Search results for "proteinuria"

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

555 hits were found for 'proteinuria'

# Family MCID Name MIFTS Score
1
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 19 4.652
2
ORT001 Orthostatic Proteinuria 28 4.250
3
MGL001 Megaloblastic Anemia 51 4.042
4
P DNT015 Dent Disease 61 3.384
5
DNN002 Donnai-Barrow Syndrome 36 2.423
6
MGL016 Megaloblastic Anemia-1, Finnish Type 31 2.339
7
P KDN018 Kidney Disease 64 0.289
8
P GLM007 Glomerulonephritis 56 0.234
9
GLM011 Glomerulosclerosis 41 0.208
10
P URF003 Urofacial Syndrome 1 51 0.191
11
P NPH012 Nephrotic Syndrome 55 0.170
12
URN009 Urinary System Disease 52 0.159
13
P FCL005 Focal Segmental Glomerulosclerosis 59 0.151
14
P AMY004 Amyloidosis 63 0.139
15
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.136
16
P MMB011 Membranous Nephropathy 53 0.136
17
c PRC016 Pre-Eclampsia 57 0.127
18
END072 Endotheliitis 41 0.127
19
c CHR089 Chronic Kidney Failure 67 0.123
20
IMP003 Impaired Renal Function Disease 36 0.123
21
P OBS005 Obesity 91 0.116
22
P MCR113 Microvascular Complications of Diabetes 3 48 0.116
23
P ECL001 Eclampsia 55 0.109
24
c MCR129 Microvascular Complications of Diabetes 1 55 0.105
25
END030 End Stage Renal Failure 53 0.101
26
P PRC031 Preeclampsia/eclampsia 1 53 0.096
27
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.092
28
FBR012 Fabry Disease 68 0.092
29
P ALP004 Alport Syndrome 68 0.092
30
MDY003 Mody, Type Ii 36 0.092
31
SCH014 Schistosomiasis 59 0.092
32
c GLM029 Glomerulosclerosis, Focal Segmental, 1 30 0.092
33
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.092
34
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.092
35
P RNL015 Renal Hypertension 47 0.092
36
MMB002 Membranous Glomerulonephritis 47 0.087
37
BLD054 Blood Protein Disease 38 0.087
38
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.082
39
c NPH055 Nephrotic Syndrome, Type 1 32 0.082
40
NPH003 Nephrocalcinosis 47 0.082
41
NPH010 Nephrosclerosis 44 0.082
42
c HYP595 Hypertension, Essential 69 0.077
43
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 40 0.077
44
P IGN003 Iga Nephropathy 1 31 0.077
45
IGG001 Iga Glomerulonephritis 46 0.077
46
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.077
47
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.077
48
URN003 Urinary Schistosomiasis 49 0.077
49
IMM001 Immune-Complex Glomerulonephritis 41 0.077
50
P HPT021 Hepatitis 74 0.071
51
NRM003 Norum Disease 53 0.071
52
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.071
53
P LKM002 Leukemia 70 0.071
54
MDY005 Mody, Type I 31 0.071
55
c GLM027 Glomerulosclerosis, Focal Segmental, 3 27 0.071
56
P FNC004 Fanconi Syndrome 54 0.071
57
INT067 Interstitial Nephritis 48 0.071
58
HLL004 Hellp Syndrome 48 0.071
59
P MYL007 Myeloma 52 0.071
60
ATM055 Autoimmune Disease 4 16 0.071
61
GLC008 Glucose Metabolism Disease 44 0.071
62
c RNL016 Renal Infectious Disease 22 0.071
63
c MLT019 Multiple Myeloma 77 0.065
64
c SYS001 Systemic Lupus Erythematosus 87 0.065
65
NLP001 Nail-Patella Syndrome 54 0.065
66
CYS010 Cystinosis 51 0.065
67
PRT036 Peritonitis 65 0.065
68
C3D001 C3 Deficiency 50 0.065
69
P GLM015 Glomerulopathy with Fibronectin Deposits 2 22 0.065
70
c NPH070 Nephrotic Syndrome, Type 6 24 0.065
71
c GLM026 Glomerulosclerosis, Focal Segmental, 2 27 0.065
72
c GLM039 Glomerulosclerosis, Focal Segmental, 6 33 0.065
73
c NPH049 Nephrotic Syndrome, Type 2 26 0.065
74
c MLG069 Malignant Hypertension 46 0.065
75
P EXN002 Exanthem 57 0.065
76
P PYL005 Pyelonephritis 52 0.065
77
P RHM011 Rheumatoid Arthritis 87 0.058
78
SCH016 Schimke Immunoosseous Dysplasia 50 0.058
79
P ART022 Arthritis 73 0.058
80
c NPH072 Nephrotic Syndrome, Type 7 30 0.058
81
P LPS004 Lupus Erythematosus 63 0.058
82
P LYM118 Lymphoma 68 0.058
83
P HYP069 Hyperparathyroidism 57 0.058
84
c GLM041 Glomerulosclerosis, Focal Segmental, 7 22 0.058
85
HMR004 Hemorrhagic Fever with Renal Syndrome 52 0.058
86
ACD009 Acid-Labile Subunit, Deficiency of 37 0.058
87
ATM052 Autoimmune Disease 1 26 0.058
88
c NPH047 Nephrotic Syndrome, Type 4 23 0.058
89
AMN006 Aminoaciduria 39 0.058
90
c NPH085 Nephrotic Syndrome 12 17 0.058
91
c CHR098 Chronic Pyelonephritis 38 0.058
92
P CLR023 Colorectal Cancer 96 0.050
93
P PHC003 Pheochromocytoma 72 0.050
94
P RNL014 Renal Cell Carcinoma 80 0.050
95
P FML161 Familial Mediterranean Fever, Ar 64 0.050
96
P KDN017 Kidney Cancer 67 0.050
97
P GCH001 Gaucher's Disease 63 0.050
98
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 32 0.050
99
LWS003 Lowe Syndrome 61 0.050
100
PPL048 Papillorenal Syndrome 36 0.050
101
GLL032 Galloway-Mowat Syndrome 52 0.050
102
VRL011 Viral Infectious Disease 56 0.050
103
P NPH005 Nephronophthisis 55 0.050
104
PRS055 Pierson Syndrome 40 0.050
105
HYP066 Hyperglycemia 61 0.050
106
c LPD019 Lipodystrophy, Partial, Acquired 32 0.050
107
EPS006 Epstein Syndrome 40 0.050
108
GDP001 Goodpasture Syndrome 47 0.050
109
FRS002 Frasier Syndrome 48 0.050
110
P HLP001 Holoprosencephaly 62 0.050
111
c CHR522 Charcot-Marie-Tooth Disease, Dominant Intermediate E 23 0.050
112
c GLM033 Glomerulosclerosis, Focal Segmental, 4 30 0.050
113
LPD008 Lipid Metabolism Disorder 42 0.050
114
c NPH054 Nephrotic Syndrome, Type 3 32 0.050
115
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 37 0.050
116
PRP030 Purpura 60 0.050
117
NPH039 Nephrotic Syndrome, Type 5, with or Without Ocular Abnormalities 21 0.050
118
c ALM001 Al Amyloidosis 45 0.050
119
c NPH074 Nephrotic Syndrome, Type 9 20 0.050
120
P CRY007 Cryoglobulinemia, Familial Mixed 24 0.050
121
c NPH073 Nephrotic Syndrome, Type 8 22 0.050
122
LPD004 Lipoid Nephrosis 49 0.050
123
LPP002 Lipoprotein Glomerulopathy 46 0.050
124
ANR004 Anuria 46 0.050
125
ATM059 Autoimmune Disease 6 23 0.050
126
RNL089 Renal Nutcracker Syndrome 18 0.050
127
P RNV001 Renovascular Hypertension 46 0.050
128
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 15 0.050
129
c SVR005 Severe Pre-Eclampsia 48 0.050
130
c IGN004 Iga Nephropathy 3 15 0.050
131
ATM053 Autoimmune Disease 2 16 0.050
132
ATM054 Autoimmune Disease 3 16 0.050
133
STR044 Steroid-Resistant Nephrotic Syndrome 34 0.050
134
CRS001 Crescentic Glomerulonephritis 41 0.050
135
P PRL003 Proliferative Glomerulonephritis 40 0.050
136
BRN106 Burns 52 0.050
137
RNL077 Renal Fibrosis 48 0.050
138
P HYP607 Hypercholesterolemia, Familial 77 0.041
139
WLS001 Wilson Disease 72 0.041
140
P LVR013 Liver Disease 76 0.041
141
WLL001 Williams-Beuren Syndrome 61 0.041
142
c GCH015 Gaucher Disease, Type I 52 0.041
143
c GCH017 Gaucher Disease, Type Iii 44 0.041
144
ACR008 Acrocallosal Syndrome 51 0.041
145
KWS002 Kawasaki Disease 70 0.041
146
CSY001 C Syndrome 49 0.041
147
P RCK004 Rickets 59 0.041
148
WGN006 Wegener Granulomatosis 63 0.041
149
NTR005 Nutritional Deficiency Disease 51 0.041
150
MJD001 Majeed Syndrome 32 0.041
151
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.041
152
RBS003 Rabson-Mendenhall Syndrome 55 0.041
153
c HPT001 Hepatitis C 68 0.041
154
DBT090 Diabetes and Deafness, Maternally Inherited 32 0.041
155
P ATR011 Atrial Fibrillation 63 0.041
156
LSH001 Leishmaniasis 63 0.041
157
MTH009 Mouth Disease 63 0.041
158
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 44 0.041
159
c ORF037 Orofaciodigital Syndrome I 43 0.041
160
c HPT016 Hepatitis B 61 0.041
161
YLL002 Yellow Fever 58 0.041
162
MCR037 Macroglossia 45 0.041
163
P HYP613 Hypophosphatemic Rickets 50 0.041
164
c HPT073 Hepatitis C Virus 72 0.041
165
P THL005 Thalassemia 61 0.041
166
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.041
167
IMM102 Immunodeficiency 14 33 0.041
168
CYS025 Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic 24 0.041
169
c SPL024 Split-Hand/foot Malformation 3 28 0.041
170
c DNT021 Dent Disease 2 37 0.041
171
HMT008 Hematuria, Benign Familial 44 0.041
172
EBL001 Ebola Hemorrhagic Fever 40 0.041
173
P FNC026 Fanconi Renotubular Syndrome 1 25 0.041
174
ATH003 Atherosclerosis 63 0.041
175
c HPT003 Hepatitis a 55 0.041
176
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.041
177
RNL007 Renal Tubular Acidosis 50 0.041
178
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.041
179
FRS004 Free Sialic Acid Storage Disorders 26 0.041
180
ALN001 Aland Island Eye Disease 45 0.041
181
LGN002 Legionellosis 61 0.041
182
P ARC016 Auriculocondylar Syndrome 1 44 0.041
183
ACQ007 Acquired Immunodeficiency Syndrome 60 0.041
184
LYM008 Lymphangiosarcoma 48 0.041
185
P PNC044 Pancreatitis 62 0.041
186
c GLM028 Glomerulosclerosis, Focal Segmental, 5 26 0.041
187
LSS003 Lassa Fever 37 0.041
188
BLK001 Balkan Nephropathy 34 0.041
189
HYP268 Hypercalciuria, Absorptive 31 0.041
190
OBS061 Obstructive Sleep Apnea 61 0.041
191
P HRT032 Heart Disease 64 0.041
192
DNS007 Dense Deposit Disease 39 0.041
193
c HYP248 Hyperprolinemia, Type I 28 0.041
194
c VRL010 Viral Hepatitis 60 0.041
195
P BCL006 B-Cell Lymphomas 64 0.041
196
SPL011 Spleen Cancer 38 0.041
197
P SLP006 Sleep Apnea 60 0.041
198
RLP001 Relapsing Polychondritis 52 0.041
199
P SPS003 Spastic Diplegia 49 0.041
200
P HYP014 Hyperuricemia 49 0.041
201
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 26 0.041
202
CNN005 Connective Tissue Disease 60 0.041
203
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 26 0.041
204
P FML035 Familial Hyperlipidemia 49 0.041
205
P THR014 Thrombocytopenia 63 0.041
206
c FCL053 Focal Segmental Glomerulosclerosis 8 21 0.041
207
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 15 0.041
208
PLS009 Plasma Cell Neoplasm 47 0.041
209
ANG016 Angiokeratoma 43 0.041
210
P THY032 Thyroiditis 57 0.041
211
c ACT071 Acute Kidney Failure 48 0.041
212
OCL043 Oculorenocerebellar Syndrome 16 0.041
213
c GLM014 Glomerulopathy with Fibronectin Deposits 1 15 0.041
214
SCK005 Sickle Cell Disease 51 0.041
215
PRP021 Peripheral Nervous System Neoplasm 49 0.041
216
MSC072 Muscle Cancer 47 0.041
217
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 23 0.041
218
c ACT027 Acute Pancreatitis 59 0.041
219
DYS180 Dyschondrosteosis and Nephritis 14 0.041
220
P AGM001 Agammaglobulinemia 63 0.041
221
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.041
222
BRS004 Breast Angiosarcoma 34 0.041
223
ADJ001 Adjustment Disorder 38 0.041
224
NRG003 Neurogenic Arthropathy 26 0.041
225
CRV068 Cervical Polyp 40 0.041
226
BLD053 Blood Platelet Disease 44 0.041
227
IMM073 Immunoglobulin a Vasculitis 29 0.041
228
MLK004 Malakoplakia 28 0.041
229
c CNG004 Congenital Epulis 34 0.041
230
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 28 0.041
231
P SKN013 Skin Benign Neoplasm 38 0.041
232
CTN012 Cutaneous Leiomyosarcoma 38 0.041
233
PLY039 Polymorphic Reticulosis 20 0.041
234
BLK002 Balkan Hemorrhagic Fever 10 0.041
235
NLP003 Nail-Patella-Like Renal Disease 11 0.041
236
SPC003 Specific Developmental Disorder 39 0.041
237
P BLD051 Blood Coagulation Disease 44 0.041
238
BNP002 Bone Epithelioid Hemangioma 18 0.041
239
PYL004 Pyelitis 39 0.041
240
MSN004 Mesenchymal Cell Neoplasm 35 0.041
241
CLC007 Calcium Metabolism Disease 39 0.041
242
c IGN002 Iga Nephropathy 2 17 0.041
243
P EXT032 Extraosseous Osteosarcoma 35 0.041
244
PDT004 Pediatric Angiosarcoma 25 0.041
245
RNL097 Renal Artery Disease 44 0.041
246
MXD006 Mixed Liposarcoma 32 0.041
247
SPL001 Spleen Angiosarcoma 19 0.041
248
SPN186 Spinal Cord Injury 62 0.041
249
THY031 Thyroid Sarcoma 27 0.041
250
HMN011 Hemangioma of Intra-Abdominal Structure 23 0.041
251
INT221 Intravascular Large B-Cell Lymphoma 37 0.041
252
P GLM006 Glomangioma 37 0.041
253
ANG017 Angiolipoma 38 0.041
254
EPT011 Epithelioid Leiomyosarcoma 39 0.041
255
BRS061 Breast Sarcoma 36 0.041
256
INT011 Interstitial Emphysema 37 0.041
257
INT055 Intravascular Fasciitis 17 0.041
258
MNN006 Meninges Hemangiopericytoma 43 0.041
259
SNL003 Senile Angioma 32 0.041
260
THY004 Thyroid Angiosarcoma 19 0.041
261
VSC008 Vascular Hemostatic Disease 30 0.041
262
ANG019 Angiomyoma 29 0.041
263
CHR010 Chorioangioma 34 0.041
264
P HYP120 Hypoaldosteronism 34 0.041
265
INF005 Infiltrating Lipoma 28 0.041
266
MYX006 Myxoid Leiomyosarcoma 39 0.041
267
GLM001 Glomeruloid Hemangioma 28 0.041
268
BRS043 Breast Leiomyosarcoma 19 0.041
269
OVR003 Ovarian Angiosarcoma 26 0.041
270
OVR061 Ovary Sarcoma 24 0.041
271
PDT001 Pediatric Lymphoma 39 0.041
272
NPH006 Nephrogenic Adenofibroma 30 0.041
273
c INT282 Integumentary System Benign Neoplasm 21 0.041
274
OCL029 Oculo Skeletal Renal Syndrome 11 0.041
275
DPL001 Deep Leiomyoma 21 0.041
276
CNV001 Conventional Angiosarcoma 16 0.041
277
CNV003 Conventional Fibrosarcoma 31 0.041
278
BRS016 Breast Myofibroblastoma 20 0.041
279
SPN017 Spindle Cell Liposarcoma 31 0.041
280
VNS002 Venous Hemangioma 36 0.041
281
BNS002 Bone Structure Disease 37 0.041
282
HBN001 Hobnail Hemangioma 18 0.041
283
CYS001 Cystic Fibrosis 87 0.029
284
P MYC007 Myocardial Infarction 80 0.029
285
P NRB001 Neuroblastoma 70 0.029
286
SCK003 Sickle Cell Anemia 72 0.029
287
CYS013 Cystinuria 63 0.029
288
HV1006 Hiv-1 80 0.029
289
KPS004 Kaposi Sarcoma 69 0.029
290
MTC097 Mitochondrial Complex Iv Deficiency 51 0.029
291
LSC001 Lesch-Nyhan Syndrome 60 0.029
292
c GLY060 Glycogen Storage Disease Ia 57 0.029
293
CYS036 Cystinosis, Nephropathic 40 0.029
294
P CRN211 Coronary Artery Disease 74 0.029
295
P RSP003 Respiratory Failure 68 0.029
296
c SPN225 Spondyloarthropathy 1 62 0.029
297
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 42 0.029
298
P CMR001 Camurati-Engelmann Disease 63 0.029
299
P SLD010 Sialidosis, Type I 41 0.029
300
GTL001 Gitelman Syndrome 60 0.029
301
CNG034 Congestive Heart Failure 72 0.029
302
ANR002 Aniridia 62 0.029
303
PRD019 Periodic Fever, Familial 48 0.029
304
GST050 Gastrointestinal System Disease 58 0.029
305
MCK007 Muckle-Wells Syndrome 62 0.029
306
CRD119 Cardiac Arrest 63 0.029
307
P MYL005 Myelofibrosis 67 0.029
308
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.029
309
DNY001 Denys-Drash Syndrome 53 0.029
310
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.029
311
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.029
312
c ALP073 Alport Syndrome, Autosomal Recessive 41 0.029
313
P PSR002 Psoriasis 63 0.029
314
c GLY016 Glycogen Storage Disease Ib 35 0.029
315
APP015 Apparent Mineralocorticoid Excess 50 0.029
316
LYM029 Lymphedema-Distichiasis Syndrome 38 0.029
317
P MTH008 Methylmalonic Acidemia 51 0.029
318
c CNG401 Congenital Heart Disease 67 0.029
319
CHL071 Child Syndrome 58 0.029
320
EPL108 Epilepsy, Progressive Myoclonic 4, with or Without Renal Failure 26 0.029
321
c ALP074 Alport Syndrome, Autosomal Dominant 37 0.029
322
c ACT210 Acute Respiratory Distress Syndrome 55 0.029
323
RNL051 Renal Cysts and Diabetes Syndrome 46 0.029
324
ADL002 Adult Syndrome 53 0.029
325
P PTS002 Ptosis 56 0.029
326
P PLY011 Polycystic Ovary Syndrome 64 0.029
327
P HYP117 Hypertriglyceridemia 65 0.029
328
P DRM010 Dermatomyositis 59 0.029
329
BLD044 Bladder Disease 50 0.029
330
P ART023 Arthropathy 63 0.029
331
BRC012 Brucellosis 66 0.029
332
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 34 0.029
333
P SJG001 Sjogren's Syndrome 55 0.029
334
PRP027 Peripheral Vascular Disease 69 0.029
335
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.029
336
P MYL006 Myeloid Leukemia 67 0.029
337
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 46 0.029
338
P AMY082 Amyloidosis, Familial Visceral 45 0.029
339
SLP005 Sleep Disorder 52 0.029
340
LVR012 Liver Cirrhosis 71 0.029
341
P ACT117 Acute Myelomonocytic Leukemia 46 0.029
342
c HML035 Hemolytic Uremic Syndrome, Atypical 2 24 0.029
343
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.029
344
MDY004 Mody, Type Iii 35 0.029
345
NRG002 Neurogenic Bladder 47 0.029
346
DFN256 Deafness and Myopia 24 0.029
347
c ACT068 Acute Cystitis 50 0.029
348
P HRP006 Herpes Simplex 65 0.029
349
c CCK006 Cockayne Syndrome, Type B 37 0.029
350
c HML034 Hemolytic Uremic Syndrome, Atypical 3 24 0.029
351
c SYS043 Systemic Lupus Erythematosus 1 29 0.029
352
HYP691 Hypomelanosis of Ito 44 0.029
353
c HYP163 Hyperlipidemia Type 3 52 0.029
354
SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 30 0.029
355
ATN011 Autoinflammation with Infantile Enterocolitis 36 0.029
356
PPL021 Papilledema 47 0.029
357
c HML032 Hemolytic Uremic Syndrome, Atypical 4 33 0.029
358
IMM065 Immunodeficiency 10 39 0.029
359
INT258 Interstitial Nephritis, Karyomegalic 21 0.029
360
c HML037 Hemolytic Uremic Syndrome, Atypical 5 24 0.029
361
c CRN139 Cornelia De Lange Syndrome 1 37 0.029
362
c ATM003 Autoimmune Thyroiditis 59 0.029
363
CNZ008 Coenzyme Q10 Deficiency, Primary, 6 23 0.029
364
KDS001 Kid Syndrome 53 0.029
365
c HML036 Hemolytic Uremic Syndrome, Atypical 6 24 0.029
366
CMP042 Complement Factor H Deficiency 40 0.029
367
INC022 Inclusion-Cell Disease 46 0.029
368
c EXS005 Exostoses, Multiple, Type 2 27 0.029
369
VSC007 Vascular Disease 51 0.029
370
NTR042 Neutrophilic Dermatosis, Acute Febrile 31 0.029
371
ETN001 Eating Disorder 59 0.029
372
P MST009 Mastocytosis 54 0.029
373
FCH003 Fechtner Syndrome 36 0.029
374
CTS003 Coats Disease 57 0.029
375
c CCK005 Cockayne Syndrome, Type a 39 0.029
376
P PNM007 Pneumonia 67 0.029
377
HYP074 Hypersensitivity Vasculitis 49 0.029
378
c NPH046 Nephrolithiasis, Type I 31 0.029
379
c HRD104 Hereditary Multiple Osteochondromas 42 0.029
380
VSC011 Vasculitis 62 0.029
381
HNC001 Henoch-Schoenlein Purpura 45 0.029
382
ONC002 Onchocerciasis 53 0.029
383
P HRD001 Hereditary Multiple Exostoses 46 0.029
384
PMP001 Pemphigus 49 0.029
385
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.029
386
P LYM026 Lymphoblastic Leukemia 60 0.029
387
c SYS004 Systemic Mastocytosis 60 0.029
388
PRL009 Prolactinoma 63 0.029
389
P RST002 Restrictive Cardiomyopathy 48 0.029
390
CNZ004 Coenzyme Q10 Deficiency, Primary, 3 20 0.029
391
P ANT006 Antiphospholipid Syndrome 60 0.029
392
c FML162 Familial Mediterranean Fever, Ad 19 0.029
393
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.029
394
MNT146 Mental Retardation, X-Linked, Syndromic, Martin-Probst Type 27 0.029
395
c TRC078 Trichohepatoenteric Syndrome 2 30 0.029
396
P CRD011 Cardiomyopathy 66 0.029
397
P PLY018 Polycythemia 58 0.029
398
IPX001 Ipex Syndrome 35 0.029
399
AMN001 Amenorrhea 51 0.029
400
c CNG415 Congenital Disorder of Glycosylation, Type Ia 46 0.029
401
ADM013 Adamantinoma of Long Bones 57 0.029
402
WLL006 Wells Syndrome 57 0.029
403
ADL030 Adult-Onset Still's Disease 57 0.029
404
DBT084 Diabetes Mellitus, Ketosis-Prone 28 0.029
405
CND002 Conduct Disorder 54 0.029
406
c HYP311 Hyperparathyroidism 3 33 0.029
407
P DBT005 Diabetes Insipidus 53 0.029
408
PRT030 Parathyroid Gland Disease 49 0.029
409
MMB001 Membranoproliferative Glomerulonephritis 44 0.029
410
P HYP004 Hypercalcemia 54 0.029
411
P VSC005 Vesicoureteral Reflux 53 0.029
412
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 16 0.029
413
PLC008 Placenta Disease 33 0.029
414
P GLY013 Glycogen Storage Disease 58 0.029
415
HPY002 H. Pylori Infection 58 0.029
416
IMM071 Immunodeficiency 12 27 0.029
417
P PLY014 Polycystic Kidney Disease 60 0.029
418
P DRR001 Diarrhea 60 0.029
419
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 26 0.029
420
INT002 Intermittent Claudication 56 0.029
421
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 19 0.029
422
c VSC025 Vesicoureteral Reflux 3 26 0.029
423
DPH001 Diphtheria 55 0.029
424
PMS001 Poems Syndrome 56 0.029
425
CRT016 Carotid Artery Disease 54 0.029
426
HDR002 Hidradenitis Suppurativa 53 0.029
427
c NPH065 Nephronophthisis 13 25 0.029
428
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 19 0.029
429
MDL009 Medullary Sponge Kidney 41 0.029
430
HYP005 Hypokalemia 52 0.029
431
c GLY017 Glycogen Storage Disease Ic 20 0.029
432
P PRG013 Paraganglioma 54 0.029
433
OHD004 Ohdo Syndrome 33 0.029
434
MRC001 Marchiafava Bignami Disease 33 0.029
435
c VSC020 Vesicoureteral Reflux 2 28 0.029
436
VSC006 Vascular Cancer 51 0.029
437
GST027 Gastric Lymphoma 54 0.029
438
P HMR012 Hemorrhagic Fever 55 0.029
439
c FCL055 Focal Segmental Glomerulosclerosis 9 19 0.029
440
CCN007 Cocoon Syndrome 32 0.029
441
c PRC045 Preeclampsia/eclampsia 5 25 0.029
442
VSC014 Vascular Hyalinosis 16 0.029
443
c NPH076 Nephrotic Syndrome, Type 10 20 0.029
444
LYM027 Lymphopenia 54 0.029
445
PLC003 Placental Site Trophoblastic Tumor 48 0.029
446
INT017 Intestinal Schistosomiasis 45 0.029
447
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 41 0.029
448
DNG002 Dengue Hemorrhagic Fever 60 0.029
449
c EXS004 Exostoses, Multiple, Type 1 22 0.029
450
MRS001 Marasmus 39 0.029
451
P CRN178 Coronary Heart Disease 6 22 0.029
452
HMX002 Heme Oxygenase-1 Deficiency 25 0.029
453
c HPT007 Hepatitis E 51 0.029
454
NPH082 Nephrosis with Deafness and Urinary Tract and Digital Malformations 14 0.029
455
GLC003 Glucose Intolerance 56 0.029
456
BCT004 Bacteriuria 48 0.029
457
c FNC049 Fanconi Renotubular Syndrome 3 15 0.029
458
c PRC034 Preeclampsia/eclampsia 4 24 0.029
459
P PNC001 Pancytopenia 53 0.029
460
MLR007 Male Reproductive System Disease 36 0.029
461
SWL001 Swallowing Disorders 33 0.029
462
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 23 0.029
463
DRF001 Dirofilariasis 38 0.029
464
HYP540 Hypertension, Diastolic 40 0.029
465
c VSC046 Vesicoureteral Reflux 8 22 0.029
466
CHR001 Churg-Strauss Syndrome 48 0.029
467
PYR004 Pyuria 33 0.029
468
PLS016 Plasma Cell Leukemia 52 0.029
469
P SDR003 Sideroblastic Anemia 40 0.029
470
SXL003 Sexual Disorder 45 0.029
471
FBR085 Fibrillary Glomerulonephritis 21 0.029
472
MCR004 Macroglobulinemia 48 0.029
473
URM002 Uremia 36 0.029
474
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.029
475
CHL070 Cholesterol Embolism 31 0.029
476
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.029
477
c SYS038 Systemic Lupus Erythematosus 2 26 0.029
478
MTB004 Metabolic Acidosis 49 0.029
479
NCR002 Necrobiosis Lipoidica 33 0.029
480
MSN001 Mesangial Proliferative Glomerulonephritis 41 0.029
481
SPS196 Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 13 0.029
482
CNG116 Congenital Nephrotic Syndrome Finnish Type 14 0.029
483
P LMY004 Leiomyosarcoma 54 0.029
484
LGH004 Light Chain Deposition Disease 43 0.029
485
OCL005 Oculocerebrorenal Syndrome 30 0.029
486
DNT019 Daentl Towsend Siegel Syndrome 15 0.029
487
CHR585 Chromosome 16p11.2 Deletion Syndrome, 220-Kb Body Mass Index Quantitative Trait Locus 16, Included 15 0.029
488
PRS047 Prostatitis 56 0.029
489
IMM053 Immunotactoid Glomerulopathy 23 0.029
490
STT004 Steatorrhea 41 0.029
491
P LPD010 Lipodystrophy 51 0.029
492
VSC009 Vascular Skin Disease 21 0.029
493
PYL007 Pylorus Cancer 19 0.029
494
c ACT075 Acute Myocardial Infarction 61 0.029
495
PMP004 Pemphigus Foliaceus 42 0.029
496
HYP025 Hyperphosphatemia 45 0.029
497
P MNC007 Monocytic Leukemia 52 0.029
498
HDR003 Hidradenitis 46 0.029
499
BNN003 Bone Inflammation Disease 46 0.029
500
ART111 Artery Disease 56 0.029
501
C3G002 C3 Glomerulopathy 26 0.029
502
P PRX033 Proximal Renal Tubular Acidosis 34 0.029
503
c RNL113 Renal Failure, Progressive, with Hypertension 18 0.029
504
SGL001 Siegler Brewer Carey Syndrome 12 0.029
505
LTZ001 Lutz Richner Landolt Syndrome 10 0.029
506
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.029
507
CST005 Castleman Disease 42 0.029
508
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 20 0.029
509
HYP114 Hypertensive Nephropathy 32 0.029
510
IMM051 Immunotactoid or Fibrillary Glomerulopathy 10 0.029
511
c NPH083 Nephrotic Syndrome 11 15 0.029
512
c NPH084 Nephrotic Syndrome 13 15 0.029
513
FBR032 Fibromuscular Dysplasia 39 0.029
514
INS009 Insulin-Resistance Type B 21 0.029
515
SPN051 Spondylitis 50 0.029
516
WLD005 Wild Type Attr Amyloidosis 18 0.029
517
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 17 0.029
518
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 19 0.029
519
DND018 Dendritic Cell Tumor 40 0.029
520
c PRC032 Preeclampsia/eclampsia 2 18 0.029
521
SPN119 Spondylarthropathy 46 0.029
522
c SYS046 Systemic Lupus Erythematosus 3 22 0.029
523
P SYS050 Systemic Lupus Erythematosus with Nephritis 2 11 0.029
524
c SYS051 Systemic Lupus Erythematosus 4 21 0.029
525
c SYS054 Systemic Lupus Erythematosus with Nephritis 3 12 0.029
526
c SYS056 Systemic Lupus Erythematosus with Nephritis 1 11 0.029
527
THL017 Thalassemia Intermedia 38 0.029
528
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 32 0.029
529
c ACT009 Acute Monocytic Leukemia 46 0.029
530
ACT040 Acute Poststreptococcal Glomerulonephritis 30 0.029
531
MLD002 Mild Pre-Eclampsia 32 0.029
532
P ACR072 Acrorenal Syndrome 21 0.029
533
c ACT042 Acute Pyelonephritis 47 0.029
534
KDN013 Kidney Hypertrophy 32 0.029
535
RTN023 Retinitis 49 0.029
536
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 18 0.029
537
c EXS006 Exostoses, Multiple, Type 3 11 0.029
538
PHC008 Pheochromocytoma-Islet Cell Tumor Syndrome 12 0.029
539
CRB009 Cerebritis 36 0.029
540
LMN004 Laminopathy Type Decaudain-Vigouroux 12 0.029
541
HYP479 Hyperinsulinism Due to Hnf4a Deficiency 11 0.029
542
IMM127 Immune System Cancer 41 0.029
543
NVD002 Nevada Syndrome 15 0.029
544
WTH001 Withdrawal Disorder 36 0.029
545
ATM012 Autoimmune Disease of Blood 36 0.029
546
P C1Q005 C1q Nephropathy 22 0.029
547
HPD002 Hepadnavirus Infection 20 0.029
548
PRM025 Primary Bacterial Infectious Disease 42 0.029
549
MNN021 Meningococcemia 35 0.029
550
THL018 Thalassemia Major 31 0.029
551
VTM003 Vitamin Metabolic Disorder 31 0.029
552
HRP008 Herpes Simiae 13 0.029
553
HRP012 Herpesvirus Simiae B Virus 10 0.029
554
PDT040 Pediatric Hypertension 30 0.029
555
CLS011 Classic Fabry Disease 9 0.029