Search results for amyloidosis, hereditary renal

640 hits were found for amyloidosis, hereditary renal

# Family MCID Name MIFTS Score
1
P AMY082 Amyloidosis, Familial Visceral 45 7.887
2
c ALM001 Al Amyloidosis 49 5.293
3
APM001 Aapoaii Amyloidosis 11 3.022
4
APM002 Aapoai Amyloidosis 11 3.006
5
AFB003 Afib Amyloidosis 10 2.567
6
P AMY004 Amyloidosis 65 0.902
7
P RNL014 Renal Cell Carcinoma 82 0.521
8
P NRP001 Neuropathy 59 0.322
9
P HPT021 Hepatitis 69 0.251
10
P KDN018 Kidney Disease 66 0.250
11
CRB009 Cerebritis 39 0.237
12
END030 End Stage Renal Failure 55 0.235
13
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.221
14
IMP003 Impaired Renal Function Disease 34 0.205
15
P KDN017 Kidney Cancer 65 0.204
16
c HRD039 Hereditary Amyloidosis 46 0.200
17
P MLT019 Multiple Myeloma 83 0.191
18
P URF003 Urofacial Syndrome 1 50 0.189
19
URN009 Urinary System Disease 50 0.188
20
P ART022 Arthritis 75 0.187
21
P PNC044 Pancreatitis 61 0.187
22
P GLM007 Glomerulonephritis 59 0.183
23
SPS057 Spasticity 42 0.180
24
c CHR089 Chronic Kidney Failure 66 0.179
25
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.174
26
END072 Endotheliitis 42 0.170
27
TBR010 Tuberculosis 70 0.167
28
PRP016 Paraplegia 49 0.165
29
P ADN016 Adenocarcinoma 69 0.164
30
RNL101 Renal Cell Carcinoma, Papillary 63 0.160
31
P NPH012 Nephrotic Syndrome 59 0.160
32
P CRD011 Cardiomyopathy 68 0.158
33
P RHM011 Rheumatoid Arthritis 89 0.158
34
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.157
35
NTR005 Nutritional Deficiency Disease 36 0.156
36
CRB085 Cerebral Hemorrhage 46 0.155
37
P LYM118 Lymphoma 69 0.150
38
P PLY019 Polyneuropathy 56 0.150
39
P PYL005 Pyelonephritis 52 0.148
40
P THY032 Thyroiditis 54 0.145
41
THR024 Thrombosis 57 0.145
42
P BLD051 Blood Coagulation Disease 42 0.144
43
P HRT032 Heart Disease 75 0.143
44
PLS009 Plasma Cell Neoplasm 48 0.141
45
P AMY084 Amyloidosis, Finnish Type 42 0.140
46
BLD054 Blood Protein Disease 37 0.138
47
VSC008 Vascular Hemostatic Disease 30 0.138
48
P RNL017 Renal Oncocytoma 47 0.137
49
PRP027 Peripheral Vascular Disease 68 0.137
50
P HMR003 Hemorrhagic Disease 57 0.135
51
c HRD088 Hereditary Neuropathies 40 0.134
52
FCT003 Factor X Deficiency 61 0.130
53
VSC006 Vascular Cancer 51 0.129
54
ATN004 Autonomic Neuropathy 45 0.129
55
RNL078 Renal Dysplasia 45 0.129
56
P MYP004 Myopathy 67 0.125
57
P LKM002 Leukemia 71 0.124
58
ADN018 Adenoma 58 0.123
59
c INH020 Inherited Metabolic Disorder 49 0.123
60
CNG034 Congestive Heart Failure 72 0.121
61
P ATX004 Ataxia 53 0.121
62
DFC004 Deficiency Anemia 64 0.120
63
PRT036 Peritonitis 63 0.120
64
PRS047 Prostatitis 56 0.120
65
CRD118 Cardiovascular Cancer 44 0.117
66
ALR002 Al-Raqad Syndrome 36 0.117
67
RTN023 Retinitis 50 0.115
68
AMY002 Amyloid Tumor 37 0.114
69
P HYP069 Hyperparathyroidism 58 0.113
70
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.113
71
ANR040 Aneurysm 57 0.113
72
CHR177 Chromophobe Renal Cell Carcinoma 56 0.112
73
GST053 Gastric Cancer 78 0.112
74
HMT002 Hematologic Cancer 64 0.111
75
P LVR013 Liver Disease 75 0.110
76
LGH004 Light Chain Deposition Disease 44 0.109
77
GNG013 Gingivitis 61 0.109
78
AND005 Androgen Insensitivity Syndrome, Mild 16 0.108
79
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.108
80
CHL068 Cholestasis 59 0.108
81
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.107
82
P OVR042 Ovarian Cancer 76 0.107
83
c HPT001 Hepatitis C 68 0.107
84
NRN002 Neuronitis 41 0.106
85
PRP021 Peripheral Nervous System Neoplasm 46 0.106
86
TRN018 Transitional Cell Carcinoma 53 0.102
87
P CRN178 Coronary Heart Disease 6 21 0.101
88
c CLL013 Cell Type Cancer 46 0.101
89
P FNC004 Fanconi Syndrome 49 0.100
90
ATN002 Autonomic Nervous System Disease 48 0.100
91
PLS010 Plasma Protein Metabolism Disease 34 0.100
92
P LPS004 Lupus Erythematosus 64 0.099
93
P PLY014 Polycystic Kidney Disease 53 0.099
94
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.098
95
P MLT074 Multiple Endocrine Neoplasia 56 0.097
96
NRM005 Neuromuscular Disease 56 0.097
97
c AMY009 Amyloidosis Aa 39 0.097
98
PRP030 Purpura 58 0.096
99
ATR060 Atrial Standstill, Digenic 51 0.096
100
DMN002 Dementia 65 0.095
101
PRP019 Peripheral Nervous System Disease 55 0.095
102
P DBT005 Diabetes Insipidus 53 0.094
103
PRT014 Protein S Deficiency 53 0.093
104
ATH003 Atherosclerosis 65 0.093
105
EPD016 Epidermolysis Bullosa 57 0.093
106
PRT011 Protein C Deficiency 52 0.093
107
PLS011 Plasmacytoma 56 0.093
108
c CRN214 Coronary Heart Disease 5 22 0.092
109
P NPH009 Nephrolithiasis 60 0.092
110
P DRR001 Diarrhea 60 0.092
111
VSC011 Vasculitis 62 0.092
112
INT067 Interstitial Nephritis 46 0.092
113
GRW007 Growth Hormone Deficiency 50 0.091
114
P LRY019 Laryngitis 54 0.091
115
NPH003 Nephrocalcinosis 48 0.090
116
c SYS001 Systemic Lupus Erythematosus 86 0.089
117
HPT074 Hepatic Adenoma, Somatic 50 0.089
118
P SPS003 Spastic Diplegia 52 0.089
119
ADJ001 Adjustment Disorder 38 0.089
120
HMT018 Hematopoietic Stem Cell Transplantation 41 0.089
121
P OBS005 Obesity 92 0.088
122
SKN016 Skin Disease 66 0.087
123
WTH001 Withdrawal Disorder 37 0.086
124
P NRV006 Nervous System Cancer 60 0.085
125
MCR037 Macroglossia 45 0.085
126
P CRV039 Cervicitis 45 0.085
127
P MYC007 Myocardial Infarction 79 0.084
128
OCL009 Ocular Cancer 59 0.084
129
BRT030 Birth Defects 43 0.084
130
ACR041 Acromelic Frontonasal Dysostosis 45 0.084
131
P PLM037 Pulmonary Hypertension 79 0.084
132
MCK007 Muckle-Wells Syndrome 61 0.084
133
c HPT073 Hepatitis C Virus 73 0.083
134
P PHC003 Pheochromocytoma 71 0.082
135
CNN005 Connective Tissue Disease 62 0.082
136
SRC014 Sarcoma 66 0.082
137
TTH006 Tooth Disease 52 0.081
138
PRM243 Primary Bone Cancer 29 0.081
139
P HYP086 Hypothyroidism 64 0.081
140
P ENC018 Encephalopathy 59 0.080
141
P PRG013 Paraganglioma 54 0.080
142
P PRP029 Porphyria 59 0.080
143
P PNM007 Pneumonia 68 0.079
144
c HPT016 Hepatitis B 64 0.078
145
FBR012 Fabry Disease 69 0.078
146
P CHR071 Charcot-Marie-Tooth Disease 67 0.077
147
INC022 Inclusion-Cell Disease 46 0.077
148
P FML161 Familial Mediterranean Fever, Ar 63 0.077
149
WLL006 Wells Syndrome 59 0.077
150
c CRN173 Coronary Heart Disease 8 18 0.077
151
SRC002 Sarcomatoid Renal Cell Carcinoma 41 0.077
152
c ATS347 Autosomal Dominant Polycystic Kidney Disease 62 0.077
153
ALN001 Aland Island Eye Disease 45 0.077
154
c CRN172 Coronary Heart Disease 3 19 0.076
155
HNM002 Hinman Syndrome 25 0.076
156
PCK002 Pick Disease 68 0.076
157
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.076
158
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.076
159
IMM025 Immunoglobulin a Deficiency 2 24 0.076
160
P BCL006 B-Cell Lymphomas 65 0.075
161
ACD009 Acid-Labile Subunit, Deficiency of 45 0.074
162
VND001 Vein Disease 47 0.073
163
P THR014 Thrombocytopenia 64 0.073
164
HMS001 Hemosiderosis 46 0.073
165
P ATR011 Atrial Fibrillation 66 0.072
166
CLT003 Colitis 60 0.072
167
ART016 Aortic Aneurysm 69 0.071
168
P INF032 Infertility 59 0.071
169
MMB001 Membranoproliferative Glomerulonephritis 46 0.071
170
GTR002 Goiter 52 0.071
171
P INT001 Intrahepatic Cholestasis 59 0.071
172
SPN051 Spondylitis 51 0.071
173
P LPR003 Leprosy 69 0.070
174
FBR019 Fibromatosis 43 0.070
175
HRT007 Heart Cancer 46 0.070
176
PPL002 Papillary Carcinoma 51 0.070
177
MRG013 Mirage Syndrome 29 0.070
178
P LYM025 Lymphedema 61 0.069
179
BRC012 Brucellosis 66 0.069
180
P PSR002 Psoriasis 61 0.069
181
P HRT017 Heart Tumor 32 0.069
182
c ADL079 Adult Heart Tumor 16 0.069
183
URN010 Urinary Tract Obstruction 55 0.069
184
BNM001 Bone Marrow Cancer 51 0.068
185
P GNG025 Gingival Fibromatosis 50 0.068
186
BLD053 Blood Platelet Disease 46 0.068
187
INS024 Insulin-Like Growth Factor I 75 0.068
188
RHM027 Rheumatic Disease 58 0.068
189
LNG099 Lung Disease 64 0.068
190
IRN001 Iron Deficiency Anemia 52 0.067
191
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.067
192
P PRD008 Periodontitis 63 0.067
193
URT039 Urticaria 57 0.067
194
P HPT023 Hepatocellular Carcinoma 92 0.067
195
P INF037 Inflammatory Bowel Disease 63 0.067
196
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.067
197
ART017 Aortic Disease 57 0.066
198
LMY002 Leiomyoma 54 0.066
199
c THR092 Thrombophilia Due to Thrombin Defect 54 0.066
200
DRM006 Dermatitis 66 0.066
201
ATN005 Autonomic Dysfunction 49 0.066
202
MTR007 Motor Peripheral Neuropathy 37 0.066
203
P ART023 Arthropathy 64 0.066
204
WLD005 Wild Type Attr Amyloidosis 22 0.065
205
DSS009 Disseminated Intravascular Coagulation 51 0.065
206
P HYP613 Hypophosphatemic Rickets 57 0.065
207
DDN006 Duodenitis 42 0.065
208
c CHR098 Chronic Pyelonephritis 36 0.065
209
SKN023 Skin Tag 44 0.065
210
SCK003 Sickle Cell Anemia 71 0.065
211
MCR088 Microscopic Polyangiitis 49 0.064
212
P PLY017 Polyarteritis Nodosa 51 0.064
213
ADL002 Adult Syndrome 52 0.064
214
c CRN177 Coronary Heart Disease 7 20 0.064
215
P PRT013 Portal Hypertension 60 0.064
216
P LMY004 Leiomyosarcoma 55 0.064
217
CLC006 Calcinosis 50 0.064
218
OST017 Osteomyelitis 61 0.063
219
PHY002 Physical Disorder 43 0.063
220
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.062
221
CRH001 Crohn's Disease 75 0.062
222
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.062
223
c ACT134 Acute Liver Failure 50 0.062
224
END035 Endocrine Gland Cancer 49 0.062
225
P ALZ034 Alzheimer Disease 92 0.062
226
PRD007 Periodontal Disease 60 0.061
227
ORL011 Oral Cancer 56 0.061
228
SQM006 Squamous Cell Carcinoma 70 0.061
229
P NRV007 Nervous System Disease 71 0.061
230
ISC006 Ischemic Heart Disease 68 0.061
231
c BSL007 Basal Cell Carcinoma 65 0.061
232
P MCR129 Microvascular Complications of Diabetes 1 54 0.061
233
STR067 Stroke, Ischemic 75 0.061
234
LPD004 Lipoid Nephrosis 48 0.060
235
P CRN035 Cranial Nerve Palsy 46 0.060
236
MDS022 Mediastinitis 41 0.060
237
RTR011 Retroperitoneal Fibrosis 39 0.060
238
SNS001 Sensorineural Hearing Loss 57 0.060
239
P MYS005 Myositis 57 0.060
240
P LYM026 Lymphoblastic Leukemia 62 0.060
241
GST050 Gastrointestinal System Disease 56 0.059
242
P SPN052 Spondyloarthropathy 60 0.059
243
PRC013 Pericarditis 51 0.059
244
MLR004 Malaria 83 0.059
245
ULC004 Ulcerative Colitis 76 0.059
246
CHL071 Child Syndrome 58 0.059
247
INC002 Inclusion Body Myositis 66 0.059
248
KDS001 Kid Syndrome 53 0.058
249
P MYL005 Myelofibrosis 67 0.058
250
HYP037 Hyperhomocysteinemia 50 0.058
251
P LYM033 Lymphoproliferative Syndrome 56 0.058
252
P MSC005 Muscular Dystrophy 65 0.058
253
MTR014 Motor Neuron Disease 58 0.058
254
PMS001 Poems Syndrome 52 0.057
255
PRD019 Periodic Fever, Familial 49 0.057
256
P CNN004 Connective Tissue Cancer 40 0.057
257
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.057
258
THY028 Thyroid Cancer 69 0.057
259
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.057
260
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.057
261
P ORL007 Oral Cavity Cancer 59 0.057
262
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.057
263
P END033 Endocarditis 54 0.057
264
SNS003 Sensory Peripheral Neuropathy 45 0.057
265
P VNS003 Venous Insufficiency 54 0.057
266
P GST049 Gastrointestinal System Cancer 60 0.057
267
CRY004 Cryoglobulinemia 46 0.056
268
KRT004 Keratitis 71 0.056
269
ADM013 Adamantinoma of Long Bones 57 0.056
270
MDL009 Medullary Sponge Kidney 41 0.056
271
ALP008 Alopecia 57 0.056
272
C3D001 C3 Deficiency 53 0.056
273
P HYP076 Hyperthyroidism 55 0.056
274
P CHL066 Cholangitis 42 0.056
275
AMN006 Aminoaciduria 40 0.056
276
ALL026 Allergic Hypersensitivity Disease 52 0.055
277
c TRC078 Trichohepatoenteric Syndrome 2 29 0.055
278
CRN030 Coronary Stenosis 51 0.055
279
CYS001 Cystic Fibrosis 83 0.055
280
DBT010 Diabetic Neuropathy 55 0.055
281
c DLT002 Dilated Cardiomyopathy 76 0.055
282
P LYM007 Lymphangioleiomyomatosis 66 0.055
283
P ALG002 Alagille Syndrome 72 0.054
284
P PRK001 Porokeratosis 45 0.054
285
P HST010 Histiocytosis 58 0.054
286
P LTR001 Lateral Sclerosis 53 0.054
287
P DYS021 Dysautonomia 44 0.054
288
P TMP003 Temporal Arteritis 60 0.054
289
HYP080 Hypogonadism 53 0.054
290
KRT009 Keratosis 52 0.054
291
PPL018 Papillary Adenocarcinoma 46 0.053
292
INT253 Intestinal Benign Neoplasm 47 0.053
293
SPC010 Speech and Communication Disorders 41 0.053
294
P SDR002 Siderosis 44 0.053
295
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.053
296
DST006 Diastolic Heart Failure 46 0.053
297
P ATP001 Atopic Dermatitis 62 0.053
298
TNS005 Tonsillitis 57 0.053
299
P FNC043 Fanconi Anemia, Complementation Group E 55 0.053
300
P PLM006 Pulmonary Alveolar Proteinosis 48 0.053
301
P ASP006 Aspergillosis 61 0.053
302
HYP056 Hypoglycemia 61 0.052
303
P ESP024 Esophagitis 61 0.052
304
P EHL001 Ehlers-Danlos Syndrome 63 0.052
305
CYS014 Cystadenocarcinoma 47 0.052
306
ANG054 Angina Pectoris 50 0.052
307
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.051
308
c CHR090 Chronic Lymphocytic Leukemia 76 0.051
309
P APL001 Aplastic Anemia 75 0.051
310
c DYS166 Dysautonomia, Familial 49 0.051
311
GST019 Gastrointestinal Stromal Tumor 73 0.051
312
P INF038 Influenza 72 0.051
313
GLT021 Glutaricaciduria, Type I 46 0.050
314
MRG003 Marginal Zone B-Cell Lymphoma 52 0.050
315
PRT019 Protein-Losing Enteropathy 42 0.050
316
RSS002 Roussy-Levy Syndrome 50 0.050
317
PRD011 Proud Syndrome 42 0.050
318
MXD005 Mixed Connective Tissue Disease 62 0.050
319
P PRM006 Primary Biliary Cirrhosis 51 0.050
320
PRC012 Pericardial Effusion 51 0.050
321
CTS003 Coats Disease 57 0.050
322
FRB001 Farber Lipogranulomatosis 53 0.050
323
SVN001 Sveinsson Choreoretinal Atrophy 26 0.050
324
CLN015 Colon Adenocarcinoma 50 0.049
325
P ATX010 Ataxia Neuropathy Spectrum 30 0.049
326
MCS002 Mucositis 55 0.049
327
P CRB059 Cerebellar Degeneration 34 0.049
328
IMM136 Immune System Disease 51 0.049
329
IRN002 Iron Metabolism Disease 41 0.049
330
KRT002 Keratomalacia 52 0.048
331
P AML002 Amelogenesis Imperfecta 45 0.048
332
P CDS001 Cadasil 55 0.048
333
ALK013 Alkaptonuria 54 0.048
334
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.048
335
GNG002 Ganglioneuroma 47 0.048
336
P NTR004 Neutropenia 59 0.048
337
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.047
338
CHR008 Choroiditis 44 0.047
339
FMR003 Femoral Neuropathy 38 0.047
340
NWC001 Newcastle Disease 54 0.047
341
P TRT010 Teratoma 52 0.047
342
P MSC007 Muscle Hypertrophy 58 0.047
343
P CYS007 Cystic Nephroma 35 0.047
344
P FML011 Familial Adenomatous Polyposis 68 0.047
345
ADL030 Adult-Onset Still's Disease 59 0.047
346
c FML303 Familial/multiple Cancer 14 0.047
347
PLS016 Plasma Cell Leukemia 42 0.047
348
BND014 Bone Development Disease 40 0.046
349
FCL012 Facial Paralysis 50 0.046
350
P CLL015 Collagen Disease 50 0.046
351
CRD137 Cardiogenic Shock 46 0.046
352
P LPS002 Liposarcoma 55 0.046
353
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.046
354
GLB003 Globe Disease 32 0.046
355
INC021 Incontinentia Pigmenti 59 0.046
356
HYP088 Hyper-Igd Syndrome 43 0.046
357
BRN022 Bronchiectasis 50 0.046
358
P SCL009 Sclerosing Cholangitis 48 0.046
359
SPN032 Spindle Cell Carcinoma 42 0.046
360
HDG012 Hodgkin Lymphoma 77 0.045
361
P AGM001 Agammaglobulinemia 64 0.045
362
ATN001 Autonomic Peripheral Neuropathy 17 0.045
363
IMM044 Immunoglobulin G Deficiency 33 0.045
364
ACR002 Acrocapitofemoral Dysplasia 33 0.045
365
CST005 Castleman Disease 41 0.045
366
P PSD003 Pseudohypoaldosteronism 44 0.045
367
EXT010 Extramedullary Plasmacytoma 49 0.045
368
P GST044 Gastritis 56 0.045
369
c BNG076 Benign Exophthalmos Syndrome 15 0.044
370
ADP007 Adie Pupil 34 0.044
371
SPN186 Spinal Cord Injury 63 0.044
372
SPL006 Splenic Infarction 35 0.044
373
CLL003 Cellulitis 51 0.044
374
SKN027 Skin Conditions 43 0.044
375
ART004 Aortic Atherosclerosis 46 0.044
376
MNN017 Mononeuropathy 40 0.044
377
CRT016 Carotid Artery Disease 57 0.043
378
P LPD010 Lipodystrophy 55 0.043
379
PLM012 Pulmonary Sarcoidosis 54 0.043
380
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 50 0.043
381
SPN119 Spondylarthropathy 42 0.043
382
P INT063 Intellectual Disability 49 0.043
383
DFF005 Diffuse Large B-Cell Lymphoma 59 0.043
384
P HYP083 Hypopituitarism 54 0.043
385
c CHR417 Chronic Graft Versus Host Disease 51 0.043
386
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 30 0.043
387
LYS002 Lysosomal Storage Disease 52 0.043
388
P GLY013 Glycogen Storage Disease 60 0.043
389
HDC001 Headache 54 0.043
390
PHS001 Phosphorus Metabolism Disease 38 0.042
391
ATM052 Autoimmune Disease 1 25 0.042
392
FLR002 Filariasis 54 0.042
393
ACT008 Actinic Keratosis 51 0.042
394
c ADL001 Adult Lymphoma 39 0.042
395
TCL003 T Cell Deficiency 45 0.042
396
KND001 Kindler Syndrome 57 0.042
397
BRS099 Breast Ductal Carcinoma 50 0.042
398
ADR005 Adrenal Carcinoma 57 0.042
399
P DRM010 Dermatomyositis 62 0.042
400
P ICH004 Ichthyosis 52 0.042
401
DSC009 Discoid Lupus Erythematosus 45 0.042
402
P PLM036 Pulmonary Fibrosis 71 0.042
403
CHD001 Chediak-Higashi Syndrome 64 0.042
404
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.042
405
CRY008 Cryopyrin-Associated Periodic Syndrome 34 0.041
406
BRN071 Brain Injury 52 0.041
407
CHL067 Cholecystitis 57 0.041
408
GST027 Gastric Lymphoma 53 0.041
409
CHR012 Chronic Granulomatous Disease 65 0.041
410
P SYP003 Syphilis 53 0.041
411
MGC001 Megacolon 45 0.041
412
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.041
413
LYM095 Lymphangiomatosis 32 0.041
414
FSC004 Fasciitis 48 0.041
415
BNN003 Bone Inflammation Disease 44 0.040
416
THR035 Thrombasthenia 39 0.040
417
P CHR084 Chromosomal Disease 32 0.040
418
ACR007 Acromegaly 66 0.040
419
PSR001 Psoriatic Arthritis 64 0.040
420
MSC072 Muscle Cancer 49 0.040
421
PPL022 Papilloma 55 0.040
422
BLD044 Bladder Disease 51 0.040
423
ANG020 Angiosarcoma 53 0.040
424
PTT006 Pituitary Adenoma 56 0.040
425
SYN036 Syncope 47 0.040
426
P ALP009 Alopecia Areata 62 0.040
427
ACN002 Acanthosis Nigricans 57 0.040
428
PNN001 Panniculitis 51 0.040
429
CRN031 Cranial Nerve Disease 40 0.040
430
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.040
431
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.040
432
CHR001 Churg-Strauss Syndrome 49 0.040
433
ARS001 Aarskog-Scott Syndrome 52 0.040
434
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.039
435
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.039
436
P WHT013 White Sponge Nevus 1 39 0.039
437
PNC033 Pancreas Adenocarcinoma 57 0.039
438
HMT008 Hematuria, Benign Familial 42 0.039
439
DWN001 Down Syndrome 66 0.039
440
c INV001 Invasive Aspergillosis 47 0.039
441
HRT012 Heart Valve Disease 40 0.039
442
INT002 Intermittent Claudication 56 0.039
443
RLP001 Relapsing Polychondritis 50 0.039
444
HNS001 Hansen's Disease 30 0.039
445
MLT113 Multicentric Castleman Disease 46 0.039
446
PST055 Postural Hypotension 36 0.039
447
P RTN008 Retinitis Pigmentosa 80 0.039
448
EVN001 Evans' Syndrome 43 0.039
449
MGL001 Megaloblastic Anemia 50 0.039
450
P CRV031 Cervical Adenocarcinoma 53 0.039
451
CRN017 Coronary Thrombosis 48 0.039
452
EXF001 Exfoliation Syndrome 57 0.038
453
P PLN008 Peeling Skin Syndrome 45 0.038
454
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.038
455
CRD119 Cardiac Arrest 61 0.038
456
P INT143 Interstitial Cystitis 57 0.038
457
LPR001 Lepromatous Leprosy 50 0.038
458
INF058 Inflammatory Myofibroblastic Tumor 47 0.038
459
INT088 Intrinsic Factor Deficiency 45 0.038
460
LPM004 Lipoma 60 0.038
461
MXD023 Mixed Cell Type Cancer 44 0.038
462
PHR003 Pharyngitis 56 0.037
463
c ATM011 Autoimmune Hepatitis 60 0.037
464
P IGN003 Iga Nephropathy 1 27 0.037
465
ATM054 Autoimmune Disease 3 15 0.037
466
PRT056 Protein R Deficiency 10 0.037
467
DSM004 Desmoid Tumor 56 0.037
468
ATR057 Atrioventricular Block 49 0.037
469
c SBC007 Subacute Thyroiditis 40 0.037
470
DNS007 Dense Deposit Disease 37 0.037
471
CHR285 Chronic Myelomonocytic Leukemia 56 0.037
472
NDL013 Nodular Regenerative Hyperplasia 50 0.037
473
MNN009 Meningoencephalitis 47 0.037
474
HYD005 Hydrocele 46 0.037
475
CRB031 Cerebral Arterial Disease 27 0.037
476
c PRM023 Pre-Malignant Neoplasm 41 0.036
477
IMP005 Impotence 51 0.036
478
KRT008 Keratopathy 44 0.036
479
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.036
480
CRV038 Cervical Squamous Cell Carcinoma 60 0.036
481
BRN014 Bronchopneumonia 45 0.036
482
P WLD002 Waldenstrom Macroglobulinemia 58 0.036
483
P INT070 Intestinal Obstruction 57 0.036
484
HPT067 Hepatocellular Adenoma 42 0.036
485
LYM004 Lymphoid Interstitial Pneumonia 33 0.036
486
HDR002 Hidradenitis Suppurativa 51 0.036
487
HDR003 Hidradenitis 45 0.036
488
P MYS003 Myasthenia Gravis 67 0.036
489
RCT015 Reactive Arthritis 63 0.036
490
OXY002 Oxyphilic Adenoma 33 0.035
491
PRV003 Perivascular Epithelioid Cell Tumor 39 0.035
492
P GLM045 Glioma 60 0.035
493
LYM006 Lymphoepithelioma-Like Carcinoma 43 0.035
494
P ACQ009 Acquired Metabolic Disease 38 0.035
495
PLM034 Pulmonary Emphysema 55 0.035
496
THY103 Thyroid Cancer, Monmedullary, 1 53 0.035
497
P ADD001 Addison's Disease 62 0.034
498
ALV010 Alveolar Soft-Part Sarcoma 54 0.034
499
CLR109 Colorectal Adenocarcinoma 51 0.034
500
ISC015 Ischemic Colitis 39 0.034
501
HMN016 Hemangioendothelioma 39 0.034
502
LCH004 Lichen Disease 36 0.034
503
MLG012 Malignant Epithelial Mesothelioma 33 0.034
504
URN008 Urinary Bladder Cancer 66 0.034
505
SMT002 Smooth Muscle Tumor 41 0.034
506
ACH005 Achalasia 52 0.034
507
MNC006 Monoclonal Gammopathy of Uncertain Significance 44 0.034
508
MRK001 Merkel Cell Carcinoma 52 0.033
509
PRG097 Paragangliomas 1, with or Without Deafness 54 0.033
510
c FML162 Familial Mediterranean Fever, Ad 23 0.033
511
P GNT008 Giant Cell Tumor 49 0.033
512
c THR037 Thrombocytopenia 2 35 0.033
513
P FBR017 Fibrosarcoma 56 0.032
514
c PLN018 Peeling Skin Syndrome 2 40 0.032
515
MCN008 Mucinous Cystadenocarcinoma 39 0.032
516
c PLN017 Peeling Skin Syndrome 1 34 0.032
517
MCN004 Mucinous Tubular and Spindle Renal Cell Carcinoma 25 0.032
518
MSL001 Measles 61 0.032
519
AMN002 Amino Acid Metabolic Disorder 47 0.032
520
LBL001 Lobular Neoplasia 46 0.032
521
P CRD194 Cardiomyopathy, Familial Hypertrophic 62 0.032
522
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.032
523
NTR003 Natural Killer Cell Leukemia 47 0.032
524
ISC002 Ischemic Optic Neuropathy 37 0.032
525
INT079 Intrahepatic Cholangiocarcinoma 56 0.032
526
BLD034 Bile Duct Carcinoma 56 0.032
527
BLD087 Bladder Cancer, Somatic 54 0.032
528
MLT006 Multidrug-Resistant Tuberculosis 46 0.032
529
P PLL002 Pellagra 45 0.032
530
LYM052 Lymphomatoid Papulosis 41 0.032
531
c PSR017 Psoriasis 2 37 0.032
532
SPN060 Spondylocarpotarsal Synostosis Syndrome 34 0.032
533
PSR005 Psoriasis, Protection Against 32 0.032
534
ABD004 Abdominal Tuberculosis 32 0.032
535
c PSR019 Psoriasis Susceptibility 13 32 0.032
536
NNS003 Non-Secretory Myeloma 28 0.032
537
c DYS033 Dysautonomia Like Disorder 16 0.032
538
CHR072 Chordoma 61 0.032
539
ING001 Inguinal Hernia 58 0.032
540
CRV047 Cervical Cancer, Somatic 65 0.031
541
P HRP006 Herpes Simplex 65 0.031
542
P ADN017 Adenofibroma 28 0.031
543
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.030
544
FND002 Fundus Dystrophy 46 0.030
545
c INS002 in Situ Carcinoma 53 0.030
546
FBR054 Fibroma 46 0.030
547
P MSN005 Mesenchymal Chondrosarcoma 38 0.030
548
FNT004 Fainting 33 0.030
549
CLR018 Clear Cell Meningioma 29 0.030
550
HRT029 Heart Tumor of the Child 15 0.030
551
P LCH002 Lichen Planus 53 0.029
552
SGN002 Signet Ring Cell Adenocarcinoma 45 0.029
553
c CNG012 Congenital Generalized Lipodystrophy 44 0.029
554
SRC027 Sarcoma, Synovial 44 0.029
555
IDP074 Idiopathic Bronchiectasis 36 0.029
556
ATM021 Autoimmune Inner Ear Disease 31 0.029
557
SKN019 Skin Melanoma 62 0.029
558
c SPN225 Spondyloarthropathy 1 62 0.029
559
SPN035 Spindle Cell Sarcoma 47 0.029
560
ADN027 Adenomyosis 46 0.029
561
ADN014 Adenomatoid Tumor 34 0.029
562
END041 Endometrial Adenocarcinoma 56 0.029
563
RHM001 Rheumatic Fever 54 0.029
564
SRS007 Sorsby Fundus Dystrophy 46 0.029
565
EMB007 Embryonal Sarcoma 46 0.029
566
CRR007 Cirrhosis, Cryptogenic 43 0.029
567
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.029
568
PRC010 Pericardial Mesothelioma 37 0.029
569
OPT008 Optic Nerve Neoplasm 36 0.029
570
P INT283 Integumentary System Cancer 33 0.029
571
PRC014 Pericardium Cancer 30 0.029
572
NDL010 Nodular Hidradenoma 25 0.029
573
ATY005 Atypical Teratoid Rhabdoid Tumor 52 0.028
574
DBT062 Diabetic Foot Ulcers 51 0.028
575
DCT002 Ductal Carcinoma in Situ 51 0.028
576
RHB001 Rhabdoid Cancer 50 0.028
577
c MLG079 Malignant Pleural Mesothelioma 50 0.028
578
DSM007 Desmoplastic Small Round Cell Tumor 47 0.028
579
P MRD002 Marden-Walker Syndrome 46 0.028
580
RFR010 Refractory Anemia 45 0.028
581
P SRT002 Sertoli Cell Tumor 36 0.028
582
ANG017 Angiolipoma 35 0.028
583
P MSN006 Mesenchymoma 33 0.028
584
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 59 0.026
585
P LRY044 Larynx Cancer 57 0.026
586
KPS002 Kaposiform Hemangioendothelioma 41 0.026
587
ADN013 Adenoid Squamous Cell Carcinoma 36 0.026
588
CTN012 Cutaneous Leiomyosarcoma 33 0.026
589
CNV003 Conventional Fibrosarcoma 30 0.026
590
C9D001 C9 Deficiency 29 0.026
591
P NSP012 Nasopharyngeal Carcinoma 66 0.026
592
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.026
593
PLM014 Pleomorphic Adenoma 52 0.026
594
END031 Endometrial Stromal Sarcoma 50 0.026
595
MCP006 Mucoepidermoid Carcinoma 48 0.026
596
P EPT012 Epithelioid Sarcoma 43 0.026
597
DDF001 Dedifferentiated Liposarcoma 43 0.026
598
CHL052 Choledochal Cyst 41 0.026
599
P SYR003 Syringoma 37 0.026
600
EXT052 Extraskeletal Ewing Sarcoma 34 0.026
601
BRS062 Breast Secretory Carcinoma 34 0.026
602
GNG006 Gingival Hypertrophy 32 0.026
603
NPH006 Nephrogenic Adenofibroma 28 0.026
604
ISL010 Isolated 17-Linked Lissencephaly 28 0.026
605
PRC011 Parachordoma 26 0.026
606
GYN003 Gynandroblastoma 26 0.026
607
INT049 Intrahepatic Bile Duct Adenoma 23 0.026
608
c THR110 Thrombocytopenia 6 20 0.026
609
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.024
610
LYM104 Lymphoma, Malt, Somatic 54 0.024
611
MST016 Mesothelioma, Somatic 51 0.024
612
c ART115 Aortic Valve Disease 1 50 0.024
613
RTC009 Reticulum Cell Sarcoma 47 0.024
614
UTR043 Uterine Sarcoma 44 0.024
615
DRM013 Dermoid Cyst 44 0.024
616
P HMN036 Hemangiopericytoma, Malignant 42 0.024
617
NDL001 Nodular Malignant Melanoma 40 0.024
618
BRS023 Breast Adenoid Cystic Carcinoma 39 0.024
619
CNJ007 Conjunctivochalasis 36 0.024
620
MLG098 Malignant Mixed Mullerian Tumor 36 0.024
621
SPN006 Spindle Cell Lipoma 35 0.024
622
ATM015 Autoimmune Disease of Gastrointestinal Tract 34 0.024
623
MCR001 Microcystic Meningioma 33 0.024
624
c MLG072 Malignant Leydig Cell Tumor 32 0.024
625
GST017 Gastric Tubular Adenocarcinoma 31 0.024
626
SPN034 Spindle Cell Synovial Sarcoma 30 0.024
627
SPS002 Spastic Entropion 27 0.024
628
FBR001 Fibrous Meningioma 27 0.024
629
OSS002 Ossifying Fibromyxoid Tumor 27 0.024
630
BPH002 Biphasic Synovial Sarcoma 27 0.024
631
EXT003 Extraskeletal Mesenchymal Chondrosarcoma 26 0.024
632
c LRG002 Large Cell Acanthoma 25 0.024
633
INT041 Intratubular Embryonal Carcinoma 24 0.024
634
MNP001 Monophasic Synovial Sarcoma 24 0.024
635
GLN006 Glandular Cystitis 23 0.024
636
c PSD084 Pseudo-Meigs Syndrome 22 0.024
637
KDN004 Kidney Hemangiopericytoma 22 0.024
638
MCN003 Mucinous Ovarian Cystadenoma 21 0.024
639
CRV037 Cervical Mucinous Adenocarcinoma 19 0.024
640
CRV014 Cervical Adenoma Malignum 16 0.024
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