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

815 hits were found for 'nephropathy'

# Family MCID Name MIFTS Score
1
DBT061 Diabetic Nephropathy 54 4.725
2
BLK001 Balkan Nephropathy 39 4.581
3
P MMB002 Membranous Glomerulonephritis 60 4.167
4
UMD001 Umod-Associated Kidney Disease 34 3.761
5
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 15 3.755
6
GTY001 Gouty Nephropathy, Familial 10 3.748
7
P FML044 Familial Juvenile Hyperuricemic Nephropathy Type 2 17 3.458
8
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 17 3.405
9
IGG001 Iga Glomerulonephritis 50 3.370
10
ACT043 Acute Urate Nephropathy 24 3.180
11
P BKV001 Bk-Virus Nephropathy 8 3.157
12
NPH037 Nephronophthisis-Like Nephropathy 1 14 3.109
13
c FML022 Familial Juvenile Hyperuricemic Nephropathy 34 2.956
14
FML076 Familial Juvenile Hyperuricaemic Nephropathy 19 2.920
15
HYP114 Hypertensive Nephropathy 34 2.903
16
c RNR002 Ren-Related Kidney Disease 20 2.864
17
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 27 2.832
18
ANG055 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle 21 2.814
19
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 23 2.505
20
DNY001 Denys-Drash Syndrome 70 2.490
21
AMY037 Amyloidosis, Hereditary Renal 26 2.445
22
NPH016 Nephropathy-Hypertension 28 2.434
23
MLT033 Multicentric Osteolysis Nephropathy 6 2.434
24
PLY043 Polyomavirus Allograft Nephropathy 2 2.434
25
ATH009 Atherosclerosis - Deafness - Diabetes - Epilepsy - Nephropathy 17 2.422
26
CTR091 Cataract - Nephropathy - Encephalopathy 13 2.408
27
ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 9 2.408
28
THN006 Thin Basement Membrane Nephropathy 37 2.125
29
P IGN002 Iga Nephropathy 2 11 2.080
30
NPH003 Nephrocalcinosis 53 2.030
31
URM003 Uromodulin-Associated Kidney Disease 21 2.030
32
c IGN003 Iga Nephropathy 1 10 2.020
33
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 7 2.009
34
FGN001 Feigenbaum Bergeron Richardson Syndrome 6 1.996
35
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 23 1.983
36
HYD039 Hydrocephalus - Blue Sclerae - Nephropathy 16 1.983
37
PRM036 Premature Atherosclerosis with Photomyoclonic Epilepsy, Deafness, Diabetes Mellitus, Nephropathy, an 2 1.983
38
ATS141 Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E 20 1.966
39
NPH066 Nephropathy Due to Cfhr5 Deficiency 16 1.966
40
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 14 1.966
41
c FML260 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 12 1.966
42
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 12 1.966
43
c FML208 Familial Renal Amyloidosis Due to Apolipoprotein Aii Variant 11 1.966
44
c FML261 Familial Renal Amyloidosis Due to Lysozyme Variant 11 1.966
45
c HYP529 Hyperuricemic Nephropathy, Familial Juvenile, 3 5 1.966
46
NPH050 Nephropathy, Progressive, with Deafness 5 1.966
47
c CL4006 Col4a5-Related Nephropathy 4 1.966
48
c CL4007 Col4a3-Related Nephropathy 4 1.966
49
c CL4008 Col4a4-Related Nephropathy 4 1.966
50
NPH022 Nephropathy Familial with Hyperuricemia 2 1.966
51
BRG002 Berger Disease 27 1.636
52
ALP004 Alport Syndrome 69 1.603
53
HMR004 Hemorrhagic Fever with Renal Syndrome 65 1.485
54
c MTR022 Maturity-Onset Diabetes of the Young, Type 5 18 1.485
55
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 36 1.476
56
c ATS015 Autosomal Dominant Alport Syndrome 46 1.465
57
DNT019 Daentl Towsend Siegel Syndrome 7 1.442
58
MCK007 Muckle-Wells Syndrome 60 1.428
59
ADN024 Adenine Phosphoribosyltransferase Deficiency 52 1.428
60
P ATS018 Autosomal Recessive Alport Syndrome 44 1.412
61
FTZ004 Fitzsimmons Walson Mellor Syndrome 14 1.412
62
P AMY038 Amyloidosis, Renal 21 1.390
63
HRR004 Herrmann Syndrome 4 1.390
64
ALL011 Allain-Babin-Demarquez Syndrome 3 1.390
65
c DBT009 Diabetes Mellitus 80 0.347
66
PRT039 Proteinuria 57 0.278
67
P HYP075 Hypertension 86 0.247
68
P GLM007 Glomerulonephritis 66 0.233
69
P TYP009 Type 2 Diabetes Mellitus 93 0.198
70
c XP2001 Xp22.3 Microdeletion Syndrome 21 0.198
71
DBT011 Diabetic Retinopathy 73 0.191
72
c TYP008 Type 1 Diabetes Mellitus 77 0.172
73
c NPH012 Nephrotic Syndrome 66 0.162
74
c KDN018 Kidney Disease 58 0.162
75
THR013 Thoracic Outlet Syndrome 54 0.162
76
PCM002 Pauci-Immune Glomerulonephritis 13 0.160
77
HYP014 Hyperuricemia 61 0.151
78
END072 Endotheliitis 47 0.149
79
PRP030 Purpura 67 0.147
80
FCL008 Focal Glomerulosclerosis 60 0.147
81
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 35 0.132
82
c HPT021 Hepatitis 75 0.130
83
P FCL005 Focal Segmental Glomerulosclerosis 70 0.127
84
NRP001 Neuropathy 61 0.127
85
CMP052 Complication in Hemodialysis 18 0.127
86
ANK002 Ankylosing Spondylitis 75 0.124
87
DBT010 Diabetic Neuropathy 68 0.122
88
MRC003 Mercury Poisoning 28 0.122
89
CRB009 Cerebritis 56 0.116
90
END030 End Stage Renal Failure 52 0.116
91
INF133 Inferior Vena Cava Interruption 27 0.116
92
MDR006 Moderate and Severe Traumatic Brain Injury 20 0.116
93
CRN131 Coronary Artery Disease, Modifier of 15 0.116
94
TNS005 Tonsillitis 62 0.113
95
P RNL028 Renal Tubular Dysgenesis 51 0.113
96
RNL015 Renal Hypertension 60 0.110
97
CRS001 Crescentic Glomerulonephritis 51 0.110
98
VSC007 Vascular Disease 72 0.107
99
P AVS004 Avascular Necrosis of the Femoral Head 49 0.107
100
INT067 Interstitial Nephritis 57 0.104
101
MMB001 Membranoproliferative Glomerulonephritis 53 0.104
102
c NPH019 Nephronophthisis 1 20 0.104
103
c MLG069 Malignant Hypertension 60 0.100
104
MNN014 Mononeuritis 48 0.100
105
P HYP090 Hyperalphalipoproteinemia 47 0.100
106
CNG380 Congenital Anomalies of Kidney and Urinary Tract 36 0.100
107
ACN002 Acanthosis Nigricans 73 0.097
108
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 45 0.097
109
LWR010 Low Renin Hypertension 34 0.097
110
IDP042 Idiopathic Recurrent Stupor 15 0.097
111
FBR012 Fabry Disease 88 0.094
112
BRN024 Bronchitis 76 0.094
113
c PRM002 Primary Hyperoxaluria 68 0.094
114
SCN006 Secondary Syphilis 55 0.094
115
P HYP117 Hypertriglyceridemia 54 0.094
116
c PRL003 Proliferative Glomerulonephritis 52 0.094
117
FBR032 Fibromuscular Dysplasia 47 0.094
118
SYN053 Syndromic Diarrhea 42 0.094
119
FML235 Familial Combined Hyperlipoproteinemia 26 0.094
120
NLP001 Nail-Patella Syndrome 70 0.090
121
c LCL006 Localized Scleroderma 68 0.090
122
P NPH009 Nephrolithiasis 59 0.090
123
VTM002 Vitamin B12 Deficiency 51 0.090
124
c HMR012 Hemorrhagic Fever 44 0.090
125
GLM037 Glioma Somatic 31 0.090
126
MYC019 Mycobacterium Marinum 25 0.090
127
CYT018 Cytochrome P450 2d6 Variant 13 0.090
128
SPS077 Sepsis 58 0.086
129
P NPH032 Nephronophthisis 4 31 0.086
130
ATH003 Atherosclerosis 71 0.082
131
WST001 West Syndrome 64 0.082
132
P RNV001 Renovascular Hypertension 58 0.082
133
c VSC005 Vesicoureteral Reflux 51 0.082
134
ART031 Aortic Coarctation 47 0.082
135
PLM019 Pleomorphic Liposarcoma 45 0.082
136
PST055 Postural Hypotension 33 0.082
137
MYC065 Myocardial Infarction, Decreased 30 0.082
138
CHL109 Childhood Apraxia of Speech 24 0.082
139
TFT003 Tufting Enteropathy 21 0.082
140
LRN002 Laron Syndrome 76 0.078
141
P ART022 Arthritis 75 0.078
142
c ESS002 Essential Hypertension 71 0.078
143
c HPT016 Hepatitis B 65 0.078
144
TRN018 Transitional Cell Carcinoma 64 0.078
145
IRN001 Iron Deficiency Anemia 61 0.078
146
P RPD001 Rapidly Progressive Glomerulonephritis 55 0.078
147
c ATN004 Autonomic Neuropathy 54 0.078
148
P FNC004 Fanconi Syndrome 53 0.078
149
NPH018 Nephrogenic Systemic Fibrosis 44 0.078
150
ACT105 Acute Mountain Sickness 40 0.078
151
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.078
152
P INF069 Infantile Neuroaxonal Dystrophy 1 32 0.078
153
HYP226 Hyporeninemic Hypoaldosteronism 27 0.078
154
IMM015 Immune Defect Due to Absence of Thymus 18 0.078
155
P ATX002 Ataxia Telangiectasia 93 0.073
156
P PLY014 Polycystic Kidney Disease 67 0.073
157
HYP066 Hyperglycemia 65 0.073
158
RTN023 Retinitis 61 0.073
159
c HPT003 Hepatitis a 60 0.073
160
P PYL005 Pyelonephritis 57 0.073
161
PRL007 Proliferative Diabetic Retinopathy 57 0.073
162
c CYS016 Cystic Kidney 56 0.073
163
NTR003 Natural Killer Cell Leukemia 56 0.073
164
ADL002 Adult Syndrome 52 0.073
165
P INS005 Insulin Resistance 48 0.073
166
DBT002 Diabetic Autonomic Neuropathy 48 0.073
167
RNL022 Renal Vascular Disease 45 0.073
168
FML089 Familial Thoracic Aortic Aneurysm and Dissection 43 0.073
169
FCT013 Factor V Leiden Thrombophilia 35 0.073
170
CRC004 Carcinoid Tumor of Lung 33 0.073
171
NNS006 Non-Suppurative Otitis Media 26 0.073
172
HNM002 Hinman Syndrome 24 0.073
173
ACD004 Acdc 23 0.073
174
MTH028 Mthfr Thermolabile Variant 13 0.073
175
P RHM011 Rheumatoid Arthritis 91 0.069
176
GLL008 Gilles De La Tourette Syndrome 73 0.069
177
P HPT001 Hepatitis C 66 0.069
178
P GT001 Gout 66 0.069
179
P AMY004 Amyloidosis 65 0.069
180
c MYL007 Myeloma 59 0.069
181
URM002 Uremia 56 0.069
182
MLR002 Miliary Tuberculosis 55 0.069
183
CNG008 Congenital Ichthyosiform Erythroderma 53 0.069
184
c CHR098 Chronic Pyelonephritis 44 0.069
185
P ATX010 Ataxia Neuropathy Spectrum 44 0.069
186
LDP002 Lead Poisoning 43 0.069
187
HYP008 Hypertensive Retinopathy 38 0.069
188
MSM007 Mesomelic Dysplasia Kantaputra Type 34 0.069
189
MNG006 Monogenic Diabetes 33 0.069
190
THL010 Thalassemia Minor 33 0.069
191
P MLR006 Male Reproductive Organ Cancer 23 0.069
192
P OBS005 Obesity 93 0.064
193
HPT023 Hepatocellular Carcinoma 89 0.064
194
TBR010 Tuberculosis 84 0.064
195
P HMP004 Hemophilia B 80 0.064
196
P LKM002 Leukemia 79 0.064
197
PRT036 Peritonitis 78 0.064
198
P PRD006 Prader-Willi Syndrome 74 0.064
199
ANT006 Antiphospholipid Syndrome 67 0.064
200
GST034 Gastroesophageal Reflux Disease 67 0.064
201
GDP001 Goodpasture Syndrome 57 0.064
202
MYC002 Mycobacterium Avium Complex Disease 57 0.064
203
NPH010 Nephrosclerosis 56 0.064
204
SNS001 Sensorineural Hearing Loss 56 0.064
205
ART004 Aortic Atherosclerosis 54 0.064
206
P THR090 Thrombocythemia 1 54 0.064
207
c NPH005 Nephronophthisis 53 0.064
208
IDP011 Idiopathic Interstitial Pneumonia 53 0.064
209
P HRM005 Hermansky-Pudlak Syndrome 1 51 0.064
210
PYM001 Pyomyositis 47 0.064
211
P ATS008 Autosomal Dominant Disease 46 0.064
212
c ALM001 Al Amyloidosis 44 0.064
213
ORL010 Oral-Facial-Digital Syndrome Type I 43 0.064
214
HYP121 Hypoalphalipoproteinemia 41 0.064
215
c TWN006 Twin Twin Transfusion Syndrome 40 0.064
216
HPT025 Hepatic Lipase Deficiency 38 0.064
217
PST041 Posterior Urethral Valves 31 0.064
218
AMN006 Aminoaciduria 29 0.064
219
BWN003 Bowenoid Papulosis 29 0.064
220
APD001 Apo a-I Deficiency 18 0.064
221
P WSK001 Wiskott-Aldrich Syndrome 87 0.058
222
CNG034 Congestive Heart Failure 81 0.058
223
P ALP006 Alpha Thalassemia 75 0.058
224
P FML018 Familial Mediterranean Fever 74 0.058
225
TKY001 Takayasu's Arteritis 72 0.058
226
c THL005 Thalassemia 68 0.058
227
PMS001 Poems Syndrome 67 0.058
228
VSC011 Vasculitis 67 0.058
229
c THY032 Thyroiditis 67 0.058
230
P PRT013 Portal Hypertension 67 0.058
231
ACQ007 Acquired Immunodeficiency Syndrome 63 0.058
232
CRY004 Cryoglobulinemia 61 0.058
233
P DWR001 Dwarfism 58 0.058
234
OST011 Osteomalacia 57 0.058
235
OCC006 Occipital Horn Syndrome 57 0.058
236
DBT004 Diabetic Polyneuropathy 57 0.058
237
HYP037 Hyperhomocysteinemia 55 0.058
238
MCR004 Macroglobulinemia 55 0.058
239
P HML001 Hemolytic-Uremic Syndrome 54 0.058
240
c DRR001 Diarrhea 54 0.058
241
PRT092 Partial Androgen Insensitivity Syndrome 53 0.058
242
P HRD057 Hereditary Pancreatitis 53 0.058
243
PRP023 Peripheral Neuropathy 53 0.058
244
P CNG095 Congenital Generalized Lipodystrophy Type 2 51 0.058
245
THR079 Thromboembolism 50 0.058
246
PRT019 Protein-Losing Enteropathy 48 0.058
247
LYS005 Loeys-Dietz Syndrome Type 1a 48 0.058
248
BRN105 Burn Scar 44 0.058
249
PYG006 Pyogenic Granuloma 41 0.058
250
NNT024 Neonatal Stroke 40 0.058
251
PRL042 Proliferating Trichilemmal Cyst 38 0.058
252
HMC014 Homocysteinemia 35 0.058
253
KRN001 Korean Hemorrhagic Fever 28 0.058
254
DYS070 Dysalbuminemic Hyperthyroxinemia 26 0.058
255
CMP061 Complete Lcat Deficiency 24 0.058
256
PSD062 Pseudoxanthoma Elasticum, Modifier of Severity of 23 0.058
257
HYP281 Hypoproteinemia, Hypercatabolic 19 0.058
258
HRD064 Hereditary Vascular Retinopathy 5 0.058
259
P ALZ001 Alzheimer's Disease 103 0.052
260
P MYC007 Myocardial Infarction 88 0.052
261
AND002 Androgen Insensitivity Syndrome 88 0.052
262
PRC016 Pre-Eclampsia 75 0.052
263
P MLR004 Malaria 73 0.052
264
CRN211 Coronary Artery Disease 72 0.052
265
c BTT002 Beta Thalassemia 70 0.052
266
c HYD006 Hydrocephalus 70 0.052
267
P ANG001 Angelman Syndrome 70 0.052
268
RLP001 Relapsing Polychondritis 69 0.052
269
ART019 Aortic Valve Stenosis 68 0.052
270
c HYP086 Hypothyroidism 68 0.052
271
c PNC044 Pancreatitis 67 0.052
272
DFC004 Deficiency Anemia 66 0.052
273
P HRD011 Hereditary Spherocytosis 66 0.052
274
EXT034 Extrinsic Allergic Alveolitis 65 0.052
275
GLB015 Glioblastoma Multiforme 64 0.052
276
c PRP029 Porphyria 64 0.052
277
c HYP069 Hyperparathyroidism 63 0.052
278
PSR002 Psoriasis 60 0.052
279
c AXN002 Axenfeld-Rieger Syndrome 60 0.052
280
P ADN016 Adenocarcinoma 60 0.052
281
c ATM011 Autoimmune Hepatitis 60 0.052
282
P RNL014 Renal Cell Carcinoma 59 0.052
283
EPD016 Epidermolysis Bullosa 59 0.052
284
RTN018 Retinal Disease 58 0.052
285
ANR008 Aneurysm Disease 57 0.052
286
RNL011 Renal Osteodystrophy 56 0.052
287
ATX019 Ataxia with Vitamin E Deficiency 55 0.052
288
CNG048 Congenital Hepatic Fibrosis 53 0.052
289
CRN030 Coronary Stenosis 53 0.052
290
DST006 Diastolic Heart Failure 52 0.052
291
CLC001 Calciphylaxis 52 0.052
292
FML026 Familial Lipoprotein Lipase Deficiency 52 0.052
293
MSN001 Mesangial Proliferative Glomerulonephritis 52 0.052
294
SCH016 Schimke Immunoosseous Dysplasia 49 0.052
295
PLY012 Polyhydramnios 49 0.052
296
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 46 0.052
297
LYM014 Lymphangitis 46 0.052
298
PRT058 Pure Autonomic Failure 44 0.052
299
TTR016 Tetra-Amelia Syndrome 43 0.052
300
VLV044 Vulvar Intraepithelial Neoplasia 42 0.052
301
P ORT004 Orthostatic Intolerance 39 0.052
302
HNC001 Henoch-Schoenlein Purpura 38 0.052
303
c NPH049 Nephrotic Syndrome, Type 2 35 0.052
304
P SLP004 Salpingo-Oophoritis 31 0.052
305
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.052
306
PLS008 Plasmodium Malariae Malaria 28 0.052
307
PRT015 Partial Third-Nerve Palsy 26 0.052
308
c HPT073 Hepatitis C Virus 25 0.052
309
c FML187 Familial Hypertension 23 0.052
310
c BNG076 Benign Exophthalmos Syndrome 21 0.052
311
c DYS055 Dystonia 10 19 0.052
312
AMY016 Amyopathic Dermatomyositis 17 0.052
313
NRG005 Neurogenic Hypertension 14 0.052
314
P AMY001 Amyotrophic Lateral Sclerosis 100 0.045
315
CDS001 Cadasil 92 0.045
316
P MLT019 Multiple Myeloma 89 0.045
317
P SYS001 Systemic Lupus Erythematosus 87 0.045
318
P HMC003 Hemochromatosis 80 0.045
319
NPH007 Nephrogenic Diabetes Insipidus 77 0.045
320
P ACT074 Acute Lymphocytic Leukemia 77 0.045
321
BHC002 Behcet's Disease 76 0.045
322
PRP027 Peripheral Vascular Disease 75 0.045
323
c LPS004 Lupus Erythematosus 73 0.045
324
MYC006 Mycosis Fungoides 71 0.045
325
ISC006 Ischemic Heart Disease 69 0.045
326
ADL030 Adult-Onset Still's Disease 68 0.045
327
GTL001 Gitelman Syndrome 67 0.045
328
P UVT001 Uveitis 67 0.045
329
BLR001 Biliary Atresia 67 0.045
330
ART021 Arteriosclerosis 65 0.045
331
NRN002 Neuronitis 64 0.045
332
c MTR004 Maturity-Onset Diabetes of the Young 63 0.045
333
PLS011 Plasmacytoma 63 0.045
334
GLC003 Glucose Intolerance 63 0.045
335
RCT015 Reactive Arthritis 62 0.045
336
URT001 Urethritis 62 0.045
337
CRB039 Cerebrovascular Disease 61 0.045
338
c ACT075 Acute Myocardial Infarction 61 0.045
339
SPN051 Spondylitis 60 0.045
340
ACR008 Acrocallosal Syndrome 59 0.045
341
INT075 Intracranial Hypertension 59 0.045
342
LYM021 Lymphadenitis 58 0.045
343
P DBT005 Diabetes Insipidus 57 0.045
344
EPL002 Epilepsy Syndrome 57 0.045
345
CNN005 Connective Tissue Disease 57 0.045
346
P SHR002 Short Stature 57 0.045
347
P ISC002 Ischemic Optic Neuropathy 57 0.045
348
P SYP003 Syphilis 56 0.045
349
P CHR092 Chronic Myeloproliferative Disease 55 0.045
350
EVN001 Evans' Syndrome 54 0.045
351
HPT014 Hepatorenal Syndrome 54 0.045
352
DBT008 Diabetic Angiopathy 54 0.045
353
P SPN052 Spondyloarthropathy 52 0.045
354
P GND004 Gonadal Dysgenesis 52 0.045
355
HMS001 Hemosiderosis 52 0.045
356
NPH004 Nephropathia Epidemica 51 0.045
357
IMM001 Immune-Complex Glomerulonephritis 50 0.045
358
ANK001 Ankylosis 50 0.045
359
c HPT007 Hepatitis E 50 0.045
360
LMY003 Leiomyomatosis 49 0.045
361
URT010 Ureteral Obstruction 49 0.045
362
RNL006 Renal Glycosuria 49 0.045
363
c PSD003 Pseudohypoaldosteronism 47 0.045
364
ACT040 Acute Poststreptococcal Glomerulonephritis 46 0.045
365
HPR003 Heparin-Induced Thrombocytopenia 45 0.045
366
LPS007 Lupus Nephritis 43 0.045
367
ENT001 Enterocele 42 0.045
368
LPD004 Lipoid Nephrosis 42 0.045
369
NPH051 Nephritis 39 0.045
370
c ACQ022 Acquired Generalized Lipodystrophy 37 0.045
371
c TRM003 Tremor 36 0.045
372
MDL019 Medullary Cystic Kidney Disease Type 1 35 0.045
373
DFF021 Diffuse Mesangial Sclerosis 35 0.045
374
PPT001 Peptic Esophagitis 34 0.045
375
PRN007 Perinephritis 33 0.045
376
ERL004 Early Yaws 33 0.045
377
HYP034 Hypertensive Encephalopathy 32 0.045
378
HRS011 Horseshoe Kidney 28 0.045
379
DFN039 Deafness-Infertility Syndrome 27 0.045
380
DFF015 Diffuse Glomerulonephritis 25 0.045
381
HRD009 Hereditary Wilms' Tumor 21 0.045
382
c MNS010 Monosomy Xp21 20 0.045
383
LKC003 Leukocyte Disease 19 0.045
384
AND005 Androgen Insensitivity Syndrome, Mild 18 0.045
385
c TTL001 Total Internal Ophthalmoplegia 17 0.045
386
c PPL028 Popliteal Pterygium Syndrome Lethal Type 14 0.045
387
OTP003 Oto-Palatal-Digital Syndrome 13 0.045
388
ANP010 Anaplastic Plasmacytoma 12 0.045
389
CL4001 Col4a1-Related Disorders 7 0.045
390
CRH001 Crohn's Disease 83 0.037
391
P APL001 Aplastic Anemia 83 0.037
392
P CRN008 Carney Complex 78 0.037
393
P CHR089 Chronic Kidney Failure 76 0.037
394
LVR012 Liver Cirrhosis 75 0.037
395
THR006 Thromboangiitis Obliterans 75 0.037
396
P BLD042 Bladder Carcinoma 73 0.037
397
BLS001 Blau Syndrome 73 0.037
398
P DRM010 Dermatomyositis 70 0.037
399
P ATM003 Autoimmune Thyroiditis 70 0.037
400
c MCP001 Mucopolysaccharidosis Iii 70 0.037
401
P TYP020 Type 1 Diabetes 69 0.037
402
DBT001 Diabetic Ketoacidosis 69 0.037
403
c THR014 Thrombocytopenia 67 0.037
404
GNG013 Gingivitis 67 0.037
405
STT001 Status Epilepticus 66 0.037
406
DSS009 Disseminated Intravascular Coagulation 66 0.037
407
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.037
408
MXD005 Mixed Connective Tissue Disease 65 0.037
409
P PRM124 Primary Hyperoxaluria Type 1 65 0.037
410
TTN003 Tetanus 63 0.037
411
ART005 Arteriovenous Malformation 63 0.037
412
GST009 Gastroschisis 63 0.037
413
PLS007 Plasmodium Falciparum Malaria 63 0.037
414
PLM001 Pulmonary Tuberculosis 63 0.037
415
c CHR090 Chronic Lymphocytic Leukemia 63 0.037
416
c ACT073 Acute Leukemia 62 0.037
417
DDN006 Duodenitis 62 0.037
418
ART001 Arterial Tortuosity Syndrome 62 0.037
419
SCK005 Sickle Cell Disease 62 0.037
420
P AGM001 Agammaglobulinemia 61 0.037
421
P INT068 Intestinal Disease 61 0.037
422
LGG001 Legg-Calve-Perthes Disease 61 0.037
423
PRT011 Protein C Deficiency 60 0.037
424
P LDD002 Liddle Syndrome 60 0.037
425
MLT001 Multiple Chemical Sensitivity 59 0.037
426
CHR001 Churg-Strauss Syndrome 59 0.037
427
P CLL015 Collagen Disease 59 0.037
428
c HRD002 Hereditary Angioedema 59 0.037
429
LPD010 Lipodystrophy 59 0.037
430
c ACT071 Acute Kidney Failure 58 0.037
431
P RNL007 Renal Tubular Acidosis 58 0.037
432
GNG012 Gingival Overgrowth 57 0.037
433
c HRM001 Hermansky-Pudlak Syndrome 57 0.037
434
c THR005 Thrombotic Thrombocytopenic Purpura 57 0.037
435
P SCL015 Scleritis 57 0.037
436
PRG009 Progressive Multifocal Leukoencephalopathy 57 0.037
437
c HYP095 Hypercholesterolemia 56 0.037
438
APP001 Apparent Mineralocorticoid Excess Syndrome 56 0.037
439
FRS002 Frasier Syndrome 55 0.037
440
URN010 Urinary Tract Obstruction 55 0.037
441
c GLY013 Glycogen Storage Disease 55 0.037
442
ANR004 Anuria 55 0.037
443
P ANG015 Angioedema 54 0.037
444
PPL006 Papillon-Lefevre Disease 54 0.037
445
RYS001 Reye Syndrome 54 0.037
446
c FML012 Familial Partial Lipodystrophy 54 0.037
447
c CTR002 Cataract 53 0.037
448
GNG008 Ganglioneuroblastoma 53 0.037
449
BCL002 B Cell Deficiency 53 0.037
450
c TYR004 Tyrosinemia 53 0.037
451
YLL001 Yellow Nail Syndrome 52 0.037
452
ANG054 Angina Pectoris 52 0.037
453
PRN011 Pernicious Anemia 52 0.037
454
SYS003 Systolic Heart Failure 51 0.037
455
c JBR001 Joubert Syndrome 51 0.037
456
FSC004 Fasciitis 50 0.037
457
P DNT009 Dentin Dysplasia 49 0.037
458
CHY002 Chylomicron Retention Disease 49 0.037
459
c ACR001 Aicardi-Goutieres Syndrome 49 0.037
460
HYP457 Hypertrophic Scars 48 0.037
461
LPT002 Lipoatrophic Diabetes 48 0.037
462
c HYD002 Hydronephrosis 48 0.037
463
GST029 Gastric Cardia Adenocarcinoma 48 0.037
464
CMP009 Complement Deficiency 47 0.037
465
LYS001 Loeys-Dietz Syndrome 46 0.037
466
NRM003 Norum Disease 46 0.037
467
CRB025 Carbohydrate Metabolic Disorder 45 0.037
468
P LSS005 Lissencephaly 1 44 0.037
469
LYM029 Lymphedema-Distichiasis Syndrome 44 0.037
470
P SNR003 Senior-Loken Syndrome 1 44 0.037
471
BRB001 Beriberi 43 0.037
472
HYP001 Hypochromic Microcytic Anemia 43 0.037
473
FLL008 Folliculitis 43 0.037
474
AND003 Andersen-Tawil Syndrome 43 0.037
475
c SNR001 Senior-Loken Syndrome 43 0.037
476
HYP266 Hypoxia 43 0.037
477
LYM012 Lymphoplasmacytic Lymphoma 42 0.037
478
CRB008 Cerebral Atherosclerosis 42 0.037
479
KLD001 Keloids 42 0.037
480
URT031 Ureteral Disease 40 0.037
481
PST087 Posterior Urethral Valve 40 0.037
482
c CNG033 Congenital Syphilis 40 0.037
483
HYP030 Hypoactive Sexual Desire Disorder 39 0.037
484
IPX001 Ipex Syndrome 39 0.037
485
c ATM007 Autoimmune Disease of Central Nervous System 38 0.037
486
ART012 Aortitis 38 0.037
487
c RNL078 Renal Dysplasia 37 0.037
488
c RSM001 Rasmussen Encephalitis 37 0.037
489
VRL011 Viral Infectious Disease 37 0.037
490
EMN001 Emanuel Syndrome 36 0.037
491
c ACT004 Acute Diarrhea 35 0.037
492
c HVY001 Heavy Chain Disease 35 0.037
493
HYP120 Hypoaldosteronism 33 0.037
494
FML059 Familial Encephalopathy with Neuroserpin Inclusion Bodies 33 0.037
495
NPH017 Nephrosis 33 0.037
496
ADS002 Adie Syndrome 33 0.037
497
RNL051 Renal Cysts and Diabetes Syndrome 32 0.037
498
MNN021 Meningococcemia 32 0.037
499
HYP456 Hyperapobetalipoproteinemia 32 0.037
500
URT036 Urethral Obstruction 31 0.037
501
c ATM022 Autoimmune Myocarditis 30 0.037
502
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 30 0.037
503
OCL022 Ocular Melanoma 29 0.037
504
P HYP078 Hypertrophy of Breast 26 0.037
505
ADP002 Adiponectin Deficiency 25 0.037
506
P GLM015 Glomerulopathy with Fibronectin Deposits 2 24 0.037
507
HMG010 Hemoglobinemia 23 0.037
508
PL2001 Pla2g6-Associated Neurodegeneration 21 0.037
509
c HMP017 Hemophilia a, Congenital 21 0.037
510
FNC002 Functional Diarrhea 18 0.037
511
PRG091 Progressively Deforming Osteogenesis Imperfecta 18 0.037
512
RTN163 Retinal Arterial Tortuosity 16 0.037
513
PRX022 Paroxysmal Choreoathetosis 15 0.037
514
ALD004 Ala Dehydratase Deficiency 12 0.037
515
LGH014 Light and Heavy Chain Deposition Disease 8 0.037
516
CRM007 Crome Syndrome 6 0.037
517
CLL035 Collagen Type Iii Glomerulopathy 4 0.037
518
MRF001 Marfan Syndrome 92 0.026
519
P PRS040 Prostate Cancer 91 0.026
520
HDG007 Hodgkin's Lymphoma 91 0.026
521
P FML021 Familial Hypercholesterolemia 87 0.026
522
KPS001 Kaposi's Sarcoma 87 0.026
523
P PRM021 Primary Pulmonary Hypertension 82 0.026
524
P RTN008 Retinitis Pigmentosa 81 0.026
525
ACR007 Acromegaly 80 0.026
526
GLN003 Glanzmann's Thrombasthenia 80 0.026
527
P MTH008 Methylmalonic Acidemia 79 0.026
528
P PNM007 Pneumonia 79 0.026
529
LSC001 Lesch-Nyhan Syndrome 79 0.026
530
INF030 Infectious Mononucleosis 78 0.026
531
TNG002 Tangier Disease 78 0.026
532
RNL002 Renal Agenesis 77 0.026
533
CRB011 Cerebrotendinous Xanthomatosis 77 0.026
534
c NNN003 Noonan Syndrome 77 0.026
535
WRN001 Werner Syndrome 75 0.026
536
P WGN002 Wegener's Granulomatosis 75 0.026
537
P LYM007 Lymphangioleiomyomatosis 74 0.026
538
c CHR065 Chronic Myeloid Leukemia 74 0.026
539
STR067 Stroke, Ischemic 74 0.026
540
P PRM006 Primary Biliary Cirrhosis 74 0.026
541
P CLC005 Celiac Disease 73 0.026
542
P CNG026 Congenital Heart Defect 73 0.026
543
c MYL006 Myeloid Leukemia 72 0.026
544
P PND002 Pendred Syndrome 72 0.026
545
P PRM005 Primary Hyperparathyroidism 72 0.026
546
ULC004 Ulcerative Colitis 72 0.026
547
P HST010 Histiocytosis 71 0.026
548
P WLF004 Wolfram Syndrome 71 0.026
549
c MNN013 Meningitis 71 0.026
550
P SYS004 Systemic Mastocytosis 70 0.026
551
P PRG006 Progressive Supranuclear Palsy 70 0.026
552
BLL006 Bullous Pemphigoid 70 0.026
553
P TMP003 Temporal Arteritis 69 0.026
554
P SYS005 Systemic Scleroderma 69 0.026
555
PSY004 Psychotic Disorder 69 0.026
556
HYP004 Hypercalcemia 69 0.026
557
c SRC013 Sarcoidosis 69 0.026
558
PLY017 Polyarteritis Nodosa 68 0.026
559
P GST044 Gastritis 68 0.026
560
MRB003 Morbid Obesity 68 0.026
561
BRR003 Barrett's Esophagus 68 0.026
562
P HML002 Hemolytic Anemia 68 0.026
563
P RTH001 Rothmund-Thomson Syndrome 67 0.026
564
P MTB001 Metabolic Syndrome X 67 0.026
565
GST033 Gestational Diabetes 67 0.026
566
P RCK004 Rickets 67 0.026
567
c JVN010 Juvenile Rheumatoid Arthritis 67 0.026
568
CMM004 Common Variable Immunodeficiency 66 0.026
569
DMN002 Dementia 66 0.026
570
P THR015 Thrombophilia 66 0.026
571
P CNG368 Congenital Adrenal Hyperplasia 66 0.026
572
P PSD087 Pseudoxanthoma Elasticum 66 0.026
573
c NRN021 Neuronal Ceroid Lipofuscinosis 66 0.026
574
LDD001 Ladd Syndrome 66 0.026
575
P CMR001 Camurati-Engelmann Disease 65 0.026
576
P BCK002 Beckwith-Wiedemann Syndrome 65 0.026
577
HST011 Histoplasmosis 65 0.026
578
P CMP010 Complex Regional Pain Syndrome 65 0.026
579
P GRF002 Graft Versus Host Disease 65 0.026
580
THR016 Thrombophlebitis 65 0.026
581
LYS003 Lysinuric Protein Intolerance 64 0.026
582
FCT006 Factor V Deficiency 64 0.026
583
P PLY019 Polyneuropathy 64 0.026
584
P DNT039 Dent's Disease 64 0.026
585
P FML020 Familial Combined Hyperlipidemia 63 0.026
586
P TYR002 Tyrosinemia Type I 63 0.026
587
P GRV001 Graves' Disease 63 0.026
588
PMP001 Pemphigus 63 0.026
589
DST005 Diastrophic Dysplasia 62 0.026
590
PHR003 Pharyngitis 62 0.026
591
PSD007 Pseudomyxoma Peritonei 62 0.026
592
PLS006 Plasmodium Vivax Malaria 62 0.026
593
SMT015 Smith Magenis Syndrome 62 0.026
594
PRS047 Prostatitis 62 0.026
595
DWN001 Down Syndrome 62 0.026
596
BRN029 Brain Disease 62 0.026
597
c VRL010 Viral Hepatitis 61 0.026
598
P MLS001 Melas Syndrome 61 0.026
599
P ANP001 Anaplastic Large Cell Lymphoma 61 0.026
600
URT039 Urticaria 61 0.026
601
ALP007 Alpha 1-Antitrypsin Deficiency 61 0.026
602
P HMC002 Homocystinuria 61 0.026
603
VTL002 Vitiligo 60 0.026
604
RTN017 Retinal Detachment 60 0.026
605
P MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.026
606
CRT049 Critical Limb Ischemia 60 0.026
607
ALP008 Alopecia 60 0.026
608
ACT049 Acute Disseminated Encephalomyelitis 60 0.026
609
P ESP024 Esophagitis 60 0.026
610
APH001 Aphthous Stomatitis 59 0.026
611
NRM002 Normal Pressure Hydrocephalus 59 0.026
612
P RTN022 Retinal Vein Occlusion 59 0.026
613
c HYP065 Hyperaldosteronism 59 0.026
614
c FML035 Familial Hyperlipidemia 59 0.026
615
c SCL016 Scleroderma 59 0.026
616
SND002 Sneddon Syndrome 58 0.026
617
LYM027 Lymphopenia 58 0.026
618
INS002 in Situ Carcinoma 58 0.026
619
LRN003 Learning Disability 58 0.026
620
P TWN001 Twin-to-Twin Transfusion Syndrome 58 0.026
621
CRT016 Carotid Artery Disease 58 0.026
622
LKD001 Leukodystrophy 58 0.026
623
c ATM010 Autoimmune Hemolytic Anemia 57 0.026
624
YLL002 Yellow Fever 57 0.026
625
HNT002 Hantavirus Pulmonary Syndrome 57 0.026
626
BRN004 Brain Edema 57 0.026
627
CRN017 Coronary Thrombosis 57 0.026
628
HLL004 Hellp Syndrome 57 0.026
629
CHR008 Choroiditis 57 0.026
630
P PSR001 Psoriatic Arthritis 57 0.026
631
c HPT015 Hepatitis D 57 0.026
632
PSD009 Pseudohermaphroditism 57 0.026
633
P CHL066 Cholangitis 57 0.026
634
SCH002 Schnitzler Syndrome 56 0.026
635
DBT062 Diabetic Foot Ulcers 56 0.026
636
P PLM006 Pulmonary Alveolar Proteinosis 56 0.026
637
PLY013 Polymyalgia Rheumatica 56 0.026
638
P LYM025 Lymphedema 56 0.026
639
PYR010 Peyronie's Disease 56 0.026
640
HYP006 Hypertensive Heart Disease 56 0.026
641
P MTR012 Mitral Valve Disease 56 0.026
642
PYR013 Pyruvate Kinase Deficiency 56 0.026
643
BRS051 Breast Disease 56 0.026
644
c PSD015 Pseudohypoparathyroidism 55 0.026
645
CNS004 Constipation 55 0.026
646
c LTR001 Lateral Sclerosis 55 0.026
647
XNT003 Xanthomatosis 55 0.026
648
CRN027 Corneal Neovascularization 55 0.026
649
ALC009 Alcoholic Liver Cirrhosis 55 0.026
650
LPC002 Lip Cancer 55 0.026
651
P MTR005 Mitral Valve Prolapse 55 0.026
652
PRR002 Pure Red-Cell Aplasia 54 0.026
653
c DNT011 Dentinogenesis Imperfecta 54 0.026
654
FBR009 Fibrous Dysplasia 54 0.026
655
CLL002 Collecting Duct Carcinoma 54 0.026
656
ART017 Aortic Disease 54 0.026
657
DFF003 Diffuse Scleroderma 54 0.026
658
FSH001 Fish-Eye Disease 54 0.026
659
P HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 54 0.026
660
LPP001 Lipoprotein Lipase Deficiency 53 0.026
661
HMG005 Hemoglobinopathy 53 0.026
662
GST045 Gastroenteritis 53 0.026
663
PRT038 Protein-Energy Malnutrition 53 0.026
664
c CNT016 Central Retinal Vein Occlusion 53 0.026
665
P HYP027 Hypobetalipoproteinemia 53 0.026
666
HYP017 Hypophosphatemia 53 0.026
667
CRN029 Coronary Arteriosclerosis 53 0.026
668
FML164 Familial Hdl Deficiency 53 0.026
669
SDR002 Siderosis 53 0.026
670
MLL005 Miller-Dieker Syndrome 52 0.026
671
WLL001 Williams-Beuren Syndrome 52 0.026
672
TCL003 T Cell Deficiency 52 0.026
673
PLY020 Polyradiculoneuropathy 52 0.026
674
NRR001 Neuroretinitis 52 0.026
675
c ACT042 Acute Pyelonephritis 52 0.026
676
P JBR004 Joubert Syndrome 2 52 0.026
677
STM007 Stomatitis 51 0.026
678
RNL029 Renal Coloboma Syndrome 51 0.026
679
c FML016 Familial Hypertriglyceridemia 51 0.026
680
MCR018 Microcytic Anemia 51 0.026
681
ACN001 Acinar Cell Carcinoma 51 0.026
682
BLS002 Blastomycosis 51 0.026
683
CNN003 Conn's Syndrome 50 0.026
684
DBT006 Diabetic Macular Edema 50 0.026
685
HYP005 Hypokalemia 50 0.026
686
c ASP011 Asphyxiating Thoracic Dystrophy 2 50 0.026
687
MNN009 Meningoencephalitis 50 0.026
688
CNG064 Congenital Chloride Diarrhea 50 0.026
689
LPD008 Lipid Metabolism Disorder 50 0.026
690
IRN002 Iron Metabolism Disease 50 0.026
691
MCL003 Macular Holes 50 0.026
692
c SCL009 Sclerosing Cholangitis 49 0.026
693
OSS010 Ossification of the Posterior Longitudinal Ligament of the Spine 49 0.026
694
NSP002 Nasopharyngitis 49 0.026
695
P ART028 Aortic Aneurysm, Familial Thoracic 4 49 0.026
696
SPR016 Spermatic Cord Torsion 49 0.026
697
STV001 Stevens-Johnson Syndrome 49 0.026
698
c MLR021 Malaria, Severe 49 0.026
699
MYC005 Myocardial Stunning 49 0.026
700
MTB004 Metabolic Acidosis 49 0.026
701
ALC010 Alcoholic Cardiomyopathy 48 0.026
702
CCH002 Coach Syndrome 48 0.026
703
GST040 Gastric Adenocarcinoma 48 0.026
704
PSD002 Pseudotumor Cerebri 47 0.026
705
c ART084 Arteriovenous Fistula 47 0.026
706
PTY003 Pityriasis Rubra Pilaris 47 0.026
707
CLD007 Cold Agglutinin Disease 47 0.026
708
CRD137 Cardiogenic Shock 47 0.026
709
P RTN016 Retinal Degeneration 47 0.026
710
c HYP011 Hyperlipoproteinemia Type Iii 47 0.026
711
c ASP005 Asphyxiating Thoracic Dystrophy 46 0.026
712
PRX001 Peroxisomal Disease 46 0.026
713
INC001 Incontinentia Pigmenti Achromians 46 0.026
714
P BRS044 Breast Adenocarcinoma 46 0.026
715
P PRG011 Progressive Myoclonus Epilepsy 46 0.026
716
CHR415 Chronic Venous Leg Ulcers 45 0.026
717
CRT004 Carotid Artery Thrombosis 45 0.026
718
c CNG012 Congenital Generalized Lipodystrophy 44 0.026
719
c SLP006 Sleep Apnea 44 0.026
720
RCR001 Recurrent Corneal Erosion 44 0.026
721
P CTN015 Cutaneous T Cell Lymphoma 44 0.026
722
c MLT074 Multiple Endocrine Neoplasia 43 0.026
723
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.026
724
CRB001 Cerebral Lymphoma 43 0.026
725
P HYP216 Hypoparathyroidism Familial Isolated 43 0.026
726
P CRN157 Coronary Heart Disease 43 0.026
727
AMY053 Amyloidosis, Secondary 43 0.026
728
CRT008 Carotid Artery Dissection 42 0.026
729
LRW002 Leri Weill Dyschondrosteosis 42 0.026
730
c HYP057 Hypervitaminosis D 42 0.026
731
P SLD005 Sialidosis Type I 42 0.026
732
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 41 0.026
733
c WLM002 Wilms Tumor 41 0.026
734
P LPD015 Lipodystrophy, Familial Partial, Type 2 41 0.026
735
ESN011 Eisenmenger Syndrome 40 0.026
736
MCR001 Microcystic Meningioma 40 0.026
737
LPP002 Lipoprotein Glomerulopathy 40 0.026
738
JBR007 Joubert Syndrome with Renal Anomalies 40 0.026
739
NCR002 Necrobiosis Lipoidica 39 0.026
740
INT071 Intestinal Perforation 39 0.026
741
EPP006 Epiphyseal Dysplasia Multiple with Early-Onset Diabetes Mellitus 39 0.026
742
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 39 0.026
743
DNN002 Donnai-Barrow Syndrome 39 0.026
744
RTN020 Retinal Vascular Disease 39 0.026
745
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 38 0.026
746
HMG020 Hmg Coa Lyase Deficiency 38 0.026
747
c BLN003 Blindness 37 0.026
748
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 37 0.026
749
c CRT018 Carotid Intimal Medial Thickness 37 0.026
750
CRB086 Cerebral Aneurysms 37 0.026
751
CYS024 Cystinosis, Ocular Nonnephropathic 37 0.026
752
c FML162 Familial Mediterranean Fever, Ad 37 0.026
753
CRP018 Cor Pulmonale 36 0.026
754
c PLY083 Polycystic Kidney Disease, Type 1 36 0.026
755
FBR063 Fibrocalculous Pancreatic Diabetes 35 0.026
756
DFN222 Deafness-Dystonia-Optic Neuronopathy Syndrome 35 0.026
757
RNL012 Renal Tuberculosis 35 0.026
758
P HYP111 Hyperprolinemia 35 0.026
759
GST007 Gastric Dilatation 34 0.026
760
IMG001 Image Syndrome 34 0.026
761
MTR001 Mature Cataract 34 0.026
762
c JBR003 Joubert Syndrome and Related Disorders 34 0.026
763
ILS001 Ileus 33 0.026
764
BRT011 Bruton-Type Agammaglobulinemia 33 0.026
765
BLD039 Bladder Adenocarcinoma 33 0.026
766
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 33 0.026
767
SLL001 Sialolithiasis 33 0.026
768
PYR026 Peyronies Disease 32 0.026
769
C3D001 C3 Deficiency 32 0.026
770
DFC001 Defective Apolipoprotein B-100 32 0.026
771
HFS001 Hfe-Associated Hereditary Hemochromatosis 31 0.026
772
ART010 Arteriolosclerosis 31 0.026
773
STR044 Steroid-Resistant Nephrotic Syndrome 31 0.026
774
ESN020 Eosinophilic Granulomatosis with Polyangiitis 30 0.026
775
c CHR096 Chronic Pulmonary Heart Disease 30 0.026
776
c FRT001 Fourth Cranial Nerve Palsy 30 0.026
777
CHR476 Chronic Angina 29 0.026
778
PYR004 Pyuria 29 0.026
779
SPS057 Spasticity 29 0.026
780
P ALP005 Alpha Chain Disease 29 0.026
781
DYS036 Dysequilibrium Syndrome 28 0.026
782
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 28 0.026
783
EXN003 Exencephaly 28 0.026
784
NTR005 Nutritional Deficiency Disease 28 0.026
785
P FML003 Familial Visceral Amyloidosis 27 0.026
786
RNL018 Renal Pelvis Carcinoma 26 0.026
787
HPR001 Hprt-Related Gout 25 0.026
788
EPD034 Epidermolysis Bullosa, Pretibial 24 0.026
789
PLM074 Pulmonary Function 24 0.026
790
MCR062 Microcephaly, Hiatal Hernia and Nephrotic Syndrome 24 0.026
791
c CNG192 Congenital Disorder of Glycosylation, Type Ik 23 0.026
792
HYP264 Hypertonia 23 0.026
793
CHL070 Cholesterol Embolism 23 0.026
794
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 23 0.026
795
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 22 0.026
796
ANT030 Antecubital Pterygium 21 0.026
797
CPL005 Capillary Disease 20 0.026
798
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 19 0.026
799
c JVN039 Juvenile Autosomal Recessive Medullary Cystic Kidney Disease 18 0.026
800
c HMC009 Hemochromatosis Type 2 18 0.026
801
DHL001 Dahlberg Borer Newcomer Syndrome 18 0.026
802
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 16 0.026
803
KDN006 Kidney Papillary Necrosis 16 0.026
804
c MCH003 Mu Chain Disease 16 0.026
805
RNL019 Renal Pelvis Transitional Cell Carcinoma 16 0.026
806
BLK002 Balkan Hemorrhagic Fever 16 0.026
807
DFN014 Deafness Nephritis Anorectal Malformation 16 0.026
808
P ACT079 Acute Proliferative Glomerulonephritis 16 0.026
809
GND003 Gonadal Disease 15 0.026
810
P ISC010 Isochromosome Yp 14 0.026
811
DYS034 Dyschondrosteosis Nephritis 14 0.026
812
ATN001 Autonomic Peripheral Neuropathy 13 0.026
813
IND008 Indomethacin Embryofetopathy 13 0.026
814
EXD002 Exudative Glomerulonephritis 9 0.026
815
LNP001 Loin Pain Hematuria Syndrome 6 0.026