Search results for rho

1187 hits were found for rho

# Family MCID Name MIFTS Score
1
c INH030 Inherited Retinal Disorder 51 5.999
2
P RTN008 Retinitis Pigmentosa 79 4.279
3
c RTN066 Retinitis Pigmentosa 4 39 4.066
4
c NGH021 Night Blindness, Congenital Stationary, Autosomal Dominant 1 34 3.905
5
RTN023 Retinitis 46 3.390
6
FND001 Fundus Albipunctatus 60 3.247
7
P CNG010 Congenital Stationary Night Blindness 54 3.221
8
P NGH001 Night Blindness 48 3.214
9
P CLR023 Colorectal Cancer 99 3.077
10
P CNR004 Cone-Rod Dystrophy 2 73 2.676
11
P CTR002 Cataract 60 2.641
12
CHL014 Cholera 59 2.333
13
P RTN016 Retinal Degeneration 53 2.333
14
RTN017 Retinal Detachment 61 2.326
15
P CND005 Cone Dystrophy 43 2.296
16
P MYP006 Myopia 55 2.267
17
c USH036 Usher Syndrome, Type I 60 2.255
18
FND002 Fundus Dystrophy 55 2.225
19
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 1.984
20
OCL006 Ocular Hypertension 53 1.984
21
c GLC092 Glaucoma, Primary Open Angle 62 1.979
22
P RTN018 Retinal Disease 53 1.933
23
P MCR115 Microvascular Complications of Diabetes 5 66 1.920
25
PTH003 Pathologic Nystagmus 52 1.888
26
OPT001 Optic Disk Drusen 34 1.878
27
P USH001 Usher Syndrome 60 1.868
28
LBR036 Leber Plus Disease 66 1.855
29
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 1.855
30
c RTN172 Retinitis Pigmentosa 1 44 1.855
31
P JBR020 Joubert Syndrome 1 72 1.841
32
P MCK013 Meckel Syndrome, Type 1 65 1.841
33
P STR022 Stargardt Disease 58 1.841
34
P STR020 Strabismus 55 1.841
35
KRT002 Keratomalacia 47 1.841
36
XRP001 Xerophthalmia 41 1.841
37
P OGC005 Oguchi Disease 39 1.841
38
HRD016 Hereditary Retinal Dystrophy 35 1.841
39
EYD002 Eye Disease 58 1.392
40
RTN020 Retinal Vascular Disease 46 1.367
41
c LTN004 Late-Onset Retinal Degeneration 59 1.347
42
CTS003 Coats Disease 53 1.347
43
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 1.347
44
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 1.347
45
RRD062 Rare Disorder with Lens Opacification 17 1.347
46
CHR081 Choroideremia 57 1.321
47
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.321
48
c EXD008 Exudative Vitreoretinopathy 1 71 1.302
49
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.302
50
P BRD002 Bardet-Biedl Syndrome 66 1.302
51
P ACH003 Achromatopsia 61 1.302
52
GYR004 Gyrate Atrophy of Choroid and Retina 57 1.302
53
ENH001 Enhanced S-Cone Syndrome 57 1.302
54
P SNR003 Senior-Loken Syndrome 1 56 1.302
55
OPT070 Optic Nerve Hypoplasia, Bilateral 56 1.302
56
MCL006 Macular Retinal Edema 55 1.302
57
c LBR004 Leber Congenital Amaurosis 1 52 1.302
58
c LBR012 Leber Congenital Amaurosis 2 51 1.302
59
TRT020 Tritanopia 49 1.302
60
c USH035 Usher Syndrome Type 2 48 1.302
61
P CLR019 Color Blindness 48 1.302
62
BLC001 Blue Cone Monochromacy 45 1.302
63
PNC056 Pineocytoma 45 1.302
64
SCT002 Scotoma 44 1.302
65
PRL047 Prolonged Electroretinal Response Suppression 42 1.302
66
VTR005 Vitreous Disease 39 1.302
67
c ACH023 Achromatopsia 4 38 1.302
68
CLR133 Colorblindness, Partial, Protan Series 37 1.302
69
CHR079 Choroid Disease 37 1.302
70
P NNP021 Nanophthalmos 36 1.302
71
c AML047 Amelogenesis Imperfecta, Type Ia 35 1.302
72
c MYS048 Myasthenic Syndrome, Congenital, 3a, Slow-Channel 35 1.302
73
CNC014 Cancer-Associated Retinopathy 34 1.302
74
STR046 Stargardt Macular Degeneration 31 1.302
75
PTT063 Pattern Dystrophy 29 1.302
76
DGN003 Degeneration of Macula and Posterior Pole 29 1.302
77
RDG001 Red-Green Color Blindness 29 1.302
78
PRP026 Peripheral Retinal Degeneration 28 1.302
79
SLR002 Solar Retinopathy 27 1.302
80
CHR077 Chorioretinal Scar 26 1.302
81
TRN011 Transient Refractive Change 25 1.302
82
c ATS009 Autosomal Genetic Disease 25 1.302
83
MLN046 Melanoma-Associated Retinopathy 24 1.302
84
c ATS168 Autosomal Dominant Congenital Stationary Night Blindness 24 1.302
85
EYD001 Eye Degenerative Disease 24 1.302
86
P PTT054 Patterned Macular Dystrophy 22 1.302
87
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.306
88
P PLM037 Pulmonary Hypertension 67 0.235
89
PRT037 Pertussis 65 0.180
90
IMP005 Impotence 52 0.178
91
P VSC007 Vascular Disease 63 0.167
92
SPN186 Spinal Cord Injury 60 0.161
93
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.149
94
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.149
95
NRR001 Neuroretinitis 42 0.146
96
P HPT023 Hepatocellular Carcinoma 100 0.144
97
P NRB001 Neuroblastoma 72 0.137
98
P BRS047 Breast Cancer 97 0.131
99
ISC004 Ischemia 58 0.127
100
P ART021 Arteriosclerosis 54 0.125
101
GLB015 Glioblastoma Multiforme 75 0.112
102
P OPN001 Open-Angle Glaucoma 49 0.110
103
ATH013 Atherosclerosis Susceptibility 65 0.105
104
P GLM045 Glioma 63 0.105
105
HYP266 Hypoxia 57 0.103
106
BNR002 Bone Resorption Disease 48 0.103
107
c MCR113 Microvascular Complications of Diabetes 3 52 0.101
108
c MCR120 Microvascular Complications of Diabetes 7 47 0.101
109
GLL048 Glial Tumor 45 0.101
110
c MCR130 Microvascular Complications of Diabetes 6 41 0.101
111
c MCR133 Microvascular Complications of Diabetes 4 41 0.101
112
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.098
113
P LTR001 Lateral Sclerosis 54 0.098
114
CRN019 Coronary Artery Vasospasm 46 0.095
115
HYP066 Hyperglycemia 61 0.093
116
CRB004 Cerebral Artery Occlusion 45 0.093
117
P MLN008 Melanoma 69 0.090
118
P PLM036 Pulmonary Fibrosis 65 0.090
119
P WSK001 Wiskott-Aldrich Syndrome 72 0.087
120
OST159 Osteogenic Sarcoma 66 0.087
121
P PNC035 Pancreatic Cancer 84 0.084
122
PRT013 Portal Hypertension 59 0.084
123
P MYT002 Myotonic Dystrophy 49 0.084
124
c PCH010 Pachyonychia Congenita 3 44 0.084
125
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.084
126
ALL014 Allergic Encephalomyelitis 38 0.084
127
P PRS040 Prostate Cancer 97 0.081
128
P OVR042 Ovarian Cancer 88 0.081
129
P BLD134 Bladder Cancer 79 0.081
130
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.081
131
P AST007 Astrocytoma 51 0.081
132
c HYP595 Hypertension, Essential 84 0.078
133
P ADN016 Adenocarcinoma 64 0.078
134
P ALZ034 Alzheimer Disease 88 0.075
135
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.075
136
P HRT032 Heart Disease 75 0.075
137
P MYC007 Myocardial Infarction 70 0.075
138
LPD008 Lipid Metabolism Disorder 62 0.075
139
SQM006 Squamous Cell Carcinoma 60 0.075
140
P LNG032 Lung Cancer 98 0.071
141
c HYP836 Hypercholesterolemia, Familial, 1 73 0.071
142
P KDN018 Kidney Disease 72 0.071
143
MSC007 Muscle Hypertrophy 64 0.071
144
TXC005 Toxic Shock Syndrome 62 0.071
145
LVR012 Liver Cirrhosis 62 0.071
146
P BCL017 B-Cell Lymphoma 58 0.071
147
P CRD246 Cardiovascular System Disease 57 0.071
148
PRS045 Prostatic Hypertrophy 53 0.071
149
PRS021 Prostatic Adenoma 51 0.071
150
NTR046 Neutrophil Migration 50 0.071
151
LWC001 Low Compliance Bladder 43 0.071
152
PLY150 Polykaryocytosis Inducer 31 0.071
153
CNG034 Congestive Heart Failure 69 0.067
154
P LYM118 Lymphoma 68 0.067
155
c PRC016 Pre-Eclampsia 63 0.067
156
P FBR017 Fibrosarcoma 56 0.067
157
PLM010 Pulmonary Edema 54 0.067
158
PRS129 Prostatic Hyperplasia, Benign 49 0.067
159
CYT002 Cytokine Deficiency 42 0.067
160
STR067 Stroke, Ischemic 81 0.064
161
INS024 Insulin-Like Growth Factor I 79 0.064
162
P LKM002 Leukemia 68 0.064
163
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.064
164
ATM095 Autoimmune Disease 62 0.064
165
c SCL052 Scleroderma, Familial Progressive 61 0.064
166
P MYL006 Myeloid Leukemia 60 0.064
167
P CYS018 Cystitis 59 0.064
168
P NRF002 Neurofibromatosis 56 0.064
169
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.064
170
c LKM061 Leukemia, Acute Myeloid 84 0.059
171
P GST053 Gastric Cancer 83 0.059
172
P RHM011 Rheumatoid Arthritis 80 0.059
173
P LKM071 Leukemia, Chronic Lymphocytic 79 0.059
174
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.059
175
P HNT016 Huntington Disease 72 0.059
176
P SYS005 Systemic Scleroderma 68 0.059
177
ANG054 Angina Pectoris 66 0.059
178
P NSP012 Nasopharyngeal Carcinoma 66 0.059
179
c SML038 Small Cell Cancer of the Lung 65 0.059
180
P NTR004 Neutropenia 63 0.059
181
ALL026 Allergic Hypersensitivity Disease 62 0.059
182
P KDN017 Kidney Cancer 60 0.059
183
P NPH012 Nephrotic Syndrome 60 0.059
184
P OPT006 Optic Nerve Disease 60 0.059
185
P NRP001 Neuropathy 56 0.059
186
P MSC003 Muscular Atrophy 52 0.059
187
VCC001 Vaccinia 49 0.059
188
CLS016 Clostridium Difficile Colitis 48 0.059
189
RNL077 Renal Fibrosis 47 0.059
190
48X005 48,xyyy 39 0.059
191
HRW001 Hair Whorl 36 0.059
192
P GLM040 Glioma Susceptibility 1 81 0.055
193
IMM167 Immune Deficiency Disease 78 0.055
194
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.055
195
SVR004 Severe Combined Immunodeficiency 73 0.055
196
P RTN024 Retinoblastoma 73 0.055
197
P THR014 Thrombocytopenia 67 0.055
198
P CRB048 Cerebral Cavernous Malformations 67 0.055
199
c ATS007 Autism Spectrum Disorder 67 0.055
200
LPP008 Lipoprotein Quantitative Trait Locus 62 0.055
201
FTT001 Fatty Liver Disease 61 0.055
202
DPH001 Diphtheria 60 0.055
203
LNG099 Lung Disease 60 0.055
204
THY029 Thyroid Carcinoma 59 0.055
205
BRN004 Brain Edema 56 0.055
206
P INF037 Inflammatory Bowel Disease 54 0.055
207
c FML008 Familial Retinoblastoma 53 0.055
208
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.055
209
ENT011 Enterocolitis 51 0.055
210
P OVR082 Overgrowth Syndrome 50 0.055
211
CRN030 Coronary Stenosis 50 0.055
212
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.055
213
MYL069 Myeloma, Multiple 85 0.050
214
OST012 Osteoarthritis 78 0.050
215
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.050
216
AST005 Asthma 76 0.050
217
ULC004 Ulcerative Colitis 73 0.050
218
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.050
219
P ATS364 Autism 70 0.050
220
c CHR684 Chronic Kidney Disease 70 0.050
221
P TBR001 Tuberous Sclerosis 70 0.050
222
P PNM007 Pneumonia 68 0.050
223
P HYP098 Hypereosinophilic Syndrome 67 0.050
224
P RHB003 Rhabdomyosarcoma 63 0.050
225
P SPN046 Spinal Muscular Atrophy 62 0.050
226
c SVR001 Severe Acute Respiratory Syndrome 62 0.050
227
CHL068 Cholestasis 61 0.050
228
c ACT071 Acute Kidney Failure 60 0.050
229
ANR040 Aneurysm 59 0.050
230
BCT022 Bacterial Infectious Disease 56 0.050
231
PRP030 Purpura 54 0.050
232
DBT010 Diabetic Neuropathy 54 0.050
233
DMY004 Demyelinating Disease 52 0.050
234
URT010 Ureteral Obstruction 45 0.050
235
P LNG064 Lung Cancer Susceptibility 3 78 0.045
236
c ATR087 Atrial Standstill 1 75 0.045
237
CRH001 Crohn's Disease 74 0.045
238
c THR092 Thrombophilia Due to Thrombin Defect 73 0.045
239
P FML011 Familial Adenomatous Polyposis 72 0.045
240
P PHC003 Pheochromocytoma 71 0.045
241
ART016 Aortic Aneurysm 69 0.045
242
P LVR013 Liver Disease 68 0.045
243
CNN005 Connective Tissue Disease 68 0.045
244
P HRP006 Herpes Simplex 65 0.045
245
BRC012 Brucellosis 64 0.045
246
MGK001 Megakaryocytic Leukemia 64 0.045
247
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.045
248
P VSC011 Vasculitis 62 0.045
249
CRC021 Carcinosarcoma 62 0.045
250
P ENC018 Encephalopathy 61 0.045
251
P ENC004 Encephalitis 61 0.045
252
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.045
253
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
254
PRN019 Perinatal Necrotizing Enterocolitis 59 0.045
255
P UVT001 Uveitis 57 0.045
256
P FCL005 Focal Segmental Glomerulosclerosis 57 0.045
257
P DRR001 Diarrhea 55 0.045
258
HYP060 Hyperinsulinism 54 0.045
259
ART140 Arteries, Anomalies of 52 0.045
260
NPH010 Nephrosclerosis 50 0.045
261
BLL004 Bullous Keratopathy 49 0.045
262
HLX001 Helix Syndrome 47 0.045
263
KRT008 Keratopathy 47 0.045
264
P VTR007 Vitreoretinopathy 46 0.045
265
ADR040 Adrenal Gland Pheochromocytoma 46 0.045
266
c MLG068 Malignant Glioma 46 0.045
267
CRT015 Carotid Artery Occlusion 45 0.045
268
P CRN026 Corneal Edema 43 0.045
269
ORL015 Oral Squamous Cell Carcinoma 43 0.045
270
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.045
271
CVR010 Cavernous Malformation 30 0.045
272
ESP021 Esophageal Cancer 90 0.039
273
c SYS001 Systemic Lupus Erythematosus 86 0.039
274
P MDL005 Medulloblastoma 77 0.039
275
c TBR025 Tuberous Sclerosis 1 77 0.039
276
KPS004 Kaposi Sarcoma 75 0.039
277
P MLT020 Multiple Sclerosis 72 0.039
278
SMT004 Smith-Lemli-Opitz Syndrome 70 0.039
279
P MYP004 Myopathy 70 0.039
280
LYM133 Lymphoma, Hodgkin, Classic 69 0.039
281
P LKM062 Leukemia, Acute Lymphoblastic 69 0.039
282
PNC129 Pancreatic Adenocarcinoma 68 0.039
283
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.039
284
CRB039 Cerebrovascular Disease 67 0.039
285
P FLL037 Follicular Lymphoma 67 0.039
286
c MGR028 Migraine with or Without Aura 1 67 0.039
287
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.039
288
P ATR011 Atrial Fibrillation 66 0.039
289
P CNJ013 Conjunctivitis 65 0.039
290
P MTR014 Motor Neuron Disease 65 0.039
291
CLN015 Colon Adenocarcinoma 65 0.039
292
P DBT009 Diabetes Mellitus 64 0.039
293
NRF007 Neurofibroma 64 0.039
294
P PRD008 Periodontitis 64 0.039
295
P PLY014 Polycystic Kidney Disease 62 0.039
296
c HPT003 Hepatitis a 62 0.039
297
c BRN108 Branchiootic Syndrome 1 62 0.039
298
P ESP024 Esophagitis 62 0.039
299
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.039
300
INT002 Intermittent Claudication 61 0.039
301
P LPS004 Lupus Erythematosus 61 0.039
302
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.039
303
c ACT027 Acute Pancreatitis 60 0.039
304
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.039
305
CHL123 Chlamydia 59 0.039
306
PLM033 Pulmonary Embolism 59 0.039
307
P BRS044 Breast Adenocarcinoma 59 0.039
308
HLC007 Helicobacter Pylori Infection 59 0.039
309
ANT024 Anthrax Disease 58 0.039
310
P MMP001 Mumps 58 0.039
311
GLS018 Glass Syndrome 57 0.039
312
MCR013 Microphthalmia 57 0.039
313
VSC002 Vascular Dementia 57 0.039
314
P CHN012 Chondrosarcoma 56 0.039
315
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.039
316
ALL006 Allergic Asthma 56 0.039
317
ERY051 Erythroleukemia, Familial 56 0.039
318
P LBR014 Leber Congenital Amaurosis 4 56 0.039
319
INT007 Intermediate Coronary Syndrome 55 0.039
320
P PMP001 Pemphigus 54 0.039
321
GLC003 Glucose Intolerance 54 0.039
322
P TRM003 Tremor 54 0.039
323
NNL006 Non-Alcoholic Steatohepatitis 54 0.039
324
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.039
325
DYS015 Dysentery 52 0.039
326
P TRT010 Teratoma 52 0.039
327
RTN003 Retinal Ischemia 50 0.039
328
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.039
329
P ECL001 Eclampsia 50 0.039
330
BLP005 Blepharitis 50 0.039
331
STM007 Stomatitis 50 0.039
332
HYP080 Hypogonadism 50 0.039
333
P CRN025 Corneal Dystrophy 49 0.039
334
BRN071 Brain Injury 49 0.039
335
c CRB191 Cerebral Cavernous Malformations 2 47 0.039
336
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.039
337
CHR074 Choriocarcinoma 47 0.039
338
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.039
339
P CHR345 Chronic Pain 44 0.039
340
c CRB094 Cerebral Cavernous Malformations 3 42 0.039
341
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.039
342
WLL004 Wallerian Degeneration 39 0.039
343
c LKM005 Leukemia, T-Cell, Chronic 34 0.039
345
RHS001 Rh Isoimmunization 32 0.039
346
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.039
347
c CRB051 Cerebral Cavernous Malformation, Familial 26 0.039
348
NRL016 Neural Tube Defects 82 0.032
349
c FNC027 Fanconi Anemia, Complementation Group a 81 0.032
350
CYS001 Cystic Fibrosis 81 0.032
351
c NRF024 Neurofibromatosis, Type I 77 0.032
352
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.032
353
ADR007 Adrenoleukodystrophy 75 0.032
354
P APL001 Aplastic Anemia 74 0.032
355
P RSP003 Respiratory Failure 74 0.032
356
BRN028 Brain Cancer 74 0.032
357
P SCH015 Schizophrenia 74 0.032
358
P FML018 Familial Mediterranean Fever 73 0.032
359
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.032
360
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.032
361
P GRF003 Graft-Versus-Host Disease 72 0.032
362
c LKM063 Leukemia, Chronic Myeloid 72 0.032
363
HMN044 Human Immunodeficiency Virus Type 1 71 0.032
364
PRP027 Peripheral Vascular Disease 71 0.032
365
P SRC025 Sarcoidosis 1 70 0.032
366
DFC004 Deficiency Anemia 70 0.032
367
GST040 Gastric Adenocarcinoma 70 0.032
368
LYM007 Lymphangioleiomyomatosis 69 0.032
369
MNT001 Mantle Cell Lymphoma 69 0.032
370
CHL065 Cholangiocarcinoma 68 0.032
371
SKN019 Skin Melanoma 68 0.032
372
BRK010 Burkitt Lymphoma 67 0.032
373
ALL003 Allergic Rhinitis 67 0.032
374
P CHR012 Chronic Granulomatous Disease 67 0.032
375
P TRN020 Turner Syndrome 67 0.032
376
c RHB024 Rhabdomyosarcoma 2 67 0.032
377
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.032
378
P MSC005 Muscular Dystrophy 66 0.032
379
P SKN015 Skin Carcinoma 66 0.032
380
HYP056 Hypoglycemia 66 0.032
381
P MNN013 Meningitis 66 0.032
382
GTL001 Gitelman Syndrome 65 0.032
383
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.032
384
KRT019 Keratitis, Hereditary 65 0.032
385
TNG002 Tangier Disease 65 0.032
386
BRR014 Barrett Esophagus 65 0.032
387
P THY023 Thymoma 65 0.032
388
P CHR071 Charcot-Marie-Tooth Disease 65 0.032
389
PRT036 Peritonitis 64 0.032
390
APN008 Apnea, Obstructive Sleep 64 0.032
391
NRM005 Neuromuscular Disease 64 0.032
392
TYP007 Typhoid Fever 63 0.032
393
PLG002 Plague 63 0.032
394
P CRN300 Coronary Heart Disease 1 63 0.032
395
SKN016 Skin Disease 63 0.032
396
P HYP055 Hypoplastic Left Heart Syndrome 63 0.032
397
P MVM001 Movement Disease 63 0.032
398
c ACT068 Acute Cystitis 63 0.032
399
HMT002 Hematologic Cancer 62 0.032
400
CLT003 Colitis 62 0.032
401
MSL001 Measles 62 0.032
402
P DRM010 Dermatomyositis 61 0.032
403
OST003 Osteonecrosis 61 0.032
404
GST033 Gestational Diabetes 61 0.032
405
VRL011 Viral Infectious Disease 61 0.032
406
P HMN010 Hemangioma 61 0.032
407
INT066 Interstitial Lung Disease 60 0.032
408
VRC005 Varicose Veins 60 0.032
409
P PTN014 Patent Ductus Arteriosus 1 60 0.032
410
ORL011 Oral Cancer 60 0.032
411
QFV001 Q Fever 60 0.032
412
STT001 Status Epilepticus 60 0.032
413
P THL005 Thalassemia 60 0.032
414
P MYC008 Myocarditis 59 0.032
415
c HPT016 Hepatitis B 59 0.032
416
PRT058 Pure Autonomic Failure 59 0.032
417
P MLN069 Melanoma, Uveal 59 0.032
418
BRN002 Bronchiolitis 59 0.032
419
P GLL022 Guillain-Barre Syndrome 59 0.032
420
P DNG005 Dengue Virus 59 0.032
421
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.032
422
GST045 Gastroenteritis 59 0.032
423
P ADM011 Adams-Oliver Syndrome 59 0.032
424
INC002 Inclusion Body Myositis 58 0.032
425
P BNC003 Bone Cancer 58 0.032
426
c DWL002 Dowling-Degos Disease 1 58 0.032
427
P PRP019 Peripheral Nervous System Disease 58 0.032
428
P INF032 Infertility 57 0.032
429
PMP006 Pemphigus Vulgaris, Familial 57 0.032
430
c CHR417 Chronic Graft Versus Host Disease 57 0.032
431
BRN056 Bronchopulmonary Dysplasia 57 0.032
432
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.032
433
P RHN004 Rhinitis 57 0.032
434
THR024 Thrombosis 57 0.032
435
c MST023 Mesothelioma, Malignant 57 0.032
436
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.032
437
TNS005 Tonsillitis 57 0.032
438
ARS001 Aarskog-Scott Syndrome 57 0.032
439
P FTL001 Fetal Alcohol Syndrome 57 0.032
440
P MYS005 Myositis 56 0.032
441
P ADL017 Adult T-Cell Leukemia 56 0.032
442
P PLY011 Polycystic Ovary Syndrome 56 0.032
443
P MLT074 Multiple Endocrine Neoplasia 56 0.032
444
EXF001 Exfoliation Syndrome 56 0.032
445
P MTC069 Mitochondrial Disorders 56 0.032
446
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.032
447
SLC006 Silicosis 56 0.032
448
P PLY019 Polyneuropathy 56 0.032
449
AGN016 Aging 56 0.032
450
P GST044 Gastritis 56 0.032
451
BRN012 Bronchiolitis Obliterans 55 0.032
452
ATR057 Atrioventricular Block 55 0.032
453
DFF005 Diffuse Large B-Cell Lymphoma 55 0.032
454
HRY003 Hairy Cell Leukemia 55 0.032
455
CRT017 Cartilage Disease 54 0.032
456
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.032
457
LYM040 Lymphoblastic Lymphoma 54 0.032
458
CLR030 Clear Cell Renal Cell Carcinoma 53 0.032
459
c CNR007 Cone-Rod Dystrophy 6 53 0.032
460
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.032
461
HYP063 Hypersplenism 53 0.032
462
GSG001 Gas Gangrene 53 0.032
463
PRP080 Peripheral Artery Disease 53 0.032
464
PRP016 Paraplegia 52 0.032
465
c VRL010 Viral Hepatitis 52 0.032
466
NRT004 Neuritis 52 0.032
467
c THY107 Thymoma, Familial 52 0.032
468
P THY032 Thyroiditis 52 0.032
469
PPT001 Peptic Esophagitis 52 0.032
470
c ACT135 Acute Graft Versus Host Disease 52 0.032
472
OCL069 Ocular Motor Apraxia 51 0.032
473
ILS001 Ileus 51 0.032
474
INT079 Intrahepatic Cholangiocarcinoma 51 0.032
475
TRM010 Traumatic Brain Injury 51 0.032
476
c VRL007 Viral Encephalitis 51 0.032
477
END086 End Stage Renal Disease 51 0.032
478
HYP081 Hypolipoproteinemia 51 0.032
479
P MMB011 Membranous Nephropathy 50 0.032
480
c PYR010 Peyronie's Disease 50 0.032
481
ALL009 Allergic Conjunctivitis 50 0.032
482
P ESN008 Eosinophilic Pneumonia 50 0.032
483
c SVR005 Severe Pre-Eclampsia 50 0.032
484
CHL122 Cholesteatoma of Middle Ear 50 0.032
485
CRT013 Carotid Stenosis 50 0.032
486
ALN001 Aland Island Eye Disease 50 0.032
487
P SCK005 Sickle Cell Disease 50 0.032
488
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.032
489
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.032
490
INT078 Intracranial Thrombosis 49 0.032
491
SCT005 Scott Syndrome 49 0.032
492
MTC005 Mitochondrial Metabolism Disease 49 0.032
493
PLM035 Pulmonary Eosinophilia 48 0.032
494
SPL018 Splenomegaly 48 0.032
495
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.032
496
SXL003 Sexual Disorder 47 0.032
497
CRN027 Corneal Neovascularization 47 0.032
498
AST006 Astigmatism 47 0.032
499
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.032
500
RYN005 Raynaud Phenomenon 47 0.032
501
P BLD051 Blood Coagulation Disease 46 0.032
502
ATN005 Autonomic Dysfunction 46 0.032
503
P BNG032 Benign Mesothelioma 46 0.032
504
c CHR421 Charcot-Marie-Tooth Disease, Type 4h 46 0.032
505
CYN002 Cyanosis, Transient Neonatal 45 0.032
506
HMR023 Hemorrhagic Cystitis 45 0.032
508
SPS057 Spasticity 45 0.032
509
FCH001 Fuchs' Endothelial Dystrophy 44 0.032
510
DMP001 Dumping Syndrome 44 0.032
511
P OVR106 Ovarian Clear Cell Carcinoma 44 0.032
512
CVD001 Covid-19 44 0.032
513
SMN007 Seminoma 43 0.032
514
P DMY001 Demyelinating Polyneuropathy 43 0.032
515
MDD018 Middle East Respiratory Syndrome 43 0.032
516
P HYP265 Hypotonia 43 0.032
517
HMP009 Haemophilus Influenzae 43 0.032
518
HYP457 Hypertrophic Scars 42 0.032
519
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.032
520
BCK006 Back Pain 42 0.032
521
ATX019 Ataxia with Vitamin E Deficiency 42 0.032
522
OLV002 Oliver Syndrome 42 0.032
523
RST023 Resting Heart Rate, Variation in 41 0.032
524
DBT002 Diabetic Autonomic Neuropathy 41 0.032
525
DFF003 Diffuse Scleroderma 41 0.032
526
c MYC083 Myoclonic Epilepsy, Familial Infantile 40 0.032
527
PRM024 Primary Angle-Closure Glaucoma 40 0.032
528
ALD013 Aldosterone-Producing Adenoma 39 0.032
529
c ATM075 Autoimmune Encephalitis 38 0.032
530
OVR094 Ovarian Epithelial Cancer 38 0.032
531
CDQ001 Cauda Equina Syndrome 38 0.032
532
GLM044 Glomerular Disease 37 0.032
533
P CRB059 Cerebellar Degeneration 37 0.032
534
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.032
535
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 35 0.032
536
PPL052 Papillomatosis, Confluent and Reticulated 33 0.032
537
c CHR054 Chronic Closed-Angle Glaucoma 32 0.032
538
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.032
539
PST092 Posttransplant Acute Limbic Encephalitis 29 0.032
540
P OVR096 Overlap Myositis 27 0.032
541
MST020 Mast Cell Activation Syndrome 26 0.032
542
PLM189 Pulmonary Arterial Hypertension Associated with Connective Tissue Disease 26 0.032
544
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.022
545
MLR004 Malaria 81 0.022
546
P RTT002 Rett Syndrome 80 0.022
547
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.022
548
c DLT002 Dilated Cardiomyopathy 79 0.022
549
PFF001 Pfeiffer Syndrome 79 0.022
550
GST019 Gastrointestinal Stromal Tumor 78 0.022
551
P PRK057 Parkinson Disease, Late-Onset 78 0.022
552
CRV035 Cervical Cancer 76 0.022
553
PHN003 Phenylketonuria 75 0.022
554
END057 Endometrial Cancer 74 0.022
555
SCK003 Sickle Cell Anemia 74 0.022
556
ANX010 Anxiety 73 0.022
557
MSC157 Muscular Dystrophy, Duchenne Type 72 0.022
558
c HPT073 Hepatitis C Virus 72 0.022
559
FBR012 Fabry Disease 72 0.022
560
AGM019 Agammaglobulinemia, X-Linked 71 0.022
561
P EPL164 Epilepsy 71 0.022
562
P AMY004 Amyloidosis 70 0.022
563
MYL009 Myelodysplastic Syndrome 70 0.022
564
MLT157 Multiple System Atrophy 1 70 0.022
565
DWN001 Down Syndrome 70 0.022
566
c GLY008 Glycogen Storage Disease Ii 70 0.022
567
MYL005 Myelofibrosis 70 0.022
568
LGH007 Leigh Syndrome 70 0.022
569
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.022
570
PTZ001 Peutz-Jeghers Syndrome 70 0.022
571
ADL002 Adult Syndrome 70 0.022
572
CRT072 Creutzfeldt-Jakob Disease 70 0.022
573
P ASP006 Aspergillosis 69 0.022
574
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.022
575
P ART022 Arthritis 69 0.022
576
ACR008 Acrocallosal Syndrome 69 0.022
577
SVR097 Severe Cutaneous Adverse Reaction 69 0.022
578
CRB037 Cerebral Palsy 69 0.022
579
P SLP006 Sleep Apnea 69 0.022
580
P HYP086 Hypothyroidism 69 0.022
581
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.022
582
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.022
583
P ANG001 Angelman Syndrome 69 0.022
584
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.022
585
P MYC084 Mycobacterium Tuberculosis 1 68 0.022
586
CMM004 Common Variable Immunodeficiency 68 0.022
587
OBS002 Obsessive-Compulsive Disorder 68 0.022
588
P MYS003 Myasthenia Gravis 68 0.022
589
P INF038 Influenza 68 0.022
590
RCK004 Rickets 68 0.022
591
P FRN006 Frontotemporal Dementia 68 0.022
592
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.022
593
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.022
594
GST092 Gastroesophageal Reflux 67 0.022
595
P CRD119 Cardiac Arrest 67 0.022
596
P HPT021 Hepatitis 67 0.022
597
P DYS007 Dyskeratosis Congenita 67 0.022
598
c INF071 Inflammatory Bowel Disease 1 67 0.022
599
FCT007 Factor Vii Deficiency 67 0.022
600
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.022
601
PSY004 Psychotic Disorder 67 0.022
602
FLL027 Fallopian Tube Carcinoma 67 0.022
603
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.022
604
MYC006 Mycosis Fungoides 66 0.022
605
P CLC063 Celiac Disease 1 66 0.022
606
P LNG028 Long Qt Syndrome 66 0.022
607
ALC007 Alcohol Dependence 66 0.022
608
GLL008 Gilles De La Tourette Syndrome 66 0.022
609
CHD001 Chediak-Higashi Syndrome 66 0.022
610
P DMN002 Dementia 66 0.022
611
c MCR129 Microvascular Complications of Diabetes 1 66 0.022
612
MYX005 Myxoid Liposarcoma 66 0.022
613
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.022
614
P HYD006 Hydrocephalus 66 0.022
615
P DRM053 Dermatitis, Atopic 66 0.022
616
MYL031 Myeloproliferative Neoplasm 66 0.022
617
KHL003 Kohlschutter-Tonz Syndrome 65 0.022
618
TTN003 Tetanus 65 0.022
619
P AGM001 Agammaglobulinemia 65 0.022
620
ACR006 Aceruloplasminemia 65 0.022
621
SRC014 Sarcoma 65 0.022
622
PPL049 Papillon-Lefevre Syndrome 65 0.022
623
P LPS002 Liposarcoma 65 0.022
624
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.022
625
DRM014 Dermatofibrosarcoma Protuberans 65 0.022
626
MRK001 Merkel Cell Carcinoma 65 0.022
627
c WLM013 Wilms Tumor 1 65 0.022
628
P PRS038 Personality Disorder 65 0.022
629
KWS002 Kawasaki Disease 65 0.022
630
P ADL010 Adult Respiratory Distress Syndrome 65 0.022
631
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.022
632
TBC004 Tobacco Addiction 64 0.022
633
c JVN010 Juvenile Rheumatoid Arthritis 64 0.022
634
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.022
635
ART002 Arts Syndrome 64 0.022
636
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.022
637
PLM031 Poliomyelitis 64 0.022
638
OST017 Osteomyelitis 64 0.022
639
c DPH024 Diaphragmatic Hernia, Congenital 63 0.022
640
P ERL057 Early Infantile Epileptic Encephalopathy 63 0.022
641
P HML002 Hemolytic Anemia 63 0.022
642
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.022
643
c MLG084 Malignant Fibrous Histiocytoma 63 0.022
644
P DST002 Distal Arthrogryposis 63 0.022
645
ACT119 Acute Promyelocytic Leukemia 63 0.022
646
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.022
647
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 0.022
648
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.022
649
c ALP101 Alpha-Thalassemia 62 0.022
650
c FNC043 Fanconi Anemia, Complementation Group E 62 0.022
651
P MCH002 Machado-Joseph Disease 62 0.022
652
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.022
653
BLL006 Bullous Pemphigoid 62 0.022
654
HYD038 Hydrops Fetalis, Nonimmune 62 0.022
655
HSH003 Hashimoto Thyroiditis 62 0.022
656
CTN007 Cutaneous Leishmaniasis 62 0.022
657
P PRM006 Primary Biliary Cirrhosis 62 0.022
658
NTR005 Nutritional Deficiency Disease 62 0.022
659
P INT143 Interstitial Cystitis 61 0.022
660
MCK005 Mckusick-Kaufman Syndrome 61 0.022
661
DRM006 Dermatitis 61 0.022
662
CHR001 Churg-Strauss Syndrome 61 0.022
663
c PNS012 Paine Syndrome 61 0.022
664
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.022
665
WST001 West Syndrome 61 0.022
666
YLL002 Yellow Fever 61 0.022
667
WLD007 Waldenstroem's Macroglobulinemia 61 0.022
668
c WLM018 Wilms Tumor 5 61 0.022
669
P PNC044 Pancreatitis 61 0.022
670
P SJG008 Sjogren Syndrome 61 0.022
671
c ART144 Arthrogryposis, Distal, Type 1a 61 0.022
672
HRP004 Herpes Zoster 60 0.022
673
SZR001 Sezary's Disease 60 0.022
674
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 0.022
675
c LPM012 Lipomatosis, Multiple 60 0.022
676
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.022
677
CRD223 Cardiac Arrhythmia 60 0.022
678
ACQ007 Acquired Immunodeficiency Syndrome 60 0.022
679
DNG002 Dengue Hemorrhagic Fever 60 0.022
680
RHM001 Rheumatic Fever 60 0.022
681
P SNS001 Sensorineural Hearing Loss 60 0.022
682
CHC001 Chickenpox 60 0.022
683
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.022
684
P GLY013 Glycogen Storage Disease 60 0.022
685
P CHR285 Chronic Myelomonocytic Leukemia 60 0.022
686
DYS164 Dyskeratosis Congenita, X-Linked 60 0.022
687
c HRD002 Hereditary Angioedema 60 0.022
688
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.022
689
P MCR010 Microcephaly 59 0.022
690
P BND020 Bone Disease 59 0.022
691
IDP011 Idiopathic Interstitial Pneumonia 59 0.022
692
P BRN022 Bronchiectasis 59 0.022
693
MTC097 Mitochondrial Complex Iv Deficiency 59 0.022
694
c DNG003 Dengue Disease 59 0.022
695
P LYM033 Lymphoproliferative Syndrome 59 0.022
696
VSL002 Visual Epilepsy 59 0.022
697
DCT002 Ductal Carcinoma in Situ 59 0.022
698
AVN001 Avian Influenza 59 0.022
699
ADN018 Adenoma 59 0.022
700
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.022
701
c ACT073 Acute Leukemia 58 0.022
702
P SYP003 Syphilis 58 0.022
703
P ANP001 Anaplastic Large Cell Lymphoma 58 0.022
704
CRY005 Cryptococcosis 58 0.022
705
PST028 Post-Traumatic Stress Disorder 58 0.022
706
P INT070 Intestinal Obstruction 58 0.022
707
RBS001 Rabies 58 0.022
708
ERY029 Erythermalgia, Primary 58 0.022
709
FBR047 Fibromyalgia 58 0.022
710
CMP010 Complex Regional Pain Syndrome 58 0.022
711
c CHL140 Chilblain Lupus 1 58 0.022
712
CRD132 Cardiac Conduction Defect 58 0.022
713
SPT004 Septic Arthritis 58 0.022
714
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.022
715
ERY003 Erythema Multiforme 58 0.022
716
P URT039 Urticaria 58 0.022
717
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.022
718
NWB001 Newborn Respiratory Distress Syndrome 58 0.022
719
DSS008 Disease of Mental Health 58 0.022
720
CRV038 Cervical Squamous Cell Carcinoma 58 0.022
721
CNS004 Constipation 58 0.022
722
LNG108 Langerhans Cell Histiocytosis 58 0.022
723
P ESP035 Esophagitis, Eosinophilic, 1 57 0.022
724
P GLM007 Glomerulonephritis 57 0.022
725
P OPT009 Optic Neuritis 57 0.022
726
P PLV020 Pelvic Organ Prolapse 57 0.022
727
P PLY041 Polymyositis 57 0.022
728
P EXN002 Exanthem 57 0.022
729
CHK001 Chikungunya 57 0.022
730
P HDC001 Headache 57 0.022
731
PRL032 Perlman Syndrome 57 0.022
732
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.022
733
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.022
734
c ACT075 Acute Myocardial Infarction 57 0.022
735
P END033 Endocarditis 57 0.022
736
P PRV006 Pervasive Developmental Disorder 57 0.022
737
c ANG068 Angioedema, Hereditary, Type I 57 0.022
738
BLR008 Bilirubin Metabolic Disorder 57 0.022
739
c LKM070 Leukemia, Acute Monocytic 57 0.022
740
HMR039 Hemorrhage, Intracerebral 57 0.022
741
CYT008 Cytomegalovirus Infection 57 0.022
742
JPN002 Japanese Encephalitis 57 0.022
743
SCH014 Schistosomiasis 57 0.022
744
CRT033 Corticobasal Degeneration 57 0.022
745
PHR003 Pharyngitis 57 0.022
746
P ANG015 Angioedema 57 0.022
747
P BPL003 Bipolar Disorder 56 0.022
748
CMR002 Coumarin Resistance 56 0.022
749
TCK001 Tick-Borne Encephalitis 56 0.022
750
TRN018 Transitional Cell Carcinoma 56 0.022
751
PLS011 Plasmacytoma 56 0.022
752
LMY014 Leiomyoma, Uterine 56 0.022
753
ADN027 Adenomyosis 56 0.022
754
c ESS001 Essential Tremor 56 0.022
755
SPN041 Spinal Cord Disease 56 0.022
756
P SZR006 Seizure Disorder 56 0.022
757
SFT003 Soft Tissue Sarcoma 56 0.022
758
SCH003 Schizophreniform Disorder 56 0.022
759
HMG005 Hemoglobinopathy 56 0.022
760
EMB004 Embryonal Carcinoma 56 0.022
761
GST050 Gastrointestinal System Disease 56 0.022
762
P SCK004 Seckel Syndrome 56 0.022
763
SML019 Smallpox 56 0.022
764
INT030 Intracranial Aneurysm 56 0.022
765
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.022
766
HYP005 Hypokalemia 55 0.022
767
VGT001 Vogt-Koyanagi-Harada Disease 55 0.022
768
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.022
769
FDB001 Foodborne Botulism 55 0.022
770
c BCT007 Bacterial Meningitis 55 0.022
771
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.022
772
P DYS193 Dystonia 11, Myoclonic 55 0.022
773
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.022
774
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.022
775
CHR100 Chronic Ulcer of Skin 55 0.022
776
P HYP076 Hyperthyroidism 55 0.022
777
HNC001 Henoch-Schoenlein Purpura 55 0.022
778
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.022
779
SYN007 Synovitis 54 0.022
780
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.022
781
RFL001 Reflex Sympathetic Dystrophy 54 0.022
782
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.022
783
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.022
784
GST037 Gastroparesis 54 0.022
785
CRY003 Cryptosporidiosis 54 0.022
786
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.022
787
PRC013 Pericarditis 54 0.022
788
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.022
789
WST005 West Nile Virus 54 0.022
790
PNC001 Pancytopenia 54 0.022
791
P TCD001 Tic Disorder 53 0.022
792
CRY001 Cryptogenic Organizing Pneumonia 53 0.022
793
RHM028 Rheumatic Heart Disease 53 0.022
794
P INS002 in Situ Carcinoma 53 0.022
795
HRT012 Heart Valve Disease 53 0.022
796
KRT006 Keratoconjunctivitis 53 0.022
797
P BND018 Band Heterotopia 53 0.022
798
PRP036 Peripheral T-Cell Lymphoma 53 0.022
799
CRH005 Crohn's Colitis 53 0.022
800
BRN038 Bronchial Disease 53 0.022
801
c PRD040 Periodontitis, Chronic 53 0.022
802
P SHR001 Short Bowel Syndrome 53 0.022
803
P HMR003 Hemorrhagic Disease 53 0.022
804
FNG017 Fungal Infectious Disease 53 0.022
805
P CTN003 Cutaneous Lupus Erythematosus 53 0.022
806
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.022
807
INT075 Intracranial Hypertension 53 0.022
808
SPN035 Spindle Cell Sarcoma 53 0.022
809
IRD001 Iridocyclitis 53 0.022
810
GST023 Gastric Ulcer 53 0.022
811
P PNC025 Panic Disorder 53 0.022
812
PRN011 Pernicious Anemia 53 0.022
813
P RTN022 Retinal Vein Occlusion 53 0.022
814
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 53 0.022
815
CHR073 Choreatic Disease 52 0.022
816
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.022
817
ESP023 Esophageal Disease 52 0.022
818
ACR041 Acromelic Frontonasal Dysostosis 52 0.022
819
P CRN276 Corneal Endothelial Dystrophy 52 0.022
820
PRS030 Persistent Fetal Circulation Syndrome 52 0.022
821
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.022
822
P HYP730 Hypogonadotropic Hypogonadism 52 0.022
823
P DDN001 Duodenal Ulcer 52 0.022
824
MRG003 Marginal Zone B-Cell Lymphoma 52 0.022
825
P RCT021 Rectum Cancer 52 0.022
826
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.022
827
END020 Endocardial Fibroelastosis 52 0.022
828
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.022
829
P MGR003 Migraine with Aura 52 0.022
830
c SPN393 Spinal Muscular Atrophy, Type I 52 0.022
831
NTR018 Neutrophilia, Hereditary 52 0.022
832
c VRL005 Viral Pneumonia 52 0.022
833
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.022
834
LMY002 Leiomyoma 52 0.022
835
SPS003 Spastic Diplegia 51 0.022
836
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.022
837
MCR088 Microscopic Polyangiitis 51 0.022
838
UNV001 Unverricht-Lundborg Syndrome 51 0.022
839
RYS001 Reye Syndrome 51 0.022
840
MYL001 Myelitis 51 0.022
841
ALK024 Alkuraya-Kucinskas Syndrome 51 0.022
842
LMB050 Limbal Stem Cell Deficiency 51 0.022
843
MGL001 Megaloblastic Anemia 51 0.022
844
THR016 Thrombophlebitis 51 0.022
845
P LSS002 Lissencephaly 51 0.022
846
SPL004 Splenic Marginal Zone Lymphoma 51 0.022
847
TNG007 Tongue Carcinoma 51 0.022
848
ASP003 Aseptic Meningitis 51 0.022
849
P CHL066 Cholangitis 51 0.022
850
CHR005 Chorioamnionitis 51 0.022
851
c ALM001 Al Amyloidosis 50 0.022
852
SCH012 Schizoaffective Disorder 50 0.022
853
LNT004 Lentigines 50 0.022
854
P FNC004 Fanconi Syndrome 50 0.022
855
P MYS079 Miyoshi Muscular Dystrophy 50 0.022
856
FSC004 Fasciitis 50 0.022
857
c INF145 Infantile Liver Failure Syndrome 1 50 0.022
858
CYT005 Cytomegalovirus Retinitis 50 0.022
859
P TMP001 Temporal Lobe Epilepsy 50 0.022
860
P OBS001 Obstructive Jaundice 50 0.022
861
BLR001 Biliary Atresia 50 0.022
862
c LRG001 Large Cell Carcinoma 50 0.022
863
HMG002 Hemoglobinuria 50 0.022
864
SCR037 Sucrase-Isomaltase Deficiency, Congenital 50 0.022
865
c INF023 Inflammatory Breast Carcinoma 50 0.022
866
TBL009 Tibial Muscular Dystrophy 50 0.022
867
DBT004 Diabetic Polyneuropathy 49 0.022
868
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.022
869
ATY042 Atypical Chronic Myeloid Leukemia 49 0.022
870
c CHR418 Chronic Leukemia 49 0.022
871
ENT004 Enthesopathy 49 0.022
872
KRT001 Keratoconjunctivitis Sicca 49 0.022
873
BRJ001 Borjeson-Forssman-Lehmann Syndrome 49 0.022
874
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.022
875
PLY024 Polymicrogyria 49 0.022
876
CMB003 Combined T Cell and B Cell Immunodeficiency 49 0.022
877
47X002 47,xyy 49 0.022
878
SPT005 Spotted Fever 49 0.022
879
MCR004 Macroglobulinemia 49 0.022
880
c FLL041 Follicular Lymphoma 1 49 0.022
881
BKR002 Baker-Gordon Syndrome 49 0.022
882
CNG069 Congenital Cytomegalovirus 49 0.022
883
MNN009 Meningoencephalitis 49 0.022
884
IMP004 Impetigo 49 0.022
885
P MGR001 Migraine Without Aura 49 0.022
886
ACT029 Acute Interstitial Pneumonia 49 0.022
887
P CTN015 Cutaneous T Cell Lymphoma 49 0.022
888
c INV001 Invasive Aspergillosis 49 0.022
889
EBL001 Ebola Hemorrhagic Fever 49 0.022
890
HST010 Histiocytosis 48 0.022
891
RYN001 Raynaud Disease 48 0.022
892
c BCT013 Bacterial Pneumonia 48 0.022
893
AMY086 Amyotrophy, Hereditary Neuralgic 48 0.022
894
NCR007 Necrotizing Fasciitis 48 0.022
895
ASP007 Aspiration Pneumonia 48 0.022
896
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.022
897
CHR563 Chronic Eosinophilic Leukemia 48 0.022
898
RFR010 Refractory Anemia 48 0.022
899
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.022
900
P RNV001 Renovascular Hypertension 48 0.022
901
P ASP001 Asperger Syndrome 48 0.022
902
DGN001 Degenerative Disc Disease 48 0.022
903
P PLY020 Polyradiculoneuropathy 48 0.022
904
PLC007 Placental Abruption 48 0.022
905
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.022
906
c PRM031 Primary Autosomal Recessive Microcephaly 47 0.022
907
PRP007 Priapism 47 0.022
908
GRM005 Germ Cell Cancer 47 0.022
909
PRL017 Prolymphocytic Leukemia 47 0.022
910
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.022
911
DRG003 Drug Dependence 47 0.022
912
DRY001 Dry Eye Syndrome 47 0.022
913
PPL002 Papillary Carcinoma 47 0.022
914
P CRN028 Corneal Ulcer 47 0.022
915
P RNL015 Renal Hypertension 47 0.022
916
P HMN032 Human Herpesvirus 8 47 0.022
917
ACT084 Acute Stress Disorder 47 0.022
918
c SPN105 Spinocerebellar Ataxia 4 47 0.022
919
RTC005 Reticulosarcoma 47 0.022
920
LYM012 Lymphoplasmacytic Lymphoma 47 0.022
921
TTR011 Tetraploidy 47 0.022
922
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.022
923
ZKF001 Zika Fever 47 0.022
924
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.022
925
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.022
926
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.022
927
P KRN004 Kernicterus 47 0.022
928
P THP004 Thiopurines, Poor Metabolism of, 1 47 0.022
929
PLS025 Plasmablastic Lymphoma 47 0.022
930
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.022
931
TST044 Testicular Torsion 47 0.022
932
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.022
933
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.022
934
AML029 Ameloblastoma 46 0.022
935
LYM019 Lymphosarcoma 46 0.022
936
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.022
937
ANT039 Antisynthetase Syndrome 46 0.022
938
CD4003 Cd40 Ligand Deficiency 46 0.022
939
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.022
940
TTH006 Tooth Disease 46 0.022
941
SMT001 Somatization Disorder 46 0.022
942
MLT075 Multifocal Motor Neuropathy 46 0.022
943
SPN020 Spondylosis 46 0.022
944
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.022
945
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.022
946
P HRT035 Heart Block, Congenital 46 0.022
947
KRT013 Keratolytic Winter Erythema 46 0.022
948
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.022
949
P LPC002 Lip Cancer 46 0.022
950
OBS003 Obsessive-Compulsive Personality Disorder 46 0.022
951
NNK001 Nonaka Myopathy 46 0.022
952
P MYC033 Myoclonus 46 0.022
953
CWP001 Cowpox 46 0.022
954
c DRR009 Diarrhea 6 46 0.022
955
ANR004 Anuria 46 0.022
956
EPD015 Epidemic Typhus 45 0.022
957
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.022
958
P TRN034 Transverse Myelitis 45 0.022
959
STP004 Staphylococcal Toxic Shock Syndrome 45 0.022
960
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.022
961
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.022
962
TRT001 Teratocarcinoma 45 0.022
963
c RTN150 Retinitis Pigmentosa 10 45 0.022
964
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.022
965
IMM003 Immunoglobulin Alpha Deficiency 45 0.022
966
DST006 Diastolic Heart Failure 45 0.022
967
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.022
968
IMM136 Immune System Disease 45 0.022
969
URL001 Urolithiasis 45 0.022
970
ACT003 Acute Kidney Tubular Necrosis 45 0.022
971
LYM051 Lymphomatoid Granulomatosis 45 0.022
972
c HMG003 Hemoglobin E Disease 45 0.022
973
ATN004 Autonomic Neuropathy 45 0.022
974
PNC085 Penicillin Allergy 45 0.022
975
INF006 Infant Botulism 45 0.022
976
ASP008 Aspiration Pneumonitis 45 0.022
977
P DFF019 Diffuse Gastric Cancer 45 0.022
978
MNT229 Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance 45 0.022
979
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.022
980
CHL149 Childhood Acute Myeloid Leukemia 44 0.022
981
PTT037 Pituitary Tumors 44 0.022
982
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.022
983
DWR001 Dwarfism 44 0.022
984
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.022
985
TNG009 Tongue Squamous Cell Carcinoma 44 0.022
986
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 44 0.022
987
OVR063 Overnutrition 44 0.022
988
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 44 0.022
989
EGG001 Egg Allergy 44 0.022
990
SYD002 Sydenham Chorea 44 0.022
991
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.022
992
P FRN036 Frontonasal Dysplasia 1 44 0.022
993
P BCT020 Bacteremia 2 44 0.022
994
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.022
995
c HRD173 Hereditary Late-Onset Parkinson Disease 44 0.022
996
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.022
997
HSD004 Hsd10 Mitochondrial Disease 44 0.022
998
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.022
999
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.022
1000
P TST026 Testicular Germ Cell Cancer 43 0.022
1001
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.022
1002
RFR003 Refractive Error 43 0.022
1003
MRG013 Mirage Syndrome 43 0.022
1004
BNM001 Bone Marrow Cancer 43 0.022
1005
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.022
1006
NNS032 Non-Syndromic X-Linked Intellectual Disability 43 0.022
1007
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.022
1008
PST020 Postpoliomyelitis Syndrome 43 0.022
1009
c SRC023 Sarcoidosis 2 43 0.022
1010
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.022
1011
P PLN008 Peeling Skin Syndrome 43 0.022
1012
c CHR056 Chronic Tic Disorder 43 0.022
1013
PMP004 Pemphigus Foliaceus 43 0.022
1014
VRL003 Variola Major 42 0.022
1015
RTN187 Retinitis Pigmentosa-Deafness Syndrome 42 0.022
1016
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.022
1017
P WST004 West Nile Encephalitis 42 0.022
1018
RTN072 Retinohepatoendocrinologic Syndrome 42 0.022
1019
CHR286 Chronic Neutrophilic Leukemia 42 0.022
1020
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.022
1021
P ATS366 Autism X-Linked 2 42 0.022
1022
MNN017 Mononeuropathy 42 0.022
1023
IDP091 Idiopathic Nephrotic Syndrome 42 0.022
1024
c PRG011 Progressive Myoclonus Epilepsy 42 0.022
1025
c PRM212 Primary Microcephaly 42 0.022
1026
MYF002 Myofascial Pain Syndrome 42 0.022
1027
SPN050 Spinocerebellar Degeneration 42 0.022
1028
FTL021 Fetal Macrosomia 42 0.022
1029
OCL052 Ocular Dominance 42 0.022
1030
ANC002 Anca-Associated Vasculitis 41 0.022
1031
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.022
1032
MSN004 Mesenchymal Cell Neoplasm 41 0.022
1033
c MCR320 Microcephaly 17, Primary, Autosomal Recessive 41 0.022
1034
CHR667 Chromosome 3pter-P25 Deletion Syndrome 41 0.022
1035
49X006 49, Xxxxy Syndrome 41 0.022
1036
INH001 Inhalation Anthrax 41 0.022
1037
c MJR024 Major Affective Disorder 9 41 0.022
1038
PLY021 Polyradiculopathy 41 0.022
1039
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.022
1040
P CRB045 Cerebellar Hypoplasia 41 0.022
1041
LRG008 Large Granular Lymphocyte Leukemia 41 0.022
1042
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 41 0.022
1043
RDN001 Reading Disorder 40 0.022
1044
IDP064 Idiopathic Neutropenia 40 0.022
1045
PLM005 Pleomorphic Lipoma 40 0.022
1046
SPR126 Superior Semicircular Canal Dehiscence 40 0.022
1047
ANG049 Angioedema Induced by Ace Inhibitors 40 0.022
1048
P PRG092 Pregnancy Loss, Recurrent 1 40 0.022
1049
NRN016 Neuronal Migration Disorders 40 0.022
1050
ACT011 Acute Contagious Conjunctivitis 40 0.022
1051
KLD004 Keloid Disorder 40 0.022
1052
PLY100 Polyploidy 40 0.022
1053
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.022
1054
SLC004 Selective Igg Deficiency Disease 40 0.022
1055
CRB086 Cerebral Aneurysms 40 0.022
1056
OCL010 Ocular Hypotension 39 0.022
1057
C1N001 C1 Inhibitor Deficiency 39 0.022
1058
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.022
1059
c GLL037 Guillain-Barre Syndrome, Familial 39 0.022
1060
SCR015 Scarlet Fever 39 0.022
1061
CRN020 Coronary Restenosis 39 0.022
1062
ALG001 Algoneurodystrophy 39 0.022
1063
P DYS021 Dysautonomia 39 0.022
1064
CRN006 Coronary Aneurysm 39 0.022
1065
CRV045 Cervical Intraepithelial Neoplasia 39 0.022
1066
c HMG029 Hemoglobin Se Disease 39 0.022
1067
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.022
1069
c SPN103 Spinocerebellar Ataxia 31 39 0.022
1070
c CHR682 Chronic Bilirubin Encephalopathy 39 0.022
1071
DBT007 Diabetic Cataract 38 0.022
1072
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.022
1073
NDL024 Nodal Marginal Zone Lymphoma 38 0.022
1074
CVT001 Cavitary Optic Disc Anomalies 38 0.022
1075
c OVR114 Ovarian Cancer 1 38 0.022
1076
PLY010 Polyclonal Hypergammaglobulinemia 38 0.022
1077
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.022
1078
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.022
1079
c MJR022 Major Affective Disorder 8 38 0.022
1080
KLD003 Keloid Formation 38 0.022
1081
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.022