Search results for amyloidosis, hereditary renal

462 hits were found for amyloidosis, hereditary renal

# Family MCID Name MIFTS Score
1
AMY082 Amyloidosis, Familial Visceral 47 8.461
2
c ALM001 Al Amyloidosis 56 5.479
3
APM002 Aapoai Amyloidosis 15 3.099
4
APM001 Aapoaii Amyloidosis 13 3.080
5
AFB003 Afib Amyloidosis 11 2.610
6
P AMY004 Amyloidosis 69 1.026
7
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.596
8
P KDN018 Kidney Disease 69 0.377
9
P NRP001 Neuropathy 63 0.376
10
URN009 Urinary System Disease 58 0.296
11
P HPT021 Hepatitis 75 0.287
12
c BLD140 Blood Group, I System 37 0.285
13
AMY087 Amyloidosis, Hereditary, Transthyretin-Related 57 0.283
14
CRB009 Cerebritis 41 0.269
15
END030 End Stage Renal Failure 59 0.261
16
c HRD039 Hereditary Amyloidosis 47 0.229
17
AGN016 Aging 65 0.227
18
c CHR089 Chronic Kidney Failure 72 0.224
19
MYL069 Myeloma, Multiple 86 0.222
20
P ADN016 Adenocarcinoma 71 0.220
21
P ART022 Arthritis 77 0.213
22
P PNC044 Pancreatitis 64 0.212
23
P GLM007 Glomerulonephritis 61 0.207
24
SPS057 Spasticity 41 0.205
25
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.201
26
END072 Endotheliitis 46 0.199
27
P FML018 Familial Mediterranean Fever 73 0.196
28
BRC012 Brucellosis 71 0.195
29
PRP016 Paraplegia 53 0.188
30
P MYC084 Mycobacterium Tuberculosis 1 69 0.184
31
P NPH012 Nephrotic Syndrome 60 0.180
32
P LYM118 Lymphoma 71 0.176
33
P PLY019 Polyneuropathy 58 0.176
34
P RHM011 Rheumatoid Arthritis 91 0.175
35
THR024 Thrombosis 61 0.174
36
P THY032 Thyroiditis 56 0.172
37
P DBT009 Diabetes Mellitus 72 0.171
38
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.169
39
ONC007 Oncocytoma 48 0.167
40
P PYL005 Pyelonephritis 56 0.166
41
P ANR048 Aniridia 1 68 0.163
42
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.162
43
ANR038 Anorexia Nervosa 1 21 0.160
44
BLD137 Blood Group--Ahonen 17 0.160
45
P RNL017 Renal Oncocytoma 49 0.160
46
P BLD051 Blood Coagulation Disease 38 0.151
47
CNG034 Congestive Heart Failure 74 0.151
48
P HMR003 Hemorrhagic Disease 61 0.149
49
VSC008 Vascular Hemostatic Disease 36 0.146
50
ATN004 Autonomic Neuropathy 46 0.146
51
P LKM002 Leukemia 75 0.144
52
PRT036 Peritonitis 67 0.143
53
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.142
54
ADN018 Adenoma 63 0.141
55
RNL012 Renal Tuberculosis 35 0.140
56
PRS047 Prostatitis 59 0.138
57
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.138
58
P ALZ034 Alzheimer Disease 95 0.137
59
P AMY084 Amyloidosis, Finnish Type 40 0.136
60
P HRT032 Heart Disease 80 0.136
61
ALR002 Al-Raqad Syndrome 30 0.135
62
P HYP069 Hyperparathyroidism 58 0.134
63
RTN023 Retinitis 52 0.134
64
FCT003 Factor X Deficiency 58 0.133
65
PLS009 Plasma Cell Neoplasm 51 0.132
66
ANR040 Aneurysm 61 0.132
67
GST053 Gastric Cancer 84 0.128
68
P MYP004 Myopathy 69 0.128
69
GNG013 Gingivitis 64 0.124
70
NRN002 Neuronitis 43 0.123
71
CHL068 Cholestasis 60 0.120
72
ALP046 Alport Syndrome, X-Linked 74 0.119
73
c HPT001 Hepatitis C 73 0.118
74
P LVR013 Liver Disease 76 0.118
75
c BRN108 Branchiootic Syndrome 1 47 0.116
76
P LPS004 Lupus Erythematosus 69 0.115
77
HPT082 Hepatic Adenomas, Familial 52 0.115
78
c AMY009 Amyloidosis Aa 48 0.114
79
TRN018 Transitional Cell Carcinoma 58 0.114
80
P PLY014 Polycystic Kidney Disease 60 0.114
81
P FNC004 Fanconi Syndrome 54 0.113
82
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.113
83
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.113
84
HMS001 Hemosiderosis 50 0.112
85
NRM005 Neuromuscular Disease 60 0.111
86
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.111
87
MCK007 Muckle-Wells Syndrome 64 0.111
88
DMN002 Dementia 68 0.110
89
NRT004 Neuritis 55 0.110
90
P MLT074 Multiple Endocrine Neoplasia 55 0.108
91
PRP030 Purpura 61 0.108
92
P DBT005 Diabetes Insipidus 54 0.107
93
VSC011 Vasculitis 66 0.107
94
INT067 Interstitial Nephritis 51 0.107
95
EPD016 Epidermolysis Bullosa 57 0.105
96
P HYP086 Hypothyroidism 62 0.105
97
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.104
98
P DRR001 Diarrhea 60 0.103
99
P LRY019 Laryngitis 57 0.102
100
c SYS001 Systemic Lupus Erythematosus 86 0.102
101
PRP019 Peripheral Nervous System Disease 53 0.101
102
SPS003 Spastic Diplegia 55 0.101
103
P ENC018 Encephalopathy 58 0.101
104
IMM158 Immune Suppression 57 0.100
105
P CRV039 Cervicitis 49 0.100
106
P MYC007 Myocardial Infarction 81 0.097
107
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.097
108
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.097
109
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.097
110
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.097
111
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.097
112
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.097
113
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.097
114
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.097
115
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.097
116
P PHC003 Pheochromocytoma 72 0.096
117
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.096
118
FBR012 Fabry Disease 72 0.094
119
CRS001 Crescentic Glomerulonephritis 44 0.093
120
ART140 Arteries, Anomalies of 51 0.092
121
HMT018 Hematopoietic Stem Cell Transplantation 58 0.092
122
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.091
123
P PRG013 Paraganglioma 57 0.091
124
SRC014 Sarcoma 68 0.091
125
P PLM037 Pulmonary Hypertension 79 0.090
126
P PRP029 Porphyria 62 0.090
127
CRP001 Carpal Tunnel Syndrome 64 0.090
128
CNN005 Connective Tissue Disease 65 0.090
129
BLD163 Blood Group, Dombrock System 23 0.089
130
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.089
131
P ATR011 Atrial Fibrillation 68 0.089
132
P PNM007 Pneumonia 70 0.087
133
c HPT073 Hepatitis C Virus 73 0.087
134
P INF032 Infertility 59 0.086
135
P ART023 Arthropathy 68 0.085
136
IRN002 Iron Metabolism Disease 45 0.084
137
ATM095 Autoimmune Disease 66 0.083
138
SPN051 Spondylitis 55 0.083
139
P NRV007 Nervous System Disease 75 0.082
140
LMY002 Leiomyoma 58 0.082
141
P THR014 Thrombocytopenia 65 0.082
142
MMB001 Membranoproliferative Glomerulonephritis 51 0.081
143
P CRN018 Coronary Artery Anomaly 69 0.081
144
P INT001 Intrahepatic Cholestasis 62 0.080
145
ISC006 Ischemic Heart Disease 73 0.080
146
c SPN225 Spondyloarthropathy 1 71 0.080
147
c HPT016 Hepatitis B 68 0.080
148
CLT003 Colitis 63 0.080
149
c MLT160 Multiple Endocrine Neoplasia, Type Iia 65 0.079
150
GTR002 Goiter 53 0.079
151
P LYM025 Lymphedema 63 0.079
152
THY111 Thyroid Carcinoma, Familial Medullary 63 0.079
153
DDN006 Duodenitis 46 0.079
154
P PSR002 Psoriasis 65 0.079
155
RHM027 Rheumatic Disease 62 0.079
156
LNG099 Lung Disease 67 0.079
157
DFC004 Deficiency Anemia 62 0.078
158
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.078
159
INS024 Insulin-Like Growth Factor I 83 0.078
160
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.078
161
ANX010 Anxiety 72 0.077
162
IRN001 Iron Deficiency Anemia 55 0.076
163
P PLY017 Polyarteritis Nodosa 51 0.076
164
URT039 Urticaria 59 0.076
165
TTH006 Tooth Disease 54 0.076
166
NRN004 Neuroendocrine Tumor 58 0.075
167
WLD005 Wild Type Attr Amyloidosis 24 0.075
168
CHN070 Cohen-Gibson Syndrome 51 0.074
169
HYP080 Hypogonadism 54 0.074
170
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.074
171
GST050 Gastrointestinal System Disease 66 0.074
172
P TMP003 Temporal Arteritis 67 0.074
173
ATN005 Autonomic Dysfunction 51 0.073
174
MCS002 Mucositis 61 0.073
175
MCR088 Microscopic Polyangiitis 58 0.073
176
c THR092 Thrombophilia Due to Thrombin Defect 61 0.073
177
INF009 Inflammatory Spondylopathy 32 0.073
178
CRH001 Crohn's Disease 80 0.072
179
CLC006 Calcinosis 51 0.072
180
P PRT013 Portal Hypertension 59 0.072
181
DRM006 Dermatitis 67 0.071
182
P LMY004 Leiomyosarcoma 59 0.071
183
P LPR021 Leprosy 3 59 0.071
184
P ALP008 Alopecia 56 0.070
185
MDS022 Mediastinitis 44 0.070
186
P LYM026 Lymphoblastic Leukemia 66 0.070
187
c PRM005 Primary Hyperparathyroidism 59 0.070
188
P PRD008 Periodontitis 67 0.070
189
ANT009 Antithrombin Iii Deficiency 58 0.069
190
P MSC005 Muscular Dystrophy 66 0.069
191
PRC013 Pericarditis 55 0.069
192
PST011 Pustulosis of Palm and Sole 47 0.069
193
P MYL005 Myelofibrosis 75 0.068
194
c BSL007 Basal Cell Carcinoma 66 0.068
195
P MYS005 Myositis 63 0.068
196
OST017 Osteomyelitis 64 0.068
197
P CTS001 Cutis Laxa 62 0.067
198
MLR004 Malaria 86 0.067
199
P HRD009 Hereditary Wilms' Tumor 46 0.067
200
P MLT020 Multiple Sclerosis 85 0.067
201
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.067
202
CRY004 Cryoglobulinemia 49 0.066
203
DSS009 Disseminated Intravascular Coagulation 56 0.066
204
P DYS021 Dysautonomia 47 0.066
205
P END033 Endocarditis 58 0.066
206
P ESP024 Esophagitis 64 0.065
207
P HYP076 Hyperthyroidism 56 0.065
208
c INT072 Intestinal Pseudo-Obstruction 57 0.065
209
WLL006 Wells Syndrome 57 0.065
210
P INF037 Inflammatory Bowel Disease 52 0.065
211
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.065
212
PRD007 Periodontal Disease 64 0.065
213
MDL009 Medullary Sponge Kidney 46 0.065
214
c INF145 Infantile Liver Failure Syndrome 1 33 0.064
215
SNS001 Sensorineural Hearing Loss 59 0.063
216
P INF038 Influenza 77 0.063
217
ULC004 Ulcerative Colitis 80 0.063
218
P RST002 Restrictive Cardiomyopathy 51 0.063
219
P FNC043 Fanconi Anemia, Complementation Group E 52 0.063
220
CYS001 Cystic Fibrosis 85 0.063
221
MTR014 Motor Neuron Disease 62 0.063
222
P LTR001 Lateral Sclerosis 58 0.062
223
SCK003 Sickle Cell Anemia 73 0.062
224
HYP056 Hypoglycemia 62 0.062
225
P HST010 Histiocytosis 60 0.062
226
FCL012 Facial Paralysis 50 0.061
227
P PRC012 Pericardial Effusion 52 0.061
228
THY028 Thyroid Cancer 72 0.061
229
DBT010 Diabetic Neuropathy 60 0.061
230
P DLT002 Dilated Cardiomyopathy 76 0.061
231
P SDR002 Siderosis 48 0.061
232
P PRK001 Porokeratosis 49 0.060
233
ADP007 Adie Pupil 41 0.060
234
PPL002 Papillary Carcinoma 51 0.060
235
ADL030 Adult-Onset Still's Disease 65 0.060
236
INC002 Inclusion Body Myositis 64 0.060
237
SKN016 Skin Disease 68 0.060
238
P ALG028 Alagille Syndrome 1 68 0.059
239
P PLM006 Pulmonary Alveolar Proteinosis 49 0.059
240
HYP088 Hyper-Igd Syndrome 49 0.059
241
CRD223 Cardiac Arrhythmia 52 0.058
242
PRT019 Protein-Losing Enteropathy 40 0.058
243
c JVN010 Juvenile Rheumatoid Arthritis 71 0.058
244
ANG054 Angina Pectoris 53 0.057
245
IMM136 Immune System Disease 57 0.057
246
P ASP006 Aspergillosis 65 0.057
247
HMT002 Hematologic Cancer 64 0.057
248
c FML116 Familial Cold Autoinflammatory Syndrome 1 56 0.057
249
CRD137 Cardiogenic Shock 45 0.056
250
P ICH004 Ichthyosis 54 0.056
251
KRT009 Keratosis 53 0.056
252
P AML002 Amelogenesis Imperfecta 46 0.056
253
P CRB059 Cerebellar Degeneration 40 0.056
254
PYL004 Pyelitis 38 0.055
255
c TRC078 Trichohepatoenteric Syndrome 2 34 0.055
256
P HYP061 Hypertrophic Cardiomyopathy 65 0.055
257
LYM019 Lymphosarcoma 58 0.055
258
HDC001 Headache 55 0.055
259
P EHL001 Ehlers-Danlos Syndrome 61 0.055
260
CHR008 Choroiditis 47 0.055
261
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.055
262
SKN027 Skin Conditions 48 0.055
263
GST019 Gastrointestinal Stromal Tumor 74 0.055
264
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.055
265
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 0.054
266
PRP027 Peripheral Vascular Disease 71 0.054
267
LPP002 Lipoprotein Glomerulopathy 44 0.054
268
MNN017 Mononeuropathy 42 0.054
269
MXD005 Mixed Connective Tissue Disease 66 0.054
270
GNG002 Ganglioneuroma 50 0.054
271
CRY008 Cryopyrin-Associated Periodic Syndrome 39 0.054
272
P GST044 Gastritis 61 0.054
273
ALK013 Alkaptonuria 56 0.053
274
P CLL015 Collagen Disease 53 0.053
275
CLL003 Cellulitis 53 0.053
276
NTR018 Neutrophilia, Hereditary 46 0.053
277
HYP190 Hypoalphalipoproteinemia, Primary 61 0.053
278
FMR003 Femoral Neuropathy 39 0.053
279
APL001 Aplastic Anemia 74 0.053
280
LPD008 Lipid Metabolism Disorder 59 0.053
281
c BSL024 Basal Cell Carcinoma 1 42 0.053
282
KRT019 Keratitis, Hereditary 62 0.052
283
MNT002 Mental Depression 60 0.052
284
P NTR004 Neutropenia 60 0.052
285
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.052
286
SVN002 Sveinsson Chorioretinal Atrophy 29 0.052
287
P SJG008 Sjogren Syndrome 58 0.052
288
c CNT035 Central Nervous System Disease 65 0.051
289
P LPD010 Lipodystrophy 57 0.051
290
AMY002 Amyloid Tumor 30 0.051
291
P SCL057 Scoliosis, Isolated 1 28 0.051
292
P AGM001 Agammaglobulinemia 70 0.051
293
EPD006 Epidermolysis Bullosa Acquisita 50 0.051
294
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.050
295
P HYP607 Hypercholesterolemia, Familial 81 0.050
296
P MYP006 Myopia 56 0.050
297
SPN119 Spondylarthropathy 46 0.050
298
P HYP083 Hypopituitarism 59 0.050
299
P PRM006 Primary Biliary Cirrhosis 55 0.050
300
PLM012 Pulmonary Sarcoidosis 58 0.050
301
P DRM010 Dermatomyositis 65 0.050
302
c ART101 Aortic Valve Disease 2 65 0.050
303
c RTN069 Retinitis Pigmentosa 7 38 0.050
304
c LKM071 Leukemia, Chronic Lymphocytic 75 0.049
305
c LKM004 Leukemia, B-Cell, Chronic 37 0.049
306
SPL006 Splenic Infarction 34 0.049
307
HLC007 Helicobacter Pylori Infection 64 0.049
308
SLP005 Sleep Disorder 59 0.049
309
P GRF003 Graft-Versus-Host Disease 72 0.049
310
ATN002 Autonomic Nervous System Disease 51 0.048
311
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 55 0.048
312
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 53 0.048
313
MGC001 Megacolon 50 0.048
314
P EXN002 Exanthem 62 0.048
315
LYM004 Lymphoid Interstitial Pneumonia 47 0.048
316
LYM024 Lymphatic System Disease 45 0.047
317
HMP001 Hemopericardium 34 0.047
318
BRN022 Bronchiectasis 55 0.047
319
CST005 Castleman Disease 44 0.047
320
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.047
321
P SYP003 Syphilis 55 0.047
322
P WHT013 White Sponge Nevus 1 46 0.047
323
P RNG031 Ring Chromosome Y Syndrome 29 0.047
324
ENT004 Enthesopathy 38 0.047
325
P CHR285 Chronic Myelomonocytic Leukemia 63 0.046
326
ARS001 Aarskog-Scott Syndrome 55 0.046
327
P RTN008 Retinitis Pigmentosa 81 0.046
328
CHD001 Chediak-Higashi Syndrome 67 0.046
329
P CRN035 Cranial Nerve Palsy 42 0.046
330
c RTN162 Retinitis Pigmentosa 2 50 0.046
331
INT002 Intermittent Claudication 61 0.046
332
P DMY001 Demyelinating Polyneuropathy 46 0.046
333
ADR005 Adrenal Carcinoma 59 0.046
334
P CHR012 Chronic Granulomatous Disease 69 0.046
335
PLS016 Plasma Cell Leukemia 43 0.046
336
PST055 Postural Hypotension 40 0.046
337
MVM001 Movement Disease 40 0.046
338
P DYS026 Dysfibrinogenemia 51 0.045
339
DWN001 Down Syndrome 70 0.045
340
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.045
341
DSC009 Discoid Lupus Erythematosus 48 0.045
342
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.045
343
ISC002 Ischemic Optic Neuropathy 48 0.045
344
ACN002 Acanthosis Nigricans 60 0.045
345
c ATR087 Atrial Standstill 1 59 0.045
346
FLR002 Filariasis 58 0.045
347
c FML344 Familial Mediterranean Fever, Autosomal Dominant 21 0.045
348
KRT008 Keratopathy 44 0.045
349
IMP005 Impotence 54 0.045
350
P ALP009 Alopecia Areata 64 0.044
351
PHR003 Pharyngitis 59 0.044
352
HDR003 Hidradenitis 47 0.044
353
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.044
354
P DRM053 Dermatitis, Atopic 68 0.044
355
FML330 Familial Lcat Deficiency 37 0.044
356
LYM133 Lymphoma, Hodgkin, Classic 78 0.043
357
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.043
358
c ACT210 Acute Respiratory Distress Syndrome 63 0.043
359
CLN015 Colon Adenocarcinoma 53 0.043
360
c INV001 Invasive Aspergillosis 51 0.043
361
HYD005 Hydrocele 51 0.043
362
MYC014 Mycobacterium Chelonae 34 0.043
363
THR035 Thrombasthenia 46 0.043
364
ALL026 Allergic Hypersensitivity Disease 59 0.043
365
MLT113 Multicentric Castleman Disease 49 0.043
366
CRT072 Creutzfeldt-Jakob Disease 65 0.043
367
RLP001 Relapsing Polychondritis 55 0.043
368
BDD001 Budd-Chiari Syndrome 58 0.043
369
HDR002 Hidradenitis Suppurativa 54 0.043
370
NDL013 Nodular Regenerative Hyperplasia 53 0.042
371
ATR057 Atrioventricular Block 52 0.042
372
P PSD087 Pseudoxanthoma Elasticum 67 0.042
373
HRY003 Hairy Cell Leukemia 60 0.042
374
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 51 0.042
375
c SRC023 Sarcoidosis 2 30 0.042
376
HNS001 Hansen's Disease 31 0.042
377
PSR001 Psoriatic Arthritis 66 0.041
378
P PTT006 Pituitary Adenoma 57 0.041
379
SYN036 Syncope 46 0.041
380
ACR007 Acromegaly 70 0.041
381
CRD119 Cardiac Arrest 63 0.041
382
P ACT008 Actinic Keratosis 56 0.041
383
JNT002 Joint Disorders 60 0.041
384
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.041
385
c MCL042 Macular Degeneration, Age-Related, 1 79 0.041
386
DCT002 Ductal Carcinoma in Situ 56 0.041
387
c NPH055 Nephrotic Syndrome, Type 1 46 0.040
388
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.040
389
c SBC007 Subacute Thyroiditis 43 0.040
390
ATM052 Autoimmune Disease 1 30 0.040
391
HNM002 Hinman Syndrome 25 0.040
392
P CLC063 Celiac Disease 1 65 0.040
393
HMN016 Hemangioendothelioma 43 0.040
394
HPT067 Hepatocellular Adenoma 43 0.040
395
RCT015 Reactive Arthritis 65 0.040
396
c PSR018 Psoriasis 13 39 0.040
397
IMM162 Immunoglobulin E Concentration, Serum 16 0.040
398
LYM006 Lymphoepithelioma-Like Carcinoma 46 0.039
399
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.039
400
c PRM196 Premature Ovarian Failure 1 68 0.039
401
EVN001 Evans' Syndrome 45 0.039
402
c CHR417 Chronic Graft Versus Host Disease 65 0.039
403
BRN071 Brain Injury 54 0.039
404
PYL006 Pyloric Stenosis 47 0.039
405
DNS007 Dense Deposit Disease 36 0.039
406
c LBR014 Leber Congenital Amaurosis 4 48 0.039
407
P INT143 Interstitial Cystitis 63 0.038
408
c CLR131 Ciliary Dyskinesia, Primary, 1 54 0.038
409
P THY023 Thymoma 65 0.038
410
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.038
411
c PCH015 Pachyonychia Congenita 1 59 0.038
412
ACH005 Achalasia 52 0.037
413
AML029 Ameloblastoma 51 0.037
414
P ESS003 Essential Thrombocythemia 71 0.037
415
LYM017 Lyme Disease 68 0.037
416
PRT058 Pure Autonomic Failure 60 0.037
417
P TRC072 Treacher Collins Syndrome 1 61 0.037
418
TBR006 Tuberculoid Leprosy 46 0.037
419
P PLL002 Pellagra 44 0.037
420
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.037
421
c ALZ056 Alzheimer Disease 3 41 0.037
422
P ANX007 Anauxetic Dysplasia 1 36 0.037
423
HSH003 Hashimoto Thyroiditis 67 0.036
424
ADN009 Adenosquamous Carcinoma 54 0.036
425
P AST055 Asthma-Related Traits 1 18 0.036
426
ACT058 Active Peptic Ulcer Disease 43 0.036
427
P FML052 Familial Cold Autoinflammatory Syndrome 55 0.036
428
ENT011 Enterocolitis 52 0.036
429
BSL008 Basal Ganglia Disease 44 0.035
430
P MYS003 Myasthenia Gravis 73 0.035
431
HYP732 Hyperalphalipoproteinemia 1 52 0.035
432
PRS115 Prosthetic Joint Infection 46 0.035
433
SMN006 Seminal Vesicle Tumor 23 0.035
434
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 46 0.035
435
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.034
436
P KRT005 Keratoacanthoma 49 0.034
437
DFF015 Diffuse Glomerulonephritis 32 0.034
438
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 51 0.034
439
c PRG018 Paragangliomas 1 57 0.033
440
P EPD003 Epidermolysis Bullosa Simplex 53 0.033
441
LYM008 Lymphangiosarcoma 51 0.033
442
FNT004 Fainting 36 0.033
443
CHY002 Chylomicron Retention Disease 54 0.032
444
PRP032 Porphyria Variegata 54 0.032
445
P ANL018 Analbuminemia 45 0.032
446
c PRM023 Pre-Malignant Neoplasm 33 0.032
447
c INS002 in Situ Carcinoma 56 0.031
448
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.031
449
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.031
450
P CHR084 Chromosomal Disease 40 0.031
451
c HYP072 Hypersensitivity Reaction Type Iii Disease 35 0.031
452
VSC002 Vascular Dementia 58 0.029
453
KPS002 Kaposiform Hemangioendothelioma 46 0.029
454
P PTY003 Pityriasis Rubra Pilaris 48 0.029
455
c LSS005 Lissencephaly 1 46 0.029
456
BRK001 Brooke-Spiegler Syndrome 45 0.029
457
CHL109 Childhood Apraxia of Speech 31 0.029
458
P AGM019 Agammaglobulinemia, X-Linked 69 0.027
459
ATH013 Atherosclerosis Susceptibility 59 0.027
460
PLV003 Pelvic Inflammatory Disease 56 0.027
461
ADR049 Adrenal Hypoplasia, Congenital 47 0.027
462
GLS007 Glossitis 46 0.027
Content
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