Search results for (2E)-Octenoyl-CoA

789 hits were found for (2E)-Octenoyl-CoA

# Family MCID Name MIFTS Score
1
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 58 42.633
2
c WRD033 Waardenburg Syndrome, Type 2e 53 32.084
3
c MSC176 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 48 28.406
4
c PNT034 Pontocerebellar Hypoplasia, Type 2e 52 24.797
5
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 66 22.497
6
c PSD092 Pseudohypoaldosteronism, Type Iie 48 20.020
7
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 61 18.415
8
IMM140 Immunodeficiency 47 56 15.692
9
GNY003 Guanylate Cyclase 2e, Pseudogene 12 10.141
10
c ART054 Arthrogryposis, Distal, Type 2e 14 9.506
11
P LMB006 Limb-Girdle Muscular Dystrophy 52 6.612
12
P MSC005 Muscular Dystrophy 67 6.458
13
P ICH004 Ichthyosis 56 4.366
14
ICH002 Ichthyosis Bullosa of Siemens 41 4.313
15
P CHR071 Charcot-Marie-Tooth Disease 64 4.155
16
TTH006 Tooth Disease 51 4.155
17
KRT009 Keratosis 53 4.050
18
P NRP001 Neuropathy 60 3.944
19
EPD002 Epidermolytic Hyperkeratosis 56 3.731
20
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.729
21
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 36 3.673
22
P QLT011 Qualitative or Quantitative Defects of Sarcoglycan 26 3.474
23
c PLM127 Pulmonary Hypertension, Primary, 3 34 3.093
24
P VNW001 Von Willebrand's Disease 65 3.039
25
P HML001 Hemolytic-Uremic Syndrome 52 2.808
26
c HYP836 Hypercholesterolemia, Familial, 1 73 2.780
27
c FML021 Familial Hypercholesterolemia 72 2.780
28
P PRP019 Peripheral Nervous System Disease 58 2.679
29
HLX001 Helix Syndrome 48 2.342
30
NRL005 Neurilemmoma 60 2.342
31
EXF002 Exfoliative Ichthyosis 25 2.291
32
ATM095 Autoimmune Disease 61 2.281
33
HRW001 Hair Whorl 35 2.281
34
SNS003 Sensory Peripheral Neuropathy 52 2.241
35
GLM045 Glioma 63 2.217
36
MSC157 Muscular Dystrophy, Duchenne Type 79 2.189
37
c CHR656 Charcot-Marie-Tooth Disease, Demyelinating, Type 1f 46 2.184
38
c DWL002 Dowling-Degos Disease 1 58 2.044
39
SJG002 Sjogren-Larsson Syndrome 54 2.005
40
c HPT073 Hepatitis C Virus 71 2.005
41
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.005
42
P NRB001 Neuroblastoma 66 2.005
43
ACT098 Acute Erythroid Leukemia 55 1.926
44
c VNW005 Von Willebrand Disease, Type 1 45 1.926
45
LPD008 Lipid Metabolism Disorder 62 1.926
46
NRR001 Neuroretinitis 42 1.921
47
RTN023 Retinitis 46 1.921
48
RPD005 Rapidly Involuting Congenital Hemangioma 46 1.882
49
HYP066 Hyperglycemia 61 1.882
50
P SCH015 Schizophrenia 74 1.843
51
P HYP750 Hypertriglyceridemia, Familial 62 1.843
52
ALL014 Allergic Encephalomyelitis 34 1.843
53
P SZR006 Seizure Disorder 70 1.792
54
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.776
55
P RTN008 Retinitis Pigmentosa 80 1.776
56
P CLR023 Colorectal Cancer 100 1.768
57
P PNC035 Pancreatic Cancer 86 1.753
58
c PCH010 Pachyonychia Congenita 3 43 1.753
59
P BCL017 B-Cell Lymphoma 59 1.753
60
P TRM003 Tremor 48 1.753
61
P HPT023 Hepatocellular Carcinoma 96 1.656
62
P LNG064 Lung Cancer Susceptibility 3 70 1.646
63
c MSC171 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 42 1.624
64
P AXN001 Axonal Neuropathy 35 1.587
65
MNN043 Meningioma, Familial 79 1.548
66
SCR001 Secretory Meningioma 40 1.548
67
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.548
68
SPN021 Spinal Meningioma 50 1.548
69
CHR178 Chromosomal Triplication 34 1.548
70
P LKM062 Leukemia, Acute Lymphoblastic 69 1.544
71
P OPT006 Optic Nerve Disease 58 1.514
72
P BRS047 Breast Cancer 98 1.444
73
P DRR001 Diarrhea 55 1.444
74
ESP021 Esophageal Cancer 83 1.426
75
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.408
77
c MSC177 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 42 1.356
78
c CHR676 Charcot-Marie-Tooth Disease, Dominant Intermediate G 24 1.355
79
c WRD029 Waardenburg Syndrome, Type 2b 29 1.315
80
c WRD031 Waardenburg Syndrome, Type 3 45 1.315
81
c WRD032 Waardenburg Syndrome, Type 2a 47 1.315
82
P WRD001 Waardenburg's Syndrome 60 1.315
83
ANS002 Aniseikonia 32 1.291
84
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 1.291
85
SCT002 Scotoma 42 1.291
86
c HPT001 Hepatitis C 62 1.291
87
ANX004 Anoxia 40 1.281
88
HGH043 High Grade Glioma 45 1.281
89
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.281
90
GST045 Gastroenteritis 58 1.281
91
EPD050 Epidermolysis Bullosa Simplex with Muscular Dystrophy 56 1.231
92
BNG077 Benign Idiopathic Neonatal Seizures 23 1.208
93
P KLZ004 Kala-Azar 1 41 1.208
94
LSH001 Leishmaniasis 64 1.208
95
SVR001 Severe Acute Respiratory Syndrome 67 1.208
96
CLN015 Colon Adenocarcinoma 65 1.208
97
HMN044 Human Immunodeficiency Virus Type 1 78 1.141
98
LBR036 Leber Plus Disease 66 1.141
99
P MSC003 Muscular Atrophy 52 1.141
100
ACQ007 Acquired Immunodeficiency Syndrome 59 1.141
101
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.141
102
P SPN046 Spinal Muscular Atrophy 63 1.141
103
NRT004 Neuritis 53 1.141
104
NRF007 Neurofibroma 64 1.141
105
c BRN108 Branchiootic Syndrome 1 62 1.131
106
P EPL164 Epilepsy 68 1.131
107
MCR013 Microphthalmia 60 1.131
108
P LNG032 Lung Cancer 98 1.118
109
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 1.118
110
CLR109 Colorectal Adenocarcinoma 50 1.118
111
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 1.118
112
GLL048 Glial Tumor 52 1.118
113
P FBR017 Fibrosarcoma 56 1.118
114
P RTN018 Retinal Disease 53 1.118
115
XLN247 X-Linked Congenital Retinoschisis 20 1.118
116
P JVN042 Juvenile Retinoschisis 39 1.118
117
MTR087 Maternal Uniparental Disomy 28 1.092
118
c MTR062 Maternal Uniparental Disomy of Chromosome 4 18 1.092
119
c ATR087 Atrial Standstill 1 74 1.092
120
c LKM063 Leukemia, Chronic Myeloid 71 1.092
121
c PLM121 Pulmonary Hypertension, Primary, 4 28 1.092
122
c TYP009 Type 2 Diabetes Mellitus 92 1.092
123
P HYP077 Hypertrichosis 46 1.092
124
DBT010 Diabetic Neuropathy 54 1.092
125
GLB002 Glioblastoma 67 1.092
126
P THY032 Thyroiditis 57 1.092
127
BRN028 Brain Cancer 74 1.092
128
P MLN008 Melanoma 76 1.092
129
STT001 Status Epilepticus 59 1.092
130
BRN071 Brain Injury 50 1.092
131
P ALZ034 Alzheimer Disease 87 1.021
132
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.021
133
P SRC025 Sarcoidosis 1 71 1.021
134
BCT022 Bacterial Infectious Disease 56 1.021
135
P MYP006 Myopia 56 1.021
136
DRM011 Dermatophytosis 52 1.021
137
VSC003 Visceral Leishmaniasis 55 1.021
138
P BRS044 Breast Adenocarcinoma 58 1.021
139
CMM005 Common Cold 56 1.021
140
GLS001 Gliosarcoma 64 1.021
141
SCH014 Schistosomiasis 56 1.021
142
P HRT032 Heart Disease 81 1.021
143
c HPT016 Hepatitis B 62 1.021
144
c RNG007 Ring Chromosome 12 27 1.021
145
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 1.021
146
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.952
147
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.952
148
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 45 0.952
149
c NRN041 Neuronopathy, Distal Hereditary Motor, Type Iib 33 0.952
150
c DST106 Distal Hereditary Motor Neuronopathy Type 2 41 0.952
151
c CHR699 Charcot-Marie-Tooth Disease Type 2a2a 28 0.952
152
P MVM001 Movement Disease 61 0.952
153
MFN001 Mfn2 Hereditary Motor and Sensory Neuropathy 13 0.952
154
DYS073 Dysphagia 53 0.952
155
P PSR002 Psoriasis 63 0.927
156
P CRN300 Coronary Heart Disease 1 73 0.913
157
END057 Endometrial Cancer 72 0.913
158
P MLT020 Multiple Sclerosis 79 0.913
159
P PRK057 Parkinson Disease, Late-Onset 80 0.913
160
P ANP001 Anaplastic Large Cell Lymphoma 61 0.913
161
LWG006 Low Grade Glioma 41 0.913
162
P LYM118 Lymphoma 67 0.913
163
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.913
164
IMM167 Immune Deficiency Disease 78 0.913
165
P GST053 Gastric Cancer 83 0.913
166
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.913
167
P PRK039 Parkinsonism 55 0.913
168
TRM010 Traumatic Brain Injury 51 0.913
169
P DBT009 Diabetes Mellitus 67 0.913
170
CRB004 Cerebral Artery Occlusion 45 0.913
171
CNT016 Central Retinal Vein Occlusion 54 0.913
172
P HPT021 Hepatitis 69 0.913
173
SVR004 Severe Combined Immunodeficiency 72 0.913
174
LVR012 Liver Cirrhosis 63 0.913
175
P GLM007 Glomerulonephritis 60 0.913
176
P HMP007 Hemophilia 52 0.913
177
HNM002 Hinman Syndrome 27 0.858
178
c BLD140 Blood Group, I System 46 0.858
179
ADP007 Adie Pupil 40 0.858
180
P NSP012 Nasopharyngeal Carcinoma 61 0.791
181
CRV035 Cervical Cancer 73 0.791
182
ANX010 Anxiety 70 0.791
183
PLY150 Polykaryocytosis Inducer 29 0.791
184
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.791
185
P URN019 Urinary Tract Infection 49 0.791
186
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.791
187
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.791
188
NRL016 Neural Tube Defects 81 0.791
189
DWN001 Down Syndrome 70 0.791
190
c SML038 Small Cell Cancer of the Lung 69 0.791
191
HND015 Hand Skill, Relative 30 0.791
192
P MYP004 Myopathy 67 0.791
193
PRM133 Primary Pulmonary Lymphoma 16 0.791
194
P LVR013 Liver Disease 69 0.791
195
PRT036 Peritonitis 65 0.791
196
ANT024 Anthrax Disease 58 0.791
197
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.791
198
TRY001 Trypanosomiasis 50 0.791
199
GST027 Gastric Lymphoma 46 0.791
200
CHG001 Chagas Disease 66 0.791
201
PTS001 Patau Syndrome 56 0.791
202
STM006 Stomach Disease 47 0.791
203
c ACT071 Acute Kidney Failure 60 0.791
204
LNG013 Lung Lymphoma 31 0.791
205
c ATS246 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c 33 0.711
206
c ATS277 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d 41 0.711
208
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.701
209
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.701
210
VSL002 Visual Epilepsy 39 0.701
211
CLF004 Cleft Lip/palate 57 0.646
212
P HRD217 Hereditary Optic Neuropathy 36 0.646
213
OBN001 Ouabain Resistance 16 0.646
214
AMN014 Aminopterin Syndrome Sine Aminopterin 32 0.646
215
c SCL052 Scleroderma, Familial Progressive 61 0.646
216
c MSC172 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8 44 0.646
217
c MYS033 Miyoshi Muscular Dystrophy 1 52 0.646
218
INS024 Insulin-Like Growth Factor I 78 0.646
219
ART002 Arts Syndrome 66 0.646
220
AGN016 Aging 54 0.646
221
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 47 0.646
222
c MSC174 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7 42 0.646
223
c THR092 Thrombophilia Due to Thrombin Defect 74 0.646
224
CHR005 Chorioamnionitis 50 0.646
225
c VNW010 Von Willebrand Disease, Type 2 48 0.646
226
TTH002 Tooth Agenesis 61 0.646
227
DFF005 Diffuse Large B-Cell Lymphoma 54 0.646
228
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.646
229
P STR022 Stargardt Disease 61 0.646
230
CLT003 Colitis 63 0.646
231
BNR002 Bone Resorption Disease 47 0.646
232
THR024 Thrombosis 56 0.646
233
P CNG010 Congenital Stationary Night Blindness 56 0.646
234
INT017 Intestinal Schistosomiasis 51 0.646
235
c LKM061 Leukemia, Acute Myeloid 83 0.646
236
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.646
237
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.646
239
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.646
240
TTH030 Teeth, Supernumerary 33 0.646
241
P PRS040 Prostate Cancer 95 0.646
242
c GLC092 Glaucoma, Primary Open Angle 62 0.646
243
PRT112 Portal Hypertension, Noncirrhotic 30 0.646
244
ORL015 Oral Squamous Cell Carcinoma 43 0.646
245
P OPN001 Open-Angle Glaucoma 55 0.646
246
BRN004 Brain Edema 54 0.646
247
P EPD003 Epidermolysis Bullosa Simplex 57 0.646
248
BNM001 Bone Marrow Cancer 46 0.646
249
NRM001 Neuromyelitis Optica 61 0.646
250
P NRC002 Narcolepsy 56 0.646
251
CLF001 Cleft Lip 53 0.646
252
CHC001 Chickenpox 57 0.646
253
YLL002 Yellow Fever 61 0.646
254
47X002 47,xyy 48 0.646
255
SKN016 Skin Disease 63 0.646
256
P SKN015 Skin Carcinoma 71 0.646
257
P RTN016 Retinal Degeneration 52 0.646
258
PPT005 Peptic Ulcer Disease 58 0.646
259
P ART022 Arthritis 71 0.646
260
OST012 Osteoarthritis 77 0.646
261
P NGH001 Night Blindness 52 0.646
262
SLP001 Sleeping Sickness 56 0.646
263
P DNG005 Dengue Virus 56 0.646
264
P DMN002 Dementia 66 0.646
265
P UVT001 Uveitis 57 0.646
266
GT001 Gout 64 0.646
267
ALL029 Allergic Disease 59 0.646
268
CRY005 Cryptococcosis 60 0.646
269
P OPT009 Optic Neuritis 57 0.646
270
P LKM002 Leukemia 67 0.646
271
DNT012 Dental Caries 53 0.646
272
P ACH003 Achromatopsia 62 0.646
273
GST033 Gestational Diabetes 61 0.646
274
CNG034 Congestive Heart Failure 69 0.646
275
ISC004 Ischemia 61 0.646
276
EMB004 Embryonal Carcinoma 56 0.646
277
P EPD016 Epidermolysis Bullosa 53 0.646
278
DRM006 Dermatitis 62 0.646
279
P PTS002 Ptosis 52 0.646
280
GST023 Gastric Ulcer 52 0.646
281
IRN002 Iron Metabolism Disease 57 0.646
282
P BNC003 Bone Cancer 58 0.646
283
DYS032 Dystrophinopathies 47 0.646
284
RFR003 Refractive Error 41 0.646
285
DPR016 Depression 65 0.646
286
P CHR345 Chronic Pain 50 0.646
287
CRD132 Cardiac Conduction Defect 60 0.635
288
ADG002 Audiogenic Seizures 25 0.635
289
INS001 Insulinoma 59 0.635
290
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.495
291
GNT176 Genetic Motor Neuron Disease 20 0.495
292
c ATS452 Autosomal Recessive Axonal Hereditary Motor and Sensory Neuropathy 18 0.495
293
SPS019 Spastic Paraparesis 38 0.495
294
c WRD010 Waardenburg Syndrome Type 4 30 0.495
295
c AXN013 Axonal Hereditary Motor and Sensory Neuropathy 13 0.495
296
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.495
297
P SPS133 Spastic Paraplegia 2, X-Linked 50 0.495
298
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 50 0.495
299
MST006 Mast Syndrome 40 0.495
300
c SPS108 Spastic Paraplegia 5a, Autosomal Recessive 42 0.495
301
c PNT044 Pontocerebellar Hypoplasia, Type 2a 41 0.495
302
ALB025 Albinism, Ocular, with Late-Onset Sensorineural Deafness 49 0.495
303
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 0.495
304
ATX047 Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, with Optic Atrophy and Mental Retardation 23 0.495
305
c SPS219 Spastic Paraplegia 17, Autosomal Dominant 42 0.495
306
c SPS125 Spastic Paraplegia 15, Autosomal Recessive 49 0.495
307
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 67 0.495
308
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 41 0.495
309
c WRD026 Waardenburg Syndrome, Type 2c 26 0.495
310
c SPS110 Spastic Paraplegia 19, Autosomal Dominant 29 0.495
311
MYP136 Myopathy, Centronuclear, X-Linked 59 0.495
312
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 49 0.495
313
c SPS127 Spastic Paraplegia 6, Autosomal Dominant 48 0.495
314
c NRN037 Neuronopathy, Distal Hereditary Motor, Type Va 49 0.495
315
c CHR649 Charcot-Marie-Tooth Disease, Axonal, Type 2d 46 0.495
316
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 49 0.495
317
NRP049 Neuropathy, Hereditary Sensory and Autonomic, Type I, with Cough and Gastroesophageal Reflux 32 0.495
318
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 47 0.495
319
P DYS193 Dystonia 11, Myoclonic 55 0.495
320
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.495
321
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.495
322
MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.495
323
TTZ003 Tietz Albinism-Deafness Syndrome 59 0.495
324
PPL049 Papillon-Lefevre Syndrome 66 0.495
325
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.495
326
c CHR353 Charcot-Marie-Tooth Disease, Axonal, Type 2l 41 0.495
327
PRP066 Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 50 0.495
328
GLD006 Goldberg-Shprintzen Syndrome 49 0.495
329
P OCL001 Ocular Albinism 48 0.495
330
P DST002 Distal Arthrogryposis 65 0.495
331
DYS001 Dyskinetic Cerebral Palsy 31 0.495
332
P PRR025 Perrault Syndrome 42 0.495
333
c SPS123 Spastic Paraplegia 32, Autosomal Recessive 33 0.495
334
c NRP039 Neuropathy, Hereditary Sensory, Type Id 39 0.495
335
c NRP029 Neuropathy, Hereditary Sensory, Type Iic 36 0.495
336
c CHR026 Charcot-Marie-Tooth Disease Type X 25 0.495
337
c CHR025 Charcot-Marie-Tooth Disease Intermediate Type 29 0.495
338
P HRD021 Hereditary Sensory Neuropathy 48 0.495
339
c SPN444 Spinal Muscular Atrophy Type 0 22 0.495
340
c AMY081 Amyotrophic Lateral Sclerosis Type 12 28 0.495
341
c AMY074 Amyotrophic Lateral Sclerosis Type 14 21 0.495
342
c AMY079 Amyotrophic Lateral Sclerosis Type 15 26 0.495
343
INT072 Intestinal Pseudo-Obstruction 62 0.495
344
c AMY022 Amyotrophic Lateral Sclerosis Type 5 33 0.495
345
c AMY023 Amyotrophic Lateral Sclerosis Type 6 34 0.495
346
c OPT023 Optic Atrophy 2 32 0.495
347
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 0.495
348
c CHR521 Charcot-Marie-Tooth Disease, Type 4b1 47 0.495
349
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 47 0.495
350
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 48 0.495
351
c AMY094 Amyotrophic Lateral Sclerosis 5, Juvenile 31 0.495
352
c PNT043 Pontocerebellar Hypoplasia, Type 4 41 0.495
353
c WRD020 Waardenburg Syndrome, Type 4a 49 0.495
354
c SPS198 Spastic Paraplegia 16, X-Linked 30 0.495
355
P PHS005 Peho Syndrome 44 0.495
356
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.495
357
c CHR626 Charcot-Marie-Tooth Disease, Axonal, Type 2a1 36 0.495
358
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.495
359
CHR629 Charcot-Marie-Tooth Disease and Deafness 50 0.495
360
c SPS117 Spastic Paraplegia 10, Autosomal Dominant 48 0.495
361
c CHR650 Charcot-Marie-Tooth Disease, Axonal, Type 2b1 45 0.495
362
c CHR651 Charcot-Marie-Tooth Disease, Axonal, Type 2b2 39 0.495
363
P HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 48 0.495
364
c SPS149 Spastic Paraplegia 8, Autosomal Dominant 48 0.495
365
P SPN408 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 51 0.495
366
NRP009 Neuropathy, Hereditary Motor and Sensory, Okinawa Type 32 0.495
367
c SPS068 Spastic Paraplegia 14, Autosomal Recessive 29 0.495
368
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 58 0.495
369
c SPS097 Spastic Paraplegia 13, Autosomal Dominant 41 0.495
370
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 36 0.495
371
c SPN326 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2 38 0.495
372
c ALZ053 Alzheimer Disease 7 32 0.495
373
c CHR519 Charcot-Marie-Tooth Disease, Type 4b2 48 0.495
374
c SPS131 Spastic Paraplegia 12, Autosomal Dominant 41 0.495
375
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 41 0.495
376
c MYP081 Myopathy, Myofibrillar, 6 41 0.495
377
c SPS071 Spastic Paraplegia 48, Autosomal Recessive 44 0.495
378
c CHR671 Charcot-Marie-Tooth Disease, Axonal, Type 2r 37 0.495
379
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.495
380
c CRT074 Cortical Dysplasia, Complex, with Other Brain Malformations 6 32 0.495
381
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.495
382
c CHR514 Charcot-Marie-Tooth Disease, Recessive Intermediate D 27 0.495
383
c CHR544 Charcot-Marie-Tooth Disease, Axonal, Type 2w 34 0.495
384
c CHR618 Charcot-Marie-Tooth Disease, Axonal, Type 2cc 28 0.495
385
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.495
386
c PNT036 Pontocerebellar Hypoplasia, Type 6 46 0.495
387
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 33 0.495
388
c CHR670 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 43 0.495
389
c SPS106 Spastic Paraplegia 54, Autosomal Recessive 42 0.495
390
c SPS119 Spastic Paraplegia 55, Autosomal Recessive 39 0.495
391
CLD014 Cole Disease 38 0.495
392
c SPS137 Spastic Paraplegia 57, Autosomal Recessive 39 0.495
393
c SPS157 Spastic Paraplegia 64, Autosomal Recessive 40 0.495
394
c SPS141 Spastic Paraplegia 61, Autosomal Recessive 37 0.495
395
c SPS228 Spastic Paraplegia 63, Autosomal Recessive 35 0.495
396
c SPS107 Spastic Paraplegia 18, Autosomal Recessive 41 0.495
397
P AMY106 Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia 44 0.495
398
c SPS096 Spastic Paraplegia 44, Autosomal Recessive 38 0.495
399
c WRD024 Waardenburg Syndrome, Type 4c 43 0.495
400
c WRD019 Waardenburg Syndrome, Type 4b 45 0.495
401
c CHR351 Charcot-Marie-Tooth Disease, Axonal, Type 2n 41 0.495
402
c SPS115 Spastic Paraplegia 41, Autosomal Dominant 29 0.495
403
c NRN018 Neuronopathy, Distal Hereditary Motor, Type Iic 34 0.495
404
c NRP040 Neuropathy, Hereditary Sensory and Autonomic, Type Ic 42 0.495
405
c CHR666 Charcot-Marie-Tooth Disease, Recessive Intermediate B 36 0.495
406
c PNT049 Pontocerebellar Hypoplasia, Type 2d 43 0.495
407
c SPS095 Spastic Paraplegia 47, Autosomal Recessive 43 0.495
408
c SPS122 Spastic Paraplegia 52, Autosomal Recessive 39 0.495
409
c CHR420 Charcot-Marie-Tooth Disease, Type 4j 48 0.495
410
c AMY085 Amyotrophic Lateral Sclerosis 9 36 0.495
411
c SPS129 Spastic Paraplegia 39, Autosomal Recessive 44 0.495
412
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 50 0.495
413
c SPS099 Spastic Paraplegia 42, Autosomal Dominant 40 0.495
414
c SPS113 Spastic Paraplegia 33, Autosomal Dominant 37 0.495
415
PHS023 Phosphoserine Aminotransferase Deficiency 41 0.495
416
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 51 0.495
417
c CHR641 Charcot-Marie-Tooth Disease, X-Linked Recessive, 2 33 0.495
418
MSS001 Masa Syndrome 60 0.495
419
SPN402 Spinal Muscular Atrophy, X-Linked 2 48 0.495
420
c PNT046 Pontocerebellar Hypoplasia, Type 5 30 0.495
421
c SPS148 Spastic Paraplegia 31, Autosomal Dominant 47 0.495
422
c SPN191 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 46 0.495
423
ALX003 Alexander Disease 61 0.495
424
c LBR004 Leber Congenital Amaurosis 1 52 0.495
425
c AMY090 Amyotrophic Lateral Sclerosis 8 43 0.495
426
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 55 0.495
427
c WRD022 Waardenburg Syndrome, Type 2d 33 0.495
428
c SPS116 Spastic Paraplegia 26, Autosomal Recessive 40 0.495
429
c CHR421 Charcot-Marie-Tooth Disease, Type 4h 46 0.495
430
c SPS124 Spastic Paraplegia 28, Autosomal Recessive 41 0.495
431
BHR001 Behr Syndrome 51 0.495
432
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 45 0.495
433
YNS002 Yunis-Varon Syndrome 50 0.495
434
HLN001 Halo Nevi 27 0.495
435
c WRD030 Waardenburg Syndrome, Type 1 53 0.495
436
c GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 48 0.495
437
PYC001 Pycnodysostosis 55 0.495
438
TLC001 Telecanthus 35 0.495
439
SCP002 Scapuloperoneal Spinal Muscular Atrophy 55 0.495
440
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 55 0.495
441
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.495
442
DLT018 Dilution, Pigmentary 25 0.495
443
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 51 0.495
444
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 0.495
445
PBL005 Piebald Trait 59 0.495
446
HTR005 Heterochromia Iridis 21 0.495
447
P HRS035 Hirschsprung Disease 1 66 0.495
448
P CMP005 Campomelic Dysplasia 65 0.495
449
c NRN040 Neuronopathy, Distal Hereditary Motor, Type Viib 45 0.495
450
c CHR371 Charcot-Marie-Tooth Disease, Dominant Intermediate C 41 0.495
451
c CHR658 Charcot-Marie-Tooth Disease, Recessive Intermediate a 38 0.495
452
c AMY063 Amyotrophic Lateral Sclerosis 20 31 0.495
453
c CHR547 Charcot-Marie-Tooth Disease, Axonal, Type 2u 38 0.495
454
c DVL055 Developmental and Epileptic Encephalopathy 29 37 0.495
455
c LKD023 Leukodystrophy, Hypomyelinating, 12 38 0.495
456
c CHR542 Charcot-Marie-Tooth Disease, Axonal, Type 2t 36 0.495
457
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.495
458
c CHR652 Charcot-Marie-Tooth Disease, Axonal, Type 2i 38 0.495
459
c CHR653 Charcot-Marie-Tooth Disease, Demyelinating, Type 1d 39 0.495
460
CHR655 Charcot-Marie-Tooth Disease, Axonal, with Vocal Cord Paresis, Autosomal Recessive 32 0.495
461
c CHR545 Charcot-Marie-Tooth Disease, Axonal, Type 2h 27 0.495
462
c CHR657 Charcot-Marie-Tooth Disease, Axonal, Type 2j 39 0.495
463
c CHR481 Charcot-Marie-Tooth Disease, Dominant Intermediate D 32 0.495
465
NNS061 Non-Syndromic Pontocerebellar Hypoplasia 20 0.495
466
P PNT019 Pontocerebellar Hypoplasia 46 0.495
467
P HYP730 Hypogonadotropic Hypogonadism 53 0.495
468
c GNT045 Giant Axonal Neuropathy 2 24 0.495
469
c HRD210 Hereditary Spastic Paraplegia 23 22 0.495
470
c ATS425 Autosomal Recessive Distal Hereditary Motor Neuronopathy 20 0.495
471
P ATS426 Autosomal Dominant Distal Hereditary Motor Neuronopathy 33 0.495
472
c HRD220 Hereditary Spastic Paraplegia 30 32 0.495
473
c HRD186 Hereditary Spastic Paraplegia 51 29 0.495
474
c HRD188 Hereditary Spastic Paraplegia 72 28 0.495
475
c CHR422 Charcot-Marie-Tooth Disease, Dominant Intermediate B 46 0.495
476
c CHR491 Charcot-Marie-Tooth Disease, Dominant Intermediate a 30 0.495
477
c CHR608 Charcot-Marie-Tooth Disease, Axonal, Type 2p 45 0.495
478
LSN001 Lesion of Sciatic Nerve 22 0.495
479
P SPN423 Spinal Muscular Atrophy with Lower Extremity Predominance 26 0.495
480
P OCL062 Ocular Albinism with Congenital Sensorineural Deafness 23 0.495
481
P DYS154 Dystonia 64 0.495
482
P KLL001 Kallmann Syndrome 65 0.495
483
P ACT008 Actinic Keratosis 54 0.495
484
CCH001 Cochlear Disease 28 0.495
485
P DST101 Distal Hereditary Motor Neuropathies 23 0.495
486
BRC011 Brachial Plexus Neuropathy 38 0.495
487
PRG001 Progressive Muscular Atrophy 41 0.495
488
ANG018 Angiomyolipoma 46 0.495
489
P CNT004 Centronuclear Myopathy 57 0.495
490
NRM005 Neuromuscular Disease 63 0.495
491
PRP016 Paraplegia 52 0.495
492
DFF013 Diffuse Meningeal Melanocytosis 20 0.495
493
c CHR522 Charcot-Marie-Tooth Disease, Dominant Intermediate E 40 0.495
494
c MLN043 Melanoma, Cutaneous Malignant 8 37 0.495
495
EPT001 Epithelioid Cell Melanoma 21 0.495
496
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 39 0.495
497
c SPS126 Spastic Paraplegia 49, Autosomal Recessive 44 0.495
498
c CHR504 Charcot-Marie-Tooth Disease, Type 4b3 45 0.495
499
ALK024 Alkuraya-Kucinskas Syndrome 45 0.495
500
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.495
501
P SNS001 Sensorineural Hearing Loss 59 0.495
502
c AMY083 Amyotrophic Lateral Sclerosis 11 39 0.495
503
c SPS109 Spastic Paraplegia 46, Autosomal Recessive 42 0.495
504
c AMY057 Amyotrophic Lateral Sclerosis 16, Juvenile 38 0.495
505
P LTR001 Lateral Sclerosis 58 0.495
506
MTR007 Motor Peripheral Neuropathy 40 0.495
507
ARG003 Argyll Robertson Pupil 23 0.495
508
c HRD010 Hereditary Spastic Paraplegia 66 0.495
509
P PPL023 Pupil Disease 26 0.495
510
MLG005 Malignant Spindle Cell Melanoma 39 0.495
511
MLN079 Melanoma in Congenital Melanocytic Nevus 37 0.495
512
c CHR571 Charcot-Marie-Tooth Disease Type 5 23 0.495
513
P MCR010 Microcephaly 60 0.495
514
SPS004 Spastic Quadriplegia 40 0.495
515
ABN004 Abnormal Pupillary Function 15 0.495
516
MLG061 Malignant Choroid Melanoma 33 0.495
517
CHL010 Childhood Kidney Cell Carcinoma 38 0.495
518
GLL012 Gallbladder Melanoma 25 0.495
519
P MTR014 Motor Neuron Disease 65 0.495
520
P PLY019 Polyneuropathy 52 0.495
521
MNN017 Mononeuropathy 41 0.495
522
MLN005 Melanoacanthoma 22 0.495
523
MGC001 Megacolon 48 0.495
524
SPS003 Spastic Diplegia 53 0.495
525
QDR001 Quadriplegia 50 0.495
526
CHR073 Choreatic Disease 54 0.495
527
OCH001 Ochronosis 40 0.495
528
HYP080 Hypogonadism 50 0.495
529
CRB037 Cerebral Palsy 67 0.495
531
ALB002 Albinism 47 0.495
532
c SPS092 Spastic Paraplegia 11 33 0.495
533
TSN004 Tsen54 Pontocerebellar Hypoplasia 15 0.495
534
P PRX014 Proximal Spinal Muscular Atrophy 42 0.495
535
c ERL012 Early-Onset Glaucoma 24 0.495
536
P ENC018 Encephalopathy 62 0.495
537
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 0.495
538
P GNT009 Giant Axonal Neuropathy 46 0.495
539
P CRB088 Cerebral Atrophy 33 0.495
540
ATN005 Autonomic Dysfunction 46 0.495
541
c HRD088 Hereditary Neuropathies 33 0.495
542
P MYC033 Myoclonus 47 0.495
543
HYP213 Hypomelanotic Disorder 22 0.495
544
ANC002 Anca-Associated Vasculitis 44 0.495
545
c ATS272 Autosomal Dominant Intermediate Charcot-Marie-Tooth 19 0.495
546
c CHR135 Charcot-Marie-Tooth Disease Type 2a 23 0.495
547
PRX008 Paroxysmal Cold Hemoglobinuria 26 0.495
548
ARC025 Arachnoid Cysts, Intracranial 37 0.457
549
c TYP008 Type 1 Diabetes Mellitus 70 0.457
550
LYM133 Lymphoma, Hodgkin, Classic 74 0.457
551
QLT002 Qualitative or Quantitative Defects of Dystrophin 19 0.457
552
ERY002 Erythema Infectiosum 35 0.457
553
APN006 Apnea of Prematurity 24 0.457
554
CYN003 Cyanide Poisoning 22 0.457
555
P OVR082 Overgrowth Syndrome 49 0.457
556
ATH013 Atherosclerosis Susceptibility 63 0.457
557
P BLD134 Bladder Cancer 79 0.457
558
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.457
559
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.457
560
P ULL002 Ullrich Congenital Muscular Dystrophy 1 57 0.457
561
P MYS003 Myasthenia Gravis 68 0.457
562
MSC152 Muscular Dystrophy, Becker Type 69 0.457
563
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 64 0.457
564
PSR001 Psoriatic Arthritis 62 0.457
565
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.457
566
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 0.457
567
c HRD138 Hereditary Motor and Sensory Neuropathy V 32 0.457
568
STR067 Stroke, Ischemic 80 0.457
569
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.457
570
P DRM053 Dermatitis, Atopic 65 0.457
571
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.457
572
RTN017 Retinal Detachment 60 0.457
573
P RHM011 Rheumatoid Arthritis 82 0.457
574
LTH043 Lithium Transport 17 0.457
575
MRF001 Marfan Syndrome 76 0.457
576
P BTH005 Bethlem Myopathy 1 62 0.457
577
P OST002 Osteoporosis 76 0.457
578
TRT017 Teratoma, Ovarian 28 0.457
579
c PCH015 Pachyonychia Congenita 1 60 0.457
580
P LKM071 Leukemia, Chronic Lymphocytic 75 0.457
581
c SYS001 Systemic Lupus Erythematosus 87 0.457
582
P OVR042 Ovarian Cancer 88 0.457
583
MNT107 Mental Retardation, Fra12a Type 20 0.457
584
GLL008 Gilles De La Tourette Syndrome 65 0.457
585
ALC007 Alcohol Dependence 66 0.457
586
c SPN225 Spondyloarthropathy 1 70 0.457
587
GST092 Gastroesophageal Reflux 61 0.457
588
c SYN084 Synpolydactyly 1 36 0.457
589
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.457
590
P CLC063 Celiac Disease 1 66 0.457
591
HYD038 Hydrops Fetalis, Nonimmune 59 0.457
592
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.457
593
P PLM037 Pulmonary Hypertension 72 0.457
594
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.457
595
P SLP006 Sleep Apnea 69 0.457
596
FTL006 Fetal Alcohol Spectrum Disorder 43 0.457
597
PRP036 Peripheral T-Cell Lymphoma 53 0.457
598
MLR004 Malaria 80 0.457
599
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.457
600
c MJR022 Major Affective Disorder 8 38 0.457
601
c MCR130 Microvascular Complications of Diabetes 6 41 0.457
602
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 27 0.457
603
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.457
604
CYN002 Cyanosis, Transient Neonatal 43 0.457
605
NDL024 Nodal Marginal Zone Lymphoma 37 0.457
606
c ATS007 Autism Spectrum Disorder 72 0.457
607
ART074 Aortic Dissection 53 0.457
608
HMN047 Human Cytomegalovirus Infection 57 0.457
609
P CTN015 Cutaneous T Cell Lymphoma 48 0.457
610
P SYN012 Synpolydactyly 38 0.457
611
P ATR011 Atrial Fibrillation 66 0.457
612
P FTL001 Fetal Alcohol Syndrome 55 0.457
613
P SML001 Small Cell Carcinoma 52 0.457
614
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 53 0.457
615
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.457
616
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.457
617
CNT105 Central Core Disease of Muscle 59 0.457
618
HSH003 Hashimoto Thyroiditis 60 0.457
619
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.457
620
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.457
621
ALV005 Alveolar Soft Part Sarcoma 61 0.457
622
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.457
623
AST006 Astigmatism 47 0.457
624
EWN003 Ewing Sarcoma 70 0.457
625
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.457
626
c LSS030 Lissencephaly 7 with Cerebellar Hypoplasia 21 0.457
627
c CHR617 Charcot-Marie-Tooth Disease, Axonal, Type 2z 35 0.457
628
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.457
629
P MJR001 Major Depressive Disorder 68 0.457
630
c MJR024 Major Affective Disorder 9 41 0.457
631
ACT119 Acute Promyelocytic Leukemia 62 0.457
632
c MCR120 Microvascular Complications of Diabetes 7 47 0.457
633
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.457
634
P DVL012 Developmental Dysplasia of the Hip 1 46 0.457
635
TBL029 Tubulin, Beta 28 0.457
636
c CHR660 Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a 35 0.457
637
P HMN036 Hemangiopericytoma, Malignant 58 0.457
638
MYL005 Myelofibrosis 71 0.457
639
OCL069 Ocular Motor Apraxia 57 0.457
640
P RTN024 Retinoblastoma 73 0.457
641
OST159 Osteogenic Sarcoma 66 0.457
642
P STR020 Strabismus 56 0.457
643
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.457
644
c HYP595 Hypertension, Essential 85 0.457
645
CRN238 Corneal Dystrophy, Epithelial Basement Membrane 32 0.457
646
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.457
647
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.457
648
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 0.457
649
P MDL005 Medulloblastoma 75 0.457
650
P GLM040 Glioma Susceptibility 1 71 0.457
651
MMM006 Mammographic Density 39 0.457
652
CHL065 Cholangiocarcinoma 58 0.457
653
DCT002 Ductal Carcinoma in Situ 58 0.457
654
PNG002 Pain Agnosia 51 0.457
655
P PTN014 Patent Ductus Arteriosus 1 59 0.457
656
DSS032 Disease by Infectious Agent 55 0.457
657
TNG009 Tongue Squamous Cell Carcinoma 43 0.457
658
ARG004 Argyria 26 0.457
659
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 40 0.457
660
TNG007 Tongue Carcinoma 52 0.457
661
MDD018 Middle East Respiratory Syndrome 44 0.457
662
PRT037 Pertussis 65 0.457
663
P LPS004 Lupus Erythematosus 61 0.457
664
P AMY004 Amyloidosis 70 0.457
665
c ACT075 Acute Myocardial Infarction 56 0.457
666
P FBR003 Fibrous Histiocytoma 43 0.457
667
CLR011 Clear Cell Ependymoma 31 0.457
668
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.457
669
NTR005 Nutritional Deficiency Disease 61 0.457
670
NRL001 Neurilemmoma of the Fifth Cranial Nerve 26 0.457
671
P RHB003 Rhabdomyosarcoma 66 0.457
672
CRV002 Cervix Uteri Carcinoma in Situ 47 0.457
673
IRD001 Iridocyclitis 53 0.457
674
MCH006 Mechanical Strabismus 40 0.457
675
P HRP006 Herpes Simplex 65 0.457
676
LRN003 Learning Disability 49 0.457
677
ULC004 Ulcerative Colitis 74 0.457
678
FTT001 Fatty Liver Disease 62 0.457
679
P HML002 Hemolytic Anemia 62 0.457
680
CLL010 Cellular Ependymoma 57 0.457
681
PST092 Posttransplant Acute Limbic Encephalitis 28 0.457
683
P ALP008 Alopecia 54 0.457
684
c PRG106 Progressive Muscular Dystrophy 32 0.457
685
P ALC033 Alcohol Use Disorder 61 0.457
686
P THR014 Thrombocytopenia 66 0.457
687
P CYS018 Cystitis 59 0.457
688
SKN022 Skin Squamous Cell Carcinoma 54 0.457
689
P OLG002 Oligodendroglioma 66 0.457
690
TRC003 Trichomoniasis 53 0.457
691
VCC001 Vaccinia 47 0.457
692
P BPL003 Bipolar Disorder 56 0.457
693
MNT002 Mental Depression 57 0.457
694
P PLM036 Pulmonary Fibrosis 66 0.457
695
P ART023 Arthropathy 61 0.457
696
P INF038 Influenza 68 0.457
697
PST011 Pustulosis of Palm and Sole 52 0.457
698
PPT002 Peptic Ulcer Perforation 34 0.457
699
SPN051 Spondylitis 51 0.457
700
EXT034 Extrinsic Allergic Alveolitis 57 0.457
701
LNG099 Lung Disease 62 0.457
702
P BNG030 Benign Ependymoma 51 0.457
703
MYL001 Myelitis 50 0.457
704
P PLY020 Polyradiculoneuropathy 46 0.457
705
DFF016 Diffuse Astrocytoma 45 0.457
706
P PRD008 Periodontitis 64 0.457
707
P INT070 Intestinal Obstruction 57 0.457
708
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.457
709
PGM003 Pigmentation Disease 45 0.457
710
P KRT007 Keratoconus 50 0.457
711
NSP002 Nasopharyngitis 45 0.457
712
P GRF003 Graft-Versus-Host Disease 71 0.457
713
c MCR113 Microvascular Complications of Diabetes 3 52 0.457
714
c MCR133 Microvascular Complications of Diabetes 4 41 0.457
715
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.457
716
THY006 Thymus Lymphoma 27 0.457
717
c DLT002 Dilated Cardiomyopathy 78 0.457
718
DNG003 Dengue Disease 65 0.457
719
P MLN007 Male Infertility 56 0.457
720
P ESP024 Esophagitis 60 0.457
721
INF009 Inflammatory Spondylopathy 30 0.457
722
DYS015 Dysentery 50 0.457
723
TST004 Testicular Lymphoma 39 0.457
724
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.457
725
P HMN010 Hemangioma 62 0.457
726
BLR008 Bilirubin Metabolic Disorder 57 0.457
727
RTN020 Retinal Vascular Disease 46 0.457
728
P HYP086 Hypothyroidism 69 0.457
729
P ADN016 Adenocarcinoma 63 0.457
730
MLG169 Malignant Astrocytoma 57 0.457
731
URT001 Urethritis 53 0.457
732
BCT004 Bacteriuria 47 0.457
733
BRC012 Brucellosis 66 0.457
734
P MYG005 Myoglobinuria 40 0.457
735
CYT005 Cytomegalovirus Retinitis 50 0.457
736
MST005 Mastitis 53 0.457
737
HMP005 Hemiplegia 54 0.457
738
P RSP003 Respiratory Failure 74 0.457
739
RBS001 Rabies 58 0.457
740
P PYL005 Pyelonephritis 57 0.457
741
PRT038 Protein-Energy Malnutrition 53 0.457
742
RCT015 Reactive Arthritis 61 0.457
743
c INF023 Inflammatory Breast Carcinoma 49 0.457
744
INT079 Intrahepatic Cholangiocarcinoma 51 0.457
745
c ESS001 Essential Tremor 57 0.457
746
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.457
747
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.457
748
P INT068 Intestinal Disease 53 0.457
749
OVR109 Ovarian Germ Cell Teratoma 32 0.457
750
P PNM007 Pneumonia 67 0.457
751
CCN002 Cocaine Abuse 49 0.457
752
P TRT010 Teratoma 51 0.457
753
PLM029 Palmoplantar Keratosis 48 0.457
754
INT066 Interstitial Lung Disease 60 0.457
755
P LRY044 Larynx Cancer 54 0.457
756
P KDN017 Kidney Cancer 61 0.457
757
P TCD001 Tic Disorder 49 0.457
758
BRS051 Breast Disease 58 0.457
759
P JNC001 Junctional Epidermolysis Bullosa 53 0.457
760
DMY004 Demyelinating Disease 50 0.457
761
PLR005 Pleuropneumonia 33 0.457
762
P EHL001 Ehlers-Danlos Syndrome 58 0.457
763
PLS007 Plasmodium Falciparum Malaria 52 0.457
764
AZS001 Azoospermia 45 0.457
765
ENT004 Enthesopathy 51 0.457
766
HYP014 Hyperuricemia 51 0.457
767
RTN021 Retinal Vascular Occlusion 45 0.457
768
SQM006 Squamous Cell Carcinoma 60 0.457
769
NRN004 Neuroendocrine Tumor 59 0.457
770
P RTN022 Retinal Vein Occlusion 54 0.457
771
PLM033 Pulmonary Embolism 58 0.457
772
P INS002 in Situ Carcinoma 53 0.457
773
HYP706 Hypermobile Ehlers-Danlos Syndrome 55 0.457
774
P MYC008 Myocarditis 59 0.457
775
HRP004 Herpes Zoster 61 0.457
776
PTH003 Pathologic Nystagmus 52 0.457
777
SFT003 Soft Tissue Sarcoma 57 0.457
778
SPL018 Splenomegaly 49 0.457
779
48X005 48,xyyy 39 0.457
780
PRN039 Paraneoplastic Syndromes 37 0.457
781
CND006 Candida Glabrata 30 0.457
782
CYT002 Cytokine Deficiency 43 0.457
783
CRV045 Cervical Intraepithelial Neoplasia 39 0.457
784
HMP009 Haemophilus Influenzae 41 0.457
785
MYC019 Mycobacterium Marinum 29 0.457
786
CHR176 Chromophil Renal Cell Carcinoma 23 0.457
787
c LMB030 Limb-Girdle Muscular Dystrophy Type 1c 27 0.457
788
LYM051 Lymphomatoid Granulomatosis 45 0.457
789
MYC015 Mycobacterium Fortuitum 28 0.457
Content
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