Search results for "proteinuria"

The MalaCard for "proteinuria" has been retired.
Searching MalaCards for entries containing "proteinuria"

533 hits were found for 'proteinuria'

# Family MCID Name MIFTS Score
1
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 19 5.342
2
MGL016 Megaloblastic Anemia-1, Finnish Type 46 4.789
3
ORT001 Orthostatic Proteinuria 29 4.371
4
P DNT015 Dent Disease 61 3.481
5
DNN002 Donnai-Barrow Syndrome 34 2.492
6
P GLM007 Glomerulonephritis 56 0.237
7
GLM011 Glomerulosclerosis 44 0.208
8
P FCL005 Focal Segmental Glomerulosclerosis 59 0.153
9
URN009 Urinary System Disease 53 0.147
10
P URF003 Urofacial Syndrome 1 52 0.147
11
P AMY004 Amyloidosis 64 0.141
12
P MMB011 Membranous Nephropathy 56 0.141
13
P PRC031 Preeclampsia/eclampsia 1 57 0.135
14
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.135
15
END072 Endotheliitis 42 0.128
16
c CHR089 Chronic Kidney Failure 66 0.125
17
IMP003 Impaired Renal Function Disease 37 0.125
18
P OBS005 Obesity 93 0.118
19
c MCR113 Microvascular Complications of Diabetes 3 49 0.118
20
P ECL001 Eclampsia 54 0.110
21
P MCR129 Microvascular Complications of Diabetes 1 57 0.106
22
c NPH055 Nephrotic Syndrome, Type 1 59 0.102
23
END030 End Stage Renal Failure 52 0.102
24
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.093
25
FBR012 Fabry Disease 69 0.093
26
P ALP004 Alport Syndrome 68 0.093
27
SCH014 Schistosomiasis 58 0.093
28
P RNL015 Renal Hypertension 47 0.093
29
MDY003 Mody, Type Ii 38 0.093
30
c GLM029 Glomerulosclerosis, Focal Segmental, 1 32 0.093
31
BLD054 Blood Protein Disease 40 0.088
32
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.088
33
IGG001 Iga Glomerulonephritis 50 0.083
34
HLL004 Hellp Syndrome 49 0.083
35
NPH010 Nephrosclerosis 42 0.083
36
P IGN003 Iga Nephropathy 1 29 0.083
37
c HYP595 Hypertension, Essential 69 0.078
38
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 52 0.078
39
URN003 Urinary Schistosomiasis 47 0.078
40
NPH003 Nephrocalcinosis 46 0.078
41
IMM001 Immune-Complex Glomerulonephritis 42 0.078
42
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.078
43
P HPT021 Hepatitis 70 0.072
44
P LKM002 Leukemia 70 0.072
45
INT067 Interstitial Nephritis 47 0.072
46
MDY005 Mody, Type I 33 0.072
47
c GLM027 Glomerulosclerosis, Focal Segmental, 3 28 0.072
48
c RNL016 Renal Infectious Disease 24 0.072
49
ATM055 Autoimmune Disease 4 18 0.072
50
c SYS001 Systemic Lupus Erythematosus 87 0.066
51
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.066
52
P MLT019 Multiple Myeloma 80 0.066
53
PRT036 Peritonitis 62 0.066
54
P EXN002 Exanthem 57 0.066
55
NLP001 Nail-Patella Syndrome 54 0.066
56
P PYL005 Pyelonephritis 52 0.066
57
NRM003 Norum Disease 52 0.066
58
CYS010 Cystinosis 51 0.066
59
c MLG069 Malignant Hypertension 47 0.066
60
c GLM026 Glomerulosclerosis, Focal Segmental, 2 28 0.066
61
c NPH049 Nephrotic Syndrome, Type 2 27 0.066
62
c GLM039 Glomerulosclerosis, Focal Segmental, 6 26 0.066
63
c NPH070 Nephrotic Syndrome, Type 6 25 0.066
64
P GLM015 Glomerulopathy with Fibronectin Deposits 2 21 0.066
65
P RHM011 Rheumatoid Arthritis 88 0.059
66
P ART022 Arthritis 75 0.059
67
P LYM118 Lymphoma 70 0.059
68
c GCH015 Gaucher Disease, Type I 66 0.059
69
P LPS004 Lupus Erythematosus 63 0.059
70
LWS003 Lowe Syndrome 61 0.059
71
HMR004 Hemorrhagic Fever with Renal Syndrome 57 0.059
72
P HYP069 Hyperparathyroidism 57 0.059
73
SCH016 Schimke Immunoosseous Dysplasia 49 0.059
74
GLC008 Glucose Metabolism Disease 47 0.059
75
AMN006 Aminoaciduria 42 0.059
76
c CHR098 Chronic Pyelonephritis 38 0.059
77
c NPH072 Nephrotic Syndrome, Type 7 32 0.059
78
ATM052 Autoimmune Disease 1 28 0.059
79
c NPH047 Nephrotic Syndrome, Type 4 25 0.059
80
c GLM041 Glomerulosclerosis, Focal Segmental, 7 24 0.059
81
c NPH085 Nephrotic Syndrome 12 19 0.059
82
P CLR023 Colorectal Cancer 97 0.051
83
HV1006 Hiv-1 82 0.051
84
P RNL014 Renal Cell Carcinoma 81 0.051
85
P PHC003 Pheochromocytoma 71 0.051
86
P KDN017 Kidney Cancer 67 0.051
87
MTH009 Mouth Disease 63 0.051
88
P FML161 Familial Mediterranean Fever, Ar 63 0.051
89
P HLP001 Holoprosencephaly 62 0.051
90
HYP066 Hyperglycemia 60 0.051
91
PRP030 Purpura 59 0.051
92
LPD008 Lipid Metabolism Disorder 58 0.051
93
P NPH005 Nephronophthisis 55 0.051
94
BRN106 Burns 52 0.051
95
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.051
96
GLL032 Galloway-Mowat Syndrome 50 0.051
97
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 50 0.051
98
GDP001 Goodpasture Syndrome 49 0.051
99
c SVR005 Severe Pre-Eclampsia 48 0.051
100
LPD004 Lipoid Nephrosis 48 0.051
101
ACD009 Acid-Labile Subunit, Deficiency of 48 0.051
102
P RNV001 Renovascular Hypertension 47 0.051
103
RNL077 Renal Fibrosis 47 0.051
104
ANR004 Anuria 46 0.051
105
LPP002 Lipoprotein Glomerulopathy 46 0.051
106
c ALM001 Al Amyloidosis 44 0.051
107
P PRL003 Proliferative Glomerulonephritis 43 0.051
108
FRS002 Frasier Syndrome 42 0.051
109
CRS001 Crescentic Glomerulonephritis 41 0.051
110
EPS006 Epstein Syndrome 40 0.051
111
PRS055 Pierson Syndrome 40 0.051
112
STR044 Steroid-Resistant Nephrotic Syndrome 38 0.051
113
P CRY007 Cryoglobulinemia, Familial Mixed 35 0.051
114
PPL048 Papillorenal Syndrome 35 0.051
115
c NPH054 Nephrotic Syndrome, Type 3 34 0.051
116
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 34 0.051
117
c LPD019 Lipodystrophy, Partial, Acquired 33 0.051
118
c GLM033 Glomerulosclerosis, Focal Segmental, 4 30 0.051
119
ATM059 Autoimmune Disease 6 26 0.051
120
NPH039 Nephrotic Syndrome, Type 5, with or Without Ocular Abnormalities 25 0.051
121
c CHR522 Charcot-Marie-Tooth Disease, Dominant Intermediate E 25 0.051
122
c NPH073 Nephrotic Syndrome, Type 8 23 0.051
123
c NPH074 Nephrotic Syndrome, Type 9 22 0.051
124
ATM053 Autoimmune Disease 2 19 0.051
125
ATM054 Autoimmune Disease 3 18 0.051
126
c IGN002 Iga Nephropathy 2 18 0.051
127
c IGN004 Iga Nephropathy 3 17 0.051
128
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 15 0.051
129
P HYP607 Hypercholesterolemia, Familial 77 0.042
130
P HRT032 Heart Disease 76 0.042
131
c HPT073 Hepatitis C Virus 72 0.042
132
P LVR013 Liver Disease 72 0.042
133
WLS001 Wilson Disease 72 0.042
134
KWS002 Kawasaki Disease 70 0.042
135
PRP027 Peripheral Vascular Disease 69 0.042
136
c HPT001 Hepatitis C 68 0.042
137
OBS061 Obstructive Sleep Apnea 66 0.042
138
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.042
139
P ATR011 Atrial Fibrillation 64 0.042
140
P BCL006 B-Cell Lymphomas 64 0.042
141
c HPT016 Hepatitis B 64 0.042
142
P AGM001 Agammaglobulinemia 64 0.042
143
P THR014 Thrombocytopenia 64 0.042
144
ATH003 Atherosclerosis 62 0.042
145
SPN186 Spinal Cord Injury 62 0.042
146
LSH001 Leishmaniasis 62 0.042
147
WGN006 Wegener Granulomatosis 62 0.042
148
PRM097 Primary Immunodeficiency Disease 61 0.042
149
P THL005 Thalassemia 61 0.042
150
WLL001 Williams-Beuren Syndrome 61 0.042
151
c VRL010 Viral Hepatitis 61 0.042
152
CNN005 Connective Tissue Disease 61 0.042
153
P SLP006 Sleep Apnea 61 0.042
154
P PNC044 Pancreatitis 60 0.042
155
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.042
156
VRL011 Viral Infectious Disease 59 0.042
157
c HPT003 Hepatitis a 59 0.042
158
LGN002 Legionellosis 59 0.042
159
P HMR003 Hemorrhagic Disease 57 0.042
160
YLL002 Yellow Fever 57 0.042
161
CND002 Conduct Disorder 56 0.042
162
c ACT027 Acute Pancreatitis 56 0.042
163
RBS003 Rabson-Mendenhall Syndrome 55 0.042
164
P THY032 Thyroiditis 54 0.042
165
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.042
166
C3D001 C3 Deficiency 53 0.042
167
P SPS003 Spastic Diplegia 53 0.042
168
P FNC026 Fanconi Renotubular Syndrome 1 51 0.042
169
P HYP613 Hypophosphatemic Rickets 51 0.042
170
P FML035 Familial Hyperlipidemia 50 0.042
171
IMM136 Immune System Disease 50 0.042
172
RNL007 Renal Tubular Acidosis 50 0.042
173
P HYP014 Hyperuricemia 50 0.042
174
c ACT071 Acute Kidney Failure 50 0.042
175
CSY001 C Syndrome 49 0.042
176
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.042
177
RLP001 Relapsing Polychondritis 49 0.042
178
SCK005 Sickle Cell Disease 49 0.042
179
PLS009 Plasma Cell Neoplasm 48 0.042
180
CRD118 Cardiovascular Cancer 47 0.042
181
BLD053 Blood Platelet Disease 46 0.042
182
c ORF037 Orofaciodigital Syndrome I 46 0.042
183
ALN001 Aland Island Eye Disease 45 0.042
184
P BLD051 Blood Coagulation Disease 45 0.042
185
MCR037 Macroglossia 45 0.042
186
HMT008 Hematuria, Benign Familial 45 0.042
187
RNL097 Renal Artery Disease 45 0.042
188
c GCH017 Gaucher Disease, Type Iii 45 0.042
189
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 45 0.042
190
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 42 0.042
191
EBL001 Ebola Hemorrhagic Fever 41 0.042
192
SPC003 Specific Developmental Disorder 40 0.042
193
NTR005 Nutritional Deficiency Disease 39 0.042
194
ADJ001 Adjustment Disorder 38 0.042
195
PYL004 Pyelitis 38 0.042
196
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.042
197
LSS003 Lassa Fever 38 0.042
198
P HYP120 Hypoaldosteronism 37 0.042
199
INT221 Intravascular Large B-Cell Lymphoma 36 0.042
200
c DNT021 Dent Disease 2 34 0.042
201
BLK001 Balkan Nephropathy 33 0.042
202
MJD001 Majeed Syndrome 33 0.042
203
VSC008 Vascular Hemostatic Disease 33 0.042
204
DBT090 Diabetes and Deafness, Maternally Inherited 33 0.042
205
IMM073 Immunoglobulin a Vasculitis 30 0.042
206
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 29 0.042
207
c GLM028 Glomerulosclerosis, Focal Segmental, 5 27 0.042
208
MLK004 Malakoplakia 27 0.042
209
c SPL024 Split-Hand/foot Malformation 3 27 0.042
210
FRS004 Free Sialic Acid Storage Disorders 26 0.042
211
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 26 0.042
212
CYS025 Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic 24 0.042
213
c HYP248 Hyperprolinemia, Type I 23 0.042
214
c FCL053 Focal Segmental Glomerulosclerosis 8 22 0.042
215
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 22 0.042
216
PRT110 Prieto Syndrome 21 0.042
217
OCL043 Oculorenocerebellar Syndrome 15 0.042
218
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 14 0.042
219
c GLM014 Glomerulopathy with Fibronectin Deposits 1 14 0.042
220
DYS180 Dyschondrosteosis and Nephritis 13 0.042
221
BLK002 Balkan Hemorrhagic Fever 11 0.042
222
OCL029 Oculo Skeletal Renal Syndrome 11 0.042
223
NLP003 Nail-Patella-Like Renal Disease 10 0.042
224
CYS001 Cystic Fibrosis 86 0.029
225
P MYC007 Myocardial Infarction 79 0.029
226
P CRN211 Coronary Artery Disease 75 0.029
227
CNG034 Congestive Heart Failure 71 0.029
228
P RSP003 Respiratory Failure 70 0.029
229
P NRB001 Neuroblastoma 69 0.029
230
SCK003 Sickle Cell Anemia 68 0.029
231
P MYL005 Myelofibrosis 67 0.029
232
P CRD011 Cardiomyopathy 67 0.029
233
P MYL006 Myeloid Leukemia 67 0.029
234
VSC007 Vascular Disease 67 0.029
235
LVR012 Liver Cirrhosis 67 0.029
236
P PNM007 Pneumonia 66 0.029
237
KPS004 Kaposi Sarcoma 66 0.029
238
P PLY011 Polycystic Ovary Syndrome 66 0.029
239
P HYP117 Hypertriglyceridemia 65 0.029
240
P HRP006 Herpes Simplex 65 0.029
241
BRC012 Brucellosis 65 0.029
242
P ALX003 Alexander Disease 64 0.029
243
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.029
244
P ART023 Arthropathy 63 0.029
245
CYS013 Cystinuria 63 0.029
246
P PSR002 Psoriasis 63 0.029
247
CRD119 Cardiac Arrest 63 0.029
248
c SPN225 Spondyloarthropathy 1 63 0.029
249
DNG002 Dengue Hemorrhagic Fever 62 0.029
250
VSC011 Vasculitis 62 0.029
251
MCK007 Muckle-Wells Syndrome 61 0.029
252
LSC001 Lesch-Nyhan Syndrome 61 0.029
253
c ACT075 Acute Myocardial Infarction 60 0.029
254
GTL001 Gitelman Syndrome 60 0.029
255
ANR002 Aniridia 60 0.029
256
P LYM026 Lymphoblastic Leukemia 60 0.029
257
ETN001 Eating Disorder 60 0.029
258
P CRN139 Cornelia De Lange Syndrome 1 60 0.029
259
P RCK004 Rickets 59 0.029
260
P CMR001 Camurati-Engelmann Disease 59 0.029
261
ADM013 Adamantinoma of Long Bones 59 0.029
262
c SYS004 Systemic Mastocytosis 59 0.029
263
P GLY013 Glycogen Storage Disease 59 0.029
264
P ANT006 Antiphospholipid Syndrome 58 0.029
265
HPY002 H. Pylori Infection 58 0.029
266
CHL071 Child Syndrome 58 0.029
267
DPH001 Diphtheria 58 0.029
268
P DRM010 Dermatomyositis 58 0.029
269
c GLY060 Glycogen Storage Disease Ia 58 0.029
270
CTS003 Coats Disease 57 0.029
271
ADL030 Adult-Onset Still's Disease 57 0.029
272
P PLY018 Polycythemia 57 0.029
273
ART111 Artery Disease 57 0.029
274
c ACT210 Acute Respiratory Distress Syndrome 57 0.029
275
WLL006 Wells Syndrome 56 0.029
276
P PTS002 Ptosis 56 0.029
277
INT002 Intermittent Claudication 56 0.029
278
PRS047 Prostatitis 56 0.029
279
PMS001 Poems Syndrome 55 0.029
280
c HYP615 Hyperparathyroidism, Familial Primary 55 0.029
281
CRT016 Carotid Artery Disease 55 0.029
282
GLC003 Glucose Intolerance 55 0.029
283
P MNC007 Monocytic Leukemia 55 0.029
284
P HMR012 Hemorrhagic Fever 55 0.029
285
GST050 Gastrointestinal System Disease 54 0.029
286
P SLD010 Sialidosis, Type I 54 0.029
287
LYM027 Lymphopenia 54 0.029
288
P VSC005 Vesicoureteral Reflux 54 0.029
289
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.029
290
VSC006 Vascular Cancer 54 0.029
291
P MST009 Mastocytosis 54 0.029
292
c HPT007 Hepatitis E 54 0.029
293
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.029
294
P LMY004 Leiomyosarcoma 53 0.029
295
ADL002 Adult Syndrome 53 0.029
296
SLP005 Sleep Disorder 53 0.029
297
GST027 Gastric Lymphoma 53 0.029
298
DNY001 Denys-Drash Syndrome 53 0.029
299
P DBT005 Diabetes Insipidus 53 0.029
300
P SJG001 Sjogren's Syndrome 53 0.029
301
KDS001 Kid Syndrome 53 0.029
302
P LPD010 Lipodystrophy 52 0.029
303
P PNC001 Pancytopenia 52 0.029
304
c ACT009 Acute Monocytic Leukemia 52 0.029
305
APP015 Apparent Mineralocorticoid Excess 52 0.029
306
HYP005 Hypokalemia 51 0.029
307
MTC097 Mitochondrial Complex Iv Deficiency 51 0.029
308
ACR008 Acrocallosal Syndrome 51 0.029
309
MSC072 Muscle Cancer 51 0.029
310
AMN001 Amenorrhea 51 0.029
311
BLD044 Bladder Disease 51 0.029
312
P DRR001 Diarrhea 51 0.029
313
MRC001 Marchiafava Bignami Disease 50 0.029
314
SPN051 Spondylitis 50 0.029
315
c ACT068 Acute Cystitis 50 0.029
316
PRD019 Periodic Fever, Familial 50 0.029
317
URM002 Uremia 50 0.029
318
NRG002 Neurogenic Bladder 50 0.029
319
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.029
320
PRP021 Peripheral Nervous System Neoplasm 50 0.029
321
ONC002 Onchocerciasis 50 0.029
322
P RST002 Restrictive Cardiomyopathy 50 0.029
323
MCR004 Macroglobulinemia 50 0.029
324
PMP001 Pemphigus 49 0.029
325
CHR001 Churg-Strauss Syndrome 49 0.029
326
PRT030 Parathyroid Gland Disease 49 0.029
327
RTN023 Retinitis 49 0.029
328
MTB004 Metabolic Acidosis 48 0.029
329
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 48 0.029
330
LYM008 Lymphangiosarcoma 48 0.029
331
PPL021 Papilledema 48 0.029
332
HYP074 Hypersensitivity Vasculitis 47 0.029
333
BCT004 Bacteriuria 47 0.029
334
RNL051 Renal Cysts and Diabetes Syndrome 47 0.029
335
SXL003 Sexual Disorder 47 0.029
336
PLC003 Placental Site Trophoblastic Tumor 47 0.029
337
HNC001 Henoch-Schoenlein Purpura 47 0.029
338
BNN003 Bone Inflammation Disease 46 0.029
339
INT017 Intestinal Schistosomiasis 46 0.029
340
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 46 0.029
341
HDR003 Hidradenitis 46 0.029
342
HYP025 Hyperphosphatemia 46 0.029
343
P AMY082 Amyloidosis, Familial Visceral 46 0.029
344
c ACT042 Acute Pyelonephritis 46 0.029
345
MMB001 Membranoproliferative Glomerulonephritis 45 0.029
346
c CNG415 Congenital Disorder of Glycosylation, Type Ia 45 0.029
347
FBR032 Fibromuscular Dysplasia 45 0.029
348
IPX001 Ipex Syndrome 45 0.029
349
P PLY026 Polycystic Kidney Disease, Autosomal Dominant 45 0.029
350
P ARC016 Auriculocondylar Syndrome 1 44 0.029
351
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.029
352
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 44 0.029
353
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.029
354
P EXS004 Exostoses, Multiple, Type 1 44 0.029
355
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.029
356
MNN006 Meninges Hemangiopericytoma 44 0.029
357
MSN001 Mesangial Proliferative Glomerulonephritis 43 0.029
358
PRM025 Primary Bacterial Infectious Disease 43 0.029
359
c HRD104 Hereditary Multiple Osteochondromas 43 0.029
360
HYP691 Hypomelanosis of Ito 42 0.029
361
LGH004 Light Chain Deposition Disease 42 0.029
362
THL018 Thalassemia Major 42 0.029
363
IMM127 Immune System Cancer 42 0.029
364
PLS016 Plasma Cell Leukemia 42 0.029
365
SPN119 Spondylarthropathy 41 0.029
366
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.029
367
CYS036 Cystinosis, Nephropathic 41 0.029
368
SCN001 Secondary Hyperparathyroidism of Renal Origin 41 0.029
369
P SML002 Small Cell Sarcoma 41 0.029
370
CRV068 Cervical Polyp 41 0.029
371
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.029
372
ATN011 Autoinflammation with Infantile Enterocolitis 41 0.029
373
HYP540 Hypertension, Diastolic 41 0.029
374
WTH001 Withdrawal Disorder 41 0.029
375
c ALP073 Alport Syndrome, Autosomal Recessive 40 0.029
376
CMP042 Complement Factor H Deficiency 40 0.029
377
MDL009 Medullary Sponge Kidney 40 0.029
378
P ACQ022 Acquired Generalized Lipodystrophy 40 0.029
379
STT004 Steatorrhea 40 0.029
380
DND018 Dendritic Cell Tumor 40 0.029
381
IMM065 Immunodeficiency 10 40 0.029
382
THL017 Thalassemia Intermedia 40 0.029
383
PDT001 Pediatric Lymphoma 40 0.029
384
P SDR003 Sideroblastic Anemia 39 0.029
385
MRS001 Marasmus 39 0.029
386
PMP004 Pemphigus Foliaceus 39 0.029
387
EPT011 Epithelioid Leiomyosarcoma 39 0.029
388
c CCK005 Cockayne Syndrome, Type a 39 0.029
389
MNN021 Meningococcemia 38 0.029
390
CRB009 Cerebritis 38 0.029
391
CST005 Castleman Disease 38 0.029
392
c ALP074 Alport Syndrome, Autosomal Dominant 38 0.029
393
CTN012 Cutaneous Leiomyosarcoma 38 0.029
394
INT011 Interstitial Emphysema 38 0.029
395
HYP268 Hypercalciuria, Absorptive 37 0.029
396
FCH003 Fechtner Syndrome 37 0.029
397
SPL011 Spleen Cancer 37 0.029
398
ATM012 Autoimmune Disease of Blood 37 0.029
399
MLR007 Male Reproductive System Disease 37 0.029
400
DRF001 Dirofilariasis 37 0.029
401
LYM029 Lymphedema-Distichiasis Syndrome 37 0.029
402
c CCK006 Cockayne Syndrome, Type B 37 0.029
403
DNS007 Dense Deposit Disease 37 0.029
404
VNS002 Venous Hemangioma 37 0.029
405
MDY004 Mody, Type Iii 37 0.029
406
BNS002 Bone Structure Disease 36 0.029
407
PLC008 Placenta Disease 36 0.029
408
c GLY016 Glycogen Storage Disease Ib 36 0.029
409
MSN004 Mesenchymal Cell Neoplasm 36 0.029
410
P EXT032 Extraosseous Osteosarcoma 35 0.029
411
CCN007 Cocoon Syndrome 35 0.029
412
BRS004 Breast Angiosarcoma 34 0.029
413
c SYS043 Systemic Lupus Erythematosus 1 34 0.029
414
P GLM006 Glomangioma 34 0.029
415
PYR004 Pyuria 34 0.029
416
SWL001 Swallowing Disorders 34 0.029
417
MLD002 Mild Pre-Eclampsia 34 0.029
418
c HYP311 Hyperparathyroidism 3 34 0.029
419
c HYP163 Hyperlipidemia Type 3 34 0.029
420
P PRX033 Proximal Renal Tubular Acidosis 33 0.029
421
CHR010 Chorioangioma 33 0.029
422
VTM003 Vitamin Metabolic Disorder 33 0.029
423
c CNG004 Congenital Epulis 33 0.029
424
INT004 Intraneural Perineurioma 33 0.029
425
KDN013 Kidney Hypertrophy 33 0.029
426
c NPH046 Nephrolithiasis, Type I 33 0.029
427
SNL003 Senile Angioma 33 0.029
428
MXD006 Mixed Liposarcoma 32 0.029
429
OHD004 Ohdo Syndrome 32 0.029
430
FML330 Familial Lcat Deficiency 32 0.029
431
HYP114 Hypertensive Nephropathy 32 0.029
432
CHL070 Cholesterol Embolism 32 0.029
433
ACT040 Acute Poststreptococcal Glomerulonephritis 32 0.029
434
CNV003 Conventional Fibrosarcoma 32 0.029
435
c TRC078 Trichohepatoenteric Syndrome 2 31 0.029
436
PDT040 Pediatric Hypertension 31 0.029
437
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 31 0.029
438
NTR042 Neutrophilic Dermatosis, Acute Febrile 30 0.029
439
NCR002 Necrobiosis Lipoidica 30 0.029
440
NPH006 Nephrogenic Adenofibroma 29 0.029
441
BRS043 Breast Leiomyosarcoma 29 0.029
442
NRG003 Neurogenic Arthropathy 29 0.029
443
SPN017 Spindle Cell Liposarcoma 29 0.029
444
C3G002 C3 Glomerulopathy 29 0.029
445
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 29 0.029
446
c EXS005 Exostoses, Multiple, Type 2 28 0.029
447
IMM071 Immunodeficiency 12 28 0.029
448
c PRC045 Preeclampsia/eclampsia 5 28 0.029
449
ANG019 Angiomyoma 28 0.029
450
BNG033 Benign Perivascular Tumor 28 0.029
451
c HML035 Hemolytic Uremic Syndrome, Atypical 2 27 0.029
452
c SYS038 Systemic Lupus Erythematosus 2 27 0.029
453
MNT146 Mental Retardation, X-Linked, Syndromic, Martin-Probst Type 27 0.029
454
c HML034 Hemolytic Uremic Syndrome, Atypical 3 27 0.029
455
GLM001 Glomeruloid Hemangioma 27 0.029
456
CRD007 Cardiovascular Organ Benign Neoplasm 27 0.029
457
INF005 Infiltrating Lipoma 27 0.029
458
THY031 Thyroid Sarcoma 27 0.029
459
c HML032 Hemolytic Uremic Syndrome, Atypical 4 27 0.029
460
c VSC025 Vesicoureteral Reflux 3 27 0.029
461
c HML037 Hemolytic Uremic Syndrome, Atypical 5 27 0.029
462
OVR061 Ovary Sarcoma 26 0.029
463
OVR003 Ovarian Angiosarcoma 26 0.029
464
c HML036 Hemolytic Uremic Syndrome, Atypical 6 26 0.029
465
c PRC034 Preeclampsia/eclampsia 4 25 0.029
466
EPL108 Epilepsy, Progressive Myoclonic 4, with or Without Renal Failure 25 0.029
467
PDT004 Pediatric Angiosarcoma 25 0.029
468
SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 25 0.029
469
HMX002 Heme Oxygenase-1 Deficiency 25 0.029
470
CNZ008 Coenzyme Q10 Deficiency, Primary, 6 24 0.029
471
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 24 0.029
472
DFN256 Deafness and Myopia 24 0.029
473
P CRN178 Coronary Heart Disease 6 24 0.029
474
c SYS046 Systemic Lupus Erythematosus 3 24 0.029
475
P C1Q005 C1q Nephropathy 23 0.029
476
CNZ004 Coenzyme Q10 Deficiency, Primary, 3 23 0.029
477
HPD002 Hepadnavirus Infection 23 0.029
478
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 23 0.029
479
c SYS051 Systemic Lupus Erythematosus 4 23 0.029
480
INS009 Insulin-Resistance Type B 22 0.029
481
VSC009 Vascular Skin Disease 22 0.029
482
HMN011 Hemangioma of Intra-Abdominal Structure 22 0.029
483
c NPH076 Nephrotic Syndrome, Type 10 22 0.029
484
c CRN174 Coronary Heart Disease 2 22 0.029
485
DPL001 Deep Leiomyoma 22 0.029
486
c VSC020 Vesicoureteral Reflux 2 22 0.029
487
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 22 0.029
488
c GLY017 Glycogen Storage Disease Ic 21 0.029
489
WLD005 Wild Type Attr Amyloidosis 21 0.029
490
c FCL055 Focal Segmental Glomerulosclerosis 9 21 0.029
491
BNP002 Bone Epithelioid Hemangioma 21 0.029
492
INT258 Interstitial Nephritis, Karyomegalic 21 0.029
493
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 21 0.029
494
c INT282 Integumentary System Benign Neoplasm 20 0.029
495
P ACR072 Acrorenal Syndrome 20 0.029
496
THY004 Thyroid Angiosarcoma 20 0.029
497
PYL007 Pylorus Cancer 20 0.029
498
c NPH065 Nephronophthisis 13 20 0.029
499
c FML162 Familial Mediterranean Fever, Ad 20 0.029
500
c RNL113 Renal Failure, Progressive, with Hypertension 19 0.029
501
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 19 0.029
502
c PRC032 Preeclampsia/eclampsia 2 19 0.029
503
c VSC046 Vesicoureteral Reflux 8 19 0.029
504
BRS016 Breast Myofibroblastoma 19 0.029
505
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 19 0.029
506
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 18 0.029
507
HBN001 Hobnail Hemangioma 18 0.029
508
RNL089 Renal Nutcracker Syndrome 17 0.029
509
INT055 Intravascular Fasciitis 17 0.029
510
SPL001 Spleen Angiosarcoma 17 0.029
511
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 16 0.029
512
c NPH083 Nephrotic Syndrome 11 16 0.029
513
CNV001 Conventional Angiosarcoma 16 0.029
514
c NPH084 Nephrotic Syndrome 13 16 0.029
515
VSC014 Vascular Hyalinosis 16 0.029
516
NVD002 Nevada Syndrome 16 0.029
517
c FNC049 Fanconi Renotubular Syndrome 3 15 0.029
518
CHR585 Chromosome 16p11.2 Deletion Syndrome, 220-Kb Body Mass Index Quantitative Trait Locus 16, Included 15 0.029
519
HRP008 Herpes Simiae 15 0.029
520
DNT019 Daentl Towsend Siegel Syndrome 14 0.029
521
NPH082 Nephrosis with Deafness and Urinary Tract and Digital Malformations 14 0.029
522
SPS196 Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 13 0.029
523
P SYS050 Systemic Lupus Erythematosus with Nephritis 2 13 0.029
524
c SYS056 Systemic Lupus Erythematosus with Nephritis 1 13 0.029
525
c SYS054 Systemic Lupus Erythematosus with Nephritis 3 13 0.029
526
HRP012 Herpesvirus Simiae B Virus 13 0.029
527
SGL001 Siegler Brewer Carey Syndrome 12 0.029
528
LMN004 Laminopathy Type Decaudain-Vigouroux 11 0.029
529
c EXS006 Exostoses, Multiple, Type 3 11 0.029
530
PHC008 Pheochromocytoma-Islet Cell Tumor Syndrome 11 0.029
531
CLS011 Classic Fabry Disease 11 0.029
532
HYP479 Hyperinsulinism Due to Hnf4a Deficiency 10 0.029
533
c ATM094 Autoimmune Disease, Multisystem, Infantile-Onset, 2 10 0.029