Search results for "nephritis"

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

591 hits were found for 'nephritis'

# Family MCID Name MIFTS Score
1
P ALP004 Alport Syndrome 68 6.376
2
INT067 Interstitial Nephritis 48 5.770
3
INT258 Interstitial Nephritis, Karyomegalic 21 5.538
4
c SYS001 Systemic Lupus Erythematosus 87 4.720
5
TBL025 Tubulointerstitial Nephritis with Uveitis 21 4.584
6
DFN014 Deafness Nephritis Anorectal Malformation 12 4.117
7
MGL007 Megalocytic Interstitial Nephritis 13 3.801
8
DYS180 Dyschondrosteosis and Nephritis 14 3.685
9
EPS006 Epstein Syndrome 40 3.224
10
P GLM015 Glomerulopathy with Fibronectin Deposits 2 22 3.140
11
P SYS050 Systemic Lupus Erythematosus with Nephritis 2 11 2.945
12
c SYS056 Systemic Lupus Erythematosus with Nephritis 1 11 2.926
13
c SYS054 Systemic Lupus Erythematosus with Nephritis 3 12 2.922
14
HMT008 Hematuria, Benign Familial 44 2.598
15
ACT041 Acute Diffuse Nephritis 7 2.598
16
FCH003 Fechtner Syndrome 36 1.898
17
P IGN003 Iga Nephropathy 1 31 1.871
18
c ALP073 Alport Syndrome, Autosomal Recessive 41 1.837
19
c ALP074 Alport Syndrome, Autosomal Dominant 37 1.837
20
SPS196 Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 13 1.813
21
FTZ004 Fitzsimmons Walson Mellor Syndrome 6 1.813
22
P LPS004 Lupus Erythematosus 63 0.389
23
P GLM007 Glomerulonephritis 56 0.351
24
P UVT001 Uveitis 60 0.343
25
PRP030 Purpura 60 0.272
26
CNN005 Connective Tissue Disease 60 0.269
27
c SYS038 Systemic Lupus Erythematosus 2 26 0.224
28
ATM053 Autoimmune Disease 2 16 0.224
29
c SYS043 Systemic Lupus Erythematosus 1 29 0.214
30
ATM052 Autoimmune Disease 1 26 0.214
31
ATM054 Autoimmune Disease 3 16 0.212
32
c SYS046 Systemic Lupus Erythematosus 3 22 0.212
33
P KDN018 Kidney Disease 64 0.204
34
P URF003 Urofacial Syndrome 1 51 0.187
35
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.182
36
ATM055 Autoimmune Disease 4 16 0.182
37
c SYS051 Systemic Lupus Erythematosus 4 21 0.182
38
P PRL003 Proliferative Glomerulonephritis 40 0.173
39
VSC011 Vasculitis 62 0.162
40
URN009 Urinary System Disease 52 0.152
41
ATM059 Autoimmune Disease 6 23 0.152
42
c SYS040 Systemic Lupus Erythematosus 10 21 0.152
43
HNC001 Henoch-Schoenlein Purpura 45 0.149
44
P MMB011 Membranous Nephropathy 53 0.146
45
P HPT021 Hepatitis 74 0.143
46
P NPH012 Nephrotic Syndrome 55 0.134
47
c SYS055 Systemic Lupus Erythematosus 12 21 0.134
48
P ART022 Arthritis 73 0.127
49
P FNC004 Fanconi Syndrome 54 0.127
50
MMB002 Membranous Glomerulonephritis 47 0.127
51
P PYL005 Pyelonephritis 52 0.124
52
ATM012 Autoimmune Disease of Blood 36 0.113
53
C3D001 C3 Deficiency 50 0.109
54
c SYS053 Systemic Lupus Erythematosus 5 20 0.109
55
CRH001 Crohn's Disease 76 0.105
56
TBR010 Tuberculosis 70 0.105
57
c SYS048 Systemic Lupus Erythematosus 8 17 0.105
58
END030 End Stage Renal Failure 53 0.101
59
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 40 0.097
60
P LYM118 Lymphoma 68 0.097
61
c RNL016 Renal Infectious Disease 22 0.097
62
END072 Endotheliitis 41 0.097
63
BRN024 Bronchitis 67 0.092
64
RNL007 Renal Tubular Acidosis 50 0.092
65
MMB001 Membranoproliferative Glomerulonephritis 44 0.092
66
GLC077 Glucocorticoid Therapy, Response to 17 0.092
67
c CHR098 Chronic Pyelonephritis 38 0.092
68
P RHM011 Rheumatoid Arthritis 87 0.088
69
c CHR089 Chronic Kidney Failure 67 0.088
70
MLK004 Malakoplakia 28 0.088
71
P LKM002 Leukemia 70 0.083
72
ACT040 Acute Poststreptococcal Glomerulonephritis 30 0.083
73
RTN023 Retinitis 49 0.083
74
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.077
75
P ESN007 Eosinophilia 61 0.077
76
LPD004 Lipoid Nephrosis 49 0.077
77
P THR014 Thrombocytopenia 63 0.077
78
IGG007 Igg4-Related Disease 39 0.077
79
ANR004 Anuria 46 0.077
80
P AMY004 Amyloidosis 63 0.077
81
c ANT034 Anterior Uveitis 49 0.077
82
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.077
83
c ACT042 Acute Pyelonephritis 47 0.077
84
GLM011 Glomerulosclerosis 41 0.077
85
c CHR090 Chronic Lymphocytic Leukemia 73 0.071
86
P KDN017 Kidney Cancer 67 0.071
87
P FCL005 Focal Segmental Glomerulosclerosis 59 0.071
88
DRM006 Dermatitis 58 0.071
89
P NPH005 Nephronophthisis 55 0.071
90
P HML002 Hemolytic Anemia 60 0.071
91
P PLY017 Polyarteritis Nodosa 54 0.071
92
P INF038 Influenza 71 0.071
93
P PNC044 Pancreatitis 62 0.071
94
P PRM006 Primary Biliary Cirrhosis 55 0.071
95
P DBT005 Diabetes Insipidus 53 0.071
96
IRD001 Iridocyclitis 40 0.071
97
P THY032 Thyroiditis 57 0.071
98
BCT015 Bacteremia 50 0.071
99
MSN001 Mesangial Proliferative Glomerulonephritis 41 0.071
100
P MYL007 Myeloma 52 0.071
101
CLT003 Colitis 56 0.071
102
c SYS065 Systemic Lupus Erythematosus 11 18 0.071
103
P CNN004 Connective Tissue Cancer 44 0.071
104
CHR008 Choroiditis 43 0.071
105
SPN051 Spondylitis 50 0.071
106
XNT001 Xanthogranulomatous Pyelonephritis 32 0.071
107
c MLT019 Multiple Myeloma 77 0.065
108
P RTN008 Retinitis Pigmentosa 78 0.065
109
HST011 Histoplasmosis 54 0.065
110
c ATM010 Autoimmune Hemolytic Anemia 59 0.065
111
CRY004 Cryoglobulinemia 47 0.065
112
BLK001 Balkan Nephropathy 34 0.065
113
P HYP004 Hypercalcemia 54 0.065
114
P PLY014 Polycystic Kidney Disease 60 0.065
115
IRT001 Iritis 36 0.065
116
NPH004 Nephropathia Epidemica 39 0.065
117
c ATM024 Autoimmune Pancreatitis 46 0.065
118
RNL012 Renal Tuberculosis 42 0.065
119
EXF003 Exfoliative Dermatitis 25 0.065
120
c SYS052 Systemic Lupus Erythematosus 13 14 0.065
121
CRS001 Crescentic Glomerulonephritis 41 0.065
122
DFF015 Diffuse Glomerulonephritis 35 0.065
123
IMM001 Immune-Complex Glomerulonephritis 41 0.065
124
c ATM007 Autoimmune Disease of Central Nervous System 29 0.065
125
IGG011 Igg4-Related Kidney Disease 14 0.065
126
RNL077 Renal Fibrosis 48 0.065
127
SKN016 Skin Disease 69 0.058
128
HV1006 Hiv-1 80 0.058
129
c SPN225 Spondyloarthropathy 1 62 0.058
130
P LVR013 Liver Disease 76 0.058
131
MLN008 Melanoma 61 0.058
132
URT039 Urticaria 58 0.058
133
ULC004 Ulcerative Colitis 74 0.058
134
ACR041 Acromelic Frontonasal Dysostosis 45 0.058
135
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.058
136
P INF032 Infertility 61 0.058
137
LSH001 Leishmaniasis 63 0.058
138
BRC012 Brucellosis 66 0.058
139
c HPT016 Hepatitis B 61 0.058
140
ATN002 Autonomic Nervous System Disease 46 0.058
141
P HRP006 Herpes Simplex 65 0.058
142
MNT001 Mantle Cell Lymphoma 72 0.058
143
P PNM007 Pneumonia 67 0.058
144
P NTR004 Neutropenia 59 0.058
145
VSC003 Visceral Leishmaniasis 56 0.058
146
P CYS018 Cystitis 54 0.058
147
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.058
148
HMG002 Hemoglobinuria 49 0.058
149
c SYS041 Systemic Lupus Erythematosus 9 21 0.058
150
VND001 Vein Disease 51 0.058
151
IGG001 Iga Glomerulonephritis 46 0.058
152
P MYC008 Myocarditis 56 0.058
153
HLL004 Hellp Syndrome 48 0.058
154
RTR011 Retroperitoneal Fibrosis 40 0.058
155
P PNV001 Panuveitis 50 0.058
156
BRT030 Birth Defects 44 0.058
157
c CHR417 Chronic Graft Versus Host Disease 50 0.058
158
ADJ001 Adjustment Disorder 38 0.058
159
ANR040 Aneurysm 56 0.058
160
PYL004 Pyelitis 39 0.058
161
c SYS045 Systemic Lupus Erythematosus 14 16 0.058
162
WTH001 Withdrawal Disorder 36 0.058
163
TXC010 Toxic Myocarditis 28 0.058
164
ATM005 Autoimmune Disease of Musculoskeletal System 14 0.058
165
P LNG032 Lung Cancer 92 0.051
166
CNG034 Congestive Heart Failure 72 0.051
167
PCK002 Pick Disease 66 0.051
168
c INF071 Inflammatory Bowel Disease 1 51 0.051
169
ALS001 Alstrom Syndrome 52 0.051
170
ART016 Aortic Aneurysm 67 0.051
171
GLL022 Guillain-Barre Syndrome 58 0.051
172
DWN001 Down Syndrome 65 0.051
173
LPT001 Leptospirosis 65 0.051
174
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.051
175
CMM004 Common Variable Immunodeficiency 68 0.051
176
c HPT001 Hepatitis C 68 0.051
177
P MYP004 Myopathy 67 0.051
178
STR008 Strongyloidiasis 51 0.051
179
ART005 Arteriovenous Malformation 63 0.051
180
P GLB002 Glioblastoma 65 0.051
181
MYH001 May-Hegglin Anomaly 41 0.051
182
c HPT003 Hepatitis a 55 0.051
183
P ENC018 Encephalopathy 59 0.051
184
SBS006 Sebastian Syndrome 36 0.051
185
CGN006 Cogan Syndrome 48 0.051
186
P NPH009 Nephrolithiasis 59 0.051
187
ACQ007 Acquired Immunodeficiency Syndrome 60 0.051
188
P MMP001 Mumps 56 0.051
189
CHL123 Chlamydia 60 0.051
190
GLB015 Glioblastoma Multiforme 63 0.051
191
c SYS061 Systemic Lupus Erythematosus 16 28 0.051
192
P ABD003 Abdominal Aortic Aneurysm 43 0.051
193
OST017 Osteomyelitis 60 0.051
194
P HYP014 Hyperuricemia 49 0.051
195
c NPH075 Nephronophthisis 18 19 0.051
196
NPH003 Nephrocalcinosis 47 0.051
197
PLS011 Plasmacytoma 57 0.051
198
ALR002 Al-Raqad Syndrome 36 0.051
199
MST005 Mastitis 53 0.051
200
PLM052 Pulmonary Arteriovenous Malformation 36 0.051
201
c INF067 Inflammatory Bowel Disease 10 31 0.051
202
PYR004 Pyuria 33 0.051
203
THY001 Thyroid Crisis 29 0.051
204
CHL070 Cholesterol Embolism 31 0.051
205
P NRP001 Neuropathy 57 0.051
206
ALT002 Aleutian Mink Disease 25 0.051
207
LCH009 Lichen Sclerosus 43 0.051
208
RNL025 Renal Hypoplasia 40 0.051
209
P END033 Endocarditis 52 0.051
210
ACR097 Acrodermatitis Chronica Atrophicans 35 0.051
211
P LMY004 Leiomyosarcoma 54 0.051
212
P GLM045 Glioma 53 0.051
213
LYM004 Lymphoid Interstitial Pneumonia 40 0.051
214
URT008 Urticaria Pigmentosa 37 0.051
215
RFR010 Refractory Anemia 43 0.051
216
P PLY041 Polymyositis 49 0.051
217
BNN003 Bone Inflammation Disease 46 0.051
218
LYM042 Lymphocytic Colitis 34 0.051
219
CHR078 Chorioretinitis 41 0.051
220
ACR005 Acrodermatitis 33 0.051
221
c PST005 Posterior Uveitis 46 0.051
222
P SCL009 Sclerosing Cholangitis 47 0.051
223
c CNT016 Central Retinal Vein Occlusion 34 0.051
224
P TCL004 T-Cell Leukemia 44 0.051
225
GRN009 Granulomatous Hepatitis 37 0.051
226
P RTN022 Retinal Vein Occlusion 36 0.051
227
BLL016 Bullous Systemic Lupus Erythematosus 23 0.051
228
c TRN014 Transient Arthritis 36 0.051
229
PRR008 Periarteritis Nodosa 28 0.051
230
IMP003 Impaired Renal Function Disease 36 0.051
231
P AXN001 Axonal Neuropathy 37 0.051
232
ATM016 Autoimmune Disease of Skin and Connective Tissue 30 0.051
233
P C1Q005 C1q Nephropathy 22 0.051
234
ACR059 Acro-Renal-Ocular Syndrome 19 0.051
235
SCK003 Sickle Cell Anemia 72 0.041
236
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.041
237
PLM033 Pulmonary Embolism 59 0.041
238
ARS001 Aarskog-Scott Syndrome 52 0.041
239
LRW001 Leri-Weill Dyschondrosteosis 42 0.041
240
URT004 Urethral Syndrome 45 0.041
241
c ART101 Aortic Valve Disease 2 56 0.041
242
CHN016 Cohen Syndrome 55 0.041
243
LGS001 Legius Syndrome 50 0.041
244
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 51 0.041
245
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 40 0.041
246
c NRF018 Neurofibromatosis, Type 1 69 0.041
247
PRP019 Peripheral Nervous System Disease 52 0.041
248
PLS030 Plasminogen Deficiency, Type I 35 0.041
249
c NML014 Nemaline Myopathy 1, Autosomal Dominant or Recessive 34 0.041
250
P NML001 Nemaline Myopathy 47 0.041
251
P CNG046 Congenital Fiber-Type Disproportion 49 0.041
252
P HYP086 Hypothyroidism 63 0.041
253
PRT036 Peritonitis 65 0.041
254
P PRV002 Periventricular Nodular Heterotopia 46 0.041
255
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.041
256
P THL005 Thalassemia 61 0.041
257
P RBL001 Rubella 54 0.041
258
P MCR113 Microvascular Complications of Diabetes 3 48 0.041
259
c NPH045 Nephronophthisis 2, Infantile 30 0.041
260
SPT004 Septic Arthritis 60 0.041
261
IMP002 Imperforate Anus 54 0.041
262
SPL012 Splenic Disease 48 0.041
263
CMP042 Complement Factor H Deficiency 40 0.041
264
P RNL028 Renal Tubular Dysgenesis 52 0.041
265
CTS003 Coats Disease 57 0.041
266
P HYP076 Hyperthyroidism 59 0.041
267
RHM027 Rheumatic Disease 55 0.041
268
HYP074 Hypersensitivity Vasculitis 49 0.041
269
c NPH046 Nephrolithiasis, Type I 31 0.041
270
SVN001 Sveinsson Choreoretinal Atrophy 28 0.041
271
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.041
272
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.041
273
c PLY059 Polycystic Kidney Disease, Adult Type I 36 0.041
274
P ANT006 Antiphospholipid Syndrome 60 0.041
275
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 19 0.041
276
c CNG464 Congenital Myopathy 49 0.041
277
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.041
278
P LPR002 Leopard Syndrome 53 0.041
279
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 33 0.041
280
c MCR120 Microvascular Complications of Diabetes 7 29 0.041
281
MYC002 Mycobacterium Avium Complex Disease 52 0.041
282
P KLZ004 Kala-Azar 1 25 0.041
283
c BRN108 Branchiootic Syndrome 1 36 0.041
284
c EPL026 Epileptic Encephalopathy, Early Infantile, 3 28 0.041
285
INT075 Intracranial Hypertension 52 0.041
286
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.041
287
c MCR130 Microvascular Complications of Diabetes 6 26 0.041
288
PLN005 Palindromic Rheumatism 43 0.041
289
SKN027 Skin Conditions 44 0.041
290
OPT010 Optic Papillitis 30 0.041
291
IMP004 Impetigo 41 0.041
292
MYL004 Myelodysplastic Myeloproliferative Cancer 46 0.041
293
c CHR086 Chronic Conjunctivitis 46 0.041
294
c MCR133 Microvascular Complications of Diabetes 4 27 0.041
295
c MCR112 Microvascular Complications of Diabetes 2 27 0.041
296
HMX002 Heme Oxygenase-1 Deficiency 25 0.041
297
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.041
298
URT001 Urethritis 39 0.041
299
PRP021 Peripheral Nervous System Neoplasm 49 0.041
300
c MLG069 Malignant Hypertension 46 0.041
301
MCR088 Microscopic Polyangiitis 47 0.041
302
CRH005 Crohn's Colitis 50 0.041
303
P ALC004 Alcohol Abuse 57 0.041
304
DYS015 Dysentery 42 0.041
305
ACT003 Acute Kidney Tubular Necrosis 31 0.041
306
PLX002 Plexiform Neurofibroma 42 0.041
307
P CTN003 Cutaneous Lupus Erythematosus 49 0.041
308
CPM001 Cap Myopathy 32 0.041
309
ENT004 Enthesopathy 29 0.041
310
NRS006 Norse 21 0.041
311
P CNT005 Central Nervous System Lymphoma 51 0.041
312
CNJ012 Conjunctival Disease 48 0.041
313
c SBC003 Subacute Bacterial Endocarditis 33 0.041
314
P LPD010 Lipodystrophy 51 0.041
315
LKC003 Leukocyte Disease 45 0.041
316
VSC009 Vascular Skin Disease 21 0.041
317
RHM009 Rheumatoid Lung Disease 41 0.041
318
IND004 Indeterminate Leprosy 32 0.041
319
NRR001 Neuroretinitis 41 0.041
320
BLN010 Balanitis 29 0.041
321
c INT274 Intermediate Congenital Nemaline Myopathy 19 0.041
322
P BLD051 Blood Coagulation Disease 44 0.041
323
CMP009 Complement Deficiency 39 0.041
324
CNG032 Congenital Structural Myopathy 28 0.041
325
KDN006 Kidney Papillary Necrosis 26 0.041
326
CHL107 Childhood-Onset Nemaline Myopathy 20 0.041
327
c SVR040 Severe Congenital Nemaline Myopathy 22 0.041
328
FTD001 Foot Drop 34 0.041
329
ADR004 Adrenal Cortical Adenocarcinoma 35 0.041
330
c SYS047 Systemic Lupus Erythematosus 7 15 0.041
331
TYP026 Typical Congenital Nemaline Myopathy 18 0.041
332
VSC008 Vascular Hemostatic Disease 30 0.041
333
c CHR093 Chronic Orbital Inflammation 30 0.041
334
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.041
335
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 19 0.041
336
GLC001 Glaucomatocyclitic Crisis 28 0.041
337
CRB009 Cerebritis 36 0.041
338
c ACT081 Acute Salpingitis 36 0.041
339
P PRM016 Primary Optic Atrophy 29 0.041
340
IMM127 Immune System Cancer 41 0.041
341
SNS023 Sensory System Cancer 45 0.041
342
THL010 Thalassemia Minor 38 0.041
343
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 14 0.041
344
URT010 Ureteral Obstruction 45 0.041
345
DFF031 Diffuse Alveolar Hemorrhage 24 0.041
346
BNS002 Bone Structure Disease 37 0.041
347
GST078 Gastrointestinal Allergy 41 0.041
348
PCM002 Pauci-Immune Glomerulonephritis 31 0.041
349
VRS001 Virus Associated Hemophagocytic Syndrome 34 0.041
350
HPT023 Hepatocellular Carcinoma 90 0.029
351
P SCH015 Schizophrenia 78 0.029
352
P AST005 Asthma 80 0.029
353
P OVR042 Ovarian Cancer 73 0.029
354
HDG012 Hodgkin Lymphoma 75 0.029
355
BRN028 Brain Cancer 69 0.029
356
P PRM019 Premature Ovarian Failure 65 0.029
357
P RFS001 Refsum Disease 60 0.029
358
P ALG002 Alagille Syndrome 70 0.029
359
P ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.029
360
PTR006 Peters Anomaly 64 0.029
361
WST001 West Syndrome 61 0.029
362
P DNT015 Dent Disease 61 0.029
363
P WSK001 Wiskott-Aldrich Syndrome 70 0.029
364
P CHR071 Charcot-Marie-Tooth Disease 66 0.029
365
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.029
366
c THR092 Thrombophilia Due to Thrombin Defect 56 0.029
367
KWS002 Kawasaki Disease 70 0.029
368
P ERY008 Erythromelalgia 50 0.029
369
P TRC086 Trichohepatoenteric Syndrome 1 46 0.029
370
P CRN108 Cranioectodermal Dysplasia 1 48 0.029
371
CYS010 Cystinosis 51 0.029
372
PRD011 Proud Syndrome 42 0.029
373
CCC001 Coccidioidomycosis 55 0.029
374
MTH039 Methylmalonic Aciduria, Mut(0) Type 34 0.029
375
P MTH008 Methylmalonic Acidemia 51 0.029
376
c CNG401 Congenital Heart Disease 67 0.029
377
CHL071 Child Syndrome 58 0.029
378
NTR005 Nutritional Deficiency Disease 51 0.029
379
PHR003 Pharyngitis 58 0.029
380
MLN007 Male Infertility 56 0.029
381
EPD016 Epidermolysis Bullosa 59 0.029
382
RCT018 Rectal Neoplasm 53 0.029
383
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.029
384
MTH009 Mouth Disease 63 0.029
385
P ART023 Arthropathy 63 0.029
386
OVR029 Ovarian Hyperstimulation Syndrome 59 0.029
387
NCT008 Nicotine Dependence, Protection Against 51 0.029
388
OBS020 Obesity, Adrenal Insufficiency, and Red Hair Due to Pomc Deficiency 29 0.029
389
ALL026 Allergic Hypersensitivity Disease 53 0.029
390
PRN038 Prune Belly Syndrome 46 0.029
391
P GT001 Gout 58 0.029
392
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.029
393
NCR004 Nocardiosis 44 0.029
394
CTS002 Cat-Scratch Disease 46 0.029
395
P CCK001 Cockayne Syndrome 58 0.029
396
c THR037 Thrombocytopenia 2 36 0.029
397
CNG048 Congenital Hepatic Fibrosis 47 0.029
398
c MDL008 Medullary Cystic Kidney Disease 1 26 0.029
399
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 31 0.029
400
BNM001 Bone Marrow Cancer 56 0.029
401
c PRM196 Premature Ovarian Failure 1 44 0.029
402
P GRV001 Graves' Disease 62 0.029
403
P INT070 Intestinal Obstruction 55 0.029
404
GDP001 Goodpasture Syndrome 47 0.029
405
ATR060 Atrial Standstill, Digenic 51 0.029
406
c HPT073 Hepatitis C Virus 72 0.029
407
ADR038 Adermatoglyphia 39 0.029
408
SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 30 0.029
409
HRT007 Heart Cancer 51 0.029
410
ERY003 Erythema Multiforme 57 0.029
411
PLY023 Polycystic Liver Disease 57 0.029
412
QFV001 Q Fever 62 0.029
413
P PRP029 Porphyria 56 0.029
414
KDS001 Kid Syndrome 53 0.029
415
P MYS005 Myositis 57 0.029
416
BLL006 Bullous Pemphigoid 59 0.029
417
SPN041 Spinal Cord Disease 50 0.029
418
VSC007 Vascular Disease 51 0.029
419
ALP008 Alopecia 56 0.029
420
P CRB042 Cerebellar Ataxia 64 0.029
421
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.029
422
RHM001 Rheumatic Fever 50 0.029
423
c GLM029 Glomerulosclerosis, Focal Segmental, 1 30 0.029
424
PNC034 Pancreas Disease 56 0.029
425
RCT015 Reactive Arthritis 65 0.029
426
c LCL006 Localized Scleroderma 60 0.029
427
ATH003 Atherosclerosis 63 0.029
428
c ATM030 Autoimmune Lymphoproliferative Syndrome, Type Ii 30 0.029
429
ADR021 Adrenocorticotropic Hormone Deficiency 43 0.029
430
P ECL001 Eclampsia 55 0.029
431
c PRM005 Primary Hyperparathyroidism 56 0.029
432
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.029
433
CLL002 Collecting Duct Carcinoma 43 0.029
434
P MNN013 Meningitis 66 0.029
435
OCY001 Oocyte Maturation Defect 31 0.029
436
P DDN001 Duodenal Ulcer 51 0.029
437
TLR001 Tularemia 46 0.029
438
WHP001 Whipple Disease 49 0.029
439
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.029
440
c PRC016 Pre-Eclampsia 57 0.029
441
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.029
442
TTH006 Tooth Disease 52 0.029
443
LNG099 Lung Disease 63 0.029
444
c ALM001 Al Amyloidosis 45 0.029
445
P PLM085 Pulmonary Hemosiderosis 45 0.029
446
P HYP069 Hyperparathyroidism 57 0.029
447
c TRC078 Trichohepatoenteric Syndrome 2 30 0.029
448
PRM013 Premature Menopause 45 0.029
449
TRN004 Trench Fever 38 0.029
450
PRT014 Protein S Deficiency 54 0.029
451
ACD009 Acid-Labile Subunit, Deficiency of 37 0.029
452
LYM021 Lymphadenitis 58 0.029
453
c THR048 Thrombocytopenia 4 29 0.029
454
P ENC004 Encephalitis 60 0.029
455
P OVR049 Ovarian Disease 54 0.029
456
P HRT032 Heart Disease 64 0.029
457
ESN015 Eosinophilic Fasciitis 46 0.029
458
P OCL002 Oculocutaneous Albinism 51 0.029
459
MTC085 Mitochondrial Complex Iii Deficiency, Nuclear Type 1 25 0.029
460
c NPH068 Nephronophthisis 16 20 0.029
461
TNS005 Tonsillitis 58 0.029
462
P CRN035 Cranial Nerve Palsy 44 0.029
463
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 19 0.029
464
c WSK002 Wiskott-Aldrich Syndrome 2 27 0.029
465
c NPH069 Nephronophthisis 15 19 0.029
466
SKN023 Skin Tag 48 0.029
467
SLD003 Sialadenitis 45 0.029
468
DPH001 Diphtheria 55 0.029
469
LMR001 Lemierre's Syndrome 43 0.029
470
c NPH077 Nephronophthisis 19 21 0.029
471
MLT016 Multicentric Reticulohistiocytosis 46 0.029
472
LRN003 Learning Disability 49 0.029
473
MLT113 Multicentric Castleman Disease 49 0.029
474
LNS003 Lens Disease 37 0.029
475
PRN009 Paranoid Schizophrenia 47 0.029
476
NWC001 Newcastle Disease 51 0.029
477
CLF028 Cleft Soft Palate 20 0.029
478
ALL006 Allergic Asthma 59 0.029
479
PLC003 Placental Site Trophoblastic Tumor 48 0.029
480
c PRM226 Primary Central Nervous System Lymphoma 51 0.029
481
c AST037 Asthma 1 35 0.029
482
c AST039 Asthma 2 28 0.029
483
c ACT071 Acute Kidney Failure 48 0.029
484
DDN006 Duodenitis 44 0.029
485
MLR002 Miliary Tuberculosis 39 0.029
486
P CRN178 Coronary Heart Disease 6 22 0.029
487
P CLL015 Collagen Disease 49 0.029
488
INT066 Interstitial Lung Disease 60 0.029
489
c PNC106 Pancreatic Agenesis 1 31 0.029
490
PNN001 Panniculitis 47 0.029
491
RLP003 Relapsing Fever 40 0.029
492
DSS008 Disease of Mental Health 48 0.029
493
HPT008 Hepatic Tuberculosis 42 0.029
494
c CRN214 Coronary Heart Disease 5 22 0.029
495
c PRM089 Premature Ovarian Failure 3 24 0.029
496
c PRM090 Premature Ovarian Failure 6 22 0.029
497
SCK005 Sickle Cell Disease 51 0.029
498
BRN014 Bronchopneumonia 45 0.029
499
C1S001 C1s Deficiency 28 0.029
500
P PNC001 Pancytopenia 53 0.029
501
HMS001 Hemosiderosis 42 0.029
502
INT253 Intestinal Benign Neoplasm 48 0.029
503
P END047 Endophthalmitis 46 0.029
504
CHR001 Churg-Strauss Syndrome 48 0.029
505
c PRM192 Premature Ovarian Failure 8 21 0.029
506
SCR015 Scarlet Fever 37 0.029
507
RCT017 Rectal Disease 35 0.029
508
PRS045 Prostatic Hypertrophy 44 0.029
509
c ACT027 Acute Pancreatitis 59 0.029
510
ANT039 Antisynthetase Syndrome 36 0.029
511
OST011 Osteomalacia 48 0.029
512
c PRM207 Premature Ovarian Failure 10 22 0.029
513
c SBC007 Subacute Thyroiditis 42 0.029
514
URM002 Uremia 36 0.029
515
P AGM001 Agammaglobulinemia 63 0.029
516
ACT201 Acute Posterior Multifocal Placoid Pigment Epitheliopathy 21 0.029
517
HYD002 Hydronephrosis 48 0.029
518
OST004 Osteitis Fibrosa 44 0.029
519
CRT012 Cortical Blindness 36 0.029
520
ALB002 Albinism 43 0.029
521
c SNR016 Senior-Loken Syndrome 9 18 0.029
522
c INH020 Inherited Metabolic Disorder 49 0.029
523
TNS004 Tonsil Cancer 42 0.029
524
CLC001 Calciphylaxis 40 0.029
525
BLN006 Blind Loop Syndrome 29 0.029
526
P ATX004 Ataxia 53 0.029
527
PSD009 Pseudohermaphroditism 39 0.029
528
PRS047 Prostatitis 56 0.029
529
IMM053 Immunotactoid Glomerulopathy 23 0.029
530
ISC006 Ischemic Heart Disease 54 0.029
531
P RPD001 Rapidly Progressive Glomerulonephritis 43 0.029
532
CRD001 Cardiac Tamponade 43 0.029
533
P HRT017 Heart Tumor 34 0.029
534
NPH010 Nephrosclerosis 44 0.029
535
THY105 Thyrocerebroretinal Syndrome 15 0.029
536
RHM007 Rheumatic Congestive Heart Failure 22 0.029
537
FSC004 Fasciitis 47 0.029
538
PRT019 Protein-Losing Enteropathy 42 0.029
539
MDS022 Mediastinitis 37 0.029
540
ALP048 Alopecia Totalis 27 0.029
541
FBR009 Fibrous Dysplasia 44 0.029
542
C1R002 C1r/c1s Deficiency, Combined 9 0.029
543
HYP266 Hypoxia 55 0.029
544
P CHL066 Cholangitis 48 0.029
545
c RNL113 Renal Failure, Progressive, with Hypertension 18 0.029
546
SPC003 Specific Developmental Disorder 39 0.029
547
P TRN034 Transverse Myelitis 43 0.029
548
DSC009 Discoid Lupus Erythematosus 40 0.029
549
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.029
550
RTN001 Retinal Vasculitis 43 0.029
551
CST005 Castleman Disease 42 0.029
552
c IGN002 Iga Nephropathy 2 17 0.029
553
c IGN004 Iga Nephropathy 3 15 0.029
554
MYL001 Myelitis 35 0.029
555
P CRV039 Cervicitis 45 0.029
556
HYP034 Hypertensive Encephalopathy 35 0.029
557
ATN003 Autonomic Nervous System Neoplasm 43 0.029
558
ACT087 Acth Deficiency 40 0.029
559
INS009 Insulin-Resistance Type B 21 0.029
560
RNL097 Renal Artery Disease 44 0.029
561
MNN032 Meningococcal Meningitis 33 0.029
562
SXD001 Sex Differentiation Disease 39 0.029
563
PRT026 Parotitis 42 0.029
564
GLC053 Glucocorticoid Deficiency 3 17 0.029
565
PRR001 Periarthritis 28 0.029
566
c MLT093 Multiple Sclerosis 2 20 0.029
567
SPN119 Spondylarthropathy 46 0.029
568
CHR077 Chorioretinal Scar 30 0.029
569
BLD054 Blood Protein Disease 38 0.029
570
CVR002 Cavernous Sinus Thrombosis 28 0.029
571
CYT017 Cytophagic Histiocytic Panniculitis 19 0.029
572
ADR009 Adrenal Cortex Disease 40 0.029
573
LTR002 Lateral Sinus Thrombosis 25 0.029
574
c HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.029
575
HYP084 Hypopyon 29 0.029
576
c INF078 Inflammatory Bowel Disease 2 23 0.029
577
c INF083 Inflammatory Bowel Disease 24 18 0.029
578
c INF086 Inflammatory Bowel Disease 3 20 0.029
579
P HYP120 Hypoaldosteronism 34 0.029
580
MYC022 Mycoplasmal Pneumonia 32 0.029
581
c ADL079 Adult Heart Tumor 17 0.029
582
CGL001 Coagulation Protein Disease 14 0.029
583
PYR005 Pyoureter 6 0.029
584
NRN002 Neuronitis 40 0.029
585
CRB086 Cerebral Aneurysms 39 0.029
586
c SML023 Small Cell Lung Cancer, Adult 17 0.029
587
c CHR096 Chronic Pulmonary Heart Disease 40 0.029
588
c FML268 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes 20 0.029
589
MLT035 Multifocal Choroiditis 29 0.029
590
BNF002 Bone Fracture 46 0.029
591
VSC047 Vascular Malformation 45 0.029