Search results for proteinuria

554 hits were found for proteinuria

# Family MCID Name MIFTS Score
1
c MGL018 Megaloblastic Anemia 1 43 5.378
2
PRT121 Proteinuria, Low Molecular Weight, with Hypercalciuria and Nephrocalcinosis 19 5.361
3
ORT001 Orthostatic Proteinuria 29 4.376
4
DNN002 Donnai-Barrow Syndrome 40 4.221
5
P DNT020 Dent Disease 1 55 3.515
6
P KDN018 Kidney Disease 69 0.315
7
c CHR089 Chronic Kidney Failure 72 0.256
8
P GLM007 Glomerulonephritis 61 0.238
9
URN009 Urinary System Disease 58 0.235
10
c MCR113 Microvascular Complications of Diabetes 3 55 0.186
11
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.184
12
c MCR130 Microvascular Complications of Diabetes 6 42 0.184
13
c MCR120 Microvascular Complications of Diabetes 7 34 0.184
14
c MCR133 Microvascular Complications of Diabetes 4 32 0.184
15
P DBT009 Diabetes Mellitus 72 0.182
16
P NPH012 Nephrotic Syndrome 60 0.165
17
P FCL005 Focal Segmental Glomerulosclerosis 60 0.165
18
c PRC016 Pre-Eclampsia 65 0.148
19
P AMY004 Amyloidosis 69 0.140
20
P MMB011 Membranous Nephropathy 55 0.137
21
END072 Endotheliitis 46 0.130
22
c BLD140 Blood Group, I System 37 0.127
23
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.113
24
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.113
25
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.113
26
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.113
27
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.113
28
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.113
29
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.113
30
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.113
31
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.113
32
END030 End Stage Renal Failure 59 0.105
33
P ECL001 Eclampsia 57 0.105
34
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.097
35
ALP046 Alport Syndrome, X-Linked 74 0.097
36
FBR012 Fabry Disease 72 0.097
37
SCH014 Schistosomiasis 62 0.092
38
P IGN003 Iga Nephropathy 1 34 0.092
39
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.092
40
P GLM015 Glomerulopathy with Fibronectin Deposits 2 30 0.092
41
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.092
42
IGG001 Iga Glomerulonephritis 52 0.087
43
NPH010 Nephrosclerosis 46 0.087
44
c NPH049 Nephrotic Syndrome, Type 2 40 0.087
45
P FML018 Familial Mediterranean Fever 73 0.082
46
ATM095 Autoimmune Disease 66 0.082
47
AGN016 Aging 65 0.082
48
c NPH055 Nephrotic Syndrome, Type 1 46 0.082
49
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.082
50
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.082
51
P HPT021 Hepatitis 75 0.077
52
P FNC004 Fanconi Syndrome 54 0.077
53
INT067 Interstitial Nephritis 51 0.077
54
URN003 Urinary Schistosomiasis 50 0.077
55
NPH003 Nephrocalcinosis 49 0.077
56
MYL069 Myeloma, Multiple 86 0.071
57
P LKM002 Leukemia 75 0.071
58
BRC012 Brucellosis 71 0.071
59
LWC002 Lowe Oculocerebrorenal Syndrome 62 0.071
60
P EXN002 Exanthem 62 0.071
61
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 0.071
62
P PYL005 Pyelonephritis 56 0.071
63
NLP001 Nail-Patella Syndrome 56 0.071
64
HLL004 Hellp Syndrome 53 0.071
65
c MLG069 Malignant Hypertension 49 0.071
66
IMM001 Immune-Complex Glomerulonephritis 39 0.071
67
P PHC003 Pheochromocytoma 72 0.065
68
PRT036 Peritonitis 67 0.065
69
HMR004 Hemorrhagic Fever with Renal Syndrome 63 0.065
70
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.065
71
CYS010 Cystinosis 55 0.065
72
FRS002 Frasier Syndrome 51 0.065
73
SCH016 Schimke Immunoosseous Dysplasia 47 0.065
74
LPD004 Lipoid Nephrosis 46 0.065
75
P PRC031 Preeclampsia/eclampsia 1 41 0.065
76
P FNC026 Fanconi Renotubular Syndrome 1 32 0.065
77
c NPH072 Nephrotic Syndrome, Type 7 28 0.065
78
c CHR522 Charcot-Marie-Tooth Disease, Dominant Intermediate E 26 0.065
79
c FCL043 Focal Segmental Glomerulosclerosis 6 21 0.065
80
c NPH074 Nephrotic Syndrome, Type 9 20 0.065
81
P RHM011 Rheumatoid Arthritis 91 0.058
82
P ART022 Arthritis 77 0.058
83
P LYM118 Lymphoma 71 0.058
84
P LPS004 Lupus Erythematosus 69 0.058
85
P MCR115 Microvascular Complications of Diabetes 5 66 0.058
86
P HYP069 Hyperparathyroidism 58 0.058
87
c ALM001 Al Amyloidosis 56 0.058
88
GDP001 Goodpasture Syndrome 55 0.058
89
PPL048 Papillorenal Syndrome 53 0.058
90
MMB001 Membranoproliferative Glomerulonephritis 51 0.058
91
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 50 0.058
92
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.058
93
ANR004 Anuria 49 0.058
94
P RNV001 Renovascular Hypertension 48 0.058
95
CYS036 Cystinosis, Nephropathic 47 0.058
96
P PRL003 Proliferative Glomerulonephritis 45 0.058
97
PRS055 Pierson Syndrome 43 0.058
98
AMN006 Aminoaciduria 41 0.058
99
OHD004 Ohdo Syndrome 41 0.058
100
c CHR098 Chronic Pyelonephritis 38 0.058
101
P HYP733 Hypercalciuria, Absorptive, 2 37 0.058
102
EPS006 Epstein Syndrome 33 0.058
103
c NPH054 Nephrotic Syndrome, Type 3 29 0.058
104
c NPH070 Nephrotic Syndrome, Type 6 20 0.058
105
c FCL085 Focal Segmental Glomerulosclerosis 7 20 0.058
106
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 20 0.058
107
c GLM014 Glomerulopathy with Fibronectin Deposits 1 18 0.058
108
NLP003 Nail-Patella-Like Renal Disease 16 0.058
109
P CLR023 Colorectal Cancer 98 0.050
110
c SYS001 Systemic Lupus Erythematosus 86 0.050
111
c HYP595 Hypertension, Essential 78 0.050
112
c HPT073 Hepatitis C Virus 73 0.050
113
c HPT001 Hepatitis C 73 0.050
114
WLS001 Wilson Disease 72 0.050
115
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.050
116
P HLP001 Holoprosencephaly 67 0.050
117
ACQ007 Acquired Immunodeficiency Syndrome 65 0.050
118
VRL011 Viral Infectious Disease 64 0.050
119
HYP066 Hyperglycemia 64 0.050
120
P GCH001 Gaucher's Disease 62 0.050
121
PRP030 Purpura 61 0.050
122
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.050
123
c GLY060 Glycogen Storage Disease Ia 57 0.050
124
P NPH005 Nephronophthisis 57 0.050
125
BRN106 Burns 57 0.050
126
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.050
127
P HYP014 Hyperuricemia 54 0.050
128
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.050
129
c SVR005 Severe Pre-Eclampsia 53 0.050
130
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 53 0.050
131
c ORF037 Orofaciodigital Syndrome I 51 0.050
132
PLS009 Plasma Cell Neoplasm 51 0.050
133
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 49 0.050
134
P ALP074 Alport Syndrome, Autosomal Dominant 47 0.050
135
P RNL015 Renal Hypertension 46 0.050
136
CRS001 Crescentic Glomerulonephritis 44 0.050
137
LPP002 Lipoprotein Glomerulopathy 44 0.050
138
P HYP120 Hypoaldosteronism 40 0.050
139
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.050
140
c LPD019 Lipodystrophy, Partial, Acquired 38 0.050
141
PYL004 Pyelitis 38 0.050
142
c GLL038 Galloway-Mowat Syndrome 1 37 0.050
143
RNL105 Renal Agenesis, Unilateral 35 0.050
144
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.050
145
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 29 0.050
146
c RNL113 Renal Failure, Progressive, with Hypertension 29 0.050
147
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 28 0.050
148
c DNT021 Dent Disease 2 26 0.050
149
CYS046 Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type 23 0.050
150
LMY010 Leiomyomatosis, Diffuse, with Alport Syndrome 23 0.050
151
c NPH073 Nephrotic Syndrome, Type 8 21 0.050
152
c FCL027 Focal Segmental Glomerulosclerosis 3 20 0.050
153
INS009 Insulin-Resistance Type B 20 0.050
154
CNZ008 Coenzyme Q10 Deficiency, Primary, 6 19 0.050
155
c NPH095 Nephrotic Syndrome, Type 11 19 0.050
156
NPH039 Nephrotic Syndrome, Type 5, with or Without Ocular Abnormalities 19 0.050
157
c FCL053 Focal Segmental Glomerulosclerosis 8 19 0.050
158
c FCL026 Focal Segmental Glomerulosclerosis 2 18 0.050
159
c IGN004 Iga Nephropathy 3 17 0.050
160
c IGN002 Iga Nephropathy 2 17 0.050
161
c ATM093 Autoimmune Disease, Multisystem, Infantile-Onset, 2 17 0.050
162
c NPH092 Nephrotic Syndrome 15 16 0.050
163
P MYC007 Myocardial Infarction 81 0.041
164
P HRT032 Heart Disease 80 0.041
165
P LVR013 Liver Disease 76 0.041
166
CNG034 Congestive Heart Failure 74 0.041
167
LVR012 Liver Cirrhosis 73 0.041
168
KWS002 Kawasaki Disease 72 0.041
169
LSH001 Leishmaniasis 71 0.041
170
WGN006 Wegener Granulomatosis 71 0.041
171
P AGM001 Agammaglobulinemia 70 0.041
172
P BCL006 B-Cell Lymphomas 70 0.041
173
c HPT016 Hepatitis B 68 0.041
174
P ATR011 Atrial Fibrillation 68 0.041
175
P ANR048 Aniridia 1 68 0.041
176
APN008 Apnea, Obstructive Sleep 67 0.041
177
SPN186 Spinal Cord Injury 67 0.041
178
LGN002 Legionellosis 65 0.041
179
P THL005 Thalassemia 65 0.041
180
P SLP006 Sleep Apnea 65 0.041
181
CNN005 Connective Tissue Disease 65 0.041
182
P THR014 Thrombocytopenia 65 0.041
183
c ACT075 Acute Myocardial Infarction 64 0.041
184
P PNC044 Pancreatitis 64 0.041
185
WLL001 Williams-Beuren Syndrome 63 0.041
186
c HPT003 Hepatitis a 63 0.041
187
CRD119 Cardiac Arrest 63 0.041
188
YLL002 Yellow Fever 63 0.041
189
c MCR129 Microvascular Complications of Diabetes 1 62 0.041
190
c ACT027 Acute Pancreatitis 61 0.041
191
THR024 Thrombosis 61 0.041
192
INT002 Intermittent Claudication 61 0.041
193
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.041
194
P HMR003 Hemorrhagic Disease 61 0.041
195
ANR040 Aneurysm 61 0.041
196
c GCH015 Gaucher Disease, Type I 57 0.041
197
IMM136 Immune System Disease 57 0.041
198
P THY032 Thyroiditis 56 0.041
199
RLP001 Relapsing Polychondritis 55 0.041
200
MTC097 Mitochondrial Complex Iv Deficiency 55 0.041
201
SPS003 Spastic Diplegia 55 0.041
202
P HYP750 Hypertriglyceridemia, Familial 55 0.041
203
SCK005 Sickle Cell Disease 54 0.041
204
DNY001 Denys-Drash Syndrome 54 0.041
205
c ACT071 Acute Kidney Failure 54 0.041
206
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 54 0.041
207
c VSC019 Vesicoureteral Reflux 1 54 0.041
208
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 53 0.041
209
c CNG415 Congenital Disorder of Glycosylation, Type Ia 53 0.041
210
FBR032 Fibromuscular Dysplasia 53 0.041
211
c CCK007 Cockayne Syndrome B 52 0.041
212
URM002 Uremia 52 0.041
213
P MGL001 Megaloblastic Anemia 52 0.041
214
P RNL007 Renal Tubular Acidosis 51 0.041
215
ART140 Arteries, Anomalies of 51 0.041
216
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 51 0.041
217
c ALP073 Alport Syndrome, Autosomal Recessive 50 0.041
218
RNL077 Renal Fibrosis 49 0.041
219
P HML033 Hemolytic Uremic Syndrome, Atypical 1 49 0.041
220
c SPL024 Split-Hand/foot Malformation 3 49 0.041
221
c CCK008 Cockayne Syndrome a 48 0.041
222
HNC001 Henoch-Schoenlein Purpura 48 0.041
223
c AMY009 Amyloidosis Aa 48 0.041
224
AMY082 Amyloidosis, Familial Visceral 47 0.041
225
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.041
226
c GCH017 Gaucher Disease, Type Iii 47 0.041
227
SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 47 0.041
228
NRM019 Neuraminidase Deficiency 47 0.041
229
EPD070 Epidermoid Cysts 46 0.041
230
c CRN139 Cornelia De Lange Syndrome 1 46 0.041
231
P HRD009 Hereditary Wilms' Tumor 46 0.041
232
EBL001 Ebola Hemorrhagic Fever 45 0.041
233
RNL051 Renal Cysts and Diabetes Syndrome 45 0.041
234
LSS003 Lassa Fever 45 0.041
235
P ACQ022 Acquired Generalized Lipodystrophy 45 0.041
236
P GLL032 Galloway-Mowat Syndrome 45 0.041
237
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.041
238
MCR037 Macroglossia 44 0.041
239
INT221 Intravascular Large B-Cell Lymphoma 42 0.041
240
CRB009 Cerebritis 41 0.041
241
DBT090 Diabetes and Deafness, Maternally Inherited 40 0.041
242
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.041
243
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 40 0.041
244
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 40 0.041
245
MRS001 Marasmus 39 0.041
246
GLC008 Glucose Metabolism Disease 38 0.041
247
FCH003 Fechtner Syndrome 38 0.041
248
P BLD051 Blood Coagulation Disease 38 0.041
249
HYP193 Hypocomplementemic Urticarial Vasculitis 38 0.041
250
VSC008 Vascular Hemostatic Disease 36 0.041
251
c GLY016 Glycogen Storage Disease Ib 36 0.041
252
DNS007 Dense Deposit Disease 36 0.041
253
c HYP072 Hypersensitivity Reaction Type Iii Disease 35 0.041
254
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 35 0.041
255
HYP114 Hypertensive Nephropathy 35 0.041
256
MJD001 Majeed Syndrome 35 0.041
257
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 34 0.041
258
MLK004 Malakoplakia 34 0.041
259
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.041
260
ACT003 Acute Kidney Tubular Necrosis 34 0.041
261
FRS004 Free Sialic Acid Storage Disorders 31 0.041
262
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 31 0.041
263
P KLZ004 Kala-Azar 1 31 0.041
264
MNT146 Mental Retardation, X-Linked, Syndromic, Martin-Probst Type 30 0.041
265
c MCR112 Microvascular Complications of Diabetes 2 30 0.041
266
URN022 Urinary Tract Infections, Recurrent 29 0.041
267
IMM073 Immunoglobulin a Vasculitis 28 0.041
268
INT258 Interstitial Nephritis, Karyomegalic 28 0.041
269
c GLY017 Glycogen Storage Disease Ic 28 0.041
270
c HYP248 Hyperprolinemia, Type I 27 0.041
271
c ALG016 Alagille Syndrome 2 26 0.041
272
INT224 Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital 26 0.041
273
c CNG378 Congenital Disorder of Glycosylation, Type Ir 26 0.041
274
c NPH047 Nephrotic Syndrome, Type 4 25 0.041
275
WLD005 Wild Type Attr Amyloidosis 24 0.041
276
c HML034 Hemolytic Uremic Syndrome, Atypical 3 22 0.041
277
c HML037 Hemolytic Uremic Syndrome, Atypical 5 22 0.041
278
c HML032 Hemolytic Uremic Syndrome, Atypical 4 22 0.041
279
PLY039 Polymorphic Reticulosis 22 0.041
280
c HML036 Hemolytic Uremic Syndrome, Atypical 6 22 0.041
281
c FCL082 Focal Segmental Glomerulosclerosis 4 22 0.041
282
CHR620 Chromosome 16p11.2 Deletion Syndrome, 220-Kb 22 0.041
283
c HML035 Hemolytic Uremic Syndrome, Atypical 2 22 0.041
284
c NPH065 Nephronophthisis 13 22 0.041
285
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 21 0.041
286
c FML344 Familial Mediterranean Fever, Autosomal Dominant 21 0.041
287
RNL089 Renal Nutcracker Syndrome 20 0.041
288
PHC017 Pheochromocytoma--Islet Cell Tumor Syndrome 20 0.041
289
OCL043 Oculorenocerebellar Syndrome 20 0.041
290
c FCL028 Focal Segmental Glomerulosclerosis 5 19 0.041
291
DYS180 Dyschondrosteosis and Nephritis 18 0.041
292
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 18 0.041
293
c NPH094 Nephrotic Syndrome 14 17 0.041
294
SPS196 Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 17 0.041
295
c FNC049 Fanconi Renotubular Syndrome 3 17 0.041
296
NNP016 Non-Progressive Predominantly Posterior Cavitating Leukoencephalopathy with Peripheral Neuropathy 17 0.041
297
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 17 0.041
298
c PTR011 Paternal Uniparental Disomy of Chromosome 1 16 0.041
299
HYP479 Hyperinsulinism Due to Hnf4a Deficiency 16 0.041
300
CNZ004 Coenzyme Q10 Deficiency, Primary, 3 15 0.041
301
OCL029 Oculo Skeletal Renal Syndrome 15 0.041
302
CHN073 Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 14 0.041
303
BLR029 Biliary Malformation with Renal Tubular Insufficiency 13 0.041
304
LPD043 Lipodystrophy, Partial, Acquired, with Low Complement Component C3, with or Without Glomerulonephritis 13 0.041
305
BLK002 Balkan Hemorrhagic Fever 8 0.041
306
CYS001 Cystic Fibrosis 85 0.029
307
c LKM063 Leukemia, Chronic Myeloid 80 0.029
308
P MYL005 Myelofibrosis 75 0.029
309
PHN003 Phenylketonuria 73 0.029
310
SCK003 Sickle Cell Anemia 73 0.029
311
P NRB001 Neuroblastoma 73 0.029
312
PRP027 Peripheral Vascular Disease 71 0.029
313
VSC007 Vascular Disease 71 0.029
314
c SPN225 Spondyloarthropathy 1 71 0.029
315
P RSP003 Respiratory Failure 71 0.029
316
P PNM007 Pneumonia 70 0.029
317
P HRP006 Herpes Simplex 70 0.029
318
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.029
319
P MYL006 Myeloid Leukemia 69 0.029
320
P CRN018 Coronary Artery Anomaly 69 0.029
321
CRB039 Cerebrovascular Disease 68 0.029
322
P ART023 Arthropathy 68 0.029
323
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.029
324
HSH003 Hashimoto Thyroiditis 67 0.029
325
DNG002 Dengue Hemorrhagic Fever 66 0.029
326
P LYM026 Lymphoblastic Leukemia 66 0.029
327
VSC011 Vasculitis 66 0.029
328
GST050 Gastrointestinal System Disease 66 0.029
329
P PLY011 Polycystic Ovary Syndrome 65 0.029
330
P DRM010 Dermatomyositis 65 0.029
331
P PSR002 Psoriasis 65 0.029
332
ADL030 Adult-Onset Still's Disease 65 0.029
333
c CHR417 Chronic Graft Versus Host Disease 65 0.029
334
SYS004 Systemic Mastocytosis 65 0.029
335
MCK007 Muckle-Wells Syndrome 64 0.029
336
OVR029 Ovarian Hyperstimulation Syndrome 64 0.029
337
PMS001 Poems Syndrome 64 0.029
338
CYS013 Cystinuria 64 0.029
339
HLC007 Helicobacter Pylori Infection 64 0.029
340
DPH001 Diphtheria 63 0.029
341
KRT001 Keratoconjunctivitis Sicca 63 0.029
342
c ACT210 Acute Respiratory Distress Syndrome 63 0.029
343
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.029
344
RCK004 Rickets 63 0.029
345
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.029
346
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.029
347
HYP056 Hypoglycemia 62 0.029
348
P CMR001 Camurati-Engelmann Disease 62 0.029
349
P HYP086 Hypothyroidism 62 0.029
350
LSC001 Lesch-Nyhan Syndrome 62 0.029
351
GTL001 Gitelman Syndrome 62 0.029
352
P GLY013 Glycogen Storage Disease 61 0.029
353
c THR092 Thrombophilia Due to Thrombin Defect 61 0.029
354
P GLL022 Guillain-Barre Syndrome 61 0.029
355
c SCL052 Scleroderma, Familial Progressive 60 0.029
356
P PLY014 Polycystic Kidney Disease 60 0.029
357
P DRR001 Diarrhea 60 0.029
358
PRT058 Pure Autonomic Failure 60 0.029
359
P HMR012 Hemorrhagic Fever 60 0.029
360
PLS011 Plasmacytoma 60 0.029
361
P PLY018 Polycythemia 60 0.029
362
c VRL010 Viral Hepatitis 59 0.029
363
PRS047 Prostatitis 59 0.029
364
SLP005 Sleep Disorder 59 0.029
365
P LMY004 Leiomyosarcoma 59 0.029
366
LPD008 Lipid Metabolism Disorder 59 0.029
367
P MNC007 Monocytic Leukemia 59 0.029
368
ANT009 Antithrombin Iii Deficiency 58 0.029
369
GLC003 Glucose Intolerance 58 0.029
370
P SJG008 Sjogren Syndrome 58 0.029
371
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.029
372
P CRN300 Coronary Heart Disease 1 57 0.029
373
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.029
374
WLL006 Wells Syndrome 57 0.029
375
HMR039 Hemorrhage, Intracerebral 57 0.029
376
P PRG013 Paraganglioma 57 0.029
377
P LPD010 Lipodystrophy 57 0.029
378
URN010 Urinary Tract Obstruction 57 0.029
379
FCL009 Focal Dermal Hypoplasia 57 0.029
380
EXT034 Extrinsic Allergic Alveolitis 57 0.029
381
P HYP726 Hypercalcemia, Infantile, 1 57 0.029
382
c ANM038 Anemia, Autoimmune Hemolytic 56 0.029
383
SLM003 Salmonellosis 56 0.029
384
LYM027 Lymphopenia 56 0.029
385
P MYP006 Myopia 56 0.029
386
ACR008 Acrocallosal Syndrome 56 0.029
387
MTH078 Methylmalonic Aciduria, Cblb Type 56 0.029
388
BLD044 Bladder Disease 55 0.029
389
SPN051 Spondylitis 55 0.029
390
c LKM070 Leukemia, Acute Monocytic 55 0.029
391
CHL028 Childhood Type Dermatomyositis 55 0.029
392
PNM001 Pneumocystosis 55 0.029
393
AMN001 Amenorrhea 55 0.029
394
P SYP003 Syphilis 55 0.029
395
P PRM006 Primary Biliary Cirrhosis 55 0.029
396
P PMP001 Pemphigus 55 0.029
397
HDR002 Hidradenitis Suppurativa 54 0.029
398
P DBT005 Diabetes Insipidus 54 0.029
399
APP015 Apparent Mineralocorticoid Excess 54 0.029
400
MCR004 Macroglobulinemia 54 0.029
401
ADR013 Adrenal Gland Hyperfunction 54 0.029
402
GST027 Gastric Lymphoma 53 0.029
403
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.029
404
NRG002 Neurogenic Bladder 53 0.029
405
HYP005 Hypokalemia 53 0.029
406
YLL001 Yellow Nail Syndrome 53 0.029
407
P OBS001 Obstructive Jaundice 53 0.029
408
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 53 0.029
409
ONC002 Onchocerciasis 53 0.029
410
PRT038 Protein-Energy Malnutrition 52 0.029
411
CRN030 Coronary Stenosis 52 0.029
412
HYP074 Hypersensitivity Vasculitis 52 0.029
413
P INF037 Inflammatory Bowel Disease 52 0.029
414
RTN023 Retinitis 52 0.029
415
CHR001 Churg-Strauss Syndrome 51 0.029
416
P RST002 Restrictive Cardiomyopathy 51 0.029
417
c ART115 Aortic Valve Disease 1 51 0.029
418
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.029
419
CHN070 Cohen-Gibson Syndrome 51 0.029
420
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 50 0.029
421
PNC001 Pancytopenia 50 0.029
422
P PTS002 Ptosis 50 0.029
423
PRT030 Parathyroid Gland Disease 50 0.029
424
URT031 Ureteral Disease 50 0.029
425
PPL021 Papilledema 50 0.029
426
HYD002 Hydronephrosis 49 0.029
427
HYP691 Hypomelanosis of Ito 49 0.029
428
c WLM018 Wilms Tumor 5 49 0.029
429
MTB004 Metabolic Acidosis 49 0.029
430
HPT014 Hepatorenal Syndrome 49 0.029
431
BCT004 Bacteriuria 49 0.029
432
RNL078 Renal Dysplasia 49 0.029
433
MNN009 Meningoencephalitis 49 0.029
434
P RNL028 Renal Tubular Dysgenesis 49 0.029
435
MNC006 Monoclonal Gammopathy of Uncertain Significance 49 0.029
436
c ACT042 Acute Pyelonephritis 48 0.029
437
HYP025 Hyperphosphatemia 48 0.029
438
PLC008 Placenta Disease 48 0.029
439
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 48 0.029
440
c BRN108 Branchiootic Syndrome 1 47 0.029
441
INT017 Intestinal Schistosomiasis 47 0.029
442
PST011 Pustulosis of Palm and Sole 47 0.029
443
HDR003 Hidradenitis 47 0.029
444
LGH004 Light Chain Deposition Disease 47 0.029
445
ULC007 Ulcerative Stomatitis 46 0.029
446
SPN119 Spondylarthropathy 46 0.029
447
PLC003 Placental Site Trophoblastic Tumor 46 0.029
448
c EXS019 Exostoses, Multiple, Type I 46 0.029
449
MDL009 Medullary Sponge Kidney 46 0.029
450
PMP004 Pemphigus Foliaceus 46 0.029
451
OBS037 Obesity-Hypoventilation Syndrome 45 0.029
452
P PRT026 Parotitis 45 0.029
453
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 45 0.029
454
P HRD001 Hereditary Multiple Exostoses 45 0.029
455
SML008 Small Intestine Lymphoma 45 0.029
456
TST044 Testicular Torsion 45 0.029
457
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.029
458
CST005 Castleman Disease 44 0.029
459
c WLM011 Wilms Tumor 6 44 0.029
460
DNB001 Danubian Endemic Familial Nephropathy 44 0.029
461
DYS015 Dysentery 43 0.029
462
P SDR003 Sideroblastic Anemia 43 0.029
463
PLS016 Plasma Cell Leukemia 43 0.029
464
MNN021 Meningococcemia 43 0.029
465
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 43 0.029
466
STT004 Steatorrhea 41 0.029
467
LYM029 Lymphedema-Distichiasis Syndrome 41 0.029
468
DRF001 Dirofilariasis 40 0.029
469
CHP002 Chops Syndrome 40 0.029
470
PRT019 Protein-Losing Enteropathy 40 0.029
471
HYP008 Hypertensive Retinopathy 39 0.029
472
RTC003 Root Caries 38 0.029
473
GRN009 Granulomatous Hepatitis 38 0.029
474
c ACT059 Acute Maxillary Sinusitis 38 0.029
475
RNL097 Renal Artery Disease 38 0.029
476
ACT040 Acute Poststreptococcal Glomerulonephritis 37 0.029
477
c ANT023 Anterior Scleritis 37 0.029
478
FML330 Familial Lcat Deficiency 37 0.029
479
HPT020 Hepatic Vascular Disease 36 0.029
480
NCR002 Necrobiosis Lipoidica 35 0.029
481
MLD002 Mild Pre-Eclampsia 35 0.029
482
RNL012 Renal Tuberculosis 35 0.029
483
c HYP073 Hypersensitivity Reaction Type Iv Disease 35 0.029
484
PYR004 Pyuria 34 0.029
485
C3G002 C3 Glomerulopathy 34 0.029
486
c TRC078 Trichohepatoenteric Syndrome 2 34 0.029
487
c CHR038 Chronic Maxillary Sinusitis 33 0.029
488
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 33 0.029
489
ASC003 Ascending Cholangitis 33 0.029
490
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.029
491
OCC001 Occupational Dermatitis 32 0.029
492
HYP540 Hypertension, Diastolic 32 0.029
493
DFF015 Diffuse Glomerulonephritis 32 0.029
494
P ACQ009 Acquired Metabolic Disease 32 0.029
495
INF009 Inflammatory Spondylopathy 32 0.029
496
c NPH031 Nephronophthisis 3 32 0.029
497
IMM149 Immunodeficiency 43 31 0.029
498
RNL001 Renal Artery Obstruction 31 0.029
499
SBD001 Subdural Empyema 31 0.029
500
CHL070 Cholesterol Embolism 31 0.029
501
ATM012 Autoimmune Disease of Blood 31 0.029
502
AMY002 Amyloid Tumor 30 0.029
503
ART010 Arteriolosclerosis 29 0.029
504
c ATR031 Atrial Septal Defect 4 29 0.029
505
c MLG039 Malignant Essential Hypertension 28 0.029
506
KDN006 Kidney Papillary Necrosis 27 0.029
507
c BNG021 Benign Essential Hypertension 27 0.029
508
NNS003 Non-Secretory Myeloma 27 0.029
509
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.029
510
HMX003 Heme Oxygenase 1 Deficiency 26 0.029
511
HYP226 Hyporeninemic Hypoaldosteronism 25 0.029
512
KDN013 Kidney Hypertrophy 25 0.029
513
DFN256 Deafness and Myopia 25 0.029
514
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 24 0.029
515
FDL001 Fiedler's Myocarditis 24 0.029
516
IMM053 Immunotactoid Glomerulopathy 23 0.029
517
LFF002 Loeffler Syndrome 23 0.029
518
P C1Q005 C1q Nephropathy 23 0.029
519
RDN004 Radin Blood Group Antigen 23 0.029
520
P ACR072 Acrorenal Syndrome 23 0.029
521
FBR085 Fibrillary Glomerulonephritis 23 0.029
522
CRK001 Cork-Handlers' Disease 22 0.029
523
ANR038 Anorexia Nervosa 1 21 0.029
524
c TYP027 Type 1 Diabetes Mellitus 10 21 0.029
525
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.029
526
c DRM055 Dermatitis, Atopic, 3 21 0.029
527
PYG002 Pyogenic Arthritis, Pyoderma Gangrenosum and Acne 20 0.029
528
OST007 Ostertagiasis 20 0.029
529
c DBT094 Diabetes Mellitus, Insulin-Dependent, 10 20 0.029
530
ATM018 Autoimmune Disease of Urogenital Tract 19 0.029
531
c NPH096 Nephrotic Syndrome, Type 12 19 0.029
532
c CHR464 Chronic Intestinal Failure 19 0.029
533
c GLL040 Galloway-Mowat Syndrome 3 18 0.029
534
SCL011 Sclerosing Keratitis 18 0.029
535
c PRC045 Preeclampsia/eclampsia 5 18 0.029
536
c GLL041 Galloway-Mowat Syndrome 4 18 0.029
537
BLD138 Blood Group--Diego System 18 0.029
538
c FCL055 Focal Segmental Glomerulosclerosis 9 18 0.029
539
c PRC034 Preeclampsia/eclampsia 4 18 0.029
540
BLD137 Blood Group--Ahonen 17 0.029
541
c GLL042 Galloway-Mowat Syndrome 5 17 0.029
542
c NPH076 Nephrotic Syndrome, Type 10 17 0.029
543
HRP008 Herpes Simiae 16 0.029
544
c NPH093 Nephrotic Syndrome, Type 13 16 0.029
545
c VSC025 Vesicoureteral Reflux 3 16 0.029
546
CHL131 Chlorpropamide-Alcohol Flushing 16 0.029
547
c VSC046 Vesicoureteral Reflux 8 16 0.029
548
CNG116 Congenital Nephrotic Syndrome Finnish Type 15 0.029
549
GLL039 Galloway-Mowat Syndrome 2, X-Linked 14 0.029
550
HPD002 Hepadnavirus Infection 14 0.029
551
c VSC020 Vesicoureteral Reflux 2 14 0.029
552
IMM051 Immunotactoid or Fibrillary Glomerulopathy 12 0.029
553
c NPH101 Nephrotic Syndrome 16 11 0.029
554
SLC010 Salcedo Syndrome 7 0.029
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