Search results for "nephropathy"

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

572 hits were found for 'nephropathy'

# Family MCID Name MIFTS Score
1
FML076 Familial Juvenile Hyperuricaemic Nephropathy 28 6.761
2
BLK001 Balkan Nephropathy 26 4.943
3
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 26 4.620
4
c HYP616 Hyperuricemic Nephropathy, Familial Juvenile 2 21 4.061
5
P HYP623 Hyperuricemic Nephropathy, Familial Juvenile 1 23 3.863
6
MLT033 Multicentric Osteolysis Nephropathy 15 3.855
7
P BKV001 Bk-Virus Nephropathy 20 3.687
8
MMB005 Membranous Glomerulonephritis, Antenatal 21 3.649
9
IGG001 Iga Glomerulonephritis 46 3.560
10
P AMY082 Amyloidosis, Familial Visceral 43 3.531
11
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 15 3.520
12
HYP114 Hypertensive Nephropathy 38 3.434
13
ACT043 Acute Urate Nephropathy 17 3.276
14
NPH037 Nephronophthisis-Like Nephropathy 1 17 3.215
15
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 18 2.952
16
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 8 2.934
17
FGN001 Feigenbaum Bergeron Richardson Syndrome 15 2.903
18
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 21 2.593
19
PLY043 Polyomavirus Allograft Nephropathy 6 2.576
20
DNY001 Denys-Drash Syndrome 61 2.566
21
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 11 2.496
22
NPH066 Nephropathy Due to Cfhr5 Deficiency 11 2.496
23
c HYP529 Hyperuricemic Nephropathy, Familial Juvenile, 3 10 2.496
24
NPH050 Nephropathy, Progressive, with Deafness 6 2.496
25
c MCR113 Microvascular Complications of Diabetes 3 22 2.480
26
P ALP004 Alport Syndrome 60 2.216
27
MMB002 Membranous Glomerulonephritis 40 2.165
28
HMT008 Hematuria, Benign Familial 28 2.140
29
NPH003 Nephrocalcinosis 41 2.099
30
MCK007 Muckle-Wells Syndrome 62 2.088
31
c ALP073 Alport Syndrome, Autosomal Recessive 40 2.060
32
BRG002 Berger Disease 26 2.060
33
DNT019 Daentl Towsend Siegel Syndrome 18 2.060
34
PRM036 Premature Atherosclerosis with Photomyoclonic Epilepsy, Deafness, Diabetes Mellitus, Nephropathy, an 2 2.060
35
HYP632 Hyperuricemia - Anemia - Renal Failure 9 2.044
36
CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 8 2.044
37
c CL4006 Col4a5-Related Nephropathy 4 2.044
38
c CL4007 Col4a3-Related Nephropathy 4 2.044
39
c CL4008 Col4a4-Related Nephropathy 4 2.044
40
ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 4 2.044
41
NPH022 Nephropathy Familial with Hyperuricemia 2 2.044
42
CRM007 Crome Syndrome 15 2.025
43
c ATS141 Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E 11 2.025
44
c FML261 Familial Renal Amyloidosis Due to Lysozyme Variant 11 2.025
45
c FML260 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 10 2.025
46
P FML208 Familial Renal Amyloidosis Due to Apolipoprotein Aii Variant 9 2.025
47
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 9 2.025
48
HMR004 Hemorrhagic Fever with Renal Syndrome 51 1.506
49
NPH004 Nephropathia Epidemica 48 1.506
50
ADN024 Adenine Phosphoribosyltransferase Deficiency 45 1.492
51
RNL051 Renal Cysts and Diabetes Syndrome 36 1.492
52
FTZ004 Fitzsimmons Walson Mellor Syndrome 13 1.476
53
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 16 1.457
54
UMD001 Umod-Associated Kidney Disease 15 1.457
55
c RNR002 Ren-Related Kidney Disease 7 1.457
56
ALL011 Allain-Babin-Demarquez Syndrome 4 1.432
57
HRR004 Herrmann Syndrome 3 1.432
58
PRT039 Proteinuria 43 0.334
59
P GLM007 Glomerulonephritis 59 0.268
60
END072 Endotheliitis 44 0.243
61
NPH051 Nephritis 46 0.227
62
P KDN018 Kidney Disease 57 0.195
63
GLM011 Glomerulosclerosis 40 0.188
64
P NPH012 Nephrotic Syndrome 60 0.175
65
PRP030 Purpura 54 0.165
66
P HPT021 Hepatitis 55 0.147
67
P NRP001 Neuropathy 52 0.144
68
P FCL005 Focal Segmental Glomerulosclerosis 58 0.138
69
END030 End Stage Renal Failure 56 0.131
70
TNS005 Tonsillitis 48 0.131
71
P HYP014 Hyperuricemia 47 0.131
72
P PRM002 Primary Hyperoxaluria 68 0.120
73
INT067 Interstitial Nephritis 38 0.120
74
MMB001 Membranoproliferative Glomerulonephritis 42 0.117
75
CRS001 Crescentic Glomerulonephritis 35 0.113
76
FBR012 Fabry Disease 76 0.109
77
c MLG069 Malignant Hypertension 54 0.109
78
THR013 Thoracic Outlet Syndrome 45 0.109
79
P TRC086 Trichohepatoenteric Syndrome 1 39 0.109
80
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.109
81
NLP001 Nail-Patella Syndrome 61 0.104
82
CRB009 Cerebritis 33 0.104
83
P BLN003 Blindness 47 0.095
84
CYS016 Cystic Kidney 44 0.095
85
RNL077 Renal Fibrosis 41 0.095
86
P ART022 Arthritis 65 0.090
87
c HPT016 Hepatitis B 60 0.090
88
P MYL007 Myeloma 53 0.090
89
P VSC005 Vesicoureteral Reflux 46 0.090
90
P FNC004 Fanconi Syndrome 44 0.090
91
VSC007 Vascular Disease 59 0.085
92
ATH003 Atherosclerosis 56 0.085
93
ACN002 Acanthosis Nigricans 55 0.085
94
P PLY014 Polycystic Kidney Disease 53 0.085
95
ATN004 Autonomic Neuropathy 41 0.085
96
P PRL003 Proliferative Glomerulonephritis 39 0.085
97
NPH017 Nephrosis 36 0.085
98
P ATX010 Ataxia Neuropathy Spectrum 29 0.085
99
TBR010 Tuberculosis 73 0.080
100
P LKM002 Leukemia 66 0.080
101
P AMY004 Amyloidosis 63 0.080
102
P GT001 Gout 56 0.080
103
P PYL005 Pyelonephritis 43 0.080
104
P RHM011 Rheumatoid Arthritis 94 0.074
105
P WSK001 Wiskott-Aldrich Syndrome 69 0.074
106
P ANG001 Angelman Syndrome 66 0.074
107
c CHR089 Chronic Kidney Failure 57 0.074
108
c HPT001 Hepatitis C 57 0.074
109
VSC011 Vasculitis 57 0.074
110
P NPH005 Nephronophthisis 54 0.074
111
HYP066 Hyperglycemia 52 0.074
112
NPH018 Nephrogenic Systemic Fibrosis 52 0.074
113
c SPN225 Spondyloarthropathy 1 48 0.074
114
RTN023 Retinitis 44 0.074
115
c ART101 Aortic Valve Disease 2 32 0.074
116
P OBS005 Obesity 94 0.067
117
P UVT001 Uveitis 57 0.067
118
TRN018 Transitional Cell Carcinoma 54 0.067
119
P RNV001 Renovascular Hypertension 52 0.067
120
P ADN016 Adenocarcinoma 49 0.067
121
P RPD001 Rapidly Progressive Glomerulonephritis 49 0.067
122
CRY004 Cryoglobulinemia 49 0.067
123
MCR004 Macroglobulinemia 48 0.067
124
OST011 Osteomalacia 45 0.067
125
NPH010 Nephrosclerosis 43 0.067
126
P HML001 Hemolytic-Uremic Syndrome 43 0.067
127
c CHR098 Chronic Pyelonephritis 40 0.067
128
LGH004 Light Chain Deposition Disease 31 0.067
129
P MYC007 Myocardial Infarction 81 0.060
130
HV1006 Hiv-1 83 0.060
131
MLR004 Malaria 81 0.060
132
P WLM002 Wilms Tumor 70 0.060
133
BRN024 Bronchitis 62 0.060
134
PRT036 Peritonitis 61 0.060
135
CRB039 Cerebrovascular Disease 59 0.060
136
P THY032 Thyroiditis 56 0.060
137
PMS001 Poems Syndrome 56 0.060
138
P ANT006 Antiphospholipid Syndrome 55 0.060
139
P PSR002 Psoriasis 54 0.060
140
c HPT073 Hepatitis C Virus 51 0.060
141
EPD016 Epidermolysis Bullosa 49 0.060
142
SNS001 Sensorineural Hearing Loss 48 0.060
143
PRT019 Protein-Losing Enteropathy 47 0.060
144
HYP037 Hyperhomocysteinemia 45 0.060
145
HNC001 Henoch-Schoenlein Purpura 44 0.060
146
LPS007 Lupus Nephritis 44 0.060
147
P DRR001 Diarrhea 44 0.060
148
RTR011 Retroperitoneal Fibrosis 39 0.060
149
ANR040 Aneurysm 35 0.060
150
P MDL021 Medullary Cystic Kidney Disease 2 24 0.060
151
c SYS001 Systemic Lupus Erythematosus 91 0.052
152
P DBT085 Diabetes Mellitus, Insulin-Dependent 83 0.052
153
P ATX030 Ataxia-Telangiectasia 76 0.052
154
c MLT019 Multiple Myeloma 75 0.052
155
P CHR090 Chronic Lymphocytic Leukemia 74 0.052
156
CDS001 Cadasil 73 0.052
157
AND015 Androgen Insensitivity 69 0.052
158
BHC002 Behcet's Disease 68 0.052
159
P LPS004 Lupus Erythematosus 67 0.052
160
MYC006 Mycosis Fungoides 62 0.052
161
c HYP595 Hypertension, Essential 66 0.052
162
STR067 Stroke, Ischemic 65 0.052
163
P HYP086 Hypothyroidism 59 0.052
164
P PNC044 Pancreatitis 59 0.052
165
P HYP069 Hyperparathyroidism 57 0.052
166
P SZR006 Seizure Disorder 56 0.052
167
MXD005 Mixed Connective Tissue Disease 56 0.052
168
ART111 Artery Disease 55 0.052
169
CLT003 Colitis 54 0.052
170
P AND016 Andersen Syndrome 54 0.052
171
P HMR012 Hemorrhagic Fever 52 0.052
172
PLM001 Pulmonary Tuberculosis 60 0.052
173
c ATM011 Autoimmune Hepatitis 51 0.052
174
P NPH009 Nephrolithiasis 51 0.052
175
P SCL015 Scleritis 50 0.052
176
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.052
177
LPD010 Lipodystrophy 49 0.052
178
CHR001 Churg-Strauss Syndrome 49 0.052
179
ART001 Arterial Tortuosity Syndrome 48 0.052
180
P SYP003 Syphilis 48 0.052
181
SPN051 Spondylitis 48 0.052
182
HPT014 Hepatorenal Syndrome 48 0.052
183
URM002 Uremia 47 0.052
184
SCH016 Schimke Immunoosseous Dysplasia 46 0.052
185
PRP023 Peripheral Neuropathy 44 0.052
186
LPD004 Lipoid Nephrosis 43 0.052
187
P HYP120 Hypoaldosteronism 42 0.052
188
LYM021 Lymphadenitis 39 0.052
189
P SPN052 Spondyloarthropathy 39 0.052
190
TTR016 Tetra-Amelia Syndrome 36 0.052
191
LMY003 Leiomyomatosis 33 0.052
192
STR044 Steroid-Resistant Nephrotic Syndrome 31 0.052
193
ADS002 Adie Syndrome 30 0.052
194
HNM002 Hinman Syndrome 26 0.052
195
c BNG076 Benign Exophthalmos Syndrome 19 0.052
196
DHL001 Dahlberg Borer Newcomer Syndrome 17 0.052
197
CLL035 Collagen Type Iii Glomerulopathy 8 0.052
198
HPT023 Hepatocellular Carcinoma 95 0.043
199
P APL001 Aplastic Anemia 76 0.043
200
P HMC003 Hemochromatosis 75 0.043
201
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.043
202
P CRN211 Coronary Artery Disease 73 0.043
203
P SCL016 Scleroderma 76 0.043
204
LVR012 Liver Cirrhosis 66 0.043
205
CRH001 Crohn's Disease 71 0.043
206
HST011 Histoplasmosis 64 0.043
207
P THL005 Thalassemia 64 0.043
208
GTL001 Gitelman Syndrome 64 0.043
209
RLP001 Relapsing Polychondritis 63 0.043
210
P PND002 Pendred Syndrome 62 0.043
211
P BCK002 Beckwith-Wiedemann Syndrome 61 0.043
212
P WLF004 Wolfram Syndrome 61 0.043
213
PLY017 Polyarteritis Nodosa 60 0.043
214
P MNN013 Meningitis 58 0.043
215
c ATM003 Autoimmune Thyroiditis 58 0.043
216
CYS010 Cystinosis 57 0.043
217
P GST044 Gastritis 56 0.043
218
LDD001 Ladd Syndrome 56 0.043
219
P THR014 Thrombocytopenia 56 0.043
220
GRV001 Graves' Disease 54 0.043
221
WLL006 Wells Syndrome 54 0.043
222
SND002 Sneddon Syndrome 54 0.043
223
SCK005 Sickle Cell Disease 54 0.043
224
P MTR004 Maturity-Onset Diabetes of the Young 54 0.043
225
DFC004 Deficiency Anemia 54 0.043
226
TTN003 Tetanus 54 0.043
227
P TYR004 Tyrosinemia 53 0.043
228
ESN015 Eosinophilic Fasciitis 52 0.043
229
P LDD002 Liddle Syndrome 52 0.043
230
GNG013 Gingivitis 52 0.043
231
P AGM001 Agammaglobulinemia 59 0.043
232
P RNL028 Renal Tubular Dysgenesis 52 0.043
233
ISC006 Ischemic Heart Disease 51 0.043
234
MYC002 Mycobacterium Avium Complex Disease 51 0.043
235
P FML161 Familial Mediterranean Fever, Ar 51 0.043
236
c ACT075 Acute Myocardial Infarction 57 0.043
237
P GLY013 Glycogen Storage Disease 51 0.043
238
c SCN006 Secondary Syphilis 51 0.043
239
MLL005 Miller-Dieker Syndrome 50 0.043
240
ASP005 Asphyxiating Thoracic Dystrophy 50 0.043
241
YLL002 Yellow Fever 50 0.043
242
RCT015 Reactive Arthritis 50 0.043
243
PLS011 Plasmacytoma 49 0.043
244
c SCN045 Secondary Amyloidosis 50 0.043
245
HYP266 Hypoxia 49 0.043
246
FRS002 Frasier Syndrome 48 0.043
247
RNL007 Renal Tubular Acidosis 48 0.043
248
CCH002 Coach Syndrome 48 0.043
249
URT001 Urethritis 48 0.043
250
DDN006 Duodenitis 48 0.043
251
DBT008 Diabetic Angiopathy 47 0.043
252
HMS001 Hemosiderosis 47 0.043
253
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 47 0.043
254
PRN011 Pernicious Anemia 46 0.043
255
ACQ007 Acquired Immunodeficiency Syndrome 46 0.043
256
c ANT034 Anterior Uveitis 45 0.043
257
PRG009 Progressive Multifocal Leukoencephalopathy 45 0.043
258
P EPL002 Epilepsy Syndrome 44 0.043
259
LYM012 Lymphoplasmacytic Lymphoma 43 0.043
260
P GND004 Gonadal Dysgenesis 43 0.043
261
MNN014 Mononeuritis 43 0.043
262
P PSD003 Pseudohypoaldosteronism 42 0.043
263
P SLD010 Sialidosis, Type I 43 0.043
264
CHY006 Chylous Ascites 40 0.043
265
GLL032 Galloway-Mowat Syndrome 41 0.043
266
WLC001 Wolcott-Rallison Syndrome 41 0.043
267
SPL018 Splenomegaly 40 0.043
268
GNG008 Ganglioneuroblastoma 40 0.043
269
URT010 Ureteral Obstruction 39 0.043
270
CYT008 Cytomegalovirus Infection 39 0.043
271
FSC004 Fasciitis 39 0.043
272
MNN009 Meningoencephalitis 39 0.043
273
P HYP599 Hypoparathyroidism, Familial Isolated 39 0.043
274
HRS011 Horseshoe Kidney 38 0.043
275
ANG054 Angina Pectoris 43 0.043
276
ART004 Aortic Atherosclerosis 38 0.043
277
c ACT004 Acute Diarrhea 37 0.043
278
CLL002 Collecting Duct Carcinoma 37 0.043
279
TBL013 Tubulointerstitial Nephritis and Uveitis 37 0.043
280
JBR006 Joubert Syndrome with Oculorenal Anomalies 36 0.043
281
NRN002 Neuronitis 36 0.043
282
INC001 Incontinentia Pigmenti Achromians 36 0.043
283
HMT018 Hematopoietic Stem Cell Transplantation 36 0.043
284
c CNG033 Congenital Syphilis 34 0.043
285
P HYP111 Hyperprolinemia 34 0.043
286
CRB086 Cerebral Aneurysms 33 0.043
287
ART012 Aortitis 33 0.043
288
VRL011 Viral Infectious Disease 31 0.043
289
ART010 Arteriolosclerosis 31 0.043
290
c JVN041 Juvenile Nephronophthisis 31 0.043
291
CLS016 Clostridium Difficile Colitis 31 0.043
292
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 29 0.043
293
BLD039 Bladder Adenocarcinoma 27 0.043
294
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.043
295
C4B001 C4b Deficiency 27 0.043
296
JBR007 Joubert Syndrome with Renal Anomalies 27 0.043
297
P ATM020 Autoimmune Enteropathy 26 0.043
298
c HYP248 Hyperprolinemia, Type I 27 0.043
299
c JVN024 Juvenile Hereditary Hemochromatosis 25 0.043
300
P GNR007 Generalized Dominant Dystrophic Epidermolysis Bullosa 24 0.043
301
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 25 0.043
302
ANT030 Antecubital Pterygium 22 0.043
303
TMR013 Tumor Necrosis Factor Receptor 1 Associated Periodic Syndrome 21 0.043
304
P GLM015 Glomerulopathy with Fibronectin Deposits 2 20 0.043
305
MDL024 Madelung Deformity 21 0.043
306
C4D002 C4a Deficiency 20 0.043
307
FTL011 Fetal Aminopterin Syndrome 18 0.043
308
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 17 0.043
309
AND005 Androgen Insensitivity Syndrome, Mild 17 0.043
310
DFN014 Deafness Nephritis Anorectal Malformation 16 0.043
311
FML277 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis with Severe Ocular Involvement 16 0.043
312
HRD064 Hereditary Vascular Retinopathy 15 0.043
313
OTP003 Oto-Palatal-Digital Syndrome 14 0.043
314
DYS034 Dyschondrosteosis Nephritis 12 0.043
315
LNP001 Loin Pain Hematuria Syndrome 11 0.043
316
P ALZ034 Alzheimer Disease 100 0.030
317
P PRS040 Prostate Cancer 84 0.030
318
P RTN008 Retinitis Pigmentosa 72 0.030
319
P CLC005 Celiac Disease 69 0.030
320
ACR007 Acromegaly 69 0.030
321
CNG034 Congestive Heart Failure 69 0.030
322
LSC001 Lesch-Nyhan Syndrome 69 0.030
323
CMM004 Common Variable Immunodeficiency 67 0.030
324
P CNG368 Congenital Adrenal Hyperplasia 66 0.030
325
P LYM007 Lymphangioleiomyomatosis 65 0.030
326
P PNM007 Pneumonia 64 0.030
327
P LGH007 Leigh Syndrome 65 0.030
328
P MYL006 Myeloid Leukemia 64 0.030
329
MGR002 Migraine 64 0.030
330
GLL008 Gilles De La Tourette Syndrome 64 0.030
331
P PRD006 Prader-Willi Syndrome 64 0.030
332
P MTH008 Methylmalonic Acidemia 63 0.030
333
P DRM010 Dermatomyositis 62 0.030
334
WRN001 Werner Syndrome 62 0.030
335
GLN010 Glanzmann Thrombasthenia 63 0.030
336
P CNG401 Congenital Heart Disease 62 0.030
337
P HYP117 Hypertriglyceridemia 61 0.030
338
P MST009 Mastocytosis 61 0.030
339
P HRM001 Hermansky-Pudlak Syndrome 60 0.030
340
BLL006 Bullous Pemphigoid 60 0.030
341
c SYS004 Systemic Mastocytosis 60 0.030
342
LYS003 Lysinuric Protein Intolerance 60 0.030
343
GST092 Gastroesophageal Reflux 60 0.030
344
PSD007 Pseudomyxoma Peritonei 59 0.030
345
c JVN010 Juvenile Rheumatoid Arthritis 59 0.030
346
PRP027 Peripheral Vascular Disease 60 0.030
347
DMN002 Dementia 58 0.030
348
c PRM005 Primary Hyperparathyroidism 58 0.030
349
ART021 Arteriosclerosis 58 0.030
350
c SYS005 Systemic Scleroderma 58 0.030
351
WLL001 Williams-Beuren Syndrome 58 0.030
352
FCT006 Factor V Deficiency 58 0.030
353
P HYP004 Hypercalcemia 57 0.030
354
c ATM010 Autoimmune Hemolytic Anemia 57 0.030
355
PLS006 Plasmodium Vivax Malaria 57 0.030
356
ACT049 Acute Disseminated Encephalomyelitis 57 0.030
357
TWN003 Townes-Brocks Syndrome 57 0.030
358
c LKM062 Leukemia, Acute Lymphoblastic 58 0.030
359
PHR003 Pharyngitis 56 0.030
360
P HML002 Hemolytic Anemia 56 0.030
361
P PRM006 Primary Biliary Cirrhosis 56 0.030
362
ULC004 Ulcerative Colitis 63 0.030
363
STT001 Status Epilepticus 56 0.030
364
P HRD011 Hereditary Spherocytosis 56 0.030
365
P HST010 Histiocytosis 55 0.030
366
URT039 Urticaria 55 0.030
367
BLD087 Bladder Cancer, Somatic 55 0.030
368
ACR008 Acrocallosal Syndrome 55 0.030
369
c VRL010 Viral Hepatitis 54 0.030
370
P ESP024 Esophagitis 54 0.030
371
EYD002 Eye Disease 54 0.030
372
P ANP001 Anaplastic Large Cell Lymphoma 53 0.030
373
ISC004 Ischemia 53 0.030
374
P KDN017 Kidney Cancer 53 0.030
375
c PNC108 Pancreatitis, Hereditary 54 0.030
376
RSD004 Rosai-Dorfman Disease 53 0.030
377
P THR005 Thrombotic Thrombocytopenic Purpura 53 0.030
378
P DBT005 Diabetes Insipidus 53 0.030
379
GLC012 Galactosialidosis 52 0.030
380
DBT010 Diabetic Neuropathy 52 0.030
381
P PLY019 Polyneuropathy 52 0.030
382
APH001 Aphthous Stomatitis 52 0.030
383
DWN001 Down Syndrome 51 0.030
384
P ANG015 Angioedema 51 0.030
385
FRB001 Farber Lipogranulomatosis 51 0.030
386
PLY041 Polymyositis 51 0.030
387
PMP001 Pemphigus 51 0.030
388
PRS047 Prostatitis 51 0.030
389
ALP008 Alopecia 51 0.030
390
P ATX004 Ataxia 50 0.030
391
GLC003 Glucose Intolerance 50 0.030
392
P INT068 Intestinal Disease 50 0.030
393
P PSR001 Psoriatic Arthritis 50 0.030
394
PST041 Posterior Urethral Valves 50 0.030
395
CNN005 Connective Tissue Disease 50 0.030
396
c HPT015 Hepatitis D 50 0.030
397
P SLP006 Sleep Apnea 50 0.030
398
HDC001 Headache 50 0.030
399
SCH002 Schnitzler Syndrome 50 0.030
400
P MLS001 Melas Syndrome 50 0.030
401
P RNL101 Renal Cell Carcinoma, Papillary 59 0.030
402
ARC007 Arachnoid Cysts 49 0.030
403
P SDR002 Siderosis 49 0.030
404
PPL002 Papillary Carcinoma 49 0.030
405
P PRT013 Portal Hypertension 49 0.030
406
FLL008 Folliculitis 49 0.030
407
MCR088 Microscopic Polyangiitis 49 0.030
408
ANR004 Anuria 48 0.030
409
P SNS014 Sinusitis 56 0.030
410
OBS061 Obstructive Sleep Apnea 48 0.030
411
PLS007 Plasmodium Falciparum Malaria 48 0.030
412
ANK001 Ankylosis 48 0.030
413
DWR001 Dwarfism 48 0.030
414
BLS002 Blastomycosis 48 0.030
415
MDL009 Medullary Sponge Kidney 48 0.030
416
P PSD015 Pseudohypoparathyroidism 47 0.030
417
PSD002 Pseudotumor Cerebri 47 0.030
418
P SPR013 Spiradenoma 47 0.030
419
P PLM006 Pulmonary Alveolar Proteinosis 47 0.030
420
PST062 Pustulosis Palmaris Et Plantaris 47 0.030
421
P EXP004 Exophthalmos 47 0.030
422
ONC003 Oncogenic Osteomalacia 47 0.030
423
P MNT147 Mental Retardation 46 0.030
424
MSN001 Mesangial Proliferative Glomerulonephritis 46 0.030
425
ART017 Aortic Disease 46 0.030
426
PLY020 Polyradiculoneuropathy 46 0.030
427
ACN001 Acinar Cell Carcinoma 46 0.030
428
c PND001 Pain Disorder 46 0.030
429
RNL078 Renal Dysplasia 46 0.030
430
PRR002 Pure Red-Cell Aplasia 46 0.030
431
PLS025 Plasmablastic Lymphoma 46 0.030
432
PLY012 Polyhydramnios 46 0.030
433
CNS004 Constipation 45 0.030
434
PLY013 Polymyalgia Rheumatica 45 0.030
435
P LYM025 Lymphedema 45 0.030
436
P LKD001 Leukodystrophy 45 0.030
437
P CHL066 Cholangitis 45 0.030
438
P HYD002 Hydronephrosis 45 0.030
439
GST045 Gastroenteritis 45 0.030
440
c HPT007 Hepatitis E 45 0.030
441
P CTN015 Cutaneous T Cell Lymphoma 45 0.030
442
CTS005 Catastrophic Antiphospholipid Syndrome 45 0.030
443
KMR001 Kimura Disease 44 0.030
444
MTR046 Maternally Inherited Diabetes and Deafness 44 0.030
445
GNG012 Gingival Overgrowth 44 0.030
446
HMP005 Hemiplegia 44 0.030
447
TRN015 Transient Cerebral Ischemia 44 0.030
448
c ATM024 Autoimmune Pancreatitis 44 0.030
449
ALC009 Alcoholic Liver Cirrhosis 43 0.030
450
c CNG012 Congenital Generalized Lipodystrophy 43 0.030
451
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 43 0.030
452
RNL011 Renal Osteodystrophy 43 0.030
453
P GGN002 Gigantism 43 0.030
454
STM007 Stomatitis 43 0.030
455
DNS007 Dense Deposit Disease 42 0.030
456
RNL015 Renal Hypertension 42 0.030
457
SPN119 Spondylarthropathy 42 0.030
458
P ENC011 Encephalomyopathy 42 0.030
459
HYP017 Hypophosphatemia 42 0.030
460
PLS016 Plasma Cell Leukemia 42 0.030
461
P SNR012 Senior-Loken Syndrome-1 43 0.030
462
BRN106 Burns 42 0.030
463
PYM001 Pyomyositis 42 0.030
464
ACT040 Acute Poststreptococcal Glomerulonephritis 41 0.030
465
P SCL009 Sclerosing Cholangitis 41 0.030
466
RTN018 Retinal Disease 41 0.030
467
TLN003 Telangiectasis 41 0.030
468
PSD009 Pseudohermaphroditism 41 0.030
469
PTY003 Pityriasis Rubra Pilaris 41 0.030
470
PMP004 Pemphigus Foliaceus 40 0.030
471
NSP002 Nasopharyngitis 40 0.030
472
CNG064 Congenital Chloride Diarrhea 40 0.030
473
HMC014 Homocysteinemia 40 0.030
474
CRT008 Carotid Artery Dissection 40 0.030
475
AMB002 Amblyopia 39 0.030
476
EVN001 Evans' Syndrome 39 0.030
477
P BRS044 Breast Adenocarcinoma 39 0.030
478
CRT004 Carotid Artery Thrombosis 39 0.030
479
IDP011 Idiopathic Interstitial Pneumonia 39 0.030
480
ATN005 Autonomic Dysfunction 39 0.030
481
MYC033 Myoclonus 39 0.030
482
UNL007 Unilateral Renal Agenesis 38 0.030
483
P RTN016 Retinal Degeneration 38 0.030
484
ARC002 Arachnoiditis 39 0.030
485
APR001 Apraxia 38 0.030
486
CRB001 Cerebral Lymphoma 38 0.030
487
ILS001 Ileus 38 0.030
488
C3D001 C3 Deficiency 38 0.030
489
BRB001 Beriberi 38 0.030
490
CMP009 Complement Deficiency 37 0.030
491
c CHR417 Chronic Graft Versus Host Disease 37 0.030
492
LYM029 Lymphedema-Distichiasis Syndrome 37 0.030
493
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 38 0.030
494
MYC019 Mycobacterium Marinum 37 0.030
495
RNL025 Renal Hypoplasia 36 0.030
496
C1Q001 C1q Deficiency 36 0.030
497
HYP008 Hypertensive Retinopathy 36 0.030
498
c HYP057 Hypervitaminosis D 35 0.030
499
c PRG011 Progressive Myoclonus Epilepsy 35 0.030
500
RTN020 Retinal Vascular Disease 35 0.030
501
SHR075 Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly 35 0.030
502
INT071 Intestinal Perforation 35 0.030
503
ESN020 Eosinophilic Granulomatosis with Polyangiitis 35 0.030
504
LNR006 Linear Iga Disease 34 0.030
505
ANG046 Angioimmunoblastic T-Cell Lymphoma 34 0.030
506
GST040 Gastric Adenocarcinoma 34 0.030
507
P HVY001 Heavy Chain Disease 33 0.030
508
AMY087 Amyloidosis, Hereditary, Transthyretin-Related 33 0.030
509
c CNG411 Congenital Disorder of Glycosylation, Type in 33 0.030
510
HYP226 Hyporeninemic Hypoaldosteronism 32 0.030
511
P PLN008 Peeling Skin Syndrome 32 0.030
512
IPX001 Ipex Syndrome 32 0.030
513
FCT013 Factor V Leiden Thrombophilia 31 0.030
514
c NPH032 Nephronophthisis 4 31 0.030
515
P MYC026 Myoclonus Epilepsy 31 0.030
516
PRP080 Peripheral Artery Disease 30 0.030
517
PSL001 Pasli Disease 30 0.030
518
MVM001 Movement Disease 30 0.030
519
PLM074 Pulmonary Function 30 0.030
520
RNL012 Renal Tuberculosis 30 0.030
521
c NPH048 Nephronophthisis 1, Juvenile 29 0.030
522
P CRB059 Cerebellar Degeneration 29 0.030
523
MLT133 Multicentric Castleman’s Disease 28 0.030
524
IDP033 Idiopathic Edema 27 0.030
525
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.030
526
EPS006 Epstein Syndrome 28 0.030
527
TFT003 Tufting Enteropathy 26 0.030
528
URT036 Urethral Obstruction 26 0.030
529
PRD012 Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis 26 0.030
530
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 25 0.030
531
ADT003 Auditory System Disease 26 0.030
532
PYR004 Pyuria 24 0.030
533
GRD004 Gardner-Diamond Syndrome 24 0.030
534
P PPL026 Papular Mucinosis 23 0.030
535
GST007 Gastric Dilatation 23 0.030
536
CHL070 Cholesterol Embolism 24 0.030
537
EPD034 Epidermolysis Bullosa, Pretibial 22 0.030
538
c MDL008 Medullary Cystic Kidney Disease 1 23 0.030
539
IRN002 Iron Metabolism Disease 22 0.030
540
IMM001 Immune-Complex Glomerulonephritis 23 0.030
541
EPL108 Epilepsy, Progressive Myoclonic 4, with or Without Renal Failure 20 0.030
542
PRP033 Properdin Deficiency 20 0.030
543
PRN007 Perinephritis 19 0.030
544
c ALP005 Alpha Chain Disease 20 0.030
545
c CRN111 Cranioectodermal Dysplasia 4 19 0.030
546
C9D001 C9 Deficiency 18 0.030
547
HPR001 Hprt-Related Gout 18 0.030
548
VRS001 Virus Associated Hemophagocytic Syndrome 18 0.030
549
c PST008 Posterior Scleritis 18 0.030
550
HVY003 Heavy Chain Deposition Disease 18 0.030
551
c GLM014 Glomerulopathy with Fibronectin Deposits 1 17 0.030
552
GLM024 Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria 16 0.030
553
ESN004 Eosinophilic Gastritis 16 0.030
554
P DMN011 Dominant Dystrophic Epidermolysis Bullosa 15 0.030
555
c ATM083 Autoimmune Lymphoproliferative Syndrome, Type Iii 16 0.030
556
c ART063 Arthrogryposis, Renal Dysfunction, and Cholestasis 2 15 0.030
557
RTN019 Retinal Telangiectasia 15 0.030
558
OCL043 Oculorenocerebellar Syndrome 15 0.030
559
ICH019 Ichthyosis Mental Retardation Dwarfism Renal Impairment 15 0.030
560
P INT105 Intellectual Disability Multi-Gene Panels 15 0.030
561
RTN163 Retinal Arterial Tortuosity 15 0.030
562
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 15 0.030
563
ATY040 Atypical Hemolytic-Uremic Syndrome with Anti-Factor H Antibodies 15 0.030
564
LGH014 Light and Heavy Chain Deposition Disease 13 0.030
565
PLS008 Plasmodium Malariae Malaria 13 0.030
566
KDN006 Kidney Papillary Necrosis 13 0.030
567
SLC010 Salcedo Syndrome 11 0.030
568
CMP053 Camptodactyly of Fingers 11 0.030
569
CNG330 Congenital Megacalycosis 9 0.030
570
NPH078 Nephrolithiasis, Uric Acid 8 0.030
571
CL4001 Col4a1-Related Disorders 6 0.030
572
EXD002 Exudative Glomerulonephritis 5 0.030