Search results for amyloidosis cerebral

657 hits were found for amyloidosis cerebral

# Family MCID Name MIFTS Score
1
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 8.969
2
P CRB019 Cerebral Amyloid Angiopathy 58 8.427
3
DMN004 Dementia, Familial Danish 33 4.069
4
GRS011 Gerstmann-Straussler Disease 42 3.758
5
DMN032 Dementia, Familial British 36 3.644
6
c HRD084 Hereditary Cerebral Amyloid Angiopathy 15 2.907
7
CRB009 Cerebritis 39 1.050
8
P AMY004 Amyloidosis 65 0.969
9
CRB085 Cerebral Hemorrhage 46 0.269
10
ANR040 Aneurysm 57 0.250
11
SPS057 Spasticity 42 0.224
12
MLR004 Malaria 83 0.214
13
THR024 Thrombosis 57 0.212
14
BRN071 Brain Injury 52 0.189
15
NRN002 Neuronitis 41 0.187
16
P LYM118 Lymphoma 69 0.181
17
P ART022 Arthritis 75 0.172
18
P ENC018 Encephalopathy 59 0.172
19
P CRB088 Cerebral Atrophy 42 0.170
20
P HPT021 Hepatitis 69 0.163
21
DMN002 Dementia 65 0.161
22
P AMY084 Amyloidosis, Finnish Type 42 0.155
23
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.154
24
P NRP001 Neuropathy 59 0.153
25
P RHM011 Rheumatoid Arthritis 89 0.151
26
END072 Endotheliitis 42 0.149
27
P CRD011 Cardiomyopathy 68 0.141
28
STR067 Stroke, Ischemic 75 0.139
29
PRP027 Peripheral Vascular Disease 68 0.138
30
NTR005 Nutritional Deficiency Disease 36 0.137
31
ATH003 Atherosclerosis 65 0.135
32
P NPH012 Nephrotic Syndrome 59 0.134
33
P PLY019 Polyneuropathy 56 0.133
34
CRB031 Cerebral Arterial Disease 27 0.126
35
FCT003 Factor X Deficiency 61 0.122
36
P HMR003 Hemorrhagic Disease 57 0.121
37
VSC006 Vascular Cancer 51 0.118
38
P CDS001 Cadasil 55 0.112
39
CRD118 Cardiovascular Cancer 44 0.111
40
P ALZ034 Alzheimer Disease 92 0.110
41
VSC008 Vascular Hemostatic Disease 30 0.110
42
GLC077 Glucocorticoid Therapy, Response to 16 0.109
43
LGH004 Light Chain Deposition Disease 44 0.107
44
P BLD051 Blood Coagulation Disease 42 0.107
45
BLD054 Blood Protein Disease 37 0.106
46
VSC011 Vasculitis 62 0.104
47
P HRT032 Heart Disease 75 0.104
48
ATN002 Autonomic Nervous System Disease 48 0.103
49
P LKM002 Leukemia 71 0.102
50
NRM005 Neuromuscular Disease 56 0.102
51
P SPS003 Spastic Diplegia 52 0.101
52
PRP019 Peripheral Nervous System Disease 55 0.101
53
ATR060 Atrial Standstill, Digenic 51 0.099
54
PRP021 Peripheral Nervous System Neoplasm 46 0.098
55
GRW007 Growth Hormone Deficiency 50 0.097
56
P THY032 Thyroiditis 54 0.096
57
HDC001 Headache 54 0.096
58
P GLM007 Glomerulonephritis 59 0.096
59
c INH020 Inherited Metabolic Disorder 49 0.096
60
HMT018 Hematopoietic Stem Cell Transplantation 41 0.095
61
P NRV007 Nervous System Disease 71 0.095
62
PLS011 Plasmacytoma 56 0.093
63
RTN023 Retinitis 50 0.093
64
PLS010 Plasma Protein Metabolism Disease 34 0.093
65
GLT021 Glutaricaciduria, Type I 46 0.092
66
HMT002 Hematologic Cancer 64 0.091
67
ALR002 Al-Raqad Syndrome 36 0.091
68
P MYP004 Myopathy 67 0.090
69
P NRV006 Nervous System Cancer 60 0.088
70
ATN003 Autonomic Nervous System Neoplasm 40 0.087
71
PRT014 Protein S Deficiency 53 0.087
72
CLT003 Colitis 60 0.085
73
P LRY019 Laryngitis 54 0.085
74
TBR010 Tuberculosis 70 0.085
75
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.084
76
P BCL006 B-Cell Lymphomas 65 0.083
77
BRT030 Birth Defects 43 0.082
78
P DRR001 Diarrhea 60 0.081
79
ATN004 Autonomic Neuropathy 45 0.081
80
CRT016 Carotid Artery Disease 57 0.081
81
PCK002 Pick Disease 68 0.081
82
P ATR011 Atrial Fibrillation 66 0.081
83
ACR041 Acromelic Frontonasal Dysostosis 45 0.081
84
IMM025 Immunoglobulin a Deficiency 2 24 0.080
85
MRG013 Mirage Syndrome 29 0.080
86
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.079
87
AND005 Androgen Insensitivity Syndrome, Mild 16 0.079
88
P CRN178 Coronary Heart Disease 6 21 0.079
89
P CRV039 Cervicitis 45 0.077
90
ULC004 Ulcerative Colitis 76 0.076
91
CNT010 Central Nervous System Hematologic Cancer 18 0.076
92
P SDR002 Siderosis 44 0.076
93
P LPS004 Lupus Erythematosus 64 0.076
94
DFC004 Deficiency Anemia 64 0.074
95
c CRN214 Coronary Heart Disease 5 22 0.074
96
CHL068 Cholestasis 59 0.073
97
BNS002 Bone Structure Disease 37 0.072
98
P KDN018 Kidney Disease 66 0.072
99
P GLM045 Glioma 60 0.072
100
SPR066 Superficial Siderosis 34 0.072
101
P PNC044 Pancreatitis 61 0.071
102
HPT074 Hepatic Adenoma, Somatic 50 0.071
103
PRT011 Protein C Deficiency 52 0.070
104
P END033 Endocarditis 54 0.070
105
BLD053 Blood Platelet Disease 46 0.070
106
OCL009 Ocular Cancer 59 0.070
107
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.070
108
CRH001 Crohn's Disease 75 0.069
109
c SYS001 Systemic Lupus Erythematosus 86 0.069
110
P CRN035 Cranial Nerve Palsy 46 0.069
111
INC021 Incontinentia Pigmenti 59 0.069
112
FCT006 Factor V Deficiency 57 0.069
113
PRD011 Proud Syndrome 42 0.068
114
HRT007 Heart Cancer 46 0.068
115
P HRT017 Heart Tumor 32 0.068
116
c ADL079 Adult Heart Tumor 16 0.068
117
END030 End Stage Renal Failure 55 0.068
118
P PNM007 Pneumonia 68 0.068
119
P ATX004 Ataxia 53 0.068
120
P LVR013 Liver Disease 75 0.068
121
c THR092 Thrombophilia Due to Thrombin Defect 54 0.067
122
P MYC007 Myocardial Infarction 79 0.066
123
P MSC005 Muscular Dystrophy 65 0.066
124
CRD119 Cardiac Arrest 61 0.066
125
ART017 Aortic Disease 57 0.065
126
c ACT134 Acute Liver Failure 50 0.065
127
P DBT005 Diabetes Insipidus 53 0.065
128
ALN001 Aland Island Eye Disease 45 0.065
129
CNG034 Congestive Heart Failure 72 0.064
130
DRM006 Dermatitis 66 0.064
131
PRP080 Peripheral Artery Disease 37 0.064
132
SCK003 Sickle Cell Anemia 71 0.064
133
WLL006 Wells Syndrome 59 0.063
134
c CRN173 Coronary Heart Disease 8 18 0.063
135
HYP037 Hyperhomocysteinemia 50 0.063
136
c DLT001 Delta Chain Disease 13 0.063
137
GTR002 Goiter 52 0.063
138
P PYL005 Pyelonephritis 52 0.063
139
c CRN172 Coronary Heart Disease 3 19 0.062
140
PRT036 Peritonitis 63 0.062
141
P SNS014 Sinusitis 60 0.062
142
P INT001 Intrahepatic Cholestasis 59 0.062
143
ATN005 Autonomic Dysfunction 49 0.061
144
BNM001 Bone Marrow Cancer 51 0.060
145
PRM243 Primary Bone Cancer 29 0.060
146
XNT001 Xanthogranulomatous Pyelonephritis 28 0.060
147
ADN018 Adenoma 58 0.060
148
IRN001 Iron Deficiency Anemia 52 0.060
149
P OBS005 Obesity 92 0.060
150
PHY002 Physical Disorder 43 0.060
151
P ASP006 Aspergillosis 61 0.059
152
P INF037 Inflammatory Bowel Disease 63 0.058
153
P CTS001 Cutis Laxa 58 0.058
154
PRT019 Protein-Losing Enteropathy 42 0.058
155
c CRN176 Coronary Heart Disease 9 18 0.058
156
P ADN016 Adenocarcinoma 69 0.058
157
P LPR003 Leprosy 69 0.058
158
P RPD001 Rapidly Progressive Glomerulonephritis 45 0.058
159
c CRN175 Coronary Heart Disease 4 19 0.057
160
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.057
161
ADJ001 Adjustment Disorder 38 0.057
162
VND001 Vein Disease 47 0.057
163
SPN186 Spinal Cord Injury 63 0.057
164
PRP030 Purpura 58 0.057
165
P INF032 Infertility 59 0.057
166
TRN018 Transitional Cell Carcinoma 53 0.057
167
PRP016 Paraplegia 49 0.056
168
P PLM037 Pulmonary Hypertension 79 0.056
169
SRC014 Sarcoma 66 0.056
170
MTR014 Motor Neuron Disease 58 0.056
171
DWN001 Down Syndrome 66 0.056
172
P HYP086 Hypothyroidism 64 0.055
173
P KDN017 Kidney Cancer 65 0.055
174
P SCK002 Sick Sinus Syndrome 50 0.055
175
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.055
176
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.055
177
P TMP003 Temporal Arteritis 60 0.055
178
RHM027 Rheumatic Disease 58 0.055
179
BNC003 Bone Cancer 58 0.055
180
P INT063 Intellectual Disability 49 0.054
181
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.054
182
c HPT001 Hepatitis C 68 0.054
183
P LYM026 Lymphoblastic Leukemia 62 0.053
184
HYP056 Hypoglycemia 61 0.053
185
HRT012 Heart Valve Disease 40 0.053
186
FBR012 Fabry Disease 69 0.053
187
DSS009 Disseminated Intravascular Coagulation 51 0.053
188
P PLY017 Polyarteritis Nodosa 51 0.053
189
CMM004 Common Variable Immunodeficiency 68 0.052
190
c ART101 Aortic Valve Disease 2 53 0.052
191
CHR008 Choroiditis 44 0.052
192
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.052
193
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.052
194
HNM002 Hinman Syndrome 25 0.052
195
c CHR089 Chronic Kidney Failure 66 0.052
196
PMS001 Poems Syndrome 52 0.052
197
FCL012 Facial Paralysis 50 0.052
198
c DLT002 Dilated Cardiomyopathy 76 0.052
199
P CHL066 Cholangitis 42 0.052
200
GST039 Gastroduodenitis 31 0.052
201
MND006 Mondor Disease 21 0.052
202
WTH001 Withdrawal Disorder 37 0.051
203
CRN030 Coronary Stenosis 51 0.051
204
c CRN177 Coronary Heart Disease 7 20 0.051
205
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.051
206
LNG099 Lung Disease 64 0.050
207
ADL030 Adult-Onset Still's Disease 59 0.050
208
SVN001 Sveinsson Choreoretinal Atrophy 26 0.050
209
MNN009 Meningoencephalitis 47 0.050
210
P THR014 Thrombocytopenia 64 0.050
211
LPD004 Lipoid Nephrosis 48 0.050
212
SNG003 Single Ventricular Heart 22 0.050
213
TXC002 Toxic Encephalopathy 51 0.050
214
CNN005 Connective Tissue Disease 62 0.049
215
P ATP001 Atopic Dermatitis 62 0.049
216
HYP088 Hyper-Igd Syndrome 43 0.049
217
GST053 Gastric Cancer 78 0.049
218
P AGM001 Agammaglobulinemia 64 0.049
219
P PRD008 Periodontitis 63 0.049
220
PRD007 Periodontal Disease 60 0.049
221
LYM012 Lymphoplasmacytic Lymphoma 44 0.049
222
ISC006 Ischemic Heart Disease 68 0.049
223
c ACT210 Acute Respiratory Distress Syndrome 57 0.049
224
P HYP083 Hypopituitarism 54 0.049
225
P LTR001 Lateral Sclerosis 53 0.049
226
c CRN174 Coronary Heart Disease 2 20 0.049
227
P PHC003 Pheochromocytoma 71 0.048
228
P FNC043 Fanconi Anemia, Complementation Group E 55 0.048
229
P HST010 Histiocytosis 58 0.048
230
HYP006 Hypertensive Heart Disease 50 0.048
231
BRC012 Brucellosis 66 0.048
232
SYN036 Syncope 47 0.048
233
HMS001 Hemosiderosis 46 0.048
234
SPC010 Speech and Communication Disorders 41 0.047
235
CRN031 Cranial Nerve Disease 40 0.047
236
P ESP024 Esophagitis 61 0.047
237
P PRP029 Porphyria 59 0.047
238
PST055 Postural Hypotension 36 0.047
239
ART016 Aortic Aneurysm 69 0.046
240
P HRP006 Herpes Simplex 65 0.046
241
P CHR071 Charcot-Marie-Tooth Disease 67 0.046
242
MTR007 Motor Peripheral Neuropathy 37 0.046
243
ATN001 Autonomic Peripheral Neuropathy 17 0.046
244
ERD001 Erdheim-Chester Disease 52 0.046
245
OST017 Osteomyelitis 61 0.046
246
P PRT013 Portal Hypertension 60 0.046
247
PRS047 Prostatitis 56 0.046
248
P APL001 Aplastic Anemia 75 0.046
249
c HPT073 Hepatitis C Virus 73 0.046
250
P PSD087 Pseudoxanthoma Elasticum 66 0.046
251
P MYS005 Myositis 57 0.046
252
ACD009 Acid-Labile Subunit, Deficiency of 45 0.046
253
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.046
254
DDN006 Duodenitis 42 0.046
255
SLP005 Sleep Disorder 53 0.046
256
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.046
257
ACR007 Acromegaly 66 0.045
258
RLP001 Relapsing Polychondritis 50 0.045
259
CHR001 Churg-Strauss Syndrome 49 0.045
260
BLS002 Blastomycosis 42 0.045
261
c MLG068 Malignant Glioma 51 0.045
262
P RNL014 Renal Cell Carcinoma 82 0.044
263
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.044
264
INC022 Inclusion-Cell Disease 46 0.044
265
DST006 Diastolic Heart Failure 46 0.044
266
CST005 Castleman Disease 41 0.044
267
MNN017 Mononeuropathy 40 0.044
268
RTR011 Retroperitoneal Fibrosis 39 0.044
269
ALP008 Alopecia 57 0.044
270
P SYP003 Syphilis 53 0.044
271
P ICH004 Ichthyosis 52 0.044
272
MCR088 Microscopic Polyangiitis 49 0.044
273
CRN017 Coronary Thrombosis 48 0.044
274
c TRC078 Trichohepatoenteric Syndrome 2 29 0.044
275
TTH006 Tooth Disease 52 0.043
276
ART004 Aortic Atherosclerosis 46 0.043
277
P MYL005 Myelofibrosis 67 0.043
278
P ART023 Arthropathy 64 0.043
279
DBT010 Diabetic Neuropathy 55 0.043
280
CRP017 Carpal Tunnel Syndrome, Familial 43 0.043
281
CRS001 Crescentic Glomerulonephritis 42 0.043
282
P HYP120 Hypoaldosteronism 36 0.043
283
MNC004 Monoclonal Paraproteinemia 34 0.043
284
IMM044 Immunoglobulin G Deficiency 33 0.043
285
HRD059 Hereditary Peripheral Nervous Disorder 11 0.043
286
MTC056 Mitochondrial Dna Depletion Syndrome 4a 48 0.043
287
ARC002 Arachnoiditis 41 0.043
288
P ALG002 Alagille Syndrome 72 0.042
289
P NMN002 Niemann-Pick Disease 65 0.042
290
DFF005 Diffuse Large B-Cell Lymphoma 59 0.042
291
HRY003 Hairy Cell Leukemia 57 0.042
292
P LMY004 Leiomyosarcoma 55 0.042
293
P HYP076 Hyperthyroidism 55 0.042
294
KRT009 Keratosis 52 0.042
295
PPL002 Papillary Carcinoma 51 0.042
296
NRM004 Neuroma 48 0.042
297
PRR002 Pure Red-Cell Aplasia 47 0.042
298
P ATX010 Ataxia Neuropathy Spectrum 30 0.042
299
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.042
300
P CNN004 Connective Tissue Cancer 40 0.042
301
CLL021 Collagenous Colitis 39 0.042
302
ADL002 Adult Syndrome 52 0.042
303
URM002 Uremia 48 0.042
304
P DYS021 Dysautonomia 44 0.042
305
HYP189 Hypoadrenalism 37 0.042
306
ALL026 Allergic Hypersensitivity Disease 52 0.042
307
c HPT016 Hepatitis B 64 0.041
308
SNS001 Sensorineural Hearing Loss 57 0.041
309
GST050 Gastrointestinal System Disease 56 0.041
310
BRN014 Bronchopneumonia 45 0.041
311
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.041
312
P CRB059 Cerebellar Degeneration 34 0.041
313
GST019 Gastrointestinal Stromal Tumor 73 0.040
314
CHR012 Chronic Granulomatous Disease 65 0.040
315
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.040
316
P INF038 Influenza 72 0.039
317
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.039
318
RDN001 Reading Disorder 34 0.039
319
BLL006 Bullous Pemphigoid 59 0.039
320
P GST044 Gastritis 56 0.039
321
ARS001 Aarskog-Scott Syndrome 52 0.039
322
BRN022 Bronchiectasis 50 0.039
323
P SCL009 Sclerosing Cholangitis 48 0.039
324
INT067 Interstitial Nephritis 46 0.039
325
P HVY001 Heavy Chain Disease 41 0.039
326
CRY008 Cryopyrin-Associated Periodic Syndrome 34 0.039
327
INS024 Insulin-Like Growth Factor I 75 0.039
328
OVR029 Ovarian Hyperstimulation Syndrome 61 0.039
329
c CHR417 Chronic Graft Versus Host Disease 51 0.039
330
CRY004 Cryoglobulinemia 46 0.039
331
NSH001 Nasu-Hakola Disease 44 0.039
332
P MYS033 Miyoshi Muscular Dystrophy 1 42 0.039
333
ISC002 Ischemic Optic Neuropathy 37 0.039
334
AMS002 Amish Infantile Epilepsy Syndrome 35 0.039
335
IMP003 Impaired Renal Function Disease 34 0.039
336
CHL071 Child Syndrome 58 0.038
337
EXF001 Exfoliation Syndrome 57 0.038
338
KDS001 Kid Syndrome 53 0.038
339
ATY005 Atypical Teratoid Rhabdoid Tumor 52 0.038
340
P PLN008 Peeling Skin Syndrome 45 0.038
341
SKN023 Skin Tag 44 0.038
342
CYS001 Cystic Fibrosis 83 0.038
343
c CHR090 Chronic Lymphocytic Leukemia 76 0.038
344
P LNG064 Lung Cancer Susceptibility 3 62 0.038
345
P DRM010 Dermatomyositis 62 0.038
346
P ALP009 Alopecia Areata 62 0.038
347
P INT070 Intestinal Obstruction 57 0.038
348
P LYM033 Lymphoproliferative Syndrome 56 0.038
349
MCS002 Mucositis 55 0.038
350
P PLM006 Pulmonary Alveolar Proteinosis 48 0.038
351
GNG002 Ganglioneuroma 47 0.038
352
c CLL013 Cell Type Cancer 46 0.038
353
SNS003 Sensory Peripheral Neuropathy 45 0.038
354
GRN017 Granulocytopenia 44 0.038
355
c SRC023 Sarcoidosis 2 33 0.038
356
GNG013 Gingivitis 61 0.037
357
P PRG013 Paraganglioma 54 0.037
358
P MYC008 Myocarditis 54 0.037
359
P PLY014 Polycystic Kidney Disease 53 0.037
360
CLC006 Calcinosis 50 0.037
361
ATR057 Atrioventricular Block 49 0.037
362
WHP001 Whipple Disease 49 0.037
363
NTR003 Natural Killer Cell Leukemia 47 0.037
364
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.037
365
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.037
366
c BNG076 Benign Exophthalmos Syndrome 15 0.037
367
P VNS003 Venous Insufficiency 54 0.037
368
CHR031 Chromoblastomycosis 42 0.037
369
BRN005 Brain Glioblastoma Multiforme 38 0.037
370
GLB003 Globe Disease 32 0.037
371
P MCR129 Microvascular Complications of Diabetes 1 54 0.035
372
NWC001 Newcastle Disease 54 0.035
373
CRB032 Cerebral Convexity Meningioma 23 0.035
374
HDG012 Hodgkin Lymphoma 77 0.035
375
c ATS347 Autosomal Dominant Polycystic Kidney Disease 62 0.035
376
c ATM011 Autoimmune Hepatitis 60 0.035
377
ADR005 Adrenal Carcinoma 57 0.035
378
PTT006 Pituitary Adenoma 56 0.035
379
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.035
380
P PRM006 Primary Biliary Cirrhosis 51 0.035
381
CLL003 Cellulitis 51 0.035
382
P CLL015 Collagen Disease 50 0.035
383
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 49 0.035
384
RTC005 Reticulosarcoma 48 0.035
385
CRD137 Cardiogenic Shock 46 0.035
386
ANR004 Anuria 45 0.035
387
EPT020 Epithelioid Hemangioendothelioma 45 0.035
388
KRT008 Keratopathy 44 0.035
389
CHR286 Chronic Neutrophilic Leukemia 43 0.035
390
DBT002 Diabetic Autonomic Neuropathy 42 0.035
391
RSD004 Rosai-Dorfman Disease 41 0.035
392
HMN016 Hemangioendothelioma 39 0.035
393
PST086 Posterior Cortical Atrophy 32 0.035
394
CLN006 Colonic Pseudo-Obstruction 31 0.035
395
GLL018 Gallbladder Cancer 63 0.035
396
ACN002 Acanthosis Nigricans 57 0.035
397
PNN001 Panniculitis 51 0.035
398
ACT008 Actinic Keratosis 51 0.035
399
VLV044 Vulvar Intraepithelial Neoplasia 47 0.035
400
P ICH001 Ichthyosis Vulgaris 46 0.035
401
ACQ017 Acquired Von Willebrand Syndrome 37 0.035
402
SPP004 Suppurative Cholangitis 33 0.035
403
MDN002 Median Neuropathy 28 0.035
404
LPM004 Lipoma 60 0.034
405
P ACR001 Aicardi-Goutieres Syndrome 54 0.034
406
ANG020 Angiosarcoma 53 0.034
407
P TRT010 Teratoma 52 0.034
408
c ART115 Aortic Valve Disease 1 50 0.034
409
MSC072 Muscle Cancer 49 0.034
410
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.034
411
SLP001 Sleeping Sickness 48 0.034
412
BND014 Bone Development Disease 40 0.034
413
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.034
414
ACR002 Acrocapitofemoral Dysplasia 33 0.034
415
c PLN021 Peeling Skin Syndrome 3 29 0.034
416
P MYS003 Myasthenia Gravis 67 0.033
417
INC002 Inclusion Body Myositis 66 0.033
418
AND015 Androgen Insensitivity 64 0.033
419
P THY023 Thymoma 57 0.033
420
ORL011 Oral Cancer 56 0.033
421
PHR003 Pharyngitis 56 0.033
422
LMY002 Leiomyoma 54 0.033
423
P CTN015 Cutaneous T Cell Lymphoma 50 0.033
424
ANG054 Angina Pectoris 50 0.033
425
END035 Endocrine Gland Cancer 49 0.033
426
c INV001 Invasive Aspergillosis 47 0.033
427
MLT006 Multidrug-Resistant Tuberculosis 46 0.033
428
MMB001 Membranoproliferative Glomerulonephritis 46 0.033
429
KRT010 Kartagener Syndrome 45 0.033
430
SRC027 Sarcoma, Synovial 44 0.033
431
c ACT076 Acute Myocarditis 42 0.033
432
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.033
433
MRT007 Martsolf Syndrome 38 0.033
434
CHN065 Choanal Atresia, Posterior 35 0.033
435
SPL006 Splenic Infarction 35 0.033
436
C5D001 C5 Deficiency 34 0.033
437
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.033
438
ABD004 Abdominal Tuberculosis 32 0.033
439
ATM021 Autoimmune Inner Ear Disease 31 0.033
440
HNS001 Hansen's Disease 30 0.033
441
ADL086 Adolescent Idiopathic Scoliosis 30 0.033
442
NCR009 Necrobiotic Xanthogranuloma 22 0.033
443
c DYS033 Dysautonomia Like Disorder 16 0.033
444
P HPT023 Hepatocellular Carcinoma 92 0.032
445
CTS003 Coats Disease 57 0.032
446
ADM013 Adamantinoma of Long Bones 57 0.032
447
P FBR017 Fibrosarcoma 56 0.032
448
ALV010 Alveolar Soft-Part Sarcoma 54 0.032
449
MGL001 Megaloblastic Anemia 50 0.032
450
FNT004 Fainting 33 0.032
451
c ALZ012 Alzheimer Disease 12 32 0.032
452
ISL010 Isolated 17-Linked Lissencephaly 28 0.032
453
SQM006 Squamous Cell Carcinoma 70 0.031
454
P ADD001 Addison's Disease 62 0.031
455
FSC004 Fasciitis 48 0.031
456
CRR007 Cirrhosis, Cryptogenic 43 0.031
457
c PLN018 Peeling Skin Syndrome 2 40 0.031
458
ADP007 Adie Pupil 34 0.031
459
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.031
460
ATM052 Autoimmune Disease 1 25 0.031
461
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.031
462
THY028 Thyroid Cancer 69 0.030
463
SKN016 Skin Disease 66 0.030
464
MYC006 Mycosis Fungoides 66 0.030
465
GLN010 Glanzmann Thrombasthenia 63 0.030
466
P LYM025 Lymphedema 61 0.030
467
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.030
468
c SYS004 Systemic Mastocytosis 60 0.030
469
CRV038 Cervical Squamous Cell Carcinoma 60 0.030
470
MRB003 Morbid Obesity 58 0.030
471
P INT143 Interstitial Cystitis 57 0.030
472
P MST009 Mastocytosis 56 0.030
473
INT079 Intrahepatic Cholangiocarcinoma 56 0.030
474
BLD087 Bladder Cancer, Somatic 54 0.030
475
KRT002 Keratomalacia 52 0.030
476
BRS099 Breast Ductal Carcinoma 50 0.030
477
HYP074 Hypersensitivity Vasculitis 48 0.030
478
SGN002 Signet Ring Cell Adenocarcinoma 45 0.030
479
SKN027 Skin Conditions 43 0.030
480
FLL013 Follicular Dendritic Cell Sarcoma 41 0.030
481
LYM052 Lymphomatoid Papulosis 41 0.030
482
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 39 0.030
483
FMR003 Femoral Neuropathy 38 0.030
484
c GST048 Gastrointestinal System Benign Neoplasm 38 0.030
485
IDP074 Idiopathic Bronchiectasis 36 0.030
486
FXF002 Fox-Fordyce Disease 36 0.030
487
c FML015 Familial Nephrotic Syndrome 36 0.030
488
SPN060 Spondylocarpotarsal Synostosis Syndrome 34 0.030
489
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.030
490
LYM023 Lymphatic System Cancer 33 0.030
491
P CHR084 Chromosomal Disease 32 0.030
492
TRT003 Tertiary Syphilis 31 0.030
493
GST014 Gastrointestinal Lymphoma 31 0.030
494
CYS015 Cystadenofibroma 30 0.030
495
FLS001 Fils Syndrome 28 0.030
496
NMN003 Niemann–pick Disease 26 0.030
497
LNG022 Lung Acinar Adenocarcinoma 24 0.030
498
CRD006 Cardiovascular Syphilis 23 0.030
499
CML001 Cumulative Trauma Disorders 18 0.030
500
MTR078 Motor Neuropathy, Peripheral, with Dysautonomia 18 0.030
501
P OVR042 Ovarian Cancer 76 0.029
502
P NSP012 Nasopharyngeal Carcinoma 66 0.029
503
URN008 Urinary Bladder Cancer 66 0.029
504
MSL001 Measles 61 0.029
505
P NTR004 Neutropenia 59 0.029
506
PLM034 Pulmonary Emphysema 55 0.029
507
HPT022 Hepatoblastoma 55 0.029
508
PPL022 Papilloma 55 0.029
509
c AFB002 Afibrinogenemia, Congenital 54 0.029
510
NRL005 Neurilemmoma 51 0.029
511
P ALT001 Alternating Hemiplegia of Childhood 50 0.029
512
END031 Endometrial Stromal Sarcoma 50 0.029
513
RHB001 Rhabdoid Cancer 50 0.029
514
EMB007 Embryonal Sarcoma 46 0.029
515
PTY003 Pityriasis Rubra Pilaris 46 0.029
516
ADN027 Adenomyosis 46 0.029
517
RNL078 Renal Dysplasia 45 0.029
518
P CHL092 Chilblain Lupus 44 0.029
519
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 44 0.029
520
DRM013 Dermoid Cyst 44 0.029
521
LVR002 Liver Angiosarcoma 43 0.029
522
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.029
523
IRN002 Iron Metabolism Disease 41 0.029
524
ANP006 Anaplastic Ependymoma 41 0.029
525
c ADL001 Adult Lymphoma 39 0.029
526
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.029
527
c ACR091 Aicardi-Goutieres Syndrome 4 35 0.029
528
c PLN017 Peeling Skin Syndrome 1 34 0.029
529
c ACR088 Aicardi-Goutieres Syndrome 3 33 0.029
530
P BNG002 Benign Meningioma 32 0.029
531
c ALZ043 Alzheimer's Disease 15 32 0.029
532
ORG010 Organ System Benign Neoplasm 31 0.029
533
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 0.029
534
c FML337 Familial Chilblain Lupus 15 0.029
535
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.026
536
P GST049 Gastrointestinal System Cancer 60 0.026
537
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 59 0.026
538
P MSC007 Muscle Hypertrophy 58 0.026
539
P LPS002 Liposarcoma 55 0.026
540
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.026
541
THY103 Thyroid Cancer, Monmedullary, 1 53 0.026
542
P LDD002 Liddle Syndrome 53 0.026
543
P TRC072 Treacher Collins Syndrome 1 52 0.026
544
IMP005 Impotence 51 0.026
545
CHL069 Cholesteatoma 49 0.026
546
INF058 Inflammatory Myofibroblastic Tumor 47 0.026
547
INT253 Intestinal Benign Neoplasm 47 0.026
548
RTC009 Reticulum Cell Sarcoma 47 0.026
549
AMN002 Amino Acid Metabolic Disorder 47 0.026
550
P MWT001 Mowat-Wilson Syndrome 46 0.026
551
P EPT012 Epithelioid Sarcoma 43 0.026
552
CLL001 Cellular Schwannoma 43 0.026
553
HMT008 Hematuria, Benign Familial 42 0.026
554
NSL006 Nasal Cavity Squamous Cell Carcinoma 38 0.026
555
c ACR090 Aicardi-Goutieres Syndrome 2 33 0.026
556
MCR001 Microcystic Meningioma 33 0.026
557
SPN017 Spindle Cell Liposarcoma 32 0.026
558
P ECT002 Ectomesenchymoma 32 0.026
559
c MLG072 Malignant Leydig Cell Tumor 32 0.026
560
CVT001 Cavitary Optic Disc Anomalies 31 0.026
561
c ACR081 Aicardi-Goutieres Syndrome 6 31 0.026
562
c ACR092 Aicardi-Goutieres Syndrome 5 30 0.026
563
SYN008 Synovium Cancer 30 0.026
564
HMM002 Haim-Munk Syndrome 30 0.026
565
c MLG133 Malignant Ectomesenchymoma 27 0.026
566
END057 Endometrial Cancer 75 0.023
567
P PLM036 Pulmonary Fibrosis 71 0.023
568
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.023
569
P FML011 Familial Adenomatous Polyposis 68 0.023
570
CRV047 Cervical Cancer, Somatic 65 0.023
571
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.023
572
CHR072 Chordoma 61 0.023
573
P ORL007 Oral Cavity Cancer 59 0.023
574
TNG009 Tongue Squamous Cell Carcinoma 59 0.023
575
TNG003 Tongue Cancer 58 0.023
576
P LRY044 Larynx Cancer 57 0.023
577
CHL067 Cholecystitis 57 0.023
578
ORL015 Oral Squamous Cell Carcinoma 57 0.023
579
PNC033 Pancreas Adenocarcinoma 57 0.023
580
END041 Endometrial Adenocarcinoma 56 0.023
581
DSM004 Desmoid Tumor 56 0.023
582
LYM104 Lymphoma, Malt, Somatic 54 0.023
583
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.023
584
PRG097 Paragangliomas 1, with or Without Deafness 54 0.023
585
VRR004 Verrucous Carcinoma 54 0.023
586
P CRV031 Cervical Adenocarcinoma 53 0.023
587
c INS002 in Situ Carcinoma 53 0.023
588
MRK001 Merkel Cell Carcinoma 52 0.023
589
MST016 Mesothelioma, Somatic 51 0.023
590
DCT002 Ductal Carcinoma in Situ 51 0.023
591
CLR109 Colorectal Adenocarcinoma 51 0.023
592
IMM136 Immune System Disease 51 0.023
593
NTR040 Neutropenia, Cyclic 51 0.023
594
MCP006 Mucoepidermoid Carcinoma 48 0.023
595
RHB009 Rhabdomyosarcoma 2, Alveolar 48 0.023
596
DSM007 Desmoplastic Small Round Cell Tumor 47 0.023
597
c MLG002 Malignant Peritoneal Mesothelioma 46 0.023
598
ACR014 Acral Lentiginous Melanoma 45 0.023
599
RFR010 Refractory Anemia 45 0.023
600
TNS004 Tonsil Cancer 44 0.023
601
BNN003 Bone Inflammation Disease 44 0.023
602
c CHL119 Cholangitis, Primary Sclerosing 44 0.023
603
P PHR004 Pharynx Cancer 44 0.023
604
FBR019 Fibromatosis 43 0.023
605
HDR006 Hidradenocarcinoma 43 0.023
606
PRT026 Parotitis 42 0.023
607
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 0.023
608
P HMN036 Hemangiopericytoma, Malignant 42 0.023
609
SPN032 Spindle Cell Carcinoma 42 0.023
610
INV006 Inverted Papilloma 41 0.023
611
SMT002 Smooth Muscle Tumor 41 0.023
612
SRC002 Sarcomatoid Renal Cell Carcinoma 41 0.023
613
c PRM023 Pre-Malignant Neoplasm 41 0.023
614
P BNG032 Benign Mesothelioma 40 0.023
615
P CYS017 Cystic Teratoma 40 0.023
616
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 40 0.023
617
PLY040 Polymorphous Low-Grade Adenocarcinoma 38 0.023
618
CRV045 Cervical Intraepithelial Neoplasia 38 0.023
619
P ACQ009 Acquired Metabolic Disease 38 0.023
620
c ALP005 Alpha Chain Disease 37 0.023
621
CYC007 Cyclic Thrombocytopenia 37 0.023
622
IMM003 Immunoglobulin Alpha Deficiency 36 0.023
623
P SRT002 Sertoli Cell Tumor 36 0.023
624
SPT007 Spitz Nevus 34 0.023
625
GBL002 Goblet Cell Carcinoid 34 0.023
626
BRS062 Breast Secretory Carcinoma 34 0.023
627
NCR003 Necrotizing Sialometaplasia 34 0.023
628
P MSN006 Mesenchymoma 33 0.023
629
PLM005 Pleomorphic Lipoma 32 0.023
630
KRT003 Keratinizing Squamous Cell Carcinoma 32 0.023
631
BRN011 Brain Stem Astrocytic Neoplasm 32 0.023
632
GLL021 Gallbladder Sarcoma 31 0.023
633
CHR463 Chronic Actinic Dermatitis 31 0.023
634
CNV003 Conventional Fibrosarcoma 30 0.023
635
PRC014 Pericardium Cancer 30 0.023
636
GLL029 Gallbladder Adenoma 30 0.023
637
ISC003 Ischemic Fasciitis 29 0.023
638
NPH006 Nephrogenic Adenofibroma 28 0.023
639
SPN009 Spindle Cell Rhabdomyosarcoma 28 0.023
640
CNJ006 Conjunctival Intraepithelial Neoplasm 28 0.023
641
PSM001 Psammomatous Meningioma 28 0.023
642
MLG011 Malignant Biphasic Mesothelioma 27 0.023
643
c ALZ014 Alzheimer Disease 16 27 0.023
644
CHN001 Chondroid Lipoma 24 0.023
645
INT041 Intratubular Embryonal Carcinoma 24 0.023
646
SRC007 Sarcomatoid Transitional Cell Carcinoma 24 0.023
647
GRM003 German Syndrome 22 0.023
648
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.023
649
RTC007 Reticular Perineurioma 20 0.023
650
c THR110 Thrombocytopenia 6 20 0.023
651
OVR002 Ovarian Serous Cystadenofibroma 17 0.023
652
ATM053 Autoimmune Disease 2 16 0.023
653
ATM054 Autoimmune Disease 3 15 0.023
654
LNR001 Leiner Disease 14 0.023
655
c FML303 Familial/multiple Cancer 14 0.023
656
CMP052 Complication in Hemodialysis 13 0.023
657
IMM004 Immunoglobulin Beta Deficiency 11 0.023
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