Search results for "nephropathy"

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

778 hits were found for 'nephropathy'

# Family MCID Name MIFTS Score
1
FML076 Familial Juvenile Hyperuricaemic Nephropathy 32 5.025
2
BLK001 Balkan Nephropathy 30 4.555
3
DBT061 Diabetic Nephropathy 40 4.545
4
MMB002 Membranous Glomerulonephritis 51 4.095
5
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 20 3.775
6
UMD001 Umod-Associated Kidney Disease 31 3.739
7
P BKV001 Bk-Virus Nephropathy 22 3.526
8
P FML044 Familial Juvenile Hyperuricemic Nephropathy Type 2 23 3.458
9
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 17 3.428
10
IGG001 Iga Glomerulonephritis 52 3.210
11
ACT043 Acute Urate Nephropathy 25 3.203
12
NPH037 Nephronophthisis-Like Nephropathy 1 15 3.130
13
c FML022 Familial Juvenile Hyperuricemic Nephropathy 34 2.979
14
HYP114 Hypertensive Nephropathy 40 2.912
15
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 10 2.853
16
c RNR002 Ren-Related Kidney Disease 18 2.823
17
ANG055 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle 17 2.812
18
THN006 Thin Basement Membrane Nephropathy 43 2.774
19
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 25 2.516
20
DNY001 Denys-Drash Syndrome 68 2.500
21
PLY043 Polyomavirus Allograft Nephropathy 6 2.500
22
MLT033 Multicentric Osteolysis Nephropathy 6 2.451
23
P AMY037 Amyloidosis, Hereditary Renal 34 2.439
24
ATH009 Atherosclerosis - Deafness - Diabetes - Epilepsy - Nephropathy 17 2.439
25
NPH016 Nephropathy-Hypertension 9 2.439
26
CTR091 Cataract - Nephropathy - Encephalopathy 14 2.424
27
ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 8 2.424
28
NPH003 Nephrocalcinosis 48 2.034
29
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 8 2.023
30
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 20 1.996
31
HYD039 Hydrocephalus - Blue Sclerae - Nephropathy 16 1.996
32
FGN001 Feigenbaum Bergeron Richardson Syndrome 6 1.996
33
PRM036 Premature Atherosclerosis with Photomyoclonic Epilepsy, Deafness, Diabetes Mellitus, Nephropathy, an 3 1.996
34
ATS141 Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E 17 1.979
35
NPH066 Nephropathy Due to Cfhr5 Deficiency 15 1.979
36
c FML261 Familial Renal Amyloidosis Due to Lysozyme Variant 13 1.979
37
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 12 1.979
38
c FML260 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 12 1.979
39
c FML208 Familial Renal Amyloidosis Due to Apolipoprotein Aii Variant 11 1.979
40
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 11 1.979
41
CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 7 1.979
42
c HYP529 Hyperuricemic Nephropathy, Familial Juvenile, 3 6 1.979
43
c CL4006 Col4a5-Related Nephropathy 6 1.979
44
c CL4007 Col4a3-Related Nephropathy 6 1.979
45
c CL4008 Col4a4-Related Nephropathy 6 1.979
46
c IGN002 Iga Nephropathy 2 5 1.979
47
P IGN003 Iga Nephropathy 1 5 1.979
48
NPH050 Nephropathy, Progressive, with Deafness 5 1.979
49
NPH022 Nephropathy Familial with Hyperuricemia 3 1.979
50
ALP004 Alport Syndrome 60 1.578
51
BRG002 Berger Disease 31 1.497
52
HMR004 Hemorrhagic Fever with Renal Syndrome 60 1.477
53
MCK007 Muckle-Wells Syndrome 66 1.453
54
P ATS015 Autosomal Dominant Alport Syndrome 52 1.453
55
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 37 1.453
56
ADN024 Adenine Phosphoribosyltransferase Deficiency 49 1.439
57
c MTR022 Maturity-Onset Diabetes of the Young, Type 5 41 1.439
58
c ATS018 Autosomal Recessive Alport Syndrome 44 1.422
59
FTZ004 Fitzsimmons Walson Mellor Syndrome 15 1.422
60
DNT019 Daentl Towsend Siegel Syndrome 7 1.422
61
c AMY038 Amyloidosis, Renal 31 1.400
62
HRR004 Herrmann Syndrome 5 1.400
63
ALL011 Allain-Babin-Demarquez Syndrome 4 1.400
64
c DBT009 Diabetes Mellitus 78 0.355
65
PRT039 Proteinuria 57 0.285
66
P HYP075 Hypertension 85 0.252
67
P GLM007 Glomerulonephritis 68 0.239
68
END072 Endotheliitis 50 0.208
69
NPH051 Nephritis 54 0.197
70
c TYP009 Type 2 Diabetes Mellitus 95 0.190
71
GLM011 Glomerulosclerosis 46 0.168
72
P TYP008 Type 1 Diabetes Mellitus 93 0.166
73
c NPH012 Nephrotic Syndrome 66 0.155
74
c KDN018 Kidney Disease 62 0.153
75
PRP030 Purpura 64 0.146
76
c HPT021 Hepatitis 64 0.133
77
NRP001 Neuropathy 61 0.130
78
P FCL005 Focal Segmental Glomerulosclerosis 72 0.125
79
DBT011 Diabetic Retinopathy 70 0.122
80
END030 End Stage Renal Failure 58 0.122
81
TNS005 Tonsillitis 57 0.116
82
P HYP014 Hyperuricemia 56 0.106
83
THR013 Thoracic Outlet Syndrome 52 0.106
84
INT067 Interstitial Nephritis 45 0.106
85
SYN053 Syndromic Diarrhea 32 0.103
86
P INS005 Insulin Resistance 66 0.100
87
MMB001 Membranoproliferative Glomerulonephritis 47 0.100
88
c PRM002 Primary Hyperoxaluria 72 0.096
89
CRS001 Crescentic Glomerulonephritis 43 0.096
90
CRB009 Cerebritis 39 0.096
91
FBR012 Fabry Disease 81 0.092
92
NLP001 Nail-Patella Syndrome 69 0.092
93
c MLG069 Malignant Hypertension 63 0.088
94
ATH003 Atherosclerosis 68 0.084
95
BLN003 Blindness 52 0.084
96
c VSC005 Vesicoureteral Reflux 50 0.084
97
P ART022 Arthritis 75 0.080
98
ANK002 Ankylosing Spondylitis 74 0.080
99
c HPT016 Hepatitis B 68 0.080
100
P CYS016 Cystic Kidney 51 0.080
101
P FNC004 Fanconi Syndrome 49 0.080
102
c ATN004 Autonomic Neuropathy 49 0.080
103
c PRL003 Proliferative Glomerulonephritis 46 0.080
104
c ESS002 Essential Hypertension 72 0.075
105
VSC007 Vascular Disease 70 0.075
106
ACN002 Acanthosis Nigricans 69 0.075
107
c PLY014 Polycystic Kidney Disease 61 0.075
108
NPH018 Nephrogenic Systemic Fibrosis 58 0.075
109
P PYL005 Pyelonephritis 54 0.075
110
RTN023 Retinitis 53 0.075
111
P ATX010 Ataxia Neuropathy Spectrum 41 0.075
112
P RHM011 Rheumatoid Arthritis 93 0.070
113
TBR010 Tuberculosis 83 0.070
114
P AMY004 Amyloidosis 67 0.070
115
P HPT001 Hepatitis C 66 0.070
116
HYP066 Hyperglycemia 62 0.070
117
c MYL007 Myeloma 61 0.070
118
NPH017 Nephrosis 42 0.070
119
P OBS005 Obesity 89 0.065
120
P LKM002 Leukemia 77 0.065
121
P ANG001 Angelman Syndrome 70 0.065
122
P GT001 Gout 65 0.065
123
ART019 Aortic Valve Stenosis 64 0.065
124
P RNV001 Renovascular Hypertension 61 0.065
125
P RPD001 Rapidly Progressive Glomerulonephritis 57 0.065
126
SNS001 Sensorineural Hearing Loss 57 0.065
127
NPH010 Nephrosclerosis 53 0.065
128
c NPH005 Nephronophthisis 50 0.065
129
c CHR098 Chronic Pyelonephritis 47 0.065
130
ANR040 Aneurysm 44 0.065
131
PRT036 Peritonitis 71 0.059
132
c THY032 Thyroiditis 66 0.059
133
VSC011 Vasculitis 66 0.059
134
TRN018 Transitional Cell Carcinoma 63 0.059
135
ART111 Artery Disease 60 0.059
136
MCR004 Macroglobulinemia 54 0.059
137
c WLM002 Wilms Tumor 51 0.059
138
HYP037 Hyperhomocysteinemia 51 0.059
139
LPD004 Lipoid Nephrosis 51 0.059
140
MNN014 Mononeuritis 51 0.059
141
PRT019 Protein-Losing Enteropathy 50 0.059
142
P HML001 Hemolytic-Uremic Syndrome 48 0.059
143
c HPT073 Hepatitis C Virus 45 0.059
144
LGH004 Light Chain Deposition Disease 36 0.059
145
c BNG076 Benign Exophthalmos Syndrome 22 0.059
146
P AMY001 Amyotrophic Lateral Sclerosis 98 0.053
147
P MYC007 Myocardial Infarction 92 0.053
148
P ATX002 Ataxia Telangiectasia 86 0.053
149
P SYS001 Systemic Lupus Erythematosus 85 0.053
150
CDS001 Cadasil 84 0.053
151
CRN211 Coronary Artery Disease 84 0.053
152
P WSK001 Wiskott-Aldrich Syndrome 78 0.053
153
P MLR004 Malaria 75 0.053
154
c PNC044 Pancreatitis 69 0.053
155
BRN024 Bronchitis 69 0.053
156
c UVT001 Uveitis 65 0.053
157
ANT006 Antiphospholipid Syndrome 65 0.053
158
CRB039 Cerebrovascular Disease 64 0.053
159
PSR002 Psoriasis 63 0.053
160
HV1006 Hiv-1 61 0.053
161
MYC002 Mycobacterium Avium Complex Disease 58 0.053
162
P ADN016 Adenocarcinoma 58 0.053
163
CRY004 Cryoglobulinemia 57 0.053
164
P NPH009 Nephrolithiasis 57 0.053
165
EPD016 Epidermolysis Bullosa 56 0.053
166
URM002 Uremia 56 0.053
167
NPH004 Nephropathia Epidemica 55 0.053
168
ART001 Arterial Tortuosity Syndrome 54 0.053
169
PRL007 Proliferative Diabetic Retinopathy 53 0.053
170
AND003 Andersen-Tawil Syndrome 53 0.053
171
LPS007 Lupus Nephritis 52 0.053
172
OST011 Osteomalacia 52 0.053
173
RTR011 Retroperitoneal Fibrosis 48 0.053
174
RNL077 Renal Fibrosis 46 0.053
175
HYP120 Hypoaldosteronism 46 0.053
176
SCH016 Schimke Immunoosseous Dysplasia 46 0.053
177
TTR016 Tetra-Amelia Syndrome 41 0.053
178
HNC001 Henoch-Schoenlein Purpura 41 0.053
179
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.053
180
STR044 Steroid-Resistant Nephrotic Syndrome 37 0.053
181
AND005 Androgen Insensitivity Syndrome, Mild 21 0.053
182
OTP003 Oto-Palatal-Digital Syndrome 16 0.053
183
P MLT019 Multiple Myeloma 82 0.046
184
AND002 Androgen Insensitivity Syndrome 80 0.046
185
HPT023 Hepatocellular Carcinoma 79 0.046
186
P HMC003 Hemochromatosis 78 0.046
187
c BTT002 Beta Thalassemia 77 0.046
188
BHC002 Behcet's Disease 76 0.046
189
LVR012 Liver Cirrhosis 75 0.046
190
P ACT074 Acute Lymphocytic Leukemia 75 0.046
191
P FML018 Familial Mediterranean Fever 74 0.046
192
HST011 Histoplasmosis 73 0.046
193
c LPS004 Lupus Erythematosus 72 0.046
194
c THL005 Thalassemia 72 0.046
195
c HYP095 Hypercholesterolemia 70 0.046
196
c HYP086 Hypothyroidism 69 0.046
197
ART021 Arteriosclerosis 67 0.046
198
MYC006 Mycosis Fungoides 66 0.046
199
c AXN002 Axenfeld-Rieger Syndrome 66 0.046
200
c MTR004 Maturity-Onset Diabetes of the Young 65 0.046
201
GTL001 Gitelman Syndrome 64 0.046
202
THR079 Thromboembolism 64 0.046
203
PMS001 Poems Syndrome 63 0.046
204
ACQ007 Acquired Immunodeficiency Syndrome 61 0.046
205
PLM001 Pulmonary Tuberculosis 60 0.046
206
c HMR012 Hemorrhagic Fever 60 0.046
207
c ATM011 Autoimmune Hepatitis 60 0.046
208
LPD010 Lipodystrophy 59 0.046
209
c ACT075 Acute Myocardial Infarction 59 0.046
210
P SYP003 Syphilis 57 0.046
211
HYP266 Hypoxia 57 0.046
212
SPN051 Spondylitis 57 0.046
213
PLS011 Plasmacytoma 57 0.046
214
HPT014 Hepatorenal Syndrome 56 0.046
215
DBT008 Diabetic Angiopathy 55 0.046
216
HMS001 Hemosiderosis 55 0.046
217
P DWR001 Dwarfism 55 0.046
218
P PRP023 Peripheral Neuropathy 52 0.046
219
P GND004 Gonadal Dysgenesis 52 0.046
220
c DRR001 Diarrhea 51 0.046
221
P SPN052 Spondyloarthropathy 49 0.046
222
URT010 Ureteral Obstruction 47 0.046
223
EPL002 Epilepsy Syndrome 45 0.046
224
DFF024 Diffuse Panbronchiolitis 45 0.046
225
P HYP111 Hyperprolinemia 45 0.046
226
ART004 Aortic Atherosclerosis 45 0.046
227
NRN002 Neuronitis 43 0.046
228
LMY003 Leiomyomatosis 39 0.046
229
ART012 Aortitis 39 0.046
230
VRL011 Viral Infectious Disease 36 0.046
231
ADS002 Adie Syndrome 35 0.046
232
MDL019 Medullary Cystic Kidney Disease Type 1 34 0.046
233
ADT003 Auditory System Disease 28 0.046
234
HNM002 Hinman Syndrome 27 0.046
235
CLL035 Collagen Type Iii Glomerulopathy 7 0.046
236
P ALZ001 Alzheimer's Disease 97 0.038
237
P APL001 Aplastic Anemia 82 0.038
238
CRH001 Crohn's Disease 74 0.038
239
GLN003 Glanzmann's Thrombasthenia 73 0.038
240
BLS001 Blau Syndrome 71 0.038
241
SPS077 Sepsis 70 0.038
242
RLP001 Relapsing Polychondritis 70 0.038
243
c THR014 Thrombocytopenia 70 0.038
244
GLL008 Gilles De La Tourette Syndrome 70 0.038
245
P DRM010 Dermatomyositis 68 0.038
246
P HYD006 Hydrocephalus 68 0.038
247
c MNN013 Meningitis 68 0.038
248
c CHR090 Chronic Lymphocytic Leukemia 67 0.038
249
PRP027 Peripheral Vascular Disease 67 0.038
250
P PRT013 Portal Hypertension 66 0.038
251
P ATM003 Autoimmune Thyroiditis 65 0.038
252
P HYP117 Hypertriglyceridemia 65 0.038
253
P CHR089 Chronic Kidney Failure 65 0.038
254
STT001 Status Epilepticus 65 0.038
255
c HYP069 Hyperparathyroidism 64 0.038
256
STR067 Stroke, Ischemic 64 0.038
257
P SHR002 Short Stature 64 0.038
258
ACT049 Acute Disseminated Encephalomyelitis 63 0.038
259
WLL006 Wells Syndrome 62 0.038
260
DFC004 Deficiency Anemia 62 0.038
261
GNG013 Gingivitis 62 0.038
262
ESN015 Eosinophilic Fasciitis 61 0.038
263
RNL015 Renal Hypertension 60 0.038
264
c AGM001 Agammaglobulinemia 60 0.038
265
ACR008 Acrocallosal Syndrome 59 0.038
266
P SCL015 Scleritis 59 0.038
267
GLB015 Glioblastoma Multiforme 59 0.038
268
c SLP006 Sleep Apnea 59 0.038
269
c GLY013 Glycogen Storage Disease 59 0.038
270
c TYR004 Tyrosinemia 58 0.038
271
SCK005 Sickle Cell Disease 58 0.038
272
P CNG401 Congenital Heart Disease 58 0.038
273
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.038
274
GLC003 Glucose Intolerance 58 0.038
275
P RNL028 Renal Tubular Dysgenesis 58 0.038
276
ANR004 Anuria 57 0.038
277
RCT015 Reactive Arthritis 57 0.038
278
P RNL007 Renal Tubular Acidosis 57 0.038
279
SCN006 Secondary Syphilis 57 0.038
280
CHR001 Churg-Strauss Syndrome 57 0.038
281
c ANG015 Angioedema 57 0.038
282
ANK001 Ankylosis 57 0.038
283
SDR002 Siderosis 56 0.038
284
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 56 0.038
285
DDN006 Duodenitis 56 0.038
286
MSN001 Mesangial Proliferative Glomerulonephritis 55 0.038
287
PSD002 Pseudotumor Cerebri 55 0.038
288
URT001 Urethritis 54 0.038
289
PRR002 Pure Red-Cell Aplasia 54 0.038
290
BLS002 Blastomycosis 54 0.038
291
c HRM001 Hermansky-Pudlak Syndrome 53 0.038
292
FRS002 Frasier Syndrome 53 0.038
293
c HYD002 Hydronephrosis 53 0.038
294
PRN011 Pernicious Anemia 53 0.038
295
OBS061 Obstructive Sleep Apnea 52 0.038
296
PST087 Posterior Urethral Valve 52 0.038
297
XLN068 X-Linked Thrombocytopenia 52 0.038
298
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.038
299
GNG012 Gingival Overgrowth 51 0.038
300
c ANT034 Anterior Uveitis 51 0.038
301
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 51 0.038
302
LPT002 Lipoatrophic Diabetes 49 0.038
303
ACT040 Acute Poststreptococcal Glomerulonephritis 49 0.038
304
c PSD003 Pseudohypoaldosteronism 49 0.038
305
PST041 Posterior Urethral Valves 48 0.038
306
RTN018 Retinal Disease 48 0.038
307
CHY006 Chylous Ascites 48 0.038
308
PYM001 Pyomyositis 47 0.038
309
CRT008 Carotid Artery Dissection 47 0.038
310
LYM021 Lymphadenitis 47 0.038
311
ANG054 Angina Pectoris 46 0.038
312
MNN009 Meningoencephalitis 46 0.038
313
SPL018 Splenomegaly 46 0.038
314
FSC004 Fasciitis 45 0.038
315
LYM012 Lymphoplasmacytic Lymphoma 44 0.038
316
HRS011 Horseshoe Kidney 44 0.038
317
ILS001 Ileus 44 0.038
318
CLL002 Collecting Duct Carcinoma 44 0.038
319
LYM029 Lymphedema-Distichiasis Syndrome 44 0.038
320
CYT008 Cytomegalovirus Infection 43 0.038
321
c SNR001 Senior-Loken Syndrome 43 0.038
322
HYP008 Hypertensive Retinopathy 43 0.038
323
c ACT004 Acute Diarrhea 43 0.038
324
MYC019 Mycobacterium Marinum 43 0.038
325
BRB001 Beriberi 42 0.038
326
c CNG033 Congenital Syphilis 40 0.038
327
HYP226 Hyporeninemic Hypoaldosteronism 39 0.038
328
CRB086 Cerebral Aneurysms 38 0.038
329
IPX001 Ipex Syndrome 37 0.038
330
HPT063 Hepatitis B Virus Infection 36 0.038
331
PRP080 Peripheral Artery Disease 34 0.038
332
PLM074 Pulmonary Function 34 0.038
333
BLD039 Bladder Adenocarcinoma 31 0.038
334
P ATM020 Autoimmune Enteropathy 30 0.038
335
GLM037 Glioma Somatic 30 0.038
336
TFT003 Tufting Enteropathy 28 0.038
337
IMM001 Immune-Complex Glomerulonephritis 28 0.038
338
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.038
339
C4B001 C4b Deficiency 26 0.038
340
c NPH019 Nephronophthisis 1 25 0.038
341
PRN007 Perinephritis 24 0.038
342
P GLM015 Glomerulopathy with Fibronectin Deposits 2 23 0.038
343
HVY003 Heavy Chain Deposition Disease 21 0.038
344
C4D002 C4a Deficiency 17 0.038
345
RTN163 Retinal Arterial Tortuosity 16 0.038
346
LGH014 Light and Heavy Chain Deposition Disease 15 0.038
347
LNP001 Loin Pain Hematuria Syndrome 14 0.038
348
HRD064 Hereditary Vascular Retinopathy 9 0.038
349
P PRS040 Prostate Cancer 87 0.027
350
KPS001 Kaposi's Sarcoma 85 0.027
351
P FML021 Familial Hypercholesterolemia 85 0.027
352
INF030 Infectious Mononucleosis 84 0.027
353
MRF001 Marfan Syndrome 83 0.027
354
P PRM021 Primary Pulmonary Hypertension 82 0.027
355
P RTN008 Retinitis Pigmentosa 80 0.027
356
ACR007 Acromegaly 79 0.027
357
CNG034 Congestive Heart Failure 78 0.027
358
P MTH008 Methylmalonic Acidemia 77 0.027
359
THR006 Thromboangiitis Obliterans 77 0.027
360
LSC001 Lesch-Nyhan Syndrome 77 0.027
361
P PNM007 Pneumonia 76 0.027
362
LRN002 Laron Syndrome 76 0.027
363
CRB011 Cerebrotendinous Xanthomatosis 75 0.027
364
P PRP003 Porphyria Cutanea Tarda 75 0.027
365
P CLC005 Celiac Disease 74 0.027
366
PRC016 Pre-Eclampsia 74 0.027
367
P LYM007 Lymphangioleiomyomatosis 73 0.027
368
KWS002 Kawasaki Disease 73 0.027
369
c MYL006 Myeloid Leukemia 72 0.027
370
P PRM006 Primary Biliary Cirrhosis 72 0.027
371
P PRD006 Prader-Willi Syndrome 71 0.027
372
c CHR065 Chronic Myeloid Leukemia 71 0.027
373
c MST009 Mastocytosis 71 0.027
374
P WGN002 Wegener's Granulomatosis 71 0.027
375
P PND002 Pendred Syndrome 70 0.027
376
RNL002 Renal Agenesis 70 0.027
377
WRN001 Werner Syndrome 70 0.027
378
ART016 Aortic Aneurysm 70 0.027
379
NPH007 Nephrogenic Diabetes Insipidus 70 0.027
380
PLY017 Polyarteritis Nodosa 69 0.027
381
P WLF004 Wolfram Syndrome 69 0.027
382
BLL006 Bullous Pemphigoid 69 0.027
383
P RTH001 Rothmund-Thomson Syndrome 68 0.027
384
c SRC013 Sarcoidosis 68 0.027
385
THR016 Thrombophlebitis 68 0.027
386
PSD012 Pseudoachondroplasia 67 0.027
387
PSD007 Pseudomyxoma Peritonei 67 0.027
388
P BCK002 Beckwith-Wiedemann Syndrome 67 0.027
389
P CMR001 Camurati-Engelmann Disease 67 0.027
390
P HML002 Hemolytic Anemia 66 0.027
391
DMN002 Dementia 66 0.027
392
P PLY011 Polycystic Ovary Syndrome 66 0.027
393
P SYS004 Systemic Mastocytosis 66 0.027
394
P SYS005 Systemic Scleroderma 66 0.027
395
P GST044 Gastritis 66 0.027
396
GST009 Gastroschisis 66 0.027
397
P BLD042 Bladder Carcinoma 66 0.027
398
P CNG368 Congenital Adrenal Hyperplasia 66 0.027
399
P THR015 Thrombophilia 66 0.027
400
MRB003 Morbid Obesity 66 0.027
401
LGG001 Legg-Calve-Perthes Disease 65 0.027
402
PYR013 Pyruvate Kinase Deficiency 65 0.027
403
EXT034 Extrinsic Allergic Alveolitis 65 0.027
404
c JVN010 Juvenile Rheumatoid Arthritis 65 0.027
405
HYP004 Hypercalcemia 65 0.027
406
PLS006 Plasmodium Vivax Malaria 65 0.027
407
c ENC004 Encephalitis 65 0.027
408
PHR003 Pharyngitis 65 0.027
409
DBT001 Diabetic Ketoacidosis 65 0.027
410
P RCK004 Rickets 64 0.027
411
c SCL016 Scleroderma 64 0.027
412
GST034 Gastroesophageal Reflux Disease 64 0.027
413
P PSD087 Pseudoxanthoma Elasticum 64 0.027
414
c NRN021 Neuronal Ceroid Lipofuscinosis 64 0.027
415
P MTR018 Maturity-Onset Diabetes of the Young, Type 1 64 0.027
416
P HRD057 Hereditary Pancreatitis 64 0.027
417
P PRG006 Progressive Supranuclear Palsy 64 0.027
418
LYS003 Lysinuric Protein Intolerance 64 0.027
419
P GRV001 Graves' Disease 64 0.027
420
c VRL010 Viral Hepatitis 64 0.027
421
ULC004 Ulcerative Colitis 63 0.027
422
P FML020 Familial Combined Hyperlipidemia 63 0.027
423
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.027
424
MXD005 Mixed Connective Tissue Disease 63 0.027
425
FCT006 Factor V Deficiency 63 0.027
426
P ESP024 Esophagitis 63 0.027
427
c GLL020 Gallbladder Disease 63 0.027
428
TTN003 Tetanus 63 0.027
429
CMM004 Common Variable Immunodeficiency 63 0.027
430
LRN003 Learning Disability 62 0.027
431
SPN027 Spinal Stenosis 62 0.027
432
TWN003 Townes-Brocks Syndrome 62 0.027
433
OCC006 Occipital Horn Syndrome 62 0.027
434
P HST010 Histiocytosis 62 0.027
435
PRT092 Partial Androgen Insensitivity Syndrome 62 0.027
436
P ANP001 Anaplastic Large Cell Lymphoma 62 0.027
437
P MTR012 Mitral Valve Disease 62 0.027
438
ART031 Aortic Coarctation 62 0.027
439
P HRD011 Hereditary Spherocytosis 62 0.027
440
NRM002 Normal Pressure Hydrocephalus 61 0.027
441
LDD001 Ladd Syndrome 61 0.027
442
URT039 Urticaria 61 0.027
443
ALP007 Alpha 1-Antitrypsin Deficiency 61 0.027
444
DBT031 Diabetes, Type 2 61 0.027
445
DWN001 Down Syndrome 61 0.027
446
DBT010 Diabetic Neuropathy 60 0.027
447
PMP001 Pemphigus 60 0.027
448
P PLY019 Polyneuropathy 60 0.027
449
c ATM010 Autoimmune Hemolytic Anemia 60 0.027
450
P GRF002 Graft Versus Host Disease 60 0.027
451
CLD007 Cold Agglutinin Disease 60 0.027
452
VTL002 Vitiligo 60 0.027
453
PRS047 Prostatitis 60 0.027
454
P PRM124 Primary Hyperoxaluria Type 1 60 0.027
455
c ACT071 Acute Kidney Failure 60 0.027
456
OLG003 Oligohydramnios 59 0.027
457
c ALM001 Al Amyloidosis 59 0.027
458
P ATY010 Atypical Hemolytic-Uremic Syndrome 59 0.027
459
c FML012 Familial Partial Lipodystrophy 59 0.027
460
SND002 Sneddon Syndrome 59 0.027
461
P MLS001 Melas Syndrome 59 0.027
462
MLT001 Multiple Chemical Sensitivity 59 0.027
463
P AVS004 Avascular Necrosis of the Femoral Head 59 0.027
464
FBR032 Fibromuscular Dysplasia 59 0.027
465
CRN017 Coronary Thrombosis 59 0.027
466
MLL005 Miller-Dieker Syndrome 59 0.027
467
ANT058 Anterior Ischemic Optic Neuropathy 59 0.027
468
P MTR005 Mitral Valve Prolapse 59 0.027
469
P PRM054 Primary Sclerosing Cholangitis 59 0.027
470
MLR002 Miliary Tuberculosis 59 0.027
471
c LCL006 Localized Scleroderma 59 0.027
472
P INT068 Intestinal Disease 58 0.027
473
YLL002 Yellow Fever 58 0.027
474
P ALP006 Alpha Thalassemia 58 0.027
475
PLY041 Polymyositis 58 0.027
476
BCT004 Bacteriuria 58 0.027
477
GLC002 Glucocorticoid-Remediable Aldosteronism 58 0.027
478
DST005 Diastrophic Dysplasia 58 0.027
479
FLL008 Folliculitis 58 0.027
480
GLC012 Galactosialidosis 58 0.027
481
HDC001 Headache 58 0.027
482
P DBT005 Diabetes Insipidus 57 0.027
483
NNS002 Nonspecific Interstitial Pneumonia 57 0.027
484
URN010 Urinary Tract Obstruction 57 0.027
485
BRN029 Brain Disease 57 0.027
486
c HYP065 Hyperaldosteronism 57 0.027
487
P SNS014 Sinusitis 57 0.027
488
BRN071 Brain Injury 57 0.027
489
c HPT015 Hepatitis D 57 0.027
490
c RTN014 Retinal Artery Occlusion 57 0.027
491
IRN001 Iron Deficiency Anemia 57 0.027
492
c CTR002 Cataract 57 0.027
493
SCH002 Schnitzler Syndrome 56 0.027
494
ACT105 Acute Mountain Sickness 56 0.027
495
DFF003 Diffuse Scleroderma 56 0.027
496
ALP008 Alopecia 56 0.027
497
ACT017 Acute Chest Syndrome 56 0.027
498
LDP002 Lead Poisoning 56 0.027
499
SMT015 Smith Magenis Syndrome 56 0.027
500
P MTB001 Metabolic Syndrome X 56 0.027
501
c HRD002 Hereditary Angioedema 56 0.027
502
EXF001 Exfoliation Syndrome 56 0.027
503
VLV044 Vulvar Intraepithelial Neoplasia 56 0.027
504
CNG048 Congenital Hepatic Fibrosis 56 0.027
505
ART017 Aortic Disease 56 0.027
506
c FML035 Familial Hyperlipidemia 55 0.027
507
c CNT016 Central Retinal Vein Occlusion 55 0.027
508
P JBR004 Joubert Syndrome 2 55 0.027
509
PRT011 Protein C Deficiency 55 0.027
510
STV001 Stevens-Johnson Syndrome 55 0.027
511
c TRM003 Tremor 55 0.027
512
DST006 Diastolic Heart Failure 55 0.027
513
MCR088 Microscopic Polyangiitis 55 0.027
514
P PSR001 Psoriatic Arthritis 55 0.027
515
PLS007 Plasmodium Falciparum Malaria 55 0.027
516
P HYP090 Hyperalphalipoproteinemia 55 0.027
517
PLY020 Polyradiculoneuropathy 55 0.027
518
CHR008 Choroiditis 55 0.027
519
CLC001 Calciphylaxis 55 0.027
520
ACN001 Acinar Cell Carcinoma 55 0.027
521
P DNT039 Dent's Disease 55 0.027
522
MDL009 Medullary Sponge Kidney 55 0.027
523
PST062 Pustulosis Palmaris Et Plantaris 54 0.027
524
P CHL066 Cholangitis 54 0.027
525
SCR002 Scurvy 54 0.027
526
PRT058 Pure Autonomic Failure 54 0.027
527
c PSD015 Pseudohypoparathyroidism 54 0.027
528
PLY012 Polyhydramnios 54 0.027
529
DBT006 Diabetic Macular Edema 54 0.027
530
P TWN001 Twin-to-Twin Transfusion Syndrome 54 0.027
531
c ART070 Aortic Valve Disease 54 0.027
532
WLL001 Williams-Beuren Syndrome 54 0.027
533
LYS001 Loeys-Dietz Syndrome 54 0.027
534
RYS001 Reye Syndrome 53 0.027
535
CNS004 Constipation 53 0.027
536
P HRM005 Hermansky-Pudlak Syndrome 1 53 0.027
537
PLS025 Plasmablastic Lymphoma 53 0.027
538
CCH002 Coach Syndrome 53 0.027
539
c LYM025 Lymphedema 53 0.027
540
APH001 Aphthous Stomatitis 53 0.027
541
c ACR001 Aicardi-Goutieres Syndrome 53 0.027
542
HNT002 Hantavirus Pulmonary Syndrome 53 0.027
543
GST045 Gastroenteritis 53 0.027
544
P CNG095 Congenital Generalized Lipodystrophy Type 2 53 0.027
545
P PLM006 Pulmonary Alveolar Proteinosis 53 0.027
546
PLY013 Polymyalgia Rheumatica 52 0.027
547
c FML016 Familial Hypertriglyceridemia 52 0.027
548
HYP121 Hypoalphalipoproteinemia 52 0.027
549
YLL001 Yellow Nail Syndrome 52 0.027
550
CNG064 Congenital Chloride Diarrhea 52 0.027
551
LKD001 Leukodystrophy 52 0.027
552
AMY053 Amyloidosis, Secondary 52 0.027
553
P ORT004 Orthostatic Intolerance 52 0.027
554
P LDD002 Liddle Syndrome 52 0.027
555
NM001 Noma 52 0.027
556
RSD004 Rosai-Dorfman Disease 52 0.027
557
c CNG012 Congenital Generalized Lipodystrophy 52 0.027
558
NNL002 Nonalcoholic Steatohepatitis 52 0.027
559
c HPT007 Hepatitis E 52 0.027
560
CTS005 Catastrophic Antiphospholipid Syndrome 52 0.027
561
PRP002 Periapical Granuloma 51 0.027
562
FML164 Familial Hdl Deficiency 51 0.027
563
c DNT009 Dentin Dysplasia 51 0.027
564
MNT147 Mental Retardation 51 0.027
565
TXC012 Toxic Epidermal Necrolysis 51 0.027
566
MYC005 Myocardial Stunning 51 0.027
567
USL001 Usual Interstitial Pneumonia 51 0.027
568
ALC009 Alcoholic Liver Cirrhosis 51 0.027
569
MCL003 Macular Holes 51 0.027
570
RNL011 Renal Osteodystrophy 51 0.027
571
ONC003 Oncogenic Osteomalacia 51 0.027
572
APP001 Apparent Mineralocorticoid Excess Syndrome 51 0.027
573
OBS006 Obstructive Lung Disease 51 0.027
574
P CTN015 Cutaneous T Cell Lymphoma 51 0.027
575
LYM027 Lymphopenia 51 0.027
576
DRG002 Drug-Induced Hepatitis 51 0.027
577
c ATM024 Autoimmune Pancreatitis 50 0.027
578
P ART028 Aortic Aneurysm, Familial Thoracic 4 50 0.027
579
PSD009 Pseudohermaphroditism 50 0.027
580
STM007 Stomatitis 50 0.027
581
PLC007 Placental Abruption 50 0.027
582
NNT024 Neonatal Stroke 50 0.027
583
HYP006 Hypertensive Heart Disease 50 0.027
584
TYP013 Type 1 Von Willebrand Disease 50 0.027
585
OCL020 Ocular Cicatricial Pemphigoid 49 0.027
586
c SCL009 Sclerosing Cholangitis 49 0.027
587
RNL006 Renal Glycosuria 49 0.027
588
DBT002 Diabetic Autonomic Neuropathy 49 0.027
589
c HYP011 Hyperlipoproteinemia Type Iii 49 0.027
590
SPN119 Spondylarthropathy 49 0.027
591
PLS016 Plasma Cell Leukemia 49 0.027
592
PRN038 Prune Belly Syndrome 49 0.027
593
ALC010 Alcoholic Cardiomyopathy 48 0.027
594
CHY002 Chylomicron Retention Disease 48 0.027
595
c CNG013 Congenital Disorder of Glycosylation Type I 48 0.027
596
CRT049 Critical Limb Ischemia 48 0.027
597
DFF021 Diffuse Mesangial Sclerosis 48 0.027
598
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 48 0.027
599
HMC014 Homocysteinemia 48 0.027
600
RFL001 Reflex Sympathetic Dystrophy 48 0.027
601
MNN021 Meningococcemia 48 0.027
602
NSP002 Nasopharyngitis 48 0.027
603
HYP017 Hypophosphatemia 48 0.027
604
ADR027 Adrenocortical Insufficiency 47 0.027
605
CNS002 Constrictive Pericarditis 47 0.027
606
c GGN002 Gigantism 47 0.027
607
LPP002 Lipoprotein Glomerulopathy 47 0.027
608
CRN027 Corneal Neovascularization 47 0.027
609
c PRN026 Porencephaly 47 0.027
610
CNN003 Conn's Syndrome 47 0.027
611
HYP005 Hypokalemia 47 0.027
612
c RNL078 Renal Dysplasia 47 0.027
613
c ACQ022 Acquired Generalized Lipodystrophy 47 0.027
614
CRT004 Carotid Artery Thrombosis 47 0.027
615
CRB008 Cerebral Atherosclerosis 47 0.027
616
GNG008 Ganglioneuroblastoma 46 0.027
617
PTY003 Pityriasis Rubra Pilaris 46 0.027
618
EVN001 Evans' Syndrome 46 0.027
619
P ATN005 Autonomic Dysfunction 46 0.027
620
MCR018 Microcytic Anemia 46 0.027
621
HPT025 Hepatic Lipase Deficiency 46 0.027
622
P SNR003 Senior-Loken Syndrome 1 46 0.027
623
FVS001 Favism 46 0.027
624
ESN011 Eisenmenger Syndrome 46 0.027
625
LWR010 Low Renin Hypertension 46 0.027
626
CRB001 Cerebral Lymphoma 46 0.027
627
PST055 Postural Hypotension 46 0.027
628
PMP004 Pemphigus Foliaceus 45 0.027
629
P CRT018 Carotid Intimal Medial Thickness 45 0.027
630
BWN003 Bowenoid Papulosis 45 0.027
631
LPD008 Lipid Metabolism Disorder 45 0.027
632
DFN221 Deafness Dystonia Syndrome 45 0.027
633
IDP011 Idiopathic Interstitial Pneumonia 45 0.027
634
BRN105 Burn Scar 45 0.027
635
MYC033 Myoclonus 45 0.027
636
FBR063 Fibrocalculous Pancreatic Diabetes 45 0.027
637
c PLY083 Polycystic Kidney Disease, Type 1 44 0.027
638
NRM003 Norum Disease 44 0.027
639
UNL007 Unilateral Renal Agenesis 44 0.027
640
ART035 Arterial Calcification of Infancy 44 0.027
641
c LTT001 Lattice Corneal Dystrophy 44 0.027
642
CRP018 Cor Pulmonale 44 0.027
643
RNL097 Renal Artery Disease 44 0.027
644
MRC003 Mercury Poisoning 44 0.027
645
URT031 Ureteral Disease 44 0.027
646
SHR067 Short-Rib Thoracic Dysplasia 2 with or Without Polydactyly 44 0.027
647
TCL003 T Cell Deficiency 44 0.027
648
CMP009 Complement Deficiency 44 0.027
649
PLC005 Placental Insufficiency 43 0.027
650
RNL029 Renal Coloboma Syndrome 43 0.027
651
ART110 Arteritic Anterior Ischemic Optic Neuropathy 43 0.027
652
HYP001 Hypochromic Microcytic Anemia 43 0.027
653
AMN006 Aminoaciduria 43 0.027
654
MCR001 Microcystic Meningioma 43 0.027
655
P RTN016 Retinal Degeneration 43 0.027
656
P SLD005 Sialidosis Type I 43 0.027
657
c CHR417 Chronic Graft Versus Host Disease 43 0.027
658
NCR002 Necrobiosis Lipoidica 43 0.027
659
P PRG011 Progressive Myoclonus Epilepsy 43 0.027
660
HMF004 Hemifacial Spasm 43 0.027
661
INC001 Incontinentia Pigmenti Achromians 43 0.027
662
DFC001 Defective Apolipoprotein B-100 42 0.027
663
LRW002 Leri Weill Dyschondrosteosis 42 0.027
664
c ACT042 Acute Pyelonephritis 42 0.027
665
DBT007 Diabetic Cataract 42 0.027
666
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 42 0.027
667
BCL002 B Cell Deficiency 42 0.027
668
INT071 Intestinal Perforation 42 0.027
669
TBL013 Tubulointerstitial Nephritis and Uveitis 42 0.027
670
MNG006 Monogenic Diabetes 42 0.027
671
P BRS044 Breast Adenocarcinoma 42 0.027
672
P HYP216 Hypoparathyroidism Familial Isolated 41 0.027
673
RTN020 Retinal Vascular Disease 41 0.027
674
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 41 0.027
675
c HYP057 Hypervitaminosis D 41 0.027
676
AMR003 Amaurosis Fugax 40 0.027
677
ANG046 Angioimmunoblastic T-Cell Lymphoma 40 0.027
678
c TRN016 Transient Hypogammaglobulinemia 40 0.027
679
INP001 Inappropriate Adh Syndrome 40 0.027
680
GST040 Gastric Adenocarcinoma 40 0.027
681
LYS015 Loeys-Dietz Syndrome, Type 1 39 0.027
682
HYP456 Hyperapobetalipoproteinemia 39 0.027
683
c HVY001 Heavy Chain Disease 39 0.027
684
LPD014 Lipodermatosclerosis 39 0.027
685
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 39 0.027
686
JBR007 Joubert Syndrome with Renal Anomalies 39 0.027
687
c MLR021 Malaria, Severe 38 0.027
688
DNN002 Donnai-Barrow Syndrome 38 0.027
689
ADP002 Adiponectin Deficiency 38 0.027
690
P TRN009 Transient Hypogammaglobulinemia of Infancy 38 0.027
691
ENC011 Encephalomyopathy 38 0.027
692
ART010 Arteriolosclerosis 37 0.027
693
OCL022 Ocular Melanoma 37 0.027
694
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 37 0.027
695
HMG010 Hemoglobinemia 37 0.027
696
SPS057 Spasticity 37 0.027
697
EPP006 Epiphyseal Dysplasia Multiple with Early-Onset Diabetes Mellitus 37 0.027
698
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 37 0.027
699
LNR006 Linear Iga Disease 36 0.027
700
ESN020 Eosinophilic Granulomatosis with Polyangiitis 36 0.027
701
c FML187 Familial Hypertension 36 0.027
702
C1Q001 C1q Deficiency 36 0.027
703
C3D001 C3 Deficiency 36 0.027
704
RNL012 Renal Tuberculosis 36 0.027
705
c MYC026 Myoclonus Epilepsy 36 0.027
706
CYS024 Cystinosis, Ocular Nonnephropathic 35 0.027
707
SRS007 Sorsby Fundus Dystrophy 35 0.027
708
c FML162 Familial Mediterranean Fever, Ad 35 0.027
709
P RNL042 Renal Hypouricemia 35 0.027
710
DYS070 Dysalbuminemic Hyperthyroxinemia 35 0.027
711
HYP264 Hypertonia 35 0.027
712
INF133 Inferior Vena Cava Interruption 35 0.027
713
HYP034 Hypertensive Encephalopathy 34 0.027
714
BRT011 Bruton-Type Agammaglobulinemia 34 0.027
715
FML235 Familial Combined Hyperlipoproteinemia 33 0.027
716
FCT013 Factor V Leiden Thrombophilia 33 0.027
717
HMG020 Hmg Coa Lyase Deficiency 33 0.027
718
P NPH032 Nephronophthisis 4 33 0.027
719
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.027
720
c CHR096 Chronic Pulmonary Heart Disease 31 0.027
721
URT036 Urethral Obstruction 31 0.027
722
CHL109 Childhood Apraxia of Speech 31 0.027
723
MYC035 Myocardial Infarction Susceptibility 30 0.027
724
NRG005 Neurogenic Hypertension 30 0.027
725
ACD004 Acdc 30 0.027
726
CHR476 Chronic Angina 30 0.027
727
HFS001 Hfe-Associated Hereditary Hemochromatosis 30 0.027
728
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 29 0.027
729
SBL004 Sea-Blue Histiocytosis 29 0.027
730
CHL070 Cholesterol Embolism 28 0.027
731
GST007 Gastric Dilatation 28 0.027
732
PYR004 Pyuria 28 0.027
733
P PPL026 Papular Mucinosis 28 0.027
734
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.027
735
c CNG192 Congenital Disorder of Glycosylation, Type Ik 27 0.027
736
KRN001 Korean Hemorrhagic Fever 26 0.027
737
c DYS055 Dystonia 10 26 0.027
738
NTR005 Nutritional Deficiency Disease 25 0.027
739
P HYP078 Hypertrophy of Breast 25 0.027
740
P ALP005 Alpha Chain Disease 25 0.027
741
PRX022 Paroxysmal Choreoathetosis 25 0.027
742
ANT030 Antecubital Pterygium 24 0.027
743
MCR062 Microcephaly, Hiatal Hernia and Nephrotic Syndrome 24 0.027
744
EPD034 Epidermolysis Bullosa, Pretibial 24 0.027
745
CNG116 Congenital Nephrotic Syndrome Finnish Type 24 0.027
746
PSD062 Pseudoxanthoma Elasticum, Modifier of Severity of 24 0.027
747
PL2001 Pla2g6-Associated Neurodegeneration 24 0.027
748
GRD004 Gardner-Diamond Syndrome 23 0.027
749
HFH001 Hfe Hemochromatosis, Modifier of 22 0.027
750
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 21 0.027
751
VRS001 Virus Associated Hemophagocytic Syndrome 21 0.027
752
KRY002 Karyomegalic Interstitial Nephritis 21 0.027
753
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 21 0.027
754
FML268 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes 21 0.027
755
HYP281 Hypoproteinemia, Hypercatabolic 20 0.027
756
PCM002 Pauci-Immune Glomerulonephritis 20 0.027
757
HPR001 Hprt-Related Gout 20 0.027
758
c AML044 Amelogenesis Imperfecta, Type Ig 19 0.027
759
PRP033 Properdin Deficiency 19 0.027
760
c DMN011 Dominant Dystrophic Epidermolysis Bullosa 19 0.027
761
P JVN039 Juvenile Autosomal Recessive Medullary Cystic Kidney Disease 18 0.027
762
IMM015 Immune Defect Due to Absence of Thymus 18 0.027
763
DHL001 Dahlberg Borer Newcomer Syndrome 18 0.027
764
ANP010 Anaplastic Plasmacytoma 18 0.027
765
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 17 0.027
766
P FML003 Familial Visceral Amyloidosis 17 0.027
767
PRD012 Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis 16 0.027
768
PLS008 Plasmodium Malariae Malaria 16 0.027
769
KDN006 Kidney Papillary Necrosis 15 0.027
770
C9D001 C9 Deficiency 15 0.027
771
DYS034 Dyschondrosteosis Nephritis 14 0.027
772
ALD004 Ala Dehydratase Deficiency 12 0.027
773
IND008 Indomethacin Embryofetopathy 12 0.027
774
DFN014 Deafness Nephritis Anorectal Malformation 12 0.027
775
GLM024 Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria 11 0.027
776
CNG330 Congenital Megacalycosis 9 0.027
777
CRM007 Crome Syndrome 7 0.027
778
EXD002 Exudative Glomerulonephritis 7 0.027