Search results for "nephropathy"

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

818 hits were found for 'nephropathy'

# Family MCID Name MIFTS Score
1
FML076 Familial Juvenile Hyperuricaemic Nephropathy 33 5.659
2
BLK001 Balkan Nephropathy 32 5.049
3
DBT061 Diabetic Nephropathy 47 4.902
4
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 30 4.319
5
MMB002 Membranous Glomerulonephritis 52 4.159
6
UMD001 Umod-Associated Kidney Disease 33 4.052
7
P BKV001 Bk-Virus Nephropathy 22 3.578
8
IGG001 Iga Glomerulonephritis 53 3.548
9
THN006 Thin Basement Membrane Nephropathy 45 3.503
10
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 18 3.484
11
c FML022 Familial Juvenile Hyperuricemic Nephropathy 34 3.345
12
ACT043 Acute Urate Nephropathy 25 3.243
13
P FML044 Familial Juvenile Hyperuricemic Nephropathy Type 2 22 3.202
14
c RNR002 Ren-Related Kidney Disease 21 3.193
15
HYP114 Hypertensive Nephropathy 41 3.040
16
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 9 2.889
17
NPH037 Nephronophthisis-Like Nephropathy 1 18 2.836
18
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 25 2.554
19
DNY001 Denys-Drash Syndrome 70 2.547
20
PLY043 Polyomavirus Allograft Nephropathy 6 2.531
21
P FML003 Familial Visceral Amyloidosis 45 2.494
22
ATH009 Atherosclerosis - Deafness - Diabetes - Epilepsy - Nephropathy 18 2.494
23
DNT019 Daentl Towsend Siegel Syndrome 19 2.483
24
MLT033 Multicentric Osteolysis Nephropathy 5 2.483
25
c NPH016 Nephropathy-Hypertension 10 2.470
26
CTR091 Cataract - Nephropathy - Encephalopathy 16 2.456
27
P ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 11 2.456
28
P IGN003 Iga Nephropathy 1 4 2.456
29
P ALP004 Alport Syndrome 63 2.171
30
BRG002 Berger Disease 31 2.088
31
NPH003 Nephrocalcinosis 48 2.070
32
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 2.048
33
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 21 2.048
34
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 8 2.048
35
FGN001 Feigenbaum Bergeron Richardson Syndrome 6 2.022
36
PRM036 Premature Atherosclerosis with Photomyoclonic Epilepsy, Deafness, Diabetes Mellitus, Nephropathy, an 3 2.022
37
P ATS141 Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E 20 2.006
38
NPH066 Nephropathy Due to Cfhr5 Deficiency 17 2.006
39
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 14 2.006
40
c FML261 Familial Renal Amyloidosis Due to Lysozyme Variant 13 2.006
41
c FML260 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 11 2.006
42
c FML208 Familial Renal Amyloidosis Due to Apolipoprotein Aii Variant 10 2.006
43
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 10 2.006
44
CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 8 2.006
45
c HYP529 Hyperuricemic Nephropathy, Familial Juvenile, 3 6 2.006
46
c CL4006 Col4a5-Related Nephropathy 6 2.006
47
c CL4007 Col4a3-Related Nephropathy 6 2.006
48
c CL4008 Col4a4-Related Nephropathy 6 2.006
49
NPH050 Nephropathy, Progressive, with Deafness 5 2.006
50
c IGN002 Iga Nephropathy 2 4 2.006
51
NPH022 Nephropathy Familial with Hyperuricemia 3 2.006
52
HMR004 Hemorrhagic Fever with Renal Syndrome 61 1.494
53
c MTR022 Maturity-Onset Diabetes of the Young, Type 5 47 1.494
54
MCK007 Muckle-Wells Syndrome 67 1.483
55
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 39 1.483
56
c ATS015 Autosomal Dominant Alport Syndrome 54 1.470
57
FTZ004 Fitzsimmons Walson Mellor Syndrome 16 1.470
58
c ATS018 Autosomal Recessive Alport Syndrome 47 1.440
59
HRR004 Herrmann Syndrome 5 1.418
60
ALL011 Allain-Babin-Demarquez Syndrome 4 1.418
61
c DBT009 Diabetes Mellitus 73 0.351
62
PRT039 Proteinuria 57 0.285
63
P HYP075 Hypertension 85 0.274
64
P GLM007 Glomerulonephritis 68 0.234
65
END072 Endotheliitis 50 0.208
66
NPH051 Nephritis 53 0.195
67
c TYP009 Type 2 Diabetes Mellitus 100 0.188
68
P TYP008 Type 1 Diabetes Mellitus 95 0.167
69
GLM011 Glomerulosclerosis 47 0.167
70
c NPH012 Nephrotic Syndrome 67 0.158
71
c KDN018 Kidney Disease 62 0.156
72
PRP030 Purpura 65 0.142
73
c HPT021 Hepatitis 63 0.127
74
NRP001 Neuropathy 61 0.127
75
P FCL005 Focal Segmental Glomerulosclerosis 72 0.125
76
DBT011 Diabetic Retinopathy 70 0.119
77
END030 End Stage Renal Failure 57 0.119
78
TNS005 Tonsillitis 56 0.113
79
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.110
80
P HYP014 Hyperuricemia 55 0.107
81
INT067 Interstitial Nephritis 45 0.104
82
P INS005 Insulin Resistance 64 0.101
83
THR013 Thoracic Outlet Syndrome 52 0.101
84
MMB001 Membranoproliferative Glomerulonephritis 47 0.101
85
CRS001 Crescentic Glomerulonephritis 43 0.097
86
CRB009 Cerebritis 38 0.097
87
SYN053 Syndromic Diarrhea 34 0.097
88
FBR012 Fabry Disease 85 0.094
89
c PRM002 Primary Hyperoxaluria 73 0.094
90
NLP001 Nail-Patella Syndrome 70 0.094
91
c MLG069 Malignant Hypertension 63 0.094
92
ANK002 Ankylosing Spondylitis 76 0.082
93
ATH003 Atherosclerosis 68 0.082
94
ACN002 Acanthosis Nigricans 64 0.082
95
BLN003 Blindness 52 0.082
96
c VSC005 Vesicoureteral Reflux 50 0.082
97
P ATX010 Ataxia Neuropathy Spectrum 47 0.082
98
P ART022 Arthritis 74 0.078
99
c HPT016 Hepatitis B 68 0.078
100
P CYS016 Cystic Kidney 50 0.078
101
P FNC004 Fanconi Syndrome 50 0.078
102
c ATN004 Autonomic Neuropathy 49 0.078
103
c PRL003 Proliferative Glomerulonephritis 46 0.078
104
TBR010 Tuberculosis 85 0.074
105
c ESS002 Essential Hypertension 73 0.074
106
P AMY004 Amyloidosis 73 0.074
107
VSC007 Vascular Disease 69 0.074
108
c MYL007 Myeloma 60 0.074
109
NPH018 Nephrogenic Systemic Fibrosis 57 0.074
110
P PYL005 Pyelonephritis 54 0.074
111
RNL077 Renal Fibrosis 48 0.074
112
NPH017 Nephrosis 42 0.074
113
P RHM011 Rheumatoid Arthritis 94 0.069
114
P LKM002 Leukemia 76 0.069
115
P ANG001 Angelman Syndrome 71 0.069
116
ART019 Aortic Valve Stenosis 63 0.069
117
c PLY014 Polycystic Kidney Disease 61 0.069
118
HYP066 Hyperglycemia 61 0.069
119
RTN023 Retinitis 53 0.069
120
P OBS005 Obesity 89 0.064
121
P WSK001 Wiskott-Aldrich Syndrome 79 0.064
122
P HPT001 Hepatitis C 66 0.064
123
P GT001 Gout 65 0.064
124
P RNV001 Renovascular Hypertension 61 0.064
125
SNS001 Sensorineural Hearing Loss 57 0.064
126
P RPD001 Rapidly Progressive Glomerulonephritis 56 0.064
127
P NPH005 Nephronophthisis 51 0.064
128
NPH010 Nephrosclerosis 51 0.064
129
c CHR098 Chronic Pyelonephritis 47 0.064
130
P ATX002 Ataxia Telangiectasia 87 0.058
131
CDS001 Cadasil 84 0.058
132
PRT036 Peritonitis 71 0.058
133
CRB039 Cerebrovascular Disease 68 0.058
134
P WLM002 Wilms Tumor 66 0.058
135
VSC011 Vasculitis 65 0.058
136
c THY032 Thyroiditis 65 0.058
137
c UVT001 Uveitis 65 0.058
138
TRN018 Transitional Cell Carcinoma 63 0.058
139
ART111 Artery Disease 63 0.058
140
P ADN016 Adenocarcinoma 58 0.058
141
CRY004 Cryoglobulinemia 58 0.058
142
ART001 Arterial Tortuosity Syndrome 55 0.058
143
PRT019 Protein-Losing Enteropathy 55 0.058
144
MCR004 Macroglobulinemia 54 0.058
145
AND003 Andersen-Tawil Syndrome 53 0.058
146
OST011 Osteomalacia 52 0.058
147
HYP037 Hyperhomocysteinemia 52 0.058
148
LPD004 Lipoid Nephrosis 50 0.058
149
P HML001 Hemolytic-Uremic Syndrome 47 0.058
150
ANR040 Aneurysm 45 0.058
151
LGH004 Light Chain Deposition Disease 35 0.058
152
c BNG076 Benign Exophthalmos Syndrome 22 0.058
153
P MYC007 Myocardial Infarction 92 0.052
154
P SYS001 Systemic Lupus Erythematosus 89 0.052
155
AND002 Androgen Insensitivity Syndrome 80 0.052
156
P MLR004 Malaria 74 0.052
157
c AXN002 Axenfeld-Rieger Syndrome 69 0.052
158
c PNC044 Pancreatitis 68 0.052
159
ANT006 Antiphospholipid Syndrome 68 0.052
160
c AMY001 Amyotrophic Lateral Sclerosis 66 0.052
161
BRN024 Bronchitis 66 0.052
162
PMS001 Poems Syndrome 64 0.052
163
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.052
164
HV1006 Hiv-1 63 0.052
165
PSR002 Psoriasis 62 0.052
166
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.052
167
P NPH009 Nephrolithiasis 59 0.052
168
MYC002 Mycobacterium Avium Complex Disease 58 0.052
169
URM002 Uremia 57 0.052
170
EPD016 Epidermolysis Bullosa 57 0.052
171
HPT014 Hepatorenal Syndrome 56 0.052
172
NPH004 Nephropathia Epidemica 54 0.052
173
PRL007 Proliferative Diabetic Retinopathy 53 0.052
174
LPS007 Lupus Nephritis 52 0.052
175
c DRR001 Diarrhea 51 0.052
176
MNN014 Mononeuritis 51 0.052
177
RTR011 Retroperitoneal Fibrosis 50 0.052
178
P HYP111 Hyperprolinemia 47 0.052
179
c HPT073 Hepatitis C Virus 47 0.052
180
HYP120 Hypoaldosteronism 46 0.052
181
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.052
182
HNC001 Henoch-Schoenlein Purpura 41 0.052
183
STR044 Steroid-Resistant Nephrotic Syndrome 36 0.052
184
AND005 Androgen Insensitivity Syndrome, Mild 21 0.052
185
OTP003 Oto-Palatal-Digital Syndrome 17 0.052
186
P LVR011 Liver Cancer 90 0.045
187
P CHR090 Chronic Lymphocytic Leukemia 88 0.045
188
P MLT019 Multiple Myeloma 88 0.045
189
P HMC003 Hemochromatosis 85 0.045
190
c BTT002 Beta Thalassemia 82 0.045
191
BHC002 Behcet's Disease 79 0.045
192
LVR012 Liver Cirrhosis 76 0.045
193
c LPS004 Lupus Erythematosus 75 0.045
194
P FML018 Familial Mediterranean Fever 75 0.045
195
BLS001 Blau Syndrome 73 0.045
196
HST011 Histoplasmosis 73 0.045
197
GTL001 Gitelman Syndrome 73 0.045
198
c HYP095 Hypercholesterolemia 72 0.045
199
c THL005 Thalassemia 71 0.045
200
ACQ007 Acquired Immunodeficiency Syndrome 70 0.045
201
c ACT074 Acute Lymphocytic Leukemia 69 0.045
202
c MTR004 Maturity-Onset Diabetes of the Young 69 0.045
203
MYC006 Mycosis Fungoides 68 0.045
204
c HYP086 Hypothyroidism 68 0.045
205
ART021 Arteriosclerosis 67 0.045
206
THR079 Thromboembolism 67 0.045
207
P CHR089 Chronic Kidney Failure 65 0.045
208
STR067 Stroke, Ischemic 64 0.045
209
c HYP069 Hyperparathyroidism 64 0.045
210
MXD005 Mixed Connective Tissue Disease 64 0.045
211
CLT003 Colitis 64 0.045
212
PLM001 Pulmonary Tuberculosis 60 0.045
213
P SCL015 Scleritis 60 0.045
214
c ATM011 Autoimmune Hepatitis 60 0.045
215
P RNL028 Renal Tubular Dysgenesis 59 0.045
216
c ACT075 Acute Myocardial Infarction 59 0.045
217
ISC006 Ischemic Heart Disease 58 0.045
218
LPD010 Lipodystrophy 58 0.045
219
P SYP003 Syphilis 57 0.045
220
CHR001 Churg-Strauss Syndrome 57 0.045
221
P HMR012 Hemorrhagic Fever 57 0.045
222
HYP266 Hypoxia 57 0.045
223
SPN051 Spondylitis 57 0.045
224
HMS001 Hemosiderosis 57 0.045
225
PLS011 Plasmacytoma 56 0.045
226
DBT008 Diabetic Angiopathy 56 0.045
227
P PRP023 Peripheral Neuropathy 51 0.045
228
P GND004 Gonadal Dysgenesis 50 0.045
229
P SZR006 Seizure Disorder 50 0.045
230
SCH016 Schimke Immunoosseous Dysplasia 48 0.045
231
LYM021 Lymphadenitis 47 0.045
232
DFF024 Diffuse Panbronchiolitis 46 0.045
233
URT010 Ureteral Obstruction 46 0.045
234
EPL002 Epilepsy Syndrome 45 0.045
235
ART004 Aortic Atherosclerosis 45 0.045
236
P SPN052 Spondyloarthropathy 45 0.045
237
HRS011 Horseshoe Kidney 44 0.045
238
P SLD005 Sialidosis Type I 44 0.045
239
NRN002 Neuronitis 43 0.045
240
TTR016 Tetra-Amelia Syndrome 43 0.045
241
LMY003 Leiomyomatosis 39 0.045
242
ART012 Aortitis 39 0.045
243
VRL011 Viral Infectious Disease 38 0.045
244
MDL019 Medullary Cystic Kidney Disease Type 1 38 0.045
245
ADS002 Adie Syndrome 35 0.045
246
ADT003 Auditory System Disease 30 0.045
247
HNM002 Hinman Syndrome 28 0.045
248
P GLM015 Glomerulopathy with Fibronectin Deposits 2 24 0.045
249
DHL001 Dahlberg Borer Newcomer Syndrome 20 0.045
250
CLL035 Collagen Type Iii Glomerulopathy 7 0.045
251
P ALZ001 Alzheimer's Disease 98 0.037
252
P APL001 Aplastic Anemia 84 0.037
253
CNG034 Congestive Heart Failure 77 0.037
254
GLN003 Glanzmann's Thrombasthenia 76 0.037
255
CRH001 Crohn's Disease 75 0.037
256
RLP001 Relapsing Polychondritis 72 0.037
257
GLL008 Gilles De La Tourette Syndrome 72 0.037
258
P PND002 Pendred Syndrome 71 0.037
259
P DRM010 Dermatomyositis 71 0.037
260
P WLF004 Wolfram Syndrome 71 0.037
261
P RTH001 Rothmund-Thomson Syndrome 70 0.037
262
c THR014 Thrombocytopenia 69 0.037
263
SPS077 Sepsis 69 0.037
264
PLY017 Polyarteritis Nodosa 69 0.037
265
P CNG401 Congenital Heart Disease 69 0.037
266
P BCK002 Beckwith-Wiedemann Syndrome 68 0.037
267
P HYP117 Hypertriglyceridemia 67 0.037
268
c MNN013 Meningitis 67 0.037
269
P BLD042 Bladder Carcinoma 67 0.037
270
PRP027 Peripheral Vascular Disease 67 0.037
271
ACT049 Acute Disseminated Encephalomyelitis 66 0.037
272
P ATM003 Autoimmune Thyroiditis 66 0.037
273
P PRT013 Portal Hypertension 65 0.037
274
P GST044 Gastritis 65 0.037
275
STT001 Status Epilepticus 65 0.037
276
P GRV001 Graves' Disease 64 0.037
277
TTN003 Tetanus 64 0.037
278
WLL006 Wells Syndrome 63 0.037
279
LDD001 Ladd Syndrome 62 0.037
280
DFC004 Deficiency Anemia 62 0.037
281
MLL005 Miller-Dieker Syndrome 62 0.037
282
SCK005 Sickle Cell Disease 61 0.037
283
ACR008 Acrocallosal Syndrome 61 0.037
284
ESN015 Eosinophilic Fasciitis 61 0.037
285
c AGM001 Agammaglobulinemia 61 0.037
286
GLC003 Glucose Intolerance 61 0.037
287
c TYR004 Tyrosinemia 61 0.037
288
GNG013 Gingivitis 60 0.037
289
SND002 Sneddon Syndrome 60 0.037
290
RNL015 Renal Hypertension 60 0.037
291
P PRM124 Primary Hyperoxaluria Type 1 60 0.037
292
c ANG015 Angioedema 60 0.037
293
YLL002 Yellow Fever 59 0.037
294
c GLY013 Glycogen Storage Disease 59 0.037
295
c SLP006 Sleep Apnea 59 0.037
296
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.037
297
ANR004 Anuria 58 0.037
298
P CNG095 Congenital Generalized Lipodystrophy Type 2 58 0.037
299
P JBR004 Joubert Syndrome 2 57 0.037
300
RCT015 Reactive Arthritis 57 0.037
301
OBS061 Obstructive Sleep Apnea 57 0.037
302
GLB015 Glioblastoma Multiforme 57 0.037
303
P SDR002 Siderosis 57 0.037
304
INC001 Incontinentia Pigmenti Achromians 56 0.037
305
SCN006 Secondary Syphilis 56 0.037
306
ANK001 Ankylosis 56 0.037
307
PSD002 Pseudotumor Cerebri 56 0.037
308
RNL007 Renal Tubular Acidosis 56 0.037
309
BLS002 Blastomycosis 56 0.037
310
FRS002 Frasier Syndrome 56 0.037
311
PST041 Posterior Urethral Valves 55 0.037
312
DDN006 Duodenitis 55 0.037
313
PRR002 Pure Red-Cell Aplasia 55 0.037
314
MSN001 Mesangial Proliferative Glomerulonephritis 55 0.037
315
PRN011 Pernicious Anemia 55 0.037
316
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.037
317
c HRM001 Hermansky-Pudlak Syndrome 54 0.037
318
P LDD002 Liddle Syndrome 54 0.037
319
P DWR001 Dwarfism 54 0.037
320
URT001 Urethritis 54 0.037
321
CCH002 Coach Syndrome 54 0.037
322
c ANT034 Anterior Uveitis 53 0.037
323
XLN068 X-Linked Thrombocytopenia 53 0.037
324
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.037
325
c HYD002 Hydronephrosis 52 0.037
326
GNG012 Gingival Overgrowth 51 0.037
327
LPT002 Lipoatrophic Diabetes 50 0.037
328
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 50 0.037
329
ACT040 Acute Poststreptococcal Glomerulonephritis 49 0.037
330
c PSD003 Pseudohypoaldosteronism 49 0.037
331
RTN018 Retinal Disease 48 0.037
332
CHY006 Chylous Ascites 48 0.037
333
PYM001 Pyomyositis 48 0.037
334
GLM037 Glioma Somatic 47 0.037
335
CRT008 Carotid Artery Dissection 47 0.037
336
ANG054 Angina Pectoris 46 0.037
337
GNG008 Ganglioneuroblastoma 46 0.037
338
SPL018 Splenomegaly 46 0.037
339
MNN009 Meningoencephalitis 46 0.037
340
LYM012 Lymphoplasmacytic Lymphoma 46 0.037
341
SHR071 Short-Rib Thoracic Dysplasia 11 with or Without Polydactyly 45 0.037
342
FSC004 Fasciitis 45 0.037
343
LYM029 Lymphedema-Distichiasis Syndrome 45 0.037
344
BRB001 Beriberi 45 0.037
345
TBL013 Tubulointerstitial Nephritis and Uveitis 44 0.037
346
P HYP216 Hypoparathyroidism Familial Isolated 44 0.037
347
ILS001 Ileus 44 0.037
348
c ACT004 Acute Diarrhea 44 0.037
349
c SNR001 Senior-Loken Syndrome 43 0.037
350
CYT008 Cytomegalovirus Infection 43 0.037
351
CLL002 Collecting Duct Carcinoma 43 0.037
352
LRW002 Leri Weill Dyschondrosteosis 43 0.037
353
MYC019 Mycobacterium Marinum 42 0.037
354
HYP008 Hypertensive Retinopathy 42 0.037
355
c CNG033 Congenital Syphilis 40 0.037
356
P EPD044 Epidermolysis Bullosa Dystrophica, Ar 40 0.037
357
c NPH048 Nephronophthisis 1, Juvenile 39 0.037
358
CYS024 Cystinosis, Ocular Nonnephropathic 39 0.037
359
CRB086 Cerebral Aneurysms 38 0.037
360
JBR007 Joubert Syndrome with Renal Anomalies 38 0.037
361
EPP006 Epiphyseal Dysplasia Multiple with Early-Onset Diabetes Mellitus 37 0.037
362
HYP226 Hyporeninemic Hypoaldosteronism 37 0.037
363
CLS016 Clostridium Difficile Colitis 37 0.037
364
ART010 Arteriolosclerosis 37 0.037
365
c FML162 Familial Mediterranean Fever, Ad 37 0.037
366
PRP080 Peripheral Artery Disease 35 0.037
367
c JVN041 Juvenile Nephronophthisis 34 0.037
368
PLM074 Pulmonary Function 34 0.037
369
BLD039 Bladder Adenocarcinoma 33 0.037
370
HPT063 Hepatitis B Virus Infection 33 0.037
371
P ATM020 Autoimmune Enteropathy 30 0.037
372
c CNG192 Congenital Disorder of Glycosylation, Type Ik 30 0.037
373
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.037
374
P PRD019 Periodic Fever, Familial 28 0.037
375
TFT003 Tufting Enteropathy 28 0.037
376
IMM001 Immune-Complex Glomerulonephritis 27 0.037
377
MCR062 Microcephaly, Hiatal Hernia and Nephrotic Syndrome 26 0.037
378
C4B001 C4b Deficiency 26 0.037
379
ANT030 Antecubital Pterygium 25 0.037
380
c NPH019 Nephronophthisis 1 25 0.037
381
PRN007 Perinephritis 24 0.037
382
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 22 0.037
383
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 22 0.037
384
c AML044 Amelogenesis Imperfecta, Type Ig 21 0.037
385
HVY003 Heavy Chain Deposition Disease 19 0.037
386
C4D002 C4a Deficiency 19 0.037
387
DYS034 Dyschondrosteosis Nephritis 15 0.037
388
LGH014 Light and Heavy Chain Deposition Disease 14 0.037
389
LNP001 Loin Pain Hematuria Syndrome 13 0.037
390
IND008 Indomethacin Embryofetopathy 13 0.037
391
DFN014 Deafness Nephritis Anorectal Malformation 12 0.037
392
HRD064 Hereditary Vascular Retinopathy 9 0.037
393
P PRS040 Prostate Cancer 97 0.026
394
HDG007 Hodgkin's Lymphoma 93 0.026
395
KPS001 Kaposi's Sarcoma 86 0.026
396
P RTN008 Retinitis Pigmentosa 86 0.026
397
P FML021 Familial Hypercholesterolemia 85 0.026
398
MRF001 Marfan Syndrome 85 0.026
399
INF030 Infectious Mononucleosis 84 0.026
400
P PRM021 Primary Pulmonary Hypertension 80 0.026
401
ACR007 Acromegaly 79 0.026
402
P PRC016 Pre-Eclampsia 79 0.026
403
THR006 Thromboangiitis Obliterans 79 0.026
404
P MTH008 Methylmalonic Acidemia 79 0.026
405
LSC001 Lesch-Nyhan Syndrome 78 0.026
406
LRN002 Laron Syndrome 77 0.026
407
P PNM007 Pneumonia 77 0.026
408
CRB011 Cerebrotendinous Xanthomatosis 76 0.026
409
P PRP003 Porphyria Cutanea Tarda 75 0.026
410
KWS002 Kawasaki Disease 75 0.026
411
P MST009 Mastocytosis 75 0.026
412
P CLC005 Celiac Disease 74 0.026
413
P ALP006 Alpha Thalassemia 74 0.026
414
c MYL006 Myeloid Leukemia 74 0.026
415
P LYM007 Lymphangioleiomyomatosis 74 0.026
416
P SRC013 Sarcoidosis 73 0.026
417
P WGN002 Wegener's Granulomatosis 73 0.026
418
c CHR065 Chronic Myeloid Leukemia 73 0.026
419
P PRD006 Prader-Willi Syndrome 73 0.026
420
c PLM037 Pulmonary Hypertension 73 0.026
421
P NPH007 Nephrogenic Diabetes Insipidus 72 0.026
422
P PRM006 Primary Biliary Cirrhosis 72 0.026
423
P CNG368 Congenital Adrenal Hyperplasia 72 0.026
424
WRN001 Werner Syndrome 71 0.026
425
P PRM005 Primary Hyperparathyroidism 70 0.026
426
ART016 Aortic Aneurysm 70 0.026
427
RNL002 Renal Agenesis 69 0.026
428
BLL006 Bullous Pemphigoid 69 0.026
429
P MTB001 Metabolic Syndrome X 69 0.026
430
PSD012 Pseudoachondroplasia 69 0.026
431
P KDN017 Kidney Cancer 69 0.026
432
P HYD006 Hydrocephalus 69 0.026
433
P CMR001 Camurati-Engelmann Disease 69 0.026
434
PYR013 Pyruvate Kinase Deficiency 68 0.026
435
PSD007 Pseudomyxoma Peritonei 68 0.026
436
P HRD011 Hereditary Spherocytosis 68 0.026
437
P PSD087 Pseudoxanthoma Elasticum 68 0.026
438
P PRG006 Progressive Supranuclear Palsy 68 0.026
439
LYS003 Lysinuric Protein Intolerance 68 0.026
440
GST034 Gastroesophageal Reflux Disease 68 0.026
441
THR016 Thrombophlebitis 68 0.026
442
P SHR002 Short Stature 68 0.026
443
P RCK004 Rickets 67 0.026
444
P PLY011 Polycystic Ovary Syndrome 67 0.026
445
MRB003 Morbid Obesity 67 0.026
446
c JVN010 Juvenile Rheumatoid Arthritis 67 0.026
447
DBT001 Diabetic Ketoacidosis 67 0.026
448
PLS006 Plasmodium Vivax Malaria 66 0.026
449
P SYS005 Systemic Scleroderma 66 0.026
450
CMM004 Common Variable Immunodeficiency 66 0.026
451
GST009 Gastroschisis 66 0.026
452
P THR015 Thrombophilia 66 0.026
453
DMN002 Dementia 66 0.026
454
P FML020 Familial Combined Hyperlipidemia 66 0.026
455
P ATM010 Autoimmune Hemolytic Anemia 66 0.026
456
FCT006 Factor V Deficiency 66 0.026
457
TRN001 Transthyretin Amyloidosis 65 0.026
458
c HML002 Hemolytic Anemia 65 0.026
459
PHR003 Pharyngitis 65 0.026
460
P ATY010 Atypical Hemolytic-Uremic Syndrome 65 0.026
461
P CRN018 Coronary Artery Anomaly 65 0.026
462
c ENC004 Encephalitis 65 0.026
463
NRM002 Normal Pressure Hydrocephalus 65 0.026
464
c SYS004 Systemic Mastocytosis 64 0.026
465
ULC004 Ulcerative Colitis 64 0.026
466
P GRF002 Graft Versus Host Disease 64 0.026
467
ALP007 Alpha 1-Antitrypsin Deficiency 64 0.026
468
c SCL016 Scleroderma 64 0.026
469
P HRD057 Hereditary Pancreatitis 64 0.026
470
HYP004 Hypercalcemia 64 0.026
471
P ACT101 Acute Lymphoblastic Leukemia 64 0.026
472
c VRL010 Viral Hepatitis 63 0.026
473
EXT034 Extrinsic Allergic Alveolitis 63 0.026
474
OCC006 Occipital Horn Syndrome 63 0.026
475
PRT092 Partial Androgen Insensitivity Syndrome 63 0.026
476
c GLL020 Gallbladder Disease 63 0.026
477
URT039 Urticaria 63 0.026
478
P MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.026
479
P ESP024 Esophagitis 63 0.026
480
P HST010 Histiocytosis 63 0.026
481
ART031 Aortic Coarctation 62 0.026
482
LRN003 Learning Disability 62 0.026
483
SPN027 Spinal Stenosis 62 0.026
484
P PPL005 Papillary Renal Cell Carcinoma 62 0.026
485
P CNG013 Congenital Disorder of Glycosylation Type I 62 0.026
486
P MTR012 Mitral Valve Disease 62 0.026
487
P ANP001 Anaplastic Large Cell Lymphoma 62 0.026
488
FBR032 Fibromuscular Dysplasia 61 0.026
489
c FML012 Familial Partial Lipodystrophy 61 0.026
490
DWN001 Down Syndrome 61 0.026
491
P AVS004 Avascular Necrosis of the Femoral Head 60 0.026
492
ACT105 Acute Mountain Sickness 60 0.026
493
GLC002 Glucocorticoid-Remediable Aldosteronism 60 0.026
494
P PRM054 Primary Sclerosing Cholangitis 60 0.026
495
P MLS001 Melas Syndrome 60 0.026
496
DBT010 Diabetic Neuropathy 60 0.026
497
P PLY019 Polyneuropathy 60 0.026
498
c ALM001 Al Amyloidosis 60 0.026
499
VTL002 Vitiligo 60 0.026
500
DST005 Diastrophic Dysplasia 60 0.026
501
CRN017 Coronary Thrombosis 60 0.026
502
c ACT071 Acute Kidney Failure 59 0.026
503
PRS047 Prostatitis 59 0.026
504
OLG003 Oligohydramnios 59 0.026
505
ALP008 Alopecia 59 0.026
506
TWN003 Townes-Brocks Syndrome 59 0.026
507
c HMP002 Hemophagocytic Lymphohistiocytosis 59 0.026
508
CLD007 Cold Agglutinin Disease 59 0.026
509
P MTR005 Mitral Valve Prolapse 59 0.026
510
GLC012 Galactosialidosis 59 0.026
511
PMP001 Pemphigus 59 0.026
512
SCR002 Scurvy 59 0.026
513
P DNT039 Dent's Disease 59 0.026
514
c LCL006 Localized Scleroderma 59 0.026
515
EXF001 Exfoliation Syndrome 59 0.026
516
MLR002 Miliary Tuberculosis 59 0.026
517
MLT001 Multiple Chemical Sensitivity 59 0.026
518
PLY041 Polymyositis 58 0.026
519
P ANT058 Anterior Ischemic Optic Neuropathy 58 0.026
520
PPL002 Papillary Carcinoma 58 0.026
521
FRB001 Farber Lipogranulomatosis 58 0.026
522
P HRM005 Hermansky-Pudlak Syndrome 1 58 0.026
523
SMT015 Smith Magenis Syndrome 58 0.026
524
BCT004 Bacteriuria 58 0.026
525
CNN005 Connective Tissue Disease 58 0.026
526
HDC001 Headache 57 0.026
527
NNS002 Nonspecific Interstitial Pneumonia 57 0.026
528
URN010 Urinary Tract Obstruction 57 0.026
529
SCH002 Schnitzler Syndrome 57 0.026
530
FLL008 Folliculitis 57 0.026
531
P INT068 Intestinal Disease 57 0.026
532
P DBT005 Diabetes Insipidus 57 0.026
533
c ISC002 Ischemic Optic Neuropathy 57 0.026
534
BRN029 Brain Disease 57 0.026
535
c HRD002 Hereditary Angioedema 57 0.026
536
c HYP065 Hyperaldosteronism 57 0.026
537
P SNS014 Sinusitis 57 0.026
538
c CNT016 Central Retinal Vein Occlusion 57 0.026
539
P PSR001 Psoriatic Arthritis 57 0.026
540
BRN071 Brain Injury 57 0.026
541
DFF003 Diffuse Scleroderma 57 0.026
542
c RTN014 Retinal Artery Occlusion 57 0.026
543
c CTR002 Cataract 57 0.026
544
c CNG025 Congenital Disorder of Glycosylation 57 0.026
545
LYS001 Loeys-Dietz Syndrome 57 0.026
546
IRN001 Iron Deficiency Anemia 56 0.026
547
ACT017 Acute Chest Syndrome 56 0.026
548
PLS007 Plasmodium Falciparum Malaria 56 0.026
549
c HPT015 Hepatitis D 56 0.026
550
TYP013 Type 1 Von Willebrand Disease 56 0.026
551
P HYP090 Hyperalphalipoproteinemia 56 0.026
552
CNG048 Congenital Hepatic Fibrosis 56 0.026
553
LDP002 Lead Poisoning 56 0.026
554
APH001 Aphthous Stomatitis 56 0.026
555
c MNT147 Mental Retardation 56 0.026
556
MCR088 Microscopic Polyangiitis 56 0.026
557
c FML035 Familial Hyperlipidemia 55 0.026
558
PRT011 Protein C Deficiency 55 0.026
559
CLC001 Calciphylaxis 55 0.026
560
ART017 Aortic Disease 55 0.026
561
STV001 Stevens-Johnson Syndrome 55 0.026
562
VLV044 Vulvar Intraepithelial Neoplasia 55 0.026
563
c TRM003 Tremor 55 0.026
564
DST006 Diastolic Heart Failure 55 0.026
565
ACN001 Acinar Cell Carcinoma 55 0.026
566
CNG064 Congenital Chloride Diarrhea 55 0.026
567
MDL009 Medullary Sponge Kidney 54 0.026
568
PLY020 Polyradiculoneuropathy 54 0.026
569
c ART070 Aortic Valve Disease 54 0.026
570
P CHL066 Cholangitis 54 0.026
571
RYS001 Reye Syndrome 54 0.026
572
HYP121 Hypoalphalipoproteinemia 54 0.026
573
c PSD015 Pseudohypoparathyroidism 54 0.026
574
PRT058 Pure Autonomic Failure 54 0.026
575
P TWN001 Twin-to-Twin Transfusion Syndrome 54 0.026
576
WLL001 Williams-Beuren Syndrome 54 0.026
577
DBT006 Diabetic Macular Edema 54 0.026
578
c ACR001 Aicardi-Goutieres Syndrome 54 0.026
579
PST062 Pustulosis Palmaris Et Plantaris 53 0.026
580
CHR008 Choroiditis 53 0.026
581
c FML016 Familial Hypertriglyceridemia 53 0.026
582
APP001 Apparent Mineralocorticoid Excess Syndrome 53 0.026
583
CNS004 Constipation 53 0.026
584
YLL001 Yellow Nail Syndrome 53 0.026
585
ONC003 Oncogenic Osteomalacia 53 0.026
586
FML164 Familial Hdl Deficiency 53 0.026
587
GST045 Gastroenteritis 53 0.026
588
P ART028 Aortic Aneurysm, Familial Thoracic 4 53 0.026
589
P PLM006 Pulmonary Alveolar Proteinosis 52 0.026
590
P ORT004 Orthostatic Intolerance 52 0.026
591
HNT002 Hantavirus Pulmonary Syndrome 52 0.026
592
c LKD001 Leukodystrophy 52 0.026
593
c LYM025 Lymphedema 52 0.026
594
OBS029 Obesity, Association with 52 0.026
595
CHY002 Chylomicron Retention Disease 52 0.026
596
PRP002 Periapical Granuloma 52 0.026
597
c CNG012 Congenital Generalized Lipodystrophy 52 0.026
598
P TXC012 Toxic Epidermal Necrolysis 52 0.026
599
NM001 Noma 52 0.026
600
c HPT007 Hepatitis E 52 0.026
601
RSD004 Rosai-Dorfman Disease 52 0.026
602
OBS006 Obstructive Lung Disease 52 0.026
603
RFL001 Reflex Sympathetic Dystrophy 52 0.026
604
NNL002 Nonalcoholic Steatohepatitis 51 0.026
605
USL001 Usual Interstitial Pneumonia 51 0.026
606
PLS025 Plasmablastic Lymphoma 51 0.026
607
CTS005 Catastrophic Antiphospholipid Syndrome 51 0.026
608
MYC005 Myocardial Stunning 51 0.026
609
ALC009 Alcoholic Liver Cirrhosis 51 0.026
610
MCL003 Macular Holes 51 0.026
611
AMY053 Amyloidosis, Secondary 51 0.026
612
RNL006 Renal Glycosuria 51 0.026
613
RNL011 Renal Osteodystrophy 51 0.026
614
P CTN015 Cutaneous T Cell Lymphoma 51 0.026
615
KMR001 Kimura Disease 51 0.026
616
DRG002 Drug-Induced Hepatitis 50 0.026
617
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 50 0.026
618
STM007 Stomatitis 50 0.026
619
PSD009 Pseudohermaphroditism 50 0.026
620
PLC007 Placental Abruption 50 0.026
621
NNT024 Neonatal Stroke 50 0.026
622
OCL020 Ocular Cicatricial Pemphigoid 50 0.026
623
LPP002 Lipoprotein Glomerulopathy 50 0.026
624
c ATM024 Autoimmune Pancreatitis 50 0.026
625
c HYP011 Hyperlipoproteinemia Type Iii 49 0.026
626
HYP006 Hypertensive Heart Disease 49 0.026
627
DFN221 Deafness Dystonia Syndrome 49 0.026
628
HYP005 Hypokalemia 49 0.026
629
BRN106 Burns 49 0.026
630
PRN038 Prune Belly Syndrome 49 0.026
631
c SCL009 Sclerosing Cholangitis 49 0.026
632
SPN119 Spondylarthropathy 49 0.026
633
ALC010 Alcoholic Cardiomyopathy 49 0.026
634
RNL097 Renal Artery Disease 48 0.026
635
DBT002 Diabetic Autonomic Neuropathy 48 0.026
636
PLS016 Plasma Cell Leukemia 48 0.026
637
CRT049 Critical Limb Ischemia 48 0.026
638
ADR027 Adrenocortical Insufficiency 48 0.026
639
HYP017 Hypophosphatemia 48 0.026
640
DFF021 Diffuse Mesangial Sclerosis 48 0.026
641
HMC014 Homocysteinemia 48 0.026
642
FVS001 Favism 48 0.026
643
NSP002 Nasopharyngitis 48 0.026
644
MNN021 Meningococcemia 48 0.026
645
P SNR003 Senior-Loken Syndrome 1 47 0.026
646
LPD008 Lipid Metabolism Disorder 47 0.026
647
CRN027 Corneal Neovascularization 47 0.026
648
HPT025 Hepatic Lipase Deficiency 47 0.026
649
PTY003 Pityriasis Rubra Pilaris 47 0.026
650
CNS002 Constrictive Pericarditis 47 0.026
651
c GGN002 Gigantism 47 0.026
652
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 47 0.026
653
c PRN026 Porencephaly 47 0.026
654
CNN003 Conn's Syndrome 47 0.026
655
c RNL078 Renal Dysplasia 47 0.026
656
ART035 Arterial Calcification of Infancy 46 0.026
657
CRT004 Carotid Artery Thrombosis 46 0.026
658
FBR063 Fibrocalculous Pancreatic Diabetes 46 0.026
659
CRB008 Cerebral Atherosclerosis 46 0.026
660
P ATN005 Autonomic Dysfunction 46 0.026
661
P CRT018 Carotid Intimal Medial Thickness 46 0.026
662
PMP004 Pemphigus Foliaceus 46 0.026
663
CRB001 Cerebral Lymphoma 46 0.026
664
P BRS044 Breast Adenocarcinoma 46 0.026
665
BRN105 Burn Scar 46 0.026
666
LWR010 Low Renin Hypertension 45 0.026
667
HYP001 Hypochromic Microcytic Anemia 45 0.026
668
MCR018 Microcytic Anemia 45 0.026
669
EVN001 Evans' Syndrome 45 0.026
670
PST055 Postural Hypotension 45 0.026
671
BWN003 Bowenoid Papulosis 45 0.026
672
c ACQ022 Acquired Generalized Lipodystrophy 45 0.026
673
IDP011 Idiopathic Interstitial Pneumonia 45 0.026
674
RNL029 Renal Coloboma Syndrome 45 0.026
675
MYC033 Myoclonus 44 0.026
676
URT031 Ureteral Disease 44 0.026
677
ART110 Arteritic Anterior Ischemic Optic Neuropathy 44 0.026
678
NRM003 Norum Disease 44 0.026
679
c PLY083 Polycystic Kidney Disease, Type 1 44 0.026
680
CMP009 Complement Deficiency 44 0.026
681
LYS015 Loeys-Dietz Syndrome, Type 1 44 0.026
682
c RTN016 Retinal Degeneration 44 0.026
683
c LTT001 Lattice Corneal Dystrophy 44 0.026
684
CRP018 Cor Pulmonale 44 0.026
685
UNL007 Unilateral Renal Agenesis 44 0.026
686
MRC003 Mercury Poisoning 44 0.026
687
ESN011 Eisenmenger Syndrome 44 0.026
688
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 43 0.026
689
PLC005 Placental Insufficiency 43 0.026
690
MCR001 Microcystic Meningioma 43 0.026
691
NCR002 Necrobiosis Lipoidica 43 0.026
692
CMP042 Complement Factor H Deficiency 43 0.026
693
P PRG011 Progressive Myoclonus Epilepsy 43 0.026
694
HMF004 Hemifacial Spasm 42 0.026
695
c ACT042 Acute Pyelonephritis 42 0.026
696
c CHR417 Chronic Graft Versus Host Disease 42 0.026
697
c HYP057 Hypervitaminosis D 42 0.026
698
DFC001 Defective Apolipoprotein B-100 42 0.026
699
DBT007 Diabetic Cataract 42 0.026
700
INT071 Intestinal Perforation 42 0.026
701
MNG006 Monogenic Diabetes 42 0.026
702
RTN020 Retinal Vascular Disease 41 0.026
703
MNN034 Mannose-Binding Lectin Deficiency 41 0.026
704
DNN002 Donnai-Barrow Syndrome 40 0.026
705
GST040 Gastric Adenocarcinoma 40 0.026
706
HYP574 Hypercholesterolemia, Familial, Modifier of 40 0.026
707
AMR003 Amaurosis Fugax 40 0.026
708
INP001 Inappropriate Adh Syndrome 40 0.026
709
CHR413 Chronic Myocardial Ischemia 40 0.026
710
c TRN016 Transient Hypogammaglobulinemia 40 0.026
711
CRB085 Cerebral Hemorrhage 40 0.026
712
ANG046 Angioimmunoblastic T-Cell Lymphoma 39 0.026
713
HYP456 Hyperapobetalipoproteinemia 39 0.026
714
PLY013 Polymyalgia Rheumatica 39 0.026
715
LPD014 Lipodermatosclerosis 39 0.026
716
P TRN009 Transient Hypogammaglobulinemia of Infancy 39 0.026
717
c HVY001 Heavy Chain Disease 39 0.026
718
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.026
719
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 38 0.026
720
c MLR021 Malaria, Severe 38 0.026
721
HMG010 Hemoglobinemia 38 0.026
722
ADP002 Adiponectin Deficiency 38 0.026
723
ENC011 Encephalomyopathy 38 0.026
724
c OBS047 Obesity, Early-Onset 38 0.026
725
C1Q001 C1q Deficiency 38 0.026
726
CRN127 Coronary Artery Disease in Familial Hypercholesterolemia, Protection Against 38 0.026
727
C3D001 C3 Deficiency 37 0.026
728
OCL022 Ocular Melanoma 37 0.026
729
SPS057 Spasticity 37 0.026
730
SRS007 Sorsby Fundus Dystrophy 37 0.026
731
P RNL042 Renal Hypouricemia 37 0.026
732
c HYP296 Hypercholesterolemia, Familial, Due to Ldlr Defect, Modifier of 36 0.026
733
LNR006 Linear Iga Disease 36 0.026
734
c PLN008 Peeling Skin Syndrome 36 0.026
735
c OBS016 Obesity, Late-Onset 36 0.026
736
IPX001 Ipex Syndrome 36 0.026
737
OBS019 Obesity, Variation in 36 0.026
738
OBS024 Obesity, Mild, Early-Onset 36 0.026
739
c OBS023 Obesity, Autosomal Dominant 36 0.026
740
c FML187 Familial Hypertension 36 0.026
741
HMG020 Hmg Coa Lyase Deficiency 36 0.026
742
c MYC026 Myoclonus Epilepsy 35 0.026
743
OBS031 Obesity, Severe, and Type Ii Diabetes 35 0.026
744
RNL012 Renal Tuberculosis 35 0.026
745
LDL001 Ldl Cholesterol Level Qtl2 35 0.026
746
DYS070 Dysalbuminemic Hyperthyroxinemia 35 0.026
747
P AMY038 Amyloidosis, Renal 35 0.026
748
HYP264 Hypertonia 35 0.026
749
HYP034 Hypertensive Encephalopathy 34 0.026
750
INF133 Inferior Vena Cava Interruption 34 0.026
751
FCT013 Factor V Leiden Thrombophilia 34 0.026
752
SHR075 Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly 33 0.026
753
c NPH032 Nephronophthisis 4 33 0.026
754
P INF069 Infantile Neuroaxonal Dystrophy 1 33 0.026
755
CHL109 Childhood Apraxia of Speech 33 0.026
756
NTR005 Nutritional Deficiency Disease 33 0.026
757
IDP033 Idiopathic Edema 32 0.026
758
CHR476 Chronic Angina 31 0.026
759
c CHR096 Chronic Pulmonary Heart Disease 31 0.026
760
URT036 Urethral Obstruction 31 0.026
761
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 31 0.026
762
NRG005 Neurogenic Hypertension 30 0.026
763
MYC035 Myocardial Infarction Susceptibility 30 0.026
764
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 30 0.026
765
ACD004 Acdc 30 0.026
766
MTH052 Methylmalonic Acidemia and Homocystinuria Cblc Type 30 0.026
767
SBL004 Sea-Blue Histiocytosis 29 0.026
768
AMY034 Amyloidosis, 3 or More Types 28 0.026
769
PYR004 Pyuria 28 0.026
770
GST007 Gastric Dilatation 28 0.026
771
PRD012 Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis 28 0.026
772
CHL070 Cholesterol Embolism 27 0.026
773
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.026
774
IRN002 Iron Metabolism Disease 27 0.026
775
c DYS055 Dystonia 10 27 0.026
776
HFS001 Hfe-Associated Hereditary Hemochromatosis 27 0.026
777
KRN001 Korean Hemorrhagic Fever 26 0.026
778
P PPL026 Papular Mucinosis 26 0.026
779
KRY002 Karyomegalic Interstitial Nephritis 26 0.026
780
PL2001 Pla2g6-Associated Neurodegeneration 24 0.026
781
PRX022 Paroxysmal Choreoathetosis 24 0.026
782
P ALP005 Alpha Chain Disease 24 0.026
783
EPD034 Epidermolysis Bullosa, Pretibial 24 0.026
784
XLN127 X-Linked Diffuse Leiomyomatosis - Alport Syndrome 24 0.026
785
CNG116 Congenital Nephrotic Syndrome Finnish Type 24 0.026
786
PSD062 Pseudoxanthoma Elasticum, Modifier of Severity of 24 0.026
787
GRD004 Gardner-Diamond Syndrome 23 0.026
788
STR080 Stroke, Hemorrhagic 23 0.026
789
HFH001 Hfe Hemochromatosis, Modifier of 23 0.026
790
HYP281 Hypoproteinemia, Hypercatabolic 22 0.026
791
c PST008 Posterior Scleritis 22 0.026
792
FML268 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes 21 0.026
793
HPR001 Hprt-Related Gout 21 0.026
794
PCM002 Pauci-Immune Glomerulonephritis 21 0.026
795
VRS001 Virus Associated Hemophagocytic Syndrome 21 0.026
796
PRM041 Primary Cortisol Resistance 21 0.026
797
ESN004 Eosinophilic Gastritis 20 0.026
798
RTN163 Retinal Arterial Tortuosity 19 0.026
799
PRP033 Properdin Deficiency 19 0.026
800
c DMN011 Dominant Dystrophic Epidermolysis Bullosa 19 0.026
801
OCL043 Oculorenocerebellar Syndrome 18 0.026
802
ANP010 Anaplastic Plasmacytoma 18 0.026
803
c CRN111 Cranioectodermal Dysplasia 4 18 0.026
804
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 17 0.026
805
EPL108 Epilepsy, Progressive Myoclonic 4, with or Without Renal Failure 17 0.026
806
PLS008 Plasmodium Malariae Malaria 16 0.026
807
KDN006 Kidney Papillary Necrosis 15 0.026
808
C9D001 C9 Deficiency 15 0.026
809
ICH053 Ichthyosis - Intellectual Disability - Dwarfism - Renal Impairment 15 0.026
810
SLC010 Salcedo Syndrome 14 0.026
811
GLM024 Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria 13 0.026
812
c ART063 Arthrogryposis, Renal Dysfunction, and Cholestasis 2 13 0.026
813
ALD004 Ala Dehydratase Deficiency 12 0.026
814
CNG330 Congenital Megacalycosis 9 0.026
815
IMM060 Immunodeficiency, Common Variable, 9 9 0.026
816
CL4001 Col4a1-Related Disorders 8 0.026
817
CRM007 Crome Syndrome 7 0.026
818
EXD002 Exudative Glomerulonephritis 7 0.026