Search results for nephritis

569 hits were found for nephritis

# Family MCID Name MIFTS Score
1
ALP046 Alport Syndrome, X-Linked 74 6.277
2
INT067 Interstitial Nephritis 51 6.122
3
c SYS001 Systemic Lupus Erythematosus 86 5.906
4
INT258 Interstitial Nephritis, Karyomegalic 28 5.545
5
TBL025 Tubulointerstitial Nephritis with Uveitis 28 4.889
6
DFN014 Deafness Nephritis Anorectal Malformation 14 4.053
7
MGL007 Megalocytic Interstitial Nephritis 14 3.741
8
DYS180 Dyschondrosteosis and Nephritis 18 3.646
9
P GLM015 Glomerulopathy with Fibronectin Deposits 2 30 3.567
10
EPS006 Epstein Syndrome 33 3.184
11
c SYS050 Systemic Lupus Erythematosus with Nephritis 2 9 3.144
12
c SYS054 Systemic Lupus Erythematosus with Nephritis 3 9 3.144
13
P SYS056 Systemic Lupus Erythematosus with Nephritis 1 9 3.144
14
ACT041 Acute Diffuse Nephritis 11 3.120
15
HMT008 Hematuria, Benign Familial 40 2.523
16
FCH003 Fechtner Syndrome 38 1.893
17
IGG001 Iga Glomerulonephritis 52 1.870
18
P IGN003 Iga Nephropathy 1 34 1.870
19
c ALP073 Alport Syndrome, Autosomal Recessive 50 1.844
20
P ALP074 Alport Syndrome, Autosomal Dominant 47 1.827
21
c RNL113 Renal Failure, Progressive, with Hypertension 29 1.808
22
SPS196 Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 17 1.784
23
FTZ004 Fitzsimmons Walson Mellor Syndrome 8 1.784
24
P LPS004 Lupus Erythematosus 69 0.421
25
P GLM007 Glomerulonephritis 61 0.380
26
P UVT001 Uveitis 61 0.352
27
P KDN018 Kidney Disease 69 0.337
28
URN009 Urinary System Disease 58 0.302
29
CNN005 Connective Tissue Disease 65 0.299
30
ATM095 Autoimmune Disease 66 0.296
31
PRP030 Purpura 61 0.293
32
VSC011 Vasculitis 66 0.169
33
P MMB011 Membranous Nephropathy 55 0.164
34
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.158
35
IMM136 Immune System Disease 57 0.152
36
HNC001 Henoch-Schoenlein Purpura 48 0.152
37
P HPT021 Hepatitis 75 0.146
38
P ART022 Arthritis 77 0.137
39
P NPH012 Nephrotic Syndrome 60 0.134
40
c CHR089 Chronic Kidney Failure 72 0.130
41
P PYL005 Pyelonephritis 56 0.130
42
P FNC004 Fanconi Syndrome 54 0.130
43
c BLD140 Blood Group, I System 37 0.130
44
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.120
45
MST021 Meester-Loeys Syndrome 29 0.112
46
END072 Endotheliitis 46 0.108
47
P PRL003 Proliferative Glomerulonephritis 45 0.108
48
CRH001 Crohn's Disease 80 0.104
49
P MYC084 Mycobacterium Tuberculosis 1 69 0.104
50
END030 End Stage Renal Failure 59 0.099
51
MMB001 Membranoproliferative Glomerulonephritis 51 0.099
52
P LYM118 Lymphoma 71 0.095
53
P RNL007 Renal Tubular Acidosis 51 0.095
54
P RHM011 Rheumatoid Arthritis 91 0.090
55
BRN024 Bronchitis 67 0.090
56
c CHR098 Chronic Pyelonephritis 38 0.090
57
P LKM002 Leukemia 75 0.085
58
RTN023 Retinitis 52 0.085
59
ANR004 Anuria 49 0.085
60
IGG007 Igg4-Related Disease 43 0.085
61
c ACT042 Acute Pyelonephritis 48 0.079
62
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.079
63
ACT040 Acute Poststreptococcal Glomerulonephritis 37 0.079
64
MLK004 Malakoplakia 34 0.079
65
P INF038 Influenza 77 0.073
66
P AMY004 Amyloidosis 69 0.073
67
P THR014 Thrombocytopenia 65 0.073
68
AGN016 Aging 65 0.073
69
CLT003 Colitis 63 0.073
70
THR024 Thrombosis 61 0.073
71
P FCL005 Focal Segmental Glomerulosclerosis 60 0.073
72
P THY032 Thyroiditis 56 0.073
73
P PRM006 Primary Biliary Cirrhosis 55 0.073
74
c ANT034 Anterior Uveitis 53 0.073
75
P INF037 Inflammatory Bowel Disease 52 0.073
76
CHR008 Choroiditis 47 0.073
77
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.073
78
CRS001 Crescentic Glomerulonephritis 44 0.073
79
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.073
80
IGG011 Igg4-Related Kidney Disease 15 0.073
81
c LKM071 Leukemia, Chronic Lymphocytic 75 0.067
82
P GRF003 Graft-Versus-Host Disease 72 0.067
83
DRM006 Dermatitis 67 0.067
84
c CHR417 Chronic Graft Versus Host Disease 65 0.067
85
P PNC044 Pancreatitis 64 0.067
86
P HML002 Hemolytic Anemia 62 0.067
87
P NPH005 Nephronophthisis 57 0.067
88
ALS001 Alstrom Syndrome 55 0.067
89
c MCR113 Microvascular Complications of Diabetes 3 55 0.067
90
P DBT005 Diabetes Insipidus 54 0.067
91
P PLY017 Polyarteritis Nodosa 51 0.067
92
RNL077 Renal Fibrosis 49 0.067
93
LPD004 Lipoid Nephrosis 46 0.067
94
P RNL045 Renal Tubular Acidosis, Distal 42 0.067
95
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.067
96
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.067
97
c LKM004 Leukemia, B-Cell, Chronic 37 0.067
98
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.067
99
ACT003 Acute Kidney Tubular Necrosis 34 0.067
100
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.067
101
MYL069 Myeloma, Multiple 86 0.060
102
P RTN008 Retinitis Pigmentosa 81 0.060
103
MLN008 Melanoma 72 0.060
104
c SPN225 Spondyloarthropathy 1 71 0.060
105
P PNM007 Pneumonia 70 0.060
106
P ANR048 Aniridia 1 68 0.060
107
SKN016 Skin Disease 68 0.060
108
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.060
109
RHM027 Rheumatic Disease 62 0.060
110
P PLY014 Polycystic Kidney Disease 60 0.060
111
P INF032 Infertility 59 0.060
112
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.060
113
P END033 Endocarditis 58 0.060
114
HST011 Histoplasmosis 56 0.060
115
SPN051 Spondylitis 55 0.060
116
CRY004 Cryoglobulinemia 49 0.060
117
c ATM024 Autoimmune Pancreatitis 49 0.060
118
c BRN108 Branchiootic Syndrome 1 47 0.060
119
IRD001 Iridocyclitis 44 0.060
120
DNB001 Danubian Endemic Familial Nephropathy 44 0.060
121
c MCR130 Microvascular Complications of Diabetes 6 42 0.060
122
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 37 0.060
123
RNL012 Renal Tuberculosis 35 0.060
124
PYR004 Pyuria 34 0.060
125
c MCR120 Microvascular Complications of Diabetes 7 34 0.060
126
XNT001 Xanthogranulomatous Pyelonephritis 32 0.060
127
c MCR133 Microvascular Complications of Diabetes 4 32 0.060
128
SBS006 Sebastian Syndrome 30 0.060
129
EXF003 Exfoliative Dermatitis 28 0.060
130
ANR038 Anorexia Nervosa 1 21 0.060
131
c NPH075 Nephronophthisis 18 21 0.060
132
THY105 Thyrocerebroretinal Syndrome 20 0.060
133
BLD137 Blood Group--Ahonen 17 0.060
134
ULC004 Ulcerative Colitis 80 0.052
135
MNT001 Mantle Cell Lymphoma 76 0.052
136
c HPT001 Hepatitis C 73 0.052
137
LSH001 Leishmaniasis 71 0.052
138
BRC012 Brucellosis 71 0.052
139
P HRP006 Herpes Simplex 70 0.052
140
c HPT016 Hepatitis B 68 0.052
141
c DNG003 Dengue Disease 66 0.052
142
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.052
143
P NRP001 Neuropathy 63 0.052
144
P HMR003 Hemorrhagic Disease 61 0.052
145
P MMP001 Mumps 61 0.052
146
ANR040 Aneurysm 61 0.052
147
URT039 Urticaria 59 0.052
148
ALL026 Allergic Hypersensitivity Disease 59 0.052
149
VSC003 Visceral Leishmaniasis 59 0.052
150
P ENC018 Encephalopathy 58 0.052
151
P MYC008 Myocarditis 58 0.052
152
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.052
153
IMM158 Immune Suppression 57 0.052
154
P CYS018 Cystitis 57 0.052
155
P HYP726 Hypercalcemia, Infantile, 1 57 0.052
156
c ANM038 Anemia, Autoimmune Hemolytic 56 0.052
157
P HYP076 Hyperthyroidism 56 0.052
158
P DNG005 Dengue Virus 56 0.052
159
P HYP014 Hyperuricemia 54 0.052
160
HLL004 Hellp Syndrome 53 0.052
161
P PNV001 Panuveitis 52 0.052
162
OST011 Osteomalacia 52 0.052
163
HMG002 Hemoglobinuria 52 0.052
164
c MLG069 Malignant Hypertension 49 0.052
165
NPH003 Nephrocalcinosis 49 0.052
166
c LBR014 Leber Congenital Amaurosis 4 48 0.052
167
PRT014 Protein S Deficiency 47 0.052
168
NRR001 Neuroretinitis 46 0.052
169
MYH001 May-Hegglin Anomaly 45 0.052
170
c WLM011 Wilms Tumor 6 44 0.052
171
RTR011 Retroperitoneal Fibrosis 43 0.052
172
c NPH030 Nephronophthisis 2 41 0.052
173
GRN009 Granulomatous Hepatitis 38 0.052
174
P BLD051 Blood Coagulation Disease 38 0.052
175
PYL004 Pyelitis 38 0.052
176
ENT004 Enthesopathy 38 0.052
177
VSC008 Vascular Hemostatic Disease 36 0.052
178
c SYS061 Systemic Lupus Erythematosus 16 35 0.052
179
c HYP072 Hypersensitivity Reaction Type Iii Disease 35 0.052
180
PLS030 Plasminogen Deficiency, Type I 33 0.052
181
TXC010 Toxic Myocarditis 30 0.052
182
PPL052 Papillomatosis, Confluent and Reticulated 26 0.052
183
P LNG032 Lung Cancer 99 0.042
184
AST005 Asthma 83 0.042
185
P LVR013 Liver Disease 76 0.042
186
CNG034 Congestive Heart Failure 74 0.042
187
GLB002 Glioblastoma 74 0.042
188
P DBT009 Diabetes Mellitus 72 0.042
189
PRP027 Peripheral Vascular Disease 71 0.042
190
CMM004 Common Variable Immunodeficiency 71 0.042
191
VSC007 Vascular Disease 71 0.042
192
DWN001 Down Syndrome 70 0.042
193
P AGM001 Agammaglobulinemia 70 0.042
194
ART016 Aortic Aneurysm 70 0.042
195
P AGM019 Agammaglobulinemia, X-Linked 69 0.042
196
GLB015 Glioblastoma Multiforme 68 0.042
197
LNG099 Lung Disease 67 0.042
198
PRT036 Peritonitis 67 0.042
199
ACQ007 Acquired Immunodeficiency Syndrome 65 0.042
200
P THL005 Thalassemia 65 0.042
201
P HYP061 Hypertrophic Cardiomyopathy 65 0.042
202
CHL123 Chlamydia 64 0.042
203
LPT001 Leptospirosis 64 0.042
204
OST017 Osteomyelitis 64 0.042
205
ART005 Arteriovenous Malformation 64 0.042
206
P SRC025 Sarcoidosis 1 63 0.042
207
c HPT003 Hepatitis a 63 0.042
208
INT066 Interstitial Lung Disease 63 0.042
209
PLM033 Pulmonary Embolism 62 0.042
210
P HYP086 Hypothyroidism 62 0.042
211
P GRV001 Graves' Disease 62 0.042
212
P EXN002 Exanthem 62 0.042
213
MCS002 Mucositis 61 0.042
214
P GLM045 Glioma 61 0.042
215
P NTR004 Neutropenia 60 0.042
216
PLS011 Plasmacytoma 60 0.042
217
P ANT006 Antiphospholipid Syndrome 59 0.042
218
SNS001 Sensorineural Hearing Loss 59 0.042
219
P LMY004 Leiomyosarcoma 59 0.042
220
MCR088 Microscopic Polyangiitis 58 0.042
221
P SJG008 Sjogren Syndrome 58 0.042
222
P PLY041 Polymyositis 57 0.042
223
P LPD010 Lipodystrophy 57 0.042
224
NPH009 Nephrolithiasis 57 0.042
225
P CNT005 Central Nervous System Lymphoma 57 0.042
226
MST005 Mastitis 56 0.042
227
SLM003 Salmonellosis 56 0.042
228
STR008 Strongyloidiasis 54 0.042
229
P TRC086 Trichohepatoenteric Syndrome 1 54 0.042
230
LGN001 Legionnaires' Disease 53 0.042
231
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.042
232
P RTN022 Retinal Vein Occlusion 53 0.042
233
INT075 Intracranial Hypertension 53 0.042
234
CGN006 Cogan Syndrome 53 0.042
235
P CRN108 Cranioectodermal Dysplasia 1 53 0.042
236
P LCT001 Lactic Acidosis 51 0.042
237
P HML001 Hemolytic-Uremic Syndrome 50 0.042
238
c CNT016 Central Retinal Vein Occlusion 50 0.042
239
RNL024 Renal Glucosuria 50 0.042
240
P TCL004 T-Cell Leukemia 50 0.042
241
c PST005 Posterior Uveitis 50 0.042
242
INT303 Intracranial Hypertension, Idiopathic 49 0.042
243
P HML033 Hemolytic Uremic Syndrome, Atypical 1 49 0.042
244
P RNL028 Renal Tubular Dysgenesis 49 0.042
245
URT010 Ureteral Obstruction 49 0.042
246
RFR010 Refractory Anemia 48 0.042
247
ASC010 Ascaris Lumbricoides Infection 48 0.042
248
SKN027 Skin Conditions 48 0.042
249
P RPD001 Rapidly Progressive Glomerulonephritis 48 0.042
250
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.042
251
SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 47 0.042
252
LYM004 Lymphoid Interstitial Pneumonia 47 0.042
253
P MTH007 Methemoglobinemia 46 0.042
254
IMP004 Impetigo 45 0.042
255
LCH009 Lichen Sclerosus 45 0.042
256
c CHR086 Chronic Conjunctivitis 44 0.042
257
MNN034 Mannose-Binding Lectin Deficiency 44 0.042
258
NRN002 Neuronitis 43 0.042
259
c NPH068 Nephronophthisis 16 42 0.042
260
CMP009 Complement Deficiency 41 0.042
261
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.042
262
CRB009 Cerebritis 41 0.042
263
PDT035 Pediatric Systemic Lupus Erythematosus 41 0.042
264
URT008 Urticaria Pigmentosa 40 0.042
265
P HYP120 Hypoaldosteronism 40 0.042
266
CMP042 Complement Factor H Deficiency 39 0.042
267
IMM001 Immune-Complex Glomerulonephritis 39 0.042
268
P AXN001 Axonal Neuropathy 38 0.042
269
LYM042 Lymphocytic Colitis 38 0.042
270
c SBC003 Subacute Bacterial Endocarditis 38 0.042
271
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.042
272
RNL025 Renal Hypoplasia 37 0.042
273
LPT014 Leptin Deficiency or Dysfunction 37 0.042
274
IRT001 Iritis 36 0.042
275
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 36 0.042
276
VRS001 Virus Associated Hemophagocytic Syndrome 36 0.042
277
ACR005 Acrodermatitis 35 0.042
278
MLT035 Multifocal Choroiditis 35 0.042
279
LGN006 Legionnaire Disease 35 0.042
280
PLM052 Pulmonary Arteriovenous Malformation 35 0.042
281
P BCT020 Bacteremia 2 34 0.042
282
ALT002 Aleutian Mink Disease 33 0.042
283
DFF015 Diffuse Glomerulonephritis 32 0.042
284
INF009 Inflammatory Spondylopathy 32 0.042
285
CHL070 Cholesterol Embolism 31 0.042
286
MTC085 Mitochondrial Complex Iii Deficiency, Nuclear Type 1 31 0.042
287
P KLZ004 Kala-Azar 1 31 0.042
288
ALR002 Al-Raqad Syndrome 30 0.042
289
c ATM097 Autoimmune Lymphoproliferative Syndrome, Type Iia 30 0.042
290
PCM002 Pauci-Immune Glomerulonephritis 30 0.042
291
THY001 Thyroid Crisis 30 0.042
292
ACR097 Acrodermatitis Chronica Atrophicans 29 0.042
293
c MDL008 Medullary Cystic Kidney Disease 1 28 0.042
294
HMX003 Heme Oxygenase 1 Deficiency 26 0.042
295
CRB190 Cerebellar Degeneration-Related Autoantigen 3 26 0.042
296
DFF031 Diffuse Alveolar Hemorrhage 25 0.042
297
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.042
298
P C1Q005 C1q Nephropathy 23 0.042
299
P ATM067 Autoimmune Polyendocrinopathy Type 3 22 0.042
300
CMB043 Combined Oxidative Phosphorylation Deficiency 9 22 0.042
301
ACT201 Acute Posterior Multifocal Placoid Pigment Epitheliopathy 21 0.042
302
c SNR016 Senior-Loken Syndrome 9 21 0.042
303
c ATM066 Autoimmune Polyendocrinopathy Type 4 21 0.042
304
INS009 Insulin-Resistance Type B 20 0.042
305
c NPH086 Nephronophthisis 20 19 0.042
306
RTN199 Retinal Venous Beading 19 0.042
307
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 18 0.042
308
CNG330 Congenital Megacalycosis 16 0.042
309
HMP028 Hemophagocytic Syndrome Associated with an Infection 15 0.042
310
CMP086 Complement Component C1r/c1s Deficiency 12 0.042
311
P MLT020 Multiple Sclerosis 85 0.030
312
GST053 Gastric Cancer 84 0.030
313
P HRT032 Heart Disease 80 0.030
314
LYM133 Lymphoma, Hodgkin, Classic 78 0.030
315
P NNN008 Noonan Syndrome 1 77 0.030
316
P WSK001 Wiskott-Aldrich Syndrome 76 0.030
317
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.030
318
PFF001 Pfeiffer Syndrome 74 0.030
319
c HPT073 Hepatitis C Virus 73 0.030
320
ISC006 Ischemic Heart Disease 73 0.030
321
P FML018 Familial Mediterranean Fever 73 0.030
322
LVR012 Liver Cirrhosis 73 0.030
323
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.030
324
P MNN013 Meningitis 71 0.030
325
P SCH015 Schizophrenia 71 0.030
326
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.030
327
c BTT014 Beta-Thalassemia 70 0.030
328
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.030
329
P MYP004 Myopathy 69 0.030
330
CRB039 Cerebrovascular Disease 68 0.030
331
c PRM196 Premature Ovarian Failure 1 68 0.030
332
P ALG028 Alagille Syndrome 1 68 0.030
333
P ART023 Arthropathy 68 0.030
334
P CHR071 Charcot-Marie-Tooth Disease 67 0.030
335
P TMP003 Temporal Arteritis 67 0.030
336
c LCL006 Localized Scleroderma 66 0.030
337
P ENC004 Encephalitis 66 0.030
338
ACR006 Aceruloplasminemia 65 0.030
339
P SLP006 Sleep Apnea 65 0.030
340
c PRC016 Pre-Eclampsia 65 0.030
341
TTN003 Tetanus 65 0.030
342
RCT015 Reactive Arthritis 65 0.030
343
OVR029 Ovarian Hyperstimulation Syndrome 64 0.030
344
BLL006 Bullous Pemphigoid 64 0.030
345
VRL011 Viral Infectious Disease 64 0.030
346
P CCK001 Cockayne Syndrome 64 0.030
347
SVR097 Severe Cutaneous Adverse Reaction 64 0.030
348
DPH001 Diphtheria 63 0.030
349
RFS006 Refsum Disease, Classic 63 0.030
350
P MYS005 Myositis 63 0.030
351
P ALC004 Alcohol Abuse 63 0.030
352
P PRP029 Porphyria 62 0.030
353
P CMR001 Camurati-Engelmann Disease 62 0.030
354
LYM021 Lymphadenitis 62 0.030
355
GTL001 Gitelman Syndrome 62 0.030
356
c ACT027 Acute Pancreatitis 61 0.030
357
HYP266 Hypoxia 61 0.030
358
INT002 Intermittent Claudication 61 0.030
359
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.030
360
c THR092 Thrombophilia Due to Thrombin Defect 61 0.030
361
TNS005 Tonsillitis 61 0.030
362
QFV001 Q Fever 61 0.030
363
P GLL022 Guillain-Barre Syndrome 61 0.030
364
HRP004 Herpes Zoster 61 0.030
365
P RBL001 Rubella 61 0.030
366
SPT004 Septic Arthritis 60 0.030
367
P DRR001 Diarrhea 60 0.030
368
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.030
369
PRP083 Porphyria, Acute Intermittent 60 0.030
370
CCC001 Coccidioidomycosis 60 0.030
371
GT001 Gout 60 0.030
372
ERY003 Erythema Multiforme 60 0.030
373
PRS047 Prostatitis 59 0.030
374
c PRM005 Primary Hyperparathyroidism 59 0.030
375
RHM001 Rheumatic Fever 59 0.030
376
PHR003 Pharyngitis 59 0.030
377
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.030
378
P HYP069 Hyperparathyroidism 58 0.030
379
P ECL001 Eclampsia 57 0.030
380
P OCL002 Oculocutaneous Albinism 57 0.030
381
URN010 Urinary Tract Obstruction 57 0.030
382
EPD016 Epidermolysis Bullosa 57 0.030
383
PLM010 Pulmonary Edema 57 0.030
384
c ALM001 Al Amyloidosis 56 0.030
385
P ALP008 Alopecia 56 0.030
386
BNF002 Bone Fracture 56 0.030
387
c HYP731 Hyperaldosteronism, Familial, Type I 56 0.030
388
MTH078 Methylmalonic Aciduria, Cblb Type 56 0.030
389
CYS010 Cystinosis 55 0.030
390
P DNT020 Dent Disease 1 55 0.030
391
P LYM033 Lymphoproliferative Syndrome 55 0.030
392
GDP001 Goodpasture Syndrome 55 0.030
393
ARS001 Aarskog-Scott Syndrome 55 0.030
394
PRN038 Prune Belly Syndrome 55 0.030
395
TTH006 Tooth Disease 54 0.030
396
SCK005 Sickle Cell Disease 54 0.030
397
c INF071 Inflammatory Bowel Disease 1 54 0.030
398
CRY005 Cryptococcosis 54 0.030
399
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 54 0.030
400
CLC001 Calciphylaxis 53 0.030
401
P CLL015 Collagen Disease 53 0.030
402
CRH005 Crohn's Colitis 53 0.030
403
P SCL009 Sclerosing Cholangitis 53 0.030
404
P CTN003 Cutaneous Lupus Erythematosus 53 0.030
405
P TRN034 Transverse Myelitis 53 0.030
406
ERY008 Erythromelalgia 53 0.030
407
P DDN001 Duodenal Ulcer 53 0.030
408
ALC009 Alcoholic Liver Cirrhosis 53 0.030
409
FBR032 Fibromuscular Dysplasia 53 0.030
410
ESN015 Eosinophilic Fasciitis 52 0.030
411
P BRT004 Bartter Disease 52 0.030
412
CRN030 Coronary Stenosis 52 0.030
413
URM002 Uremia 52 0.030
414
P CHL066 Cholangitis 52 0.030
415
HPT082 Hepatic Adenomas, Familial 52 0.030
416
MYL001 Myelitis 52 0.030
417
CHR001 Churg-Strauss Syndrome 51 0.030
418
P GLM040 Glioma Susceptibility 1 51 0.030
419
CTS002 Cat-Scratch Disease 51 0.030
420
ART140 Arteries, Anomalies of 51 0.030
421
c PRM226 Primary Central Nervous System Lymphoma 51 0.030
422
c ART115 Aortic Valve Disease 1 51 0.030
423
P END047 Endophthalmitis 51 0.030
424
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 51 0.030
425
PRS045 Prostatic Hypertrophy 51 0.030
426
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.030
427
WHP001 Whipple Disease 50 0.030
428
PNC001 Pancytopenia 50 0.030
429
c RTN162 Retinitis Pigmentosa 2 50 0.030
430
HMS001 Hemosiderosis 50 0.030
431
ANS023 Anus, Imperforate 50 0.030
432
P CRV039 Cervicitis 49 0.030
433
HYD002 Hydronephrosis 49 0.030
434
SLD003 Sialadenitis 49 0.030
435
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.030
436
c WLM018 Wilms Tumor 5 49 0.030
437
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.030
438
MLT113 Multicentric Castleman Disease 49 0.030
439
PRN009 Paranoid Schizophrenia 49 0.030
440
HPT014 Hepatorenal Syndrome 49 0.030
441
CYS039 Cystic Kidney Disease 49 0.030
442
FBR009 Fibrous Dysplasia 49 0.030
443
RNL078 Renal Dysplasia 49 0.030
444
FSC004 Fasciitis 48 0.030
445
P PLM085 Pulmonary Hemosiderosis 48 0.030
446
DSC009 Discoid Lupus Erythematosus 48 0.030
447
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.030
448
CHC001 Chickenpox 48 0.030
449
KMR001 Kimura Disease 48 0.030
450
PNN001 Panniculitis 48 0.030
451
CHN016 Cohen Syndrome 48 0.030
452
LMR001 Lemierre's Syndrome 47 0.030
453
MLT016 Multicentric Reticulohistiocytosis 47 0.030
454
RTN001 Retinal Vasculitis 47 0.030
455
DST006 Diastolic Heart Failure 47 0.030
456
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.030
457
P RNL015 Renal Hypertension 46 0.030
458
SPN119 Spondylarthropathy 46 0.030
459
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.030
460
NPH010 Nephrosclerosis 46 0.030
461
PLC003 Placental Site Trophoblastic Tumor 46 0.030
462
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.030
463
ANT039 Antisynthetase Syndrome 46 0.030
464
BNN003 Bone Inflammation Disease 46 0.030
465
DDN006 Duodenitis 46 0.030
466
ALB002 Albinism 45 0.030
467
PRM013 Premature Menopause 45 0.030
468
P PRT026 Parotitis 45 0.030
469
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.030
470
MNN032 Meningococcal Meningitis 45 0.030
471
CRD001 Cardiac Tamponade 45 0.030
472
BRN014 Bronchopneumonia 45 0.030
473
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.030
474
OST004 Osteitis Fibrosa 45 0.030
475
TLR001 Tularemia 44 0.030
476
NRN008 Neuronal Intranuclear Inclusion Disease 44 0.030
477
INT071 Intestinal Perforation 44 0.030
478
DCB001 Decubitus Ulcer 44 0.030
479
DNR002 Duane-Radial Ray Syndrome 44 0.030
480
CST005 Castleman Disease 44 0.030
481
SYS003 Systolic Heart Failure 44 0.030
482
MDS022 Mediastinitis 44 0.030
483
TRN004 Trench Fever 44 0.030
484
P FNG006 Feingold Syndrome 1 44 0.030
485
MRG013 Mirage Syndrome 44 0.030
486
NCR004 Nocardiosis 43 0.030
487
RLP003 Relapsing Fever 43 0.030
488
CLL002 Collecting Duct Carcinoma 43 0.030
489
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 43 0.030
490
c SBC007 Subacute Thyroiditis 43 0.030
491
c NPH019 Nephronophthisis 1 42 0.030
492
PSD009 Pseudohermaphroditism 42 0.030
493
LGN005 Ligneous Conjunctivitis 42 0.030
494
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.030
495
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.030
496
P CRN035 Cranial Nerve Palsy 42 0.030
497
CRB086 Cerebral Aneurysms 42 0.030
498
P CNG048 Congenital Hepatic Fibrosis 41 0.030
499
CHR078 Chorioretinitis 41 0.030
500
LRW001 Leri-Weill Dyschondrosteosis 41 0.030
501
LYM029 Lymphedema-Distichiasis Syndrome 41 0.030
502
SCR015 Scarlet Fever 40 0.030
503
c HYP758 Hyperuricemic Nephropathy, Familial Juvenile, 1 40 0.030
504
MLR002 Miliary Tuberculosis 40 0.030
505
c NPH049 Nephrotic Syndrome, Type 2 40 0.030
506
PRT019 Protein-Losing Enteropathy 40 0.030
507
PPT001 Peptic Esophagitis 40 0.030
508
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.030
509
HYP008 Hypertensive Retinopathy 39 0.030
510
GLC008 Glucose Metabolism Disease 38 0.030
511
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.030
512
RNL097 Renal Artery Disease 38 0.030
513
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.030
514
PPT002 Peptic Ulcer Perforation 38 0.030
515
HPT008 Hepatic Tuberculosis 37 0.030
516
LNS003 Lens Disease 37 0.030
517
P GRM010 Germ Cells Tumors 37 0.030
518
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.030
519
GNR003 Generalized Atherosclerosis 35 0.030
520
RHM035 Rheumatic Fever-Related Antigen 34 0.030
521
CRT012 Cortical Blindness 34 0.030
522
c FNC059 Fanconi-Like Syndrome 34 0.030
523
MYC022 Mycoplasmal Pneumonia 34 0.030
524
c CTR174 Cataract 40 33 0.030
525
HYP084 Hypopyon 33 0.030
526
PLM151 Pulmonary Arteriovenous Fistulas 33 0.030
527
HYP540 Hypertension, Diastolic 32 0.030
528
PRG023 Progeroid Short Stature with Pigmented Nevi 32 0.030
529
P ACQ009 Acquired Metabolic Disease 32 0.030
530
CHR077 Chorioretinal Scar 32 0.030
531
RNL001 Renal Artery Obstruction 31 0.030
532
ALP048 Alopecia Totalis 31 0.030
533
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.030
534
CLF028 Cleft Soft Palate 30 0.030
535
ATM052 Autoimmune Disease 1 30 0.030
536
c SRC023 Sarcoidosis 2 30 0.030
537
PDT040 Pediatric Hypertension 30 0.030
538
ORT001 Orthostatic Proteinuria 29 0.030
539
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 29 0.030
540
SVN002 Sveinsson Chorioretinal Atrophy 29 0.030
541
c ATR031 Atrial Septal Defect 4 29 0.030
542
IMM073 Immunoglobulin a Vasculitis 28 0.030
543
P STR035 Streptococcal Group a Invasive Disease 28 0.030
544
CVR002 Cavernous Sinus Thrombosis 28 0.030
545
P SCL057 Scoliosis, Isolated 1 28 0.030
546
KDN006 Kidney Papillary Necrosis 27 0.030
547
c BNG021 Benign Essential Hypertension 27 0.030
548
PRR001 Periarthritis 27 0.030
549
c TRN014 Transient Arthritis 27 0.030
550
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.030
551
MDL024 Madelung Deformity 26 0.030
552
HYP226 Hyporeninemic Hypoaldosteronism 25 0.030
553
LTR002 Lateral Sinus Thrombosis 24 0.030
554
IMM053 Immunotactoid Glomerulopathy 23 0.030
555
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 21 0.030
556
CYT017 Cytophagic Histiocytic Panniculitis 21 0.030
557
MYH004 Myh9 Related Thrombocytopenia 20 0.030
558
c NPH077 Nephronophthisis 19 20 0.030
559
ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 20 0.030
560
c CTR025 Cataract, Total Congenital 20 0.030
561
CMP091 Complement Component C1s Deficiency 20 0.030
562
c NPH069 Nephronophthisis 15 19 0.030
563
IGG016 Igg4-Related Dacryoadenitis and Sialadenitis 18 0.030
564
c IGN002 Iga Nephropathy 2 17 0.030
565
IMM162 Immunoglobulin E Concentration, Serum 16 0.030
566
c PSD047 Pseudo-Turner Syndrome 15 0.030
567
APM002 Aapoai Amyloidosis 15 0.030
568
BRK013 Birk-Landau-Perez Syndrome 13 0.030
569
PYR005 Pyoureter 6 0.030
Content
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