Search results for SQSTM1

620 hits were found for SQSTM1

# Family MCID Name MIFTS Score
1
c PGT007 Paget Disease of Bone 3 39 47.475
2
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 64 43.025
3
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 40 40.472
4
P PGT001 Paget's Disease of Bone 60 39.967
5
c PGT009 Paget Disease of Bone 2, Early-Onset 34 36.327
6
c AMY091 Amyotrophic Lateral Sclerosis 1 87 34.383
7
PCK003 Pick Disease of Brain 70 29.371
8
NRD027 Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy, Childhood-Onset 24 26.606
9
MYP120 Myopathy, Distal, with Rimmed Vacuoles 34 21.076
10
P LTR001 Lateral Sclerosis 57 20.478
11
NNK001 Nonaka Myopathy 58 19.946
12
SPS188 Spastic Paraplegia-Paget Disease of Bone Syndrome 25 18.688
13
FRN006 Frontotemporal Dementia 68 18.656
14
P DMN002 Dementia 65 17.244
15
P HPT023 Hepatocellular Carcinoma 95 16.031
16
P ALZ034 Alzheimer Disease 87 15.340
17
P MYP004 Myopathy 67 15.313
18
P OVR042 Ovarian Cancer 88 15.300
19
P DYS154 Dystonia 64 14.635
20
P HNT016 Huntington Disease 73 13.613
21
P PRS040 Prostate Cancer 95 13.523
22
P PRK057 Parkinson Disease, Late-Onset 79 13.331
23
P MTR014 Motor Neuron Disease 65 12.776
24
MMM001 Mammary Paget's Disease 53 12.766
25
LVR012 Liver Cirrhosis 62 11.608
26
INC002 Inclusion Body Myositis 56 10.832
27
P MSC003 Muscular Atrophy 52 10.640
28
MLT177 Multisystem Proteinopathy 31 10.393
29
c HRD026 Hereditary Ataxia 46 10.222
30
MLT157 Multiple System Atrophy 1 69 10.172
31
CYS010 Cystinosis 61 10.172
32
FML345 Familial Expansile Osteolysis 46 9.736
33
ACT119 Acute Promyelocytic Leukemia 62 9.579
34
P SPN046 Spinal Muscular Atrophy 62 9.544
35
PRS037 Periostitis 40 9.498
36
c AMY088 Amyotrophic Lateral Sclerosis 3 33 9.388
37
P MCH002 Machado-Joseph Disease 62 9.388
38
WLN001 Welander Distal Myopathy 35 8.413
39
MYC013 Mycobacterium Abscessus 42 7.313
40
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 6.638
41
DMN031 Dementia, Lewy Body 65 6.638
42
DNN001 Danon Disease 59 6.638
43
c SPN325 Spinocerebellar Ataxia, Autosomal Recessive 20 47 6.638
44
c DMN049 Diamond-Blackfan Anemia 20 31 6.638
46
c PRK085 Parkinson Disease 1, Autosomal Dominant 50 6.638
47
c SPN191 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 47 6.638
48
DSS008 Disease of Mental Health 74 6.638
49
P BRS044 Breast Adenocarcinoma 58 6.638
50
P BRS047 Breast Cancer 97 2.567
51
SQM006 Squamous Cell Carcinoma 59 2.458
52
ORL015 Oral Squamous Cell Carcinoma 43 2.184
53
P BND020 Bone Disease 60 2.137
54
GLB002 Glioblastoma 67 2.008
55
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.833
56
FTT001 Fatty Liver Disease 61 1.794
57
NNL006 Non-Alcoholic Steatohepatitis 54 1.770
59
BNR002 Bone Resorption Disease 47 1.719
60
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.716
61
P PNC035 Pancreatic Cancer 87 1.671
62
P LNG032 Lung Cancer 98 1.668
63
P MYS079 Miyoshi Muscular Dystrophy 53 1.608
64
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.592
65
P MYL006 Myeloid Leukemia 60 1.570
66
c LKM061 Leukemia, Acute Myeloid 83 1.538
67
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.516
68
GLM045 Glioma 62 1.505
69
GLL048 Glial Tumor 51 1.505
70
P BCL017 B-Cell Lymphoma 57 1.457
71
P MYS005 Myositis 55 1.444
72
MYL069 Myeloma, Multiple 76 1.403
73
OST159 Osteogenic Sarcoma 66 1.391
74
P CLR023 Colorectal Cancer 100 1.370
75
AGN016 Aging 53 1.326
76
P GST053 Gastric Cancer 82 1.290
77
ORL011 Oral Cancer 60 1.252
78
ATH013 Atherosclerosis Susceptibility 63 1.238
79
P LKM002 Leukemia 65 1.238
80
c SML038 Small Cell Cancer of the Lung 68 1.223
81
KPS004 Kaposi Sarcoma 76 1.210
82
P MLN008 Melanoma 75 1.163
83
P LNG064 Lung Cancer Susceptibility 3 69 1.146
84
P PRK039 Parkinsonism 55 1.146
85
P TBR001 Tuberous Sclerosis 69 1.109
86
P KDN017 Kidney Cancer 60 1.109
87
c TBR025 Tuberous Sclerosis 1 84 1.089
88
ALK017 Alk-Positive Large B-Cell Lymphoma 19 1.089
89
P NRB001 Neuroblastoma 66 1.081
90
THY029 Thyroid Carcinoma 55 1.057
91
SPL018 Splenomegaly 47 1.044
92
P PRN023 Prion Disease 60 1.018
93
c OPT053 Optic Atrophy 1 62 1.005
94
P LVR013 Liver Disease 68 1.005
95
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.005
96
P ENC004 Encephalitis 61 1.005
97
P NSP012 Nasopharyngeal Carcinoma 60 0.991
98
CYT002 Cytokine Deficiency 43 0.988
99
P EYD002 Eye Disease 57 0.976
100
LYS002 Lysosomal Storage Disease 51 0.976
101
MSL001 Measles 61 0.976
102
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.961
103
MTH009 Mouth Disease 57 0.961
104
LNG039 Lung Squamous Cell Carcinoma 57 0.961
105
CHL068 Cholestasis 61 0.953
106
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.946
107
END057 Endometrial Cancer 76 0.946
108
PPL002 Papillary Carcinoma 46 0.946
109
APH002 Aphasia 55 0.929
110
c BRN108 Branchiootic Syndrome 1 63 0.929
111
HLX001 Helix Syndrome 47 0.929
112
P PNM007 Pneumonia 64 0.929
113
PLY150 Polykaryocytosis Inducer 29 0.912
114
SPN035 Spindle Cell Sarcoma 51 0.912
115
END062 Endometrial Hyperplasia 47 0.912
116
SRC014 Sarcoma 64 0.912
117
PRG007 Progressive Bulbar Palsy 33 0.912
118
DYS073 Dysphagia 53 0.912
119
CYS001 Cystic Fibrosis 77 0.894
120
TXC005 Toxic Shock Syndrome 61 0.894
121
P MYC084 Mycobacterium Tuberculosis 1 68 0.876
122
FBR009 Fibrous Dysplasia 48 0.876
123
c PRC016 Pre-Eclampsia 64 0.876
124
P OVR082 Overgrowth Syndrome 41 0.876
125
NRN008 Neuronal Intranuclear Inclusion Disease 45 0.873
126
PLY114 Polyglucosan Body Myopathy 2 25 0.873
127
c TRM029 Tremor, Hereditary Essential, 6 19 0.873
128
c FRN060 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 6 28 0.872
129
c FRN059 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 49 0.872
130
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.855
131
P FBR003 Fibrous Histiocytoma 43 0.855
132
STM007 Stomatitis 52 0.855
133
CRH001 Crohn's Disease 80 0.855
134
APR001 Apraxia 51 0.834
135
CRH005 Crohn's Colitis 53 0.834
136
P INC029 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 1 38 0.834
137
MLD018 Mild Cognitive Impairment 48 0.834
138
P PRP019 Peripheral Nervous System Disease 57 0.834
139
PST011 Pustulosis of Palm and Sole 52 0.834
140
P SKN015 Skin Carcinoma 71 0.834
141
JPN002 Japanese Encephalitis 61 0.834
142
BRN028 Brain Cancer 73 0.834
143
UDD002 Udd Distal Myopathy - Tibial Muscular Dystrophy 9 0.834
144
P PSR002 Psoriasis 63 0.834
145
P AMY004 Amyloidosis 69 0.834
146
c ATS432 Autosomal Dominant Distal Myopathy 24 0.834
147
ATS010 Autosomal Recessive Disease 42 0.810
148
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.810
149
P LKM062 Leukemia, Acute Lymphoblastic 69 0.810
150
PRP016 Paraplegia 52 0.810
151
P ADN016 Adenocarcinoma 63 0.810
152
P PLM036 Pulmonary Fibrosis 65 0.810
153
P NMN002 Niemann-Pick Disease 60 0.810
154
P NRP001 Neuropathy 59 0.810
155
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.784
156
c TYP009 Type 2 Diabetes Mellitus 91 0.784
157
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.784
158
P BLD134 Bladder Cancer 79 0.784
159
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.784
160
P MYF003 Myofibrillar Myopathy 50 0.784
161
P PLY041 Polymyositis 58 0.784
162
P VSC007 Vascular Disease 62 0.784
163
CLR030 Clear Cell Renal Cell Carcinoma 53 0.784
164
SYN007 Synovitis 54 0.784
165
PLC002 Plica Syndrome 35 0.784
166
OST012 Osteoarthritis 77 0.784
167
P MSC005 Muscular Dystrophy 66 0.784
169
GLC084 Glaucoma, Normal Tension 45 0.755
170
c CRB191 Cerebral Cavernous Malformations 2 45 0.755
171
c CRB094 Cerebral Cavernous Malformations 3 41 0.755
172
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.755
173
P CRB048 Cerebral Cavernous Malformations 63 0.755
174
c NMN016 Niemann-Pick Disease, Type B 56 0.755
175
ATM095 Autoimmune Disease 61 0.755
176
INF058 Inflammatory Myofibroblastic Tumor 45 0.755
177
CHR073 Choreatic Disease 53 0.755
178
OVR094 Ovarian Epithelial Cancer 39 0.755
179
P ENC018 Encephalopathy 62 0.755
180
P DRM053 Dermatitis, Atopic 65 0.720
181
c ERL056 Early-Onset Parkinson's Disease 39 0.720
182
SLC006 Silicosis 55 0.720
183
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.720
184
GST040 Gastric Adenocarcinoma 66 0.720
185
PRK046 Parkin Type of Early-Onset Parkinson Disease 21 0.720
186
P RRN010 Rare Neurodegenerative Disease 14 0.720
187
MLR004 Malaria 77 0.674
188
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 60 0.674
189
P DRR001 Diarrhea 55 0.674
190
NLX003 Neu-Laxova Syndrome 2 47 0.674
191
c LRG001 Large Cell Carcinoma 48 0.674
192
ADN018 Adenoma 58 0.674
193
GST045 Gastroenteritis 58 0.674
194
BLR001 Biliary Atresia 55 0.674
195
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.674
196
BRN071 Brain Injury 50 0.633
197
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.564
198
P CHN012 Chondrosarcoma 56 0.564
199
P PSD003 Pseudohypoaldosteronism 45 0.564
200
P DRM010 Dermatomyositis 61 0.564
201
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.564
202
PRT058 Pure Autonomic Failure 58 0.564
203
TRM010 Traumatic Brain Injury 50 0.517
204
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.505
205
HYP266 Hypoxia 56 0.492
206
ISC004 Ischemia 61 0.467
207
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.397
208
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.397
209
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.397
210
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.397
211
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.397
212
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.397
213
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.397
214
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.397
215
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.397
216
TBL029 Tubulin, Beta 28 0.381
217
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.365
218
c ATR087 Atrial Standstill 1 74 0.365
219
CRB004 Cerebral Artery Occlusion 45 0.365
220
HYP066 Hyperglycemia 60 0.348
221
c MCR133 Microvascular Complications of Diabetes 4 41 0.330
222
c MCR113 Microvascular Complications of Diabetes 3 52 0.330
223
c MCR130 Microvascular Complications of Diabetes 6 41 0.330
224
c MCR120 Microvascular Complications of Diabetes 7 47 0.330
225
HMN044 Human Immunodeficiency Virus Type 1 76 0.330
226
c HPT016 Hepatitis B 62 0.330
227
c THY107 Thymoma, Familial 42 0.311
228
P THY023 Thymoma 64 0.311
229
c DLT002 Dilated Cardiomyopathy 79 0.311
230
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.291
231
c LKM063 Leukemia, Chronic Myeloid 70 0.291
232
LPD008 Lipid Metabolism Disorder 61 0.291
233
P HPT021 Hepatitis 68 0.291
234
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.270
235
c MCR115 Microvascular Complications of Diabetes 5 65 0.270
236
c HRD010 Hereditary Spastic Paraplegia 65 0.270
237
P HRP006 Herpes Simplex 65 0.270
238
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.246
239
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 52 0.246
240
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.246
241
c PCH010 Pachyonychia Congenita 3 43 0.246
242
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.246
243
SVR004 Severe Combined Immunodeficiency 70 0.246
244
NWC001 Newcastle Disease 47 0.246
245
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.246
246
SPN027 Spinal Stenosis 58 0.246
247
DGN001 Degenerative Disc Disease 48 0.246
248
ULC004 Ulcerative Colitis 74 0.246
249
ALL014 Allergic Encephalomyelitis 34 0.246
250
47X002 47,xyy 47 0.246
251
PLY100 Polyploidy 36 0.246
252
c FNC029 Fanconi Anemia, Complementation Group I 55 0.220
253
P INF037 Inflammatory Bowel Disease 53 0.220
254
c PGT011 Paget Disease of Bone 6 25 0.220
255
P PHC003 Pheochromocytoma 70 0.220
256
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.220
257
ADR040 Adrenal Gland Pheochromocytoma 45 0.220
258
CNG034 Congestive Heart Failure 69 0.220
259
IRN002 Iron Metabolism Disease 56 0.220
260
P CRN025 Corneal Dystrophy 49 0.220
261
PNC129 Pancreatic Adenocarcinoma 64 0.220
262
c ACT073 Acute Leukemia 59 0.220
263
LMY002 Leiomyoma 51 0.220
264
OCL006 Ocular Hypertension 53 0.220
265
P RTN016 Retinal Degeneration 52 0.220
266
P TRM003 Tremor 50 0.220
267
SPS019 Spastic Paraparesis 38 0.220
268
SPN186 Spinal Cord Injury 60 0.220
269
c ACT134 Acute Liver Failure 57 0.220
270
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.191
271
PRT251 Proteinuria, Chronic Benign 58 0.191
272
RNL077 Renal Fibrosis 46 0.191
273
P RTN024 Retinoblastoma 72 0.191
274
DSS032 Disease by Infectious Agent 55 0.191
275
c SPS125 Spastic Paraplegia 15, Autosomal Recessive 51 0.191
276
LMY014 Leiomyoma, Uterine 55 0.191
277
c PGT008 Paget Disease of Bone 5, Juvenile-Onset 46 0.191
278
IMM167 Immune Deficiency Disease 76 0.191
279
P RTN008 Retinitis Pigmentosa 79 0.191
280
ESP021 Esophageal Cancer 84 0.191
281
P GLM040 Glioma Susceptibility 1 70 0.191
282
PLY068 Polysubstance Abuse 41 0.191
283
AML029 Ameloblastoma 46 0.191
284
P HMR003 Hemorrhagic Disease 59 0.191
285
c ATM011 Autoimmune Hepatitis 62 0.191
286
P GCH001 Gaucher's Disease 69 0.191
287
MLG169 Malignant Astrocytoma 57 0.191
288
P OST001 Osteopetrosis 70 0.191
289
URT010 Ureteral Obstruction 44 0.191
290
CTN004 Cutaneous Fibrous Histiocytoma 39 0.191
291
OVR063 Overnutrition 42 0.191
292
P PLY011 Polycystic Ovary Syndrome 57 0.191
293
ART074 Aortic Dissection 53 0.191
294
NRR001 Neuroretinitis 42 0.191
295
SVR001 Severe Acute Respiratory Syndrome 68 0.191
296
NRM005 Neuromuscular Disease 62 0.191
297
P PNC044 Pancreatitis 61 0.191
298
GLC003 Glucose Intolerance 53 0.191
299
P FNC004 Fanconi Syndrome 60 0.191
300
MST005 Mastitis 52 0.191
301
PRM013 Premature Menopause 57 0.191
302
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.191
303
P THR014 Thrombocytopenia 66 0.191
304
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.191
305
CRM001 Crimean-Congo Hemorrhagic Fever 51 0.191
306
P ART022 Arthritis 70 0.191
307
RTN023 Retinitis 45 0.191
308
P DBT009 Diabetes Mellitus 67 0.191
309
LNG099 Lung Disease 62 0.191
310
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.191
311
c CHR684 Chronic Kidney Disease 73 0.191
312
c LKM005 Leukemia, T-Cell, Chronic 33 0.191
313
ODN006 Odontoma 32 0.191
314
c SPS025 Spastic Paraplegia 15 30 0.191
315
FCL042 Facial Onset Sensory and Motor Neuronopathy 22 0.191
316
P CHR345 Chronic Pain 50 0.191
317
CLT003 Colitis 63 0.156
318
P SCL048 Sclerosteosis 58 0.156
319
c MJR022 Major Affective Disorder 8 37 0.156
320
c NMN014 Niemann-Pick Disease, Type C2 49 0.156
321
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 63 0.156
322
MYL009 Myelodysplastic Syndrome 67 0.156
323
P LYM118 Lymphoma 66 0.156
324
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.156
325
P RHM011 Rheumatoid Arthritis 81 0.156
326
MCL075 Macular Dystrophy, Corneal 55 0.156
327
DWN001 Down Syndrome 70 0.156
328
c MGR028 Migraine with or Without Aura 1 63 0.156
329
c MCL013 Mucolipidosis Iv 64 0.156
330
OCL069 Ocular Motor Apraxia 57 0.156
331
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.156
332
STR067 Stroke, Ischemic 79 0.156
333
BRT054 Brittle Bone Disorder 74 0.156
334
c MJR024 Major Affective Disorder 9 40 0.156
335
c FRN061 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 8 12 0.156
336
MSC007 Muscle Hypertrophy 64 0.156
337
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.156
338
P SPP010 Suppressor of Tumorigenicity 3 50 0.156
339
VCS001 Vici Syndrome 57 0.156
340
c NMN015 Niemann-Pick Disease, Type C1 68 0.156
341
P LPR021 Leprosy 3 71 0.156
342
P GRF003 Graft-Versus-Host Disease 71 0.156
343
c SPS126 Spastic Paraplegia 49, Autosomal Recessive 45 0.156
344
LGN006 Legionnaire Disease 52 0.156
345
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.156
346
c HYP836 Hypercholesterolemia, Familial, 1 73 0.156
347
c MST023 Mesothelioma, Malignant 56 0.156
348
CRV035 Cervical Cancer 72 0.156
349
PRS129 Prostatic Hyperplasia, Benign 48 0.156
350
OST003 Osteonecrosis 60 0.156
351
THR024 Thrombosis 56 0.156
352
P RSP003 Respiratory Failure 73 0.156
353
P MCL001 Mucolipidosis 49 0.156
354
CLR109 Colorectal Adenocarcinoma 50 0.156
355
HYP060 Hyperinsulinism 53 0.156
356
P BNG032 Benign Mesothelioma 53 0.156
357
P BNG095 Benign Giant Cell Tumor 43 0.156
358
THY122 Thyroid Gland Cancer 59 0.156
359
KRT009 Keratosis 52 0.156
360
GRN055 Granular Corneal Dystrophy 36 0.156
361
BCT022 Bacterial Infectious Disease 55 0.156
362
HYP026 Hypoglycemic Coma 37 0.156
363
BRN004 Brain Edema 54 0.156
364
P BPL003 Bipolar Disorder 56 0.156
365
PRS021 Prostatic Adenoma 43 0.156
366
INT066 Interstitial Lung Disease 60 0.156
367
ANV001 Anovulation 46 0.156
368
c ACT027 Acute Pancreatitis 60 0.156
369
BNG036 Bone Giant Cell Tumor 48 0.156
370
P HYP061 Hypertrophic Cardiomyopathy 68 0.156
371
PRM236 Primary Biliary Cholangitis 62 0.156
372
P ADL010 Adult Respiratory Distress Syndrome 70 0.156
373
RTN003 Retinal Ischemia 48 0.156
374
PRS045 Prostatic Hypertrophy 53 0.156
375
PRS047 Prostatitis 57 0.156
376
CNT028 Central Retinal Artery Occlusion 42 0.156
377
BRN026 Branch Retinal Artery Occlusion 41 0.156
378
SCR011 Scrapie 39 0.156
379
BRN024 Bronchitis 67 0.156
380
ACQ007 Acquired Immunodeficiency Syndrome 58 0.156
381
END086 End Stage Renal Disease 54 0.156
382
P PRD008 Periodontitis 63 0.156
383
P RTN014 Retinal Artery Occlusion 46 0.156
384
HNS001 Hansen's Disease 32 0.156
385
MYC019 Mycobacterium Marinum 29 0.156
386
MLG079 Malignant Pleural Mesothelioma 42 0.156
387
HYP056 Hypoglycemia 65 0.156
388
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.156
389
OST115 Osteonecrosis of the Jaw 40 0.156
390
MSC193 Muscular Lipidosis 23 0.156
391
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.156
392
c ATS007 Autism Spectrum Disorder 71 0.110
393
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.110
395
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.110
396
MTB004 Metabolic Acidosis 48 0.110
397
c SPN304 Spinocerebellar Ataxia 8 47 0.110
398
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 57 0.110
399
ALV005 Alveolar Soft Part Sarcoma 61 0.110
400
P FML023 Familial Hemiplegic Migraine 53 0.110
401
c AMY023 Amyotrophic Lateral Sclerosis Type 6 36 0.110
402
TNG009 Tongue Squamous Cell Carcinoma 43 0.110
403
P PRS062 Persistent Hyperplastic Primary Vitreous 48 0.110
404
P HRD021 Hereditary Sensory Neuropathy 48 0.110
405
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.110
406
c WLM013 Wilms Tumor 1 65 0.110
407
P ATS364 Autism 72 0.110
408
c PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 39 0.110
409
P NNN008 Noonan Syndrome 1 76 0.110
410
P OST002 Osteoporosis 76 0.110
411
c PRD039 Periodontitis, Aggressive, 1 47 0.110
412
LYM133 Lymphoma, Hodgkin, Classic 69 0.110
413
PPL049 Papillon-Lefevre Syndrome 65 0.110
414
HMM002 Haim-Munk Syndrome 35 0.110
415
MLB001 Mulibrey Nanism 51 0.110
416
P ALK019 Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 1 17 0.110
417
PNM010 Pneumothorax, Primary Spontaneous 58 0.110
418
P CMR001 Camurati-Engelmann Disease 58 0.110
419
SMT008 Smith-Magenis Syndrome 53 0.110
420
c GCH015 Gaucher Disease, Type I 67 0.110
421
c GLY008 Glycogen Storage Disease Ii 72 0.110
422
RTC012 Reticuloendotheliosis, X-Linked 35 0.110
423
P RTT002 Rett Syndrome 79 0.110
424
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.110
425
c SPN225 Spondyloarthropathy 1 70 0.110
426
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.110
427
INS024 Insulin-Like Growth Factor I 77 0.110
428
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.110
429
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 49 0.110
430
MYP153 Myopathy, Myofibrillar, 9, with Early Respiratory Failure 52 0.110
431
SPP011 Suppression of Tumorigenicity 12 61 0.110
432
SCK003 Sickle Cell Anemia 74 0.110
433
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.110
434
ANX010 Anxiety 70 0.110
435
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 36 0.110
436
PRP027 Peripheral Vascular Disease 71 0.110
437
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.110
438
P FML011 Familial Adenomatous Polyposis 70 0.110
439
HYP025 Hyperphosphatemia 47 0.110
440
DYS001 Dyskinetic Cerebral Palsy 31 0.110
441
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 47 0.110
442
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.110
443
c RTN129 Retinitis Pigmentosa 49 38 0.110
444
KSH004 Kashin-Beck Disease 37 0.110
445
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.110
446
SYD002 Sydenham Chorea 34 0.110
447
FTL006 Fetal Alcohol Spectrum Disorder 43 0.110
448
P ATX030 Ataxia-Telangiectasia 80 0.110
449
KRT019 Keratitis, Hereditary 66 0.110
450
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.110
451
SMT004 Smith-Lemli-Opitz Syndrome 69 0.110
452
P FRG001 Fragile X Syndrome 70 0.110
453
FBR012 Fabry Disease 71 0.110
454
c TBR026 Tuberous Sclerosis 2 71 0.110
455
P MYC007 Myocardial Infarction 69 0.110
456
GST019 Gastrointestinal Stromal Tumor 78 0.110
457
c AMY105 Amyotrophic Lateral Sclerosis 6 with or Without Frontotemporal Dementia 34 0.110
458
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.110
459
PLT004 Platelet Glycoprotein Iv Deficiency 55 0.110
460
LPT014 Leptin Deficiency or Dysfunction 77 0.110
461
c TRM017 Tremor, Hereditary Essential, 4 35 0.110
462
c CRD182 Ceroid Lipofuscinosis, Neuronal, 10 50 0.110
463
P DNG005 Dengue Virus 55 0.110
464
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 43 0.110
465
MLD001 Melioidosis 67 0.110
466
HRN029 Hearing Loss, Noise-Induced 37 0.110
467
P LKM071 Leukemia, Chronic Lymphocytic 74 0.110
468
THY111 Thyroid Carcinoma, Familial Medullary 67 0.110
469
c SPN294 Spinocerebellar Ataxia 1 53 0.110
470
P MLN069 Melanoma, Uveal 59 0.110
471
PRR007 Perry Syndrome 53 0.110
472
P SPN301 Spinocerebellar Ataxia 2 59 0.110
473
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.110
474
c SPN299 Spinocerebellar Ataxia 20 33 0.110
475
c HMP013 Hemophagocytic Lymphohistiocytosis, Familial, 3 47 0.110
476
WST005 West Nile Virus 55 0.110
477
HLC007 Helicobacter Pylori Infection 67 0.110
478
P VTL001 Vitelliform Macular Dystrophy 46 0.110
479
P FTL001 Fetal Alcohol Syndrome 55 0.110
480
c HRD201 Hereditary Sensory and Autonomic Neuropathy Type 1 44 0.110
481
P CRB045 Cerebellar Hypoplasia 40 0.110
482
ZKF001 Zika Fever 51 0.110
483
GST105 Gastroesophageal Adenocarcinoma 42 0.110
484
MMM007 Mammary Analogue Secretory Carcinoma 33 0.110
485
P NPH012 Nephrotic Syndrome 61 0.110
486
P PLY014 Polycystic Kidney Disease 71 0.110
487
DBT081 Diabetic Encephalopathy 36 0.110
488
LMB062 Limb Ischemia 55 0.110
489
P FLL037 Follicular Lymphoma 66 0.110
490
QFV001 Q Fever 61 0.110
491
BRR014 Barrett Esophagus 66 0.110
492
HND002 Hand, Foot and Mouth Disease 50 0.110
493
P CYS018 Cystitis 58 0.110
494
P HYP069 Hyperparathyroidism 62 0.110
495
PST028 Post-Traumatic Stress Disorder 58 0.110
496
P GRN010 Granular Cell Tumor 40 0.110
497
GNG005 Gangliocytoma 54 0.110
498
HYP068 Hyperostosis 47 0.110
499
DRG002 Drug-Induced Hepatitis 42 0.110
500
HYP080 Hypogonadism 49 0.110
501
SPH010 Sphingolipidosis 47 0.110
502
NRL005 Neurilemmoma 60 0.110
503
P TCD001 Tic Disorder 50 0.110
504
P GLY013 Glycogen Storage Disease 59 0.110
505
RTN020 Retinal Vascular Disease 45 0.110
506
NRT004 Neuritis 53 0.110
507
P BNC003 Bone Cancer 58 0.110
508
P BRD002 Bardet-Biedl Syndrome 66 0.110
509
P LMY004 Leiomyosarcoma 62 0.110
510
CRB037 Cerebral Palsy 66 0.110
511
PNM008 Pneumothorax 54 0.110
512
P ICH004 Ichthyosis 56 0.110
513
HMS001 Hemosiderosis 48 0.110
514
c BRD016 Bardet-Biedl Syndrome 4 44 0.110
515
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.110
516
P ALC033 Alcohol Use Disorder 67 0.110
517
P MVM001 Movement Disease 61 0.110
518
GNG002 Ganglioneuroma 52 0.110
519
P BNG030 Benign Ependymoma 51 0.110
520
CLL010 Cellular Ependymoma 58 0.110
521
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.110
522
FBR047 Fibromyalgia 57 0.110
523
SPN051 Spondylitis 51 0.110
524
P KDN018 Kidney Disease 71 0.110
525
P HRT032 Heart Disease 84 0.110
526
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.110
527
MDD018 Middle East Respiratory Syndrome 44 0.110
528
STT001 Status Epilepticus 58 0.110
529
P OVR049 Ovarian Disease 50 0.110
530
PRN022 Perineurioma 36 0.110
531
APC004 Apocrine Adenocarcinoma 37 0.110
532
ADN012 Adenocarcinoma in Situ 41 0.110
533
PLM031 Poliomyelitis 62 0.110
534
P GST044 Gastritis 55 0.110
535
MRK001 Merkel Cell Carcinoma 64 0.110
536
THY125 Thyroid Gland Medullary Carcinoma 48 0.110
537
LCL004 Localized Osteosarcoma 35 0.110
538
TST015 Testicular Disease 42 0.110
539
ORC001 Orchitis 43 0.110
540
P ART023 Arthropathy 59 0.110
541
c SCN007 Secondary Hyperparathyroidism 50 0.110
542
NRL002 Neurilemmomatosis 52 0.110
543
DMY004 Demyelinating Disease 50 0.110
544
P RHB003 Rhabdomyosarcoma 66 0.110
545
P CHR012 Chronic Granulomatous Disease 69 0.110
546
ART016 Aortic Aneurysm 68 0.110
547
ATN004 Autonomic Neuropathy 42 0.110
548
HYP043 Hyperandrogenism 47 0.110
549
GST033 Gestational Diabetes 60 0.110
550
OST011 Osteomalacia 52 0.110
551
MCR013 Microphthalmia 59 0.110
552
P HYP040 Hypospadias 51 0.110
553
c HPT003 Hepatitis a 63 0.110
554
RCK004 Rickets 64 0.110
555
PRV004 Periventricular Leukomalacia 52 0.110
556
CVD001 Covid-19 59 0.110
557
CMM005 Common Cold 55 0.110
558
P AGG001 Aggressive Periodontitis 55 0.110
559
CRY003 Cryptosporidiosis 55 0.110
560
AZS001 Azoospermia 45 0.110
561
NPH003 Nephrocalcinosis 49 0.110
562
P CRD246 Cardiovascular System Disease 55 0.110
563
ALC010 Alcoholic Cardiomyopathy 42 0.110
564
INF009 Inflammatory Spondylopathy 30 0.110
565
TLN003 Telangiectasis 51 0.110
566
PRC013 Pericarditis 53 0.110
567
P CTR002 Cataract 59 0.110
568
P RTN018 Retinal Disease 53 0.110
569
ACT084 Acute Stress Disorder 53 0.110
570
CRB039 Cerebrovascular Disease 65 0.110
571
HPT022 Hepatoblastoma 54 0.110
572
ANT024 Anthrax Disease 57 0.110
573
GSG001 Gas Gangrene 52 0.110
574
OST016 Osteochondrosis 52 0.110
575
ORL004 Oral Submucous Fibrosis 56 0.110
576
c SPS092 Spastic Paraplegia 11 37 0.110
577
SKN019 Skin Melanoma 70 0.110
578
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.110
579
P MYC008 Myocarditis 59 0.110
580
P OST009 Osteochondritis Dissecans 61 0.110
581
P INF038 Influenza 68 0.110
582
P CHL066 Cholangitis 51 0.110
583
NRF007 Neurofibroma 63 0.110
584
P NRV007 Nervous System Disease 65 0.110
585
CHC001 Chickenpox 56 0.110
586
CRT015 Carotid Artery Occlusion 45 0.110
587
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.110
588
IDP022 Idiopathic Spinal Cord Herniation 17 0.110
589
c SPS230 Spastic Paraplegia Type 49 10 0.110
590
PTT037 Pituitary Tumors 44 0.110
591
P SZR006 Seizure Disorder 69 0.110
592
BCK006 Back Pain 43 0.110
593
MCP033 Mucopolysaccharidoses 44 0.110
594
ANR040 Aneurysm 60 0.110
595
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.110
596
P CRB059 Cerebellar Degeneration 36 0.110
597
PRN029 Parainfluenza Virus Type 3 32 0.110
598
CHR178 Chromosomal Triplication 33 0.110
599
CRT033 Corticobasal Degeneration 48 0.110
600
NCR015 Necrotizing Autoimmune Myopathy 32 0.110
601
CHM008 Chmp2b Frontotemporal Dementia 12 0.110
602
c CRB051 Cerebral Cavernous Malformation, Familial 41 0.110
603
P RRH023 Rare Hereditary Hemochromatosis 52 0.110
605
FNG016 Fungal Keratitis 40 0.110
606
CMB094 Combined Dystonia 14 0.110
607
c PSD047 Pseudo-Turner Syndrome 52 0.110
608
OCL015 Oculomotor Apraxia 39 0.110
609
IDP069 Idiopathic Avascular Necrosis 23 0.110
610
CNG506 Congenital Amyoplasia 27 0.110
611
LYS029 Lysosomal Disease 30 0.110
612
P RRT020 Rare Tumor 39 0.110
613
c CHR417 Chronic Graft Versus Host Disease 55 0.110
614
HRD141 Hereditary Proximal Myopathy with Early Respiratory Failure 25 0.110
615
CVR010 Cavernous Malformation 29 0.110
616
CRB090 Cerebral Hypoxia 42 0.110
617
HDN002 Head Injury 44 0.110
618
SPS057 Spasticity 43 0.110
619
PST092 Posttransplant Acute Limbic Encephalitis 29 0.110
620
PRM329 Premature Aging 36 0.110
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