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

898 hits were found for 'nephropathy'

# ++ Fam MCID Name MIFTS Score
1
BLK001 Balkan Nephropathy 37 4.557
2
DBT061 Diabetic Nephropathy 50 4.507
3
P MMB002 Membranous Glomerulonephritis 56 4.157
4
c HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 12 3.749
5
UMD001 Umod-Associated Kidney Disease 24 3.743
6
GTY001 Gouty Nephropathy, Familial 7 3.743
7
P FML044 Familial Juvenile Hyperuricemic Nephropathy Type 2 10 3.430
8
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 12 3.403
9
ACT043 Acute Urate Nephropathy 23 3.174
10
IGG001 Iga Glomerulonephritis 39 3.160
11
c BKV001 Bk-Virus Nephropathy 7 3.152
12
NPH037 Nephronophthisis-Like Nephropathy 1 10 3.106
13
HYP114 Hypertensive Nephropathy 34 3.008
14
FML076 Familial Juvenile Hyperuricaemic Nephropathy 22 2.985
15
c FML022 Familial Juvenile Hyperuricemic Nephropathy 31 2.946
16
RNR002 Ren-Related Kidney Disease 18 2.895
17
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 17 2.828
18
P ANG055 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle 11 2.810
19
NPH016 Nephropathy-Hypertension 33 2.717
20
DNY001 Denys-Drash Syndrome 58 2.485
21
PLY043 Polyomavirus Allograft Nephropathy 5 2.485
22
AMY037 Amyloidosis, Hereditary Renal 29 2.442
23
MLT033 Multicentric Osteolysis Nephropathy 5 2.442
24
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 13 2.419
25
ATH009 Atherosclerosis - Deafness - Diabetes - Epilepsy - Nephropathy 11 2.419
26
CTR091 Cataract - Nephropathy - Encephalopathy 9 2.406
27
ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 4 2.406
28
THN006 Thin Basement Membrane Nephropathy 37 2.335
29
URM003 Uromodulin-Associated Kidney Disease 15 2.152
30
IGN002 Iga Nephropathy 2 9 2.147
31
IGN003 Iga Nephropathy 1 10 2.059
32
NPH003 Nephrocalcinosis 52 2.026
33
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 6 2.005
34
FGN001 Feigenbaum Bergeron Richardson Syndrome 3 1.994
35
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 12 1.980
36
HYD039 Hydrocephalus - Blue Sclerae - Nephropathy 8 1.980
37
PRM036 Premature Atherosclerosis with Photomyoclonic Epilepsy, Deafness, Diabetes Mellitus, Nephropathy, an 0 1.980
38
ATS141 Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E 11 1.965
39
NPH066 Nephropathy Due to Cfhr5 Deficiency 10 1.965
40
FML259 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 9 1.965
41
FML260 Familial Renal Amyloidosis Due to Lysozyme Variant 7 1.965
42
FML208 Familial Renal Amyloidosis Due to Apolipoprotein Aii Variant 7 1.965
43
FML258 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 7 1.965
44
P NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 7 1.965
45
c HYP529 Hyperuricemic Nephropathy, Familial Juvenile, 3 3 1.965
46
c NPH050 Nephropathy, Progressive, with Deafness 3 1.965
47
CL4006 Col4a5-Related Nephropathy 1 1.965
48
CL4007 Col4a3-Related Nephropathy 1 1.965
49
CL4008 Col4a4-Related Nephropathy 1 1.965
50
c NPH022 Nephropathy Familial with Hyperuricemia 0 1.965
51
BRG002 Berger Disease 30 1.707
52
ALP004 Alport Syndrome 55 1.592
53
c MTR022 Maturity-Onset Diabetes of the Young, Type 5 16 1.480
54
RTN138 Retinal Vasculopathy with Cerebral Leukodystrophy 27 1.471
55
P ATS015 Autosomal Dominant Alport Syndrome 43 1.461
56
MCK007 Muckle-Wells Syndrome 55 1.450
57
HMR004 Hemorrhagic Fever with Renal Syndrome 46 1.450
58
DNT019 Daentl Towsend Siegel Syndrome 4 1.439
59
ADN024 Adenine Phosphoribosyltransferase Deficiency 42 1.425
60
c ATS018 Autosomal Recessive Alport Syndrome 38 1.410
61
AMY038 Amyloidosis, Renal 37 1.410
62
FTZ004 Fitzsimmons Walson Mellor Syndrome 9 1.410
63
HRR004 Herrmann Syndrome 3 1.389
64
ALL011 Allain-Babin-Demarquez Syndrome 2 1.389
65
c DBT009 Diabetes Mellitus 68 0.334
66
NSY001 N Syndrome 57 0.301
67
P PRT039 Proteinuria 51 0.268
68
P GLM007 Glomerulonephritis 60 0.227
69
P HYP075 Hypertension 76 0.203
70
END072 Endotheliitis 51 0.201
71
c XP2001 Xp22.3 Microdeletion Syndrome 17 0.189
72
NPH051 Nephritis 55 0.184
73
INF133 Inferior Vena Cava Interruption 29 0.166
74
P PCM002 Pauci-Immune Glomerulonephritis 19 0.157
75
c NPH012 Nephrotic Syndrome 57 0.155
76
THR013 Thoracic Outlet Syndrome 53 0.155
77
ANK002 Ankylosing Spondylitis 75 0.153
78
c KDN018 Kidney Disease 52 0.153
79
DBT011 Diabetic Retinopathy 66 0.151
80
14Q004 14q22q23 Microdeletion Syndrome 25 0.147
81
3Q2005 3q26q27 Microdeletion Syndrome 14 0.147
82
HYP014 Hyperuricemia 58 0.145
83
PRP030 Purpura 60 0.140
84
FCL008 Focal Glomerulosclerosis 57 0.140
85
P INS005 Insulin Resistance 62 0.134
86
FML089 Familial Thoracic Aortic Aneurysm and Dissection 39 0.134
87
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 34 0.131
88
IDP042 Idiopathic Recurrent Stupor 15 0.131
89
P FCL005 Focal Segmental Glomerulosclerosis 64 0.126
90
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 33 0.126
91
NRP001 Neuropathy 54 0.121
92
CRB009 Cerebritis 46 0.121
93
CMP052 Complication in Hemodialysis 16 0.121
94
MRC003 Mercury Poisoning 37 0.116
95
c HPT021 Hepatitis 65 0.114
96
CNG379 Congenital Anomalies of Kidney and Urinary Tract 25 0.114
97
c LCL006 Localized Scleroderma 64 0.111
98
c MLG069 Malignant Hypertension 53 0.111
99
CRN131 Coronary Artery Disease, Modifier of 12 0.111
100
MDR006 Moderate and Severe Traumatic Brain Injury 11 0.111
101
RNL028 Renal Tubular Dysgenesis 49 0.108
102
21Q001 21q22.11q22.12 Microdeletion Syndrome 13 0.108
103
CRS001 Crescentic Glomerulonephritis 50 0.105
104
P TYP020 Type 1 Diabetes 73 0.102
105
BRN024 Bronchitis 71 0.102
106
VSC007 Vascular Disease 69 0.102
107
P CRT049 Critical Limb Ischemia 58 0.102
108
P NPH009 Nephrolithiasis 57 0.102
109
ACN002 Acanthosis Nigricans 70 0.099
110
DBT010 Diabetic Neuropathy 59 0.099
111
P MMB001 Membranoproliferative Glomerulonephritis 52 0.099
112
NPH018 Nephrogenic Systemic Fibrosis 50 0.099
113
INT067 Interstitial Nephritis 49 0.099
114
c NPH019 Nephronophthisis 1 20 0.099
115
HMR012 Hemorrhagic Fever 58 0.096
116
MNN014 Mononeuritis 40 0.096
117
P AVS004 Avascular Necrosis of the Femoral Head 40 0.096
118
JVN024 Juvenile Hereditary Hemochromatosis 28 0.096
119
14Q001 14q12 Microdeletion Syndrome 23 0.096
120
c 2P1003 2p13.2 Microdeletion Syndrome 11 0.096
121
P HYP117 Hypertriglyceridemia 63 0.093
122
GLL008 Gilles De La Tourette Syndrome 60 0.093
123
CNG008 Congenital Ichthyosiform Erythroderma 51 0.093
124
LWR010 Low Renin Hypertension 34 0.093
125
c DST058 Distal Monosomy 12p 16 0.093
126
MNS013 Monosomy 13q34 14 0.093
127
FBR012 Fabry Disease 74 0.089
128
c ESS002 Essential Hypertension 64 0.089
129
c PRM002 Primary Hyperoxaluria 63 0.089
130
FBR032 Fibromuscular Dysplasia 54 0.089
131
SCN006 Secondary Syphilis 53 0.089
132
RNL015 Renal Hypertension 52 0.089
133
ACT105 Acute Mountain Sickness 50 0.089
134
c PRL003 Proliferative Glomerulonephritis 49 0.089
135
MYC019 Mycobacterium Marinum 37 0.089
136
17Q001 17q21.31 Microdeletion Syndrome 29 0.089
137
FML235 Familial Combined Hyperlipoproteinemia 26 0.089
138
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 23 0.089
139
MCR071 Microdeletion 15q11.2 21 0.089
140
ATX002 Ataxia Telangiectasia 81 0.086
141
SPS077 Sepsis 67 0.086
142
P HPT001 Hepatitis C 66 0.086
143
NLP001 Nail-Patella Syndrome 58 0.086
144
P HYP090 Hyperalphalipoproteinemia 43 0.086
145
VTM002 Vitamin B12 Deficiency 35 0.086
146
GLM037 Glioma Somatic 27 0.086
147
NNS006 Non-Suppurative Otitis Media 24 0.086
148
10P002 10p11.21p12.31 Microdeletion Syndrome 14 0.086
149
CYT018 Cytochrome P450 2d6 Variant 12 0.086
150
WST001 West Syndrome 64 0.082
151
TNS005 Tonsillitis 57 0.082
152
c HPT073 Hepatitis C Virus 43 0.082
153
HYP226 Hyporeninemic Hypoaldosteronism 33 0.082
154
c 2Q3005 2q31.1 Microdeletion Syndrome 22 0.082
155
c NPH032 Nephronophthisis 4 22 0.082
156
17Q007 17q11 Microdeletion Syndrome 21 0.082
157
12P001 12p12.1 Microdeletion Syndrome 15 0.082
158
c TYP008 Type 1 Diabetes Mellitus 71 0.078
159
ATH003 Atherosclerosis 69 0.078
160
ART031 Aortic Coarctation 56 0.078
161
P RNV001 Renovascular Hypertension 56 0.078
162
P FNC004 Fanconi Syndrome 52 0.078
163
PST055 Postural Hypotension 42 0.078
164
MYC065 Myocardial Infarction, Decreased 33 0.078
165
HNM001 Hinman's Syndrome 28 0.078
166
TFT003 Tufting Enteropathy 26 0.078
167
CHL109 Childhood Apraxia of Speech 19 0.078
168
P ART022 Arthritis 75 0.074
169
CNG034 Congestive Heart Failure 74 0.074
170
LRN002 Laron Syndrome 65 0.074
171
TRN018 Transitional Cell Carcinoma 61 0.074
172
IRN001 Iron Deficiency Anemia 58 0.074
173
c ATN004 Autonomic Neuropathy 52 0.074
174
P RPD001 Rapidly Progressive Glomerulonephritis 51 0.074
175
EVN001 Evans' Syndrome 50 0.074
176
ADL002 Adult Syndrome 50 0.074
177
JCB001 Jacobsen Syndrome 49 0.074
178
19Q001 19q13.11 Microdeletion Syndrome 21 0.074
179
P PLY014 Polycystic Kidney Disease 62 0.070
180
HYP066 Hyperglycemia 59 0.070
181
c HPT003 Hepatitis a 57 0.070
182
HML001 Hemolytic-Uremic Syndrome 52 0.070
183
NTR003 Natural Killer Cell Leukemia 52 0.070
184
c VSC005 Vesicoureteral Reflux 51 0.070
185
P PYL005 Pyelonephritis 51 0.070
186
CYS016 Cystic Kidney 50 0.070
187
THL010 Thalassemia Minor 40 0.070
188
RNL022 Renal Vascular Disease 35 0.070
189
c ATX010 Ataxia Neuropathy Spectrum 33 0.070
190
FCT013 Factor V Leiden Thrombophilia 31 0.070
191
CRC004 Carcinoid Tumor of Lung 26 0.070
192
ACD004 Acdc 25 0.070
193
c CHR266 Chromosome 8p23.1 Deletion 21 0.070
194
MTH028 Mthfr Thermolabile Variant 17 0.070
195
P IMM015 Immune Defect Due to Absence of Thymus 14 0.070
196
P RHM011 Rheumatoid Arthritis 83 0.066
197
P TYP009 Type 2 Diabetes Mellitus 80 0.066
198
P WSK001 Wiskott-Aldrich Syndrome 76 0.066
199
P ANG001 Angelman Syndrome 67 0.066
200
GT001 Gout 66 0.066
201
P AMY004 Amyloidosis 65 0.066
202
ART019 Aortic Valve Stenosis 64 0.066
203
LPS007 Lupus Nephritis 55 0.066
204
URM002 Uremia 54 0.066
205
PRL007 Proliferative Diabetic Retinopathy 54 0.066
206
c MYL007 Myeloma 53 0.066
207
MLR002 Miliary Tuberculosis 53 0.066
208
c WLM002 Wilms Tumor 50 0.066
209
c ALM001 Al Amyloidosis 49 0.066
210
LDP002 Lead Poisoning 47 0.066
211
NPH017 Nephrosis 45 0.066
212
DBT002 Diabetic Autonomic Neuropathy 44 0.066
213
c CHR098 Chronic Pyelonephritis 37 0.066
214
MNG006 Monogenic Diabetes 37 0.066
215
17Q004 17q12 Microdeletion Syndrome 32 0.066
216
APD001 Apo a-I Deficiency 26 0.066
217
MLR006 Male Reproductive Organ Cancer 21 0.066
218
TBR010 Tuberculosis 82 0.061
219
LKM002 Leukemia 70 0.061
220
P PRD006 Prader-Willi Syndrome 69 0.061
221
P HMP004 Hemophilia B 66 0.061
222
RLP001 Relapsing Polychondritis 66 0.061
223
GST034 Gastroesophageal Reflux Disease 65 0.061
224
ANT006 Antiphospholipid Syndrome 64 0.061
225
MYC002 Mycobacterium Avium Complex Disease 56 0.061
226
SNS001 Sensorineural Hearing Loss 55 0.061
227
RTN023 Retinitis 53 0.061
228
NPH010 Nephrosclerosis 53 0.061
229
GDP001 Goodpasture Syndrome 51 0.061
230
ART004 Aortic Atherosclerosis 51 0.061
231
c TWN006 Twin Twin Transfusion Syndrome 51 0.061
232
c DRR001 Diarrhea 49 0.061
233
P THR090 Thrombocythemia 1 48 0.061
234
c NPH005 Nephronophthisis 48 0.061
235
IDP011 Idiopathic Interstitial Pneumonia 47 0.061
236
HMC014 Homocysteinemia 46 0.061
237
P ATS008 Autosomal Dominant Disease 45 0.061
238
HYP121 Hypoalphalipoproteinemia 44 0.061
239
PYM001 Pyomyositis 44 0.061
240
P HRM005 Hermansky-Pudlak Syndrome 1 44 0.061
241
1P3001 1p36 Deletion Syndrome 44 0.061
242
PST041 Posterior Urethral Valves 42 0.061
243
AMN006 Aminoaciduria 41 0.061
244
BWN003 Bowenoid Papulosis 39 0.061
245
HPT025 Hepatic Lipase Deficiency 38 0.061
246
HYP008 Hypertensive Retinopathy 35 0.061
247
LGH004 Light Chain Deposition Disease 34 0.061
248
MSM007 Mesomelic Dysplasia Kantaputra Type 32 0.061
249
P SLP004 Salpingo-Oophoritis 30 0.061
250
c ERL004 Early Yaws 29 0.061
251
ORL010 Oral-Facial-Digital Syndrome Type I 29 0.061
252
12Q001 12q15q21.1 Microdeletion Syndrome 14 0.061
253
HRD064 Hereditary Vascular Retinopathy 6 0.061
254
AND002 Androgen Insensitivity Syndrome 75 0.055
255
P FML018 Familial Mediterranean Fever 73 0.055
256
THL005 Thalassemia 69 0.055
257
P PRT013 Portal Hypertension 65 0.055
258
TKY001 Takayasu's Arteritis 65 0.055
259
VSC011 Vasculitis 65 0.055
260
THR079 Thromboembolism 63 0.055
261
ACQ007 Acquired Immunodeficiency Syndrome 62 0.055
262
PMS001 Poems Syndrome 61 0.055
263
CRY004 Cryoglobulinemia 59 0.055
264
P DWR001 Dwarfism 59 0.055
265
ANR008 Aneurysm Disease 57 0.055
266
OCC006 Occipital Horn Syndrome 57 0.055
267
c AXN002 Axenfeld-Rieger Syndrome 57 0.055
268
OST011 Osteomalacia 56 0.055
269
KDS001 Kid Syndrome 55 0.055
270
HYP037 Hyperhomocysteinemia 55 0.055
271
MCR004 Macroglobulinemia 54 0.055
272
HRD057 Hereditary Pancreatitis 53 0.055
273
c EPD016 Epidermolysis Bullosa 53 0.055
274
PYG006 Pyogenic Granuloma 52 0.055
275
DBT004 Diabetic Polyneuropathy 52 0.055
276
NNT024 Neonatal Stroke 47 0.055
277
CRN030 Coronary Stenosis 47 0.055
278
PRP023 Peripheral Neuropathy 46 0.055
279
PRT019 Protein-Losing Enteropathy 46 0.055
280
PRT092 Partial Androgen Insensitivity Syndrome 45 0.055
281
HYP120 Hypoaldosteronism 42 0.055
282
BRN105 Burn Scar 41 0.055
283
PRL042 Proliferating Trichilemmal Cyst 40 0.055
284
c 3Q2003 3q29 Microdeletion Syndrome 37 0.055
285
P LYS005 Loeys-Dietz Syndrome Type 1a 36 0.055
286
c DBT031 Diabetes, Type 2 36 0.055
287
DYS070 Dysalbuminemic Hyperthyroxinemia 29 0.055
288
12Q002 12q14 Microdeletion Syndrome 28 0.055
289
2Q3003 2q32q33 Microdeletion Syndrome 25 0.055
290
c 2Q2001 2q23.1 Microdeletion Syndrome 25 0.055
291
KRN001 Korean Hemorrhagic Fever 24 0.055
292
c 4Q2001 4q21 Microdeletion Syndrome 24 0.055
293
10Q001 10q22.3q23.3 Microdeletion Syndrome 19 0.055
294
CMP061 Complete Lcat Deficiency 17 0.055
295
HYP281 Hypoproteinemia, Hypercatabolic 16 0.055
296
PSD062 Pseudoxanthoma Elasticum, Modifier of Severity of 14 0.055
297
OTP003 Oto-Palatal-Digital Syndrome 13 0.055
298
P ALZ001 Alzheimer's Disease 93 0.050
299
P MYC007 Myocardial Infarction 82 0.050
300
HPT023 Hepatocellular Carcinoma 69 0.050
301
BTT002 Beta Thalassemia 69 0.050
302
CRN211 Coronary Artery Disease, 68 0.050
303
P MLR004 Malaria 66 0.050
304
DFC004 Deficiency Anemia 65 0.050
305
PRC016 Pre-Eclampsia 64 0.050
306
P HYD006 Hydrocephalus 60 0.050
307
P ADN016 Adenocarcinoma 60 0.050
308
P HRD011 Hereditary Spherocytosis 59 0.050
309
GLB015 Glioblastoma Multiforme 57 0.050
310
c PRP029 Porphyria 56 0.050
311
c ATM011 Autoimmune Hepatitis 56 0.050
312
EXT034 Extrinsic Allergic Alveolitis 55 0.050
313
CNG048 Congenital Hepatic Fibrosis 52 0.050
314
PSR002 Psoriasis 51 0.050
315
RNL014 Renal Cell Carcinoma 51 0.050
316
FML026 Familial Lipoprotein Lipase Deficiency 50 0.050
317
RNL011 Renal Osteodystrophy 50 0.050
318
DST006 Diastolic Heart Failure 50 0.050
319
P CLC001 Calciphylaxis 49 0.050
320
RTN018 Retinal Disease 49 0.050
321
PLY012 Polyhydramnios 49 0.050
322
MSN001 Mesangial Proliferative Glomerulonephritis 49 0.050
323
P ORT004 Orthostatic Intolerance 48 0.050
324
PRT058 Pure Autonomic Failure 48 0.050
325
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 45 0.050
326
VLV044 Vulvar Intraepithelial Neoplasia 45 0.050
327
LYM014 Lymphangitis 42 0.050
328
RTR011 Retroperitoneal Fibrosis 42 0.050
329
STR044 Steroid-Resistant Nephrotic Syndrome 40 0.050
330
ATX019 Ataxia with Vitamin E Deficiency 40 0.050
331
SCH016 Schimke Immunoosseous Dysplasia 40 0.050
332
LPD004 Lipoid Nephrosis 40 0.050
333
HRS011 Horseshoe Kidney 39 0.050
334
c ACQ022 Acquired Generalized Lipodystrophy 36 0.050
335
TTR016 Tetra-Amelia Syndrome 36 0.050
336
ART012 Aortitis 36 0.050
337
HNC001 Henoch-Schoenlein Purpura 35 0.050
338
MNT053 Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations 29 0.050
339
c FML187 Familial Hypertension 29 0.050
340
AMY016 Amyopathic Dermatomyositis 25 0.050
341
NRG005 Neurogenic Hypertension 24 0.050
342
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.050
343
P HYP078 Hypertrophy of Breast 20 0.050
344
PRT015 Partial Third-Nerve Palsy 19 0.050
345
c DYS055 Dystonia 10 17 0.050
346
c BNG076 Benign Exophthalmos Syndrome 17 0.050
347
c 9P1001 9p13 Microdeletion Syndrome 13 0.050
348
c 5Q3002 5q31.3 Microdeletion Syndrome 13 0.050
349
P AMY001 Amyotrophic Lateral Sclerosis 87 0.043
350
P SYS001 Systemic Lupus Erythematosus 83 0.043
351
CDS001 Cadasil 80 0.043
352
P OBS005 Obesity 79 0.043
353
P MLT019 Multiple Myeloma 76 0.043
354
P HMC003 Hemochromatosis 73 0.043
355
PRP027 Peripheral Vascular Disease 71 0.043
356
ACT074 Acute Lymphocytic Leukemia 69 0.043
357
LVR012 Liver Cirrhosis 69 0.043
358
MYC006 Mycosis Fungoides 68 0.043
359
P UVT001 Uveitis 66 0.043
360
c LPS004 Lupus Erythematosus 65 0.043
361
c HYP095 Hypercholesterolemia 65 0.043
362
P SHR002 Short Stature 64 0.043
363
ART021 Arteriosclerosis 63 0.043
364
ISC006 Ischemic Heart Disease 62 0.043
365
GLC003 Glucose Intolerance 62 0.043
366
ADL030 Adult-Onset Still's Disease 61 0.043
367
c THY032 Thyroiditis 61 0.043
368
P BLR001 Biliary Atresia 60 0.043
369
c ACT075 Acute Myocardial Infarction 59 0.043
370
DSS009 Disseminated Intravascular Coagulation 59 0.043
371
c HYP086 Hypothyroidism 59 0.043
372
SPN051 Spondylitis 59 0.043
373
RCT015 Reactive Arthritis 58 0.043
374
c HYP069 Hyperparathyroidism 57 0.043
375
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.043
376
HPR003 Heparin-Induced Thrombocytopenia 55 0.043
377
c SYP003 Syphilis 55 0.043
378
GTL001 Gitelman Syndrome 54 0.043
379
INT075 Intracranial Hypertension 53 0.043
380
ACR008 Acrocallosal Syndrome 53 0.043
381
CRB039 Cerebrovascular Disease 53 0.043
382
P ISC002 Ischemic Optic Neuropathy 52 0.043
383
P EPL002 Epilepsy Syndrome 52 0.043
384
PLS011 Plasmacytoma 52 0.043
385
c HPT007 Hepatitis E 52 0.043
386
HMS001 Hemosiderosis 51 0.043
387
ANK001 Ankylosis 51 0.043
388
CNN005 Connective Tissue Disease 51 0.043
389
c TRM003 Tremor 50 0.043
390
LYM021 Lymphadenitis 50 0.043
391
AMY053 Amyloidosis, Secondary 50 0.043
392
HPT014 Hepatorenal Syndrome 49 0.043
393
URT010 Ureteral Obstruction 48 0.043
394
CRB086 Cerebral Aneurysms 48 0.043
395
P CHR092 Chronic Myeloproliferative Disease 48 0.043
396
PST087 Posterior Urethral Valve 47 0.043
397
RNL078 Renal Dysplasia 47 0.043
398
P GND004 Gonadal Dysgenesis 47 0.043
399
IMM001 Immune-Complex Glomerulonephritis 47 0.043
400
DBT008 Diabetic Angiopathy 47 0.043
401
c PSD003 Pseudohypoaldosteronism 46 0.043
402
NPH004 Nephropathia Epidemica 45 0.043
403
DFF024 Diffuse Panbronchiolitis 44 0.043
404
LMY003 Leiomyomatosis 43 0.043
405
ACT040 Acute Poststreptococcal Glomerulonephritis 43 0.043
406
FLL008 Folliculitis 43 0.043
407
RNL006 Renal Glycosuria 41 0.043
408
END030 End Stage Renal Failure 40 0.043
409
DFF021 Diffuse Mesangial Sclerosis 40 0.043
410
CHL079 Children's Interstitial Lung Disease 39 0.043
411
ENT001 Enterocele 39 0.043
412
P HYP111 Hyperprolinemia 38 0.043
413
EMN001 Emanuel Syndrome 34 0.043
414
PPT001 Peptic Esophagitis 32 0.043
415
HYP034 Hypertensive Encephalopathy 30 0.043
416
15Q001 15q13.3 Microdeletion 29 0.043
417
DFN039 Deafness-Infertility Syndrome 24 0.043
418
16Q001 16q24.3 Microdeletion Syndrome 23 0.043
419
DFF015 Diffuse Glomerulonephritis 21 0.043
420
AND005 Androgen Insensitivity Syndrome, Mild 19 0.043
421
HRD009 Hereditary Wilms' Tumor 19 0.043
422
ANP010 Anaplastic Plasmacytoma 17 0.043
423
c TTL001 Total Internal Ophthalmoplegia 17 0.043
424
LKC003 Leukocyte Disease 14 0.043
425
c PPL028 Popliteal Pterygium Syndrome Lethal Type 12 0.043
426
CL4001 Col4a1-Related Disorders 6 0.043
427
APL001 Aplastic Anemia 77 0.035
428
BLD042 Bladder Carcinoma 70 0.035
429
P CRN008 Carney Complex 68 0.035
430
P CHR089 Chronic Kidney Failure 68 0.035
431
GLN003 Glanzmann's Thrombasthenia 68 0.035
432
THR006 Thromboangiitis Obliterans 67 0.035
433
PRT036 Peritonitis 67 0.035
434
DBT001 Diabetic Ketoacidosis 67 0.035
435
c THR014 Thrombocytopenia 66 0.035
436
P ATM003 Autoimmune Thyroiditis 66 0.035
437
P CNG026 Congenital Heart Defect 65 0.035
438
STT001 Status Epilepticus 64 0.035
439
ACT073 Acute Leukemia 62 0.035
440
PLM001 Pulmonary Tuberculosis 62 0.035
441
ART005 Arteriovenous Malformation 62 0.035
442
HMP002 Hemophagocytic Lymphohistiocytosis 62 0.035
443
URT039 Urticaria 61 0.035
444
LMY002 Leiomyoma 61 0.035
445
HYP266 Hypoxia 60 0.035
446
MXD005 Mixed Connective Tissue Disease 60 0.035
447
TTN003 Tetanus 60 0.035
448
c MCP001 Mucopolysaccharidosis Iii 59 0.035
449
P DRM010 Dermatomyositis 59 0.035
450
c HPT015 Hepatitis D 59 0.035
451
BLS001 Blau Syndrome 59 0.035
452
P CRN157 Coronary Heart Disease 59 0.035
453
PLS007 Plasmodium Falciparum Malaria 59 0.035
454
PRT011 Protein C Deficiency 59 0.035
455
SCK005 Sickle Cell Disease 58 0.035
456
P AGM001 Agammaglobulinemia 58 0.035
457
c PNC044 Pancreatitis 58 0.035
458
MLT001 Multiple Chemical Sensitivity 58 0.035
459
GST009 Gastroschisis 58 0.035
460
c HRD002 Hereditary Angioedema 58 0.035
461
RNL007 Renal Tubular Acidosis 57 0.035
462
SLP006 Sleep Apnea 57 0.035
463
LGG001 Legg-Calve-Perthes Disease 56 0.035
464
CHR001 Churg-Strauss Syndrome 56 0.035
465
CHR090 Chronic Lymphocytic Leukemia 56 0.035
466
c THR005 Thrombotic Thrombocytopenic Purpura 55 0.035
467
c HRM001 Hermansky-Pudlak Syndrome 55 0.035
468
WLL006 Wells Syndrome 55 0.035
469
c BLN003 Blindness 54 0.035
470
ESN015 Eosinophilic Fasciitis 54 0.035
471
P ANG015 Angioedema 54 0.035
472
LPD010 Lipodystrophy 53 0.035
473
ANR004 Anuria 53 0.035
474
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.035
475
c ACT071 Acute Kidney Failure 53 0.035
476
LDD002 Liddle Syndrome 52 0.035
477
P CLL015 Collagen Disease 52 0.035
478
c TYR004 Tyrosinemia 52 0.035
479
P SPN052 Spondyloarthropathy 52 0.035
480
KLD001 Keloids 52 0.035
481
ART001 Arterial Tortuosity Syndrome 52 0.035
482
PRN011 Pernicious Anemia 52 0.035
483
URN010 Urinary Tract Obstruction 52 0.035
484
SND002 Sneddon Syndrome 51 0.035
485
c FML012 Familial Partial Lipodystrophy 51 0.035
486
P INT068 Intestinal Disease 51 0.035
487
P SCL015 Scleritis 50 0.035
488
BCL002 B Cell Deficiency 50 0.035
489
GNG012 Gingival Overgrowth 50 0.035
490
FRS002 Frasier Syndrome 50 0.035
491
SPL018 Splenomegaly 50 0.035
492
RYS001 Reye Syndrome 50 0.035
493
c GLY013 Glycogen Storage Disease 49 0.035
494
c JBR001 Joubert Syndrome 49 0.035
495
SYS003 Systolic Heart Failure 48 0.035
496
c CTR002 Cataract 48 0.035
497
c HYD002 Hydronephrosis 48 0.035
498
ANG054 Angina Pectoris 48 0.035
499
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 48 0.035
500
YLL001 Yellow Nail Syndrome 47 0.035
501
ILS001 Ileus 47 0.035
502
P DNT009 Dentin Dysplasia 46 0.035
503
CHY002 Chylomicron Retention Disease 46 0.035
504
HYP457 Hypertrophic Scars 46 0.035
505
c RSM001 Rasmussen Encephalitis 46 0.035
506
c ACR001 Aicardi-Goutieres Syndrome 46 0.035
507
APP001 Apparent Mineralocorticoid Excess Syndrome 45 0.035
508
LPT002 Lipoatrophic Diabetes 45 0.035
509
GST029 Gastric Cardia Adenocarcinoma 44 0.035
510
c LYS001 Loeys-Dietz Syndrome 44 0.035
511
P PRM124 Primary Hyperoxaluria Type 1 44 0.035
512
FSC004 Fasciitis 44 0.035
513
GNG008 Ganglioneuroblastoma 43 0.035
514
RCR001 Recurrent Corneal Erosion 43 0.035
515
MNN021 Meningococcemia 42 0.035
516
CHR101 Char Syndrome 42 0.035
517
CRT008 Carotid Artery Dissection 41 0.035
518
CHY006 Chylous Ascites 40 0.035
519
BRB001 Beriberi 40 0.035
520
c ATM022 Autoimmune Myocarditis 40 0.035
521
LYM012 Lymphoplasmacytic Lymphoma 40 0.035
522
CLS008 Clostridium Difficile 40 0.035
523
c SNR001 Senior-Loken Syndrome 40 0.035
524
CRB008 Cerebral Atherosclerosis 39 0.035
525
HYP030 Hypoactive Sexual Desire Disorder 39 0.035
526
AND003 Andersen-Tawil Syndrome 39 0.035
527
NRM003 Norum Disease 39 0.035
528
OCL022 Ocular Melanoma 38 0.035
529
PLM074 Pulmonary Function 38 0.035
530
P SNR003 Senior-Loken Syndrome 1 37 0.035
531
CRB025 Carbohydrate Metabolic Disorder 37 0.035
532
P LYM029 Lymphedema-Distichiasis Syndrome 36 0.035
533
HYP456 Hyperapobetalipoproteinemia 35 0.035
534
HYP001 Hypochromic Microcytic Anemia 35 0.035
535
IPX001 Ipex Syndrome 35 0.035
536
VRL011 Viral Infectious Disease 35 0.035
537
c ACT004 Acute Diarrhea 34 0.035
538
c CNG033 Congenital Syphilis 34 0.035
539
ADP002 Adiponectin Deficiency 33 0.035
540
URT031 Ureteral Disease 32 0.035
541
ADS002 Adie Syndrome 32 0.035
542
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 31 0.035
543
PRN007 Perinephritis 30 0.035
544
SLL001 Sialolithiasis 30 0.035
545
HMG010 Hemoglobinemia 30 0.035
546
DFC001 Defective Apolipoprotein B-100 30 0.035
547
c HVY001 Heavy Chain Disease 27 0.035
548
c HMP017 Hemophilia a, Congenital 26 0.035
549
CCM003 Cecum Cancer 25 0.035
550
PRX022 Paroxysmal Choreoathetosis 25 0.035
551
c FML056 Familial Deafness 24 0.035
552
MDL019 Medullary Cystic Kidney Disease Type 1 24 0.035
553
6Q1001 6q16 Deletion Syndrome 24 0.035
554
P FML059 Familial Encephalopathy with Neuroserpin Inclusion Bodies 23 0.035
555
c ATM007 Autoimmune Disease of Central Nervous System 22 0.035
556
MNS009 Monosomy 13q14 22 0.035
557
P ATM020 Autoimmune Enteropathy 22 0.035
558
c NPH049 Nephrotic Syndrome, Type 2 21 0.035
559
RNL051 Renal Cysts and Diabetes Syndrome 19 0.035
560
P 19P001 19p13.12 Microdeletion Syndrome 19 0.035
561
c INS009 Insulin-Resistance Type B 16 0.035
562
PL2001 Pla2g6-Associated Neurodegeneration 14 0.035
563
21Q002 21q22.13q22.2 Microdeletion Syndrome 14 0.035
564
PRG091 Progressively Deforming Osteogenesis Imperfecta 13 0.035
565
LNP001 Loin Pain Hematuria Syndrome 12 0.035
566
RTN163 Retinal Arterial Tortuosity 11 0.035
567
ANT002 Anti-Basement Membrane Glomerulonephritis 11 0.035
568
LGH014 Light and Heavy Chain Deposition Disease 5 0.035
569
CRM007 Crome Syndrome 4 0.035
570
MRF001 Marfan Syndrome 78 0.025
571
CRH001 Crohn's Disease 78 0.025
572
P PRS040 Prostate Cancer 76 0.025
573
P RTN008 Retinitis Pigmentosa 76 0.025
574
P FML021 Familial Hypercholesterolemia 76 0.025
575
ACR007 Acromegaly 75 0.025
576
P PRM021 Primary Pulmonary Hypertension 74 0.025
577
c NNN003 Noonan Syndrome 73 0.025
578
ULC004 Ulcerative Colitis 71 0.025
579
P CLC005 Celiac Disease 71 0.025
580
P PRM006 Primary Biliary Cirrhosis 69 0.025
581
HYP004 Hypercalcemia 69 0.025
582
STR067 Stroke, Ischemic 69 0.025
583
WRN001 Werner Syndrome 68 0.025
584
RNL002 Renal Agenesis 68 0.025
585
LSC001 Lesch-Nyhan Syndrome 68 0.025
586
P PNM007 Pneumonia 67 0.025
587
LYM007 Lymphangioleiomyomatosis 67 0.025
588
P WGN002 Wegener's Granulomatosis 67 0.025
589
c MST009 Mastocytosis 67 0.025
590
CHR065 Chronic Myeloid Leukemia 67 0.025
591
PRT014 Protein S Deficiency 67 0.025
592
CRB011 Cerebrotendinous Xanthomatosis 66 0.025
593
P PRM005 Primary Hyperparathyroidism 66 0.025
594
INF030 Infectious Mononucleosis 65 0.025
595
P THR015 Thrombophilia 65 0.025
596
P SYS004 Systemic Mastocytosis 65 0.025
597
BLL006 Bullous Pemphigoid 65 0.025
598
P RCK004 Rickets 65 0.025
599
NPH007 Nephrogenic Diabetes Insipidus 65 0.025
600
CMM004 Common Variable Immunodeficiency 64 0.025
601
P TMP003 Temporal Arteritis 64 0.025
602
TNG002 Tangier Disease 64 0.025
603
MYL006 Myeloid Leukemia 64 0.025
604
P GRF002 Graft Versus Host Disease 64 0.025
605
CNG368 Congenital Adrenal Hyperplasia 64 0.025
606
P PRG006 Progressive Supranuclear Palsy 63 0.025
607
P SYS005 Systemic Scleroderma 63 0.025
608
P RTH001 Rothmund-Thomson Syndrome 63 0.025
609
P GRV001 Graves' Disease 63 0.025
610
c HPT016 Hepatitis B 62 0.025
611
c JVN010 Juvenile Rheumatoid Arthritis 62 0.025
612
PLY017 Polyarteritis Nodosa 62 0.025
613
PSY004 Psychotic Disorder 62 0.025
614
c MNN013 Meningitis 62 0.025
615
P BCK002 Beckwith-Wiedemann Syndrome 62 0.025
616
BRR003 Barrett's Esophagus 62 0.025
617
P MTH008 Methylmalonic Acidemia 62 0.025
618
P HMC002 Homocystinuria 61 0.025
619
PLY041 Polymyositis 61 0.025
620
THR016 Thrombophlebitis 61 0.025
621
P WLF004 Wolfram Syndrome 61 0.025
622
P HST010 Histiocytosis 61 0.025
623
P DMN002 Dementia 61 0.025
624
PND002 Pendred Syndrome 60 0.025
625
MRB003 Morbid Obesity 60 0.025
626
PMP001 Pemphigus 60 0.025
627
HML002 Hemolytic Anemia 60 0.025
628
c SRC013 Sarcoidosis 60 0.025
629
BRN029 Brain Disease 60 0.025
630
GST033 Gestational Diabetes 59 0.025
631
P GST044 Gastritis 59 0.025
632
ALP008 Alopecia 59 0.025
633
ACT020 Acute T Cell Leukemia 59 0.025
634
P FML020 Familial Combined Hyperlipidemia 59 0.025
635
VTL002 Vitiligo 59 0.025
636
P CST002 Castleman's Disease 58 0.025
637
DST005 Diastrophic Dysplasia 58 0.025
638
MLT074 Multiple Endocrine Neoplasia 58 0.025
639
SMT015 Smith Magenis Syndrome 58 0.025
640
MCR088 Microscopic Polyangiitis 58 0.025
641
PSD007 Pseudomyxoma Peritonei 58 0.025
642
c VRL010 Viral Hepatitis 57 0.025
643
PHR003 Pharyngitis 57 0.025
644
P CMP010 Complex Regional Pain Syndrome 57 0.025
645
MLL005 Miller-Dieker Syndrome 57 0.025
646
P PRM054 Primary Sclerosing Cholangitis 57 0.025
647
P CMR001 Camurati-Engelmann Disease 57 0.025
648
P PMP005 Pemphigus Vulgaris 57 0.025
649
P DBT005 Diabetes Insipidus 56 0.025
650
c NRN021 Neuronal Ceroid Lipofuscinosis 56 0.025
651
CRD137 Cardiogenic Shock 56 0.025
652
ACT049 Acute Disseminated Encephalomyelitis 56 0.025
653
P PSD087 Pseudoxanthoma Elasticum 56 0.025
654
APH001 Aphthous Stomatitis 56 0.025
655
URT001 Urethritis 56 0.025
656
PLS006 Plasmodium Vivax Malaria 56 0.025
657
P MTB001 Metabolic Syndrome X 56 0.025
658
P PSR001 Psoriatic Arthritis 56 0.025
659
P ANP001 Anaplastic Large Cell Lymphoma 56 0.025
660
BRN004 Brain Edema 55 0.025
661
THR009 Thrombocytopenia-Absent Radius Syndrome 55 0.025
662
ATM010 Autoimmune Hemolytic Anemia 55 0.025
663
LYS003 Lysinuric Protein Intolerance 55 0.025
664
CRN017 Coronary Thrombosis 55 0.025
665
P PLM006 Pulmonary Alveolar Proteinosis 55 0.025
666
LDD001 Ladd Syndrome 54 0.025
667
LRN003 Learning Disability 54 0.025
668
P MTR018 Maturity-Onset Diabetes of the Young, Type 1 54 0.025
669
P MTR005 Mitral Valve Prolapse 54 0.025
670
HST011 Histoplasmosis 54 0.025
671
NRM002 Normal Pressure Hydrocephalus 54 0.025
672
P PLY019 Polyneuropathy 54 0.025
673
PYR013 Pyruvate Kinase Deficiency 54 0.025
674
HNT002 Hantavirus Pulmonary Syndrome 54 0.025
675
GLL031 Guillain-Barr� Syndrome 54 0.025
676
HLL004 Hellp Syndrome 54 0.025
677
P SNS014 Sinusitis 54 0.025
678
P XNT003 Xanthomatosis 54 0.025
679
RTN017 Retinal Detachment 53 0.025
680
c FML035 Familial Hyperlipidemia 53 0.025
681
TWN003 Townes-Brocks Syndrome 53 0.025
682
YLL002 Yellow Fever 53 0.025
683
P RTN022 Retinal Vein Occlusion 53 0.025
684
c SCL016 Scleroderma 53 0.025
685
P LKD001 Leukodystrophy 53 0.025
686
HYP017 Hypophosphatemia 52 0.025
687
CLD007 Cold Agglutinin Disease 52 0.025
688
P ATN005 Autonomic Dysfunction 52 0.025
689
CNN003 Conn's Syndrome 52 0.025
690
HPY002 H. Pylori Infection 52 0.025
691
DBT062 Diabetic Foot Ulcers 52 0.025
692
ALC009 Alcoholic Liver Cirrhosis 52 0.025
693
LYM027 Lymphopenia 51 0.025
694
PLY013 Polymyalgia Rheumatica 51 0.025
695
TCL003 T Cell Deficiency 51 0.025
696
STM007 Stomatitis 51 0.025
697
P HYP027 Hypobetalipoproteinemia 51 0.025
698
P ESP024 Esophagitis 51 0.025
699
HYP006 Hypertensive Heart Disease 51 0.025
700
FBR009 Fibrous Dysplasia 51 0.025
701
c MNT147 Mental Retardation 51 0.025
702
ART017 Aortic Disease 51 0.025
703
c ATM024 Autoimmune Pancreatitis 51 0.025
704
PYR010 Peyronie's Disease 51 0.025
705
SDR002 Siderosis 50 0.025
706
LPC002 Lip Cancer 50 0.025
707
PMP004 Pemphigus Foliaceus 50 0.025
708
LPP001 Lipoprotein Lipase Deficiency 50 0.025
709
c HYP065 Hyperaldosteronism 50 0.025
710
c CNT016 Central Retinal Vein Occlusion 50 0.025
711
TCL004 T-Cell Leukemia 50 0.025
712
HYP005 Hypokalemia 50 0.025
713
P CHL066 Cholangitis 50 0.025
714
CYT008 Cytomegalovirus Infection 50 0.025
715
c DNT011 Dentinogenesis Imperfecta 50 0.025
716
CNS004 Constipation 50 0.025
717
P MLS001 Melas Syndrome 50 0.025
718
CRT016 Carotid Artery Disease 49 0.025
719
MNN009 Meningoencephalitis 49 0.025
720
P LYM025 Lymphedema 49 0.025
721
PLS016 Plasma Cell Leukemia 49 0.025
722
c MTR004 Maturity-Onset Diabetes of the Young 49 0.025
723
TXC012 Toxic Epidermal Necrolysis 49 0.025
724
c CHR417 Chronic Graft Versus Host Disease 49 0.025
725
c SCL009 Sclerosing Cholangitis 49 0.025
726
PSD009 Pseudohermaphroditism 49 0.025
727
SCH002 Schnitzler Syndrome 49 0.025
728
c ACT042 Acute Pyelonephritis 49 0.025
729
c PSD015 Pseudohypoparathyroidism 49 0.025
730
BRS051 Breast Disease 48 0.025
731
STV001 Stevens-Johnson Syndrome 48 0.025
732
BLS002 Blastomycosis 48 0.025
733
ACN001 Acinar Cell Carcinoma 48 0.025
734
NTR021 Nutrition Disease 48 0.025
735
CLL002 Collecting Duct Carcinoma 48 0.025
736
c FML016 Familial Hypertriglyceridemia 48 0.025
737
NRR001 Neuroretinitis 48 0.025
738
c MTR012 Mitral Valve Disease 48 0.025
739
MTB004 Metabolic Acidosis 48 0.025
740
CRN027 Corneal Neovascularization 48 0.025
741
GLC012 Galactosialidosis 48 0.025
742
HMG005 Hemoglobinopathy 47 0.025
743
PRP036 Peripheral T-Cell Lymphoma 47 0.025
744
MYC033 Myoclonus 47 0.025
745
DFF003 Diffuse Scleroderma 47 0.025
746
SPR016 Spermatic Cord Torsion 47 0.025
747
MCR018 Microcytic Anemia 46 0.025
748
GST045 Gastroenteritis 46 0.025
749
WLL001 Williams-Beuren Syndrome 46 0.025
750
MYC005 Myocardial Stunning 46 0.025
751
DBT006 Diabetic Macular Edema 46 0.025
752
CRN029 Coronary Arteriosclerosis 45 0.025
753
MCL003 Macular Holes 45 0.025
754
PLY020 Polyradiculoneuropathy 45 0.025
755
P JBR004 Joubert Syndrome 2 45 0.025
756
MDL009 Medullary Sponge Kidney 45 0.025
757
PLS025 Plasmablastic Lymphoma 45 0.025
758
P BRS044 Breast Adenocarcinoma 45 0.025
759
PRT038 Protein-Energy Malnutrition 45 0.025
760
ESN011 Eisenmenger Syndrome 44 0.025
761
RSD004 Rosai-Dorfman Disease 44 0.025
762
c ASP005 Asphyxiating Thoracic Dystrophy 44 0.025
763
SPN119 Spondylarthropathy 44 0.025
764
PRN038 Prune Belly Syndrome 44 0.025
765
GRD002 Gardner Syndrome 44 0.025
766
IRN002 Iron Metabolism Disease 44 0.025
767
ALC010 Alcoholic Cardiomyopathy 44 0.025
768
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.025
769
FML164 Familial Hdl Deficiency 43 0.025
770
PSD002 Pseudotumor Cerebri 43 0.025
771
P PRG011 Progressive Myoclonus Epilepsy 43 0.025
772
P CNG095 Congenital Generalized Lipodystrophy Type 2 42 0.025
773
SPS057 Spasticity 42 0.025
774
CCH002 Coach Syndrome 42 0.025
775
c ANT034 Anterior Uveitis 42 0.025
776
P ADR027 Adrenocortical Insufficiency 42 0.025
777
c CNG012 Congenital Generalized Lipodystrophy 42 0.025
778
RNL029 Renal Coloboma Syndrome 42 0.025
779
CRD053 Cardiovascular Disease Risk Factor 42 0.025
780
ENC011 Encephalomyopathy 41 0.025
781
CMP009 Complement Deficiency 41 0.025
782
FSH001 Fish-Eye Disease 41 0.025
783
LPD008 Lipid Metabolism Disorder 41 0.025
784
c RTN016 Retinal Degeneration 41 0.025
785
PTY003 Pityriasis Rubra Pilaris 41 0.025
786
GST040 Gastric Adenocarcinoma 41 0.025
787
OSS010 Ossification of the Posterior Longitudinal Ligament of the Spine 40 0.025
788
CRT004 Carotid Artery Thrombosis 40 0.025
789
CRP018 Cor Pulmonale 40 0.025
790
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 40 0.025
791
c MYC026 Myoclonus Epilepsy 40 0.025
792
P ART028 Aortic Aneurysm, Familial Thoracic 4 39 0.025
793
INC001 Incontinentia Pigmenti Achromians 39 0.025
794
c CRT018 Carotid Intimal Medial Thickness 39 0.025
795
CRB001 Cerebral Lymphoma 39 0.025
796
KRT010 Kartagener Syndrome 39 0.025
797
LPP002 Lipoprotein Glomerulopathy 39 0.025
798
P TWN001 Twin-to-Twin Transfusion Syndrome 39 0.025
799
P ASP011 Asphyxiating Thoracic Dystrophy 2 39 0.025
800
CNG064 Congenital Chloride Diarrhea 38 0.025
801
EXN003 Exencephaly 38 0.025
802
P HYP058 Hypervitaminosis a 38 0.025
803
UNL007 Unilateral Renal Agenesis 38 0.025
804
NCR002 Necrobiosis Lipoidica 37 0.025
805
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.025
806
HPT063 Hepatitis B Virus Infection 36 0.025
807
P FNG005 Feingold Syndrome 36 0.025
808
MCR001 Microcystic Meningioma 35 0.025
809
c PLY083 Polycystic Kidney Disease, Type 1 35 0.025
810
P HYP216 Hypoparathyroidism Familial Isolated 35 0.025
811
BLD054 Blood Protein Disease 35 0.025
812
AMY002 Amyloid Tumor 35 0.025
813
FBR063 Fibrocalculous Pancreatic Diabetes 34 0.025
814
P 2Q3002 2q37 Microdeletion Syndrome 34 0.025
815
c HYP011 Hyperlipoproteinemia Type Iii 34 0.025
816
HYP264 Hypertonia 34 0.025
817
P PTT002 Potter's Syndrome 33 0.025
818
RNL012 Renal Tuberculosis 33 0.025
819
GST007 Gastric Dilatation 33 0.025
820
CHR415 Chronic Venous Leg Ulcers 33 0.025
821
DNN002 Donnai-Barrow Syndrome 33 0.025
822
BRT011 Bruton-Type Agammaglobulinemia 32 0.025
823
MTR001 Mature Cataract 32 0.025
824
DYS036 Dysequilibrium Syndrome 32 0.025
825
c FML162 Familial Mediterranean Fever, Ad 32 0.025
826
CYS024 Cystinosis, Ocular Nonnephropathic 32 0.025
827
INT071 Intestinal Perforation 32 0.025
828
URT036 Urethral Obstruction 31 0.025
829
HMC004 Homocysteine Plasma Level 31 0.025
830
P SLD005 Sialidosis Type I 31 0.025
831
THR027 Thoracic Aortic Aneurysms and Aortic Dissections 31 0.025
832
BLD039 Bladder Adenocarcinoma 31 0.025
833
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 31 0.025
834
c EPP006 Epiphyseal Dysplasia Multiple with Early-Onset Diabetes Mellitus 30 0.025
835
c JBR007 Joubert Syndrome with Renal Anomalies 30 0.025
836
ART010 Arteriolosclerosis 29 0.025
837
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 29 0.025
838
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 28 0.025
839
HMG020 Hmg Coa Lyase Deficiency 28 0.025
840
PYR004 Pyuria 27 0.025
841
RNL042 Renal Hypouricemia 27 0.025
842
HFS001 Hfe-Associated Hereditary Hemochromatosis 27 0.025
843
DFN222 Deafness-Dystonia-Optic Neuronopathy Syndrome 27 0.025
844
PYR026 Peyronies Disease 26 0.025
845
P ALP005 Alpha Chain Disease 26 0.025
846
c FRT001 Fourth Cranial Nerve Palsy 26 0.025
847
c 2P2001 2p21 Microdeletion Syndrome 25 0.025
848
LRW003 L�ri-Weill Dyschondrosteosis 25 0.025
849
CHR476 Chronic Angina 24 0.025
850
EPD034 Epidermolysis Bullosa, Pretibial 24 0.025
851
c CHR096 Chronic Pulmonary Heart Disease 24 0.025
852
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 23 0.025
853
P PPL026 Papular Mucinosis 23 0.025
854
LPD027 Lip Disease 23 0.025
855
P CHR259 Chromosome 6q25 Microdeletion Syndrome 22 0.025
856
c FML003 Familial Visceral Amyloidosis 21 0.025
857
ESN020 Eosinophilic Granulomatosis with Polyangiitis 21 0.025
858
c JBR003 Joubert Syndrome and Related Disorders 21 0.025
859
c MCH003 Mu Chain Disease 20 0.025
860
ANT030 Antecubital Pterygium 20 0.025
861
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 19 0.025
862
RNL018 Renal Pelvis Carcinoma 19 0.025
863
GRD004 Gardner-Diamond Syndrome 18 0.025
864
MCR062 Microcephaly, Hiatal Hernia and Nephrotic Syndrome 18 0.025
865
CHL070 Cholesterol Embolism 18 0.025
866
KRY002 Karyomegalic Interstitial Nephritis 17 0.025
867
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 16 0.025
868
HVY003 Heavy Chain Deposition Disease 16 0.025
869
BLK002 Balkan Hemorrhagic Fever 16 0.025
870
PRP033 Properdin Deficiency 15 0.025
871
KDN006 Kidney Papillary Necrosis 15 0.025
872
c DMN011 Dominant Dystrophic Epidermolysis Bullosa 15 0.025
873
P ISC010 Isochromosome Yp 14 0.025
874
c CNG192 Congenital Disorder of Glycosylation, Type Ik 14 0.025
875
HPR001 Hprt-Related Gout 14 0.025
876
NPH026 Nephrotic Syndrome, Idiopathic, Steroid-Resistant 14 0.025
877
P ACT079 Acute Proliferative Glomerulonephritis 14 0.025
878
P JVN038 Juvenile Autosomal Recessive Medullary Cystic Kidney Disease 14 0.025
879
PST042 Posterior Valve Urethra 14 0.025
880
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 13 0.025
881
CPL005 Capillary Disease 13 0.025
882
DHL001 Dahlberg Borer Newcomer Syndrome 13 0.025
883
LYM061 Lymphocytic Leukemia, Acute T-Cell 12 0.025
884
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 12 0.025
885
PLS008 Plasmodium Malariae Malaria 12 0.025
886
GND003 Gonadal Disease 12 0.025
887
DHY008 Dihydroxyadeninuria 12 0.025
888
DFN014 Deafness Nephritis Anorectal Malformation 11 0.025
889
RNL019 Renal Pelvis Transitional Cell Carcinoma 11 0.025
890
ATN001 Autonomic Peripheral Neuropathy 10 0.025
891
c FML153 Familial Wilms Tumor 9 0.025
892
DYS034 Dyschondrosteosis Nephritis 9 0.025
893
c DFN131 Deafness, Autosomal Dominant 1 8 0.025
894
EXD002 Exudative Glomerulonephritis 8 0.025
895
IND008 Indomethacin Embryofetopathy 8 0.025
896
P DBT040 Diabetes Mellitus, Insulin-Dependent, 2 7 0.025
897
c CNG330 Congenital Megacalycosis 6 0.025
898
c DFN251 Deafness, Autosomal Dominant 11 5 0.025