Search results for proteinuria

520 hits were found for proteinuria

# Family MCID Name MIFTS Score
1
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 21 5.221
2
ORT001 Orthostatic Proteinuria 26 4.275
3
MGL001 Megaloblastic Anemia 49 4.060
4
P DNT015 Dent Disease 61 3.431
5
DNN002 Donnai-Barrow Syndrome 38 3.393
6
MGL016 Megaloblastic Anemia-1, Finnish Type 32 2.380
7
P KDN018 Kidney Disease 65 0.323
8
P GLM007 Glomerulonephritis 55 0.243
9
URN009 Urinary System Disease 49 0.239
10
P NPH012 Nephrotic Syndrome 59 0.168
11
P FCL005 Focal Segmental Glomerulosclerosis 60 0.165
12
P AMY004 Amyloidosis 64 0.145
13
END072 Endotheliitis 41 0.135
14
c PRC016 Pre-Eclampsia 56 0.131
15
IMP003 Impaired Renal Function Disease 36 0.131
16
P PRC031 Preeclampsia/eclampsia 1 55 0.128
17
c CHR089 Chronic Kidney Failure 65 0.124
18
P OBS005 Obesity 91 0.121
19
P MMB011 Membranous Nephropathy 50 0.117
20
P ECL001 Eclampsia 51 0.113
21
FBR012 Fabry Disease 71 0.104
22
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.100
23
P ALP004 Alport Syndrome 70 0.100
24
END030 End Stage Renal Failure 51 0.100
25
c GLM029 Glomerulosclerosis, Focal Segmental, 1 48 0.100
26
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 23 0.100
27
SCH014 Schistosomiasis 56 0.095
28
MDY003 Mody, Type Ii 40 0.095
29
c NPH055 Nephrotic Syndrome, Type 1 36 0.095
30
P IGN003 Iga Nephropathy 1 31 0.095
31
P GLM015 Glomerulopathy with Fibronectin Deposits 2 26 0.095
32
P RNL015 Renal Hypertension 47 0.090
33
BLD054 Blood Protein Disease 39 0.090
34
HLL004 Hellp Syndrome 48 0.085
35
IGG001 Iga Glomerulonephritis 48 0.085
36
NPH010 Nephrosclerosis 42 0.085
37
P HPT021 Hepatitis 68 0.080
38
P EXN002 Exanthem 57 0.080
39
P FNC004 Fanconi Syndrome 48 0.080
40
NPH003 Nephrocalcinosis 47 0.080
41
URN003 Urinary Schistosomiasis 46 0.080
42
IMM001 Immune-Complex Glomerulonephritis 41 0.080
43
P MLT019 Multiple Myeloma 82 0.074
44
P LKM002 Leukemia 72 0.074
45
MTH009 Mouth Disease 62 0.074
46
NLP001 Nail-Patella Syndrome 55 0.074
47
NRM003 Norum Disease 51 0.074
48
GLC008 Glucose Metabolism Disease 44 0.074
49
c NPH072 Nephrotic Syndrome, Type 7 34 0.074
50
MDY005 Mody, Type I 34 0.074
51
c GLM039 Glomerulosclerosis, Focal Segmental, 6 29 0.074
52
c NPH070 Nephrotic Syndrome, Type 6 27 0.074
53
c RNL016 Renal Infectious Disease 23 0.074
54
ATM055 Autoimmune Disease 4 18 0.074
55
P ART022 Arthritis 72 0.067
56
P PHC003 Pheochromocytoma 72 0.067
57
PRT036 Peritonitis 60 0.067
58
LWS003 Lowe Syndrome 59 0.067
59
CYS010 Cystinosis 53 0.067
60
IMM136 Immune System Disease 53 0.067
61
P PYL005 Pyelonephritis 52 0.067
62
SCH016 Schimke Immunoosseous Dysplasia 47 0.067
63
c MLG069 Malignant Hypertension 46 0.067
64
INT067 Interstitial Nephritis 45 0.067
65
GLL032 Galloway-Mowat Syndrome 45 0.067
66
CYS036 Cystinosis, Nephropathic 42 0.067
67
c NPH049 Nephrotic Syndrome, Type 2 29 0.067
68
c CHR522 Charcot-Marie-Tooth Disease, Dominant Intermediate E 29 0.067
69
c GLM026 Glomerulosclerosis, Focal Segmental, 2 28 0.067
70
c GLM027 Glomerulosclerosis, Focal Segmental, 3 27 0.067
71
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.067
72
c GLM041 Glomerulosclerosis, Focal Segmental, 7 25 0.067
73
c NPH074 Nephrotic Syndrome, Type 9 23 0.067
74
c IGN002 Iga Nephropathy 2 21 0.067
75
P RHM011 Rheumatoid Arthritis 87 0.060
76
P LYM118 Lymphoma 69 0.060
77
P LPS004 Lupus Erythematosus 63 0.060
78
ADL002 Adult Syndrome 57 0.060
79
P HYP069 Hyperparathyroidism 56 0.060
80
c ALM001 Al Amyloidosis 56 0.060
81
PPL048 Papillorenal Syndrome 51 0.060
82
PRS055 Pierson Syndrome 50 0.060
83
GDP001 Goodpasture Syndrome 49 0.060
84
P AMY082 Amyloidosis, Familial Visceral 46 0.060
85
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 45 0.060
86
EPS006 Epstein Syndrome 41 0.060
87
AMN006 Aminoaciduria 40 0.060
88
P CRY007 Cryoglobulinemia, Familial Mixed 37 0.060
89
c NPH054 Nephrotic Syndrome, Type 3 36 0.060
90
BNS002 Bone Structure Disease 36 0.060
91
c CHR098 Chronic Pyelonephritis 35 0.060
92
c NPH073 Nephrotic Syndrome, Type 8 26 0.060
93
c NPH047 Nephrotic Syndrome, Type 4 25 0.060
94
c IGN004 Iga Nephropathy 3 22 0.060
95
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 18 0.060
96
c GLM014 Glomerulopathy with Fibronectin Deposits 1 16 0.060
97
P CLR023 Colorectal Cancer 95 0.052
98
c SYS001 Systemic Lupus Erythematosus 86 0.052
99
P RNL014 Renal Cell Carcinoma 80 0.052
100
WLS001 Wilson Disease 73 0.052
101
c HPT073 Hepatitis C Virus 70 0.052
102
P HLP001 Holoprosencephaly 65 0.052
103
P GCH001 Gaucher's Disease 63 0.052
104
c HPT001 Hepatitis C 62 0.052
105
HYP066 Hyperglycemia 59 0.052
106
VRL011 Viral Infectious Disease 59 0.052
107
PRP030 Purpura 57 0.052
108
HMR004 Hemorrhagic Fever with Renal Syndrome 56 0.052
109
c ACT027 Acute Pancreatitis 56 0.052
110
P HYP613 Hypophosphatemic Rickets 55 0.052
111
P NPH005 Nephronophthisis 54 0.052
112
CND002 Conduct Disorder 53 0.052
113
BRN106 Burns 52 0.052
114
P HYP014 Hyperuricemia 50 0.052
115
FRS002 Frasier Syndrome 49 0.052
116
c SVR005 Severe Pre-Eclampsia 48 0.052
117
c ORF037 Orofaciodigital Syndrome I 48 0.052
118
P RNV001 Renovascular Hypertension 46 0.052
119
LPP002 Lipoprotein Glomerulopathy 45 0.052
120
ANR004 Anuria 44 0.052
121
P SLD010 Sialidosis, Type I 44 0.052
122
c ALP074 Alport Syndrome, Autosomal Dominant 44 0.052
123
P PRL003 Proliferative Glomerulonephritis 43 0.052
124
LPD004 Lipoid Nephrosis 43 0.052
125
CRS001 Crescentic Glomerulonephritis 41 0.052
126
c LPD019 Lipodystrophy, Partial, Acquired 35 0.052
127
c DNT021 Dent Disease 2 35 0.052
128
c NPH046 Nephrolithiasis, Type I 34 0.052
129
c GLM033 Glomerulosclerosis, Focal Segmental, 4 29 0.052
130
ATM059 Autoimmune Disease 6 27 0.052
131
INS009 Insulin-Resistance Type B 26 0.052
132
EPL108 Epilepsy, Progressive Myoclonic 4, with or Without Renal Failure 26 0.052
133
NLL002 Null Syndrome 26 0.052
134
NPH039 Nephrotic Syndrome, Type 5, with or Without Ocular Abnormalities 25 0.052
135
CNZ008 Coenzyme Q10 Deficiency, Primary, 6 25 0.052
136
c FNC026 Fanconi Renotubular Syndrome 1 24 0.052
137
CYS025 Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic 24 0.052
138
c FCL053 Focal Segmental Glomerulosclerosis 8 23 0.052
139
c NPH095 Nephrotic Syndrome, Type 11 20 0.052
140
c NPH092 Nephrotic Syndrome 15 19 0.052
141
ATM053 Autoimmune Disease 2 18 0.052
142
ATM054 Autoimmune Disease 3 18 0.052
143
P MYC007 Myocardial Infarction 77 0.043
144
P HRT032 Heart Disease 75 0.043
145
P LVR013 Liver Disease 72 0.043
146
KWS002 Kawasaki Disease 67 0.043
147
LSH001 Leishmaniasis 66 0.043
148
P ATR011 Atrial Fibrillation 65 0.043
149
OBS061 Obstructive Sleep Apnea 65 0.043
150
ATH003 Atherosclerosis 65 0.043
151
P AGM001 Agammaglobulinemia 64 0.043
152
P BCL006 B-Cell Lymphomas 64 0.043
153
PRM097 Primary Immunodeficiency Disease 64 0.043
154
P THR014 Thrombocytopenia 63 0.043
155
c HPT016 Hepatitis B 62 0.043
156
SPN186 Spinal Cord Injury 62 0.043
157
WLL001 Williams-Beuren Syndrome 62 0.043
158
P HYP117 Hypertriglyceridemia 61 0.043
159
P THL005 Thalassemia 61 0.043
160
BRC012 Brucellosis 61 0.043
161
CNN005 Connective Tissue Disease 61 0.043
162
P FML161 Familial Mediterranean Fever, Ar 61 0.043
163
WGN006 Wegener Granulomatosis 61 0.043
164
P SLP006 Sleep Apnea 60 0.043
165
P PNC044 Pancreatitis 60 0.043
166
ACQ007 Acquired Immunodeficiency Syndrome 60 0.043
167
ADL030 Adult-Onset Still's Disease 60 0.043
168
c ACT075 Acute Myocardial Infarction 59 0.043
169
LGN002 Legionellosis 59 0.043
170
YLL002 Yellow Fever 57 0.043
171
RBS003 Rabson-Mendenhall Syndrome 57 0.043
172
c HPT003 Hepatitis a 56 0.043
173
c ACT210 Acute Respiratory Distress Syndrome 56 0.043
174
c GLY060 Glycogen Storage Disease Ia 55 0.043
175
P HMR003 Hemorrhagic Disease 55 0.043
176
ART111 Artery Disease 55 0.043
177
c GCH015 Gaucher Disease, Type I 54 0.043
178
P THY032 Thyroiditis 53 0.043
179
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.043
180
P SPS003 Spastic Diplegia 52 0.043
181
RLP001 Relapsing Polychondritis 51 0.043
182
MTC097 Mitochondrial Complex Iv Deficiency 51 0.043
183
PMS001 Poems Syndrome 51 0.043
184
SCK005 Sickle Cell Disease 51 0.043
185
P RNL100 Renal Hypodysplasia/aplasia 1 50 0.043
186
RNL007 Renal Tubular Acidosis 48 0.043
187
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 48 0.043
188
c CNG415 Congenital Disorder of Glycosylation, Type Ia 48 0.043
189
c MCP040 Mucopolysaccharidosis-Plus Syndrome 48 0.043
190
c GCH017 Gaucher Disease, Type Iii 47 0.043
191
PLS009 Plasma Cell Neoplasm 47 0.043
192
RNL051 Renal Cysts and Diabetes Syndrome 46 0.043
193
BLD053 Blood Platelet Disease 46 0.043
194
RNL077 Renal Fibrosis 46 0.043
195
MMB001 Membranoproliferative Glomerulonephritis 46 0.043
196
P HML033 Hemolytic Uremic Syndrome, Atypical 1 46 0.043
197
c ALP073 Alport Syndrome, Autosomal Recessive 45 0.043
198
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.043
199
MCR037 Macroglossia 45 0.043
200
c ACT042 Acute Pyelonephritis 44 0.043
201
BCT004 Bacteriuria 44 0.043
202
SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 43 0.043
203
RPR002 Reproductive System Disease 43 0.043
204
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 43 0.043
205
ESN020 Eosinophilic Granulomatosis with Polyangiitis 43 0.043
206
c SPL024 Split-Hand/foot Malformation 3 43 0.043
207
THR024 Thrombosis 43 0.043
208
EBL001 Ebola Hemorrhagic Fever 43 0.043
209
c CCK005 Cockayne Syndrome, Type a 42 0.043
210
c CRN139 Cornelia De Lange Syndrome 1 42 0.043
211
P ACQ022 Acquired Generalized Lipodystrophy 42 0.043
212
MSN001 Mesangial Proliferative Glomerulonephritis 41 0.043
213
c CCK006 Cockayne Syndrome, Type B 40 0.043
214
FCH003 Fechtner Syndrome 39 0.043
215
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 39 0.043
216
c GLY016 Glycogen Storage Disease Ib 39 0.043
217
CRB009 Cerebritis 39 0.043
218
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 38 0.043
219
ADJ001 Adjustment Disorder 38 0.043
220
SPC003 Specific Developmental Disorder 38 0.043
221
INT221 Intravascular Large B-Cell Lymphoma 38 0.043
222
OHD004 Ohdo Syndrome 36 0.043
223
P HYP120 Hypoaldosteronism 36 0.043
224
DNS007 Dense Deposit Disease 35 0.043
225
MJD001 Majeed Syndrome 35 0.043
226
DBT090 Diabetes and Deafness, Maternally Inherited 35 0.043
227
PYL004 Pyelitis 35 0.043
228
HYP193 Hypocomplementemic Urticarial Vasculitis 34 0.043
229
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 34 0.043
230
IMM073 Immunoglobulin a Vasculitis 33 0.043
231
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 33 0.043
232
HYP114 Hypertensive Nephropathy 33 0.043
233
BLK001 Balkan Nephropathy 32 0.043
234
VSC008 Vascular Hemostatic Disease 32 0.043
235
MLK004 Malakoplakia 31 0.043
236
FRS004 Free Sialic Acid Storage Disorders 30 0.043
237
MNT146 Mental Retardation, X-Linked, Syndromic, Martin-Probst Type 29 0.043
238
c HML035 Hemolytic Uremic Syndrome, Atypical 2 28 0.043
239
c HML034 Hemolytic Uremic Syndrome, Atypical 3 28 0.043
240
c HML032 Hemolytic Uremic Syndrome, Atypical 4 28 0.043
241
c HML037 Hemolytic Uremic Syndrome, Atypical 5 28 0.043
242
ATM052 Autoimmune Disease 1 27 0.043
243
c HML036 Hemolytic Uremic Syndrome, Atypical 6 27 0.043
244
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 27 0.043
245
INT224 Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital 26 0.043
246
c GLM028 Glomerulosclerosis, Focal Segmental, 5 26 0.043
247
c GLY017 Glycogen Storage Disease Ic 25 0.043
248
WLD005 Wild Type Attr Amyloidosis 25 0.043
249
c HYP248 Hyperprolinemia, Type I 24 0.043
250
INT258 Interstitial Nephritis, Karyomegalic 24 0.043
251
CNZ004 Coenzyme Q10 Deficiency, Primary, 3 24 0.043
252
c NPH096 Nephrotic Syndrome, Type 12 23 0.043
253
c FML162 Familial Mediterranean Fever, Ad 22 0.043
254
c NPH065 Nephronophthisis 13 21 0.043
255
c RNL113 Renal Failure, Progressive, with Hypertension 21 0.043
256
PRT110 Prieto Syndrome 21 0.043
257
CHR620 Chromosome 16p11.2 Deletion Syndrome, 220-Kb 20 0.043
258
c NPH094 Nephrotic Syndrome 14 20 0.043
259
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 19 0.043
260
OCL043 Oculorenocerebellar Syndrome 18 0.043
261
RNL089 Renal Nutcracker Syndrome 17 0.043
262
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 17 0.043
263
c FNC049 Fanconi Renotubular Syndrome 3 17 0.043
264
DYS180 Dyschondrosteosis and Nephritis 17 0.043
265
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 17 0.043
266
c ATM093 Autoimmune Disease, Multisystem, Infantile-Onset, 2 16 0.043
267
HYP479 Hyperinsulinism Due to Hnf4a Deficiency 15 0.043
268
LMN004 Laminopathy Type Decaudain-Vigouroux 14 0.043
269
OCL029 Oculo Skeletal Renal Syndrome 14 0.043
270
NLP003 Nail-Patella-Like Renal Disease 12 0.043
271
CYS001 Cystic Fibrosis 86 0.030
272
HV1006 Hiv-1 80 0.030
273
P DBT085 Diabetes Mellitus, Insulin-Dependent 79 0.030
274
P CRN211 Coronary Artery Disease 73 0.030
275
PHN003 Phenylketonuria 72 0.030
276
SCK003 Sickle Cell Anemia 71 0.030
277
P NRB001 Neuroblastoma 71 0.030
278
CNG034 Congestive Heart Failure 70 0.030
279
P RSP003 Respiratory Failure 68 0.030
280
PCK002 Pick Disease 68 0.030
281
P CRD011 Cardiomyopathy 67 0.030
282
P ANR002 Aniridia 66 0.030
283
LVR012 Liver Cirrhosis 66 0.030
284
CHG001 Chagas Disease 66 0.030
285
P PNM007 Pneumonia 66 0.030
286
c HYP595 Hypertension, Essential 66 0.030
287
VSC007 Vascular Disease 65 0.030
288
ALX003 Alexander Disease 65 0.030
289
PRP027 Peripheral Vascular Disease 65 0.030
290
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.030
291
P MYL006 Myeloid Leukemia 64 0.030
292
P PSR002 Psoriasis 64 0.030
293
P PLY011 Polycystic Ovary Syndrome 63 0.030
294
P CNJ013 Conjunctivitis 63 0.030
295
MCK007 Muckle-Wells Syndrome 63 0.030
296
CYS013 Cystinuria 63 0.030
297
P INF037 Inflammatory Bowel Disease 62 0.030
298
VSC011 Vasculitis 62 0.030
299
P ART023 Arthropathy 62 0.030
300
LSC001 Lesch-Nyhan Syndrome 62 0.030
301
P HRP006 Herpes Simplex 62 0.030
302
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.030
303
GTL001 Gitelman Syndrome 61 0.030
304
HYP056 Hypoglycemia 60 0.030
305
P LYM026 Lymphoblastic Leukemia 60 0.030
306
SYS004 Systemic Mastocytosis 60 0.030
307
HPY002 H. Pylori Infection 60 0.030
308
DNG002 Dengue Hemorrhagic Fever 60 0.030
309
CHL071 Child Syndrome 59 0.030
310
P CMR001 Camurati-Engelmann Disease 59 0.030
311
P DRM010 Dermatomyositis 59 0.030
312
P GLY013 Glycogen Storage Disease 59 0.030
313
P DRR001 Diarrhea 59 0.030
314
CRD119 Cardiac Arrest 59 0.030
315
OST017 Osteomyelitis 58 0.030
316
c VRL010 Viral Hepatitis 58 0.030
317
WLL006 Wells Syndrome 58 0.030
318
CTS003 Coats Disease 58 0.030
319
DPH001 Diphtheria 57 0.030
320
P THR005 Thrombotic Thrombocytopenic Purpura 57 0.030
321
KDS001 Kid Syndrome 57 0.030
322
P RCK004 Rickets 57 0.030
323
LPD008 Lipid Metabolism Disorder 57 0.030
324
P PLY018 Polycythemia 56 0.030
325
PRD019 Periodic Fever, Familial 56 0.030
326
P MTH008 Methylmalonic Acidemia 56 0.030
327
TNS005 Tonsillitis 56 0.030
328
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 55 0.030
329
INT002 Intermittent Claudication 55 0.030
330
TXC005 Toxic Shock Syndrome 55 0.030
331
ACR008 Acrocallosal Syndrome 55 0.030
332
PRS047 Prostatitis 55 0.030
333
GLC003 Glucose Intolerance 54 0.030
334
RHM001 Rheumatic Fever 54 0.030
335
P PRG013 Paraganglioma 54 0.030
336
P LMY004 Leiomyosarcoma 54 0.030
337
P MNC007 Monocytic Leukemia 54 0.030
338
SLP005 Sleep Disorder 54 0.030
339
LYM027 Lymphopenia 54 0.030
340
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.030
341
GST050 Gastrointestinal System Disease 53 0.030
342
P LPD010 Lipodystrophy 53 0.030
343
PHR003 Pharyngitis 53 0.030
344
CSY001 C Syndrome 53 0.030
345
GST027 Gastric Lymphoma 52 0.030
346
THL018 Thalassemia Major 52 0.030
347
P HMR012 Hemorrhagic Fever 52 0.030
348
P BRN009 Burning Mouth Syndrome 52 0.030
349
P PLY014 Polycystic Kidney Disease 52 0.030
350
APP015 Apparent Mineralocorticoid Excess 52 0.030
351
P PTS002 Ptosis 52 0.030
352
c ACT009 Acute Monocytic Leukemia 52 0.030
353
P VSC005 Vesicoureteral Reflux 52 0.030
354
CYS005 Cysticercosis 52 0.030
355
P DBT005 Diabetes Insipidus 52 0.030
356
c INT064 Intermediate Uveitis 51 0.030
357
MCN007 Meconium Aspiration Syndrome 51 0.030
358
HDR002 Hidradenitis Suppurativa 51 0.030
359
SPN051 Spondylitis 51 0.030
360
SLM003 Salmonellosis 51 0.030
361
CRH005 Crohn's Colitis 50 0.030
362
TRY001 Trypanosomiasis 50 0.030
363
SCH002 Schnitzler Syndrome 50 0.030
364
NRG002 Neurogenic Bladder 50 0.030
365
ASP003 Aseptic Meningitis 50 0.030
366
BLD044 Bladder Disease 50 0.030
367
PNC001 Pancytopenia 49 0.030
368
P AGG001 Aggressive Periodontitis 49 0.030
369
SPH001 Sapho Syndrome 49 0.030
370
PMP001 Pemphigus 49 0.030
371
AMN001 Amenorrhea 49 0.030
372
P RST002 Restrictive Cardiomyopathy 49 0.030
373
DBT084 Diabetes Mellitus, Ketosis-Prone 49 0.030
374
RTN023 Retinitis 49 0.030
375
MCR004 Macroglobulinemia 48 0.030
376
ONC002 Onchocerciasis 48 0.030
377
EXT010 Extramedullary Plasmacytoma 48 0.030
378
c ACT071 Acute Kidney Failure 48 0.030
379
P DDN001 Duodenal Ulcer 48 0.030
380
RGH009 Right Atrial Isomerism 48 0.030
381
BRN056 Bronchopulmonary Dysplasia 48 0.030
382
URM002 Uremia 48 0.030
383
MTB004 Metabolic Acidosis 47 0.030
384
PRT030 Parathyroid Gland Disease 47 0.030
385
PPL021 Papilledema 47 0.030
386
CHR001 Churg-Strauss Syndrome 47 0.030
387
PRT082 Preterm Premature Rupture of the Membranes 47 0.030
388
PRR002 Pure Red-Cell Aplasia 46 0.030
389
P HRD001 Hereditary Multiple Exostoses 46 0.030
390
FBR032 Fibromuscular Dysplasia 46 0.030
391
HYP025 Hyperphosphatemia 46 0.030
392
PLR001 Pleural Tuberculosis 46 0.030
393
c ACT068 Acute Cystitis 45 0.030
394
c AMY009 Amyloidosis Aa 45 0.030
395
NCR007 Necrotizing Fasciitis 45 0.030
396
CRD118 Cardiovascular Cancer 45 0.030
397
BNN003 Bone Inflammation Disease 45 0.030
398
PLP001 Pulpitis 44 0.030
399
FSC004 Fasciitis 44 0.030
400
HNC001 Henoch-Schoenlein Purpura 44 0.030
401
HYP691 Hypomelanosis of Ito 44 0.030
402
MNC006 Monoclonal Gammopathy of Uncertain Significance 43 0.030
403
TCL002 T-Cell Large Granular Lymphocyte Leukemia 43 0.030
404
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 43 0.030
405
NSS002 Neisseria Meningitidis Infection 43 0.030
406
PHY002 Physical Disorder 43 0.030
407
HDR003 Hidradenitis 43 0.030
408
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 42 0.030
409
PMP004 Pemphigus Foliaceus 42 0.030
410
CLN003 Clonorchiasis 42 0.030
411
LGH004 Light Chain Deposition Disease 42 0.030
412
PLC003 Placental Site Trophoblastic Tumor 42 0.030
413
SPN119 Spondylarthropathy 42 0.030
414
SXL003 Sexual Disorder 42 0.030
415
IMP004 Impetigo 42 0.030
416
RNL097 Renal Artery Disease 42 0.030
417
ACT200 Acute Monoblastic Leukemia 42 0.030
418
INT017 Intestinal Schistosomiasis 42 0.030
419
c ACT159 Acute Transverse Myelitis 42 0.030
420
MDL009 Medullary Sponge Kidney 42 0.030
421
NM001 Noma 42 0.030
422
ART008 Arteriosclerosis Obliterans 42 0.030
423
LSS003 Lassa Fever 41 0.030
424
P CPL003 Capillary Leak Syndrome 41 0.030
425
c HYP073 Hypersensitivity Reaction Type Iv Disease 41 0.030
426
PLS016 Plasma Cell Leukemia 41 0.030
427
LYM029 Lymphedema-Distichiasis Syndrome 41 0.030
428
TRC003 Trichomoniasis 40 0.030
429
HYP540 Hypertension, Diastolic 40 0.030
430
P SDR003 Sideroblastic Anemia 40 0.030
431
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 40 0.030
432
STT004 Steatorrhea 40 0.030
433
THL017 Thalassemia Intermedia 40 0.030
434
CST005 Castleman Disease 39 0.030
435
STR077 Streptococcal Toxic-Shock Syndrome 39 0.030
436
URM005 Uremic Pruritus 38 0.030
437
DNT008 Denture Stomatitis 38 0.030
438
DRF001 Dirofilariasis 38 0.030
439
PCH007 Pouchitis 38 0.030
440
MNN021 Meningococcemia 38 0.030
441
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 38 0.030
442
MDY004 Mody, Type Iii 37 0.030
443
ATM012 Autoimmune Disease of Blood 37 0.030
444
SCR015 Scarlet Fever 36 0.030
445
c HYP311 Hyperparathyroidism 3 36 0.030
446
FNS001 Funisitis 36 0.030
447
MRS001 Marasmus 36 0.030
448
IMM065 Immunodeficiency 10 36 0.030
449
HYD003 Hydrarthrosis 36 0.030
450
OST008 Osteosclerotic Myeloma 35 0.030
451
MRR003 Murray Valley Encephalitis 35 0.030
452
PPL019 Papillary Conjunctivitis 35 0.030
453
RCR001 Recurrent Corneal Erosion 35 0.030
454
P PRX033 Proximal Renal Tubular Acidosis 34 0.030
455
P ARC016 Auriculocondylar Syndrome 1 34 0.030
456
ACT040 Acute Poststreptococcal Glomerulonephritis 34 0.030
457
c TRC078 Trichohepatoenteric Syndrome 2 34 0.030
458
FML330 Familial Lcat Deficiency 34 0.030
459
BGS001 Bagassosis 34 0.030
460
CRY008 Cryopyrin-Associated Periodic Syndrome 33 0.030
461
MLD002 Mild Pre-Eclampsia 32 0.030
462
c SYS043 Systemic Lupus Erythematosus 1 32 0.030
463
PNN005 Panencephalitis, Subacute Sclerosing 32 0.030
464
c ACT036 Acute Cholangitis 32 0.030
465
NCR002 Necrobiosis Lipoidica 32 0.030
466
c ALG016 Alagille Syndrome 2 32 0.030
467
PLY010 Polyclonal Hypergammaglobulinemia 31 0.030
468
PYR004 Pyuria 31 0.030
469
KDN013 Kidney Hypertrophy 31 0.030
470
LST003 Listeria Meningitis 31 0.030
471
VTM003 Vitamin Metabolic Disorder 31 0.030
472
PDT040 Pediatric Hypertension 31 0.030
473
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 30 0.030
474
IMM071 Immunodeficiency 12 30 0.030
475
CMM006 Commensal Bacterial Infectious Disease 30 0.030
476
CHL070 Cholesterol Embolism 30 0.030
477
c NPH031 Nephronophthisis 3 30 0.030
478
NLL001 Null-Cell Leukemia 30 0.030
479
TYP027 Type 1 Diabetes Mellitus 10 30 0.030
480
C3G002 C3 Glomerulopathy 29 0.030
481
c PRC045 Preeclampsia/eclampsia 5 28 0.030
482
CNG116 Congenital Nephrotic Syndrome Finnish Type 27 0.030
483
TXC003 Toxicodendron Dermatitis 27 0.030
484
HMX002 Heme Oxygenase-1 Deficiency 27 0.030
485
c SYS038 Systemic Lupus Erythematosus 2 27 0.030
486
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 26 0.030
487
DFN256 Deafness and Myopia 26 0.030
488
c JVN047 Juvenile Spondyloarthropathy 25 0.030
489
c PRC034 Preeclampsia/eclampsia 4 25 0.030
490
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 25 0.030
491
P C1Q005 C1q Nephropathy 24 0.030
492
IMM053 Immunotactoid Glomerulopathy 23 0.030
493
c EXS004 Exostoses, Multiple, Type 1 23 0.030
494
c VSC025 Vesicoureteral Reflux 3 23 0.030
495
HPD002 Hepadnavirus Infection 22 0.030
496
P CRN178 Coronary Heart Disease 6 22 0.030
497
c SYS051 Systemic Lupus Erythematosus 4 22 0.030
498
c FCL055 Focal Segmental Glomerulosclerosis 9 22 0.030
499
PYG002 Pyogenic Arthritis, Pyoderma Gangrenosum and Acne 22 0.030
500
c VSC020 Vesicoureteral Reflux 2 22 0.030
501
c NPH076 Nephrotic Syndrome, Type 10 21 0.030
502
c VSC046 Vesicoureteral Reflux 8 21 0.030
503
PYL007 Pylorus Cancer 20 0.030
504
FBR085 Fibrillary Glomerulonephritis 20 0.030
505
P ACR072 Acrorenal Syndrome 19 0.030
506
c PRC032 Preeclampsia/eclampsia 2 18 0.030
507
c NPH093 Nephrotic Syndrome, Type 13 18 0.030
508
NVD002 Nevada Syndrome 16 0.030
509
PHC008 Pheochromocytoma-Islet Cell Tumor Syndrome 15 0.030
510
HRP008 Herpes Simiae 15 0.030
511
c PTR011 Paternal Uniparental Disomy of Chromosome 1 15 0.030
512
c EXS006 Exostoses, Multiple, Type 3 13 0.030
513
c SYS056 Systemic Lupus Erythematosus with Nephritis 1 13 0.030
514
HRP012 Herpesvirus Simiae B Virus 13 0.030
515
P SYS050 Systemic Lupus Erythematosus with Nephritis 2 13 0.030
516
TSY001 Tau Syndrome 12 0.030
517
CLS011 Classic Fabry Disease 12 0.030
518
IMM051 Immunotactoid or Fibrillary Glomerulopathy 9 0.030
519
BLK002 Balkan Hemorrhagic Fever 7 0.030
520
SLC010 Salcedo Syndrome 5 0.030
Content
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