Search results for "paralysis"

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

1209 hits were found for 'paralysis'

# Family MCID Name MIFTS Score
1
P HYP370 Hypokalemic Periodic Paralysis, Type 1 51 7.145
2
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 45 6.689
3
P AND016 Andersen Syndrome 57 4.697
4
NRM009 Normokalemic Periodic Paralysis 29 4.095
5
c INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 28 4.072
6
FCL012 Facial Paralysis 50 3.785
7
c THY083 Thyrotoxic Periodic Paralysis 2 19 3.776
8
P THY054 Thyrotoxic Periodic Paralysis 46 3.724
9
TCK002 Tick Paralysis 28 3.608
10
P SPS154 Spastic Paralysis, Infantile Onset Ascending 21 3.476
11
FML036 Familial Periodic Paralysis 39 3.297
12
PRM028 Paramyotonia Congenita 51 3.275
13
OCL003 Oculomotor Nerve Paralysis 26 3.251
14
LRY047 Laryngeal Abductor Paralysis 23 3.246
15
c HYP606 Hypokalemic Periodic Paralysis, Type 2 32 3.198
16
c THY084 Thyrotoxic Periodic Paralysis 1 20 2.930
17
BLL003 Bell's Palsy 47 2.647
18
PRN008 Peroneal Nerve Paralysis 20 2.518
19
MBS002 Moebius Syndrome 44 2.507
20
KRT022 Keratoderma Palmoplantar Spastic Paralysis 8 2.495
21
P PRK057 Parkinson Disease, Late-Onset 72 2.474
22
PLM031 Poliomyelitis 59 2.263
23
P CRN035 Cranial Nerve Palsy 44 2.097
24
KLM001 Klumpke Paralysis 10 2.091
25
CNG241 Congenital Laryngeal Palsy 6 2.062
26
GLS003 Glossopharyngeal Nerve Paralysis 8 2.042
27
LRY021 Laryngeal Adductor Paralysis 8 2.034
28
FML082 Familial Partial Paralysis 8 2.034
29
GNC003 Geniculate Herpes Zoster 34 2.017
30
c HYP142 Hyperkalemic Periodic Paralysis Type 1 12 2.017
31
VCL007 Vocal Cord Paralysis and Ptosis 11 2.017
32
PSD001 Pseudobulbar Palsy 33 2.007
33
KRT067 Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy 14 2.007
34
CNG302 Congenital Hereditary Facial Paralysis with Variable Hearing Loss 7 2.007
35
TCK005 Tucker Syndrome 13 2.007
36
c NRN025 Neuronopathy, Distal Hereditary Motor, Type Viia 25 1.995
37
TDD001 Todd's Paralysis 10 1.575
38
MYT015 Myotonia Congenita, Atypical, Acetazolamide-Responsive 40 1.479
39
c FML159 Familial Periodic Paralyses 14 1.463
40
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 15 1.454
41
P HRN001 Horner's Syndrome 45 1.444
42
PRL008 Paralytic Ileus 37 1.444
43
PRD032 Periodic Paralysis with Transient Compartment-Like Syndrome 4 1.444
44
FML160 Familial Spastic Paralysis 7 1.444
45
LRY023 Laryngeal Abductor Paralysis Mental Retardation 2 1.444
46
P NRP022 Neuropathy, Distal Hereditary Motor, Type Viib 25 1.432
47
CYC001 Cycloplegia 30 1.432
48
PRL020 Paralysis Agitans, Juvenile, of Hunt 6 1.432
49
KRN002 Kearns-Sayre Syndrome 60 1.419
50
GLL022 Guillain-Barre Syndrome 58 1.419
51
TRP002 Tropical Spastic Paraparesis 55 1.419
52
P SPS003 Spastic Diplegia 49 1.419
53
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 25 1.402
54
ABD002 Abducens Nerve Disease 22 1.402
55
THR010 Third Cranial Nerve Disease 27 1.402
56
BLN017 Balint Syndrome 18 1.402
57
c FCL030 Facial Paresis, Hereditary Congenital, 1 14 1.402
58
MRK002 Marek Disease 35 1.402
59
c AND007 Andersen Syndrome Type 1 13 1.402
60
c DST092 Distal Hereditary Motor Neuropathy Type 7 12 1.402
61
RNL007 Renal Tubular Acidosis 50 0.139
62
HYP005 Hypokalemia 52 0.132
63
P MYP004 Myopathy 67 0.127
64
P LRY019 Laryngitis 55 0.127
65
SPS057 Spasticity 41 0.112
66
P NRP001 Neuropathy 57 0.108
67
P GRV001 Graves' Disease 62 0.106
68
P NRV007 Nervous System Disease 71 0.101
69
P THY032 Thyroiditis 57 0.099
70
ALR002 Al-Raqad Syndrome 36 0.097
71
MYT011 Myotonia 40 0.097
72
P RSP003 Respiratory Failure 68 0.095
73
ADN018 Adenoma 59 0.092
74
NRM005 Neuromuscular Disease 56 0.090
75
NRN002 Neuronitis 40 0.090
76
OTT002 Otitis Media 66 0.087
77
BTL001 Botulism 52 0.085
78
BNF002 Bone Fracture 46 0.085
79
P MSC033 Muscle Disorders 52 0.082
80
ANR040 Aneurysm 56 0.082
81
P PTS002 Ptosis 56 0.079
82
P HYP076 Hyperthyroidism 59 0.079
83
PRP016 Paraplegia 49 0.079
84
LYM017 Lyme Disease 64 0.076
85
P MSC003 Muscular Atrophy 51 0.076
86
P CRV039 Cervicitis 45 0.076
87
CRN031 Cranial Nerve Disease 39 0.073
88
NRM004 Neuroma 47 0.073
89
P PRD017 Periodic Paralyses 27 0.073
90
MSC004 Muscle Tissue Disease 35 0.073
91
ACS001 Acoustic Neuroma 56 0.070
92
DYS073 Dysphagia 51 0.070
93
P EPL164 Epilepsy 60 0.070
94
P ALT001 Alternating Hemiplegia of Childhood 52 0.067
95
P HPT021 Hepatitis 74 0.067
96
P HRP006 Herpes Simplex 65 0.067
97
P MNN013 Meningitis 66 0.067
98
TTH006 Tooth Disease 52 0.067
99
HYP017 Hypophosphatemia 43 0.067
100
P ATX004 Ataxia 53 0.067
101
EPL031 Epileptic Hemiplegia 4 0.067
102
CRB037 Cerebral Palsy 54 0.063
103
HRP004 Herpes Zoster 56 0.063
104
P LYM118 Lymphoma 68 0.063
105
LCK001 Locked-in Syndrome 37 0.063
106
HMP005 Hemiplegia 52 0.063
107
LRY017 Laryngeal Disease 33 0.063
108
NRT004 Neuritis 52 0.063
109
CRB009 Cerebritis 36 0.063
110
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.060
111
P CHR071 Charcot-Marie-Tooth Disease 66 0.060
112
CHL069 Cholesteatoma 51 0.060
113
MVM001 Movement Disease 45 0.060
114
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.060
115
VGS001 Vagus Nerve Disease 17 0.060
116
LGP001 Lagophthalmos 27 0.060
117
ECT005 Ectropion 38 0.060
118
FDB001 Foodborne Botulism 34 0.060
119
c PRG001 Progressive Muscular Atrophy 39 0.060
120
WND001 Wound Botulism 31 0.060
121
SPN186 Spinal Cord Injury 62 0.060
122
STR067 Stroke, Ischemic 74 0.056
123
P MYS003 Myasthenia Gravis 64 0.056
124
CRD119 Cardiac Arrest 63 0.056
125
MLT021 Multiple System Atrophy 71 0.056
126
MLK003 Melkersson-Rosenthal Syndrome 52 0.056
127
QDR001 Quadriplegia 51 0.056
128
CNV002 Conversion Disorder 45 0.056
129
WST005 West Nile Virus 50 0.056
130
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.056
131
P PLY019 Polyneuropathy 53 0.056
132
AYM001 Ayme-Gripp Syndrome 40 0.056
133
MTR014 Motor Neuron Disease 57 0.056
134
ARC002 Arachnoiditis 38 0.056
135
SWL001 Swallowing Disorders 33 0.056
136
PRL013 Paralytic Poliomyelitis 27 0.056
137
PRT026 Parotitis 42 0.056
138
c SYS001 Systemic Lupus Erythematosus 87 0.052
139
MLG056 Malignant Hyperthermia 60 0.052
140
TBR010 Tuberculosis 70 0.052
141
MTH009 Mouth Disease 63 0.052
142
P HYP086 Hypothyroidism 63 0.052
143
SPN041 Spinal Cord Disease 50 0.052
144
P PNM007 Pneumonia 67 0.052
145
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.052
146
ARC007 Arachnoid Cysts 39 0.052
147
STT002 Status Asthmaticus 43 0.052
148
P FNC004 Fanconi Syndrome 54 0.052
149
SPC005 Speech Disorder 41 0.052
150
MST019 Mastoiditis 31 0.052
151
ATN005 Autonomic Dysfunction 44 0.052
152
PTT006 Pituitary Adenoma 54 0.052
153
MYL001 Myelitis 35 0.052
154
SPN185 Spinal Cord Infarction 36 0.052
155
PRP083 Porphyria, Acute Intermittent 54 0.047
156
P SPN046 Spinal Muscular Atrophy 62 0.047
157
ART016 Aortic Aneurysm 67 0.047
158
CRB039 Cerebrovascular Disease 49 0.047
159
c HPT001 Hepatitis C 68 0.047
160
P ATR011 Atrial Fibrillation 63 0.047
161
P LPS004 Lupus Erythematosus 63 0.047
162
P LKM002 Leukemia 70 0.047
163
P SJG001 Sjogren's Syndrome 55 0.047
164
c GRV008 Graves Disease 1 44 0.047
165
GTR002 Goiter 54 0.047
166
c MYS064 Myasthenic Syndrome, Congenital, 16 34 0.047
167
SPT005 Spotted Fever 56 0.047
168
TLR001 Tularemia 46 0.047
169
PTN002 Patent Ductus Arteriosus 50 0.047
170
SNS001 Sensorineural Hearing Loss 52 0.047
171
MLL002 Miller Fisher Syndrome 43 0.047
172
P OTT001 Otitis Externa 48 0.047
173
THY025 Thymus Cancer 52 0.047
174
P HRT032 Heart Disease 64 0.047
175
P HYP065 Hyperaldosteronism 52 0.047
176
P LBY004 Labyrinthitis 39 0.047
177
P AMY004 Amyloidosis 63 0.047
178
c MLG069 Malignant Hypertension 46 0.047
179
c SBC007 Subacute Thyroiditis 42 0.047
180
SPP008 Suppurative Otitis Media 45 0.047
181
MDS022 Mediastinitis 37 0.047
182
MNN009 Meningoencephalitis 42 0.047
183
FTD001 Foot Drop 34 0.047
184
MDD008 Middle Ear Adenoma 21 0.047
185
TXN001 Toxin-Mediated Infectious Botulism 9 0.047
186
ERB002 Erb's Palsy 7 0.047
187
HPT023 Hepatocellular Carcinoma 90 0.042
188
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.042
189
P NRB001 Neuroblastoma 70 0.042
190
P NRC002 Narcolepsy 62 0.042
191
CNR002 Cone-Rod Dystrophy 65 0.042
192
c THR092 Thrombophilia Due to Thrombin Defect 56 0.042
193
c HRD010 Hereditary Spastic Paraplegia 66 0.042
194
GLN010 Glanzmann Thrombasthenia 64 0.042
195
STT001 Status Epilepticus 59 0.042
196
P STR020 Strabismus 55 0.042
197
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 56 0.042
198
RSP006 Respiratory System Disease 61 0.042
199
P TMT001 Timothy Syndrome 58 0.042
200
c AFB002 Afibrinogenemia, Congenital 51 0.042
201
FCT006 Factor V Deficiency 62 0.042
202
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.042
203
VNW007 Von Willebrand Disease 57 0.042
204
c HMP029 Hemophilia a 61 0.042
205
P LNG028 Long Qt Syndrome 67 0.042
206
c ATM010 Autoimmune Hemolytic Anemia 59 0.042
207
P MSC005 Muscular Dystrophy 64 0.042
208
VNB005 Van Buchem Disease 46 0.042
209
VNW005 Von Willebrand Disease, Type 1 48 0.042
210
P MYT023 Myotonia Congenita 39 0.042
211
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.042
212
c BRG005 Brugada Syndrome 1 42 0.042
213
NRP016 Neuropathy, Recurrent, with Pressure Palsies 30 0.042
214
SRC014 Sarcoma 66 0.042
215
P HMN010 Hemangioma 62 0.042
216
HPT074 Hepatic Adenoma, Somatic 35 0.042
217
P HMP007 Hemophilia 55 0.042
218
P ENC018 Encephalopathy 59 0.042
219
FZL002 Fazio-Londe Disease 25 0.042
220
P MMP001 Mumps 56 0.042
221
BRW004 Brown-Sequard Syndrome 32 0.042
222
P DBT005 Diabetes Insipidus 53 0.042
223
CLR007 Colorado Tick Fever 33 0.042
224
HMM003 Hemimegalencephaly 47 0.042
225
P SYR001 Syringomyelia 44 0.042
226
CNT025 Central Pontine Myelinolysis 43 0.042
227
SPL011 Spleen Cancer 38 0.042
228
HYP068 Hyperostosis 39 0.042
229
P THR003 Thoracic Aortic Aneurysm 57 0.042
230
ADR008 Adrenal Adenoma 49 0.042
231
DPH021 Diaphragm Disease 45 0.042
232
BLB003 Bulbar Polio 18 0.042
233
FCT001 Factor Viii Deficiency 41 0.042
234
P MYC008 Myocarditis 56 0.042
235
PTR001 Petrositis 25 0.042
236
c PLM022 Pulmonary Valve Insufficiency 37 0.042
237
c SHR030 Short Qt Syndrome 45 0.042
238
GNC005 Geniculate Ganglionitis 27 0.042
239
FCL011 Facial Nerve Disease 37 0.042
240
NRL005 Neurilemmoma 47 0.042
241
FMR003 Femoral Neuropathy 34 0.042
242
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.042
243
ACQ017 Acquired Von Willebrand Syndrome 35 0.042
244
ASP003 Aseptic Meningitis 51 0.042
245
FSC004 Fasciitis 47 0.042
246
PRS120 Persistent Idiopathic Facial Pain 20 0.042
247
c FML191 Familial Long Qt Syndrome 39 0.042
248
P BLD051 Blood Coagulation Disease 44 0.042
249
BNP002 Bone Epithelioid Hemangioma 18 0.042
250
CRT008 Carotid Artery Dissection 38 0.042
251
c ADL069 Adult Intestinal Botulism 12 0.042
252
SKL006 Skull Base Neoplasm 24 0.042
253
CVR002 Cavernous Sinus Thrombosis 28 0.042
254
c INH004 Inherited Blood Coagulation Disease 38 0.042
255
P MLD013 Mild Hemophilia a 28 0.042
256
FBR024 Fibrocartilaginous Embolism 13 0.042
257
OTP003 Oto-Palatal-Digital Syndrome 14 0.042
258
ANG054 Angina Pectoris 48 0.042
259
ITR001 Iatrogenic Botulism 14 0.042
260
FNT004 Fainting 33 0.042
261
TYP015 Type 2b Von Willebrand Disease 29 0.042
262
TYP016 Type 2m Von Willebrand Disease 18 0.042
263
TYP017 Type 2n Von Willebrand Disease 19 0.042
264
ABD009 Abducens Palsy 17 0.042
265
PNT023 Pontine Hemorrhage 17 0.042
266
P BRS047 Breast Cancer 100 0.037
267
MLR004 Malaria 80 0.037
268
HDG012 Hodgkin Lymphoma 75 0.037
269
P KDN017 Kidney Cancer 67 0.037
270
CNT098 Central Core Disease 68 0.037
271
TRG002 Trigeminal Neuralgia 56 0.037
272
GTL001 Gitelman Syndrome 60 0.037
273
c LNG044 Long Qt Syndrome 1 59 0.037
274
P NRN017 Neuronopathy, Distal Hereditary Motor, Type Vi 36 0.037
275
NRL016 Neural Tube Defects 76 0.037
276
CPR001 Coproporphyria 54 0.037
277
PLM033 Pulmonary Embolism 59 0.037
278
CNG368 Congenital Adrenal Hyperplasia 60 0.037
279
c PSD092 Pseudohypoaldosteronism, Type Iie 33 0.037
280
P TRN020 Turner Syndrome 64 0.037
281
MYH012 Myhre Syndrome 37 0.037
282
INS024 Insulin-Like Growth Factor I 75 0.037
283
HML015 Hemolytic Anemia Due to Triosephosphate Isomerase Deficiency 46 0.037
284
FCT003 Factor X Deficiency 62 0.037
285
P CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 39 0.037
286
LPT001 Leptospirosis 65 0.037
287
c CNG401 Congenital Heart Disease 67 0.037
288
PHR003 Pharyngitis 58 0.037
289
NRC019 Neurocutaneous Melanosis, Somatic 38 0.037
290
RCT018 Rectal Neoplasm 53 0.037
291
HMF006 Hemifacial Microsomia 54 0.037
292
P HYP117 Hypertriglyceridemia 65 0.037
293
PRP019 Peripheral Nervous System Disease 52 0.037
294
EYL005 Eyelid Disease 41 0.037
295
ART005 Arteriovenous Malformation 63 0.037
296
YLL002 Yellow Fever 58 0.037
297
SLP005 Sleep Disorder 52 0.037
298
P INT070 Intestinal Obstruction 55 0.037
299
c SPS078 Spastic Paraplegia 7 34 0.037
300
MCN017 Meconium Ileus 53 0.037
301
c NRC009 Narcolepsy 1 28 0.037
302
MSL001 Measles 61 0.037
303
LCR004 La Crosse Encephalitis 43 0.037
304
P MYS005 Myositis 57 0.037
305
OLV001 Olivopontocerebellar Atrophy 53 0.037
306
RBS001 Rabies 55 0.037
307
P CRB042 Cerebellar Ataxia 64 0.037
308
BBS001 Babesiosis 45 0.037
309
SPC010 Speech and Communication Disorders 42 0.037
310
RHB003 Rhabdomyosarcoma 55 0.037
311
P HMR005 Hemorrhoid 45 0.037
312
P NRV006 Nervous System Cancer 62 0.037
313
TLS001 Tolosa-Hunt Syndrome 33 0.037
314
RCK002 Rocky Mountain Spotted Fever 44 0.037
315
EHR002 Ehrlichiosis 44 0.037
316
WST004 West Nile Encephalitis 38 0.037
317
TRC023 Trichinosis 44 0.037
318
XRP001 Xerophthalmia 36 0.037
319
P ADN016 Adenocarcinoma 69 0.037
320
c PRK045 Parkinson Disease 5 43 0.037
321
P ENC004 Encephalitis 60 0.037
322
P INT068 Intestinal Disease 60 0.037
323
P SCL018 Scoliosis 56 0.037
324
EXT056 External Ear Disease 40 0.037
325
PLM010 Pulmonary Edema 56 0.037
326
GST045 Gastroenteritis 59 0.037
327
P SYP003 Syphilis 51 0.037
328
MYL003 Myeloid Sarcoma 48 0.037
329
c BRN108 Branchiootic Syndrome 1 36 0.037
330
EXC003 Excessive Tearing 39 0.037
331
TBS001 Tabes Dorsalis 32 0.037
332
RBF003 Riboflavin Transporter Deficiency 23 0.037
333
RLP003 Relapsing Fever 40 0.037
334
RNL011 Renal Osteodystrophy 48 0.037
335
GLC003 Glucose Intolerance 56 0.037
336
ASP007 Aspiration Pneumonia 46 0.037
337
PRT029 Parathyroid Adenoma 46 0.037
338
HDC001 Headache 52 0.037
339
NSP002 Nasopharyngitis 39 0.037
340
OPT009 Optic Neuritis 48 0.037
341
MCP006 Mucoepidermoid Carcinoma 50 0.037
342
HYP006 Hypertensive Heart Disease 49 0.037
343
PRS053 Parsonage Turner Syndrome 18 0.037
344
P PRS062 Persistent Hyperplastic Primary Vitreous 38 0.037
345
P PRX033 Proximal Renal Tubular Acidosis 34 0.037
346
PRL006 Paralytic Lagophthalmos 19 0.037
347
FCL003 Facial Hemiatrophy 30 0.037
348
c SCN006 Secondary Syphilis 41 0.037
349
UVP001 Uveoparotid Fever 12 0.037
350
ECT004 Ecthyma 37 0.037
351
EPD005 Epidural Abscess 32 0.037
352
OST006 Osteoblastoma 33 0.037
353
TCK004 Tick Infestation 23 0.037
354
UPP004 Upper Respiratory Tract Disease 48 0.037
355
STR002 Streptococcal Meningitis 34 0.037
356
P ATR081 Atrial Standstill 29 0.037
357
CRB029 Cerebellopontine Angle Tumor 33 0.037
358
END051 Endolymphatic Sac Tumor 24 0.037
359
P OST028 Osteochondroma 45 0.037
360
PRS037 Periostitis 31 0.037
361
P HYP120 Hypoaldosteronism 34 0.037
362
INH013 Inhalational Botulism 12 0.037
363
PRR008 Periarteritis Nodosa 28 0.037
364
P AXN001 Axonal Neuropathy 37 0.037
365
BRN071 Brain Injury 51 0.037
366
PST055 Postural Hypotension 36 0.037
367
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.030
368
PTZ001 Peutz-Jeghers Syndrome 71 0.030
369
OBS002 Obsessive-Compulsive Disorder 66 0.030
370
P GCH001 Gaucher's Disease 63 0.030
371
ALC007 Alcohol Dependence 66 0.030
372
c LPD037 Lipodystrophy, Familial Partial, 2 52 0.030
373
PRG097 Paragangliomas 1, with or Without Deafness 51 0.030
374
ANX002 Anxiety Disorder 67 0.030
375
MSM014 Mismatch Repair Cancer Syndrome 60 0.030
376
FCT007 Factor Vii Deficiency 60 0.030
377
BRN082 Bernard-Soulier Syndrome, Type C 51 0.030
378
P CMR001 Camurati-Engelmann Disease 63 0.030
379
WLL001 Williams-Beuren Syndrome 61 0.030
380
CNG034 Congestive Heart Failure 72 0.030
381
ETH011 Ethylmalonic Encephalopathy 57 0.030
382
KRT004 Keratitis 70 0.030
383
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.030
384
P LPR003 Leprosy 70 0.030
385
P ESS003 Essential Thrombocythemia 66 0.030
386
P SZR006 Seizure Disorder 56 0.030
387
c FNC027 Fanconi Anemia, Complementation Group a 71 0.030
388
c MYT020 Myotonic Dystrophy 2 56 0.030
389
LDD001 Ladd Syndrome 60 0.030
390
TWN003 Townes-Brocks Syndrome 55 0.030
391
PRD019 Periodic Fever, Familial 48 0.030
392
KWS002 Kawasaki Disease 70 0.030
393
P BRD002 Bardet-Biedl Syndrome 64 0.030
394
P HYP620 Hypoprothrombinemia 50 0.030
395
MCK007 Muckle-Wells Syndrome 62 0.030
396
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.030
397
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.030
398
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.030
399
P PNC025 Panic Disorder 60 0.030
400
FCT022 Factor Xi Deficiency, Autosomal Recessive 55 0.030
401
PSD029 Pseudocholinesterase Deficiency 40 0.030
402
RPP001 Rapp-Hodgkin Syndrome 52 0.030
403
P SDD001 Sudden Infant Death Syndrome 60 0.030
404
CYS010 Cystinosis 51 0.030
405
c FML001 Familial Atrial Fibrillation 59 0.030
406
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.030
407
VHW001 Vohwinkel Syndrome 47 0.030
408
PNM010 Pneumothorax, Primary Spontaneous 34 0.030
409
P PRC031 Preeclampsia/eclampsia 1 53 0.030
410
c OST131 Osteopetrosis, Autosomal Dominant 2 40 0.030
411
MST016 Mesothelioma, Somatic 52 0.030
412
WGN006 Wegener Granulomatosis 63 0.030
413
c PRK027 Parkinson Disease 15, Autosomal Recessive 43 0.030
414
URB001 Urbach-Wiethe Disease 48 0.030
415
c HMP004 Hemophilia B 61 0.030
416
PRP056 Porphyria, Acute Hepatic 36 0.030
417
PPL046 Popliteal Pterygium Syndrome 1 47 0.030
418
BRN003 Branchiooculofacial Syndrome 51 0.030
419
FCT004 Factor Xii Deficiency 51 0.030
420
ANT024 Anthrax Disease 50 0.030
421
SND002 Sneddon Syndrome 45 0.030
422
APP015 Apparent Mineralocorticoid Excess 50 0.030
423
P BDD001 Budd-Chiari Syndrome 52 0.030
424
BRK001 Brooke-Spiegler Syndrome 47 0.030
425
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.030
426
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 47 0.030
427
IRR002 Irritable Bowel Syndrome 58 0.030
428
c PRG020 Paragangliomas 3 32 0.030
429
RHB022 Rhabdoid Tumors, Somatic 30 0.030
430
P CNJ013 Conjunctivitis 65 0.030
431
STR081 Stormorken Syndrome 50 0.030
432
c ACT210 Acute Respiratory Distress Syndrome 55 0.030
433
ADL002 Adult Syndrome 53 0.030
434
BHC003 Behcet Syndrome 60 0.030
435
c PRG019 Paragangliomas 2 32 0.030
436
P BRG001 Brugada Syndrome 59 0.030
437
ATS001 Autistic Disorder 60 0.030
438
P ANR007 Anorexia Nervosa 63 0.030
439
P CNG001 Congenital Myasthenic Syndrome 52 0.030
440
P NML001 Nemaline Myopathy 47 0.030
441
CHR066 Chronic Fatigue Syndrome 63 0.030
442
P ART023 Arthropathy 63 0.030
443
THR013 Thoracic Outlet Syndrome 48 0.030
444
c GLC062 Glaucoma 1, Open Angle, E 46 0.030
445
BRN107 Branchiootorenal Syndrome 1, with or Without Cataracts 37 0.030
446
THR016 Thrombophlebitis 55 0.030
447
P MYP087 Myopathy, Tubular Aggregate, 1 43 0.030
448
PLY119 Polymicrogyria, Bilateral Perisylvian 31 0.030
449
MTC018 Metachondromatosis 30 0.030
450
BRT002 Birt-Hogg-Dube Syndrome 51 0.030
451
PRP027 Peripheral Vascular Disease 69 0.030
452
P KLP003 Klippel-Feil Syndrome 47 0.030
453
HNT002 Hantavirus Pulmonary Syndrome 51 0.030
454
PRT036 Peritonitis 65 0.030
455
FRC001 Fructose-1,6-Bisphosphatase Deficiency 41 0.030
456
P EMR001 Emery-Dreifuss Muscular Dystrophy 57 0.030
457
P HML002 Hemolytic Anemia 60 0.030
458
P PLY017 Polyarteritis Nodosa 54 0.030
459
SCT005 Scott Syndrome 51 0.030
460
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 40 0.030
461
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 26 0.030
462
RYN001 Raynaud Disease 41 0.030
463
TNG004 Tongue Disease 40 0.030
464
PST028 Post-Traumatic Stress Disorder 55 0.030
465
ATR060 Atrial Standstill, Digenic 51 0.030
466
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.030
467
MDD011 Mood Disorder 60 0.030
468
P HYP055 Hypoplastic Left Heart Syndrome 60 0.030
469
EYD002 Eye Disease 62 0.030
470
SPT004 Septic Arthritis 60 0.030
471
MLT145 Multiple Enchondromatosis, Maffucci Type 48 0.030
472
P WLD002 Waldenstrom Macroglobulinemia 62 0.030
473
P PRP029 Porphyria 56 0.030
474
JPN002 Japanese Encephalitis 51 0.030
475
SML020 Small Patella Syndrome 36 0.030
476
SPL012 Splenic Disease 48 0.030
477
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 32 0.030
478
P PRS038 Personality Disorder 60 0.030
479
SCR008 Scrub Typhus 55 0.030
480
PLM029 Palmoplantar Keratosis 40 0.030
481
c BSL007 Basal Cell Carcinoma 66 0.030
482
P PRM001 Primary Cutaneous Amyloidosis 54 0.030
483
c HYP555 Hypertriglyceridemia, Transient Infantile 26 0.030
484
PRP030 Purpura 60 0.030
485
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.030
486
GST037 Gastroparesis 54 0.030
487
P OPN001 Open-Angle Glaucoma 47 0.030
488
TCK001 Tick-Borne Encephalitis 49 0.030
489
c HRD104 Hereditary Multiple Osteochondromas 42 0.030
490
P BRN042 Branchiootic Syndrome 36 0.030
491
NRL004 Neuroleptic Malignant Syndrome 48 0.030
492
P HML001 Hemolytic-Uremic Syndrome 50 0.030
493
P NRM001 Neuromyelitis Optica 55 0.030
494
P TXP001 Toxoplasmosis 61 0.030
495
WHP001 Whipple Disease 49 0.030
496
PLS006 Plasmodium Vivax Malaria 52 0.030
497
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.030
498
c PND001 Pain Disorder 53 0.030
499
c PTS008 Ptosis, Congenital 29 0.030
500
c MTR002 Mitral Valve Insufficiency 42 0.030
501
P ANT006 Antiphospholipid Syndrome 60 0.030
502
HMF009 Hemifacial Hyperplasia 31 0.030
503
LYM008 Lymphangiosarcoma 48 0.030
504
c BRG008 Brugada Syndrome 6 27 0.030
505
RHB001 Rhabdoid Cancer 52 0.030
506
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.030
507
AMY061 Amyotrophic Lateral Sclerosis 14, with or Without Frontotemporal Dementia 21 0.030
508
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.030
509
P MLG086 Malignant Hyperthermia Susceptibility 45 0.030
510
HMR002 Hemarthrosis 47 0.030
511
HRT008 Heart Conduction Disease 43 0.030
512
ORL005 Oral Candidiasis 47 0.030
513
SPR010 Sporotrichosis 48 0.030
514
c CNG464 Congenital Myopathy 49 0.030
515
PRT014 Protein S Deficiency 54 0.030
516
P THR015 Thrombophilia 59 0.030
517
ACT058 Active Peptic Ulcer Disease 44 0.030
518
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.030
519
CND002 Conduct Disorder 54 0.030
520
c LNG096 Long Qt Syndrome 15 42 0.030
521
c CNT035 Central Nervous System Disease 60 0.030
522
VLV011 Vulvovaginal Candidiasis 47 0.030
523
STL001 St. Louis Encephalitis 46 0.030
524
c LNG098 Long Qt Syndrome 14 42 0.030
525
SPH001 Sapho Syndrome 48 0.030
526
P ABD003 Abdominal Aortic Aneurysm 43 0.030
527
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.030
528
P VNS003 Venous Insufficiency 53 0.030
529
APH002 Aphasia 52 0.030
530
DSS009 Disseminated Intravascular Coagulation 52 0.030
531
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.030
532
c SPS092 Spastic Paraplegia 11 24 0.030
533
RLP001 Relapsing Polychondritis 52 0.030
534
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.030
535
ANT018 Anthracosis 41 0.030
536
P INT063 Intellectual Disability 46 0.030
537
P CTR002 Cataract 57 0.030
538
INT075 Intracranial Hypertension 52 0.030
539
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.030
540
PHB001 Phobic Disorder 38 0.030
541
HYD001 Hydranencephaly 35 0.030
542
END030 End Stage Renal Failure 53 0.030
543
BLM002 Bulimia Nervosa 54 0.030
544
FCT005 Factor Xiii Deficiency 42 0.030
545
P BRN120 Bronchus Cancer 43 0.030
546
MLT113 Multicentric Castleman Disease 49 0.030
547
P ADV001 Advanced Sleep Phase Syndrome 42 0.030
548
P PRG013 Paraganglioma 54 0.030
549
P PRN026 Porencephaly 47 0.030
550
HPR003 Heparin-Induced Thrombocytopenia 45 0.030
551
PRN009 Paranoid Schizophrenia 47 0.030
552
c HMG003 Hemoglobin E Disease 44 0.030
553
NWC001 Newcastle Disease 51 0.030
554
NPH003 Nephrocalcinosis 47 0.030
555
DLY005 Delayed Sleep Phase Syndrome 37 0.030
556
P BRN006 Branchiootorenal Syndrome 39 0.030
557
MBM001 Meibomian Cyst 31 0.030
558
CBB002 Cobb Syndrome 30 0.030
559
APP009 Appendix Adenocarcinoma 40 0.030
560
P ACR093 Acrofrontofacionasal Dysostosis 22 0.030
561
PRT012 Prothrombin Deficiency 43 0.030
562
SPR007 Superior Mesenteric Artery Syndrome 37 0.030
563
VND001 Vein Disease 51 0.030
564
CLN019 Colonic Disease 50 0.030
565
FBR086 Fibrolamellar Carcinoma 41 0.030
566
MYT003 Myotonic Disease 33 0.030
567
PLR006 Pleural Cancer 46 0.030
568
SPN331 Spondyloocular Syndrome 27 0.030
569
DNG002 Dengue Hemorrhagic Fever 60 0.030
570
P CMP008 Compartment Syndrome 46 0.030
571
TRC025 Tracheal Cancer 37 0.030
572
PRD002 Periodic Limb Movement Disorder 42 0.030
573
INF006 Infant Botulism 42 0.030
574
CTN006 Cutaneous Paget's Disease 23 0.030
575
c URT035 Urethral Benign Neoplasm 34 0.030
576
PST021 Postpartum Depression 49 0.030
577
PST095 Post-Thrombotic Syndrome 48 0.030
578
SST001 Sost-Related Sclerosing Bone Dysplasia 34 0.030
579
DSS008 Disease of Mental Health 48 0.030
580
MNT002 Mental Depression 52 0.030
581
SPN020 Spondylosis 48 0.030
582
MNN017 Mononeuropathy 37 0.030
583
c MLG036 Malignant Spiradenoma 33 0.030
584
BRS062 Breast Secretory Carcinoma 35 0.030
585
HLL004 Hellp Syndrome 48 0.030
586
PPL022 Papilloma 54 0.030
587
LVD002 Livedoid Vasculopathy 33 0.030
588
P GRS003 Griscelli Syndrome 48 0.030
589
INT253 Intestinal Benign Neoplasm 48 0.030
590
P TRT010 Teratoma 49 0.030
591
AGR002 Agoraphobia 41 0.030
592
P ALC004 Alcohol Abuse 57 0.030
593
SPS016 Spasmodic Dysphonia 29 0.030
594
c CNG021 Congenital Toxoplasmosis 46 0.030
595
c LTH030 Lethal Congenital Contracture Syndrome 8 15 0.030
596
c LTH032 Lethal Congenital Contracture Syndrome 7 16 0.030
597
OST011 Osteomalacia 48 0.030
598
PLC007 Placental Abruption 46 0.030
599
P RNV001 Renovascular Hypertension 46 0.030
600
PRT011 Protein C Deficiency 52 0.030
601
PWS001 Powassan Encephalitis 16 0.030
602
ATR057 Atrioventricular Block 49 0.030
603
c FML249 Familial Amyloidosis, Finnish Type 25 0.030
604
ANK001 Ankylosis 52 0.030
605
END040 Endogenous Depression 51 0.030
606
HDR006 Hidradenocarcinoma 42 0.030
607
c ADL023 Adult Medulloblastoma 52 0.030
608
SWT002 Sweat Gland Cancer 40 0.030
609
PRM003 Premature Ejaculation 45 0.030
610
c INH020 Inherited Metabolic Disorder 49 0.030
611
ADJ001 Adjustment Disorder 38 0.030
612
OVR044 Ovarian Carcinosarcoma 42 0.030
613
DYS009 Dysthymic Disorder 37 0.030
614
KRN001 Korean Hemorrhagic Fever 39 0.030
615
PRL014 Paralytic Squint 25 0.030
616
CLF001 Cleft Lip 48 0.030
617
GNR004 Generalized Anxiety Disorder 49 0.030
618
PRP009 Peripartum Cardiomyopathy 41 0.030
619
KDN015 Kidney Angiomyolipoma 39 0.030
620
VTM001 Vitamin K Deficiency Hemorrhagic Disease 37 0.030
621
c CNT015 Central Sleep Apnea 43 0.030
622
ENT005 Entropion 30 0.030
623
BLD053 Blood Platelet Disease 44 0.030
624
INT042 Internuclear Ophthalmoplegia 36 0.030
625
PRT018 Portal Vein Thrombosis 48 0.030
626
OPP004 Oppositional Defiant Disorder 42 0.030
627
GLM046 Glomus Vagale Tumor 14 0.030
628
ADN009 Adenosquamous Carcinoma 50 0.030
629
P CLL020 Collagenopathy Type 2 Alpha 1 13 0.030
630
BLD005 Bile Duct Mucoepidermoid Carcinoma 31 0.030
631
BLD019 Bile Duct Cystadenocarcinoma 32 0.030
632
c ACQ042 Acquired Hemophilia a 39 0.030
633
P BRS017 Breast Adenomyoepithelioma 27 0.030
634
QLT001 Qualitative Platelet Defect 30 0.030
635
KLP001 Kleptomania 36 0.030
636
CRD001 Cardiac Tamponade 43 0.030
637
ANL012 Anal Gland Adenocarcinoma 31 0.030
638
GST052 Gestational Choriocarcinoma 45 0.030
639
ISC004 Ischemia 56 0.030
640
OVR059 Ovary Adenocarcinoma 37 0.030
641
PRC005 Pericardial Tuberculosis 37 0.030
642
P PRP034 Purpura Fulminans 41 0.030
643
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 28 0.030
644
MNN005 Meningovascular Neurosyphilis 24 0.030
645
SPN032 Spindle Cell Carcinoma 44 0.030
646
PRP028 Peripheral Vertigo 42 0.030
647
ATY002 Atypical Choroid Plexus Papilloma 36 0.030
648
OXY002 Oxyphilic Adenoma 30 0.030
649
SPN033 Spontaneous Ocular Nystagmus 37 0.030
650
PSY003 Psychosexual Disorder 30 0.030
651
PRC010 Pericardial Mesothelioma 37 0.030
652
c BRN046 Branchiootorenal Spectrum Disorders 25 0.030
653
ISC015 Ischemic Colitis 38 0.030
654
LCH001 Leech Infestation 35 0.030
655
PRL042 Proliferating Trichilemmal Cyst 33 0.030
656
SCH004 Schizoid Personality Disorder 24 0.030
657
TRN003 Transverse Colon Cancer 38 0.030
658
CTS005 Catastrophic Antiphospholipid Syndrome 39 0.030
659
CRB017 Cerebral Falx Meningioma 18 0.030
660
c ACQ014 Acquired Hemophilia 42 0.030
661
BRS058 Breast Myoepithelial Neoplasm 23 0.030
662
CCM001 Cecum Adenocarcinoma 38 0.030
663
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.030
664
P INT006 Intestinal Botulism 19 0.030
665
PPL009 Papillary Craniopharyngioma 37 0.030
666
PRC014 Pericardium Cancer 31 0.030
667
SRT004 Serotonin Syndrome 47 0.030
668
P TRN034 Transverse Myelitis 43 0.030
669
VSC004 Vasculogenic Impotence 32 0.030
670
CNT009 Central Core Myopathy 33 0.030
671
BRS063 Breast Squamous Cell Carcinoma 36 0.030
672
OVR054 Ovarian Mucinous Neoplasm 35 0.030
673
VRT001 Vertebral Artery Occlusion 35 0.030
674
CTN009 Cutaneous Adenocystic Carcinoma 30 0.030
675
PNC018 Pancreatic Serous Cystadenoma 31 0.030
676
NDL005 Nodular Medulloblastoma 37 0.030
677
SDD007 Sudden Cardiac Death 46 0.030
678
SRC011 Sarcocystosis 35 0.030
679
VLV021 Vulval Paget's Disease 23 0.030
680
ATY001 Atypical Depressive Disorder 34 0.030
681
CRT015 Carotid Artery Occlusion 43 0.030
682
CYS014 Cystadenocarcinoma 47 0.030
683
ALC003 Alcoholic Psychosis 35 0.030
684
c ACT072 Acute Laryngitis 37 0.030
685
XNT002 Xanthogranulomatous Cholecystitis 30 0.030
686
ACT043 Acute Urate Nephropathy 33 0.030
687
ODN006 Odontoma 34 0.030
688
BLB001 Bulbospinal Polio 7 0.030
689
DST006 Diastolic Heart Failure 45 0.030
690
GLL015 Gallbladder Squamous Cell Carcinoma 27 0.030
691
GST017 Gastric Tubular Adenocarcinoma 30 0.030
692
ANS010 Anus Adenocarcinoma 28 0.030
693
ANT022 Anterior Cranial Fossa Meningioma 26 0.030
694
CRB006 Cribriform Carcinoma 42 0.030
695
P EXT032 Extraosseous Osteosarcoma 35 0.030
696
ACT181 Acute Motor Axonal Neuropathy 19 0.030
697
ADN008 Adenosquamous Pancreas Carcinoma 32 0.030
698
BRD004 Borderline Personality Disorder 46 0.030
699
LCR001 Lacrimal Duct Obstruction 33 0.030
700
PNC002 Pancreatic Mucinous Cystadenoma 35 0.030
701
RNL097 Renal Artery Disease 44 0.030
702
P PNM006 Pneumoconiosis 51 0.030
703
MTL002 Metal Metabolism Disorder 37 0.030
704
RTT004 Rete Testis Adenocarcinoma 27 0.030
705
THY024 Thymus Adenocarcinoma 28 0.030
706
URT016 Urethral Diverticulum 31 0.030
707
URT030 Ureteral Benign Neoplasm 20 0.030
708
URT032 Urethra Adenocarcinoma 28 0.030
709
VLV031 Vulva Adenocarcinoma 22 0.030
710
WST006 Westphal Disease 11 0.030
711
CRT009 Critical Illness Polyneuropathy 38 0.030
712
CYS015 Cystadenofibroma 29 0.030
713
INT004 Intraneural Perineurioma 33 0.030
714
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 37 0.030
715
PRS015 Prostate Signet Ring Cell Adenocarcinoma 15 0.030
716
SGT001 Sagittal Sinus Thrombosis 32 0.030
717
TRN019 Transitional Papilloma 32 0.030
718
FRN014 Fournier Gangrene 33 0.030
719
HNS001 Hansen's Disease 30 0.030
720
c KDN016 Kidney Benign Neoplasm 36 0.030
721
OTM001 Otomycosis 37 0.030
722
P RNL015 Renal Hypertension 47 0.030
723
c MLG053 Malignant Ovarian Brenner Tumor 38 0.030
724
c MLT009 Multiple Cranial Nerve Palsy 29 0.030
725
MRN001 Marantic Endocarditis 34 0.030
726
NCR003 Necrotizing Sialometaplasia 35 0.030
727
SPN015 Spinal Polio 11 0.030
728
SYN036 Syncope 45 0.030
729
CHR077 Chorioretinal Scar 30 0.030
730
BLD054 Blood Protein Disease 38 0.030
731
CTN002 Cutaneous Mucoepidermoid Carcinoma 23 0.030
732
FXP001 Foxp2-Related Speech and Language Disorders 15 0.030
733
CHL040 Cholangiolocellular Carcinoma 35 0.030
734
CHN001 Chondroid Lipoma 26 0.030
735
P CHR342 Chiari Malformation 36 0.030
736
BLR005 Biliary Papillomatosis 34 0.030
737
c BPL002 Bipolar I Disorder 45 0.030
738
PRS004 Prostate Squamous Cell Carcinoma 32 0.030
739
MCN003 Mucinous Ovarian Cystadenoma 21 0.030
740
MLG011 Malignant Biphasic Mesothelioma 26 0.030
741
SMN006 Seminal Vesicle Tumor 26 0.030
742
SNT005 Sinoatrial Node Disease 34 0.030
743
c SVR056 Severe Hemophilia a 44 0.030
744
SYS003 Systolic Heart Failure 42 0.030
745
URT024 Urethra Clear Cell Adenocarcinoma 22 0.030
746
c CHR088 Chronic Inflammation of Lacrimal Passage 15 0.030
747
MCN004 Mucinous Tubular and Spindle Renal Cell Carcinoma 26 0.030
748
THY009 Thyroid Lymphoma 48 0.030
749
CYS003 Cystitis Cystica 31 0.030
750
c ACT037 Acute Dacryocystitis 33 0.030
751
CLC003 Cloacogenic Carcinoma 32 0.030
752
SCR001 Secretory Meningioma 36 0.030
753
SLR002 Solar Retinopathy 18 0.030
754
SPS019 Spastic Paraparesis 34 0.030
755
THY043 Thymic Hyperplasia 32 0.030
756
VLL006 Villous Adenoma 32 0.030
757
c ATS282 Autosomal Recessive Malignant Osteopetrosis 35 0.030
758
BLD032 Bile Duct Adenocarcinoma 39 0.030
759
CRV026 Cervical Clear Cell Adenocarcinoma 34 0.030
760
P DMY001 Demyelinating Polyneuropathy 41 0.030
761
FML040 Female Urethral Cancer 20 0.030
762
CLR005 Clear Cell Chondrosarcoma 38 0.030
763
c ACT159 Acute Transverse Myelitis 27 0.030
764
CHN009 Chondroid Chordoma 29 0.030
765
c CHR098 Chronic Pyelonephritis 38 0.030
766
BLT003 Blue Toe Syndrome 33 0.030
767
BNG033 Benign Perivascular Tumor 28 0.030
768
LPD007 Lipoadenoma 29 0.030
769
c LRG002 Large Cell Acanthoma 25 0.030
770
LVR006 Liver Lymphoma 29 0.030
771
RNL104 Renal Hypodysplasia 29 0.030
772
P ORF002 Orofacial Cleft 38 0.030
773
MLG012 Malignant Epithelial Mesothelioma 35 0.030
774
MSN003 Mesenteric Vascular Occlusion 34 0.030
775
NNG001 Non-Gestational Choriocarcinoma 26 0.030
776
NPH006 Nephrogenic Adenofibroma 30 0.030
777
SBS005 Substance-Induced Psychosis 26 0.030
778
SMN005 Seminal Vesicle Adenocarcinoma 23 0.030
779
THY007 Thymus Lipoma 24 0.030
780
CRN004 Corneal Abscess 19 0.030
781
INT050 Intestinal Impaction 28 0.030
782
ATS009 Autosomal Genetic Disease 38 0.030
783
CRD007 Cardiovascular Organ Benign Neoplasm 27 0.030
784
ECC005 Eccrine Adenocarcinoma 25 0.030
785
ALX002 Alexithymia 37 0.030
786
ART031 Aortic Coarctation 42 0.030
787
ADN015 Adenoid Basal Cell Carcinoma 36 0.030
788
c CHR060 Chronic Dacryocystitis 22 0.030
789
OST115 Osteonecrosis of the Jaw 37 0.030
790
PNG002 Pain Agnosia 26 0.030
791
IMM006 Immune System Organ Benign Neoplasm 26 0.030
792
NDL010 Nodular Hidradenoma 24 0.030
793
c SVR057 Severe Hemophilia B 30 0.030
794
c FML028 Familial Renal Oncocytoma 15 0.030
795
GLM002 Glomangiomatosis 14 0.030
796
P GNT005 Giant Hemangioma 34 0.030
797
OVR017 Ovarian Cystic Teratoma 36 0.030
798
OVR021 Ovarian Lymphoma 33 0.030
799
MCN006 Mucinous Adenofibroma 15 0.030
800
RTT005 Rete Testis Neoplasm 23 0.030
801
ART110 Arteritic Anterior Ischemic Optic Neuropathy 32 0.030
802
CRB132 Cerebral Sinovenous Thrombosis 30 0.030
803
c FML294 Familial Short Qt Syndrome 24 0.030
804
CNT067 Central Cord Syndrome 22 0.030
805
c HRD020 Hereditary Renal Cell Carcinoma 30 0.030
806
P HYP265 Hypotonia 39 0.030
807
INF027 Infiltrative Basal Cell Carcinoma 26 0.030
808
MYP026 Myopathy - Thyrotoxic 6 0.030
809
SYR004 Syringobulbia 13 0.030
810
ERB001 Erb-Duchenne and Dejerine-Klumpke Palsies 1 0.030
811
c ERL020 Early-Onset Schizophrenia 44 0.030
812
BRC057 Brachial Plexus Birth Injuries 6 0.030
813
HMC014 Homocysteinemia 32 0.030
814
HMP020 Hemiplegia Alterans 1 0.030
815
THR035 Thrombasthenia 41 0.030
816
P AST005 Asthma 80 0.021
817
c MLT019 Multiple Myeloma 77 0.021
818
INC002 Inclusion Body Myositis 64 0.021
819
P CLR023 Colorectal Cancer 96 0.021
820
P TYS001 Tay-Sachs Disease 72 0.021
821
c GLY008 Glycogen Storage Disease Ii 59 0.021
822
P SPN301 Spinocerebellar Ataxia 2 57 0.021
823
MTC056 Mitochondrial Dna Depletion Syndrome 4a 45 0.021
824
P OST002 Osteoporosis 63 0.021
825
P MTC003 Metachromatic Leukodystrophy 71 0.021
826
BRN028 Brain Cancer 69 0.021
827
WLF001 Wolff-Parkinson-White Syndrome 58 0.021
828
P MCH002 Machado-Joseph Disease 63 0.021
829
THY028 Thyroid Cancer 71 0.021
830
MVD001 Moved to 60 0.021
831
P FNG005 Feingold Syndrome 43 0.021
832
TRY002 Troyer Syndrome 44 0.021
833
P ADD001 Addison's Disease 60 0.021
834
PRP032 Porphyria Variegata 51 0.021
835
c DLT002 Dilated Cardiomyopathy 75 0.021
836
CHD001 Chediak-Higashi Syndrome 66 0.021
837
GST092 Gastroesophageal Reflux 62 0.021
838
c CRB103 Cerebral Cavernous Malformations-1 48 0.021
839
MLN008 Melanoma 61 0.021
840
RBR001 Roberts Syndrome 61 0.021
841
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.021
842
P ALX003 Alexander Disease 64 0.021
843
P KDN018 Kidney Disease 64 0.021
844
c TYR012 Tyrosinemia, Type I 54 0.021
845
P EPS003 Episodic Ataxia 58 0.021
846
c CWD006 Cowden Syndrome 1 43 0.021
847
CRB011 Cerebrotendinous Xanthomatosis 60 0.021
848
GST050 Gastrointestinal System Disease 58 0.021
849
P ALP004 Alport Syndrome 68 0.021
850
HJD001 Hajdu-Cheney Syndrome 60 0.021
851
P CRN012 Craniometaphyseal Dysplasia 49 0.021
852
ADT003 Auditory System Disease 49 0.021
853
P MYL005 Myelofibrosis 67 0.021
854
P PRM175 Primary Familial Brain Calcification 43 0.021
855
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 39 0.021
856
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.021
857
RNL026 Renal Tubular Acidosis with Deafness 24 0.021
858
CHN016 Cohen Syndrome 55 0.021
859
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 31 0.021
860
PRD011 Proud Syndrome 42 0.021
861
P SYS005 Systemic Scleroderma 60 0.021
862
c OST126 Osteopetrosis, Autosomal Recessive 1 34 0.021
863
CHR222 Chromosome 1p36 Deletion Syndrome 43 0.021
864
c NRF019 Neurofibromatosis, Type 2 62 0.021
865
OST022 Osteopathia Striata with Cranial Sclerosis 34 0.021
866
c PRG021 Paragangliomas 4 42 0.021
867
c DYS119 Dystonia 9 39 0.021
868
P MYM002 Moyamoya Disease 60 0.021
869
P RNL066 Renal Tubular Acidosis, Distal, Ad 29 0.021
870
CCC001 Coccidioidomycosis 55 0.021
871
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.021
872
DND001 Dandy-Walker Syndrome 42 0.021
873
MYP093 Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset 24 0.021
874
ACR041 Acromelic Frontonasal Dysostosis 45 0.021
875
P BPL003 Bipolar Disorder 58 0.021
876
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 27 0.021
877
STF001 Stiff-Person Syndrome 54 0.021
878
c FML023 Familial Hemiplegic Migraine 55 0.021
879
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 27 0.021
880
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 42 0.021
881
BLD044 Bladder Disease 50 0.021
882
c GM2005 Gm2-Gangliosidosis, Ab Variant 32 0.021
883
P WRD001 Waardenburg's Syndrome 56 0.021
884
c MYP081 Myopathy, Myofibrillar, 6 25 0.021
885
ALL026 Allergic Hypersensitivity Disease 53 0.021
886
DYG001 Dyggve-Melchior-Clausen Disease 25 0.021
887
PST020 Postpoliomyelitis Syndrome 38 0.021
888
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.021
889
P SCH018 Schizencephaly 51 0.021
890
c CHR579 Chiari Malformation Type Ii 38 0.021
891
c AMY090 Amyotrophic Lateral Sclerosis 8 39 0.021
892
ABL002 Ablepharon-Macrostomia Syndrome 51 0.021
893
P IDP010 Idiopathic Generalized Epilepsy 61 0.021
894
c HPT016 Hepatitis B 61 0.021
895
CTS002 Cat-Scratch Disease 46 0.021
896
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 38 0.021
897
c AMY085 Amyotrophic Lateral Sclerosis 9 41 0.021
898
P INF038 Influenza 71 0.021
899
ABD010 Abdominal Wall Defect 37 0.021
900
STF002 Stiff Skin Syndrome 51 0.021
901
KRT001 Keratoconjunctivitis Sicca 58 0.021
902
c INT072 Intestinal Pseudo-Obstruction 45 0.021
903
c AMY083 Amyotrophic Lateral Sclerosis 11 37 0.021
904
MLY001 Molybdenum Cofactor Deficiency 40 0.021
905
CHR072 Chordoma 60 0.021
906
BRW009 Brown-Vialetto-Van Laere Syndrome 1 23 0.021
907
SPN040 Spinal Cancer 43 0.021
908
c ATM003 Autoimmune Thyroiditis 59 0.021
909
BNC003 Bone Cancer 44 0.021
910
c SPS025 Spastic Paraplegia 15 23 0.021
911
CMB042 Combined Oxidative Phosphorylation Deficiency 16 22 0.021
912
c SPS079 Spastic Paraplegia 2 29 0.021
913
NNT012 Neonatal Jaundice 49 0.021
914
CHK001 Chikungunya 49 0.021
915
P EXP004 Exophthalmos 56 0.021
916
MNT001 Mantle Cell Lymphoma 72 0.021
917
P MTR012 Mitral Valve Disease 59 0.021
918
c CRB094 Cerebral Cavernous Malformations 3 29 0.021
919
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.021
920
P ENC008 Encephalocele 48 0.021
921
P HYP024 Hypoparathyroidism 52 0.021
922
c AMY062 Amyotrophic Lateral Sclerosis 12 33 0.021
923
DRY001 Dry Eye Syndrome 37 0.021
924
c NRC017 Narcolepsy 7 24 0.021
925
c CNG413 Congenital Short Bowel Syndrome 34 0.021
926
P OST001 Osteopetrosis 63 0.021
927
ACT012 Acute Hemorrhagic Conjunctivitis 37 0.021
928
OPT006 Optic Nerve Disease 47 0.021
929
c AMY067 Amyotrophic Lateral Sclerosis 18 38 0.021
930
ALN001 Aland Island Eye Disease 45 0.021
931
P AML002 Amelogenesis Imperfecta 43 0.021
932
OCL009 Ocular Cancer 61 0.021
933
PMP001 Pemphigus 49 0.021
934
GLT018 Glut1 Deficiency Syndrome 1 30 0.021
935
P ESP024 Esophagitis 62 0.021
936
MLG141 Malignant Atrophic Papulosis 30 0.021
937
MLR010 Melorheostosis with Osteopoikilosis 25 0.021
938
P GST049 Gastrointestinal System Cancer 59 0.021
939
NSD001 Nose Disease 51 0.021
940
PRL009 Prolactinoma 63 0.021
941
c CNG112 Congenital Muscular Dystrophy Type 1a 23 0.021
942
PTN001 Patent Foramen Ovale 55 0.021
943
TRN015 Transient Cerebral Ischemia 57 0.021
944
EST005 Esotropia 39 0.021
945
AMY068 Amyotrophic Lateral Sclerosis 15, with or Without Frontotemporal Dementia 21 0.021
946
PLG002 Plague 49 0.021
947
CYS008 Cystic Echinococcosis 48 0.021
948
PGT009 Paget Disease of Bone 2, Early-Onset 21 0.021
949
CYS039 Cystic Kidney Disease 49 0.021
950
SLV012 Salivary Gland Adenoid Cystic Carcinoma 52 0.021
951
c AMY059 Amyotrophic Lateral Sclerosis 19 36 0.021
952
CHL123 Chlamydia 60 0.021
953
c TRC078 Trichohepatoenteric Syndrome 2 30 0.021
954
c CLR077 Colorectal Cancer 10 33 0.021
955
P CRD011 Cardiomyopathy 66 0.021
956
P MSC007 Muscle Hypertrophy 55 0.021
957
c SPS013 Spastic Paraplegia 8 25 0.021
958
c SPN364 Spinocerebellar Ataxia, X-Linked 3 18 0.021
959
CSL001 Causalgia 42 0.021
960
LYM021 Lymphadenitis 58 0.021
961
SLV005 Silver Spastic Paraplegia Syndrome 24 0.021
962
c SPS159 Spastic Paraplegia 9b, Autosomal Recessive 23 0.021
963
c ACT073 Acute Leukemia 61 0.021
964
PTT009 Pituitary Gland Disease 45 0.021
965
WLL006 Wells Syndrome 57 0.021
966
GYN001 Gynecomastia 49 0.021
967
P LRY016 Laryngeal Carcinoma 60 0.021
968
MMB001 Membranoproliferative Glomerulonephritis 44 0.021
969
P HYP004 Hypercalcemia 54 0.021
970
ART017 Aortic Disease 57 0.021
971
BRB001 Beriberi 40 0.021
972
PNM005 Pneumonic Plague 33 0.021
973
c AMY057 Amyotrophic Lateral Sclerosis 16, Juvenile 22 0.021
974
BLR001 Biliary Atresia 52 0.021
975
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 23 0.021
976
c AMY063 Amyotrophic Lateral Sclerosis 20 27 0.021
977
P FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 22 0.021
978
FRY001 Frey Syndrome 38 0.021
979
BRS064 Bursitis 40 0.021
980
CVR006 Cavernous Hemangioma 46 0.021
981
LMB010 Lambert Syndrome 35 0.021
982
P OLG002 Oligodendroglioma 55 0.021
983
PNM008 Pneumothorax 51 0.021
984
THY030 Thyroid Gland Disease 52 0.021
985
MYL057 Myelopathy, Htlv-1-Associated 28 0.021
986
TRP004 Tropical Sprue 36 0.021
987
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 21 0.021
988
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 25 0.021
989
DPH001 Diphtheria 55 0.021
990
CDQ001 Cauda Equina Syndrome 40 0.021
991
P HYP083 Hypopituitarism 50 0.021
992
c SPS091 Spastic Paraplegia 4 22 0.021
993
c MLT124 Multiple Sclerosis 5 24 0.021
994
LYM022 Lymphangioma 55 0.021
995
MDL009 Medullary Sponge Kidney 41 0.021
996
TRC040 Tracheoesophageal Fistula 41 0.021
997
DSM004 Desmoid Tumor 55 0.021
998
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 28 0.021
999
P HYP014 Hyperuricemia 49 0.021
1000
MYX004 Myxedema 36 0.021
1001
CRT017 Cartilage Disease 44 0.021
1002
c CLR085 Colorectal Cancer 1 39 0.021
1003
MRR003 Murray Valley Encephalitis 41 0.021
1004
P APL006 Aplasia Cutis Congenita 48 0.021
1005
P FBR017 Fibrosarcoma 55 0.021
1006
c MRR010 Mirror Movements 2 20 0.021
1007
P INT030 Intracranial Aneurysm 52 0.021
1008
THY049 Thyroid Cancer, Anaplastic 25 0.021
1009
EXS001 Exostosis 42 0.021
1010
PRG102 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 2 20 0.021
1011
LPD027 Lip Disease 35 0.021
1012
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 20 0.021
1013
BTN005 Biotin-Thiamine-Responsive Basal Ganglia Disease 17 0.021
1014
CCN007 Cocoon Syndrome 32 0.021
1015
PRN011 Pernicious Anemia 41 0.021
1016
MGC001 Megacolon 50 0.021
1017
ALV002 Alveolar Echinococcosis 50 0.021
1018
WYB001 Wyburn Mason's Syndrome 23 0.021
1019
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 30 0.021
1020
CNM001 Canomad Syndrome 13 0.021
1021
PRC013 Pericarditis 52 0.021
1022
P LTR001 Lateral Sclerosis 50 0.021
1023
ANR004 Anuria 46 0.021
1024
STS002 Situs Inversus 43 0.021
1025
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 38 0.021
1026
DND013 Dandy-Walker Malformation with Postaxial Polydactyly 17 0.021
1027
P SML001 Small Cell Carcinoma 54 0.021
1028
c ACT071 Acute Kidney Failure 48 0.021
1029
MLT075 Multifocal Motor Neuropathy 40 0.021
1030
c SCP001 Sc Phocomelia Syndrome 36 0.021
1031
DDN006 Duodenitis 44 0.021
1032
TXC002 Toxic Encephalopathy 52 0.021
1033
P CRN178 Coronary Heart Disease 6 22 0.021
1034
HTS001 Hiatus Hernia 40 0.021
1035
FBR028 Fibrosing Mediastinitis 24 0.021
1036
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 25 0.021
1037
c NRN027 Neuronopathy, Distal Hereditary Motor, Type I 16 0.021
1038
SPN029 Spondylolysis 39 0.021
1039
DVL001 Developmental Coordination Disorder 36 0.021
1040
PNT009 Pontine Tegmental Cap Dysplasia 24 0.021
1041
MGL013 Megalencephaly 50 0.021
1042
WST003 West Nile Fever 29 0.021
1043
c CLR075 Colorectal Cancer 3 37 0.021
1044
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 45 0.021
1045
c VRL004 Viral Labyrinthitis 23 0.021
1046
PRP021 Peripheral Nervous System Neoplasm 49 0.021
1047
NRG004 Neurogenic Diabetes Insipidus 26 0.021
1048
MSC072 Muscle Cancer 47 0.021
1049
NCR007 Necrotizing Fasciitis 43 0.021
1050
SCT002 Scotoma 37 0.021
1051
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 36 0.021
1052
BRN004 Brain Edema 51 0.021
1053
ESP020 Esophageal Atresia 48 0.021
1054