Search results for amyloidosis cerebral

515 hits were found for amyloidosis cerebral

# Family MCID Name MIFTS Score
1
CRB193 Cerebral Amyloid Angiopathy, App-Related 36 9.825
2
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 8.924
3
P CRB174 Cerebral Amyloid Angiopathy, Itm2b-Related, 2 36 4.006
4
GRS011 Gerstmann-Straussler Disease 48 3.979
5
c CRB176 Cerebral Amyloid Angiopathy, Itm2b-Related, 1 35 3.561
6
HRD084 Hereditary Cerebral Amyloid Angiopathy 15 2.951
7
CRB009 Cerebritis 41 1.152
8
P AMY004 Amyloidosis 69 1.096
9
CRB085 Cerebral Hemorrhage 47 0.283
10
ANR040 Aneurysm 61 0.277
11
P ALZ034 Alzheimer Disease 95 0.250
12
SPS057 Spasticity 41 0.249
13
THR024 Thrombosis 61 0.243
14
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.233
15
MLR004 Malaria 86 0.231
16
AGN016 Aging 65 0.226
17
P ENC018 Encephalopathy 58 0.226
18
NRN002 Neuronitis 43 0.205
19
BRN071 Brain Injury 54 0.203
20
P LYM118 Lymphoma 71 0.200
21
c HRD039 Hereditary Amyloidosis 47 0.198
22
P ART022 Arthritis 77 0.193
23
DMN002 Dementia 68 0.182
24
c CNT035 Central Nervous System Disease 65 0.182
25
P HPT021 Hepatitis 75 0.181
26
P NRP001 Neuropathy 63 0.181
27
P NRV007 Nervous System Disease 75 0.177
28
P FML018 Familial Mediterranean Fever 73 0.176
29
BRC012 Brucellosis 71 0.170
30
P RHM011 Rheumatoid Arthritis 91 0.168
31
END072 Endotheliitis 46 0.167
32
c BLD140 Blood Group, I System 37 0.163
33
c THR092 Thrombophilia Due to Thrombin Defect 61 0.156
34
P PLY019 Polyneuropathy 58 0.154
35
P AMY084 Amyloidosis, Finnish Type 40 0.148
36
P NPH012 Nephrotic Syndrome 60 0.147
37
FCT003 Factor X Deficiency 58 0.134
38
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.130
39
P BLD051 Blood Coagulation Disease 38 0.120
40
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.119
41
PLS009 Plasma Cell Neoplasm 51 0.119
42
P HMR003 Hemorrhagic Disease 61 0.118
43
VSC008 Vascular Hemostatic Disease 36 0.118
44
ART140 Arteries, Anomalies of 51 0.118
45
P ANR048 Aniridia 1 68 0.118
46
ANR038 Anorexia Nervosa 1 21 0.118
47
BLD137 Blood Group--Ahonen 17 0.118
48
P LKM002 Leukemia 75 0.117
49
VSC011 Vasculitis 66 0.116
50
HDC001 Headache 55 0.115
51
P HRT032 Heart Disease 80 0.113
52
P THY032 Thyroiditis 56 0.112
53
SPS003 Spastic Diplegia 55 0.112
54
P MYP006 Myopia 56 0.107
55
P GLM007 Glomerulonephritis 61 0.105
56
PLS011 Plasmacytoma 60 0.105
57
c AMY060 Amyloidosis, Primary Localized Cutaneous, 1 32 0.104
58
NRM005 Neuromuscular Disease 60 0.104
59
NRT004 Neuritis 55 0.104
60
LGH004 Light Chain Deposition Disease 47 0.104
61
RTN023 Retinitis 52 0.102
62
PRP019 Peripheral Nervous System Disease 53 0.097
63
P LRY019 Laryngitis 57 0.096
64
CLT003 Colitis 63 0.095
65
P MLT020 Multiple Sclerosis 85 0.095
66
ALR002 Al-Raqad Syndrome 30 0.095
67
P MYP004 Myopathy 69 0.094
68
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.094
69
P ATR011 Atrial Fibrillation 68 0.094
70
P BCL006 B-Cell Lymphomas 70 0.094
71
P DRR001 Diarrhea 60 0.091
72
HMT018 Hematopoietic Stem Cell Transplantation 58 0.089
73
HPT082 Hepatic Adenomas, Familial 52 0.088
74
P MYC084 Mycobacterium Tuberculosis 1 69 0.088
75
P KDN018 Kidney Disease 69 0.087
76
ANX010 Anxiety 72 0.086
77
ULC004 Ulcerative Colitis 80 0.086
78
P DBT009 Diabetes Mellitus 72 0.086
79
CRP001 Carpal Tunnel Syndrome 64 0.086
80
P SDR002 Siderosis 48 0.085
81
ATN004 Autonomic Neuropathy 46 0.085
82
P CRV039 Cervicitis 49 0.085
83
CNG034 Congestive Heart Failure 74 0.083
84
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.083
85
P PNC044 Pancreatitis 64 0.083
86
P LPS004 Lupus Erythematosus 69 0.083
87
SPR066 Superficial Siderosis 40 0.081
88
HMR039 Hemorrhage, Intracerebral 57 0.080
89
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.080
90
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.079
91
VSC002 Vascular Dementia 58 0.078
92
CRH001 Crohn's Disease 80 0.078
93
PRT036 Peritonitis 67 0.078
94
CRD119 Cardiac Arrest 63 0.078
95
P END033 Endocarditis 58 0.078
96
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.077
97
P PNM007 Pneumonia 70 0.076
98
CRT016 Carotid Artery Disease 58 0.075
99
c SYS001 Systemic Lupus Erythematosus 86 0.075
100
INC021 Incontinentia Pigmenti 57 0.075
101
c SPN225 Spondyloarthropathy 1 71 0.074
102
c INF145 Infantile Liver Failure Syndrome 1 33 0.073
103
P MYC007 Myocardial Infarction 81 0.073
104
P TMP003 Temporal Arteritis 67 0.072
105
P HYP086 Hypothyroidism 62 0.072
106
SCK003 Sickle Cell Anemia 73 0.071
107
c ACT134 Acute Liver Failure 52 0.071
108
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.071
109
P DBT005 Diabetes Insipidus 54 0.071
110
P MSC005 Muscular Dystrophy 66 0.070
111
P CTS001 Cutis Laxa 62 0.069
112
P PYL005 Pyelonephritis 56 0.069
113
GTR002 Goiter 53 0.069
114
P INF032 Infertility 59 0.069
115
END030 End Stage Renal Failure 59 0.069
116
DRM006 Dermatitis 67 0.068
117
P SNS014 Sinusitis 62 0.068
118
ATN005 Autonomic Dysfunction 51 0.067
119
IRN001 Iron Deficiency Anemia 55 0.067
120
BLD163 Blood Group, Dombrock System 23 0.067
121
PRT019 Protein-Losing Enteropathy 40 0.067
122
RHM027 Rheumatic Disease 62 0.066
123
XNT001 Xanthogranulomatous Pyelonephritis 32 0.066
124
P ASP006 Aspergillosis 65 0.066
125
P LVR013 Liver Disease 76 0.066
126
DFC004 Deficiency Anemia 62 0.066
127
PRP030 Purpura 61 0.065
128
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.065
129
LNG099 Lung Disease 67 0.064
130
ADN018 Adenoma 63 0.064
131
c CHR089 Chronic Kidney Failure 72 0.064
132
P INF037 Inflammatory Bowel Disease 52 0.064
133
PMS001 Poems Syndrome 64 0.063
134
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.062
135
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.062
136
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.062
137
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.062
138
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.062
139
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.062
140
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.062
141
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.062
142
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.062
143
DWN001 Down Syndrome 70 0.062
144
P PLY017 Polyarteritis Nodosa 51 0.062
145
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.061
146
P SCK002 Sick Sinus Syndrome 53 0.061
147
P RPD001 Rapidly Progressive Glomerulonephritis 48 0.061
148
ADL030 Adult-Onset Still's Disease 65 0.061
149
TRN018 Transitional Cell Carcinoma 58 0.061
150
CRT072 Creutzfeldt-Jakob Disease 65 0.060
151
PRP016 Paraplegia 53 0.060
152
c HPT001 Hepatitis C 73 0.060
153
ATM095 Autoimmune Disease 66 0.060
154
CMM004 Common Variable Immunodeficiency 71 0.060
155
SPN186 Spinal Cord Injury 67 0.060
156
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.060
157
ISC006 Ischemic Heart Disease 73 0.059
158
FBR012 Fabry Disease 72 0.059
159
P ADN016 Adenocarcinoma 71 0.059
160
PRS047 Prostatitis 59 0.059
161
P CRN018 Coronary Artery Anomaly 69 0.058
162
P PHC003 Pheochromocytoma 72 0.058
163
P LYM026 Lymphoblastic Leukemia 66 0.058
164
c ART101 Aortic Valve Disease 2 65 0.058
165
HYP056 Hypoglycemia 62 0.058
166
P LPR021 Leprosy 3 59 0.058
167
PRC013 Pericarditis 55 0.058
168
P ALP008 Alopecia 56 0.058
169
DSS009 Disseminated Intravascular Coagulation 56 0.058
170
P DLT002 Dilated Cardiomyopathy 76 0.057
171
P AGM001 Agammaglobulinemia 70 0.057
172
P ART023 Arthropathy 68 0.057
173
P CHL066 Cholangitis 52 0.057
174
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.057
175
GST039 Gastroduodenitis 33 0.057
176
CHR008 Choroiditis 47 0.057
177
APH002 Aphasia 58 0.057
178
P THR014 Thrombocytopenia 65 0.056
179
SRC014 Sarcoma 68 0.056
180
c ACT210 Acute Respiratory Distress Syndrome 63 0.056
181
MNN009 Meningoencephalitis 49 0.056
182
HRT012 Heart Valve Disease 45 0.056
183
IRN002 Iron Metabolism Disease 45 0.056
184
P CRN035 Cranial Nerve Palsy 42 0.056
185
P PRD008 Periodontitis 67 0.055
186
OST017 Osteomyelitis 64 0.055
187
PRD007 Periodontal Disease 64 0.055
188
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.055
189
P PLM037 Pulmonary Hypertension 79 0.055
190
c JVN010 Juvenile Rheumatoid Arthritis 71 0.055
191
DDN006 Duodenitis 46 0.055
192
CNN005 Connective Tissue Disease 65 0.054
193
FCL012 Facial Paralysis 50 0.054
194
AMY002 Amyloid Tumor 30 0.054
195
ALP046 Alport Syndrome, X-Linked 74 0.054
196
MCS002 Mucositis 61 0.054
197
TNS005 Tonsillitis 61 0.054
198
LYM012 Lymphoplasmacytic Lymphoma 50 0.054
199
P HYP083 Hypopituitarism 59 0.053
200
P LTR001 Lateral Sclerosis 58 0.053
201
SYN036 Syncope 46 0.053
202
MNT002 Mental Depression 60 0.053
203
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.053
204
FCT006 Factor V Deficiency 52 0.053
205
MNN017 Mononeuropathy 42 0.053
206
P PRP029 Porphyria 62 0.053
207
MTR014 Motor Neuron Disease 62 0.053
208
NRM004 Neuroma 51 0.053
209
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.053
210
P HST010 Histiocytosis 60 0.053
211
P FNC043 Fanconi Anemia, Complementation Group E 52 0.051
212
PST055 Postural Hypotension 40 0.051
213
MVM001 Movement Disease 40 0.051
214
HMS001 Hemosiderosis 50 0.051
215
P CHR071 Charcot-Marie-Tooth Disease 67 0.051
216
DST006 Diastolic Heart Failure 47 0.050
217
GST050 Gastrointestinal System Disease 66 0.050
218
ANT009 Antithrombin Iii Deficiency 58 0.050
219
ERD001 Erdheim-Chester Disease 57 0.050
220
c HPT073 Hepatitis C Virus 73 0.050
221
P PSD087 Pseudoxanthoma Elasticum 67 0.050
222
P ESP024 Esophagitis 64 0.050
223
BDD001 Budd-Chiari Syndrome 58 0.050
224
P DYS021 Dysautonomia 47 0.050
225
CRD137 Cardiogenic Shock 45 0.049
226
CST005 Castleman Disease 44 0.049
227
CHR001 Churg-Strauss Syndrome 51 0.049
228
BLS002 Blastomycosis 44 0.049
229
SLP005 Sleep Disorder 59 0.048
230
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.048
231
APL001 Aplastic Anemia 74 0.048
232
P ALG028 Alagille Syndrome 1 68 0.048
233
MCR088 Microscopic Polyangiitis 58 0.048
234
P SYP003 Syphilis 55 0.048
235
P ICH004 Ichthyosis 54 0.048
236
P INF038 Influenza 77 0.047
237
P ESS003 Essential Thrombocythemia 71 0.047
238
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.047
239
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.047
240
ACR007 Acromegaly 70 0.047
241
RLP001 Relapsing Polychondritis 55 0.047
242
ART004 Aortic Atherosclerosis 48 0.047
243
GST053 Gastric Cancer 84 0.047
244
P MYL005 Myelofibrosis 75 0.047
245
c DWL002 Dowling-Degos Disease 1 50 0.047
246
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 53 0.046
247
ATN002 Autonomic Nervous System Disease 51 0.046
248
CLL021 Collagenous Colitis 43 0.046
249
SVN002 Sveinsson Chorioretinal Atrophy 29 0.046
250
P NMN002 Niemann-Pick Disease 68 0.046
251
PCK003 Pick Disease of Brain 66 0.046
252
DFF005 Diffuse Large B-Cell Lymphoma 64 0.046
253
P MYS005 Myositis 63 0.046
254
P HYP076 Hyperthyroidism 56 0.046
255
FRN006 Frontotemporal Dementia 70 0.046
256
SCH014 Schistosomiasis 62 0.046
257
c BRN108 Branchiootic Syndrome 1 47 0.046
258
ARC002 Arachnoiditis 45 0.046
259
INS024 Insulin-Like Growth Factor I 83 0.046
260
c HPT016 Hepatitis B 68 0.046
261
ISC002 Ischemic Optic Neuropathy 48 0.046
262
BRN014 Bronchopneumonia 45 0.046
263
HYP189 Hypoadrenalism 43 0.046
264
ALN001 Aland Island Eye Disease 39 0.046
265
SLT014 Salt and Pepper Developmental Regression Syndrome 37 0.046
266
CRN036 Craniopharyngioma 63 0.045
267
P GRF003 Graft-Versus-Host Disease 72 0.044
268
P PRG013 Paraganglioma 57 0.044
269
TXC002 Toxic Encephalopathy 55 0.044
270
URM002 Uremia 52 0.044
271
CRY004 Cryoglobulinemia 49 0.044
272
P CHR012 Chronic Granulomatous Disease 69 0.044
273
P DRM010 Dermatomyositis 65 0.044
274
HRY003 Hairy Cell Leukemia 60 0.044
275
P INT070 Intestinal Obstruction 55 0.044
276
PRR002 Pure Red-Cell Aplasia 52 0.044
277
ACH005 Achalasia 52 0.044
278
HYP006 Hypertensive Heart Disease 51 0.044
279
GNG002 Ganglioneuroma 50 0.044
280
KRT008 Keratopathy 44 0.044
281
P SCL057 Scoliosis, Isolated 1 28 0.044
282
PRP027 Peripheral Vascular Disease 71 0.044
283
CNC002 Cinca Syndrome 62 0.043
284
P GST044 Gastritis 61 0.043
285
ARS001 Aarskog-Scott Syndrome 55 0.043
286
ACQ017 Acquired Von Willebrand Syndrome 40 0.043
287
FML330 Familial Lcat Deficiency 37 0.043
288
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 36 0.043
289
P CLC063 Celiac Disease 1 65 0.043
290
c CHR417 Chronic Graft Versus Host Disease 65 0.043
291
OVR029 Ovarian Hyperstimulation Syndrome 64 0.043
292
P PLY014 Polycystic Kidney Disease 60 0.043
293
SNS001 Sensorineural Hearing Loss 59 0.043
294
URN009 Urinary System Disease 58 0.043
295
TTH006 Tooth Disease 54 0.043
296
LPD016 Lipoid Proteinosis of Urbach and Wiethe 54 0.043
297
P CRB059 Cerebellar Degeneration 40 0.043
298
CYS001 Cystic Fibrosis 85 0.042
299
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.042
300
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.042
301
PHR003 Pharyngitis 59 0.042
302
P PLM006 Pulmonary Alveolar Proteinosis 49 0.042
303
GRN017 Granulocytopenia 49 0.042
304
KRT010 Kartagener Syndrome 46 0.042
305
c LKD015 Leukodystrophy, Hypomyelinating, 3 44 0.042
306
RTR011 Retroperitoneal Fibrosis 43 0.042
307
c SRC023 Sarcoidosis 2 30 0.042
308
c LSS005 Lissencephaly 1 46 0.041
309
c ALZ056 Alzheimer Disease 3 41 0.041
310
P HYP607 Hypercholesterolemia, Familial 81 0.041
311
c LKM071 Leukemia, Chronic Lymphocytic 75 0.041
312
GST019 Gastrointestinal Stromal Tumor 74 0.041
313
GNG013 Gingivitis 64 0.041
314
LNG108 Langerhans Cell Histiocytosis 63 0.041
315
P LMY004 Leiomyosarcoma 59 0.041
316
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.041
317
KRT009 Keratosis 53 0.041
318
CLC006 Calcinosis 51 0.041
319
PPL002 Papillary Carcinoma 51 0.041
320
WHP001 Whipple Disease 50 0.041
321
HMN016 Hemangioendothelioma 43 0.041
322
ADP007 Adie Pupil 41 0.041
323
PST086 Posterior Cortical Atrophy 38 0.041
324
c LKM004 Leukemia, B-Cell, Chronic 37 0.041
325
CLN006 Colonic Pseudo-Obstruction 36 0.041
326
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.041
327
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.041
328
SNL009 Senile Plaque Formation 26 0.041
329
P ANX007 Anauxetic Dysplasia 1 36 0.040
330
c TRC078 Trichohepatoenteric Syndrome 2 34 0.040
331
P RNG031 Ring Chromosome Y Syndrome 29 0.040
332
P EXN002 Exanthem 62 0.039
333
IMM158 Immune Suppression 57 0.039
334
IMM136 Immune System Disease 57 0.039
335
FNT004 Fainting 36 0.039
336
GLN010 Glanzmann Thrombasthenia 66 0.039
337
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.039
338
P MYC008 Myocarditis 58 0.039
339
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.039
340
P PRM006 Primary Biliary Cirrhosis 55 0.039
341
P CLL015 Collagen Disease 53 0.039
342
ANG054 Angina Pectoris 53 0.039
343
CLL003 Cellulitis 53 0.039
344
ATR057 Atrioventricular Block 52 0.039
345
P EPT020 Epithelioid Hemangioendothelioma 50 0.039
346
RTC005 Reticulosarcoma 49 0.039
347
CHR286 Chronic Neutrophilic Leukemia 49 0.039
348
RSD004 Rosai-Dorfman Disease 48 0.039
349
P MYS033 Miyoshi Muscular Dystrophy 1 48 0.039
350
THR035 Thrombasthenia 46 0.039
351
NTR003 Natural Killer Cell Leukemia 45 0.039
352
SPL006 Splenic Infarction 34 0.039
353
TNG002 Tangier Disease 65 0.038
354
P ALP009 Alopecia Areata 64 0.038
355
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 0.038
356
ALK013 Alkaptonuria 56 0.038
357
HYP074 Hypersensitivity Vasculitis 52 0.038
358
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.038
359
MNC006 Monoclonal Gammopathy of Uncertain Significance 49 0.038
360
HYP081 Hypolipoproteinemia 49 0.038
361
ONC007 Oncocytoma 48 0.038
362
P ICH001 Ichthyosis Vulgaris 47 0.038
363
ARC023 Arcus Corneae 40 0.038
364
c AFB002 Afibrinogenemia, Congenital 61 0.037
365
P MYS003 Myasthenia Gravis 73 0.036
366
SKN016 Skin Disease 68 0.036
367
P THY023 Thymoma 65 0.036
368
HLC007 Helicobacter Pylori Infection 64 0.036
369
c ATM011 Autoimmune Hepatitis 63 0.036
370
P TRC072 Treacher Collins Syndrome 1 61 0.036
371
ADR005 Adrenal Carcinoma 59 0.036
372
LMY002 Leiomyoma 58 0.036
373
NRN004 Neuroendocrine Tumor 58 0.036
374
P PTT006 Pituitary Adenoma 57 0.036
375
P CTN015 Cutaneous T Cell Lymphoma 56 0.036
376
MMB001 Membranoproliferative Glomerulonephritis 51 0.036
377
c INV001 Invasive Aspergillosis 51 0.036
378
ANR004 Anuria 49 0.036
379
c ACT076 Acute Myocarditis 48 0.036
380
MLT006 Multidrug-Resistant Tuberculosis 48 0.036
381
SKN027 Skin Conditions 48 0.036
382
PYL006 Pyloric Stenosis 47 0.036
383
CHN065 Choanal Atresia, Posterior 43 0.036
384
MRT007 Martsolf Syndrome 41 0.036
385
FMR003 Femoral Neuropathy 39 0.036
386
ABD004 Abdominal Tuberculosis 31 0.036
387
NCR009 Necrobiotic Xanthogranuloma 26 0.036
388
CLF051 Cleft Larynx, Posterior 24 0.036
389
IMM162 Immunoglobulin E Concentration, Serum 16 0.036
390
JNT002 Joint Disorders 60 0.035
391
P VNS003 Venous Insufficiency 53 0.035
392
BSL008 Basal Ganglia Disease 44 0.035
393
SPC010 Speech and Communication Disorders 40 0.035
394
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.035
395
LYM017 Lyme Disease 68 0.033
396
DMN031 Dementia, Lewy Body 66 0.033
397
PRT058 Pure Autonomic Failure 60 0.033
398
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.033
399
LYM019 Lymphosarcoma 58 0.033
400
GLL018 Gallbladder Cancer 67 0.033
401
INC002 Inclusion Body Myositis 64 0.033
402
P LYM025 Lymphedema 63 0.033
403
INT002 Intermittent Claudication 61 0.033
404
MRB003 Morbid Obesity 61 0.033
405
P SJG008 Sjogren Syndrome 58 0.033
406
AND002 Androgen Insensitivity Syndrome 57 0.033
407
SCH002 Schnitzler Syndrome 54 0.033
408
c CLR131 Ciliary Dyskinesia, Primary, 1 54 0.033
409
NDL013 Nodular Regenerative Hyperplasia 53 0.033
410
CRD223 Cardiac Arrhythmia 52 0.033
411
HYP732 Hyperalphalipoproteinemia 1 52 0.033
412
HMR002 Hemarthrosis 51 0.033
413
P PLM085 Pulmonary Hemosiderosis 48 0.033
414
SCT005 Scott Syndrome 48 0.033
415
PRS115 Prosthetic Joint Infection 46 0.033
416
LCH004 Lichen Disease 42 0.033
417
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.033
418
P HVY001 Heavy Chain Disease 41 0.033
419
ISC015 Ischemic Colitis 39 0.033
420
PYL004 Pyelitis 38 0.033
421
IMM003 Immunoglobulin Alpha Deficiency 37 0.033
422
ATM021 Autoimmune Inner Ear Disease 34 0.033
423
HNS001 Hansen's Disease 31 0.033
424
FCL084 Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature 30 0.033
425
NNS003 Non-Secretory Myeloma 27 0.033
426
HNM002 Hinman Syndrome 25 0.033
427
HSH003 Hashimoto Thyroiditis 67 0.031
428
VRC005 Varicose Veins 64 0.031
429
P NTR004 Neutropenia 60 0.031
430
P ALT001 Alternating Hemiplegia of Childhood 48 0.031
431
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.031
432
BSL006 Basaloid Squamous Cell Carcinoma 43 0.031
433
c ERL006 Early-Onset Familial Alzheimer Disease 38 0.031
434
ENT004 Enthesopathy 38 0.031
435
HMP001 Hemopericardium 34 0.031
436
HMM002 Haim-Munk Syndrome 31 0.031
437
MDD008 Middle Ear Adenoma 23 0.031
438
SNS004 Sensory Organ Benign Neoplasm 15 0.031
439
c MCL042 Macular Degeneration, Age-Related, 1 79 0.029
440
LYM133 Lymphoma, Hodgkin, Classic 78 0.029
441
CNR004 Cone-Rod Dystrophy 2 69 0.029
442
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.029
443
c SCL052 Scleroderma, Familial Progressive 60 0.029
444
c ALZ049 Alzheimer Disease 2 59 0.029
445
LPD008 Lipid Metabolism Disorder 59 0.029
446
ALL026 Allergic Hypersensitivity Disease 59 0.029
447
PPL022 Papilloma 58 0.029
448
IMP005 Impotence 54 0.029
449
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.029
450
P CHL069 Cholesteatoma 52 0.029
451
P OTT001 Otitis Externa 51 0.029
452
P MWT001 Mowat-Wilson Syndrome 47 0.029
453
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.029
454
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 46 0.029
455
LYM024 Lymphatic System Disease 45 0.029
456
P ANL018 Analbuminemia 45 0.029
457
DCB001 Decubitus Ulcer 44 0.029
458
c ALZ054 Alzheimer Disease 4 43 0.029
459
KWS001 Kwashiorkor 43 0.029
460
LTH045 Lutheran Suppressor, X-Linked 41 0.029
461
P FML043 Familial Idiopathic Basal Ganglia Calcification 40 0.029
462
P BRN120 Bronchus Cancer 39 0.029
463
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.029
464
GTP001 Gait Apraxia 38 0.029
465
ATY002 Atypical Choroid Plexus Papilloma 37 0.029
466
NSL006 Nasal Cavity Squamous Cell Carcinoma 35 0.029
467
CRY036 Cryptogenic Cirrhosis 34 0.029
468
CRV026 Cervical Clear Cell Adenocarcinoma 30 0.029
469
c INT282 Integumentary System Benign Neoplasm 20 0.029
470
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.025
471
ABT001 Abetalipoproteinemia 64 0.025
472
CRV038 Cervical Squamous Cell Carcinoma 61 0.025
473
ATH013 Atherosclerosis Susceptibility 59 0.025
474
P HYP724 Hyperlipoproteinemia, Type Iii 59 0.025
475
c SPN294 Spinocerebellar Ataxia 1 58 0.025
476
DCT002 Ductal Carcinoma in Situ 56 0.025
477
c INS002 in Situ Carcinoma 56 0.025
478
PLV003 Pelvic Inflammatory Disease 56 0.025
479
BLD131 Bladder Urothelial Carcinoma 55 0.025
480
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.025
481
PRP032 Porphyria Variegata 54 0.025
482
LYM008 Lymphangiosarcoma 51 0.025
483
P DYS026 Dysfibrinogenemia 51 0.025
484
c HYP739 Hyperlipoproteinemia, Type Iv 51 0.025
485
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 51 0.025
486
SPR010 Sporotrichosis 50 0.025
487
c GMM003 Gamma Heavy Chain Disease 49 0.025
488
P KRT005 Keratoacanthoma 49 0.025
489
P FML035 Familial Hyperlipidemia 48 0.025
490
HPT025 Hepatic Lipase Deficiency 48 0.025
491
NTR018 Neutrophilia, Hereditary 46 0.025
492
c NPH055 Nephrotic Syndrome, Type 1 46 0.025
493
LYM006 Lymphoepithelioma-Like Carcinoma 46 0.025
494
KPS002 Kaposiform Hemangioendothelioma 46 0.025
495
ACT058 Active Peptic Ulcer Disease 43 0.025
496
DYS015 Dysentery 43 0.025
497
ERY004 Erysipelas 43 0.025
498
CMP007 Complement Component 5 Deficiency 40 0.025
499
P CHR084 Chromosomal Disease 40 0.025
500
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 40 0.025
501
BRS056 Breast Metaplastic Carcinoma 38 0.025
502
HYP737 Hyperhidrosis, Gustatory 36 0.025
503
PRC010 Pericardial Mesothelioma 35 0.025
504
c HYP072 Hypersensitivity Reaction Type Iii Disease 35 0.025
505
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.025
506
c THY107 Thymoma, Familial 34 0.025
507
c PRM023 Pre-Malignant Neoplasm 33 0.025
508
DFF015 Diffuse Glomerulonephritis 32 0.025
509
c PRM093 Premature Ovarian Failure 7 32 0.025
510
c RNL113 Renal Failure, Progressive, with Hypertension 29 0.025
511
FBR089 Fibrosclerosis, Multifocal 28 0.025
512
c MYS011 Myasthenia Gravis Congenital 28 0.025
513
NDL010 Nodular Hidradenoma 28 0.025
514
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.025
515
P AST055 Asthma-Related Traits 1 18 0.025
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