Search results for Sphingosine

938 hits were found for Sphingosine

# Family MCID Name MIFTS Score
1
SPH021 Sphingosine Phosphate Lyase Insufficiency Syndrome 15 20.612
2
PRT037 Pertussis 65 16.945
3
P MLT020 Multiple Sclerosis 79 10.405
4
LYM027 Lymphopenia 56 9.817
5
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 7.887
6
ALL014 Allergic Encephalomyelitis 34 7.684
7
RLP002 Relapsing-Remitting Multiple Sclerosis 56 7.634
8
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 6.774
9
GLB002 Glioblastoma 67 6.734
10
GLM045 Glioma 63 6.708
11
ISC004 Ischemia 61 6.695
12
GLL048 Glial Tumor 52 6.648
13
P NRB001 Neuroblastoma 66 6.296
14
HYP266 Hypoxia 57 6.278
15
ATM095 Autoimmune Disease 61 6.256
16
CLT003 Colitis 63 5.925
17
P INF037 Inflammatory Bowel Disease 53 5.760
18
P DRM053 Dermatitis, Atopic 65 5.594
19
ATH013 Atherosclerosis Susceptibility 63 5.455
20
PLM010 Pulmonary Edema 55 5.428
21
BNR002 Bone Resorption Disease 47 5.340
22
CYT002 Cytokine Deficiency 43 5.309
23
P HPT023 Hepatocellular Carcinoma 96 5.266
24
P BRS047 Breast Cancer 98 5.116
25
ULC004 Ulcerative Colitis 74 5.039
26
CRB004 Cerebral Artery Occlusion 45 5.037
27
P OVR042 Ovarian Cancer 88 4.959
28
P MYL006 Myeloid Leukemia 61 4.878
29
SKN016 Skin Disease 63 4.838
30
P PHC003 Pheochromocytoma 69 4.793
31
ADR040 Adrenal Gland Pheochromocytoma 46 4.793
32
P PNM007 Pneumonia 67 4.769
33
FTT001 Fatty Liver Disease 62 4.690
34
P AST005 Asthma 76 4.664
35
RNL077 Renal Fibrosis 46 4.634
36
c MCR130 Microvascular Complications of Diabetes 6 41 4.582
37
c MCR120 Microvascular Complications of Diabetes 7 47 4.582
38
c MCR113 Microvascular Complications of Diabetes 3 52 4.582
39
c MCR133 Microvascular Complications of Diabetes 4 41 4.582
40
CYS001 Cystic Fibrosis 78 4.552
41
P NPH012 Nephrotic Syndrome 60 4.534
42
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.533
43
c PCH010 Pachyonychia Congenita 3 43 4.522
44
c LKM061 Leukemia, Acute Myeloid 83 4.461
45
LPD008 Lipid Metabolism Disorder 62 4.452
46
P RTN024 Retinoblastoma 73 4.418
47
P GST053 Gastric Cancer 83 4.397
48
CHL014 Cholera 62 4.280
49
P GCH001 Gaucher's Disease 70 4.230
50
SVR004 Severe Combined Immunodeficiency 72 4.225
51
P BCL017 B-Cell Lymphoma 59 4.198
52
P RHM011 Rheumatoid Arthritis 82 4.095
53
P ICH004 Ichthyosis 56 4.085
54
SPH010 Sphingolipidosis 47 4.083
55
P ADL010 Adult Respiratory Distress Syndrome 71 4.061
56
c PLM164 Pulmonary Hypertension, Primary, 1 76 4.049
57
P SCK005 Sickle Cell Disease 56 4.035
58
P PLM036 Pulmonary Fibrosis 66 4.007
59
BRN071 Brain Injury 50 3.925
60
P LYM118 Lymphoma 67 3.909
61
P PNC035 Pancreatic Cancer 86 3.892
62
P ALZ034 Alzheimer Disease 87 3.878
63
c NPH102 Nephrotic Syndrome, Type 14 44 3.859
64
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.848
65
P PSR002 Psoriasis 63 3.840
66
PST011 Pustulosis of Palm and Sole 52 3.840
67
DMY004 Demyelinating Disease 50 3.840
68
P CLR023 Colorectal Cancer 100 3.836
69
SQM006 Squamous Cell Carcinoma 60 3.800
70
DRM006 Dermatitis 62 3.800
72
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.735
73
P LKM002 Leukemia 67 3.671
74
BRN004 Brain Edema 54 3.633
75
P NMN002 Niemann-Pick Disease 60 3.615
76
P VSC007 Vascular Disease 63 3.600
77
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.552
78
P PLM037 Pulmonary Hypertension 72 3.490
79
P ART022 Arthritis 71 3.488
80
P INF038 Influenza 68 3.487
81
OST159 Osteogenic Sarcoma 66 3.486
82
ALL029 Allergic Disease 59 3.470
83
c PRM340 Primary Adrenal Insufficiency 38 3.455
84
P LNG064 Lung Cancer Susceptibility 3 70 3.415
85
DFF005 Diffuse Large B-Cell Lymphoma 54 3.413
86
LNG099 Lung Disease 62 3.377
87
P MYC007 Myocardial Infarction 70 3.350
88
THY029 Thyroid Carcinoma 51 3.338
89
P END044 Endometriosis 62 3.322
90
AGN016 Aging 54 3.315
91
PRT251 Proteinuria, Chronic Benign 57 3.299
92
MYL069 Myeloma, Multiple 77 3.297
93
P ADN016 Adenocarcinoma 63 3.293
94
c BCT013 Bacterial Pneumonia 48 3.290
95
P LPS004 Lupus Erythematosus 61 3.279
96
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.252
97
PLY150 Polykaryocytosis Inducer 29 3.220
98
PRT036 Peritonitis 65 3.217
99
c ACT134 Acute Liver Failure 59 3.215
100
P LVR013 Liver Disease 69 3.179
101
ESP021 Esophageal Cancer 83 3.178
102
HYP066 Hyperglycemia 61 3.172
103
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.146
104
P BRS044 Breast Adenocarcinoma 58 3.138
105
47X002 47,xyy 48 3.112
106
c LKM063 Leukemia, Chronic Myeloid 71 3.097
107
c PRC016 Pre-Eclampsia 65 3.083
108
FRB001 Farber Lipogranulomatosis 58 3.053
109
P PRS040 Prostate Cancer 95 3.049
110
c SML038 Small Cell Cancer of the Lung 69 3.037
111
SVR001 Severe Acute Respiratory Syndrome 67 3.014
112
P GLM007 Glomerulonephritis 60 3.012
113
CVD001 Covid-19 57 3.012
114
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.008
115
PLM134 Pulmonary Fibrosis, Idiopathic 76 3.006
116
ACT098 Acute Erythroid Leukemia 55 2.993
117
c HYP836 Hypercholesterolemia, Familial, 1 73 2.993
118
FBR012 Fabry Disease 70 2.986
119
P MSC005 Muscular Dystrophy 67 2.968
120
P LKM062 Leukemia, Acute Lymphoblastic 69 2.966
121
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.959
122
c SCN036 Secondary Progressive Multiple Sclerosis 55 2.953
123
P NRP001 Neuropathy 60 2.918
124
P LKM071 Leukemia, Chronic Lymphocytic 75 2.912
125
P DNG005 Dengue Virus 56 2.912
126
P CHR345 Chronic Pain 50 2.890
127
48X005 48,xyyy 39 2.880
128
P EST001 Estrogen-Receptor Positive Breast Cancer 49 2.877
129
c FML015 Familial Nephrotic Syndrome 48 2.855
130
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.847
131
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.847
132
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.847
133
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.847
134
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.847
135
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.847
136
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.847
137
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.847
138
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.847
139
P LKD001 Leukodystrophy 59 2.844
140
P LNG032 Lung Cancer 98 2.830
141
BCT022 Bacterial Infectious Disease 56 2.827
142
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.806
143
URT010 Ureteral Obstruction 45 2.789
144
P DBT009 Diabetes Mellitus 67 2.789
145
P MLN008 Melanoma 76 2.764
146
P PNC044 Pancreatitis 61 2.757
147
c SYS001 Systemic Lupus Erythematosus 87 2.739
148
TXC005 Toxic Shock Syndrome 62 2.739
149
CHL065 Cholangiocarcinoma 58 2.730
150
INT079 Intrahepatic Cholangiocarcinoma 51 2.730
151
CRH001 Crohn's Disease 80 2.726
152
P KLZ004 Kala-Azar 1 41 2.721
153
LSH001 Leishmaniasis 64 2.721
154
c TYP009 Type 2 Diabetes Mellitus 92 2.692
155
P HNT016 Huntington Disease 73 2.692
156
INS001 Insulinoma 59 2.692
157
c NMN015 Niemann-Pick Disease, Type C1 68 2.677
158
ADN018 Adenoma 59 2.677
159
P RHN004 Rhinitis 57 2.643
160
NNL006 Non-Alcoholic Steatohepatitis 54 2.600
161
TRM010 Traumatic Brain Injury 51 2.600
162
c HNT011 Huntington Disease-Like 3 34 2.596
163
ART140 Arteries, Anomalies of 53 2.590
164
LPP008 Lipoprotein Quantitative Trait Locus 65 2.590
165
GLC003 Glucose Intolerance 54 2.590
166
CHL068 Cholestasis 61 2.590
167
INS024 Insulin-Like Growth Factor I 78 2.556
168
ATR057 Atrioventricular Block 54 2.556
169
P GLM040 Glioma Susceptibility 1 71 2.546
170
P THR014 Thrombocytopenia 66 2.546
171
MLG169 Malignant Astrocytoma 57 2.546
172
c ATM075 Autoimmune Encephalitis 40 2.539
173
ALL003 Allergic Rhinitis 67 2.511
174
P VSC011 Vasculitis 61 2.509
175
P KRB001 Krabbe Disease 69 2.500
176
ALL006 Allergic Asthma 56 2.490
177
P ENC004 Encephalitis 61 2.490
178
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.457
179
BRK010 Burkitt Lymphoma 66 2.457
180
P LTR001 Lateral Sclerosis 58 2.457
181
P PRD008 Periodontitis 64 2.439
182
MCL006 Macular Retinal Edema 57 2.436
183
SPN186 Spinal Cord Injury 61 2.418
184
LYM009 Lymphocytic Choriomeningitis 46 2.387
185
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.383
186
c HNT004 Huntington Disease-Like 2 52 2.383
187
c ACT027 Acute Pancreatitis 60 2.377
188
FDL002 Food Allergy 47 2.358
189
KPS004 Kaposi Sarcoma 77 2.333
190
CHG001 Chagas Disease 66 2.333
191
SPL018 Splenomegaly 49 2.333
192
c ACT071 Acute Kidney Failure 60 2.318
193
OVR094 Ovarian Epithelial Cancer 39 2.318
194
PLC002 Plica Syndrome 35 2.316
195
SYN007 Synovitis 55 2.316
196
MLR004 Malaria 80 2.295
197
c CHR684 Chronic Kidney Disease 69 2.277
198
P RHB003 Rhabdomyosarcoma 66 2.274
199
P MSC003 Muscular Atrophy 52 2.266
200
MSC157 Muscular Dystrophy, Duchenne Type 79 2.263
201
END086 End Stage Renal Disease 52 2.227
202
P KDN018 Kidney Disease 72 2.218
203
c SCL052 Scleroderma, Familial Progressive 61 2.156
204
STR067 Stroke, Ischemic 80 2.156
205
MNT001 Mantle Cell Lymphoma 67 2.156
206
CRB039 Cerebrovascular Disease 66 2.156
207
P GRF003 Graft-Versus-Host Disease 71 2.135
208
ANC002 Anca-Associated Vasculitis 44 2.131
209
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.123
210
P DRR001 Diarrhea 55 2.101
211
c ACT075 Acute Myocardial Infarction 56 2.098
212
PNC129 Pancreatic Adenocarcinoma 65 2.098
213
P PRP019 Peripheral Nervous System Disease 58 2.098
215
RTN020 Retinal Vascular Disease 46 2.093
216
P MYC008 Myocarditis 59 2.093
217
RHB024 Rhabdomyosarcoma 2 67 2.069
218
P RTN016 Retinal Degeneration 52 2.069
219
MSL001 Measles 61 2.069
220
c MCR115 Microvascular Complications of Diabetes 5 65 2.036
221
P FBR017 Fibrosarcoma 56 2.036
222
P EYD002 Eye Disease 57 2.036
223
BRN056 Bronchopulmonary Dysplasia 56 2.036
224
LMY002 Leiomyoma 51 2.024
225
P ART021 Arteriosclerosis 54 2.024
226
KLD004 Keloid Disorder 39 2.024
227
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.013
228
P HRT032 Heart Disease 81 2.013
229
P CRN300 Coronary Heart Disease 1 73 1.988
230
HLX001 Helix Syndrome 48 1.972
231
IMP005 Impotence 52 1.972
232
SJG002 Sjogren-Larsson Syndrome 54 1.961
233
c MST023 Mesothelioma, Malignant 56 1.954
234
THR024 Thrombosis 56 1.954
235
PRM013 Premature Menopause 58 1.954
236
P BNG032 Benign Mesothelioma 53 1.954
237
c TYP008 Type 1 Diabetes Mellitus 70 1.952
238
P HYP098 Hypereosinophilic Syndrome 66 1.952
239
P CYS018 Cystitis 59 1.935
240
P BLD134 Bladder Cancer 79 1.904
241
SPP011 Suppression of Tumorigenicity 12 61 1.904
242
DFC004 Deficiency Anemia 74 1.893
243
P MTC003 Metachromatic Leukodystrophy 71 1.893
244
c NMN014 Niemann-Pick Disease, Type C2 49 1.893
245
CLR030 Clear Cell Renal Cell Carcinoma 54 1.893
246
P MYP004 Myopathy 67 1.882
247
NRT004 Neuritis 53 1.882
248
c THY107 Thymoma, Familial 42 1.831
249
EST002 Estrogen-Receptor Negative Breast Cancer 45 1.831
250
P SKN015 Skin Carcinoma 71 1.831
251
CRY005 Cryptococcosis 60 1.831
252
P THY023 Thymoma 64 1.831
253
HYP080 Hypogonadism 50 1.831
254
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.829
255
DSS032 Disease by Infectious Agent 55 1.829
256
P FLL037 Follicular Lymphoma 74 1.829
257
P INT143 Interstitial Cystitis 60 1.828
258
SND001 Sandhoff Disease 66 1.826
259
NRL016 Neural Tube Defects 81 1.826
260
DSS009 Disseminated Intravascular Coagulation 57 1.826
261
ANG020 Angiosarcoma 64 1.789
262
c PRM108 Primary Progressive Multiple Sclerosis 51 1.768
263
MDD018 Middle East Respiratory Syndrome 44 1.768
264
CHC001 Chickenpox 57 1.768
265
P OST002 Osteoporosis 76 1.760
266
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.760
267
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.760
268
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.760
269
c BRN108 Branchiootic Syndrome 1 62 1.753
270
DNG002 Dengue Hemorrhagic Fever 60 1.753
271
P TYS001 Tay-Sachs Disease 69 1.706
272
P HRP006 Herpes Simplex 65 1.706
273
GTR002 Goiter 53 1.706
274
ANT081 Antigen Defined by Monoclonal Antibody T87 14 1.688
275
MRG003 Marginal Zone B-Cell Lymphoma 52 1.688
276
P PLY014 Polycystic Kidney Disease 69 1.688
277
DGN001 Degenerative Disc Disease 49 1.688
278
SPN035 Spindle Cell Sarcoma 54 1.688
279
P CRN024 Corneal Disease 44 1.688
280
SRC014 Sarcoma 65 1.688
281
P BND020 Bone Disease 59 1.688
282
LVR012 Liver Cirrhosis 63 1.688
283
LYS002 Lysosomal Storage Disease 51 1.685
284
PRT013 Portal Hypertension 59 1.669
285
P OVR046 Ovarian Cyst 46 1.669
286
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.642
287
TRT001 Teratocarcinoma 42 1.642
288
P GNG009 Gangliosidosis 44 1.637
289
P SZR006 Seizure Disorder 70 1.610
290
P NSP012 Nasopharyngeal Carcinoma 61 1.610
291
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 1.610
292
CHK001 Chikungunya 60 1.610
293
c ACT073 Acute Leukemia 58 1.610
294
P TRM003 Tremor 48 1.610
295
OST012 Osteoarthritis 77 1.610
296
CMB007 Combined Immunodeficiency 57 1.610
297
P HYP086 Hypothyroidism 69 1.610
298
CNG034 Congestive Heart Failure 69 1.610
299
c HPT016 Hepatitis B 62 1.610
300
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.575
301
TNG009 Tongue Squamous Cell Carcinoma 43 1.575
302
P PRK057 Parkinson Disease, Late-Onset 80 1.574
303
MTB004 Metabolic Acidosis 48 1.574
304
CHD004 Chudley-Mccullough Syndrome 48 1.574
305
P OPT009 Optic Neuritis 57 1.574
306
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.574
307
NDL007 Nodular Goiter 48 1.574
308
P APL001 Aplastic Anemia 73 1.525
309
P CHN012 Chondrosarcoma 57 1.525
310
HYP114 Hypertensive Nephropathy 36 1.525
312
P ECL001 Eclampsia 52 1.525
313
PST028 Post-Traumatic Stress Disorder 59 1.525
314
ANX004 Anoxia 40 1.501
315
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.501
316
c NMN013 Niemann-Pick Disease, Type a 63 1.501
317
HRW001 Hair Whorl 35 1.501
318
P ACN011 Acne 57 1.501
319
SFT003 Soft Tissue Sarcoma 57 1.501
320
P PLY041 Polymyositis 59 1.468
321
P HMR003 Hemorrhagic Disease 59 1.468
322
CNT047 Contact Dermatitis 57 1.468
323
CHL123 Chlamydia 58 1.432
324
OVR029 Ovarian Hyperstimulation Syndrome 63 1.432
325
c ATR087 Atrial Standstill 1 74 1.432
326
LMY014 Leiomyoma, Uterine 56 1.432
327
ORL015 Oral Squamous Cell Carcinoma 43 1.432
328
P PLM034 Pulmonary Emphysema 58 1.432
329
ILS001 Ileus 50 1.432
330
P CHR071 Charcot-Marie-Tooth Disease 64 1.432
331
SKN005 Skin Atrophy 41 1.432
332
TTH006 Tooth Disease 51 1.432
333
MCR013 Microphthalmia 60 1.432
334
INT066 Interstitial Lung Disease 60 1.432
335
ANK001 Ankylosis 51 1.432
336
VSC002 Vascular Dementia 60 1.432
337
SYS003 Systolic Heart Failure 49 1.432
338
P ENC018 Encephalopathy 62 1.432
339
SPN019 Spondylolisthesis 52 1.423
340
P MJR001 Major Depressive Disorder 68 1.423
341
P EMB005 Embryonal Rhabdomyosarcoma 53 1.423
342
MNT002 Mental Depression 57 1.423
343
OST003 Osteonecrosis 61 1.423
344
P GRV001 Graves' Disease 55 1.423
345
P HPT021 Hepatitis 69 1.423
346
CLN015 Colon Adenocarcinoma 65 1.423
347
MNN009 Meningoencephalitis 48 1.423
348
P INF032 Infertility 57 1.423
349
P KDN017 Kidney Cancer 61 1.423
350
STT001 Status Epilepticus 59 1.423
351
P BNC003 Bone Cancer 58 1.423
352
HYP060 Hyperinsulinism 54 1.423
353
DPR016 Depression 65 1.423
354
P ATS364 Autism 69 1.339
355
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.339
356
EWN003 Ewing Sarcoma 70 1.339
357
c HPT073 Hepatitis C Virus 71 1.339
358
P SPP010 Suppressor of Tumorigenicity 3 51 1.339
359
P EPL164 Epilepsy 68 1.339
360
c HPT001 Hepatitis C 62 1.339
361
P ART023 Arthropathy 61 1.339
362
SLP001 Sleeping Sickness 56 1.339
363
P RSP003 Respiratory Failure 74 1.339
364
EMB004 Embryonal Carcinoma 56 1.339
365
P OST001 Osteopetrosis 71 1.339
366
c ACT135 Acute Graft Versus Host Disease 51 1.339
367
STM007 Stomatitis 54 1.339
368
P SCH015 Schizophrenia 74 1.325
369
PRS047 Prostatitis 58 1.325
370
CRT013 Carotid Stenosis 51 1.325
371
P CRD119 Cardiac Arrest 67 1.325
372
c ESS001 Essential Tremor 57 1.325
373
PLS007 Plasmodium Falciparum Malaria 52 1.325
374
ANR040 Aneurysm 61 1.325
375
P PLY019 Polyneuropathy 52 1.317
376
P OVR082 Overgrowth Syndrome 49 1.256
377
LPG001 Lipogranulomatosis 29 1.256
378
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.251
379
CRD132 Cardiac Conduction Defect 60 1.245
380
c RTN047 Retinitis Pigmentosa 18 46 1.245
381
ANX010 Anxiety 70 1.245
382
P MCR129 Microvascular Complications of Diabetes 1 68 1.245
383
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.245
384
c PNC106 Pancreatic Agenesis 1 51 1.245
385
LRG008 Large Granular Lymphocyte Leukemia 34 1.245
386
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.245
387
SYS071 Systemic Autoimmune Disease 35 1.245
388
SKN022 Skin Squamous Cell Carcinoma 54 1.245
389
ACT084 Acute Stress Disorder 54 1.245
390
P SNS001 Sensorineural Hearing Loss 59 1.245
391
c MCR112 Microvascular Complications of Diabetes 2 42 1.245
392
RSP002 Respiratory Syncytial Virus Infectious Disease 52 1.245
393
BRN028 Brain Cancer 74 1.245
394
THR004 Thrombocytosis 53 1.245
395
ATN004 Autonomic Neuropathy 42 1.245
396
P GLL018 Gallbladder Cancer 53 1.245
397
PNC034 Pancreas Disease 50 1.245
398
HML018 Homologous Wasting Disease 21 1.245
399
HMP009 Haemophilus Influenzae 41 1.245
400
ILT001 Ileitis 48 1.199
401
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.199
402
P MDL005 Medulloblastoma 75 1.199
403
CRN030 Coronary Stenosis 50 1.199
404
ALL010 Allergic Contact Dermatitis 56 1.199
405
P UVT001 Uveitis 57 1.191
406
TTN003 Tetanus 65 1.191
407
c GM1007 Gm1 Gangliosidosis 65 1.191
408
PLG002 Plague 58 1.191
409
LYM133 Lymphoma, Hodgkin, Classic 74 1.138
410
P RTT002 Rett Syndrome 79 1.138
411
c OPT053 Optic Atrophy 1 62 1.138
412
PRP027 Peripheral Vascular Disease 71 1.138
414
c MJR022 Major Affective Disorder 8 38 1.138
415
c ATS007 Autism Spectrum Disorder 72 1.138
416
P FTL001 Fetal Alcohol Syndrome 55 1.138
417
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 29 1.138
418
KLD003 Keloid Formation 34 1.138
419
HSH003 Hashimoto Thyroiditis 60 1.138
420
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.138
421
c MJR024 Major Affective Disorder 9 41 1.138
422
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 31 1.138
423
c GLC092 Glaucoma, Primary Open Angle 62 1.138
424
P OPN001 Open-Angle Glaucoma 55 1.138
425
VSC003 Visceral Leishmaniasis 55 1.138
426
HPT022 Hepatoblastoma 54 1.138
427
DBT010 Diabetic Neuropathy 54 1.138
428
IGG001 Iga Glomerulonephritis 50 1.138
429
NRN001 Neuroendocrine Carcinoma 47 1.138
430
P PRT096 Peritoneal Mesothelioma 49 1.138
431
P BPL003 Bipolar Disorder 56 1.138
432
THY123 Thyroid Gland Follicular Carcinoma 55 1.138
433
MRK001 Merkel Cell Carcinoma 64 1.138
434
P THY032 Thyroiditis 57 1.138
435
NSP002 Nasopharyngitis 45 1.138
436
THY006 Thymus Lymphoma 27 1.138
437
P MLN007 Male Infertility 56 1.138
438
P FCL005 Focal Segmental Glomerulosclerosis 57 1.138
439
PPL022 Papilloma 53 1.138
440
P HYP069 Hyperparathyroidism 62 1.138
441
SQM002 Squamous Cell Papilloma 46 1.138
442
SNS003 Sensory Peripheral Neuropathy 52 1.138
443
CRN027 Corneal Neovascularization 47 1.138
444
PRP030 Purpura 54 1.138
445
MNN017 Mononeuropathy 41 1.138
446
ART006 Arthus Reaction 40 1.138
447
P BRN022 Bronchiectasis 60 1.138
448
CRB090 Cerebral Hypoxia 42 1.138
449
BLR013 Biliary Tract Cancer 43 1.138
450
PNC060 Punctate Porokeratosis 28 1.138
451
END057 Endometrial Cancer 72 1.123
452
ATS010 Autosomal Recessive Disease 42 1.123
453
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 1.123
454
P MLG056 Malignant Hyperthermia 66 1.123
455
P MNN013 Meningitis 65 1.123
456
HPT004 Hepatic Coma 43 1.034
457
HPT019 Hepatic Encephalopathy 59 1.034
458
P ESS003 Essential Thrombocythemia 69 1.034
459
c HMC039 Hemochromatosis, Type 1 73 1.012
460
P WSK001 Wiskott-Aldrich Syndrome 72 1.012
461
P SJG008 Sjogren Syndrome 61 1.012
462
PSR001 Psoriatic Arthritis 62 1.012
463
CRV035 Cervical Cancer 73 1.012
464
P MYC084 Mycobacterium Tuberculosis 1 68 1.012
465
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.012
466
MYL009 Myelodysplastic Syndrome 67 1.012
467
LMB062 Limb Ischemia 55 1.012
468
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 1.012
469
P URN019 Urinary Tract Infection 49 1.012
470
P CRB045 Cerebellar Hypoplasia 40 1.012
471
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.012
472
LGN006 Legionnaire Disease 52 1.012
473
CLR109 Colorectal Adenocarcinoma 50 1.012
474
OCL006 Ocular Hypertension 53 1.012
475
ADN001 Adenosine Deaminase Deficiency 59 1.012
476
P OLG002 Oligodendroglioma 66 1.012
477
PHG002 Phagocyte Bactericidal Dysfunction 34 1.012
478
P MST009 Mastocytosis 64 1.012
479
ART016 Aortic Aneurysm 68 1.012
480
MYF001 Myofibroma 42 1.012
481
EXT034 Extrinsic Allergic Alveolitis 57 1.012
482
PYR009 Pyridoxine Deficiency Anemia 35 1.012
483
HMT002 Hematologic Cancer 61 1.012
484
RCK004 Rickets 68 1.012
485
TCK001 Tick-Borne Encephalitis 59 1.012
486
P HYP061 Hypertrophic Cardiomyopathy 69 1.012
487
PNC001 Pancytopenia 53 1.012
488
LWC001 Low Compliance Bladder 45 1.012
489
c ACT068 Acute Cystitis 61 1.012
490
CNS004 Constipation 56 1.012
491
BLR008 Bilirubin Metabolic Disorder 57 1.012
492
P NPH005 Nephronophthisis 56 1.012
493
BRC012 Brucellosis 66 1.012
494
P MCR010 Microcephaly 60 1.012
495
BRN024 Bronchitis 67 1.012
496
P SCL048 Sclerosteosis 58 1.012
497
c SVR005 Severe Pre-Eclampsia 50 1.012
499
ATN005 Autonomic Dysfunction 46 1.012
500
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 1.012
501
P TRN020 Turner Syndrome 67 0.975
502
SMT004 Smith-Lemli-Opitz Syndrome 70 0.973
503
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.973
504
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.973
505
P HYP750 Hypertriglyceridemia, Familial 62 0.973
506
ICH054 Ichthyosis, X-Linked 52 0.973
507
P SPN046 Spinal Muscular Atrophy 63 0.973
508
P HYD006 Hydrocephalus 61 0.973
509
P DMY001 Demyelinating Polyneuropathy 41 0.973
510
ERL001 Early Myoclonic Encephalopathy 62 0.973
511
c GM2006 Gm2 Gangliosidosis 46 0.973
512
c CHR417 Chronic Graft Versus Host Disease 55 0.973
513
RST023 Resting Heart Rate, Variation in 40 0.888
514
P MCL001 Mucolipidosis 49 0.888
515
c CHR711 Chronic Asthma 41 0.888
516
ENT011 Enterocolitis 55 0.888
517
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.888
518
LPD009 Lipid Storage Disease 45 0.888
520
P PLY018 Polycythemia 56 0.888
521
CHL147 Chlamydia Pneumonia 47 0.888
522
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.888
523
MDD011 Mood Disorder 62 0.888
524
ACD003 Acid Sphingomyelinase Deficiency 32 0.888
525
PRN019 Perinatal Necrotizing Enterocolitis 60 0.888
526
HPT070 Hepatosplenic T-Cell Lymphoma 36 0.867
527
c GCH015 Gaucher Disease, Type I 68 0.848
528
P DBT005 Diabetes Insipidus 54 0.848
529
P VTR007 Vitreoretinopathy 46 0.848
530
CRT072 Creutzfeldt-Jakob Disease 68 0.848
531
ALC007 Alcohol Dependence 66 0.848
532
GST092 Gastroesophageal Reflux 61 0.848
533
ANG054 Angina Pectoris 66 0.848
534
ADR016 Adrenal Cortical Carcinoma 62 0.848
535
PRP080 Peripheral Artery Disease 54 0.848
536
P SLP006 Sleep Apnea 69 0.848
537
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 0.848
538
BRR014 Barrett Esophagus 66 0.848
539
MCR191 Microscopic Colitis 46 0.848
540
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 0.848
541
HMN047 Human Cytomegalovirus Infection 57 0.848
542
P LYM033 Lymphoproliferative Syndrome 59 0.848
543
c ATM022 Autoimmune Myocarditis 36 0.848
544
P PLV020 Pelvic Organ Prolapse 58 0.848
545
c PSR017 Psoriasis 2 53 0.848
546
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.848
547
c WLM013 Wilms Tumor 1 66 0.848
548
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.848
549
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 0.848
550
P SLV026 Salivary Gland Carcinoma 58 0.848
551
P OVR106 Ovarian Clear Cell Carcinoma 44 0.848
552
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.848
553
SCH012 Schizoaffective Disorder 50 0.848
554
CMP010 Complex Regional Pain Syndrome 60 0.848
555
P MVM001 Movement Disease 61 0.848
556
HMG002 Hemoglobinuria 50 0.848
557
P VNT002 Ventricular Septal Defect 58 0.848
558
ADR004 Adrenal Cortical Adenocarcinoma 38 0.848
559
PLM001 Pulmonary Tuberculosis 69 0.848
560
P EPT012 Epithelioid Sarcoma 41 0.848
561
MLG079 Malignant Pleural Mesothelioma 42 0.848
562
DFF016 Diffuse Astrocytoma 45 0.848
563
IMP004 Impetigo 48 0.848
564
P DRM010 Dermatomyositis 61 0.848
565
KRN001 Korean Hemorrhagic Fever 35 0.848
566
c ATM104 Autoimmune Vasculitis 37 0.848
567
DNG003 Dengue Disease 65 0.848
568
P NTR004 Neutropenia 63 0.848
569
P HMN010 Hemangioma 62 0.848
570
HNT002 Hantavirus Pulmonary Syndrome 55 0.848
571
c ATM011 Autoimmune Hepatitis 63 0.848
572
RTR008 Root Resorption 44 0.848
573
INT030 Intracranial Aneurysm 55 0.848
574
HNC001 Henoch-Schoenlein Purpura 54 0.848
575
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.848
576
c INF023 Inflammatory Breast Carcinoma 49 0.848
577
GST050 Gastrointestinal System Disease 55 0.848
578
ORL004 Oral Submucous Fibrosis 56 0.848
579
P CYS039 Cystic Kidney Disease 53 0.848
580
VSC006 Vascular Cancer 46 0.848
581
ORL011 Oral Cancer 60 0.848
582
BRN049 Brain Tumor, Childhood 28 0.848
583
PRS129 Prostatic Hyperplasia, Benign 49 0.794
584
P MYS003 Myasthenia Gravis 68 0.794
585
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.794
586
P MTR004 Maturity-Onset Diabetes of the Young 68 0.794
587
P FML011 Familial Adenomatous Polyposis 71 0.794
588
HYP001 Hypochromic Microcytic Anemia 37 0.794
589
P HRD021 Hereditary Sensory Neuropathy 48 0.794
590
KSH004 Kashin-Beck Disease 38 0.794
591
ECT026 Ectopic Pregnancy 48 0.794
592
P SLL003 Salla Disease 45 0.794
593
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.794
594
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.794
595
c HYP595 Hypertension, Essential 85 0.794
596
FCS014 Fucosidase Regulator 15 0.794
597
PCK003 Pick Disease of Brain 69 0.794
598
HPT067 Hepatocellular Adenoma 43 0.794
600
INT007 Intermediate Coronary Syndrome 54 0.794
601
P HML002 Hemolytic Anemia 62 0.794
602
P SYS005 Systemic Scleroderma 74 0.794
603
LKD026 Leukodystrophy, Progressive, Early Childhood-Onset 24 0.794
604
PRS021 Prostatic Adenoma 43 0.794
605
PRS045 Prostatic Hypertrophy 53 0.794
606
P HYP076 Hyperthyroidism 53 0.794
607
P TMP001 Temporal Lobe Epilepsy 49 0.794
608
HRP004 Herpes Zoster 61 0.794
609
HYD038 Hydrops Fetalis, Nonimmune 59 0.762
610
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.762
611
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.762
612
c LYM150 Lymphatic Malformation 7 38 0.762
613
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.762
614
c NPH055 Nephrotic Syndrome, Type 1 52 0.762
615
IMM039 Immune Hydrops Fetalis 33 0.762
616
c DRR009 Diarrhea 6 45 0.762
617
VSL002 Visual Epilepsy 39 0.762
618
P PTS002 Ptosis 52 0.762
619
c PNS012 Paine Syndrome 60 0.690
620
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.690
621
THR123 Thrombotic Microangiopathy 40 0.688
622
P RTN008 Retinitis Pigmentosa 80 0.688
623
CD4008 Cd4/cd8 T-Cell Ratio 19 0.688
624
c ATM099 Autoimmune Uveitis 45 0.688
625
NPH113 Nephroma 37 0.688
626
c HRD201 Hereditary Sensory and Autonomic Neuropathy Type 1 43 0.688
627
CLR108 Colorectal Adenoma 64 0.688
628
PLY001 Polycythemia Vera 69 0.688
629
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 53 0.688
630
NRR001 Neuroretinitis 42 0.688
631
OST017 Osteomyelitis 63 0.688
632
ARG004 Argyria 26 0.688
633
c LKD031 Leukodystrophy, Hypomyelinating, 18 25 0.688
634
FML063 Familial Glucocorticoid Deficiency 58 0.688
635
RTN023 Retinitis 46 0.688
636
c VRL010 Viral Hepatitis 53 0.688
637
VCC001 Vaccinia 47 0.688
638
CNN005 Connective Tissue Disease 67 0.688
639
P PLY020 Polyradiculoneuropathy 46 0.688
640
c FTL071 Fetal Akinesia Deformation Sequence 3 30 0.688
641
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.688
642
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.688
643
c DLT002 Dilated Cardiomyopathy 78 0.688
644
TRN018 Transitional Cell Carcinoma 56 0.688
645
DPH001 Diphtheria 59 0.688
646
c PRM005 Primary Hyperparathyroidism 59 0.688
647
P PLY011 Polycystic Ovary Syndrome 57 0.688
648
c FML021 Familial Hypercholesterolemia 72 0.688
649
GST023 Gastric Ulcer 52 0.688
650
P CRD246 Cardiovascular System Disease 56 0.688
651
c MLG002 Malignant Peritoneal Mesothelioma 42 0.562
652
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 41 0.562
653
P SKL032 Skeletal Muscle Disease 25 0.562
654
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.562
655
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.562
656
c MCL013 Mucolipidosis Iv 65 0.562
657
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.562
658
RTN017 Retinal Detachment 60 0.562
659
SPN252 Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy 45 0.562
660
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 52 0.562
661
HMN044 Human Immunodeficiency Virus Type 1 78 0.562
662
HYP457 Hypertrophic Scars 42 0.562
663
SRN001 Serine Deficiency 24 0.562
664
FRS012 First-Degree Atrioventricular Block 39 0.562
665
BCT021 Bacterial Sepsis 43 0.562
666
CHL159 Childhood-Onset Asthma 30 0.562
667
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.562
668
RHM028 Rheumatic Heart Disease 56 0.562
669
IMM167 Immune Deficiency Disease 78 0.562
670
c DPH024 Diaphragmatic Hernia, Congenital 64 0.562
671
P SPN301 Spinocerebellar Ataxia 2 59 0.562
672
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.562
673
MRG013 Mirage Syndrome 44 0.562
674
c DFN263 Deafness, Autosomal Recessive 68 25 0.562
675
DNH001 Donohue Syndrome 61 0.562
676
c DFN111 Deafness, Autosomal Recessive 35 35 0.562
677
ICH020 Ichthyosis Prematurity Syndrome 40 0.562
678
MYL005 Myelofibrosis 71 0.562
679
SBC001 Subacute Sclerosing Panencephalitis 53 0.562
680
STR033 Storm Syndrome 27 0.562
681
TST044 Testicular Torsion 45 0.562
682
P SCL018 Scoliosis 57 0.562
683
PRM329 Premature Aging 36 0.562
684
P AMY004 Amyloidosis 70 0.562
685
AMB001 Amebiasis 57 0.562
686
VRL011 Viral Infectious Disease 61 0.562
687
P CHL066 Cholangitis 52 0.562
688
CHR074 Choriocarcinoma 46 0.562
689
P CRV031 Cervical Adenocarcinoma 48 0.562
690
P GST044 Gastritis 55 0.562
691
MTH009 Mouth Disease 57 0.562
692
NRM005 Neuromuscular Disease 63 0.562
693
ACT049 Acute Disseminated Encephalomyelitis 48 0.562
694
CHL045 Choline Deficiency Disease 39 0.562
695
PNT038 Peanut Allergy 46 0.562
696
TRY001 Trypanosomiasis 50 0.562
697
P GLL022 Guillain-Barre Syndrome 60 0.562
698
PRV004 Periventricular Leukomalacia 52 0.562
699
DNT012 Dental Caries 53 0.562
700
BLR001 Biliary Atresia 55 0.562
701
KRT009 Keratosis 53 0.562
702
HGH043 High Grade Glioma 45 0.562
703
GST033 Gestational Diabetes 61 0.562
704
SPS004 Spastic Quadriplegia 40 0.562
705
STR008 Strongyloidiasis 52 0.562
706
P CRN026 Corneal Edema 42 0.562
707
P PRN023 Prion Disease 60 0.562
708
P CNJ013 Conjunctivitis 66 0.562
709
PLS009 Plasma Cell Neoplasm 64 0.562
710
P RTN018 Retinal Disease 53 0.562
711
GLY031 Glycoproteinosis 49 0.562
712
MMM001 Mammary Paget's Disease 53 0.562
713
NWC001 Newcastle Disease 47 0.562
714
QDR001 Quadriplegia 50 0.562
715
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.562
716
HST011 Histoplasmosis 55 0.562
717
P RTN022 Retinal Vein Occlusion 54 0.562
718
P ACT105 Acute Mountain Sickness 52 0.562
719
HDN002 Head Injury 44 0.562
720
P CRB088 Cerebral Atrophy 33 0.562
721
DYS073 Dysphagia 53 0.562
722
DDN006 Duodenitis 50 0.562
723
P RRT020 Rare Tumor 39 0.451
724
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.451
725
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.451
726
SKN019 Skin Melanoma 71 0.451
727
P RRH023 Rare Hereditary Hemochromatosis 54 0.451
728
EPD006 Epidermolysis Bullosa Acquisita 48 0.451
729
HMS001 Hemosiderosis 48 0.451
730
c SCN007 Secondary Hyperparathyroidism 51 0.451
731
P EPD016 Epidermolysis Bullosa 53 0.451
732
FCS002 Fucosidosis 62 0.397
733
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.397
734
P DCR003 Dacryoadenitis 44 0.397
735
ADR022 Adrenomyeloneuropathy 39 0.397
736
ERY014 Erythrokeratoderma 26 0.397
737
PLY100 Polyploidy 36 0.397
738
GLM044 Glomerular Disease 35 0.397
739
SDD008 Sudden Sensorineural Hearing Loss 41 0.397
740
P SCH017 Schindler Disease 37 0.397
741
HYP855 Hyperpigmentation of the Skin 26 0.397
742
THY128 Thyroid Tumor 35 0.397
743
c AMY088 Amyotrophic Lateral Sclerosis 3 31 0.397
744
c STR040 Stargardt Disease 3 34 0.397
745
c DWL002 Dowling-Degos Disease 1 58 0.397
746
ADR007 Adrenoleukodystrophy 73 0.397
747
FRG010 Fragile X Tremor/ataxia Syndrome 44 0.397
748
c 46X049 46,xy Sex Reversal 2 49 0.397
749
P LPR021 Leprosy 3 71 0.397
750
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.397
751
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 0.397
752
LYM007 Lymphangioleiomyomatosis 68 0.397
753
c PRK025 Parkinson Disease 10 33 0.397
754
c PRM196 Premature Ovarian Failure 1 59 0.397
755
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 0.397
756
P MYS005 Myositis 56 0.397
757
c NRP033 Neuropathy, Hereditary Sensory and Autonomic, Type Ia 43 0.397
758
CLF027 Cleft Palate, Isolated 64 0.397
759
c BLD146 Blood Group, P1pk System 28 0.397
760
c THR092 Thrombophilia Due to Thrombin Defect 74 0.397
761
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.397
762
VLV047 Volvulus of Midgut 52 0.397
763
ABT001 Abetalipoproteinemia 68 0.397
764
c MGR028 Migraine with or Without Aura 1 64 0.397
765
c CNG415 Congenital Disorder of Glycosylation, Type Ia 59 0.397
766
c SKN065 Skin/hair/eye Pigmentation, Variation in, 1 27 0.397
767
CHR005 Chorioamnionitis 50 0.397
768
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.397
769
THR099 Third-Degree Atrioventricular Block 42 0.397
770
PRP036 Peripheral T-Cell Lymphoma 53 0.397
771
HMR023 Hemorrhagic Cystitis 43 0.397
772
DRG013 Drug-Induced Lupus Erythematosus 49 0.397
773
PYR010 Peyronie's Disease 50 0.397
774
ATM100 Autoimmune Optic Neuritis 28 0.397
775
DVR006 Diversion Colitis 28 0.397
776
P ATR011 Atrial Fibrillation 66 0.397
777
RSP021 Respiratory Allergy 41 0.397
778
MLD018 Mild Cognitive Impairment 48 0.397
779
HLC007 Helicobacter Pylori Infection 67 0.397
780
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 0.397
781
WLS001 Wilson Disease 70 0.397
782
LKC009 Leukocyte Adhesion Deficiency, Type I 70 0.397
783
ICH001 Ichthyosis Vulgaris 53 0.397
784
c PRG020 Paragangliomas 3 39 0.397
785
c DMN005 Diamond-Blackfan Anemia 2 28 0.397
786
c HNT010 Huntington Disease-Like 1 55 0.397
787
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.397
788
SCK003 Sickle Cell Anemia 74 0.397
789
GLC106 Glucocorticoid Resistance, Generalized 48 0.397
790
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.397
791
KWS002 Kawasaki Disease 65 0.397
792
c CNG411 Congenital Disorder of Glycosylation, Type in 67 0.397
793
ACT119 Acute Promyelocytic Leukemia 62 0.397
794
c NRP040 Neuropathy, Hereditary Sensory and Autonomic, Type Ic 42 0.397
795
c CHL119 Cholangitis, Primary Sclerosing 58 0.397
796
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 50 0.397
797
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.397
798
GLC042 Glucocorticoid Deficiency 1 50 0.397
799
GLC053 Glucocorticoid Deficiency 3 20 0.397
800
CHD001 Chediak-Higashi Syndrome 67 0.397
801
CHR072 Chordoma 57 0.397
802
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 0.397
803
WHM001 Whim Syndrome 60 0.397
804
OCL069 Ocular Motor Apraxia 57 0.397
805
SCT005 Scott Syndrome 50 0.397
806
c TBR025 Tuberous Sclerosis 1 84 0.397
807
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.397
808
MLT157 Multiple System Atrophy 1 69 0.397
809
AMY086 Amyotrophy, Hereditary Neuralgic 45 0.397
810
P PYR039 Peyronie Disease 39 0.397
812
HYP020 Hyperprolactinemia 63 0.397
813
c SPS160 Spastic Paraplegia 73, Autosomal Dominant 38 0.397
814
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.397
815
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.397
816
PNG002 Pain Agnosia 51 0.397
817
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.397
818
AGG012 Aggressive Nk-Cell Leukemia 46 0.397
819
CRR012 Cirrhotic Cardiomyopathy 22 0.397
820
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.397
821
IMM200 Immunodeficiency 62 19 0.397
822
PRC002 Paracoccidioidomycosis 54 0.397
823
CRY014 Cryptococcal Meningitis 48 0.397
824
ACT003 Acute Kidney Tubular Necrosis 46 0.397
825
P PRK039 Parkinsonism 55 0.397
826
CWP001 Cowpox 45 0.397
827
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 0.397
828
CTN007 Cutaneous Leishmaniasis 62 0.397
829
URM002 Uremia 47 0.397
830
AVN001 Avian Influenza 61 0.397
831
MLL001 Molluscum Contagiosum 48 0.397
832
NRM001 Neuromyelitis Optica 61 0.397
833
P NRC002 Narcolepsy 56 0.397
834
IRD001 Iridocyclitis 53 0.397
835
RSC001 Rosacea 55 0.397
836
ACH005 Achalasia 55 0.397
837
CHR066 Chronic Fatigue Syndrome 60 0.397
838
P RRN010 Rare Neurodegenerative Disease 14 0.397
839
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.397
840
P PTT006 Pituitary Adenoma 55 0.397
841
DDN004 Duodenogastric Reflux 31 0.397
842
CHL067 Cholecystitis 60 0.397
843
ANG018 Angiomyolipoma 46 0.397
844
GLL017 Gallbladder Adenocarcinoma 42 0.397
845
GST040 Gastric Adenocarcinoma 67 0.397
846
EXT010 Extramedullary Plasmacytoma 46 0.397
847
PLS011 Plasmacytoma 56 0.397
848
LNG039 Lung Squamous Cell Carcinoma 57 0.397
849
P PNC025 Panic Disorder 52 0.397
850
c VRL007 Viral Encephalitis 50 0.397
851
CLR003 Clear Cell Adenocarcinoma 50 0.397
852
ANT024 Anthrax Disease 58 0.397
853
MYL001 Myelitis 50 0.397
854
MCN008 Mucinous Cystadenocarcinoma 39 0.397
855
KDN015 Kidney Angiomyolipoma 46 0.397
856
P KRT007 Keratoconus 50 0.397
857
SLC006 Silicosis 56 0.397
858
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.397
859
PRM004 Primary Amebic Meningoencephalitis 27 0.397
860
EPS001 Epstein-Barr Virus Hepatitis 32 0.397
861
BLD171 Blood Group, Lewis System 20 0.397
862
PLV003 Pelvic Inflammatory Disease 55 0.397
863
XRP001 Xerophthalmia 41 0.397
864
SLD003 Sialadenitis 48 0.397
865
AMY003 Amyotrophic Neuralgia 41 0.397
866
TLN003 Telangiectasis 51 0.397
867
P DMN002 Dementia 66 0.397
868
RTN003 Retinal Ischemia 49 0.397
869
PRM236 Primary Biliary Cholangitis 60 0.397
870
END041 Endometrial Adenocarcinoma 64 0.397
871
c BSL007 Basal Cell Carcinoma 68 0.397
872
P HYP035 Hypophosphatasia 62 0.397
873
P SCL009 Sclerosing Cholangitis 48 0.397
874
SPP004 Suppurative Cholangitis 23 0.397
875
P DDN001 Duodenal Ulcer 53 0.397
876
P BRS053 Breast Fibroadenoma 49 0.397
877
CCC002 Coccidiosis 50 0.397
878
BCL002 B Cell Deficiency 41 0.397
879
P CRN037 Craniosynostosis 68 0.397
880
CYS014 Cystadenocarcinoma 51 0.397
881
P TBR001 Tuberous Sclerosis 69 0.397
882
P AGM001 Agammaglobulinemia 68 0.397
883
c ATM089 Autoimmune Neuropathy 28 0.397
884
KHN001 Kuhnt-Junius Degeneration 48 0.397
885
LYM017 Lyme Disease 62 0.397
886
GRD001 Giardiasis 46 0.397
887
c MLG069 Malignant Hypertension 46 0.397
888
KRT002 Keratomalacia 55 0.397
889
P END033 Endocarditis 58 0.397
890
c INH020 Inherited Metabolic Disorder 48 0.397
891
P PRL003 Proliferative Glomerulonephritis 43 0.397
892
IMM001 Immune-Complex Glomerulonephritis 36 0.397
893
P INT068 Intestinal Disease 53 0.397
894
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.397
895
PLC008 Placenta Disease 49 0.397
896
CRT015 Carotid Artery Occlusion 45 0.397
897
P TRT010 Teratoma 51 0.397
898
SRS001 Serous Cystadenocarcinoma 52 0.397
899
ANP005 Anaplastic Astrocytoma 57 0.397
900
P MLT074 Multiple Endocrine Neoplasia 59 0.397
901
P TCD001 Tic Disorder 49 0.397
902
THY025 Thymus Cancer 55 0.397
903
c CNT035 Central Nervous System Disease 54 0.397
904
P LRY019 Laryngitis 53 0.397
905
GST045 Gastroenteritis 58 0.397
906
INC003 Inclusion Conjunctivitis 35 0.397
907
DNT008 Denture Stomatitis 35 0.397
908
P EHL001 Ehlers-Danlos Syndrome 58 0.397
909
P URT039 Urticaria 58 0.397
910
P NRM002 Normal Pressure Hydrocephalus 49 0.397
911
KRT001 Keratoconjunctivitis Sicca 50 0.397
912
TLR001 Tularemia 56 0.397
913
HDR002 Hidradenitis Suppurativa 54 0.397
914
HDR003 Hidradenitis 50 0.397
915
ENC005 Encephalomalacia 44 0.397
916
CRB037 Cerebral Palsy 67 0.397
917
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.397
918
c JVN010 Juvenile Rheumatoid Arthritis 66 0.397
919
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.397
920
GRN017 Granulocytopenia 42 0.397
921
HYP056 Hypoglycemia 65 0.397
922
IRR002 Irritable Bowel Syndrome 65 0.397
923
HNS001 Hansen's Disease 32 0.397
924
HRP009 Herpes Simplex Encephalitis 58 0.397
925
c LKM005 Leukemia, T-Cell, Chronic 34 0.397
926
P HDC001 Headache 57 0.397
927
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.397
928
MCP033 Mucopolysaccharidoses 44 0.397
929
PRN039 Paraneoplastic Syndromes 37 0.397
930
SRF006 Surfactant Dysfunction 33 0.397
931
P MYC033 Myoclonus 47 0.397
932
CND006 Candida Glabrata 30 0.397
933
c CNG216 Congenital Hydrocephalus 53 0.397
934
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.397
935
EXN003 Exencephaly 30 0.397
936
P NRV007 Nervous System Disease 67 0.397
937
c HMN022 Human T-Cell Leukemia Virus Type 2 33 0.397
938
PDT025 Pediatric Multiple Sclerosis 35 0.397
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