Search results for deoxyguanosine

917 hits were found for deoxyguanosine

# Family MCID Name MIFTS Score
1
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 32.085
2
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 3.520
3
HLX001 Helix Syndrome 47 2.958
4
P LVR013 Liver Disease 68 2.596
5
P PRD008 Periodontitis 64 2.528
6
P MTC010 Mitochondrial Dna Depletion Syndrome 46 2.370
7
XRD010 Xeroderma Pigmentosum, Variant Type 72 2.331
8
c MCR133 Microvascular Complications of Diabetes 4 41 2.080
9
c MCR113 Microvascular Complications of Diabetes 3 52 2.080
10
c MCR130 Microvascular Complications of Diabetes 6 41 2.080
11
c MCR120 Microvascular Complications of Diabetes 7 47 2.080
12
P DBT009 Diabetes Mellitus 67 1.953
13
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.945
14
HMS001 Hemosiderosis 48 1.877
15
P RRH023 Rare Hereditary Hemochromatosis 53 1.870
16
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.788
17
P HRP006 Herpes Simplex 65 1.770
18
P HYP265 Hypotonia 42 1.723
19
PTH003 Pathologic Nystagmus 52 1.723
20
P SKN015 Skin Carcinoma 71 1.720
21
MDD018 Middle East Respiratory Syndrome 44 1.648
22
c TYP009 Type 2 Diabetes Mellitus 92 1.644
23
P CCK001 Cockayne Syndrome 68 1.635
24
c PRD040 Periodontitis, Chronic 52 1.622
25
P INF032 Infertility 60 1.602
26
FTT001 Fatty Liver Disease 61 1.537
27
ISC004 Ischemia 61 1.537
28
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.530
29
c HPT016 Hepatitis B 62 1.528
30
HYP056 Hypoglycemia 65 1.526
31
P MYP004 Myopathy 67 1.518
32
c HMC039 Hemochromatosis, Type 1 73 1.487
33
P HPT021 Hepatitis 68 1.483
34
ALL029 Allergic Disease 61 1.468
35
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.465
36
P BLD134 Bladder Cancer 79 1.447
37
P BNG032 Benign Mesothelioma 53 1.441
38
P END044 Endometriosis 62 1.429
39
HYP066 Hyperglycemia 60 1.425
40
P LKM062 Leukemia, Acute Lymphoblastic 69 1.410
41
CHL068 Cholestasis 61 1.376
42
AGN016 Aging 54 1.374
43
P CLR023 Colorectal Cancer 100 1.361
44
LVR012 Liver Cirrhosis 62 1.330
45
P LNG064 Lung Cancer Susceptibility 3 70 1.294
46
P HPT023 Hepatocellular Carcinoma 95 1.291
47
VRC001 Varicocele 48 1.291
48
URT049 Urate Oxidase, Pseudogene 24 1.254
49
P PLM036 Pulmonary Fibrosis 65 1.252
50
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.252
51
48X005 48,xyyy 39 1.236
52
P ATR011 Atrial Fibrillation 66 1.230
53
ORL011 Oral Cancer 60 1.216
54
P MTC133 Mitochondrial Myopathy 51 1.208
55
STM007 Stomatitis 52 1.208
56
c ACT073 Acute Leukemia 59 1.191
57
P MTC069 Mitochondrial Disorders 57 1.191
58
URM002 Uremia 47 1.174
59
c DLT002 Dilated Cardiomyopathy 79 1.156
60
TRN018 Transitional Cell Carcinoma 56 1.137
61
P THY032 Thyroiditis 56 1.137
62
HLC007 Helicobacter Pylori Infection 67 1.127
63
P KDN018 Kidney Disease 72 1.127
64
c MCR115 Microvascular Complications of Diabetes 5 65 1.114
65
P OPN001 Open-Angle Glaucoma 55 1.101
66
P ADN016 Adenocarcinoma 63 1.101
67
MYM001 Myoma 54 1.092
68
ART140 Arteries, Anomalies of 52 1.088
70
c GLC092 Glaucoma, Primary Open Angle 61 1.088
71
LPP008 Lipoprotein Quantitative Trait Locus 65 1.074
72
P SRC025 Sarcoidosis 1 70 1.065
73
CRD003 Cardiac Sarcoidosis 44 1.065
74
c CHR684 Chronic Kidney Disease 74 1.060
75
P HYP086 Hypothyroidism 69 1.059
76
SKN016 Skin Disease 62 1.059
77
NNL006 Non-Alcoholic Steatohepatitis 54 1.051
78
c HYP836 Hypercholesterolemia, Familial, 1 73 1.032
79
ESP021 Esophageal Cancer 84 1.028
80
c LKM061 Leukemia, Acute Myeloid 83 1.028
81
P LKM071 Leukemia, Chronic Lymphocytic 74 1.013
82
c SYS001 Systemic Lupus Erythematosus 86 1.011
83
HRW001 Hair Whorl 35 1.011
84
P MLN008 Melanoma 75 1.011
85
P LCT001 Lactic Acidosis 50 1.011
86
CHC001 Chickenpox 56 1.011
87
THY029 Thyroid Carcinoma 54 1.011
88
P MLN007 Male Infertility 56 1.003
89
P MDL005 Medulloblastoma 75 0.992
90
P HYP076 Hyperthyroidism 53 0.992
91
END057 Endometrial Cancer 71 0.982
92
P BRS047 Breast Cancer 97 0.973
93
PRT112 Portal Hypertension, Noncirrhotic 29 0.973
94
c PRG128 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 4 28 0.973
95
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.973
96
GST033 Gestational Diabetes 61 0.973
97
HPT022 Hepatoblastoma 54 0.973
98
PRS129 Prostatic Hyperplasia, Benign 48 0.960
99
PRS021 Prostatic Adenoma 43 0.960
100
PRS045 Prostatic Hypertrophy 52 0.960
101
CRV035 Cervical Cancer 72 0.952
102
CLN015 Colon Adenocarcinoma 64 0.952
103
CHL065 Cholangiocarcinoma 58 0.949
104
INT079 Intrahepatic Cholangiocarcinoma 51 0.949
105
P GST044 Gastritis 55 0.949
106
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.937
107
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.933
108
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.933
109
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.933
110
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.933
111
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.933
112
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.933
113
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.933
114
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.933
115
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.933
116
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.933
117
c VRL010 Viral Hepatitis 52 0.928
118
LMY002 Leiomyoma 51 0.928
119
THY030 Thyroid Gland Disease 50 0.928
120
P GRV001 Graves' Disease 54 0.928
121
P PLY011 Polycystic Ovary Syndrome 57 0.928
122
PRP083 Porphyria, Acute Intermittent 64 0.926
123
P PRP029 Porphyria 60 0.926
124
P ALZ034 Alzheimer Disease 87 0.913
125
GLL048 Glial Tumor 52 0.913
126
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.913
127
c LKM005 Leukemia, T-Cell, Chronic 33 0.913
128
HMC038 Hemochromatosis, Neonatal 33 0.902
129
CRN030 Coronary Stenosis 50 0.902
130
c ACT134 Acute Liver Failure 57 0.902
131
c PRC016 Pre-Eclampsia 64 0.901
132
LPD008 Lipid Metabolism Disorder 61 0.901
133
GLM045 Glioma 62 0.901
134
END086 End Stage Renal Disease 54 0.888
135
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.888
136
c MJR024 Major Affective Disorder 9 40 0.874
137
c MJR022 Major Affective Disorder 8 37 0.874
138
P BPL003 Bipolar Disorder 56 0.874
139
KRN002 Kearns-Sayre Syndrome 63 0.874
141
c HPT001 Hepatitis C 61 0.860
142
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.860
143
ORL015 Oral Squamous Cell Carcinoma 43 0.845
144
c HPT073 Hepatitis C Virus 71 0.845
145
PPL022 Papilloma 53 0.845
146
SQM002 Squamous Cell Papilloma 45 0.845
147
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.845
148
P NRP001 Neuropathy 59 0.845
149
P CRD119 Cardiac Arrest 68 0.830
150
P HNT016 Huntington Disease 73 0.830
151
HRY003 Hairy Cell Leukemia 61 0.830
152
DPR016 Depression 65 0.830
153
VCC001 Vaccinia 49 0.814
154
P SZR006 Seizure Disorder 69 0.814
155
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.797
156
P CTN015 Cutaneous T Cell Lymphoma 48 0.797
157
P ANP001 Anaplastic Large Cell Lymphoma 61 0.797
158
P DRM053 Dermatitis, Atopic 65 0.797
159
c OST125 Osteopetrosis, Autosomal Dominant 1 34 0.797
160
HYP060 Hyperinsulinism 53 0.797
161
P VSC007 Vascular Disease 62 0.797
162
SQM006 Squamous Cell Carcinoma 59 0.797
163
P CRN300 Coronary Heart Disease 1 73 0.797
164
STR067 Stroke, Ischemic 79 0.797
165
CYT002 Cytokine Deficiency 43 0.797
166
LKP003 Leukoplakia 39 0.797
167
P CTR002 Cataract 59 0.797
168
MYL009 Myelodysplastic Syndrome 67 0.779
169
P PRK039 Parkinsonism 55 0.779
170
CLR109 Colorectal Adenocarcinoma 50 0.779
171
c SML038 Small Cell Cancer of the Lung 69 0.779
172
P LRY044 Larynx Cancer 53 0.779
173
P ECL001 Eclampsia 52 0.779
174
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.779
175
DRM006 Dermatitis 62 0.779
176
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 53 0.759
177
c ATR087 Atrial Standstill 1 74 0.759
178
CNG034 Congestive Heart Failure 69 0.759
179
ACQ007 Acquired Immunodeficiency Syndrome 58 0.759
180
P KDN017 Kidney Cancer 60 0.759
181
BRS051 Breast Disease 58 0.759
182
P LPS004 Lupus Erythematosus 61 0.759
183
MYC006 Mycosis Fungoides 65 0.738
184
c MTC062 Mitochondrial Dna Depletion Syndrome 2 43 0.738
185
PRT013 Portal Hypertension 59 0.738
186
P MLT020 Multiple Sclerosis 79 0.738
187
P LYM118 Lymphoma 69 0.738
188
BLM001 Bloom Syndrome 65 0.738
189
KRT009 Keratosis 52 0.738
190
IRN002 Iron Metabolism Disease 56 0.738
191
P GLM007 Glomerulonephritis 59 0.738
192
PST011 Pustulosis of Palm and Sole 52 0.738
193
P LCH002 Lichen Planus 55 0.738
194
LNG099 Lung Disease 62 0.738
195
BWN006 Bowen's Disease 32 0.738
196
P PSR002 Psoriasis 63 0.738
197
ALL006 Allergic Asthma 56 0.738
198
ORL012 Oral Leukoplakia 35 0.738
199
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.715
200
RCK004 Rickets 65 0.715
201
P OST002 Osteoporosis 77 0.715
202
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.715
203
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.715
204
LWC001 Low Compliance Bladder 44 0.715
205
CHL014 Cholera 62 0.715
206
IGG001 Iga Glomerulonephritis 50 0.715
207
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.715
208
P NPH012 Nephrotic Syndrome 62 0.715
209
DPH001 Diphtheria 59 0.715
210
P RHB003 Rhabdomyosarcoma 66 0.715
211
P GLL018 Gallbladder Cancer 53 0.715
212
OST159 Osteogenic Sarcoma 66 0.715
214
SKN019 Skin Melanoma 70 0.715
215
HVY002 Heavy Metal Poisoning 22 0.715
216
ORL013 Oral Lichen Planus 45 0.715
217
P TYR004 Tyrosinemia 49 0.715
218
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 0.715
219
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.711
220
P ADL017 Adult T-Cell Leukemia 54 0.688
221
TNS005 Tonsillitis 57 0.688
222
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.688
223
HYP114 Hypertensive Nephropathy 35 0.688
224
HSH003 Hashimoto Thyroiditis 60 0.688
225
P PTS002 Ptosis 52 0.688
226
ACT098 Acute Erythroid Leukemia 55 0.688
227
P MCR010 Microcephaly 59 0.688
228
c BSL007 Basal Cell Carcinoma 68 0.688
229
P AGG001 Aggressive Periodontitis 55 0.688
230
TXC005 Toxic Shock Syndrome 62 0.688
231
GNG013 Gingivitis 59 0.688
232
MDD011 Mood Disorder 62 0.688
233
LNG030 Lung Adenoma 37 0.688
234
SPL018 Splenomegaly 47 0.688
235
BRN056 Bronchopulmonary Dysplasia 57 0.688
236
P MNN013 Meningitis 65 0.688
237
CRB004 Cerebral Artery Occlusion 46 0.659
238
P RTN024 Retinoblastoma 72 0.656
239
BTT016 Batten-Turner Congenital Myopathy 53 0.656
240
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.656
241
DSS032 Disease by Infectious Agent 55 0.656
242
c INF194 Infantile Liver Failure Syndrome 30 0.656
243
DRM046 Dermal Ridges-off-the-End 20 0.656
244
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.656
245
MTG002 Mutagen Sensitivity 35 0.656
246
KRT019 Keratitis, Hereditary 66 0.656
247
P OPT006 Optic Nerve Disease 57 0.656
248
BRN002 Bronchiolitis 57 0.656
249
BRN024 Bronchitis 67 0.656
250
c ATM011 Autoimmune Hepatitis 62 0.656
251
BRN028 Brain Cancer 73 0.656
252
PTT037 Pituitary Tumors 44 0.656
253
CLF001 Cleft Lip 54 0.656
254
ORL004 Oral Submucous Fibrosis 56 0.656
255
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.656
256
c ACT075 Acute Myocardial Infarction 55 0.656
257
c BCT007 Bacterial Meningitis 55 0.656
258
P HRD217 Hereditary Optic Neuropathy 36 0.656
259
c GLY004 Glycogen Storage Disease V 62 0.615
260
ADN027 Adenomyosis 59 0.615
261
P GRF003 Graft-Versus-Host Disease 71 0.615
262
P SML001 Small Cell Carcinoma 52 0.615
263
TNG007 Tongue Carcinoma 55 0.615
264
PRM013 Premature Menopause 57 0.615
265
HPT067 Hepatocellular Adenoma 42 0.615
266
FML037 Female Breast Cancer 51 0.615
267
MTB004 Metabolic Acidosis 48 0.615
268
LNT004 Lentigines 45 0.615
269
EXF001 Exfoliation Syndrome 56 0.615
270
BLR028 Biliary Atresia, Extrahepatic 36 0.615
271
P URN019 Urinary Tract Infection 49 0.615
272
BRN012 Bronchiolitis Obliterans 56 0.615
273
FBR047 Fibromyalgia 58 0.615
274
END040 Endogenous Depression 54 0.615
275
PYR004 Pyuria 36 0.615
276
ASP003 Aseptic Meningitis 51 0.615
277
P SDR002 Siderosis 42 0.615
278
GNG003 Gingival Recession 50 0.615
279
PRT018 Portal Vein Thrombosis 50 0.615
280
BLD131 Bladder Urothelial Carcinoma 59 0.615
281
FDL002 Food Allergy 47 0.615
282
P GLY013 Glycogen Storage Disease 59 0.615
283
HMT002 Hematologic Cancer 61 0.615
284
NRL005 Neurilemmoma 60 0.615
285
PHN003 Phenylketonuria 76 0.615
286
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.615
287
CHL045 Choline Deficiency Disease 39 0.615
288
PPL014 Papillary Transitional Carcinoma 25 0.615
289
SYS003 Systolic Heart Failure 49 0.615
290
ORL006 Oral Mucosa Leukoplakia 22 0.615
291
AMN006 Aminoaciduria 37 0.615
292
CHR066 Chronic Fatigue Syndrome 60 0.615
293
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 32 0.615
294
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.615
295
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 0.615
296
XRD026 Xeroderma Pigmentosum-Cockayne Syndrome Complex 34 0.615
297
RFR010 Refractory Anemia 49 0.615
298
PRT251 Proteinuria, Chronic Benign 58 0.517
299
c RNG022 Ring Chromosome 6 28 0.516
300
c RNG023 Ring Chromosome 7 43 0.516
301
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.507
302
P NRB001 Neuroblastoma 66 0.507
303
HYP266 Hypoxia 56 0.507
304
BRN071 Brain Injury 50 0.497
305
ATH013 Atherosclerosis Susceptibility 63 0.487
306
P LKM002 Leukemia 66 0.466
307
P BCL017 B-Cell Lymphoma 57 0.456
308
ADN018 Adenoma 58 0.445
309
TLN003 Telangiectasis 51 0.445
310
P ATX030 Ataxia-Telangiectasia 80 0.433
311
HMN044 Human Immunodeficiency Virus Type 1 76 0.433
312
SVR004 Severe Combined Immunodeficiency 71 0.433
313
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.410
314
RNL077 Renal Fibrosis 46 0.410
315
P LTR001 Lateral Sclerosis 58 0.410
316
TRM010 Traumatic Brain Injury 50 0.410
317
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.398
318
P SLP006 Sleep Apnea 69 0.385
319
CLT003 Colitis 63 0.385
320
IMP005 Impotence 52 0.358
321
P INF037 Inflammatory Bowel Disease 53 0.344
322
GLC003 Glucose Intolerance 53 0.344
323
P LNG032 Lung Cancer 98 0.344
324
BRN004 Brain Edema 54 0.344
325
CMB007 Combined Immunodeficiency 56 0.330
326
BNR002 Bone Resorption Disease 47 0.330
327
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.330
328
LYM027 Lymphopenia 56 0.330
329
P ENC018 Encephalopathy 62 0.330
330
P RTN016 Retinal Degeneration 52 0.330
331
ULC004 Ulcerative Colitis 74 0.330
332
P AST005 Asthma 76 0.314
333
DWN001 Down Syndrome 70 0.314
334
c TYP008 Type 1 Diabetes Mellitus 77 0.314
335
IMM167 Immune Deficiency Disease 77 0.314
336
P PRP019 Peripheral Nervous System Disease 57 0.314
337
P EYD002 Eye Disease 57 0.314
338
ADN001 Adenosine Deaminase Deficiency 59 0.314
339
DBT010 Diabetic Neuropathy 54 0.314
340
BRR014 Barrett Esophagus 66 0.298
341
c HYP595 Hypertension, Essential 84 0.298
342
c MST023 Mesothelioma, Malignant 56 0.298
343
PPT005 Peptic Ulcer Disease 58 0.298
344
PRM329 Premature Aging 36 0.298
345
c FNC027 Fanconi Anemia, Complementation Group a 81 0.281
346
P MJR001 Major Depressive Disorder 68 0.281
347
c WLM013 Wilms Tumor 1 65 0.281
348
MNT002 Mental Depression 56 0.281
349
RTN003 Retinal Ischemia 48 0.281
350
ANR040 Aneurysm 60 0.281
351
ANX004 Anoxia 40 0.281
352
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.263
353
P GST053 Gastric Cancer 82 0.263
354
ATS010 Autosomal Recessive Disease 42 0.263
355
OST003 Osteonecrosis 61 0.263
356
P MYC007 Myocardial Infarction 69 0.263
357
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.263
358
PPL052 Papillomatosis, Confluent and Reticulated 34 0.263
359
P ATS364 Autism 72 0.263
360
TST015 Testicular Disease 42 0.263
361
P FBR017 Fibrosarcoma 55 0.263
362
TRN015 Transient Cerebral Ischemia 62 0.263
363
P NSP012 Nasopharyngeal Carcinoma 60 0.263
365
CRT015 Carotid Artery Occlusion 45 0.263
366
P ATR005 Atrophic Gastritis 50 0.263
367
MLD018 Mild Cognitive Impairment 48 0.243
368
NRR001 Neuroretinitis 42 0.243
369
P PRK057 Parkinson Disease, Late-Onset 79 0.243
370
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.243
371
P RHM011 Rheumatoid Arthritis 81 0.243
372
CLR108 Colorectal Adenoma 63 0.243
373
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.243
374
P RSP003 Respiratory Failure 74 0.243
375
STT001 Status Epilepticus 58 0.243
376
GLB002 Glioblastoma 67 0.243
377
P DMN002 Dementia 65 0.243
378
P ESP024 Esophagitis 60 0.243
379
P NTR004 Neutropenia 62 0.243
380
ART016 Aortic Aneurysm 69 0.243
381
RTN023 Retinitis 45 0.243
382
P ART021 Arteriosclerosis 53 0.243
383
P MYC008 Myocarditis 59 0.243
384
ATN005 Autonomic Dysfunction 45 0.243
385
P MSC003 Muscular Atrophy 52 0.243
386
P MSC005 Muscular Dystrophy 66 0.243
387
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.243
388
GST092 Gastroesophageal Reflux 60 0.222
389
CYS001 Cystic Fibrosis 77 0.222
390
WRN001 Werner Syndrome 69 0.222
391
ANX010 Anxiety 70 0.222
392
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.222
393
ALC007 Alcohol Dependence 65 0.222
394
ADR040 Adrenal Gland Pheochromocytoma 45 0.222
395
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.222
396
P HYP750 Hypertriglyceridemia, Familial 62 0.222
397
P PHC003 Pheochromocytoma 70 0.222
398
NRL016 Neural Tube Defects 81 0.222
399
c FML021 Familial Hypercholesterolemia 71 0.222
400
CMP010 Complex Regional Pain Syndrome 59 0.222
401
P RTN018 Retinal Disease 53 0.222
402
HYP014 Hyperuricemia 51 0.222
403
c ACT071 Acute Kidney Failure 60 0.222
404
BLR008 Bilirubin Metabolic Disorder 57 0.222
405
SPP011 Suppression of Tumorigenicity 12 61 0.222
406
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.222
407
P PNC035 Pancreatic Cancer 86 0.222
408
P MYL006 Myeloid Leukemia 60 0.222
409
VSC002 Vascular Dementia 59 0.222
410
OST012 Osteoarthritis 77 0.222
411
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.199
412
P PRS040 Prostate Cancer 95 0.199
413
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.199
414
CPR004 Coproporphyria, Hereditary 57 0.199
415
PRP082 Porphyria, Congenital Erythropoietic 56 0.199
416
P PLM037 Pulmonary Hypertension 69 0.199
417
c PCH010 Pachyonychia Congenita 3 43 0.199
418
MCR013 Microphthalmia 60 0.199
419
APN008 Apnea, Obstructive Sleep 66 0.199
420
c ATS007 Autism Spectrum Disorder 72 0.199
421
P FML011 Familial Adenomatous Polyposis 71 0.199
422
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.199
423
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.199
424
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.199
425
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.199
426
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.199
427
P PRP003 Porphyria Cutanea Tarda 66 0.199
428
VRG001 Variegate Porphyria 55 0.199
429
P ALC033 Alcohol Use Disorder 67 0.199
430
P BND020 Bone Disease 60 0.199
431
P SPN046 Spinal Muscular Atrophy 62 0.199
432
P PLY019 Polyneuropathy 53 0.199
433
GT001 Gout 63 0.199
434
NPH009 Nephrolithiasis 54 0.199
435
CRB039 Cerebrovascular Disease 65 0.199
436
URT010 Ureteral Obstruction 45 0.199
437
PRP016 Paraplegia 52 0.199
438
P PNC044 Pancreatitis 61 0.199
439
HYP080 Hypogonadism 49 0.199
440
P HYP069 Hyperparathyroidism 62 0.199
441
SCH014 Schistosomiasis 56 0.199
442
P THR014 Thrombocytopenia 66 0.199
443
P CYS018 Cystitis 59 0.199
444
ASB001 Asbestosis 47 0.199
445
P ADL010 Adult Respiratory Distress Syndrome 71 0.199
446
c SCN007 Secondary Hyperparathyroidism 51 0.199
447
GST040 Gastric Adenocarcinoma 66 0.199
448
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.199
449
MTC005 Mitochondrial Metabolism Disease 45 0.199
450
SPN186 Spinal Cord Injury 61 0.199
451
P INF038 Influenza 68 0.199
452
P ART022 Arthritis 70 0.199
453
MTY003 Mutyh Polyposis 38 0.199
454
47X002 47,xyy 48 0.199
455
ASB003 Asbestos Intoxication 32 0.199
456
P PNM006 Pneumoconiosis 55 0.172
457
P OVR042 Ovarian Cancer 88 0.172
458
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.172
459
P EXN002 Exanthem 58 0.172
460
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.172
461
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.172
462
c FML347 Familial Adenomatous Polyposis 2 56 0.172
463
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.172
464
ATM095 Autoimmune Disease 61 0.172
465
CLF027 Cleft Palate, Isolated 64 0.172
466
SRC014 Sarcoma 64 0.172
467
P EPL164 Epilepsy 70 0.172
468
LYM040 Lymphoblastic Lymphoma 53 0.172
469
CYT005 Cytomegalovirus Retinitis 50 0.172
470
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.172
471
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.172
472
BLR001 Biliary Atresia 55 0.172
473
OPS001 Opisthorchiasis 41 0.172
474
P DRR001 Diarrhea 55 0.172
475
c ACT027 Acute Pancreatitis 60 0.172
476
P OVR046 Ovarian Cyst 44 0.172
477
TCL003 T Cell Deficiency 44 0.172
478
PPT001 Peptic Esophagitis 51 0.172
479
P RNV001 Renovascular Hypertension 49 0.172
480
AZS001 Azoospermia 45 0.172
481
CHL123 Chlamydia 58 0.172
482
P HYP061 Hypertrophic Cardiomyopathy 69 0.172
483
PLM010 Pulmonary Edema 54 0.172
484
PLR008 Pleurisy 49 0.172
485
SLC006 Silicosis 55 0.172
486
ANT018 Anthracosis 51 0.172
487
NPH010 Nephrosclerosis 50 0.172
488
P HRT032 Heart Disease 84 0.172
489
P PTT006 Pituitary Adenoma 55 0.172
490
INT025 Intermittent Explosive Disorder 39 0.172
491
MSC157 Muscular Dystrophy, Duchenne Type 79 0.172
492
P THL005 Thalassemia 56 0.172
493
P INS002 in Situ Carcinoma 53 0.172
494
CRV002 Cervix Uteri Carcinoma in Situ 48 0.172
495
CRH001 Crohn's Disease 80 0.172
496
INT078 Intracranial Thrombosis 50 0.172
497
P SLP005 Sleep Disorder 62 0.172
498
P PLM034 Pulmonary Emphysema 58 0.172
499
CRV045 Cervical Intraepithelial Neoplasia 38 0.172
500
P ATT003 Attenuated Familial Adenomatous Polyposis 57 0.172
501
PLC008 Placenta Disease 49 0.172
502
GRW007 Growth Hormone Deficiency 47 0.172
503
MYH016 Myh-Associated Polyposis 38 0.172
504
c CCK007 Cockayne Syndrome B 56 0.141
505
OCL069 Ocular Motor Apraxia 57 0.141
506
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 0.141
507
P SPP010 Suppressor of Tumorigenicity 3 51 0.141
508
P MYS003 Myasthenia Gravis 68 0.141
509
P RTN008 Retinitis Pigmentosa 79 0.141
510
LSC001 Lesch-Nyhan Syndrome 62 0.141
511
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.141
512
HMC014 Homocysteinemia 52 0.141
513
P TMR010 Tumor Predisposition Syndrome 69 0.141
514
MND025 Mandibulofacial Dysostosis with Alopecia 39 0.141
515
HMN047 Human Cytomegalovirus Infection 59 0.141
516
P KRT007 Keratoconus 50 0.141
517
BCT022 Bacterial Infectious Disease 56 0.141
518
NSP002 Nasopharyngitis 45 0.141
519
URL001 Urolithiasis 45 0.141
520
P PLY041 Polymyositis 59 0.141
521
INT395 Intracranial Meningioma 48 0.141
522
P MTH007 Methemoglobinemia 46 0.141
523
P FRD001 Friedreich Ataxia 62 0.141
524
BRN032 Brain Glioma 45 0.141
525
INT029 Interleukin-7 Receptor Alpha Deficiency 28 0.141
526
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.141
527
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 59 0.141
528
MLR004 Malaria 78 0.141
529
ALL003 Allergic Rhinitis 66 0.141
530
GLB001 Gilbert Syndrome 53 0.141
531
INT051 Intussusception 53 0.141
532
LMY014 Leiomyoma, Uterine 55 0.141
533
c EXD008 Exudative Vitreoretinopathy 1 71 0.141
534
c SCL052 Scleroderma, Familial Progressive 60 0.141
535
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.141
536
HRN029 Hearing Loss, Noise-Induced 37 0.141
537
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.141
538
ACT209 Acatalasemia 44 0.141
539
ACT003 Acute Kidney Tubular Necrosis 46 0.141
540
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.141
541
CRD223 Cardiac Arrhythmia 63 0.141
542
c DPH024 Diaphragmatic Hernia, Congenital 64 0.141
543
c TBR025 Tuberous Sclerosis 1 84 0.141
544
INT030 Intracranial Aneurysm 55 0.141
545
THY006 Thymus Lymphoma 27 0.141
546
THR024 Thrombosis 56 0.141
547
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.141
548
PRP027 Peripheral Vascular Disease 71 0.141
549
DFC004 Deficiency Anemia 74 0.141
550
CLB002 Clubfoot 51 0.141
551
CRT013 Carotid Stenosis 51 0.141
552
P TBR001 Tuberous Sclerosis 69 0.141
553
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.141
554
P SBS003 Substance Abuse 54 0.141
555
P HML002 Hemolytic Anemia 62 0.141
556
GST029 Gastric Cardia Adenocarcinoma 29 0.141
557
P INT068 Intestinal Disease 53 0.141
558
ACT084 Acute Stress Disorder 53 0.141
559
KRT002 Keratomalacia 54 0.141
560
PST028 Post-Traumatic Stress Disorder 59 0.141
561
ACR007 Acromegaly 70 0.141
562
P RCT021 Rectum Cancer 54 0.141
563
P KRN004 Kernicterus 47 0.141
564
NNT012 Neonatal Jaundice 53 0.141
565
P CRN025 Corneal Dystrophy 49 0.141
566
DBT004 Diabetic Polyneuropathy 50 0.141
567
c CHR087 Chronic Cystitis 37 0.141
568
P RTN022 Retinal Vein Occlusion 54 0.141
569
P PRT096 Peritoneal Mesothelioma 49 0.141
570
GTR002 Goiter 52 0.141
571
OLG003 Oligohydramnios 51 0.141
572
CRN027 Corneal Neovascularization 47 0.141
573
FCH001 Fuchs' Endothelial Dystrophy 48 0.141
574
END011 Endometriosis of Ovary 40 0.141
575
TTN003 Tetanus 64 0.141
576
P RHN004 Rhinitis 57 0.141
577
c ACT076 Acute Myocarditis 47 0.141
578
THY123 Thyroid Gland Follicular Carcinoma 53 0.141
579
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.141
580
MNN043 Meningioma, Familial 79 0.141
581
c RNG019 Ring Chromosome 3 19 0.141
582
NRM005 Neuromuscular Disease 63 0.141
583
SPN035 Spindle Cell Sarcoma 51 0.141
584
HML018 Homologous Wasting Disease 21 0.141
585
P VSC011 Vasculitis 61 0.141
586
SCB001 Scabies 49 0.141
587
P PLY018 Polycythemia 56 0.141
588
PRS042 Prostate Disease 42 0.141
589
CLR030 Clear Cell Renal Cell Carcinoma 54 0.141
590
SCR001 Secretory Meningioma 40 0.141
591
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.141
592
HDN002 Head Injury 44 0.141
593
SRC001 Sarcomatoid Mesothelioma 31 0.141
594
P FBR031 Febrile Seizures 52 0.141
595
MTC004 Mitochondrial Encephalomyopathy 43 0.141
596
P AMY004 Amyloidosis 69 0.141
597
CHL061 Childhood Leukemia 47 0.141
598
c SPR009 Sporadic Breast Cancer 42 0.141
599
P ALP008 Alopecia 53 0.141
601
IRR002 Irritable Bowel Syndrome 65 0.141
602
P MYT002 Myotonic Dystrophy 51 0.141
603
P ENC004 Encephalitis 61 0.141
604
P ORL007 Oral Cavity Cancer 52 0.141
605
ELS001 Eales Disease 45 0.141
606
EXN003 Exencephaly 30 0.141
607
NDL013 Nodular Regenerative Hyperplasia 46 0.141
608
P PRG139 Progeroid Syndrome 29 0.141
609
INH023 Inherited Cancer-Predisposing Syndrome 53 0.141
610
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.141
611
GLM044 Glomerular Disease 34 0.141
613
P SCH015 Schizophrenia 74 0.099
614
ERY029 Erythermalgia, Primary 58 0.099
615
P CHN012 Chondrosarcoma 56 0.099
616
P FNC044 Fanconi Anemia, Complementation Group C 56 0.099
617
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.099
618
c TYR013 Tyrosinemia, Type Ii 48 0.099
619
c SPN393 Spinal Muscular Atrophy, Type I 51 0.099
620
PLY001 Polycythemia Vera 69 0.099
621
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.099
622
c SPN395 Spinal Muscular Atrophy, Type Ii 55 0.099
623
MYL005 Myelofibrosis 70 0.099
624
c ANM038 Anemia, Autoimmune Hemolytic 63 0.099
625
INS024 Insulin-Like Growth Factor I 77 0.099
626
TYR015 Tyrosinosis 20 0.099
627
c XRD031 Xeroderma Pigmentosum, Complementation Group F 55 0.099
628
PRX085 Preaxial Hallucal Polydactyly 28 0.099
629
c BRN108 Branchiootic Syndrome 1 63 0.099
630
c LKM063 Leukemia, Chronic Myeloid 71 0.099
631
c LNG109 Lung Cancer Susceptibility 1 26 0.099
632
c FNC025 Fanconi Anemia, Complementation Group J 52 0.099
633
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.099
634
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.099
635
WST005 West Nile Virus 55 0.099
636
KSH001 Keshan Disease 31 0.099
637
ACT119 Acute Promyelocytic Leukemia 62 0.099
638
c BRS111 Breast-Ovarian Cancer, Familial 2 54 0.099
639
c MCR112 Microvascular Complications of Diabetes 2 42 0.099
640
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.099
641
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.099
642
MSC007 Muscle Hypertrophy 64 0.099
643
CHR515 Chronic Atrial and Intestinal Dysrhythmia 44 0.099
644
KSH004 Kashin-Beck Disease 37 0.099
645
P RST001 Restless Legs Syndrome 52 0.099
646
P MLT008 Multinodular Goiter 42 0.099
647
P FTL001 Fetal Alcohol Syndrome 55 0.099
648
CHR005 Chorioamnionitis 50 0.099
650
EXR010 Exercise-Induced Bronchoconstriction 34 0.099
651
P SNS001 Sensorineural Hearing Loss 59 0.099
652
P LKD001 Leukodystrophy 58 0.099
653
THL010 Thalassemia Minor 31 0.099
654
MCS002 Mucositis 55 0.099
655
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 0.099
656
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.099
657
END062 Endometrial Hyperplasia 48 0.099
658
SLP001 Sleeping Sickness 56 0.099
659
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.099
660
c MGR028 Migraine with or Without Aura 1 64 0.099
661
PLY150 Polykaryocytosis Inducer 29 0.099
662
MLN071 Melanoma Tumor Antigen Gp90 17 0.099
663
P MYS005 Myositis 56 0.099
664
OBS002 Obsessive-Compulsive Disorder 68 0.099
665
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.099
666
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.099
667
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.099
668
P GLC113 Galactosemia I 65 0.099
669
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.099
670
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.099
671
P LPR021 Leprosy 3 71 0.099
672
P NJM001 Nijmegen Breakage Syndrome 75 0.099
673
CTR172 Citrullinemia, Classic 64 0.099
674
CYS019 Cystathioninuria 46 0.099
675
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.099
676
c DWL002 Dowling-Degos Disease 1 58 0.099
677
RTN017 Retinal Detachment 60 0.099
678
P CLC063 Celiac Disease 1 66 0.099
679
c CCK008 Cockayne Syndrome a 59 0.099
680
P FML018 Familial Mediterranean Fever 73 0.099
681
HMR023 Hemorrhagic Cystitis 43 0.099
682
PNG002 Pain Agnosia 51 0.099
683
CLN044 Colon Adenoma 44 0.099
684
END075 Endocervical Adenocarcinoma 37 0.099
685
LMB062 Limb Ischemia 55 0.099
686
WTH001 Withdrawal Disorder 47 0.099
687
HYP025 Hyperphosphatemia 47 0.099
689
VTM002 Vitamin B12 Deficiency 48 0.099
690
HYP017 Hypophosphatemia 49 0.099
691
PRP080 Peripheral Artery Disease 54 0.099
692
RSP021 Respiratory Allergy 41 0.099
693
FBR054 Fibroma 44 0.099
694
c SPR162 Spermatogenic Failure 50 42 0.099
695
P MYC084 Mycobacterium Tuberculosis 1 68 0.099
696
P APL001 Aplastic Anemia 73 0.099
697
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.099
698
P MCR129 Microvascular Complications of Diabetes 1 68 0.099
699
c ATX040 Ataxia-Telangiectasia-Like Disorder 1 50 0.099
700
TMR017 Tumoral Calcinosis, Normophosphatemic, Familial 31 0.099
701
RGD003 Rigid Spine Muscular Dystrophy 1 56 0.099
702
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.099
703
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.099
704
CNN008 Cinnamon Odor, Pleasantness of 13 0.099
705
INC002 Inclusion Body Myositis 57 0.099
706
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 0.099
707
P CRC039 Coarctation of Aorta 46 0.099
709
ANS021 Anisocoria 25 0.099
710
PHS025 Phosphatase, Acid, of Tissues 28 0.099
711
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.099
712
PCK003 Pick Disease of Brain 69 0.099
713
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.099
714
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.099
715
P HMN032 Human Herpesvirus 8 47 0.099
716
c BTT014 Beta-Thalassemia 72 0.099
717
P MMB011 Membranous Nephropathy 50 0.099
718
TRC010 Trichotillomania 50 0.099
719
PTN004 Patent Ductus Venosus 31 0.099
720
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.099
721
SHR107 Short Stature-Obesity Syndrome 25 0.099
722
P SJG008 Sjogren Syndrome 61 0.099
723
LPT014 Leptin Deficiency or Dysfunction 77 0.099
724
BRD004 Borderline Personality Disorder 53 0.099
725
P CRN026 Corneal Edema 42 0.099
726
BLL004 Bullous Keratopathy 47 0.099
727
P HML001 Hemolytic-Uremic Syndrome 52 0.099
728
HND015 Hand Skill, Relative 29 0.099
729
LCH016 Lichen Sclerosus Et Atrophicus 41 0.099
730
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.099
731
MLT157 Multiple System Atrophy 1 69 0.099
732
TBC004 Tobacco Addiction 63 0.099
733
TST044 Testicular Torsion 45 0.099
734
BRC012 Brucellosis 66 0.099
735
AVD001 Avoidant Personality Disorder 49 0.099
736
P PRS038 Personality Disorder 65 0.099
737
P ANG015 Angioedema 56 0.099
738
c ACT249 Acute Asthma 40 0.099
739
INT394 Intermittent Asthma 21 0.099
740
DRY001 Dry Eye Syndrome 49 0.099
741
P MYG005 Myoglobinuria 40 0.099
742
ADN067 Adenoid Hypertrophy 39 0.099
743
ECT026 Ectopic Pregnancy 47 0.099
744
CHR100 Chronic Ulcer of Skin 57 0.099
745
DYS015 Dysentery 50 0.099
746
MNN017 Mononeuropathy 41 0.099
747
MNN009 Meningoencephalitis 48 0.099
748
CLN003 Clonorchiasis 42 0.099
749
NWB001 Newborn Respiratory Distress Syndrome 56 0.099
750
P MGR001 Migraine Without Aura 48 0.099
751
P UVT001 Uveitis 57 0.099
752
c ACT068 Acute Cystitis 61 0.099
753
BRS099 Breast Ductal Carcinoma 61 0.099
754
IDP011 Idiopathic Interstitial Pneumonia 59 0.099
755
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.099
756
P ANT006 Antiphospholipid Syndrome 55 0.099
757
MCN001 Mucinous Adenocarcinoma 49 0.099
758
CRV040 Cervix Carcinoma 50 0.099
759
ANG009 Angiomatous Meningioma 25 0.099
760
P ACN011 Acne 55 0.099
761
TBL003 Tubular Adenocarcinoma 40 0.099
762
PTT009 Pituitary Gland Disease 53 0.099
763
SCH003 Schizophreniform Disorder 54 0.099
764
ENT004 Enthesopathy 51 0.099
765
DNT012 Dental Caries 53 0.099
766
KRT008 Keratopathy 46 0.099
767
P LMY004 Leiomyosarcoma 62 0.099
768
P HMN010 Hemangioma 61 0.099
769
SYN007 Synovitis 54 0.099
770
RTN020 Retinal Vascular Disease 45 0.099
771
c MLG084 Malignant Fibrous Histiocytoma 62 0.099
772
CNT016 Central Retinal Vein Occlusion 54 0.099
773
SNS003 Sensory Peripheral Neuropathy 51 0.099
774
P GLL022 Guillain-Barre Syndrome 59 0.099
775
NVS001 Neovascular Glaucoma 52 0.099
776
P CRD246 Cardiovascular System Disease 55 0.099
777
SBC014 Subclavian Steal Syndrome 30 0.099
778
URN003 Urinary Schistosomiasis 45 0.099
779
OLG001 Oligospermia 45 0.099
780
PLR005 Pleuropneumonia 33 0.099
781
c BPL002 Bipolar I Disorder 47 0.099
782
PRS047 Prostatitis 58 0.099
783
CRB033 Cerebral Degeneration 36 0.099
784
P BRS053 Breast Fibroadenoma 48 0.099
785
NDL007 Nodular Goiter 48 0.099
786
DBT007 Diabetic Cataract 35 0.099
787
P OBS001 Obstructive Jaundice 49 0.099
788
ANG005 Anogenital Venereal Wart 55 0.099
789
PLC002 Plica Syndrome 35 0.099
790
NRG002 Neurogenic Bladder 55 0.099
791
PRM236 Primary Biliary Cholangitis 62 0.099
792
GST023 Gastric Ulcer 52 0.099
793
IRN001 Iron Deficiency Anemia 58 0.099
794
ESN006 Eosinophilic Meningitis 36 0.099
795
PNC129 Pancreatic Adenocarcinoma 65 0.099
796
PLC005 Placental Insufficiency 56 0.099
797
INS001 Insulinoma 59 0.099
798
NNS002 Nonspecific Interstitial Pneumonia 42 0.099
799
HGH043 High Grade Glioma 46 0.099
800
INT066 Interstitial Lung Disease 60 0.099
801
P OLG002 Oligodendroglioma 66 0.099
802
P CHR012 Chronic Granulomatous Disease 69 0.099
803
INT002 Intermittent Claudication 61 0.099
804
LNG031 Lung Benign Neoplasm 51 0.099
805
LNG039 Lung Squamous Cell Carcinoma 57 0.099
806
CRT004 Carotid Artery Thrombosis 39 0.099
807
P BRS044 Breast Adenocarcinoma 58 0.099
808
MDD003 Middle Cerebral Artery Infarction 37 0.099
809
SKN005 Skin Atrophy 41 0.099
810
MCL006 Macular Retinal Edema 56 0.099
811
APP009 Appendix Adenocarcinoma 47 0.099
812
CRV038 Cervical Squamous Cell Carcinoma 56 0.099
813
ADR005 Adrenal Carcinoma 61 0.099
814
CNS004 Constipation 56 0.099
815
P TMP001 Temporal Lobe Epilepsy 49 0.099
816
PLG002 Plague 58 0.099
817
DMY004 Demyelinating Disease 50 0.099
818
P THY023 Thymoma 64 0.099
819
SKN020 Skin Papilloma 40 0.099
820
ART002 Arts Syndrome 66 0.099
821
INC021 Incontinentia Pigmenti 63 0.099
822
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.099
823
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.099
824
ORT008 Orotic Aciduria 56 0.099
825
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 0.099
826
SBC001 Subacute Sclerosing Panencephalitis 53 0.099
827
MMM006 Mammographic Density 39 0.099
828
RST023 Resting Heart Rate, Variation in 40 0.099
829
c THY107 Thymoma, Familial 42 0.099
830
c XNT010 Xanthinuria, Type I 52 0.099
831
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.099
832
c SPR086 Spermatogenic Failure 3 47 0.099
833
c RNG024 Ring Chromosome 8 28 0.099
834
AML001 Amelanotic Melanoma 37 0.099
835
P SYS005 Systemic Scleroderma 73 0.099
836
PRP030 Purpura 54 0.099
837
ANG018 Angiomyolipoma 45 0.099
838
PST106 Post-Cardiac Arrest Syndrome 31 0.099
839
P FBR003 Fibrous Histiocytoma 43 0.099
840
P MRC003 Mercury Poisoning 48 0.099
841
SFT003 Soft Tissue Sarcoma 57 0.099
842
HRP004 Herpes Zoster 60 0.099
843
RFR002 Refractory Hairy Cell Leukemia 34 0.099
844
RDT001 Radiation Cystitis 31 0.099
845
P TRM003 Tremor 50 0.099
846
ACT191 Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion 18 0.099
847
P MYC033 Myoclonus 46 0.099
848
SPS057 Spasticity 43 0.099
849
DGN001 Degenerative Disc Disease 48 0.099
850
DYS032 Dystrophinopathies 47 0.099
851
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 38 0.099
852
P BRN022 Bronchiectasis 59 0.099
853
P MTR014 Motor Neuron Disease 65 0.099
854
PRP017 Periapical Periodontitis 46 0.099
855
FNC007 Functioning Pituitary Adenoma 42 0.099
856
KDN013 Kidney Hypertrophy 33 0.099
857
APH001 Aphthous Stomatitis 57 0.099
858
P HDC001 Headache 56 0.099
859
HYP264 Hypertonia 36 0.099
860
SPN050 Spinocerebellar Degeneration 39 0.099
861
c RNG015 Ring Chromosome 2 22 0.099
862
CHR178 Chromosomal Triplication 34 0.099
863
P CRB059 Cerebellar Degeneration 36 0.099
864
c PRG011 Progressive Myoclonus Epilepsy 40 0.099
865
PRT036 Peritonitis 65 0.099
866
ANP009 Anaplastic Oligodendroglioma 41 0.099
867
TRN002 Transitional Meningioma 25 0.099
868
APP008 Appendicitis 62 0.099
869
KDN015 Kidney Angiomyolipoma 46 0.099
870
MLG079 Malignant Pleural Mesothelioma 42 0.099
871
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.099
872
MSL001 Measles 61 0.099
873
SBC016 Subacute Delirium 42 0.099
874
HRN003 Heroin Dependence 44 0.099
876
P ALP009 Alopecia Areata 59 0.099
877
P CHL066 Cholangitis 51 0.099
878
PST021 Postpartum Depression 50 0.099
879
GNT003 Genital Herpes 54 0.099
880
DCB001 Decubitus Ulcer 61 0.099
881
c FML053 Familial Colorectal Cancer 47 0.099
882
GNT019 Giant Cell Myocarditis 29 0.099
883
HMN016 Hemangioendothelioma 35 0.099
884
HPR003 Heparin-Induced Thrombocytopenia 47 0.099
885
NSS002 Neisseria Meningitidis Infection 47 0.099
886
P FML187 Familial Hypertension 34 0.099
887
HMP009 Haemophilus Influenzae 41 0.099
888
MYC019 Mycobacterium Marinum 29 0.099
889
CGH002 Cough Headache 16 0.099
890
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.099
891
DWR001 Dwarfism 45 0.099
892
HNS001 Hansen's Disease 32 0.099
893
P MYC026 Myoclonus Epilepsy 35 0.099
894
P TXP001 Toxoplasmosis 60 0.099
895
P HYP098 Hypereosinophilic Syndrome 66 0.099
896
MCR004 Macroglobulinemia 48 0.099
897
c PRM015 Primary Cerebellar Degeneration 30 0.099
898
OCL006 Ocular Hypertension 53 0.099
899
PRQ002 Paraquat Poisoning 28 0.099
900
THY128 Thyroid Tumor 33 0.099
901
c PRM038 Primary Agammaglobulinemia 47 0.099
902
PST092 Posttransplant Acute Limbic Encephalitis 29 0.099
903
CLF004 Cleft Lip/palate 57 0.099
904
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 0.099
905
MNG007 Manganese Poisoning 28 0.099
906
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.099
907
FXD003 Fixed Drug Eruption 34 0.099
908
EXR008 Exercise-Induced Malignant Hyperthermia 20 0.099
909
OST115 Osteonecrosis of the Jaw 40 0.099
910
ARG004 Argyria 26 0.099
911
c ERL020 Early-Onset Schizophrenia 43 0.099
912
TRG022 Triglyceride Deposit Cardiomyovasculopathy 19 0.099
913
GNT167 Genetic Obesity 32 0.099
914
NNF007 Non-Functioning Pituitary Adenoma 39 0.099
915
PNM013 Pneumococcal Meningitis 43 0.099
916
P ACT241 Acute Bilirubin Encephalopathy 25 0.099
917
PLY100 Polyploidy 36 0.099
Content
Loading form....