenital 28 0.057
170
c SCN048 Secondary Syringomyelia 22 0.057
171
c SYS001 Systemic Lupus Erythematosus 86 0.052
172
P HRT032 Heart Disease 80 0.052
173
P LKM002 Leukemia 75 0.052
174
ART016 Aortic Aneurysm 70 0.052
175
P AMY004 Amyloidosis 69 0.052
176
P MSC005 Muscular Dystrophy 66 0.052
177
RSP006 Respiratory System Disease 63 0.052
178
CRD119 Cardiac Arrest 63 0.052
179
GTL001 Gitelman Syndrome 62 0.052
180
P PTT006 Pituitary Adenoma 57 0.052
181
CPR004 Coproporphyria, Hereditary 54 0.052
182
P DBT005 Diabetes Insipidus 54 0.052
183
GTR002 Goiter 53 0.052
184
SPP008 Suppurative Otitis Media 50 0.052
185
P PTN014 Patent Ductus Arteriosus 1 45 0.052
186
P MYT023 Myotonia Congenita 44 0.052
187
c SBC007 Subacute Thyroiditis 43 0.052
188
CRT008 Carotid Artery Dissection 42 0.052
189
PNG002 Pain Agnosia 41 0.052
190
P SPN408 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 41 0.052
191
THY043 Thymic Hyperplasia 38 0.052
192
MST019 Mastoiditis 33 0.052
193
c NRC009 Narcolepsy 1 23 0.052
194
TXN001 Toxin-Mediated Infectious Botulism 12 0.052
195
ERB002 Erb's Palsy 8 0.052
196
c HPT001 Hepatitis C 73 0.047
197
WGN006 Wegener Granulomatosis 71 0.047
198
P LPS004 Lupus Erythematosus 69 0.047
199
P MYC084 Mycobacterium Tuberculosis 1 69 0.047
200
P NRM001 Neuromyelitis Optica 67 0.047
201
GST050 Gastrointestinal System Disease 66 0.047
202
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.047
203
NRL005 Neurilemmoma 64 0.047
204
P MYS005 Myositis 63 0.047
205
THR024 Thrombosis 61 0.047
206
PHR003 Pharyngitis 59 0.047
207
ANK001 Ankylosis 56 0.047
208
c CHR320 Chiari Malformation Type I 56 0.047
209
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.047
210
SPN041 Spinal Cord Disease 54 0.047
211
HYP068 Hyperostosis 52 0.047
212
ATN005 Autonomic Dysfunction 51 0.047
213
P SYR001 Syringomyelia 49 0.047
214
MNN009 Meningoencephalitis 49 0.047
215
TLR001 Tularemia 44 0.047
216
MDS022 Mediastinitis 44 0.047
217
WST004 West Nile Encephalitis 42 0.047
218
P LBY004 Labyrinthitis 41 0.047
219
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.047
220
ARC007 Arachnoid Cysts 39 0.047
221
FTD001 Foot Drop 35 0.047
222
TBS001 Tabes Dorsalis 33 0.047
223
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.047
224
BRW004 Brown-Sequard Syndrome 30 0.047
225
FZL002 Fazio-Londe Disease 25 0.047
226
MDD008 Middle Ear Adenoma 23 0.047
227
BLD163 Blood Group, Dombrock System 23 0.047
228
c LTH032 Lethal Congenital Contracture Syndrome 7 20 0.047
229
ITR001 Iatrogenic Botulism 16 0.047
230
c ADL069 Adult Intestinal Botulism 15 0.047
231
FBR024 Fibrocartilaginous Embolism 14 0.047
232
INH013 Inhalational Botulism 14 0.047
233
P HPT023 Hepatocellular Carcinoma 94 0.040
234
MLR004 Malaria 86 0.040
235
STR067 Stroke, Ischemic 84 0.040
236
P NRB001 Neuroblastoma 73 0.040
237
ADR007 Adrenoleukodystrophy 72 0.040
238
P TRN020 Turner Syndrome 69 0.040
239
CNR004 Cone-Rod Dystrophy 2 69 0.040
240
P ATR011 Atrial Fibrillation 68 0.040
241
SRC014 Sarcoma 68 0.040
242
P ENC004 Encephalitis 66 0.040
243
ISC004 Ischemia 66 0.040
244
GST045 Gastroenteritis 65 0.040
245
P INT068 Intestinal Disease 65 0.040
246
LPT001 Leptospirosis 64 0.040
247
WLL001 Williams-Beuren Syndrome 63 0.040
248
RBS001 Rabies 63 0.040
249
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.040
250
P MCH002 Machado-Joseph Disease 63 0.040
251
P SPN046 Spinal Muscular Atrophy 63 0.040
252
MTR014 Motor Neuron Disease 62 0.040
253
P HMN010 Hemangioma 61 0.040
254
P MMP001 Mumps 61 0.040
255
STT001 Status Epilepticus 60 0.040
256
SNS001 Sensorineural Hearing Loss 59 0.040
257
P MYC008 Myocarditis 58 0.040
258
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.040
259
P EPS003 Episodic Ataxia 57 0.040
260
c PRG018 Paragangliomas 1 57 0.040
261
P SCL018 Scoliosis 56 0.040
262
P INT070 Intestinal Obstruction 55 0.040
263
ASP003 Aseptic Meningitis 54 0.040
264
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.040
265
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.040
266
P TRN034 Transverse Myelitis 53 0.040
267
THY025 Thymus Cancer 52 0.040
268
P OLV001 Olivopontocerebellar Atrophy 51 0.040
269
ADR008 Adrenal Adenoma 51 0.040
270
VNB005 Van Buchem Disease 51 0.040
271
PRT029 Parathyroid Adenoma 50 0.040
272
ASP007 Aspiration Pneumonia 49 0.040
273
FSC004 Fasciitis 48 0.040
274
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.040
275
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.040
276
LCR004 La Crosse Encephalitis 45 0.040
277
RLP003 Relapsing Fever 43 0.040
278
SPR007 Superior Mesenteric Artery Syndrome 42 0.040
279
ADP007 Adie Pupil 41 0.040
280
PRP056 Porphyria, Acute Hepatic 41 0.040
281
MYH012 Myhre Syndrome 41 0.040
282
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.040
283
P HYP265 Hypotonia 40 0.040
284
INT042 Internuclear Ophthalmoplegia 40 0.040
285
MLG086 Malignant Hyperthermia Susceptibility 38 0.040
286
PRL008 Paralytic Ileus 38 0.040
287
MLN073 Melanosis, Neurocutaneous 38 0.040
288
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.040
289
GLT018 Glut1 Deficiency Syndrome 1 37 0.040
290
c OST126 Osteopetrosis, Autosomal Recessive 1 36 0.040
291
TLS001 Tolosa-Hunt Syndrome 35 0.040
292
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 35 0.040
293
SPN185 Spinal Cord Infarction 33 0.040
294
FCL003 Facial Hemiatrophy 31 0.040
295
BRW009 Brown-Vialetto-Van Laere Syndrome 1 31 0.040
296
CLR007 Colorado Tick Fever 31 0.040
297
EPD005 Epidural Abscess 31 0.040
298
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 31 0.040
299
HYP048 Hypotropia 31 0.040
300
HYP047 Hypertropia 30 0.040
301
ABD009 Abducens Palsy 29 0.040
302
MTC018 Metachondromatosis 28 0.040
303
CVR002 Cavernous Sinus Thrombosis 28 0.040
304
MYT003 Myotonic Disease 27 0.040
305
PTR001 Petrositis 25 0.040
306
P RNL115 Renal Tubular Acidosis, Proximal 24 0.040
307
c PRG020 Paragangliomas 3 23 0.040
308
c PRG019 Paragangliomas 2 22 0.040
309
PRS053 Parsonage Turner Syndrome 22 0.040
310
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 22 0.040
311
c LTH030 Lethal Congenital Contracture Syndrome 8 20 0.040
312
CNT067 Central Cord Syndrome 19 0.040
313
SKL006 Skull Base Neoplasm 19 0.040
314
PNT023 Pontine Hemorrhage 18 0.040
315
BLB003 Bulbar Polio 17 0.040
316
MYP026 Myopathy - Thyrotoxic 10 0.040
317
P BRS047 Breast Cancer 100 0.033
318
P PRS040 Prostate Cancer 88 0.033
319
INS024 Insulin-Like Growth Factor I 83 0.033
320
NRL016 Neural Tube Defects 79 0.033
321
P FNC027 Fanconi Anemia, Complementation Group a 78 0.033
322
P BLD134 Bladder Cancer 78 0.033
323
P INF038 Influenza 77 0.033
324
P DLT002 Dilated Cardiomyopathy 76 0.033
325
SQM006 Squamous Cell Carcinoma 74 0.033
326
GLB002 Glioblastoma 74 0.033
327
ANX010 Anxiety 72 0.033
328
KWS002 Kawasaki Disease 72 0.033
329
P ADN016 Adenocarcinoma 71 0.033
330
CRB037 Cerebral Palsy 70 0.033
331
P MJR001 Major Depressive Disorder 70 0.033
332
P NRF023 Neurofibromatosis, Type Ii 69 0.033
333
BHC003 Behcet Syndrome 68 0.033
334
c HRD010 Hereditary Spastic Paraplegia 68 0.033
335
P ART023 Arthropathy 68 0.033
336
P CNJ013 Conjunctivitis 67 0.033
337
PRT036 Peritonitis 67 0.033
338
P LYM026 Lymphoblastic Leukemia 66 0.033
339
ACR006 Aceruloplasminemia 65 0.033
340
P TXP001 Toxoplasmosis 65 0.033
341
P WLD002 Waldenstrom Macroglobulinemia 65 0.033
342
MCK007 Muckle-Wells Syndrome 64 0.033
343
MSL001 Measles 64 0.033
344
c GLY008 Glycogen Storage Disease Ii 64 0.033
345
ART005 Arteriovenous Malformation 64 0.033
346
CRB011 Cerebrotendinous Xanthomatosis 64 0.033
347
P LNG028 Long Qt Syndrome 63 0.033
348
DPH001 Diphtheria 63 0.033
349
YLL002 Yellow Fever 63 0.033
350
P PRP029 Porphyria 62 0.033
351
P GCH001 Gaucher's Disease 62 0.033
352
P CMR001 Camurati-Engelmann Disease 62 0.033
353
P HML002 Hemolytic Anemia 62 0.033
354
HYP266 Hypoxia 61 0.033
355
P BRD002 Bardet-Biedl Syndrome 61 0.033
356
P GLM007 Glomerulonephritis 61 0.033
357
BRN056 Bronchopulmonary Dysplasia 61 0.033
358
c LNG044 Long Qt Syndrome 1 61 0.033
359
P RHB003 Rhabdomyosarcoma 61 0.033
360
P BPL003 Bipolar Disorder 61 0.033
361
TRG002 Trigeminal Neuralgia 60 0.033
362
PRS047 Prostatitis 59 0.033
363
JPN002 Japanese Encephalitis 59 0.033
364
PRD013 Periodic Fever, Familial, Autosomal Dominant 59 0.033
365
P LPR021 Leprosy 3 59 0.033
366
APH002 Aphasia 58 0.033
367
P GRS003 Griscelli Syndrome 58 0.033
368
HMF006 Hemifacial Microsomia 58 0.033
369
GLC003 Glucose Intolerance 58 0.033
370
c BRD014 Bardet-Biedl Syndrome 2 58 0.033
371
c CNG021 Congenital Toxoplasmosis 57 0.033
372
P PRG013 Paraganglioma 57 0.033
373
WLF001 Wolff-Parkinson-White Syndrome 57 0.033
374
P TWN003 Townes-Brocks Syndrome 57 0.033
375
SPT005 Spotted Fever 57 0.033
376
CNT105 Central Core Disease of Muscle 57 0.033
377
c ANM038 Anemia, Autoimmune Hemolytic 56 0.033
378
c BRD011 Bardet-Biedl Syndrome 10 56 0.033
379
PLS006 Plasmodium Vivax Malaria 56 0.033
380
CYS010 Cystinosis 55 0.033
381
RLP001 Relapsing Polychondritis 55 0.033
382
P CNG001 Congenital Myasthenic Syndrome 55 0.033
383
CHR288 Chronic Recurrent Multifocal Osteomyelitis 55 0.033
384
HDC001 Headache 55 0.033
385
RBR001 Roberts Syndrome 55 0.033
386
TCK001 Tick-Borne Encephalitis 55 0.033
387
STR020 Strabismus 55 0.033
388
c BRD013 Bardet-Biedl Syndrome 12 55 0.033
389
c TYR012 Tyrosinemia, Type I 55 0.033
390
c BRD012 Bardet-Biedl Syndrome 11 55 0.033
391
P SYP003 Syphilis 55 0.033
392
c LPD015 Lipodystrophy, Familial Partial, Type 2 55 0.033
393
P PNM006 Pneumoconiosis 55 0.033
394
P SZR006 Seizure Disorder 55 0.033
395
P HYP014 Hyperuricemia 54 0.033
396
BRN071 Brain Injury 54 0.033
397
P ICH004 Ichthyosis 54 0.033
398
P TRM003 Tremor 54 0.033
399
SPH001 Sapho Syndrome 54 0.033
400
PRP032 Porphyria Variegata 54 0.033
401
ART001 Arterial Tortuosity Syndrome 53 0.033
402
OPT009 Optic Neuritis 53 0.033
403
THY049 Thyroid Cancer, Anaplastic 53 0.033
404
PRP019 Peripheral Nervous System Disease 53 0.033
405
P SCH018 Schizencephaly 53 0.033
406
P BRT004 Bartter Disease 52 0.033
407
OST011 Osteomalacia 52 0.033
408
GRW007 Growth Hormone Deficiency 52 0.033
409
INF006 Infant Botulism 52 0.033
410
SPN020 Spondylosis 52 0.033
411
MMB001 Membranoproliferative Glomerulonephritis 51 0.033
412
MYL003 Myeloid Sarcoma 51 0.033
413
P PLY017 Polyarteritis Nodosa 51 0.033
414
TRS021 Triosephosphate Isomerase Deficiency 51 0.033
415
BBS001 Babesiosis 51 0.033
416
P OST028 Osteochondroma 51 0.033
417
P PNB001 Pineoblastoma 51 0.033
418
P HMR005 Hemorrhoid 51 0.033
419
P OTT001 Otitis Externa 51 0.033
420
MLT145 Multiple Enchondromatosis, Maffucci Type 51 0.033
421
RHB001 Rhabdoid Cancer 51 0.033
422
WHP001 Whipple Disease 50 0.033
423
NWC001 Newcastle Disease 50 0.033
424
P MYM013 Moyamoya Disease 1 50 0.033
425
THR013 Thoracic Outlet Syndrome 50 0.033
426
RNL011 Renal Osteodystrophy 49 0.033
427
P HMP006 Hemiplegic Migraine 49 0.033
428
c MLG069 Malignant Hypertension 49 0.033
429
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.033
430
NPH003 Nephrocalcinosis 49 0.033
431
PRM020 Premenstrual Tension 49 0.033
432
P CRN013 Craniodiaphyseal Dysplasia 48 0.033
433
ENC010 Encephalocraniocutaneous Lipomatosis 48 0.033
434
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.033
435
c HRD039 Hereditary Amyloidosis 47 0.033
436
P NML001 Nemaline Myopathy 47 0.033
437
PTT004 Pituitary Apoplexy 47 0.033
438
GYN001 Gynecomastia 47 0.033
439
HMM003 Hemimegalencephaly 47 0.033
440
P RSM001 Rasmussen Encephalitis 46 0.033
441
P DMY001 Demyelinating Polyneuropathy 46 0.033
442
THY009 Thyroid Lymphoma 46 0.033
443
c EXS019 Exostoses, Multiple, Type I 46 0.033
444
CHR222 Chromosome 1p36 Deletion Syndrome 46 0.033
445
NSP002 Nasopharyngitis 46 0.033
446
P AML002 Amelogenesis Imperfecta 46 0.033
447
P KLP003 Klippel-Feil Syndrome 46 0.033
448
EHR002 Ehrlichiosis 45 0.033
449
P CHR342 Chiari Malformation 45 0.033
450
VST004 Vestibular Disease 45 0.033
451
TRC023 Trichinosis 45 0.033
452
c ACT159 Acute Transverse Myelitis 45 0.033
453
MYX004 Myxedema 44 0.033
454
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.033
455
NRS003 Neurosyphilis 44 0.033
456
P FNG006 Feingold Syndrome 1 44 0.033
457
CRT009 Critical Illness Polyneuropathy 44 0.033
458
STL001 St. Louis Encephalitis 43 0.033
459
c FML191 Familial Long Qt Syndrome 43 0.033
460
c OST131 Osteopetrosis, Autosomal Dominant 2 43 0.033
461
c CHR579 Chiari Malformation Type Ii 42 0.033
462
UPP004 Upper Respiratory Tract Disease 42 0.033
463
RCK002 Rocky Mountain Spotted Fever 42 0.033
464
P PRS062 Persistent Hyperplastic Primary Vitreous 41 0.033
465
CDQ001 Cauda Equina Syndrome 41 0.033
466
STR002 Streptococcal Meningitis 40 0.033
467
c SCN006 Secondary Syphilis 40 0.033
468
PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.033
469
NTV001 Native American Myopathy 40 0.033
470
PST055 Postural Hypotension 40 0.033
471
ANT018 Anthracosis 39 0.033
472
c SZR022 Seizures, Benign Familial Neonatal, 1 39 0.033
473
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.033
474
LTR003 Lateral Medullary Syndrome 38 0.033
475
CRB029 Cerebellopontine Angle Tumor 38 0.033
476
P AXN001 Axonal Neuropathy 38 0.033
477
ECT004 Ecthyma 38 0.033
478
HYP193 Hypocomplementemic Urticarial Vasculitis 38 0.033
479
TRP004 Tropical Sprue 38 0.033
480
PSD029 Pseudocholinesterase Deficiency 38 0.033
481
SPN040 Spinal Cancer 37 0.033
482
c ATS282 Autosomal Recessive Malignant Osteopetrosis 37 0.033
483
c PSD092 Pseudohypoaldosteronism, Type Iie 37 0.033
484
SWL001 Swallowing Disorders 36 0.033
485
HYD001 Hydranencephaly 36 0.033
486
XRP001 Xerophthalmia 35 0.033
487
ENT005 Entropion 35 0.033
488
SPN331 Spondyloocular Syndrome 34 0.033
489
PLY161 Polymicrogyria, Bilateral Perisylvian, X-Linked 34 0.033
490
CRY032 Carey-Fineman-Ziter Syndrome 33 0.033
491
SPS016 Spasmodic Dysphonia 33 0.033
492
PRS037 Periostitis 33 0.033
493
LRY007 Laryngeal Tuberculosis 33 0.033
494
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.033
495
ANT013 Anterior Spinal Artery Syndrome 33 0.033
496
OST006 Osteoblastoma 32 0.033
497
PRN016 Peroneal Neuropathy 32 0.033
498
EXP002 Exposure Keratitis 32 0.033
499
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 31 0.033
500
HSH002 Hashimoto's Encephalitis 31 0.033
501
CNT009 Central Core Myopathy 31 0.033
502
HNS001 Hansen's Disease 31 0.033
503
MTL002 Metal Metabolism Disorder 30 0.033
504
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 30 0.033
505
CBB002 Cobb Syndrome 29 0.033
506
PRP013 Paraphimosis 29 0.033
507
DYS045 Dysosteosclerosis 28 0.033
508
c CHR671 Charcot-Marie-Tooth Disease, Axonal, Type 2r 28 0.033
509
P STR035 Streptococcal Group a Invasive Disease 28 0.033
510
PRL014 Paralytic Squint 27 0.033
511
TCK004 Tick Infestation 27 0.033
512
MYP093 Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset 27 0.033
513
c MYP081 Myopathy, Myofibrillar, 6 26 0.033
514
c SPS092 Spastic Paraplegia 11 26 0.033
515
MNN005 Meningovascular Neurosyphilis 26 0.033
516
RBF003 Riboflavin Transporter Deficiency 25 0.033
517
INF021 Infant Gynecomastia 25 0.033
518
P INT006 Intestinal Botulism 23 0.033
519
c SPN364 Spinocerebellar Ataxia, X-Linked 3 23 0.033
520
c FML249 Familial Amyloidosis, Finnish Type 23 0.033
521
PRS120 Persistent Idiopathic Facial Pain 22 0.033
522
c HRN024 Horner Syndrome, Congenital 21 0.033
523
ACT181 Acute Motor Axonal Neuropathy 21 0.033
524
AMY104 Amyotrophic Lateral Sclerosis 15 with or Without Frontotemporal Dementia 21 0.033
525
FCL074 Facial Spasm 21 0.033
526
PRL006 Paralytic Lagophthalmos 20 0.033
527
MXD001 Mixed Cerebral Palsy 20 0.033
528
BNP002 Bone Epithelioid Hemangioma 20 0.033
529
c ICH014 Ichthyosis Lamellar 1 20 0.033
530
AMY107 Amyotrophic Lateral Sclerosis 14 with or Without Frontotemporal Dementia 19 0.033
531
MLG143 Malignant Hyperthermia of Anesthesia 18 0.033
532
EXT039 Extrapontine Myelinolysis 18 0.033
533
PWS001 Powassan Encephalitis 17 0.033
534
FML325 Familial Cervical Artery Dissection 17 0.033
535
AND005 Androgen Insensitivity Syndrome, Mild 16 0.033
536
c RNL117 Renal Tubular Acidosis Iii 15 0.033
537
DFN310 Deafness, Conductive Stapedial, with Ear Malformation and Facial Palsy 15 0.033
538
GLM046 Glomus Vagale Tumor 15 0.033
539
SYR004 Syringobulbia 15 0.033
540
MBS006 Moebius Syndrome-Axonal Neuropathy-Hypogonadotropic Hypogonadism Syndrome 13 0.033
541
BDR001 Bidirectional Tachycardia 12 0.033
542
UVP001 Uveoparotid Fever 11 0.033
543
MSC144 Muscular Atrophy, Malignant Neurogenic 10 0.033
544
BLB001 Bulbospinal Polio 7 0.033
545
SPN015 Spinal Polio 6 0.033
546
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.033
547
HMP020 Hemiplegia Alterans 1 0.033
548
P CLR023 Colorectal Cancer 98 0.023
549
MYL069 Myeloma, Multiple 86 0.023
550
GST053 Gastric Cancer 84 0.023
551
AST005 Asthma 83 0.023
552
P ATX030 Ataxia-Telangiectasia 80 0.023
553
LYM133 Lymphoma, Hodgkin, Classic 78 0.023
554
MNT001 Mantle Cell Lymphoma 76 0.023
555
P MYL005 Myelofibrosis 75 0.023
556
P OST002 Osteoporosis 75 0.023
557
VNH007 Von Hippel-Lindau Syndrome 72 0.023
558
P MTC003 Metachromatic Leukodystrophy 72 0.023
559
P PHC003 Pheochromocytoma 72 0.023
560
MLN008 Melanoma 72 0.023
561
P DBT009 Diabetes Mellitus 72 0.023
562
VSC007 Vascular Disease 71 0.023
563
P TYS001 Tay-Sachs Disease 71 0.023
564
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.023
565
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.023
566
P OST001 Osteopetrosis 70 0.023
567
P KDN018 Kidney Disease 69 0.023
568
c HPT016 Hepatitis B 68 0.023
569
P NMN002 Niemann-Pick Disease 68 0.023
570
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.023
571
P SYS005 Systemic Scleroderma 67 0.023
572
CHD001 Chediak-Higashi Syndrome 67 0.023
573
HSH003 Hashimoto Thyroiditis 67 0.023
574
P TMP003 Temporal Arteritis 67 0.023
575
P CWD001 Cowden Disease 67 0.023
576
P PRD006 Prader-Willi Syndrome 66 0.023
577
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.023
578
P THY023 Thymoma 65 0.023
579
CRT072 Creutzfeldt-Jakob Disease 65 0.023
580
CHL123 Chlamydia 64 0.023
581
HJD001 Hajdu-Cheney Syndrome 64 0.023
582
c ACT075 Acute Myocardial Infarction 64 0.023
583
GST092 Gastroesophageal Reflux 64 0.023
584
P ESP024 Esophagitis 64 0.023
585
KRT001 Keratoconjunctivitis Sicca 63 0.023
586
DSM004 Desmoid Tumor 63 0.023
587
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.023
588
PLM033 Pulmonary Embolism 62 0.023
589
KRT019 Keratitis, Hereditary 62 0.023
590
P XRD010 Xeroderma Pigmentosum, Variant Type 62 0.023
591
LYM021 Lymphadenitis 62 0.023
592
P EXN002 Exanthem 62 0.023
593
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.023
594
NRV006 Nervous System Cancer 61 0.023
595
P BRG001 Brugada Syndrome 61 0.023
596
STF001 Stiff-Person Syndrome 61 0.023
597
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 0.023
598
CHR072 Chordoma 61 0.023
599
P FBR017 Fibrosarcoma 61 0.023
600
c ACT073 Acute Leukemia 61 0.023
601
CHK001 Chikungunya 61 0.023
602
P GLM045 Glioma 61 0.023
603
P CTR002 Cataract 60 0.023
604
MNT002 Mental Depression 60 0.023
605
P DRR001 Diarrhea 60 0.023
606
CCC001 Coccidioidomycosis 60 0.023
607
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 60 0.023
608
SPN027 Spinal Stenosis 60 0.023
609
RGD003 Rigid Spine Muscular Dystrophy 1 59 0.023
610
c ATR087 Atrial Standstill 1 59 0.023
611
CHR103 Charge Syndrome 59 0.023
612
SLP005 Sleep Disorder 59 0.023
613
P MTR012 Mitral Valve Disease 59 0.023
614
END030 End Stage Renal Failure 59 0.023
615
STR039 Sturge-Weber Syndrome 59 0.023
616
P OLG002 Oligodendroglioma 59 0.023
617
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.023
618
BNC003 Bone Cancer 59 0.023
619
P HYP083 Hypopituitarism 59 0.023
620
PTN001 Patent Foramen Ovale 58 0.023
621
CMP005 Campomelic Dysplasia 58 0.023
622
MCR088 Microscopic Polyangiitis 58 0.023
623
P SML001 Small Cell Carcinoma 58 0.023
624
P LTR001 Lateral Sclerosis 58 0.023
625
P EPL140 Epilepsy, Idiopathic Generalized 58 0.023
626
P END033 Endocarditis 58 0.023
627
ALX003 Alexander Disease 58 0.023
628
ESP023 Esophageal Disease 58 0.023
629
FCT003 Factor X Deficiency 58 0.023
630
c INT072 Intestinal Pseudo-Obstruction 57 0.023
631
P WRD001 Waardenburg's Syndrome 57 0.023
632
ART017 Aortic Disease 57 0.023
633
P CRB048 Cerebral Cavernous Malformations 57 0.023
634
CNS004 Constipation 57 0.023
635
ATY005 Atypical Teratoid Rhabdoid Tumor 57 0.023
636
PLM010 Pulmonary Edema 57 0.023
637
P HYP726 Hypercalcemia, Infantile, 1 57 0.023
638
PNM008 Pneumothorax 57 0.023
639
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 56 0.023
640
PTT009 Pituitary Gland Disease 56 0.023
641
BLR001 Biliary Atresia 56 0.023
642
P MYP006 Myopia 56 0.023
643
KRT006 Keratoconjunctivitis 56 0.023
644
GST037 Gastroparesis 56 0.023
645
P SPN301 Spinocerebellar Ataxia 2 56 0.023
646
GST009 Gastroschisis 55 0.023
647
CLN019 Colonic Disease 55 0.023
648
PLG002 Plague 55 0.023
649
MGR028 Migraine with or Without Aura 1 55 0.023
650
P HYP750 Hypertriglyceridemia, Familial 55 0.023
651
PRC013 Pericarditis 55 0.023
652
c LYM130 Lymphedema, Hereditary, Ii 55 0.023
653
TXC002 Toxic Encephalopathy 55 0.023
654
P PMP001 Pemphigus 55 0.023
655
P HYP024 Hypoparathyroidism 55 0.023
656
c FML001 Familial Atrial Fibrillation 55 0.023
657
INT007 Intermediate Coronary Syndrome 55 0.023
658
P MGL013 Megalencephaly 54 0.023
659
SLV012 Salivary Gland Adenoid Cystic Carcinoma 54 0.023
660
P JRV004 Jervell and Lange-Nielsen Syndrome 1 54 0.023
661
c CWD006 Cowden Syndrome 1 54 0.023
662
P CNV004 Canavan Disease 54 0.023
663
ESP020 Esophageal Atresia 54 0.023
664
c OST164 Osteoporosis, Juvenile 54 0.023
665
c ACT071 Acute Kidney Failure 54 0.023
666
LYM022 Lymphangioma 53 0.023
667
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 53 0.023
668
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.023
669
P CRD132 Cardiac Conduction Defect 53 0.023
670
STF002 Stiff Skin Syndrome 53 0.023
671
c PNS012 Paine Syndrome 52 0.023
672
ACT049 Acute Disseminated Encephalomyelitis 52 0.023
673
APR001 Apraxia 52 0.023
674
ATR057 Atrioventricular Block 52 0.023
675
TMT001 Timothy Syndrome 52 0.023
676
OST016 Osteochondrosis 52 0.023
677
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 51 0.023
678
DRY001 Dry Eye Syndrome 51 0.023
679
MCP006 Mucoepidermoid Carcinoma 51 0.023
680
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.023
681
THY030 Thyroid Gland Disease 51 0.023
682
GSG001 Gas Gangrene 51 0.023
683
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 51 0.023
684
CTS002 Cat-Scratch Disease 51 0.023
685
c FML023 Familial Hemiplegic Migraine 51 0.023
686
HYP006 Hypertensive Heart Disease 51 0.023
687
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.023
688
PRN011 Pernicious Anemia 50 0.023
689
KLD001 Keloids 50 0.023
690
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 50 0.023
691
P PRN026 Porencephaly 50 0.023
692
EXP004 Exophthalmos 50 0.023
693
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.023
694
PLN006 Poland Syndrome 50 0.023
695
NRP060 Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive 50 0.023
696
P APL006 Aplasia Cutis Congenita 50 0.023
697
MGC001 Megacolon 50 0.023
698
c VRL012 Viral Meningitis 49 0.023
699
c LNG047 Long Qt Syndrome 2 49 0.023
700
NCR007 Necrotizing Fasciitis 49 0.023
701
MTB004 Metabolic Acidosis 49 0.023
702
P GNT008 Giant Cell Tumor 49 0.023
703
OST022 Osteopathia Striata with Cranial Sclerosis 49 0.023
704
ANX004 Anoxia 49 0.023
705
CYS039 Cystic Kidney Disease 49 0.023
706
FBR009 Fibrous Dysplasia 49 0.023
707
ANR004 Anuria 49 0.023
708
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 49 0.023
709
MTP034 Metaphyseal Chondrodysplasia, Jansen Type 49 0.023
710
P MYP087 Myopathy, Tubular Aggregate, 1 48 0.023
711
c HYP293 Hypophosphatasia, Adult 48 0.023
712
CNJ012 Conjunctival Disease 48 0.023
713
c HYP292 Hypophosphatasia, Infantile 48 0.023
714
P ENC008 Encephalocele 48 0.023
715
STS002 Situs Inversus 48 0.023
716
CVR006 Cavernous Hemangioma 48 0.023
717
c ART120 Arthrogryposis, Distal, Type 3 47 0.023
718
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 47 0.023
719
CRN024 Corneal Disease 47 0.023
720
NNF007 Non-Functioning Pituitary Adenoma 47 0.023
721
TRC040 Tracheoesophageal Fistula 47 0.023
722
SYN036 Syncope 46 0.023
723
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 46 0.023
724
TKL001 Tukel Syndrome 46 0.023
725
c LNG048 Long Qt Syndrome 3 46 0.023
726
EXS001 Exostosis 46 0.023
727
MDL009 Medullary Sponge Kidney 46 0.023
728
BCK006 Back Pain 46 0.023
729
ATN004 Autonomic Neuropathy 46 0.023
730
DDN006 Duodenitis 46 0.023
731
MTR010 Mature Teratoma 46 0.023
732
P TRT019 Torticollis 45 0.023
733
HRT012 Heart Valve Disease 45 0.023
734
AMB002 Amblyopia 45 0.023
735
EVN001 Evans' Syndrome 45 0.023
736
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 45 0.023
737
MLT075 Multifocal Motor Neuropathy 45 0.023
738
GRD001 Giardiasis 45 0.023
739
BRN080 Brain Ischemia 45 0.023
740
DVR002 Diverticulitis 44 0.023
741
ANG002 Angiostrongyliasis 44 0.023
742
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 44 0.023
743
P MLT008 Multinodular Goiter 44 0.023
744
TRN004 Trench Fever 44 0.023
745
RHY001 Rhyns Syndrome 44 0.023
746
P PLL002 Pellagra 44 0.023
747
ALX001 Alexia 44 0.023
748
c SCN005 Secondary Hypertrophic Osteoarthropathy 44 0.023
749
SPC005 Speech Disorder 44 0.023
750
EST005 Esotropia 43 0.023
751
c LNG050 Long Qt Syndrome 5 43 0.023
752
LCR008 Lacrimal Apparatus Disease 43 0.023
753
c AMY090 Amyotrophic Lateral Sclerosis 8 43 0.023
754
PLS016 Plasma Cell Leukemia 43 0.023
755
SPN029 Spondylolysis 43 0.023
756
MLR003 Melorheostosis 43 0.023
757
c SHR030 Short Qt Syndrome 42 0.023
758
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 42 0.023
759
SCT002 Scotoma 42 0.023
760
RMS001 Rem Sleep Behavior Disorder 42 0.023
761
TSH001 Tsh Producing Pituitary Tumor 42 0.023
762
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.023
763
SPN369 Spinal Disease 42 0.023
764
MRR003 Murray Valley Encephalitis 42 0.023
765
MNN017 Mononeuropathy 42 0.023
766
BRS064 Bursitis 42 0.023
767
PRX014 Proximal Spinal Muscular Atrophy 42 0.023
768
c LNG051 Long Qt Syndrome 6 42 0.023
769
c SPS219 Spastic Paraplegia 17, Autosomal Dominant 42 0.023
770
MYP001 Myoepithelioma 42 0.023
771
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 42 0.023
772
LKD025 Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 42 0.023
773
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.023
774
PNM010 Pneumothorax, Primary Spontaneous 41 0.023
775
P SPS133 Spastic Paraplegia 2, X-Linked 41 0.023
776
SPN050 Spinocerebellar Degeneration 41 0.023
777
DND001 Dandy-Walker Syndrome 41 0.023
778
PLM029 Palmoplantar Keratosis 41 0.023
779
c BRN131 Branchiootorenal Syndrome 1 41 0.023
780
BRB001 Beriberi 40 0.023
781
P FML043 Familial Idiopathic Basal Ganglia Calcification 40 0.023
782
SCR015 Scarlet Fever 40 0.023
783
P HYP120 Hypoaldosteronism 40 0.023
784
MVM001 Movement Disease 40 0.023
785
c HRD088 Hereditary Neuropathies 40 0.023
786
SPC010 Speech and Communication Disorders 40 0.023
787
c SCP001 Sc Phocomelia Syndrome 40 0.023
788
NRX001 Neuroaxonal Dystrophy 40 0.023
789
PRM237 Primary Hypomagnesemia 40 0.023
790
c LNG053 Long Qt Syndrome 9 40 0.023
791
BSL009 Basal Ganglia Calcification 39 0.023
792
PST020 Postpoliomyelitis Syndrome 39 0.023
793
c GM2005 Gm2-Gangliosidosis, Ab Variant 39 0.023
794
c CNG413 Congenital Short Bowel Syndrome 39 0.023
795
c LNG057 Long Qt Syndrome 13 39 0.023
796
P CNT036 Central Nervous System Germ Cell Tumor 39 0.023
797
ALD013 Aldosterone-Producing Adenoma 39 0.023
798
NRT001 Neurotic Disorder 39 0.023
799
NRM006 Neuromuscular Junction Disease 39 0.023
800
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 39 0.023
801
EYL005 Eyelid Disease 39 0.023
802
LKS001 Leukostasis 39 0.023
803
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.023
804
ACT012 Acute Hemorrhagic Conjunctivitis 38 0.023
805
AGR018 Agraphia 38 0.023
806
CLC011 Cloacal Exstrophy 38 0.023
807
RCT017 Rectal Disease 38 0.023
808
c AMY067 Amyotrophic Lateral Sclerosis 18 38 0.023
809
c CRB094 Cerebral Cavernous Malformations 3 38 0.023
810
P MNN007 Meningocele 38 0.023
811
CSL001 Causalgia 38 0.023
812
MNN042 Meningioma, Radiation-Induced 38 0.023
813
c CHR098 Chronic Pyelonephritis 38 0.023
814
CLC004 Calcific Tendinitis 38 0.023
815
DRS001 Dressler's Syndrome 37 0.023
816
MLY001 Molybdenum Cofactor Deficiency 37 0.023
817
P GLM006 Glomangioma 37 0.023
818
PLX004 Plexopathy 37 0.023
819
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 37 0.023
820
THR099 Third-Degree Atrioventricular Block 37 0.023
821
AMY106 Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia 37 0.023
822
NRV004 Nerve Compression Syndrome 37 0.023
823
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 37 0.023
824
NCR003 Necrotizing Sialometaplasia 36 0.023
825
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.023
826
HMN035 Hemangioma-Thrombocytopenia Syndrome 36 0.023
827
HYP737 Hyperhidrosis, Gustatory 36 0.023
828
PLS002 Peliosis Hepatis 36 0.023
829
PNM005 Pneumonic Plague 36 0.023
830
AMY005 Amyloid Neuropathy 36 0.023
831
FNT004 Fainting 36 0.023
832
PLY024 Polymicrogyria 36 0.023
833
P LTT001 Lattice Corneal Dystrophy 36 0.023
834
PNC032 Pancoast Tumor 36 0.023
835
c LNG056 Long Qt Syndrome 12 36 0.023
836
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 36 0.023
837
AMY086 Amyotrophy, Hereditary Neuralgic 35 0.023
838
BRN026 Branch Retinal Artery Occlusion 35 0.023
839
MLN002 Melanomatosis 35 0.023
840
SCR016 Scrotal Carcinoma 35 0.023
841
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 35 0.023
842
CNR001 Coenurosis 35 0.023
843
AMY003 Amyotrophic Neuralgia 35 0.023
844
MDS018 Mediastinal Cancer 35 0.023
845
c LBR011 Leber Congenital Amaurosis 16 35 0.023
846
MYC014 Mycobacterium Chelonae 34 0.023
847
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.023
848
BRC010 Brachial Plexus Lesion 34 0.023
849
HYP034 Hypertensive Encephalopathy 34 0.023
850
c THY107 Thymoma, Familial 34 0.023
851
BRN036 Brain Stem Infarction 34 0.023
852
c APL023 Aplasia Cutis Congenita, Nonsyndromic 34 0.023
853
END034 Endocrine Exophthalmos 34 0.023
854
P ATR081 Atrial Standstill 34 0.023
855
c FML294 Familial Short Qt Syndrome 34 0.023
856
JPN001 Japanese Spotted Fever 34 0.023
857
c TRC078 Trichohepatoenteric Syndrome 2 34 0.023
858
CRV030 Cervical Adenitis 33 0.023
859
c INF145 Infantile Liver Failure Syndrome 1 33 0.023
860
c NRP055 Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive 33 0.023
861
SPS019 Spastic Paraparesis 33 0.023
862
c AMY085 Amyotrophic Lateral Sclerosis 9 33 0.023
863
CLV002 Clivus Chordoma 33 0.023
864
LMB010 Lambert Syndrome 33 0.023
865
EXT035 Extrinsic Cardiomyopathy 33 0.023
866
SRC001 Sarcomatoid Mesothelioma 33 0.023
867
MYS001 Myositis Ossificans 33 0.023
868
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.023
869
TST020 Testis Seminoma 32 0.023
870
c AMY059 Amyotrophic Lateral Sclerosis 19 32 0.023
871
HRT008 Heart Conduction Disease 32 0.023
872
AST003 Asthenopia 32 0.023
873
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.023
874
HYP264 Hypertonia 32 0.023
875
ANT022 Anterior Cranial Fossa Meningioma 32 0.023
876
c PSD090 Pseudohypoaldosteronism, Type Iia 32 0.023
877
c CNG112 Congenital Muscular Dystrophy Type 1a 31 0.023
878
DYG001 Dyggve-Melchior-Clausen Disease 31 0.023
879
c AMY057 Amyotrophic Lateral Sclerosis 16, Juvenile 31 0.023
880
c AMY083 Amyotrophic Lateral Sclerosis 11 31 0.023
881
CRN225 Cranio-Facial Dystonia 31 0.023
882
BNR001 Bone Remodeling Disease 31 0.023
883
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 31 0.023
884
HMD003 Hemidystonia 31 0.023
885
AMY002 Amyloid Tumor 30 0.023
886
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 30 0.023
887
ISC005 Ischemic Bone Disease 30 0.023
888
c PRN053 Porencephaly 1 30 0.023
889
c PRM195 Primary Lateral Sclerosis, Juvenile 30 0.023
890
c SRC023 Sarcoidosis 2 30 0.023
891
TXC010 Toxic Myocarditis 30 0.023
892
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 30 0.023
893
ANS018 Anismus 29 0.023
894
c ACR044 Acroosteolysis Dominant Type 29 0.023
895
INT084 Intrinsic Cardiomyopathy 29 0.023
896
ATX010 Ataxia Neuropathy Spectrum 29 0.023
897
PNT009 Pontine Tegmental Cap Dysplasia 29 0.023
898
c CNG133 Congenital Varicella Syndrome 29 0.023
899
PMP008 Pemphigus Vegetans 29 0.023
900
DSC004 Discitis 28 0.023
901
GRN004 Granulomatous Amebic Encephalitis 28 0.023
902
FNT005 Fontaine Progeroid Syndrome 28 0.023
903
END013 Endometrial Small Cell Carcinoma 28 0.023
904
CRB005 Cerebral Arteritis 28 0.023
905
DNT046 Dental Abscess 28 0.023
906
FBR028 Fibrosing Mediastinitis 28 0.023
907
HML042 Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy 28 0.023
908
BRN031 Brain Germinoma 28 0.023
909
VST003 Vestibular Nystagmus 28 0.023
910
TBR003 Tuberculous Epididymitis 27 0.023
911
END051 Endolymphatic Sac Tumor 27 0.023
912
WYB001 Wyburn Mason's Syndrome 27 0.023
913
LPN001 Louping Ill 27 0.023
914
EXT053 Extragonadal Nonseminomatous Germ Cell Tumor 27 0.023
915
TRG006 Trigger Thumb 27 0.023
916
ACC003 Accommodative Esotropia 27 0.023
917
ATR055 Atrial Septal Aneurysm 27 0.023
918
c CHR094 Chronic Polyneuropathy 26 0.023
919
c SPS159 Spastic Paraplegia 9b, Autosomal Recessive 26 0.023
920
GNT004 Gnathomiasis 26 0.023
921
BRC002 Brachial Plexus Neuritis 26 0.023
922
SBS002 Substernal Goiter 25 0.023
923
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 0.023
924
EXT025 Extragonadal Germ Cell Cancer 25 0.023
925
c PRG021 Paragangliomas 4 25 0.023
926
c HYP699 Hyperekplexia 1 25 0.023
927
c AMY063 Amyotrophic Lateral Sclerosis 20 25 0.023
928
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 25 0.023
929
STR017 Sternum Cancer 25 0.023
930
c AMY094 Amyotrophic Lateral Sclerosis 5, Juvenile 24 0.023
931
AMT001 Ametropic Amblyopia 24 0.023
932
LTR002 Lateral Sinus Thrombosis 24 0.023
933
SPH007 Sphenoid Sinusitis 24 0.023
934
PGT009 Paget Disease of Bone 2, Early-Onset 24 0.023
935
MTC021 Mitochondrial Complex V Deficiency 24 0.023
936
c AMY062 Amyotrophic Lateral Sclerosis 12 24 0.023
937
FNC005 Functional Colonic Disease 24 0.023
938
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 24 0.023
939
c CRD219 Cardiomyopathy, Infantile Hypertrophic 23 0.023
940
c SPS025 Spastic Paraplegia 15 23 0.023
941
HTR005 Heterochromia Iridis 23 0.023
942
P FRM004 Foramen Magnum Meningioma 23 0.023
943
DND013 Dandy-Walker Malformation with Postaxial Polydactyly 23 0.023
944
SPN187 Spinocerebellar Atrophy 23 0.023
945
HYP018 Hyperglobulinemic Purpura 23 0.023
946
ISL119 Isolated Optic Neuritis 23 0.023
947
MLR023 Melorheostosis, Isolated 23 0.023
948
CRP004 Corpus Luteum Cyst 23 0.023
949
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 22 0.023
950
P INT103 Intrauterine Infections 22 0.023
951
P JVN024 Juvenile Hereditary Hemochromatosis 22 0.023
952
PRG102 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 2 22 0.023
953
RNL118 Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness 22 0.023
954
c CNG129 Congenital Torticollis 22 0.023
955
c MYS064 Myasthenic Syndrome, Congenital, 16 22 0.023
956
ATL010 Atlantoaxial Subluxation 21 0.023
957
PRG128 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 4 21 0.023
958
c SPS091 Spastic Paraplegia 4 21 0.023
959
MNR004 Mounier-Kuhn Syndrome 21 0.023
960
ETH012 Ethylene Glycol Poisoning 21 0.023
961
P SNS011 Sinus Cancer 21 0.023
962
SPR038 Supranuclear Ocular Palsy 21 0.023
963
c FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 21 0.023
964
c NRN041 Neuronopathy, Distal Hereditary Motor, Type Iib 21 0.023
965
AMY105 Amyotrophic Lateral Sclerosis 6 with or Without Frontotemporal Dementia 21 0.023
966
CMB042 Combined Oxidative Phosphorylation Deficiency 16 21 0.023
967
BTN005 Biotin-Thiamine-Responsive Basal Ganglia Disease 20 0.023
968
INT095 Internal Carotid Agenesis 20 0.023
969
P PHC014 Phocomelia 20 0.023
970
PRS033 Parasitic Ectoparasitic Infectious Disease 20 0.023
971
LVR006 Liver Lymphoma 20 0.023
972
FCD002 Faciodigitogenital Syndrome, Autosomal Recessive 19 0.023
973
c SPS013 Spastic Paraplegia 8 19 0.023
974
c NRN035 Neuronopathy, Distal Hereditary Motor, Type Iia 19 0.023
975
c VRL004 Viral Labyrinthitis 19 0.023
976
c NRP029 Neuropathy, Hereditary Sensory, Type Iic 19 0.023
977
SPN092 Spinal Shock 19 0.023
978
ISL082 Isolated Atp Synthase Deficiency 19 0.023
979
c SPS037 Spastic Paraplegia 31 18 0.023
980
INF036 Inflammatory and Toxic Neuropathy 18 0.023
981
c NRC017 Narcolepsy 7 18 0.023
982
PRG129 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 3 18 0.023
983
DND020 Dandy-Walker Malformation with Mental Retardation, Macrocephaly, Myopia, and Brachytelephalangy 17 0.023
984
NNF008 Non-Functioning Paraganglioma 17 0.023
985
ORB003 Orbital Tenonitis 17 0.023
986
CHR159 Charlie M Syndrome 17 0.023
987
c NRC011 Narcolepsy 3 17 0.023
988
AMY099 Amyotrophic Lateral Sclerosis 22 with or Without Frontotemporal Dementia 17 0.023
989
BMF002 Bamforth Syndrome 15 0.023
990
TRG017 Trigeminal Trophic Syndrome 15 0.023
991
ALT004 Alternating Esotropia 15 0.023
992
MLL006 Mollaret Meningitis 14 0.023
993
DST013 Distal Myopathy with Vocal Cord Weakness 14 0.023
994
CNM001 Canomad Syndrome 14 0.023
995
ANL005 Anal Spasm 14 0.023
996
HNT018 Hunter-Macdonald Syndrome 14 0.023
997
ACT231 Acute Flaccid Myelitis 13 0.023
998
P PRL012 Purulent Acute Otitis Media 12 0.023
999
PST054 Postinfectious Encephalomyelitis 12 0.023
1000
c INF052 Infantile Scoliosis 12 0.023
1001
SPH008 Sphenoidal Sinus Cancer 11 0.023
1002
PLC012 Pleoconial Myopathy with Salt Craving 10 0.023
1003
OPH018 Ophthalmoplegia Totalis with Ptosis and Miosis 9 0.023
1004
GNR012 Generalized Gangliosidoses 8 0.023
1005
LYM055 Lyme Disease - Neurological Complications 7 0.023
1006
CNT066 Central Cervical Cord Syndrome 6 0.023
1007
ATR076 Atrophic Muscular Disease 6 0.023
1008
WST006 Westphal Disease 6 0.023
1009
LPS008 Lupus - Neurological Sequelae 5 0.023
1010
BRN069 Brain and Spinal Tumors 5 0.023
1011
VSC023 Vasculitis Syndromes of the Central and Peripheral Nervous Systems 4 0.023
1012
IMM028 Immune-Mediated Encephalomyelitis 4 0.023
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