Search results for "nephropathy"

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

805 hits were found for 'nephropathy'

# Family MCID Name MIFTS Score
1
FML076 Familial Juvenile Hyperuricaemic Nephropathy 33 5.662
2
BLK001 Balkan Nephropathy 31 5.050
3
DBT061 Diabetic Nephropathy 47 4.916
4
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 28 4.321
5
MMB002 Membranous Glomerulonephritis 53 4.161
6
UMD001 Umod-Associated Kidney Disease 31 4.046
7
P BKV001 Bk-Virus Nephropathy 23 3.582
8
IGG001 Iga Glomerulonephritis 54 3.550
9
THN006 Thin Basement Membrane Nephropathy 45 3.506
10
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 18 3.475
11
c FML022 Familial Juvenile Hyperuricemic Nephropathy 34 3.347
12
ACT043 Acute Urate Nephropathy 25 3.244
13
P FML044 Familial Juvenile Hyperuricemic Nephropathy Type 2 23 3.203
14
c RNR002 Ren-Related Kidney Disease 19 3.194
15
HYP114 Hypertensive Nephropathy 42 3.043
16
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 9 2.890
17
NPH037 Nephronophthisis-Like Nephropathy 1 15 2.837
18
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 25 2.555
19
DNY001 Denys-Drash Syndrome 69 2.532
20
PLY043 Polyomavirus Allograft Nephropathy 6 2.532
21
P FML003 Familial Visceral Amyloidosis 42 2.484
22
MLT033 Multicentric Osteolysis Nephropathy 5 2.484
23
DNT019 Daentl Towsend Siegel Syndrome 18 2.471
24
ATH009 Atherosclerosis - Deafness - Diabetes - Epilepsy - Nephropathy 17 2.471
25
NPH016 Nephropathy-Hypertension 8 2.471
26
CTR091 Cataract - Nephropathy - Encephalopathy 15 2.457
27
ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 8 2.457
28
P IGN003 Iga Nephropathy 1 4 2.457
29
ALP004 Alport Syndrome 61 2.172
30
BRG002 Berger Disease 32 2.089
31
NPH003 Nephrocalcinosis 49 2.071
32
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 8 2.049
33
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 2.037
34
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 20 2.023
35
FGN001 Feigenbaum Bergeron Richardson Syndrome 6 2.023
36
PRM036 Premature Atherosclerosis with Photomyoclonic Epilepsy, Deafness, Diabetes Mellitus, Nephropathy, an 3 2.023
37
ATS141 Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E 17 2.006
38
NPH066 Nephropathy Due to Cfhr5 Deficiency 16 2.006
39
c FML261 Familial Renal Amyloidosis Due to Lysozyme Variant 13 2.006
40
c FML260 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 12 2.006
41
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 11 2.006
42
c FML208 Familial Renal Amyloidosis Due to Apolipoprotein Aii Variant 11 2.006
43
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 11 2.006
44
CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 7 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 1.495
53
c MTR022 Maturity-Onset Diabetes of the Young, Type 5 47 1.483
54
MCK007 Muckle-Wells Syndrome 67 1.471
55
P ATS015 Autosomal Dominant Alport Syndrome 54 1.471
56
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 38 1.471
57
c ATS018 Autosomal Recessive Alport Syndrome 45 1.440
58
FTZ004 Fitzsimmons Walson Mellor Syndrome 15 1.440
59
HRR004 Herrmann Syndrome 5 1.419
60
ALL011 Allain-Babin-Demarquez Syndrome 4 1.419
61
c DBT009 Diabetes Mellitus 74 0.354
62
PRT039 Proteinuria 58 0.287
63
P HYP075 Hypertension 87 0.276
64
P GLM007 Glomerulonephritis 69 0.236
65
END072 Endotheliitis 51 0.210
66
NPH051 Nephritis 54 0.196
67
c TYP009 Type 2 Diabetes Mellitus 100 0.189
68
P TYP008 Type 1 Diabetes Mellitus 96 0.168
69
GLM011 Glomerulosclerosis 48 0.168
70
c NPH012 Nephrotic Syndrome 67 0.159
71
c KDN018 Kidney Disease 63 0.157
72
PRP030 Purpura 66 0.144
73
c HPT021 Hepatitis 64 0.128
74
NRP001 Neuropathy 62 0.128
75
P FCL005 Focal Segmental Glomerulosclerosis 70 0.126
76
DBT011 Diabetic Retinopathy 71 0.120
77
END030 End Stage Renal Failure 58 0.120
78
TNS005 Tonsillitis 57 0.114
79
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.111
80
P HYP014 Hyperuricemia 56 0.108
81
INT067 Interstitial Nephritis 45 0.105
82
P INS005 Insulin Resistance 65 0.102
83
THR013 Thoracic Outlet Syndrome 52 0.102
84
MMB001 Membranoproliferative Glomerulonephritis 48 0.102
85
CRS001 Crescentic Glomerulonephritis 44 0.098
86
CRB009 Cerebritis 39 0.098
87
SYN053 Syndromic Diarrhea 34 0.098
88
FBR012 Fabry Disease 86 0.095
89
c PRM002 Primary Hyperoxaluria 74 0.095
90
c MLG069 Malignant Hypertension 64 0.095
91
NLP001 Nail-Patella Syndrome 70 0.091
92
ANK002 Ankylosing Spondylitis 77 0.083
93
ATH003 Atherosclerosis 69 0.083
94
ACN002 Acanthosis Nigricans 63 0.083
95
BLN003 Blindness 53 0.083
96
c VSC005 Vesicoureteral Reflux 51 0.083
97
P ATX010 Ataxia Neuropathy Spectrum 43 0.083
98
P ART022 Arthritis 75 0.079
99
c HPT016 Hepatitis B 70 0.079
100
P CYS016 Cystic Kidney 51 0.079
101
P FNC004 Fanconi Syndrome 50 0.079
102
c ATN004 Autonomic Neuropathy 50 0.079
103
c PRL003 Proliferative Glomerulonephritis 46 0.079
104
TBR010 Tuberculosis 87 0.074
105
c ESS002 Essential Hypertension 73 0.074
106
VSC007 Vascular Disease 70 0.074
107
P AMY004 Amyloidosis 68 0.074
108
c MYL007 Myeloma 61 0.074
109
NPH018 Nephrogenic Systemic Fibrosis 58 0.074
110
P PYL005 Pyelonephritis 55 0.074
111
RNL077 Renal Fibrosis 49 0.074
112
NPH017 Nephrosis 42 0.074
113
P RHM011 Rheumatoid Arthritis 94 0.069
114
P LKM002 Leukemia 77 0.069
115
P ANG001 Angelman Syndrome 70 0.069
116
ART019 Aortic Valve Stenosis 64 0.069
117
HYP066 Hyperglycemia 62 0.069
118
c PLY014 Polycystic Kidney Disease 62 0.069
119
RTN023 Retinitis 54 0.069
120
P OBS005 Obesity 91 0.064
121
P WSK001 Wiskott-Aldrich Syndrome 79 0.064
122
P HPT001 Hepatitis C 67 0.064
123
P GT001 Gout 66 0.064
124
P RNV001 Renovascular Hypertension 62 0.064
125
SNS001 Sensorineural Hearing Loss 57 0.064
126
P RPD001 Rapidly Progressive Glomerulonephritis 57 0.064
127
P NPH005 Nephronophthisis 52 0.064
128
NPH010 Nephrosclerosis 52 0.064
129
c CHR098 Chronic Pyelonephritis 48 0.064
130
P ATX002 Ataxia Telangiectasia 87 0.059
131
CDS001 Cadasil 84 0.059
132
PRT036 Peritonitis 72 0.059
133
CRB039 Cerebrovascular Disease 69 0.059
134
VSC011 Vasculitis 66 0.059
135
c THY032 Thyroiditis 66 0.059
136
c UVT001 Uveitis 66 0.059
137
P WLM002 Wilms Tumor 66 0.059
138
TRN018 Transitional Cell Carcinoma 64 0.059
139
ART111 Artery Disease 62 0.059
140
P ADN016 Adenocarcinoma 59 0.059
141
CRY004 Cryoglobulinemia 59 0.059
142
MCR004 Macroglobulinemia 55 0.059
143
ART001 Arterial Tortuosity Syndrome 55 0.059
144
AND003 Andersen-Tawil Syndrome 54 0.059
145
OST011 Osteomalacia 53 0.059
146
HYP037 Hyperhomocysteinemia 53 0.059
147
LPD004 Lipoid Nephrosis 51 0.059
148
PRT019 Protein-Losing Enteropathy 51 0.059
149
P HML001 Hemolytic-Uremic Syndrome 48 0.059
150
ANR040 Aneurysm 46 0.059
151
LGH004 Light Chain Deposition Disease 35 0.059
152
c BNG076 Benign Exophthalmos Syndrome 22 0.059
153
P MYC007 Myocardial Infarction 93 0.052
154
P SYS001 Systemic Lupus Erythematosus 88 0.052
155
AND002 Androgen Insensitivity Syndrome 80 0.052
156
P MLR004 Malaria 75 0.052
157
c PNC044 Pancreatitis 69 0.052
158
c AXN002 Axenfeld-Rieger Syndrome 67 0.052
159
BRN024 Bronchitis 67 0.052
160
c AMY001 Amyotrophic Lateral Sclerosis 67 0.052
161
ANT006 Antiphospholipid Syndrome 66 0.052
162
PMS001 Poems Syndrome 64 0.052
163
HV1006 Hiv-1 64 0.052
164
PSR002 Psoriasis 63 0.052
165
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.052
166
MYC002 Mycobacterium Avium Complex Disease 59 0.052
167
P NPH009 Nephrolithiasis 58 0.052
168
URM002 Uremia 58 0.052
169
EPD016 Epidermolysis Bullosa 58 0.052
170
HPT014 Hepatorenal Syndrome 57 0.052
171
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.052
172
NPH004 Nephropathia Epidemica 55 0.052
173
PRL007 Proliferative Diabetic Retinopathy 54 0.052
174
LPS007 Lupus Nephritis 53 0.052
175
c DRR001 Diarrhea 52 0.052
176
MNN014 Mononeuritis 51 0.052
177
RTR011 Retroperitoneal Fibrosis 48 0.052
178
c HPT073 Hepatitis C Virus 48 0.052
179
HYP120 Hypoaldosteronism 47 0.052
180
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.052
181
HNC001 Henoch-Schoenlein Purpura 41 0.052
182
STR044 Steroid-Resistant Nephrotic Syndrome 37 0.052
183
AND005 Androgen Insensitivity Syndrome, Mild 21 0.052
184
OTP003 Oto-Palatal-Digital Syndrome 17 0.052
185
P LVR011 Liver Cancer 91 0.045
186
P CHR090 Chronic Lymphocytic Leukemia 89 0.045
187
P MLT019 Multiple Myeloma 88 0.045
188
P HMC003 Hemochromatosis 83 0.045
189
BHC002 Behcet's Disease 79 0.045
190
c BTT002 Beta Thalassemia 78 0.045
191
LVR012 Liver Cirrhosis 77 0.045
192
c LPS004 Lupus Erythematosus 77 0.045
193
P FML018 Familial Mediterranean Fever 76 0.045
194
HST011 Histoplasmosis 73 0.045
195
c HYP095 Hypercholesterolemia 73 0.045
196
c THL005 Thalassemia 72 0.045
197
ACQ007 Acquired Immunodeficiency Syndrome 71 0.045
198
GTL001 Gitelman Syndrome 70 0.045
199
c ACT074 Acute Lymphocytic Leukemia 70 0.045
200
c MTR004 Maturity-Onset Diabetes of the Young 70 0.045
201
MYC006 Mycosis Fungoides 69 0.045
202
c HYP086 Hypothyroidism 69 0.045
203
ART021 Arteriosclerosis 68 0.045
204
P CHR089 Chronic Kidney Failure 66 0.045
205
THR079 Thromboembolism 66 0.045
206
c HYP069 Hyperparathyroidism 65 0.045
207
STR067 Stroke, Ischemic 65 0.045
208
CLT003 Colitis 64 0.045
209
PLM001 Pulmonary Tuberculosis 61 0.045
210
P SCL015 Scleritis 61 0.045
211
c ATM011 Autoimmune Hepatitis 61 0.045
212
c ACT075 Acute Myocardial Infarction 60 0.045
213
LPD010 Lipodystrophy 59 0.045
214
P SYP003 Syphilis 58 0.045
215
ISC006 Ischemic Heart Disease 58 0.045
216
CHR001 Churg-Strauss Syndrome 58 0.045
217
P HMR012 Hemorrhagic Fever 58 0.045
218
HYP266 Hypoxia 58 0.045
219
SPN051 Spondylitis 58 0.045
220
HMS001 Hemosiderosis 57 0.045
221
PLS011 Plasmacytoma 57 0.045
222
DBT008 Diabetic Angiopathy 57 0.045
223
P PRP023 Peripheral Neuropathy 52 0.045
224
P GND004 Gonadal Dysgenesis 51 0.045
225
P SZR006 Seizure Disorder 51 0.045
226
LYM021 Lymphadenitis 48 0.045
227
SCH016 Schimke Immunoosseous Dysplasia 47 0.045
228
URT010 Ureteral Obstruction 47 0.045
229
P HYP111 Hyperprolinemia 46 0.045
230
DFF024 Diffuse Panbronchiolitis 46 0.045
231
EPL002 Epilepsy Syndrome 46 0.045
232
ART004 Aortic Atherosclerosis 46 0.045
233
P SPN052 Spondyloarthropathy 46 0.045
234
HRS011 Horseshoe Kidney 45 0.045
235
NRN002 Neuronitis 44 0.045
236
TTR016 Tetra-Amelia Syndrome 42 0.045
237
LMY003 Leiomyomatosis 40 0.045
238
ART012 Aortitis 39 0.045
239
VRL011 Viral Infectious Disease 39 0.045
240
ADS002 Adie Syndrome 35 0.045
241
MDL019 Medullary Cystic Kidney Disease Type 1 35 0.045
242
ADT003 Auditory System Disease 30 0.045
243
HNM002 Hinman Syndrome 28 0.045
244
CLL035 Collagen Type Iii Glomerulopathy 7 0.045
245
P ALZ001 Alzheimer's Disease 100 0.037
246
P APL001 Aplastic Anemia 83 0.037
247
CNG034 Congestive Heart Failure 78 0.037
248
CRH001 Crohn's Disease 76 0.037
249
GLN003 Glanzmann's Thrombasthenia 74 0.037
250
BLS001 Blau Syndrome 73 0.037
251
RLP001 Relapsing Polychondritis 72 0.037
252
P DRM010 Dermatomyositis 71 0.037
253
GLL008 Gilles De La Tourette Syndrome 71 0.037
254
c THR014 Thrombocytopenia 71 0.037
255
SPS077 Sepsis 70 0.037
256
P RTH001 Rothmund-Thomson Syndrome 70 0.037
257
P CNG401 Congenital Heart Disease 69 0.037
258
c MNN013 Meningitis 68 0.037
259
P BLD042 Bladder Carcinoma 68 0.037
260
PRP027 Peripheral Vascular Disease 68 0.037
261
ACT049 Acute Disseminated Encephalomyelitis 67 0.037
262
P HYP117 Hypertriglyceridemia 67 0.037
263
P ATM003 Autoimmune Thyroiditis 67 0.037
264
P PRT013 Portal Hypertension 66 0.037
265
P GST044 Gastritis 66 0.037
266
STT001 Status Epilepticus 66 0.037
267
TTN003 Tetanus 65 0.037
268
MXD005 Mixed Connective Tissue Disease 64 0.037
269
DFC004 Deficiency Anemia 63 0.037
270
WLL006 Wells Syndrome 63 0.037
271
SCK005 Sickle Cell Disease 62 0.037
272
GLC003 Glucose Intolerance 62 0.037
273
c TYR004 Tyrosinemia 62 0.037
274
ESN015 Eosinophilic Fasciitis 61 0.037
275
GNG013 Gingivitis 61 0.037
276
RNL015 Renal Hypertension 61 0.037
277
c ANG015 Angioedema 61 0.037
278
ACR008 Acrocallosal Syndrome 60 0.037
279
c GLY013 Glycogen Storage Disease 60 0.037
280
c SLP006 Sleep Apnea 59 0.037
281
c THR005 Thrombotic Thrombocytopenic Purpura 59 0.037
282
ANR004 Anuria 59 0.037
283
P RNL028 Renal Tubular Dysgenesis 59 0.037
284
OBS061 Obstructive Sleep Apnea 58 0.037
285
P SDR002 Siderosis 58 0.037
286
GLB015 Glioblastoma Multiforme 58 0.037
287
RCT015 Reactive Arthritis 57 0.037
288
SCN006 Secondary Syphilis 57 0.037
289
ANK001 Ankylosis 57 0.037
290
RNL007 Renal Tubular Acidosis 57 0.037
291
BLS002 Blastomycosis 57 0.037
292
PST041 Posterior Urethral Valves 56 0.037
293
DDN006 Duodenitis 56 0.037
294
PRR002 Pure Red-Cell Aplasia 56 0.037
295
MSN001 Mesangial Proliferative Glomerulonephritis 56 0.037
296
PSD002 Pseudotumor Cerebri 55 0.037
297
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 55 0.037
298
c HRM001 Hermansky-Pudlak Syndrome 55 0.037
299
P DWR001 Dwarfism 55 0.037
300
FRS002 Frasier Syndrome 55 0.037
301
URT001 Urethritis 55 0.037
302
c ANT034 Anterior Uveitis 54 0.037
303
P LDD002 Liddle Syndrome 54 0.037
304
PRN011 Pernicious Anemia 53 0.037
305
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.037
306
c HYD002 Hydronephrosis 52 0.037
307
GNG012 Gingival Overgrowth 52 0.037
308
LPT002 Lipoatrophic Diabetes 51 0.037
309
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 51 0.037
310
XLN068 X-Linked Thrombocytopenia 51 0.037
311
P GRV001 Graves' Disease 51 0.037
312
ACT040 Acute Poststreptococcal Glomerulonephritis 50 0.037
313
c PSD003 Pseudohypoaldosteronism 49 0.037
314
RTN018 Retinal Disease 49 0.037
315
PYM001 Pyomyositis 48 0.037
316
CHY006 Chylous Ascites 48 0.037
317
CRT008 Carotid Artery Dissection 48 0.037
318
ANG054 Angina Pectoris 47 0.037
319
GNG008 Ganglioneuroblastoma 47 0.037
320
SPL018 Splenomegaly 47 0.037
321
MNN009 Meningoencephalitis 47 0.037
322
LYM012 Lymphoplasmacytic Lymphoma 46 0.037
323
GLM037 Glioma Somatic 46 0.037
324
FSC004 Fasciitis 46 0.037
325
BRB001 Beriberi 45 0.037
326
ILS001 Ileus 45 0.037
327
c ACT004 Acute Diarrhea 44 0.037
328
LYM029 Lymphedema-Distichiasis Syndrome 44 0.037
329
c SNR001 Senior-Loken Syndrome 44 0.037
330
CYT008 Cytomegalovirus Infection 44 0.037
331
CLL002 Collecting Duct Carcinoma 44 0.037
332
MYC019 Mycobacterium Marinum 43 0.037
333
HYP008 Hypertensive Retinopathy 43 0.037
334
TBL013 Tubulointerstitial Nephritis and Uveitis 43 0.037
335
c NPH048 Nephronophthisis 1, Juvenile 42 0.037
336
c CNG033 Congenital Syphilis 41 0.037
337
HPT063 Hepatitis B Virus Infection 39 0.037
338
CRB086 Cerebral Aneurysms 39 0.037
339
HYP226 Hyporeninemic Hypoaldosteronism 38 0.037
340
ART010 Arteriolosclerosis 38 0.037
341
CLS016 Clostridium Difficile Colitis 37 0.037
342
PRP080 Peripheral Artery Disease 36 0.037
343
PLM074 Pulmonary Function 34 0.037
344
c JVN041 Juvenile Nephronophthisis 34 0.037
345
BLD039 Bladder Adenocarcinoma 34 0.037
346
P ATM020 Autoimmune Enteropathy 31 0.037
347
TFT003 Tufting Enteropathy 28 0.037
348
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.037
349
IMM001 Immune-Complex Glomerulonephritis 27 0.037
350
C4B001 C4b Deficiency 26 0.037
351
c NPH019 Nephronophthisis 1 25 0.037
352
PRN007 Perinephritis 24 0.037
353
P GLM015 Glomerulopathy with Fibronectin Deposits 2 23 0.037
354
HVY003 Heavy Chain Deposition Disease 20 0.037
355
C4D002 C4a Deficiency 17 0.037
356
LGH014 Light and Heavy Chain Deposition Disease 15 0.037
357
LNP001 Loin Pain Hematuria Syndrome 13 0.037
358
HRD064 Hereditary Vascular Retinopathy 9 0.037
359
P PRS040 Prostate Cancer 98 0.026
360
HDG007 Hodgkin's Lymphoma 93 0.026
361
KPS001 Kaposi's Sarcoma 87 0.026
362
P RTN008 Retinitis Pigmentosa 86 0.026
363
P FML021 Familial Hypercholesterolemia 86 0.026
364
MRF001 Marfan Syndrome 85 0.026
365
INF030 Infectious Mononucleosis 84 0.026
366
ACR007 Acromegaly 80 0.026
367
THR006 Thromboangiitis Obliterans 79 0.026
368
P MTH008 Methylmalonic Acidemia 79 0.026
369
P PRC016 Pre-Eclampsia 78 0.026
370
LSC001 Lesch-Nyhan Syndrome 78 0.026
371
P PNM007 Pneumonia 78 0.026
372
P PRM021 Primary Pulmonary Hypertension 77 0.026
373
LRN002 Laron Syndrome 77 0.026
374
CRB011 Cerebrotendinous Xanthomatosis 76 0.026
375
KWS002 Kawasaki Disease 76 0.026
376
P PRP003 Porphyria Cutanea Tarda 75 0.026
377
c MYL006 Myeloid Leukemia 75 0.026
378
P SRC013 Sarcoidosis 75 0.026
379
P ALP006 Alpha Thalassemia 75 0.026
380
P MST009 Mastocytosis 75 0.026
381
P LYM007 Lymphangioleiomyomatosis 74 0.026
382
P WGN002 Wegener's Granulomatosis 74 0.026
383
P PRM006 Primary Biliary Cirrhosis 73 0.026
384
c CHR065 Chronic Myeloid Leukemia 73 0.026
385
c PLM037 Pulmonary Hypertension 73 0.026
386
P CLC005 Celiac Disease 73 0.026
387
P PRD006 Prader-Willi Syndrome 72 0.026
388
WRN001 Werner Syndrome 72 0.026
389
P PRM005 Primary Hyperparathyroidism 71 0.026
390
ART016 Aortic Aneurysm 71 0.026
391
P WLF004 Wolfram Syndrome 70 0.026
392
P MTB001 Metabolic Syndrome X 70 0.026
393
NPH007 Nephrogenic Diabetes Insipidus 70 0.026
394
P KDN017 Kidney Cancer 70 0.026
395
BLL006 Bullous Pemphigoid 70 0.026
396
P CNG368 Congenital Adrenal Hyperplasia 70 0.026
397
RNL002 Renal Agenesis 70 0.026
398
PLY017 Polyarteritis Nodosa 69 0.026
399
THR016 Thrombophlebitis 69 0.026
400
P RCK004 Rickets 68 0.026
401
P PLY011 Polycystic Ovary Syndrome 68 0.026
402
P CMR001 Camurati-Engelmann Disease 68 0.026
403
PSD007 Pseudomyxoma Peritonei 68 0.026
404
P HYD006 Hydrocephalus 68 0.026
405
MRB003 Morbid Obesity 68 0.026
406
PSD012 Pseudoachondroplasia 68 0.026
407
P SHR002 Short Stature 68 0.026
408
P BCK002 Beckwith-Wiedemann Syndrome 68 0.026
409
PLS006 Plasmodium Vivax Malaria 68 0.026
410
CMM004 Common Variable Immunodeficiency 67 0.026
411
P THR015 Thrombophilia 67 0.026
412
P PND002 Pendred Syndrome 67 0.026
413
DMN002 Dementia 67 0.026
414
P HRD011 Hereditary Spherocytosis 67 0.026
415
PYR013 Pyruvate Kinase Deficiency 67 0.026
416
GST009 Gastroschisis 66 0.026
417
c JVN010 Juvenile Rheumatoid Arthritis 66 0.026
418
c HML002 Hemolytic Anemia 66 0.026
419
PHR003 Pharyngitis 66 0.026
420
P HRD057 Hereditary Pancreatitis 66 0.026
421
GST034 Gastroesophageal Reflux Disease 66 0.026
422
P SYS005 Systemic Scleroderma 66 0.026
423
DBT001 Diabetic Ketoacidosis 66 0.026
424
P FML020 Familial Combined Hyperlipidemia 66 0.026
425
c ENC004 Encephalitis 66 0.026
426
P PSD087 Pseudoxanthoma Elasticum 66 0.026
427
ULC004 Ulcerative Colitis 65 0.026
428
P GRF002 Graft Versus Host Disease 65 0.026
429
c SCL016 Scleroderma 65 0.026
430
P PRG006 Progressive Supranuclear Palsy 65 0.026
431
HYP004 Hypercalcemia 65 0.026
432
LYS003 Lysinuric Protein Intolerance 65 0.026
433
c VRL010 Viral Hepatitis 64 0.026
434
FCT006 Factor V Deficiency 64 0.026
435
EXT034 Extrinsic Allergic Alveolitis 64 0.026
436
c GLL020 Gallbladder Disease 64 0.026
437
URT039 Urticaria 64 0.026
438
P ESP024 Esophagitis 64 0.026
439
P HST010 Histiocytosis 64 0.026
440
CRN018 Coronary Artery Anomaly 63 0.026
441
LRN003 Learning Disability 63 0.026
442
SPN027 Spinal Stenosis 63 0.026
443
P MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.026
444
P ACT101 Acute Lymphoblastic Leukemia 63 0.026
445
P MTR012 Mitral Valve Disease 63 0.026
446
P ANP001 Anaplastic Large Cell Lymphoma 63 0.026
447
ALP007 Alpha 1-Antitrypsin Deficiency 62 0.026
448
PRT092 Partial Androgen Insensitivity Syndrome 62 0.026
449
OCC006 Occipital Horn Syndrome 62 0.026
450
P ATY010 Atypical Hemolytic-Uremic Syndrome 62 0.026
451
ART031 Aortic Coarctation 62 0.026
452
TRN001 Transthyretin Amyloidosis 62 0.026
453
LDD001 Ladd Syndrome 62 0.026
454
NRM002 Normal Pressure Hydrocephalus 62 0.026
455
P ATM010 Autoimmune Hemolytic Anemia 62 0.026
456
c FML012 Familial Partial Lipodystrophy 62 0.026
457
DWN001 Down Syndrome 62 0.026
458
ACT105 Acute Mountain Sickness 61 0.026
459
DBT010 Diabetic Neuropathy 61 0.026
460
c AGM001 Agammaglobulinemia 61 0.026
461
P PLY019 Polyneuropathy 61 0.026
462
P PPL005 Papillary Renal Cell Carcinoma 61 0.026
463
c ALM001 Al Amyloidosis 61 0.026
464
VTL002 Vitiligo 61 0.026
465
CRN017 Coronary Thrombosis 60 0.026
466
c ACT071 Acute Kidney Failure 60 0.026
467
PRS047 Prostatitis 60 0.026
468
MLL005 Miller-Dieker Syndrome 60 0.026
469
OLG003 Oligohydramnios 60 0.026
470
P CNG013 Congenital Disorder of Glycosylation Type I 60 0.026
471
c HMP002 Hemophagocytic Lymphohistiocytosis 60 0.026
472
SND002 Sneddon Syndrome 60 0.026
473
P MLS001 Melas Syndrome 60 0.026
474
PMP001 Pemphigus 60 0.026
475
P PRM054 Primary Sclerosing Cholangitis 60 0.026
476
FBR032 Fibromuscular Dysplasia 60 0.026
477
MLR002 Miliary Tuberculosis 60 0.026
478
MLT001 Multiple Chemical Sensitivity 60 0.026
479
P AVS004 Avascular Necrosis of the Femoral Head 59 0.026
480
c SYS004 Systemic Mastocytosis 59 0.026
481
P MTR005 Mitral Valve Prolapse 59 0.026
482
P ANT058 Anterior Ischemic Optic Neuropathy 59 0.026
483
DST005 Diastrophic Dysplasia 59 0.026
484
PPL002 Papillary Carcinoma 59 0.026
485
c LCL006 Localized Scleroderma 59 0.026
486
P PRM124 Primary Hyperoxaluria Type 1 59 0.026
487
CLD007 Cold Agglutinin Disease 59 0.026
488
TWN003 Townes-Brocks Syndrome 59 0.026
489
YLL002 Yellow Fever 59 0.026
490
BCT004 Bacteriuria 59 0.026
491
GLC002 Glucocorticoid-Remediable Aldosteronism 59 0.026
492
PLY041 Polymyositis 59 0.026
493
CNN005 Connective Tissue Disease 58 0.026
494
HDC001 Headache 58 0.026
495
GLC012 Galactosialidosis 58 0.026
496
P HRM005 Hermansky-Pudlak Syndrome 1 58 0.026
497
NNS002 Nonspecific Interstitial Pneumonia 58 0.026
498
SCR002 Scurvy 58 0.026
499
URN010 Urinary Tract Obstruction 58 0.026
500
FLL008 Folliculitis 58 0.026
501
P DBT005 Diabetes Insipidus 58 0.026
502
P INT068 Intestinal Disease 58 0.026
503
BRN029 Brain Disease 58 0.026
504
c HRD002 Hereditary Angioedema 58 0.026
505
c HYP065 Hyperaldosteronism 58 0.026
506
P SNS014 Sinusitis 58 0.026
507
c CNT016 Central Retinal Vein Occlusion 58 0.026
508
P PSR001 Psoriatic Arthritis 58 0.026
509
BRN071 Brain Injury 58 0.026
510
c RTN014 Retinal Artery Occlusion 58 0.026
511
P CNG095 Congenital Generalized Lipodystrophy Type 2 58 0.026
512
LYS001 Loeys-Dietz Syndrome 57 0.026
513
IRN001 Iron Deficiency Anemia 57 0.026
514
SMT015 Smith Magenis Syndrome 57 0.026
515
ACT017 Acute Chest Syndrome 57 0.026
516
EXF001 Exfoliation Syndrome 57 0.026
517
PLS007 Plasmodium Falciparum Malaria 57 0.026
518
ALP008 Alopecia 57 0.026
519
c HPT015 Hepatitis D 57 0.026
520
c CTR002 Cataract 57 0.026
521
SCH002 Schnitzler Syndrome 57 0.026
522
DFF003 Diffuse Scleroderma 57 0.026
523
c ISC002 Ischemic Optic Neuropathy 57 0.026
524
CNG048 Congenital Hepatic Fibrosis 57 0.026
525
LDP002 Lead Poisoning 57 0.026
526
APH001 Aphthous Stomatitis 56 0.026
527
c FML035 Familial Hyperlipidemia 56 0.026
528
PRT011 Protein C Deficiency 56 0.026
529
P JBR004 Joubert Syndrome 2 56 0.026
530
CLC001 Calciphylaxis 56 0.026
531
ART017 Aortic Disease 56 0.026
532
STV001 Stevens-Johnson Syndrome 56 0.026
533
VLV044 Vulvar Intraepithelial Neoplasia 56 0.026
534
P HYP090 Hyperalphalipoproteinemia 56 0.026
535
c TRM003 Tremor 56 0.026
536
MCR088 Microscopic Polyangiitis 56 0.026
537
P DNT039 Dent's Disease 56 0.026
538
DST006 Diastolic Heart Failure 55 0.026
539
ACN001 Acinar Cell Carcinoma 55 0.026
540
TYP013 Type 1 Von Willebrand Disease 55 0.026
541
PLY020 Polyradiculoneuropathy 55 0.026
542
INC001 Incontinentia Pigmenti Achromians 55 0.026
543
c ART070 Aortic Valve Disease 55 0.026
544
P CHL066 Cholangitis 55 0.026
545
RYS001 Reye Syndrome 55 0.026
546
MDL009 Medullary Sponge Kidney 55 0.026
547
c PSD015 Pseudohypoparathyroidism 55 0.026
548
PRT058 Pure Autonomic Failure 55 0.026
549
P TWN001 Twin-to-Twin Transfusion Syndrome 55 0.026
550
DBT006 Diabetic Macular Edema 54 0.026
551
c ACR001 Aicardi-Goutieres Syndrome 54 0.026
552
CHR008 Choroiditis 54 0.026
553
PST062 Pustulosis Palmaris Et Plantaris 54 0.026
554
c FML016 Familial Hypertriglyceridemia 54 0.026
555
CNS004 Constipation 54 0.026
556
ONC003 Oncogenic Osteomalacia 54 0.026
557
GST045 Gastroenteritis 54 0.026
558
WLL001 Williams-Beuren Syndrome 54 0.026
559
P PLM006 Pulmonary Alveolar Proteinosis 53 0.026
560
CCH002 Coach Syndrome 53 0.026
561
HNT002 Hantavirus Pulmonary Syndrome 53 0.026
562
PLY013 Polymyalgia Rheumatica 53 0.026
563
c LYM025 Lymphedema 53 0.026
564
YLL001 Yellow Nail Syndrome 53 0.026
565
PRP002 Periapical Granuloma 53 0.026
566
c CNG012 Congenital Generalized Lipodystrophy 53 0.026
567
P TXC012 Toxic Epidermal Necrolysis 53 0.026
568
NM001 Noma 53 0.026
569
c HPT007 Hepatitis E 53 0.026
570
RSD004 Rosai-Dorfman Disease 53 0.026
571
OBS006 Obstructive Lung Disease 53 0.026
572
RFL001 Reflex Sympathetic Dystrophy 52 0.026
573
CNG064 Congenital Chloride Diarrhea 52 0.026
574
NNL002 Nonalcoholic Steatohepatitis 52 0.026
575
OBS029 Obesity, Association with 52 0.026
576
FML164 Familial Hdl Deficiency 52 0.026
577
USL001 Usual Interstitial Pneumonia 52 0.026
578
PLS025 Plasmablastic Lymphoma 52 0.026
579
CTS005 Catastrophic Antiphospholipid Syndrome 52 0.026
580
MYC005 Myocardial Stunning 52 0.026
581
HYP121 Hypoalphalipoproteinemia 52 0.026
582
MNT147 Mental Retardation 52 0.026
583
ALC009 Alcoholic Liver Cirrhosis 52 0.026
584
MCL003 Macular Holes 52 0.026
585
P ORT004 Orthostatic Intolerance 52 0.026
586
AMY053 Amyloidosis, Secondary 52 0.026
587
RNL011 Renal Osteodystrophy 51 0.026
588
P CTN015 Cutaneous T Cell Lymphoma 51 0.026
589
KMR001 Kimura Disease 51 0.026
590
P ART028 Aortic Aneurysm, Familial Thoracic 4 51 0.026
591
APP001 Apparent Mineralocorticoid Excess Syndrome 51 0.026
592
DRG002 Drug-Induced Hepatitis 51 0.026
593
LKD001 Leukodystrophy 51 0.026
594
STM007 Stomatitis 51 0.026
595
PSD009 Pseudohermaphroditism 51 0.026
596
PLC007 Placental Abruption 51 0.026
597
NNT024 Neonatal Stroke 51 0.026
598
OCL020 Ocular Cicatricial Pemphigoid 51 0.026
599
c ATM024 Autoimmune Pancreatitis 50 0.026
600
c HYP011 Hyperlipoproteinemia Type Iii 50 0.026
601
HYP006 Hypertensive Heart Disease 50 0.026
602
HYP005 Hypokalemia 50 0.026
603
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 50 0.026
604
BRN106 Burns 50 0.026
605
c SCL009 Sclerosing Cholangitis 50 0.026
606
CHY002 Chylomicron Retention Disease 49 0.026
607
SPN119 Spondylarthropathy 49 0.026
608
ALC010 Alcoholic Cardiomyopathy 49 0.026
609
RNL097 Renal Artery Disease 49 0.026
610
DBT002 Diabetic Autonomic Neuropathy 49 0.026
611
RNL006 Renal Glycosuria 49 0.026
612
PLS016 Plasma Cell Leukemia 49 0.026
613
CRT049 Critical Limb Ischemia 49 0.026
614
ADR027 Adrenocortical Insufficiency 49 0.026
615
HYP017 Hypophosphatemia 49 0.026
616
DFF021 Diffuse Mesangial Sclerosis 49 0.026
617
HMC014 Homocysteinemia 49 0.026
618
PRN038 Prune Belly Syndrome 49 0.026
619
NSP002 Nasopharyngitis 48 0.026
620
MNN021 Meningococcemia 48 0.026
621
LPD008 Lipid Metabolism Disorder 48 0.026
622
CRN027 Corneal Neovascularization 48 0.026
623
LPP002 Lipoprotein Glomerulopathy 48 0.026
624
CNS002 Constrictive Pericarditis 48 0.026
625
c GGN002 Gigantism 48 0.026
626
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 48 0.026
627
c PRN026 Porencephaly 48 0.026
628
CNN003 Conn's Syndrome 48 0.026
629
c RNL078 Renal Dysplasia 48 0.026
630
FVS001 Favism 48 0.026
631
PTY003 Pityriasis Rubra Pilaris 47 0.026
632
ART035 Arterial Calcification of Infancy 47 0.026
633
CRT004 Carotid Artery Thrombosis 47 0.026
634
CRB008 Cerebral Atherosclerosis 47 0.026
635
P SNR003 Senior-Loken Syndrome 1 47 0.026
636
P ATN005 Autonomic Dysfunction 47 0.026
637
P CRT018 Carotid Intimal Medial Thickness 47 0.026
638
HPT025 Hepatic Lipase Deficiency 47 0.026
639
DFN221 Deafness Dystonia Syndrome 47 0.026
640
CRB001 Cerebral Lymphoma 46 0.026
641
P BRS044 Breast Adenocarcinoma 46 0.026
642
BRN105 Burn Scar 46 0.026
643
LWR010 Low Renin Hypertension 46 0.026
644
MCR018 Microcytic Anemia 46 0.026
645
EVN001 Evans' Syndrome 46 0.026
646
PST055 Postural Hypotension 46 0.026
647
PMP004 Pemphigus Foliaceus 46 0.026
648
BWN003 Bowenoid Papulosis 46 0.026
649
c ACQ022 Acquired Generalized Lipodystrophy 46 0.026
650
IDP011 Idiopathic Interstitial Pneumonia 46 0.026
651
MYC033 Myoclonus 45 0.026
652
URT031 Ureteral Disease 45 0.026
653
ART110 Arteritic Anterior Ischemic Optic Neuropathy 45 0.026
654
NRM003 Norum Disease 45 0.026
655
CMP009 Complement Deficiency 45 0.026
656
HYP001 Hypochromic Microcytic Anemia 45 0.026
657
c LTT001 Lattice Corneal Dystrophy 45 0.026
658
CRP018 Cor Pulmonale 45 0.026
659
SHR071 Short-Rib Thoracic Dysplasia 11 with or Without Polydactyly 45 0.026
660
UNL007 Unilateral Renal Agenesis 45 0.026
661
FBR063 Fibrocalculous Pancreatic Diabetes 45 0.026
662
MRC003 Mercury Poisoning 45 0.026
663
c PLY083 Polycystic Kidney Disease, Type 1 45 0.026
664
ESN011 Eisenmenger Syndrome 45 0.026
665
PLC005 Placental Insufficiency 44 0.026
666
MCR001 Microcystic Meningioma 44 0.026
667
P RTN016 Retinal Degeneration 44 0.026
668
NCR002 Necrobiosis Lipoidica 44 0.026
669
P HYP216 Hypoparathyroidism Familial Isolated 43 0.026
670
RNL029 Renal Coloboma Syndrome 43 0.026
671
LYS015 Loeys-Dietz Syndrome, Type 1 43 0.026
672
P PRG011 Progressive Myoclonus Epilepsy 43 0.026
673
HMF004 Hemifacial Spasm 43 0.026
674
c ACT042 Acute Pyelonephritis 43 0.026
675
P SLD005 Sialidosis Type I 43 0.026
676
c CHR417 Chronic Graft Versus Host Disease 43 0.026
677
c HYP057 Hypervitaminosis D 43 0.026
678
DFC001 Defective Apolipoprotein B-100 43 0.026
679
DBT007 Diabetic Cataract 43 0.026
680
LRW002 Leri Weill Dyschondrosteosis 43 0.026
681
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 43 0.026
682
INT071 Intestinal Perforation 42 0.026
683
MNG006 Monogenic Diabetes 42 0.026
684
RTN020 Retinal Vascular Disease 41 0.026
685
MNN034 Mannose-Binding Lectin Deficiency 41 0.026
686
GST040 Gastric Adenocarcinoma 41 0.026
687
CMP042 Complement Factor H Deficiency 41 0.026
688
AMR003 Amaurosis Fugax 41 0.026
689
INP001 Inappropriate Adh Syndrome 41 0.026
690
c TRN016 Transient Hypogammaglobulinemia 40 0.026
691
SRS007 Sorsby Fundus Dystrophy 40 0.026
692
ANG046 Angioimmunoblastic T-Cell Lymphoma 40 0.026
693
HYP574 Hypercholesterolemia, Familial, Modifier of 40 0.026
694
HYP456 Hyperapobetalipoproteinemia 40 0.026
695
LPD014 Lipodermatosclerosis 40 0.026
696
DNN002 Donnai-Barrow Syndrome 40 0.026
697
CHR413 Chronic Myocardial Ischemia 39 0.026
698
P EPD044 Epidermolysis Bullosa Dystrophica, Ar 39 0.026
699
P TRN009 Transient Hypogammaglobulinemia of Infancy 39 0.026
700
CRB085 Cerebral Hemorrhage 39 0.026
701
c HVY001 Heavy Chain Disease 39 0.026
702
c MLR021 Malaria, Severe 39 0.026
703
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 39 0.026
704
HMG010 Hemoglobinemia 39 0.026
705
ADP002 Adiponectin Deficiency 39 0.026
706
ENC011 Encephalomyopathy 39 0.026
707
c OBS047 Obesity, Early-Onset 39 0.026
708
CYS024 Cystinosis, Ocular Nonnephropathic 38 0.026
709
CRN127 Coronary Artery Disease in Familial Hypercholesterolemia, Protection Against 38 0.026
710
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.026
711
JBR007 Joubert Syndrome with Renal Anomalies 38 0.026
712
OCL022 Ocular Melanoma 38 0.026
713
c OBS016 Obesity, Late-Onset 38 0.026
714
SPS057 Spasticity 38 0.026
715
OBS019 Obesity, Variation in 37 0.026
716
c HYP296 Hypercholesterolemia, Familial, Due to Ldlr Defect, Modifier of 37 0.026
717
OBS024 Obesity, Mild, Early-Onset 37 0.026
718
OBS023 Obesity, Autosomal Dominant 37 0.026
719
OBS031 Obesity, Severe, and Type Ii Diabetes 37 0.026
720
IPX001 Ipex Syndrome 37 0.026
721
c FML162 Familial Mediterranean Fever, Ad 37 0.026
722
EPP006 Epiphyseal Dysplasia Multiple with Early-Onset Diabetes Mellitus 37 0.026
723
c FML187 Familial Hypertension 36 0.026
724
C1Q001 C1q Deficiency 36 0.026
725
LNR006 Linear Iga Disease 36 0.026
726
c MYC026 Myoclonus Epilepsy 36 0.026
727
RNL012 Renal Tuberculosis 36 0.026
728
C3D001 C3 Deficiency 36 0.026
729
LDL001 Ldl Cholesterol Level Qtl2 36 0.026
730
P RNL042 Renal Hypouricemia 36 0.026
731
DYS070 Dysalbuminemic Hyperthyroxinemia 36 0.026
732
P AMY038 Amyloidosis, Renal 35 0.026
733
HYP264 Hypertonia 35 0.026
734
HYP034 Hypertensive Encephalopathy 35 0.026
735
INF133 Inferior Vena Cava Interruption 35 0.026
736
FCT013 Factor V Leiden Thrombophilia 34 0.026
737
HMG020 Hmg Coa Lyase Deficiency 33 0.026
738
P PLN008 Peeling Skin Syndrome 33 0.026
739
NTR005 Nutritional Deficiency Disease 33 0.026
740
IDP033 Idiopathic Edema 32 0.026
741
CHR476 Chronic Angina 32 0.026
742
ACD004 Acdc 31 0.026
743
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.026
744
c CHR096 Chronic Pulmonary Heart Disease 31 0.026
745
URT036 Urethral Obstruction 31 0.026
746
CHL109 Childhood Apraxia of Speech 31 0.026
747
c NPH032 Nephronophthisis 4 31 0.026
748
NRG005 Neurogenic Hypertension 31 0.026
749
MYC035 Myocardial Infarction Susceptibility 31 0.026
750
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 30 0.026
751
SBL004 Sea-Blue Histiocytosis 29 0.026
752
AMY034 Amyloidosis, 3 or More Types 29 0.026
753
c CNG192 Congenital Disorder of Glycosylation, Type Ik 28 0.026
754
PYR004 Pyuria 28 0.026
755
GST007 Gastric Dilatation 28 0.026
756
CHL070 Cholesterol Embolism 28 0.026
757
MDR006 Moderate and Severe Traumatic Brain Injury 28 0.026
758
IRN002 Iron Metabolism Disease 28 0.026
759
PRD019 Periodic Fever, Familial 27 0.026
760
c DYS055 Dystonia 10 27 0.026
761
PRD012 Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis 27 0.026
762
HFS001 Hfe-Associated Hereditary Hemochromatosis 27 0.026
763
KRN001 Korean Hemorrhagic Fever 27 0.026
764
P PPL026 Papular Mucinosis 26 0.026
765
PL2001 Pla2g6-Associated Neurodegeneration 25 0.026
766
PRX022 Paroxysmal Choreoathetosis 25 0.026
767
ANT030 Antecubital Pterygium 25 0.026
768
P ALP005 Alpha Chain Disease 25 0.026
769
MCR062 Microcephaly, Hiatal Hernia and Nephrotic Syndrome 24 0.026
770
CNG116 Congenital Nephrotic Syndrome Finnish Type 24 0.026
771
PSD062 Pseudoxanthoma Elasticum, Modifier of Severity of 24 0.026
772
EPD034 Epidermolysis Bullosa, Pretibial 24 0.026
773
GRD004 Gardner-Diamond Syndrome 24 0.026
774
KRY002 Karyomegalic Interstitial Nephritis 24 0.026
775
STR080 Stroke, Hemorrhagic 23 0.026
776
HFH001 Hfe Hemochromatosis, Modifier of 23 0.026
777
c PST008 Posterior Scleritis 22 0.026
778
FML268 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes 22 0.026
779
PCM002 Pauci-Immune Glomerulonephritis 22 0.026
780
VRS001 Virus Associated Hemophagocytic Syndrome 21 0.026
781
c AML044 Amelogenesis Imperfecta, Type Ig 21 0.026
782
PRM041 Primary Cortisol Resistance 21 0.026
783
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 21 0.026
784
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 21 0.026
785
HYP281 Hypoproteinemia, Hypercatabolic 21 0.026
786
ESN004 Eosinophilic Gastritis 20 0.026
787
HPR001 Hprt-Related Gout 20 0.026
788
PRP033 Properdin Deficiency 19 0.026
789
c DMN011 Dominant Dystrophic Epidermolysis Bullosa 19 0.026
790
DHL001 Dahlberg Borer Newcomer Syndrome 18 0.026
791
ANP010 Anaplastic Plasmacytoma 18 0.026
792
RTN163 Retinal Arterial Tortuosity 18 0.026
793
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 17 0.026
794
PLS008 Plasmodium Malariae Malaria 16 0.026
795
KDN006 Kidney Papillary Necrosis 16 0.026
796
C9D001 C9 Deficiency 14 0.026
797
DYS034 Dyschondrosteosis Nephritis 14 0.026
798
ALD004 Ala Dehydratase Deficiency 12 0.026
799
IND008 Indomethacin Embryofetopathy 12 0.026
800
DFN014 Deafness Nephritis Anorectal Malformation 12 0.026
801
GLM024 Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria 11 0.026
802
CNG330 Congenital Megacalycosis 9 0.026
803
CL4001 Col4a1-Related Disorders 8 0.026
804
CRM007 Crome Syndrome 7 0.026
805
EXD002 Exudative Glomerulonephritis 7 0.026