Search results for "proteinuria"

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

1029 hits were found for 'proteinuria'

# Family MCID Name MIFTS Score
1
PRT069 Proteinuria, Low Molecular Weight, with Hypercalciuric Nephrocalcinosis 19 4.766
2
MGL001 Megaloblastic Anemia 49 4.758
3
ORT001 Orthostatic Proteinuria 26 4.112
4
DNN002 Donnai-Barrow Syndrome 34 2.456
5
P DNT015 Dent Disease 53 2.441
6
URN009 Urinary System Disease 35 0.160
7
P PRM002 Primary Hyperoxaluria 55 0.141
8
P KDN018 Kidney Disease 49 0.141
9
P BRS047 Breast Cancer 100 0.105
10
P LKM002 Leukemia 63 0.101
11
c CHR089 Chronic Kidney Failure 58 0.096
12
P LYM118 Lymphoma 57 0.096
13
IMP003 Impaired Renal Function Disease 27 0.091
14
c MCR113 Microvascular Complications of Diabetes 3 48 0.088
15
END072 Endotheliitis 41 0.088
16
P GLM044 Glomerular Disease 33 0.082
17
P NPH012 Nephrotic Syndrome 55 0.076
18
c PRC016 Pre-Eclampsia 48 0.076
19
P LNG032 Lung Cancer 91 0.073
20
P HPT021 Hepatitis 63 0.073
21
P GLM007 Glomerulonephritis 50 0.073
22
P PRC031 Preeclampsia/eclampsia 1 49 0.073
23
P DBT085 Diabetes Mellitus, Insulin-Dependent 77 0.069
24
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 76 0.069
25
P ART022 Arthritis 63 0.069
26
P ADN016 Adenocarcinoma 59 0.069
27
END030 End Stage Renal Failure 50 0.069
28
P MMB011 Membranous Nephropathy 41 0.069
29
MDY003 Mody, Type Ii 31 0.069
30
c GLM029 Glomerulosclerosis, Focal Segmental, 1 26 0.069
31
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 13 0.069
32
PRS047 Prostatitis 53 0.066
33
P PNC044 Pancreatitis 53 0.066
34
BLD054 Blood Protein Disease 28 0.066
35
RTN023 Retinitis 42 0.062
36
RNL015 Renal Hypertension 40 0.062
37
NRN002 Neuronitis 36 0.062
38
GLC008 Glucose Metabolism Disease 35 0.062
39
c NPH055 Nephrotic Syndrome, Type 1 31 0.062
40
P RHM011 Rheumatoid Arthritis 87 0.058
41
c HYP595 Hypertension, Essential 62 0.058
42
P LRY019 Laryngitis 50 0.058
43
P THY032 Thyroiditis 49 0.058
44
P CRV039 Cervicitis 41 0.058
45
P HYP071 Hypersensitivity Reaction Type Ii Disease 38 0.058
46
P IGN003 Iga Nephropathy 1 27 0.058
47
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 20 0.058
48
P ALP004 Alport Syndrome 66 0.054
49
SRC014 Sarcoma 61 0.054
50
P CRD011 Cardiomyopathy 59 0.054
51
P LPS004 Lupus Erythematosus 59 0.054
52
c MTB001 Metabolic Syndrome X 53 0.054
53
NRM003 Norum Disease 50 0.054
54
CRB009 Cerebritis 44 0.054
55
GLM011 Glomerulosclerosis 36 0.054
56
MDY005 Mody, Type I 27 0.054
57
c GLM027 Glomerulosclerosis, Focal Segmental, 3 23 0.054
58
c RNL016 Renal Infectious Disease 10 0.054
59
ATM055 Autoimmune Disease 4 8 0.054
60
HPT023 Hepatocellular Carcinoma 87 0.049
61
c SYS001 Systemic Lupus Erythematosus 84 0.049
62
P OST012 Osteoarthritis 72 0.049
63
P LVR013 Liver Disease 60 0.049
64
P FCL005 Focal Segmental Glomerulosclerosis 55 0.049
65
P MNN013 Meningitis 55 0.049
66
P ESP024 Esophagitis 54 0.049
67
P ENC004 Encephalitis 50 0.049
68
GMM002 Gamma Chain Deficiency 48 0.049
69
P EXN002 Exanthem 48 0.049
70
P ECL001 Eclampsia 47 0.049
71
P NRP001 Neuropathy 47 0.049
72
HLL004 Hellp Syndrome 42 0.049
73
IGG001 Iga Glomerulonephritis 41 0.049
74
c GLM039 Glomerulosclerosis, Focal Segmental, 6 28 0.049
75
c NPH049 Nephrotic Syndrome, Type 2 24 0.049
76
P GLM015 Glomerulopathy with Fibronectin Deposits 2 24 0.049
77
c GLM026 Glomerulosclerosis, Focal Segmental, 2 22 0.049
78
c NPH070 Nephrotic Syndrome, Type 6 20 0.049
79
c CHR090 Chronic Lymphocytic Leukemia 69 0.044
80
TBR010 Tuberculosis 65 0.044
81
P BCL006 B-Cell Lymphomas 59 0.044
82
P PNM007 Pneumonia 56 0.044
83
LWS003 Lowe Syndrome 54 0.044
84
HMR004 Hemorrhagic Fever with Renal Syndrome 54 0.044
85
ADN018 Adenoma 53 0.044
86
VSC011 Vasculitis 53 0.044
87
GLL032 Galloway-Mowat Syndrome 51 0.044
88
ISC004 Ischemia 49 0.044
89
CLT003 Colitis 49 0.044
90
GST053 Gastric Cancer 44 0.044
91
LPP002 Lipoprotein Glomerulopathy 40 0.044
92
URT001 Urethritis 37 0.044
93
SCH016 Schimke Immunoosseous Dysplasia 37 0.044
94
c DNT021 Dent Disease 2 32 0.044
95
c NPH072 Nephrotic Syndrome, Type 7 24 0.044
96
ATM052 Autoimmune Disease 1 21 0.044
97
c NPH047 Nephrotic Syndrome, Type 4 21 0.044
98
c GLM041 Glomerulosclerosis, Focal Segmental, 7 20 0.044
99
P CLR023 Colorectal Cancer 91 0.038
100
P PRS040 Prostate Cancer 87 0.038
101
P OBS005 Obesity 87 0.038
102
P RNL014 Renal Cell Carcinoma 81 0.038
103
HV1006 Hiv-1 78 0.038
104
P RTN008 Retinitis Pigmentosa 75 0.038
105
HDG012 Hodgkin Lymphoma 73 0.038
106
c MLT019 Multiple Myeloma 71 0.038
107
P LYN001 Lynch Syndrome 69 0.038
108
FBR012 Fabry Disease 67 0.038
109
GLC006 Galactosemia 67 0.038
110
THY028 Thyroid Cancer 65 0.038
111
ATT013 Attention Deficit-Hyperactivity Disorder 65 0.038
112
P MYL006 Myeloid Leukemia 61 0.038
113
P KDN017 Kidney Cancer 59 0.038
114
P PSR002 Psoriasis 58 0.038
115
NLP001 Nail-Patella Syndrome 58 0.038
116
P AST007 Astrocytoma 57 0.038
117
MSL001 Measles 57 0.038
118
P FML161 Familial Mediterranean Fever, Ar 56 0.038
119
LGN002 Legionellosis 56 0.038
120
P GCH001 Gaucher's Disease 56 0.038
121
ACQ007 Acquired Immunodeficiency Syndrome 55 0.038
122
P RSP003 Respiratory Failure 55 0.038
123
P CND004 Candidiasis 55 0.038
124
P LYM026 Lymphoblastic Leukemia 55 0.038
125
P MYP004 Myopathy 54 0.038
126
BRN012 Bronchiolitis Obliterans 53 0.038
127
P NSP012 Nasopharyngeal Carcinoma 53 0.038
128
ETN001 Eating Disorder 52 0.038
129
BRN002 Bronchiolitis 51 0.038
130
FRS002 Frasier Syndrome 51 0.038
131
DMN002 Dementia 51 0.038
132
MTH009 Mouth Disease 51 0.038
133
LNG099 Lung Disease 50 0.038
134
RLP001 Relapsing Polychondritis 49 0.038
135
GDP001 Goodpasture Syndrome 48 0.038
136
NSP002 Nasopharyngitis 48 0.038
137
CNN005 Connective Tissue Disease 48 0.038
138
VRL011 Viral Infectious Disease 48 0.038
139
c HPT003 Hepatitis a 47 0.038
140
LPD008 Lipid Metabolism Disorder 47 0.038
141
ANR040 Aneurysm 46 0.038
142
P HYP613 Hypophosphatemic Rickets 46 0.038
143
ORL005 Oral Candidiasis 43 0.038
144
c SVR005 Severe Pre-Eclampsia 42 0.038
145
MMB002 Membranous Glomerulonephritis 41 0.038
146
FBR054 Fibroma 41 0.038
147
PRS055 Pierson Syndrome 40 0.038
148
CHR008 Choroiditis 39 0.038
149
PPL048 Papillorenal Syndrome 38 0.038
150
SPL007 Splenic Abscess 34 0.038
151
c NPH054 Nephrotic Syndrome, Type 3 32 0.038
152
c LPD019 Lipodystrophy, Partial, Acquired 31 0.038
153
MLK004 Malakoplakia 30 0.038
154
c GLM033 Glomerulosclerosis, Focal Segmental, 4 22 0.038
155
c CHR522 Charcot-Marie-Tooth Disease, Dominant Intermediate E 22 0.038
156
c NPH074 Nephrotic Syndrome, Type 9 20 0.038
157
NPH039 Nephrotic Syndrome, Type 5, with or Without Ocular Abnormalities 20 0.038
158
c NPH073 Nephrotic Syndrome, Type 8 20 0.038
159
ATM059 Autoimmune Disease 6 17 0.038
160
ATM053 Autoimmune Disease 2 8 0.038
161
ATM054 Autoimmune Disease 3 8 0.038
162
CYS001 Cystic Fibrosis 84 0.031
163
P MYC007 Myocardial Infarction 77 0.031
164
P HYP607 Hypercholesterolemia, Familial 74 0.031
165
c DLT002 Dilated Cardiomyopathy 72 0.031
166
P FLL037 Follicular Lymphoma 70 0.031
167
P NRB001 Neuroblastoma 69 0.031
168
P OVR042 Ovarian Cancer 69 0.031
169
SCK003 Sickle Cell Anemia 66 0.031
170
P KRT004 Keratitis 66 0.031
171
SVR004 Severe Combined Immunodeficiency 65 0.031
172
c HPT001 Hepatitis C 65 0.031
173
P ESS003 Essential Thrombocythemia 65 0.031
174
CNG034 Congestive Heart Failure 64 0.031
175
KWS002 Kawasaki Disease 63 0.031
176
P HLP001 Holoprosencephaly 63 0.031
177
P PLM036 Pulmonary Fibrosis 62 0.031
178
c HPT073 Hepatitis C Virus 62 0.031
179
P END044 Endometriosis 62 0.031
180
VNW001 Von Willebrand's Disease 61 0.031
181
PRG004 Progeria 60 0.031
182
PSR001 Psoriatic Arthritis 60 0.031
183
PRT036 Peritonitis 59 0.031
184
P AGM001 Agammaglobulinemia 59 0.031
185
P ASP006 Aspergillosis 58 0.031
186
P HYD006 Hydrocephalus 58 0.031
187
P HMN010 Hemangioma 57 0.031
188
c HPT016 Hepatitis B 57 0.031
189
P PRD008 Periodontitis 57 0.031
190
YLL002 Yellow Fever 57 0.031
191
WGN006 Wegener Granulomatosis 57 0.031
192
ATH003 Atherosclerosis 56 0.031
193
P HYP061 Hypertrophic Cardiomyopathy 55 0.031
194
DRM006 Dermatitis 55 0.031
195
P THL005 Thalassemia 55 0.031
196
MLN008 Melanoma 55 0.031
197
P CHN012 Chondrosarcoma 54 0.031
198
WLL001 Williams-Beuren Syndrome 54 0.031
199
P OST009 Osteochondritis Dissecans 54 0.031
200
P MSC005 Muscular Dystrophy 54 0.031
201
DNY001 Denys-Drash Syndrome 54 0.031
202
c VRL010 Viral Hepatitis 54 0.031
203
P THR014 Thrombocytopenia 54 0.031
204
P HMP002 Hemophagocytic Lymphohistiocytosis 53 0.031
205
HYP066 Hyperglycemia 53 0.031
206
CYS010 Cystinosis 53 0.031
207
P CNJ013 Conjunctivitis 52 0.031
208
OST017 Osteomyelitis 52 0.031
209
P NTR004 Neutropenia 52 0.031
210
HRY003 Hairy Cell Leukemia 52 0.031
211
PPL022 Papilloma 52 0.031
212
P HYP086 Hypothyroidism 51 0.031
213
P RBL001 Rubella 51 0.031
214
P PLY018 Polycythemia 51 0.031
215
P DYS154 Dystonia 51 0.031
216
DBT010 Diabetic Neuropathy 51 0.031
217
RBS003 Rabson-Mendenhall Syndrome 51 0.031
218
P MLS001 Melas Syndrome 50 0.031
219
P LRY016 Laryngeal Carcinoma 50 0.031
220
c FML108 Familial Breast Cancer 50 0.031
221
P MYL007 Myeloma 50 0.031
222
SML019 Smallpox 49 0.031
223
ECH003 Echinococcosis 49 0.031
224
SPN027 Spinal Stenosis 48 0.031
225
BLR001 Biliary Atresia 48 0.031
226
P OSS001 Ossifying Fibroma 47 0.031
227
CND002 Conduct Disorder 47 0.031
228
P MCR010 Microcephaly 47 0.031
229
STL001 St. Louis Encephalitis 47 0.031
230
c GCH015 Gaucher Disease, Type I 47 0.031
231
P CTR002 Cataract 47 0.031
232
P FML035 Familial Hyperlipidemia 47 0.031
233
P MYT002 Myotonic Dystrophy 47 0.031
234
P OTT001 Otitis Externa 47 0.031
235
CYS008 Cystic Echinococcosis 46 0.031
236
P END033 Endocarditis 46 0.031
237
GLS001 Gliosarcoma 46 0.031
238
RTN017 Retinal Detachment 46 0.031
239
P FBR031 Febrile Seizures 46 0.031
240
HMT018 Hematopoietic Stem Cell Transplantation 46 0.031
241
URM002 Uremia 46 0.031
242
P SYP003 Syphilis 46 0.031
243
CTS003 Coats Disease 45 0.031
244
P DRR001 Diarrhea 45 0.031
245
KRT009 Keratosis 44 0.031
246
P PYL005 Pyelonephritis 44 0.031
247
P TRM003 Tremor 44 0.031
248
P PRG013 Paraganglioma 44 0.031
249
P THY054 Thyrotoxic Periodic Paralysis 43 0.031
250
HYD012 Hydrops Fetalis 43 0.031
251
c ORF037 Orofaciodigital Syndrome I 43 0.031
252
MRG003 Marginal Zone B-Cell Lymphoma 42 0.031
253
NRL004 Neuroleptic Malignant Syndrome 42 0.031
254
P HRD001 Hereditary Multiple Exostoses 42 0.031
255
P GRN010 Granular Cell Tumor 42 0.031
256
MTR046 Maternally Inherited Diabetes and Deafness 42 0.031
257
P SPS003 Spastic Diplegia 42 0.031
258
INF034 Infective Endocarditis 41 0.031
259
STS002 Situs Inversus 41 0.031
260
HYP017 Hypophosphatemia 40 0.031
261
LPM005 Lipomatosis 40 0.031
262
PYD002 Pyoderma 40 0.031
263
PLR005 Pleuropneumonia 40 0.031
264
c GCH017 Gaucher Disease, Type Iii 39 0.031
265
ASC002 Ascariasis 39 0.031
266
CSY001 C Syndrome 39 0.031
267
DNT012 Dental Caries 39 0.031
268
HMN014 Human Immunodeficiency Virus Infectious Disease 39 0.031
269
NTR005 Nutritional Deficiency Disease 39 0.031
270
DYS018 Dysostosis 38 0.031
271
VTM002 Vitamin B12 Deficiency 38 0.031
272
PST010 Pasteurellosis 38 0.031
273
P SYR001 Syringomyelia 38 0.031
274
EBL001 Ebola Hemorrhagic Fever 37 0.031
275
GLC036 Glucagonoma 37 0.031
276
LSS003 Lassa Fever 37 0.031
277
GLM004 Gliomatosis Cerebri 37 0.031
278
P BLD051 Blood Coagulation Disease 37 0.031
279
EPD005 Epidural Abscess 36 0.031
280
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 36 0.031
281
BLD053 Blood Platelet Disease 35 0.031
282
P OVR046 Ovarian Cyst 35 0.031
283
ESN020 Eosinophilic Granulomatosis with Polyangiitis 35 0.031
284
PLP001 Pulpitis 34 0.031
285
MJD001 Majeed Syndrome 33 0.031
286
WLL004 Wallerian Degeneration 33 0.031
287
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 33 0.031
288
RNL097 Renal Artery Disease 33 0.031
289
STR044 Steroid-Resistant Nephrotic Syndrome 33 0.031
290
CLC007 Calcium Metabolism Disease 32 0.031
291
CHL052 Choledochal Cyst 32 0.031
292
ACT100 Acute Febrile Neutrophilic Dermatosis 31 0.031
293
IPX001 Ipex Syndrome 31 0.031
294
ADJ001 Adjustment Disorder 30 0.031
295
OCH001 Ochronosis 30 0.031
296
PRN039 Paraneoplastic Syndromes 30 0.031
297
SPC003 Specific Developmental Disorder 30 0.031
298
URT037 Urethral Stricture 30 0.031
299
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 28 0.031
300
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 28 0.031
301
PYR004 Pyuria 28 0.031
302
FRS004 Free Sialic Acid Storage Disorders 28 0.031
303
BNS002 Bone Structure Disease 27 0.031
304
IMM073 Immunoglobulin a Vasculitis 23 0.031
305
c FNC026 Fanconi Renotubular Syndrome 1 23 0.031
306
MYC014 Mycobacterium Chelonae 22 0.031
307
c GLM028 Glomerulosclerosis, Focal Segmental, 5 22 0.031
308
VSC008 Vascular Hemostatic Disease 21 0.031
309
CYS025 Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic 20 0.031
310
c FCL053 Focal Segmental Glomerulosclerosis 8 17 0.031
311
DNT019 Daentl Towsend Siegel Syndrome 17 0.031
312
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 16 0.031
313
NPH024 Nephrosis Deafness Urinary Tract Digital Malformation 15 0.031
314
OCL043 Oculorenocerebellar Syndrome 15 0.031
315
c GLM014 Glomerulopathy with Fibronectin Deposits 1 15 0.031
316
PRT055 Prieto X-Linked Mental Retardation Syndrome 14 0.031
317
SGL001 Siegler Brewer Carey Syndrome 13 0.031
318
c IGN002 Iga Nephropathy 2 12 0.031
319
FGN001 Feigenbaum Bergeron Richardson Syndrome 11 0.031
320
OCL029 Oculo Skeletal Renal Syndrome 11 0.031
321
BLK002 Balkan Hemorrhagic Fever 10 0.031
322
c SCN053 Secondary Glomerular Disease 7 0.031
323
P PNC035 Pancreatic Cancer 82 0.022
324
P SCH015 Schizophrenia 76 0.022
325
P OST002 Osteoporosis 76 0.022
326
ULC004 Ulcerative Colitis 70 0.022
327
P PHC003 Pheochromocytoma 70 0.022
328
P CRN211 Coronary Artery Disease 69 0.022
329
WLS001 Wilson Disease 68 0.022
330
PHN003 Phenylketonuria 68 0.022
331
P TYS001 Tay-Sachs Disease 68 0.022
332
P OST005 Osteogenesis Imperfecta 67 0.022
333
P INF038 Influenza 67 0.022
334
P LPR003 Leprosy 66 0.022
335
CRZ001 Crouzon Syndrome 66 0.022
336
KPS004 Kaposi Sarcoma 66 0.022
337
P PRP003 Porphyria Cutanea Tarda 65 0.022
338
c CNG401 Congenital Heart Disease 64 0.022
339
MLT021 Multiple System Atrophy 64 0.022
340
BRK010 Burkitt Lymphoma 63 0.022
341
P NRC002 Narcolepsy 62 0.022
342
P PRM019 Premature Ovarian Failure 62 0.022
343
P MYL005 Myelofibrosis 62 0.022
344
ACR007 Acromegaly 62 0.022
345
c SPN225 Spondyloarthropathy 1 61 0.022
346
ESP021 Esophageal Cancer 61 0.022
347
P OST001 Osteopetrosis 61 0.022
348
OTT002 Otitis Media 60 0.022
349
ALC007 Alcohol Dependence 60 0.022
350
P ANG001 Angelman Syndrome 60 0.022
351
ART016 Aortic Aneurysm 60 0.022
352
P TBR001 Tuberous Sclerosis 60 0.022
353
DRM014 Dermatofibrosarcoma Protuberans 60 0.022
354
P HRP006 Herpes Simplex 59 0.022
355
P PLZ001 Pelizaeus-Merzbacher Disease 59 0.022
356
ANX002 Anxiety Disorder 59 0.022
357
P HYP055 Hypoplastic Left Heart Syndrome 59 0.022
358
PRP027 Peripheral Vascular Disease 59 0.022
359
c BSL007 Basal Cell Carcinoma 59 0.022
360
P ATS007 Autism Spectrum Disorder 59 0.022
361
c ATM003 Autoimmune Thyroiditis 59 0.022
362
BRC012 Brucellosis 59 0.022
363
P PNC025 Panic Disorder 59 0.022
364
P WLF004 Wolfram Syndrome 59 0.022
365
P TRN020 Turner Syndrome 59 0.022
366
P CMR001 Camurati-Engelmann Disease 58 0.022
367
PNC041 Pancreatic Ductal Adenocarcinoma 58 0.022
368
P HRT032 Heart Disease 58 0.022
369
P MYS003 Myasthenia Gravis 58 0.022
370
ATP002 Atopy 58 0.022
371
TYP007 Typhoid Fever 58 0.022
372
P PLY011 Polycystic Ovary Syndrome 58 0.022
373
P HYP117 Hypertriglyceridemia 58 0.022
374
BRN028 Brain Cancer 58 0.022
375
LPT001 Leptospirosis 58 0.022
376
P NRN021 Neuronal Ceroid Lipofuscinosis 58 0.022
377
SKN016 Skin Disease 58 0.022
378
P MYM002 Moyamoya Disease 58 0.022
379
P TXP001 Toxoplasmosis 57 0.022
380
P CNG015 Congenital Diaphragmatic Hernia 57 0.022
381
P ORT004 Orthostatic Intolerance 57 0.022
382
P SYS005 Systemic Scleroderma 57 0.022
383
LVR012 Liver Cirrhosis 57 0.022
384
ABT001 Abetalipoproteinemia 57 0.022
385
P HML002 Hemolytic Anemia 57 0.022
386
c ATM011 Autoimmune Hepatitis 56 0.022
387
c CNG006 Congenital Hypothyroidism 56 0.022
388
P GLB002 Glioblastoma 56 0.022
389
c HRD002 Hereditary Angioedema 56 0.022
390
TTN003 Tetanus 56 0.022
391
P EHL001 Ehlers-Danlos Syndrome 56 0.022
392
P EHL033 Ehlers-Danlos Syndrome, Classic Type 56 0.022
393
OVR029 Ovarian Hyperstimulation Syndrome 55 0.022
394
SHW002 Shwachman-Diamond Syndrome 55 0.022
395
HYP121 Hypoalphalipoproteinemia 55 0.022
396
P ADD001 Addison's Disease 55 0.022
397
VSC007 Vascular Disease 55 0.022
398
GLB015 Glioblastoma Multiforme 55 0.022
399
EPD016 Epidermolysis Bullosa 55 0.022
400
SHG001 Shigellosis 55 0.022
401
P PRP029 Porphyria 55 0.022
402
P LCH002 Lichen Planus 55 0.022
403
CRB039 Cerebrovascular Disease 55 0.022
404
PRL009 Prolactinoma 55 0.022
405
HRP004 Herpes Zoster 55 0.022
406
P HYP069 Hyperparathyroidism 54 0.022
407
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.022
408
CHL014 Cholera 54 0.022
409
c MLG054 Malignant Histiocytosis 54 0.022
410
P SPN046 Spinal Muscular Atrophy 54 0.022
411
MXD005 Mixed Connective Tissue Disease 54 0.022
412
P ATP001 Atopic Dermatitis 54 0.022
413
GLL018 Gallbladder Cancer 54 0.022
414
P HYP035 Hypophosphatasia 54 0.022
415
ALP008 Alopecia 54 0.022
416
ASP005 Asphyxiating Thoracic Dystrophy 54 0.022
417
P GLY013 Glycogen Storage Disease 53 0.022
418
P RCK004 Rickets 53 0.022
419
FTT001 Fatty Liver Disease 53 0.022
420
ART021 Arteriosclerosis 53 0.022
421
P ANT006 Antiphospholipid Syndrome 53 0.022
422
P SJG001 Sjogren's Syndrome 53 0.022
423
c GLY060 Glycogen Storage Disease Ia 53 0.022
424
P ABD003 Abdominal Aortic Aneurysm 53 0.022
425
P GT001 Gout 53 0.022
426
TNG003 Tongue Cancer 53 0.022
427
RHM001 Rheumatic Fever 53 0.022
428
P GRV001 Graves' Disease 53 0.022
429
P UVT001 Uveitis 53 0.022
430
P HST010 Histiocytosis 53 0.022
431
LMY002 Leiomyoma 53 0.022
432
PST028 Post-Traumatic Stress Disorder 53 0.022
433
CHR003 Cherubism 53 0.022
434
P SCH018 Schizencephaly 53 0.022
435
DBN001 Dubin-Johnson Syndrome 53 0.022
436
RBS001 Rabies 52 0.022
437
c XRD019 Xeroderma Pigmentosum, Group C 52 0.022
438
KRT001 Keratoconjunctivitis Sicca 52 0.022
439
LYS003 Lysinuric Protein Intolerance 52 0.022
440
KRN002 Kearns-Sayre Syndrome 52 0.022
441
P ESN007 Eosinophilia 52 0.022
442
HPY002 H. Pylori Infection 52 0.022
443
FCL014 Focal Epilepsy 51 0.022
444
c ACT075 Acute Myocardial Infarction 51 0.022
445
P ART023 Arthropathy 51 0.022
446
P SPN052 Spondyloarthropathy 51 0.022
447
PLM033 Pulmonary Embolism 51 0.022
448
TST014 Testicular Cancer 51 0.022
449
P LPS002 Liposarcoma 51 0.022
450
CRD119 Cardiac Arrest 51 0.022
451
FDL002 Food Allergy 51 0.022
452
ORL015 Oral Squamous Cell Carcinoma 51 0.022
453
LYM021 Lymphadenitis 51 0.022
454
P MMP001 Mumps 50 0.022
455
P LMY004 Leiomyosarcoma 50 0.022
456
OLL001 Ollier Disease 50 0.022
457
ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.022
458
ACN002 Acanthosis Nigricans 50 0.022
459
P CMP010 Complex Regional Pain Syndrome 50 0.022
460
P ACH003 Achromatopsia 50 0.022
461
P RNL100 Renal Hypodysplasia/aplasia 1 50 0.022
462
CHR029 Choroid Plexus Papilloma 50 0.022
463
P HYP004 Hypercalcemia 49 0.022
464
P INT068 Intestinal Disease 49 0.022
465
DSS009 Disseminated Intravascular Coagulation 49 0.022
466
INS001 Insulinoma 49 0.022
467
JPN002 Japanese Encephalitis 49 0.022
468
P DGR001 Digeorge Syndrome 49 0.022
469
P SML001 Small Cell Carcinoma 49 0.022
470
BRN056 Bronchopulmonary Dysplasia 49 0.022
471
P TRT010 Teratoma 49 0.022
472
PLM034 Pulmonary Emphysema 49 0.022
473
c ACT073 Acute Leukemia 49 0.022
474
ART111 Artery Disease 49 0.022
475
P PRS038 Personality Disorder 49 0.022
476
FCT004 Factor Xii Deficiency 49 0.022
477
VRR004 Verrucous Carcinoma 48 0.022
478
STR008 Strongyloidiasis 48 0.022
479
c BCT007 Bacterial Meningitis 48 0.022
480
CST005 Castleman Disease 48 0.022
481
P MST009 Mastocytosis 48 0.022
482
MRK001 Merkel Cell Carcinoma 48 0.022
483
VSC002 Vascular Dementia 48 0.022
484
ORL004 Oral Submucous Fibrosis 48 0.022
485
MCR094 Microvillus Inclusion Disease 48 0.022
486
PRC013 Pericarditis 48 0.022
487
P MYP006 Myopia 48 0.022
488
GSG001 Gas Gangrene 48 0.022
489
MTR014 Motor Neuron Disease 48 0.022
490
c MLG079 Malignant Pleural Mesothelioma 48 0.022
491
P CPL006 Capillary Hemangioma 48 0.022
492
ALL009 Allergic Conjunctivitis 48 0.022
493
P OPN001 Open-Angle Glaucoma 48 0.022
494
CLN015 Colon Adenocarcinoma 48 0.022
495
EXF001 Exfoliation Syndrome 48 0.022
496
GST050 Gastrointestinal System Disease 48 0.022
497
ANG020 Angiosarcoma 48 0.022
498
SFT003 Soft Tissue Sarcoma 48 0.022
499
BLM002 Bulimia Nervosa 48 0.022
500
CHC001 Chickenpox 48 0.022
501
PTN001 Patent Foramen Ovale 48 0.022
502
P NPH009 Nephrolithiasis 48 0.022
503
VGN023 Vaginitis 47 0.022
504
PRT014 Protein S Deficiency 47 0.022
505
P ANG015 Angioedema 47 0.022
506
MTC097 Mitochondrial Complex Iv Deficiency 47 0.022
507
P EPD003 Epidermolysis Bullosa Simplex 47 0.022
508
P AGG001 Aggressive Periodontitis 47 0.022
509
CHL067 Cholecystitis 47 0.022
510
CYT008 Cytomegalovirus Infection 47 0.022
511
GST033 Gestational Diabetes 47 0.022
512
P SHR029 Short Syndrome 47 0.022
513
GLC003 Glucose Intolerance 47 0.022
514
DPH001 Diphtheria 47 0.022
515
PRP030 Purpura 47 0.022
516
P SCH070 Schwannomatosis 47 0.022
517
CCT002 Cicatricial Pemphigoid 47 0.022
518
P HMR012 Hemorrhagic Fever 47 0.022
519
ACT008 Actinic Keratosis 47 0.022
520
KRT006 Keratoconjunctivitis 47 0.022
521
MLR003 Melorheostosis 47 0.022
522
PTN002 Patent Ductus Arteriosus 47 0.022
523
OMP004 Omphalocele 47 0.022
524
c PST041 Posterior Urethral Valves 47 0.022
525
c MLG069 Malignant Hypertension 47 0.022
526
ANN002 Anencephaly 46 0.022
527
CYS014 Cystadenocarcinoma 46 0.022
528
CCC002 Coccidiosis 46 0.022
529
LYM008 Lymphangiosarcoma 46 0.022
530
c HPT007 Hepatitis E 46 0.022
531
CNS004 Constipation 46 0.022
532
HYP135 Hypophosphatemic Rickets with Hypercalciuria 46 0.022
533
PTT006 Pituitary Adenoma 46 0.022
534
SYN007 Synovitis 46 0.022
535
TMP001 Temporal Lobe Epilepsy 46 0.022
536
KLN001 Klinefelter's Syndrome 46 0.022
537
c HPT015 Hepatitis D 46 0.022
538
HYP074 Hypersensitivity Vasculitis 46 0.022
539
c ACT210 Acute Respiratory Distress Syndrome 46 0.022
540
MMB001 Membranoproliferative Glomerulonephritis 46 0.022
541
P GLM045 Glioma 46 0.022
542
HYP266 Hypoxia 46 0.022
543
PLY013 Polymyalgia Rheumatica 46 0.022
544
MGC001 Megacolon 45 0.022
545
MCR191 Microscopic Colitis 45 0.022
546
CHL071 Child Syndrome 45 0.022
547
HDC001 Headache 45 0.022
548
URN010 Urinary Tract Obstruction 45 0.022
549
HYP080 Hypogonadism 45 0.022
550
PRG009 Progressive Multifocal Leukoencephalopathy 45 0.022
551
THR100 Thrombocytopenic Purpura, Autoimmune 45 0.022
552
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.022
553
PYD001 Pyoderma Gangrenosum 45 0.022
554
P LTR001 Lateral Sclerosis 45 0.022
555
CRT049 Critical Limb Ischemia 45 0.022
556
P MNC007 Monocytic Leukemia 45 0.022
557
PLM017 Pulmonary Alveolar Microlithiasis 45 0.022
558
P NPH005 Nephronophthisis 45 0.022
559
P ACT135 Acute Graft Versus Host Disease 45 0.022
560
PRN014 Paronychia 45 0.022
561
TRM010 Traumatic Brain Injury 45 0.022
562
c ANT034 Anterior Uveitis 45 0.022
563
FLT001 Felty's Syndrome 45 0.022
564
TLR001 Tularemia 45 0.022
565
RNL051 Renal Cysts and Diabetes Syndrome 45 0.022
566
PMP001 Pemphigus 45 0.022
567
P CNT005 Central Nervous System Lymphoma 45 0.022
568
ADN002 Adenoiditis 45 0.022
569
PPL049 Papillon-Lefevre Syndrome 45 0.022
570
MTN003 Motion Sickness 45 0.022
571
SPN020 Spondylosis 45 0.022
572
INT075 Intracranial Hypertension 45 0.022
573
P SCL015 Scleritis 45 0.022
574
NCR004 Nocardiosis 45 0.022
575
CHL068 Cholestasis 45 0.022
576
CLF001 Cleft Lip 44 0.022
577
ASP001 Asperger Syndrome 44 0.022
578
NRM004 Neuroma 44 0.022
579
KDS001 Kid Syndrome 44 0.022
580
SBS003 Substance Abuse 44 0.022
581
OST011 Osteomalacia 44 0.022
582
NPH004 Nephropathia Epidemica 44 0.022
583
NRM005 Neuromuscular Disease 44 0.022
584
ACR012 Aicardi Syndrome 44 0.022
585
EPT020 Epithelioid Hemangioendothelioma 44 0.022
586
c GLY016 Glycogen Storage Disease Ib 44 0.022
587
PRD019 Periodic Fever, Familial 44 0.022
588
HPT009 Hepatopulmonary Syndrome 44 0.022
589
HYP141 Hyperphenylalaninemia 44 0.022
590
P PLR021 Pleural Mesothelioma 44 0.022
591
ADN001 Adenosine Deaminase Deficiency 44 0.022
592
HND002 Hand, Foot and Mouth Disease 44 0.022
593
P PNL012 Penile Cancer 44 0.022
594
RTN018 Retinal Disease 44 0.022
595
TRC023 Trichinosis 44 0.022
596
CRB016 Carbuncle 43 0.022
597
PYR010 Peyronie's Disease 43 0.022
598
ANG018 Angiomyolipoma 43 0.022
599
SPN051 Spondylitis 43 0.022
600
CYT005 Cytomegalovirus Retinitis 43 0.022
601
P ENC018 Encephalopathy 43 0.022
602
c HYP163 Hyperlipidemia Type 3 43 0.022
603
BLL004 Bullous Keratopathy 43 0.022
604
KRT008 Keratopathy 43 0.022
605
c CNG415 Congenital Disorder of Glycosylation, Type Ia 43 0.022
606
FCL012 Facial Paralysis 43 0.022
607
EBS001 Ebstein Anomaly 43 0.022
608
P END046 Endometritis 43 0.022
609
PLS009 Plasma Cell Neoplasm 43 0.022
610
BRN071 Brain Injury 43 0.022
611
LMB062 Limb Ischemia 43 0.022
612
P SLD010 Sialidosis, Type I 43 0.022
613
OLG003 Oligohydramnios 43 0.022
614
c CNG124 Congenital Rubella 43 0.022
615
PST021 Postpartum Depression 43 0.022
616
c ACT071 Acute Kidney Failure 43 0.022
617
P CRN028 Corneal Ulcer 43 0.022
618
DVR002 Diverticulitis 43 0.022
619
SYN005 Synostosis 42 0.022
620
ZLL002 Zollinger-Ellison Syndrome 42 0.022
621
RST001 Restless Legs Syndrome 42 0.022
622
CHR285 Chronic Myelomonocytic Leukemia 42 0.022
623
CCN001 Cocaine Dependence 42 0.022
624
FRZ001 Frozen Shoulder 42 0.022
625
ASB001 Asbestosis 42 0.022
626
c PRM226 Primary Central Nervous System Lymphoma 42 0.022
627
c GRV008 Graves Disease 1 42 0.022
628
PNM001 Pneumocystosis 42 0.022
629
ANK001 Ankylosis 42 0.022
630
P STR020 Strabismus 42 0.022
631
P SCK005 Sickle Cell Disease 42 0.022
632
VSC006 Vascular Cancer 42 0.022
633
P MSC003 Muscular Atrophy 42 0.022
634
BCT004 Bacteriuria 42 0.022
635
P XLN190 X-Linked Hypophosphatemic Rickets 42 0.022
636
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 42 0.022
637
c INV001 Invasive Aspergillosis 42 0.022
638
ADL002 Adult Syndrome 42 0.022
639
c CNG021 Congenital Toxoplasmosis 42 0.022
640
CRT016 Carotid Artery Disease 42 0.022
641
P PLY041 Polymyositis 42 0.022
642
ALB002 Albinism 42 0.022
643
CDQ001 Cauda Equina Syndrome 42 0.022
644
P PRT029 Parathyroid Adenoma 41 0.022
645
CHR074 Choriocarcinoma 41 0.022
646
P AML002 Amelogenesis Imperfecta 41 0.022
647
SCL003 Social Phobia 41 0.022
648
FLL008 Folliculitis 41 0.022
649
CRB086 Cerebral Aneurysms 41 0.022
650
RNL011 Renal Osteodystrophy 41 0.022
651
NRL005 Neurilemmoma 41 0.022
652
FSC004 Fasciitis 41 0.022
653
P ACH011 Achondrogenesis 41 0.022
654
P CTN003 Cutaneous Lupus Erythematosus 41 0.022
655
c CHR418 Chronic Leukemia 41 0.022
656
P PRP023 Peripheral Neuropathy 41 0.022
657
P CHN014 Chondrodysplasia Punctata 41 0.022
658
MLT012 Multiple Symmetric Lipomatosis 41 0.022
659
THR013 Thoracic Outlet Syndrome 41 0.022
660
NDL013 Nodular Regenerative Hyperplasia 41 0.022
661
c ALP073 Alport Syndrome, Autosomal Recessive 41 0.022
662
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 41 0.022
663
BRS050 Breast Cyst 41 0.022
664
PHC013 Phaeochromocytoma 41 0.022
665
TNC002 Tinea Capitis 41 0.022
666
P SCL009 Sclerosing Cholangitis 41 0.022
667
CNN003 Conn's Syndrome 40 0.022
668
BYS001 Byssinosis 40 0.022
669
CYS005 Cysticercosis 40 0.022
670
RNL077 Renal Fibrosis 40 0.022
671
NPH003 Nephrocalcinosis 40 0.022
672
P AMY082 Amyloidosis, Familial Visceral 40 0.022
673
PTT037 Pituitary Tumors 40 0.022
674
PYM001 Pyomyositis 40 0.022
675
ART008 Arteriosclerosis Obliterans 40 0.022
676
P CHL066 Cholangitis 40 0.022
677
c ACT068 Acute Cystitis 40 0.022
678
SMN007 Seminoma 40 0.022
679
PNM008 Pneumothorax 40 0.022
680
P PSD015 Pseudohypoparathyroidism 40 0.022
681
P PRM018 Primary Hypertrophic Osteoarthropathy 40 0.022
682
HNC001 Henoch-Schoenlein Purpura 40 0.022
683
PRT030 Parathyroid Gland Disease 40 0.022
684
GRD001 Giardiasis 40 0.022
685
PRC003 Proctitis 40 0.022
686
SKL014 Skeletal Dysplasia 40 0.022
687
DSC009 Discoid Lupus Erythematosus 40 0.022
688
PMP004 Pemphigus Foliaceus 40 0.022
689
CHL004 Cholelithiasis 39 0.022
690
c CHR417 Chronic Graft Versus Host Disease 39 0.022
691
C3D001 C3 Deficiency 39 0.022
692
DST006 Diastolic Heart Failure 39 0.022
693
ANG011 Angiodysplasia 39 0.022
694
FBR003 Fibrous Histiocytoma 39 0.022
695
ESN015 Eosinophilic Fasciitis 39 0.022
696
BRC084 Brca1 Hereditary Breast and Ovarian Cancer Syndrome 39 0.022
697
c BPL002 Bipolar I Disorder 39 0.022
698
P BLP003 Blepharospasm 39 0.022
699
LMY003 Leiomyomatosis 39 0.022
700
DSQ001 Desquamative Interstitial Pneumonia 39 0.022
701
P KRT005 Keratoacanthoma 39 0.022
702
ART035 Arterial Calcification of Infancy 39 0.022
703
FSC002 Fascioliasis 39 0.022
704
c ADN012 Adenocarcinoma in Situ 39 0.022
705
PRM024 Primary Angle-Closure Glaucoma 39 0.022
706
CHN005 Choanal Atresia 39 0.022
707
RSD004 Rosai-Dorfman Disease 39 0.022
708
BNN003 Bone Inflammation Disease 39 0.022
709
DDN006 Duodenitis 39 0.022
710
FCH003 Fechtner Syndrome 39 0.022
711
HMZ003 Homozygous Familial Hypercholesterolemia 39 0.022
712
CLS010 Cluster Headache 39 0.022
713
APR001 Apraxia 38 0.022
714
DND002 Dendritic Cell Sarcoma 38 0.022
715
INT221 Intravascular Large B-Cell Lymphoma 38 0.022
716
P CTN015 Cutaneous T Cell Lymphoma 38 0.022
717
P PLN008 Peeling Skin Syndrome 38 0.022
718
PYL004 Pyelitis 38 0.022
719
c CCK006 Cockayne Syndrome, Type B 38 0.022
720
CLC006 Calcinosis 38 0.022
721
CHR177 Chromophobe Renal Cell Carcinoma 38 0.022
722
TRP014 Triploidy 38 0.022
723
CNT025 Central Pontine Myelinolysis 38 0.022
724
THR035 Thrombasthenia 38 0.022
725
c ACT042 Acute Pyelonephritis 38 0.022
726
MDD003 Middle Cerebral Artery Infarction 38 0.022
727
MLT002 Multiple Symmetrical Lipomatosis 38 0.022
728
ESN006 Eosinophilic Meningitis 38 0.022
729
c HRD104 Hereditary Multiple Osteochondromas 38 0.022
730
ANM001 Anemia of Prematurity 38 0.022
731
SYN058 Synucleinopathy 38 0.022
732
ETH008 Ethmoid Sinus Cancer 38 0.022
733
CVR006 Cavernous Hemangioma 38 0.022
734
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 38 0.022
735
LYM029 Lymphedema-Distichiasis Syndrome 37 0.022
736
SMN008 Semantic Dementia 37 0.022
737
BNF002 Bone Fracture 37 0.022
738
LKM001 Leukemoid Reaction 37 0.022
739
c ALP074 Alport Syndrome, Autosomal Dominant 37 0.022
740
P MNN007 Meningocele 37 0.022
741
CLL003 Cellulitis 37 0.022
742
PRT026 Parotitis 37 0.022
743
SPN029 Spondylolysis 37 0.022
744
HDN002 Head Injury 37 0.022
745
GLM008 Glomus Tumor 37 0.022
746
BLL003 Bell's Palsy 37 0.022
747
PLC008 Placenta Disease 37 0.022
748
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 37 0.022
749
PLC001 Placenta Accreta 37 0.022
750
HST009 Histiocytoma 37 0.022
751
P CNG003 Congenital Dyserythropoietic Anemia 37 0.022
752
SKL017 Skeletal Dysplasias 37 0.022
753
ASP007 Aspiration Pneumonia 37 0.022
754
P CYS036 Cystinosis, Nephropathic 36 0.022
755
HRM002 Hermaphroditism 36 0.022
756
RTN001 Retinal Vasculitis 36 0.022
757
c HYP073 Hypersensitivity Reaction Type Iv Disease 36 0.022
758
ALC005 Alcoholic Pancreatitis 36 0.022
759
P ART084 Arteriovenous Fistula 36 0.022
760
GNG005 Gangliocytoma 36 0.022
761
CHR034 Chromophobe Adenoma 36 0.022
762
TRT001 Teratocarcinoma 36 0.022
763
APH002 Aphasia 36 0.022
764
EPC002 Epicondylitis 36 0.022
765
FLL031 Follicular Adenoma 35 0.022
766
RTR011 Retroperitoneal Fibrosis 35 0.022
767
SQM002 Squamous Cell Papilloma 35 0.022
768
OCL005 Oculocerebrorenal Syndrome 35 0.022
769
MYC033 Myoclonus 35 0.022
770
INT071 Intestinal Perforation 35 0.022
771
DMP001 Dumping Syndrome 35 0.022
772
P PRX033 Proximal Renal Tubular Acidosis 35 0.022
773
EPS006 Epstein Syndrome 35 0.022
774
CRY021 Cryoglobulinemic Vasculitis 35 0.022
775
TTN001 Tetanus Neonatorum 35 0.022
776
DNS007 Dense Deposit Disease 35 0.022
777
P MNN018 Mannosidosis 35 0.022
778
P CHR102 Charcot-Marie-Tooth Neuropathy 35 0.022
779
FLL013 Follicular Dendritic Cell Sarcoma 35 0.022
780
LRY029 Laryngomalacia 35 0.022
781
PHS001 Phosphorus Metabolism Disease 35 0.022
782
PTT004 Pituitary Apoplexy 34 0.022
783
INT067 Interstitial Nephritis 34 0.022
784
GST020 Gastric Antral Vascular Ectasia 34 0.022
785
SKN027 Skin Conditions 34 0.022
786
TXC001 Toxic Megacolon 34 0.022
787
IMM001 Immune-Complex Glomerulonephritis 34 0.022
788
SPT006 Septooptic Dysplasia 34 0.022
789
PNG001 Pinguecula 34 0.022
790
SPR012 Separation Anxiety Disorder 34 0.022
791
DXR001 Doxorubicin Induced Cardiomyopathy 34 0.022
792
OCL020 Ocular Cicatricial Pemphigoid 34 0.022
793
ABD004 Abdominal Tuberculosis 34 0.022
794
INC022 Inclusion-Cell Disease 34 0.022
795
MYS004 Myiasis 34 0.022
796
MYX013 Myxofibrosarcoma 34 0.022
797
MLN003 Melancholia 34 0.022
798
c ANT023 Anterior Scleritis 34 0.022
799
c CCK005 Cockayne Syndrome, Type a 34 0.022
800
c CNG033 Congenital Syphilis 34 0.022
801
CNS002 Constrictive Pericarditis 34 0.022
802
ACT087 Acth Deficiency 34 0.022
803
PNM010 Pneumothorax, Primary Spontaneous 34 0.022
804
P MSN005 Mesenchymal Chondrosarcoma 34 0.022
805
P HYP111 Hyperprolinemia 34 0.022
806
c CRN139 Cornelia De Lange Syndrome 1 34 0.022
807
SCR015 Scarlet Fever 34 0.022
808
SCN001 Secondary Hyperparathyroidism of Renal Origin 33 0.022
809
GST007 Gastric Dilatation 33 0.022
810
ERY004 Erysipelas 33 0.022
811
HYD005 Hydrocele 33 0.022
812
PRM025 Primary Bacterial Infectious Disease 33 0.022
813
DRM013 Dermoid Cyst 33 0.022
814
PST086 Posterior Cortical Atrophy 33 0.022
815
EXT022 Exotropia 33 0.022
816
FBR019 Fibromatosis 33 0.022
817
P CNG024 Congenital Nystagmus 33 0.022
818
PRP036 Peripheral T-Cell Lymphoma 33 0.022
819
ONC003 Oncogenic Osteomalacia 33 0.022
820
BND016 Bone Diseases 33 0.022
821
LRY004 Laryngotracheitis 33 0.022
822
GNG002 Ganglioneuroma 33 0.022
823
WBR001 Weber Syndrome 33 0.022
824
HPT004 Hepatic Coma 33 0.022
825
PRX077 Peroxisomal Biogenesis Disorders 33 0.022
826
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 33 0.022
827
MNR003 Mineral Metabolism Disease 33 0.022
828
LYM014 Lymphangitis 32 0.022
829
DCB001 Decubitus Ulcer 32 0.022
830
RHM009 Rheumatoid Lung Disease 32 0.022
831
LNT002 Lentigo Maligna Melanoma 32 0.022
832
HMN016 Hemangioendothelioma 32 0.022
833
TRT003 Tertiary Syphilis 32 0.022
834
P HRN001 Horner's Syndrome 32 0.022
835
CMP001 Composite Lymphoma 32 0.022
836
SXL003 Sexual Disorder 32 0.022
837
VRT001 Vertebral Artery Occlusion 32 0.022
838
ANC002 Anca-Associated Vasculitis 32 0.022
839
MCN008 Mucinous Cystadenocarcinoma 32 0.022
840
ACL001 Acalculous Cholecystitis 31 0.022
841
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 31 0.022
842
FBR008 Fibrillary Astrocytoma 31 0.022
843
WTH001 Withdrawal Disorder 31 0.022
844
HYP540 Hypertension, Diastolic 31 0.022
845
SYD001 Sydenham's Chorea 31 0.022
846
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 31 0.022
847
IMM127 Immune System Cancer 31 0.022
848
CMP042 Complement Factor H Deficiency 31 0.022
849
CRB004 Cerebral Artery Occlusion 31 0.022
850
DPN001 Dependent Personality Disorder 31 0.022
851
c HML032 Hemolytic Uremic Syndrome, Atypical 4 31 0.022
852
MLN001 Melanotic Neuroectodermal Tumor 31 0.022
853
MLN012 Melanoma and Neural System Tumor Syndrome 31 0.022
854
OBS004 Obstructive Hydrocephalus 30 0.022
855
RDL002 Radioulnar Synostosis 30 0.022
856
IDP073 Idiopathic Hypercalciuria 30 0.022
857
MLN013 Melanoma Metastasis 30 0.022
858
MDY004 Mody, Type Iii 30 0.022
859
P CMM008 Communicating Hydrocephalus 30 0.022
860
CMB021 Combined Pituitary Hormone Deficiency 30 0.022
861
c FCL055 Focal Segmental Glomerulosclerosis 9 30 0.022
862
ATN005 Autonomic Dysfunction 30 0.022
863
GLC001 Glaucomatocyclitic Crisis 30 0.022
864
RTT001 Ritter's Disease 30 0.022
865
SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 30 0.022
866
PYG002 Pyogenic Arthritis, Pyoderma Gangrenosum and Acne 30 0.022
867
MTN002 Mite Infestation 30 0.022
868
PLV001 Pelvic Lipomatosis 29 0.022
869
P DYS021 Dysautonomia 29 0.022
870
RPR002 Reproductive System Disease 29 0.022
871
CYC008 Cyclic Vomiting Syndrome 29 0.022
872
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 29 0.022
873
BLR002 Bile Reflux 29 0.022
874
MLD002 Mild Pre-Eclampsia 29 0.022
875
DRM005 Dermoid Cyst of Ovary 29 0.022
876
BLN010 Balanitis 29 0.022
877
c HYP311 Hyperparathyroidism 3 29 0.022
878
MYB001 Myoblastoma 29 0.022
879
MYC015 Mycobacterium Fortuitum 29 0.022
880
MGL016 Megaloblastic Anemia-1, Finnish Type 29 0.022
881
SPC001 Space Motion Sickness 29 0.022
882
CNG069 Congenital Cytomegalovirus 28 0.022
883
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 28 0.022
884
c SYS043 Systemic Lupus Erythematosus 1 28 0.022
885
CPL001 Capillariasis 28 0.022
886
LPN001 Louping Ill 28 0.022
887
ACN019 Acanthamoeba Keratitis 28 0.022
888
PHC006 Phacomatosis Pigmentovascularis 28 0.022
889
CVR002 Cavernous Sinus Thrombosis 27 0.022
890
c PRM032 Primary Congenital Glaucoma 27 0.022
891
ATM012 Autoimmune Disease of Blood 27 0.022
892
DBT084 Diabetes Mellitus, Ketosis-Prone 27 0.022
893
c HYP248 Hyperprolinemia, Type I 27 0.022
894
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 27 0.022
895
HRS011 Horseshoe Kidney 27 0.022
896
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 27 0.022
897
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 27 0.022
898
ISC001 Ischemic Neuropathy 27 0.022
899
ANG037 Angiomatosis 27 0.022
900
SPS016 Spasmodic Dysphonia 27 0.022
901
HMX002 Heme Oxygenase-1 Deficiency 27 0.022
902
MRC001 Marchiafava Bignami Disease 26 0.022
903
HYP114 Hypertensive Nephropathy 26 0.022
904
CLR018 Clear Cell Meningioma 26 0.022
905
OVR013 Ovarian Mucinous Cystadenocarcinoma 26 0.022
906
SBC002 Subclavian Artery Aneurysm 26 0.022
907
c NPH065 Nephronophthisis 13 26 0.022
908
ACT120 Acute Zonal Occult Outer Retinopathy 26 0.022
909
URT011 Urethral Calculus 26 0.022
910
ULC006 Ulceroglandular Tularemia 26 0.022
911
AMN009 Amniotic Band Syndrome 26 0.022
912
c NPH046 Nephrolithiasis, Type I 25 0.022
913
MLT084 Multicystic Dysplastic Kidney 25 0.022
914
NRG001 Neurogenic Bowel 25 0.022
915
NCR009 Necrobiotic Xanthogranuloma 25 0.022
916
EPL108 Epilepsy, Progressive Myoclonic 4, with or Without Renal Failure 25 0.022
917
c CNT101 Central Congenital Hypothyroidism 25 0.022
918
INT065 Interstitial Keratitis 25 0.022
919
DND018 Dendritic Cell Tumor 24 0.022
920
IMM065 Immunodeficiency 10 24 0.022
921
PRS064 Persistent Vegetative State 24 0.022
922
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 24 0.022
923
PDT040 Pediatric Hypertension 24 0.022
924
MLR007 Male Reproductive System Disease 24 0.022
925
VTM003 Vitamin Metabolic Disorder 24 0.022
926
SPN156 Spontaneous Coronary Artery Dissection 24 0.022
927
c VSC020 Vesicoureteral Reflux 2 24 0.022
928
P SPR036 Supernumerary Nipples 24 0.022
929
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 23 0.022
930
SCR024 Sacrococcygeal Teratoma 23 0.022
931
c HML034 Hemolytic Uremic Syndrome, Atypical 3 23 0.022
932
C3G002 C3 Glomerulopathy 23 0.022
933
HRP011 Herpes Zoster Ophthalmicus 23 0.022
934
ADG002 Audiogenic Seizures 23 0.022
935
IDP077 Idiopathic Membranous Glomerulonephritis 23 0.022
936
c VSC025 Vesicoureteral Reflux 3 23 0.022
937
INT258 Interstitial Nephritis, Karyomegalic 23 0.022
938
c HML036 Hemolytic Uremic Syndrome, Atypical 6 23 0.022
939
MNT146 Mental Retardation, X-Linked, Syndromic, Martin-Probst Type 23 0.022
940
c HML037 Hemolytic Uremic Syndrome, Atypical 5 23 0.022
941
LRY027 Laryngeal Papillomatosis 23 0.022
942
c EXS005 Exostoses, Multiple, Type 2 23 0.022
943
c HML035 Hemolytic Uremic Syndrome, Atypical 2 23 0.022
944
PYR035 Pyrimidine Metabolic Disorder 23 0.022
945
HYD034 Hydromyelia 22 0.022
946
IMM053 Immunotactoid Glomerulopathy 22 0.022
947
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 22 0.022
948
c TRC078 Trichohepatoenteric Syndrome 2 22 0.022
949
PRR008 Periarteritis Nodosa 22 0.022
950
NNT021 Neonatal Meningitis 22 0.022
951
DCR002 Dacryocystocele 21 0.022
952
NRN022 Neurenteric Cyst 21 0.022
953
CVR001 Cavernous Sinus Meningioma 21 0.022
954
ULC008 Ulcerative Proctitis 21 0.022
955
MCH006 Mechanical Strabismus 21 0.022
956
CNZ008 Coenzyme Q10 Deficiency, Primary, 6 20 0.022
957
DFN256 Deafness and Myopia 20 0.022
958
FBR085 Fibrillary Glomerulonephritis 20 0.022
959
c EXS004 Exostoses, Multiple, Type 1 20 0.022
960
c GLY017 Glycogen Storage Disease Ic 20 0.022
961
TRC037 Tracheobronchomalacia 20 0.022
962
CLF025 Cleft Lip +/- Cleft Palate 20 0.022
963
c PRC045 Preeclampsia/eclampsia 5 20 0.022
964
ALP035 Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 20 0.022
965
SWL001 Swallowing Disorders 20 0.022
966
CYC007 Cyclic Thrombocytopenia 20 0.022
967
c SYS038 Systemic Lupus Erythematosus 2 20 0.022
968
c FML162 Familial Mediterranean Fever, Ad 19 0.022
969
LMB011 Limb Deficiencies Distal with Micrognathia 19 0.022
970
SHK001 Shaken Baby Syndrome 19 0.022
971
MLG087 Malignant Cylindroma 19 0.022
972
BRN097 Brainstem Auditory Evoked Responses 19 0.022
973
P SNS011 Sinus Cancer 19 0.022
974
RHM013 Rheumatoid Nodulosis 18 0.022
975
EXG001 Exogenous Ochronosis 17 0.022
976
c PRC034 Preeclampsia/eclampsia 4 17 0.022
977
IMM071 Immunodeficiency 12 17 0.022
978
CNZ004 Coenzyme Q10 Deficiency, Primary, 3 17 0.022
979
c NPH076 Nephrotic Syndrome, Type 10 17 0.022
980
AMN012 Aminoacidopathies 17 0.022
981
ALP085 Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome 17 0.022
982
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 17 0.022
983
c VSC046 Vesicoureteral Reflux 8 17 0.022
984
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 17 0.022
985
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 17 0.022
986
RNL089 Renal Nutcracker Syndrome 16 0.022
987
FBR024 Fibrocartilaginous Embolism 16 0.022
988
HYP666 Hypoparathyroidism-Deafness-Renal Disease Syndrome 16 0.022
989
c SYS046 Systemic Lupus Erythematosus 3 16 0.022
990
WND005 Wound Myiasis 16 0.022
991
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 16 0.022
992
HPD002 Hepadnavirus Infection 15 0.022
993
c FNC049 Fanconi Renotubular Syndrome 3 15 0.022
994
SPR064 Supernumerary Breasts 14 0.022
995
BCK018 Bickerstaff Brainstem Encephalitis 14 0.022
996
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 14 0.022
997
MTS004 Metastatic Insulinoma 14 0.022
998
c SYS051 Systemic Lupus Erythematosus 4 14 0.022
999
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 14 0.022
1000
P CRN178 Coronary Heart Disease 6 13 0.022
1001
TFT002 Tufted Hair Folliculitis 13 0.022
1002
ATH011 Atherosclerosis-Deafness-Diabetes-Epilepsy-Nephropathy Syndrome 13 0.022
1003
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 12 0.022
1004
PYL007 Pylorus Cancer 12 0.022
1005
AML051 Aml with Myelodysplasia-Related Features 12 0.022
1006
ASB003 Asbestos Intoxication 12 0.022
1007
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 12 0.022
1008
STP007 Staphylococcal Scarlet Fever 12 0.022
1009
PHC008 Pheochromocytoma-Islet Cell Tumor Syndrome 12 0.022
1010
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 12 0.022
1011
RTN184 Retinal Ischemic Syndrome-Digestive Tract Small Vessel Hyalinosis-Diffuse Cerebral Calcifications Syndrome 12 0.022
1012
FTZ004 Fitzsimmons Walson Mellor Syndrome 12 0.022
1013
CNG116 Congenital Nephrotic Syndrome Finnish Type 11 0.022
1014
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 11 0.022
1015
c PRC032 Preeclampsia/eclampsia 2 11 0.022
1016
MLT102 Multicentric Carpo-Tarsal Osteolysis with or Without Nephropathy 11 0.022
1017
DYS034 Dyschondrosteosis Nephritis 10 0.022
1018
SLC010 Salcedo Syndrome 10 0.022
1019
VSC009 Vascular Skin Disease 10 0.022
1020
IMM051 Immunotactoid or Fibrillary Glomerulopathy 9 0.022
1021
VSC014 Vascular Hyalinosis 9 0.022
1022
LTZ001 Lutz Richner Landolt Syndrome 9 0.022
1023
NVD002 Nevada Syndrome 8 0.022
1024
HRP008 Herpes Simiae 8 0.022
1025
c EXS006 Exostoses, Multiple, Type 3 7 0.022
1026
c SYS054 Systemic Lupus Erythematosus with Nephritis 3 7 0.022
1027
P SYS050 Systemic Lupus Erythematosus with Nephritis 2 6 0.022
1028
c SYS056 Systemic Lupus Erythematosus with Nephritis 1 6 0.022
1029
HRP012 Herpesvirus Simiae B Virus 4 0.022