Search results for heme

1646 hits were found for heme

# Family MCID Name MIFTS Score
1
HMX003 Heme Oxygenase 1 Deficiency 27 42.288
2
P PRP029 Porphyria 60 21.518
3
c PRT132 Protoporphyria, Erythropoietic, 1 61 17.996
4
P ATS324 Autosomal Erythropoietic Protoporphyria 25 11.774
5
IRN002 Iron Metabolism Disease 56 10.140
6
DFC004 Deficiency Anemia 74 9.100
7
ISC004 Ischemia 61 7.386
8
HLX001 Helix Syndrome 47 7.232
9
BLR008 Bilirubin Metabolic Disorder 57 6.282
10
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 6.212
11
P SCK005 Sickle Cell Disease 56 6.013
12
PRP083 Porphyria, Acute Intermittent 64 5.669
13
ACT078 Acute Porphyria 50 5.653
14
IRN001 Iron Deficiency Anemia 58 5.619
15
HYP266 Hypoxia 56 5.534
16
P RRH023 Rare Hereditary Hemochromatosis 52 5.516
17
PRP082 Porphyria, Congenital Erythropoietic 56 5.450
18
ACT098 Acute Erythroid Leukemia 55 5.280
19
HMS001 Hemosiderosis 48 4.855
20
c ACT071 Acute Kidney Failure 60 4.801
21
P HML002 Hemolytic Anemia 62 4.782
22
VRG001 Variegate Porphyria 55 4.675
23
ATH013 Atherosclerosis Susceptibility 63 4.544
24
MLR004 Malaria 77 4.495
25
P SDR003 Sideroblastic Anemia 49 4.418
26
c PRC016 Pre-Eclampsia 64 4.247
27
HMP009 Haemophilus Influenzae 41 4.244
28
P PRP003 Porphyria Cutanea Tarda 66 3.969
29
P THL005 Thalassemia 56 3.903
30
P VSC007 Vascular Disease 62 3.882
31
LPP008 Lipoprotein Quantitative Trait Locus 65 3.825
32
P PLM037 Pulmonary Hypertension 69 3.796
33
P CRD246 Cardiovascular System Disease 55 3.743
34
P MYC084 Mycobacterium Tuberculosis 1 68 3.642
35
P PRD008 Periodontitis 63 3.497
36
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.474
37
CTN011 Cutaneous Porphyria 45 3.467
38
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.434
39
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 3.419
40
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 3.419
41
HYP066 Hyperglycemia 60 3.335
42
P ALZ034 Alzheimer Disease 87 3.300
43
CPR004 Coproporphyria, Hereditary 57 3.288
44
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.258
45
48X005 48,xyyy 39 3.214
46
P ADL010 Adult Respiratory Distress Syndrome 70 3.188
47
FTT001 Fatty Liver Disease 61 3.081
48
HLT001 Holt-Oram Syndrome 66 3.078
49
PRT251 Proteinuria, Chronic Benign 58 3.071
50
CHG001 Chagas Disease 65 3.037
51
BRN071 Brain Injury 50 2.999
52
SCK003 Sickle Cell Anemia 74 2.974
53
CYT002 Cytokine Deficiency 43 2.961
54
CLT003 Colitis 63 2.954
55
P LVR013 Liver Disease 68 2.939
56
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 2.908
57
P MYC007 Myocardial Infarction 69 2.905
58
P NRB001 Neuroblastoma 66 2.885
59
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.881
60
c ACT027 Acute Pancreatitis 60 2.872
61
LNG099 Lung Disease 62 2.869
62
NNT012 Neonatal Jaundice 53 2.793
63
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.793
64
c TYP009 Type 2 Diabetes Mellitus 91 2.780
65
CRB004 Cerebral Artery Occlusion 45 2.757
66
P PNC044 Pancreatitis 61 2.756
67
RNL077 Renal Fibrosis 46 2.740
68
HMG005 Hemoglobinopathy 55 2.733
69
P ANR048 Aniridia 1 66 2.697
70
c INH020 Inherited Metabolic Disorder 47 2.695
71
BCT022 Bacterial Infectious Disease 55 2.623
72
c ACT075 Acute Myocardial Infarction 55 2.597
73
P PRK057 Parkinson Disease, Late-Onset 79 2.546
74
P KDN018 Kidney Disease 71 2.493
76
AGN016 Aging 53 2.458
77
TRM010 Traumatic Brain Injury 50 2.453
78
NNL006 Non-Alcoholic Steatohepatitis 54 2.451
79
P DBT009 Diabetes Mellitus 67 2.451
80
P KLZ004 Kala-Azar 1 41 2.444
81
LSH001 Leishmaniasis 63 2.444
82
ART140 Arteries, Anomalies of 52 2.434
83
c HMC039 Hemochromatosis, Type 1 73 2.428
84
ALL014 Allergic Encephalomyelitis 34 2.426
85
c MCR133 Microvascular Complications of Diabetes 4 41 2.419
86
c MCR113 Microvascular Complications of Diabetes 3 52 2.419
87
c MCR130 Microvascular Complications of Diabetes 6 41 2.419
88
c MCR120 Microvascular Complications of Diabetes 7 47 2.419
89
P CRN300 Coronary Heart Disease 1 73 2.414
90
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.401
91
P PLM036 Pulmonary Fibrosis 65 2.399
92
c PRD040 Periodontitis, Chronic 52 2.388
93
CHL068 Cholestasis 61 2.379
94
BRN004 Brain Edema 54 2.352
95
ART016 Aortic Aneurysm 68 2.341
96
c HPT001 Hepatitis C 61 2.319
97
LVR012 Liver Cirrhosis 62 2.313
98
PRT013 Portal Hypertension 59 2.313
99
SPN186 Spinal Cord Injury 60 2.264
100
TXC005 Toxic Shock Syndrome 61 2.261
101
c ACT134 Acute Liver Failure 57 2.254
102
ANT024 Anthrax Disease 57 2.239
103
P PHC003 Pheochromocytoma 70 2.228
104
ADR040 Adrenal Gland Pheochromocytoma 45 2.228
105
P MYL006 Myeloid Leukemia 60 2.220
106
c ANM036 Anemia, Sideroblastic, 1 56 2.214
107
c BTT014 Beta-Thalassemia 72 2.213
108
P BCL017 B-Cell Lymphoma 57 2.195
109
PRT037 Pertussis 49 2.165
110
P INF037 Inflammatory Bowel Disease 53 2.165
111
ANR040 Aneurysm 60 2.162
112
c PLM164 Pulmonary Hypertension, Primary, 1 75 2.158
113
PPL052 Papillomatosis, Confluent and Reticulated 34 2.090
114
c LKM063 Leukemia, Chronic Myeloid 70 2.069
115
MYL009 Myelodysplastic Syndrome 67 2.066
116
ENT011 Enterocolitis 55 2.066
117
P LNG064 Lung Cancer Susceptibility 3 69 2.054
118
ANX004 Anoxia 40 2.045
119
HMG002 Hemoglobinuria 50 2.042
120
P HPT021 Hepatitis 68 2.037
121
GST037 Gastroparesis 52 2.035
122
PLM010 Pulmonary Edema 54 2.018
123
PST036 Posterior Column Ataxia with Retinitis Pigmentosa 38 1.999
124
c CHR684 Chronic Kidney Disease 73 1.992
125
THR024 Thrombosis 56 1.979
126
P INF038 Influenza 68 1.970
127
P LKM002 Leukemia 65 1.965
128
LMB062 Limb Ischemia 55 1.951
129
GLB002 Glioblastoma 67 1.944
130
47X002 47,xyy 47 1.939
131
GLL048 Glial Tumor 51 1.933
132
GLM045 Glioma 62 1.927
133
OTT002 Otitis Media 70 1.920
134
HYP001 Hypochromic Microcytic Anemia 36 1.920
135
P DMN001 Diamond-Blackfan Anemia 73 1.916
136
MCR018 Microcytic Anemia 46 1.914
137
c HYP595 Hypertension, Essential 84 1.907
138
MLD018 Mild Cognitive Impairment 48 1.898
139
BNR002 Bone Resorption Disease 47 1.894
140
PRT036 Peritonitis 65 1.886
141
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 52 1.883
142
P SLP006 Sleep Apnea 69 1.876
143
CRB039 Cerebrovascular Disease 65 1.868
144
P DNG005 Dengue Virus 55 1.822
145
c HPT073 Hepatitis C Virus 70 1.803
146
c BRS111 Breast-Ovarian Cancer, Familial 2 53 1.787
147
PRN019 Perinatal Necrotizing Enterocolitis 60 1.786
148
P HPT023 Hepatocellular Carcinoma 95 1.780
149
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.775
150
P ART021 Arteriosclerosis 53 1.769
151
P ECL001 Eclampsia 52 1.762
152
c ATR087 Atrial Standstill 1 74 1.756
153
c HYP836 Hypercholesterolemia, Familial, 1 73 1.755
154
STR067 Stroke, Ischemic 79 1.753
155
P LNG032 Lung Cancer 98 1.750
156
c LKM061 Leukemia, Acute Myeloid 83 1.749
157
P PNC035 Pancreatic Cancer 87 1.742
158
INT066 Interstitial Lung Disease 60 1.735
159
P HML001 Hemolytic-Uremic Syndrome 52 1.725
160
SPL018 Splenomegaly 47 1.702
161
P END044 Endometriosis 62 1.691
162
P DRM053 Dermatitis, Atopic 65 1.689
163
P HMC002 Homocystinuria 52 1.687
164
c MCR115 Microvascular Complications of Diabetes 5 65 1.685
165
ACT003 Acute Kidney Tubular Necrosis 46 1.675
166
P TYR004 Tyrosinemia 49 1.675
167
P GLM007 Glomerulonephritis 59 1.666
168
BRN056 Bronchopulmonary Dysplasia 57 1.665
169
IMP005 Impotence 52 1.663
170
ORL011 Oral Cancer 60 1.661
171
P BLD134 Bladder Cancer 79 1.657
172
P TRN020 Turner Syndrome 67 1.657
173
SKN016 Skin Disease 63 1.657
174
LGH007 Leigh Syndrome 70 1.651
175
c SML038 Small Cell Cancer of the Lung 68 1.650
176
P RSP003 Respiratory Failure 73 1.650
177
P NRP001 Neuropathy 59 1.648
178
URT010 Ureteral Obstruction 44 1.644
179
DPH001 Diphtheria 59 1.638
180
HRM022 Hair Morphology 1 11 1.618
181
P RHN004 Rhinitis 56 1.612
182
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 1.607
183
P AST005 Asthma 75 1.605
184
RTN003 Retinal Ischemia 48 1.604
185
SVR004 Severe Combined Immunodeficiency 70 1.604
186
END086 End Stage Renal Disease 54 1.604
187
DSS032 Disease by Infectious Agent 55 1.589
188
ATM095 Autoimmune Disease 61 1.589
189
ALL006 Allergic Asthma 55 1.588
190
ORL015 Oral Squamous Cell Carcinoma 43 1.571
191
AMN017 Aminolevulinic Acid Dehydratase Deficiency Porphyria 8 1.565
192
URM002 Uremia 47 1.561
193
ESP021 Esophageal Cancer 84 1.553
194
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.546
195
P GST053 Gastric Cancer 82 1.546
196
SQM006 Squamous Cell Carcinoma 59 1.546
197
GST033 Gestational Diabetes 60 1.526
198
P LTR001 Lateral Sclerosis 57 1.524
199
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.518
200
P GRF003 Graft-Versus-Host Disease 71 1.515
201
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.513
202
P VSC011 Vasculitis 61 1.513
203
SVR001 Severe Acute Respiratory Syndrome 68 1.505
204
P PRP056 Porphyria, Acute Hepatic 49 1.502
205
c VRL010 Viral Hepatitis 52 1.496
207
MYL069 Myeloma, Multiple 76 1.487
208
c PRT135 Protoporphyria, Erythropoietic, 2 18 1.478
209
ULC004 Ulcerative Colitis 74 1.466
210
P PLY018 Polycythemia 56 1.464
211
P BRS047 Breast Cancer 97 1.458
212
P KRN004 Kernicterus 47 1.458
213
PLS007 Plasmodium Falciparum Malaria 52 1.458
214
ALL003 Allergic Rhinitis 66 1.450
215
LPD008 Lipid Metabolism Disorder 61 1.450
216
P CLR023 Colorectal Cancer 100 1.442
217
KPS004 Kaposi Sarcoma 76 1.442
218
DYS015 Dysentery 49 1.437
219
P GLM040 Glioma Susceptibility 1 70 1.433
220
MLG169 Malignant Astrocytoma 57 1.433
221
PLC008 Placenta Disease 48 1.433
222
OST012 Osteoarthritis 77 1.433
223
P PRP019 Peripheral Nervous System Disease 57 1.424
224
P CRG003 Crigler-Najjar Syndrome, Type I 64 1.423
225
CYS001 Cystic Fibrosis 77 1.423
226
P HRT032 Heart Disease 84 1.423
227
PRT094 Protoporphyria, Erythropoietic, X-Linked 28 1.417
228
P PRK039 Parkinsonism 55 1.409
229
P RNV001 Renovascular Hypertension 48 1.407
230
P PNM007 Pneumonia 64 1.407
231
PST040 Posterior Column Ataxia 23 1.401
232
SLP001 Sleeping Sickness 56 1.401
233
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.398
234
ALL029 Allergic Disease 61 1.398
235
P HYP061 Hypertrophic Cardiomyopathy 68 1.394
236
PRP080 Peripheral Artery Disease 54 1.380
237
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 1.379
238
P HNT016 Huntington Disease 73 1.379
239
P SZR006 Seizure Disorder 69 1.379
240
P RHM011 Rheumatoid Arthritis 81 1.370
241
P ENC018 Encephalopathy 62 1.367
242
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.363
243
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.363
244
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.363
245
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.363
246
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.363
247
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.363
248
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.363
249
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.363
250
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.363
251
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.363
252
DSS009 Disseminated Intravascular Coagulation 56 1.355
253
P PRR002 Pure Red-Cell Aplasia 46 1.355
254
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 36 1.355
255
PST092 Posttransplant Acute Limbic Encephalitis 29 1.334
256
IMM167 Immune Deficiency Disease 76 1.329
257
P CHR345 Chronic Pain 50 1.329
258
P PRS040 Prostate Cancer 95 1.329
259
P PSR002 Psoriasis 63 1.317
260
P CHR012 Chronic Granulomatous Disease 69 1.315
261
VSC003 Visceral Leishmaniasis 54 1.312
262
SPN035 Spindle Cell Sarcoma 51 1.311
263
SRC014 Sarcoma 64 1.311
264
NRR001 Neuroretinitis 42 1.305
265
P ADN016 Adenocarcinoma 63 1.305
266
RTN023 Retinitis 45 1.305
267
P CRD119 Cardiac Arrest 68 1.302
268
GLC003 Glucose Intolerance 53 1.302
269
P RTN008 Retinitis Pigmentosa 79 1.298
270
ATS010 Autosomal Recessive Disease 42 1.290
271
MCR017 Macrocytic Anemia 44 1.284
272
HMC014 Homocysteinemia 52 1.282
273
P LPS004 Lupus Erythematosus 61 1.282
274
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.274
275
MCR013 Microphthalmia 59 1.274
276
SCH014 Schistosomiasis 56 1.274
277
TRN015 Transient Cerebral Ischemia 62 1.273
278
DBT010 Diabetic Neuropathy 54 1.273
279
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.266
280
THR004 Thrombocytosis 52 1.263
281
CHR074 Choriocarcinoma 46 1.263
282
THR016 Thrombophlebitis 50 1.258
283
MTC150 Mitochondrial Complex V Deficiency, Mitochondrial Type 1 29 1.250
284
c CRD219 Cardiomyopathy, Infantile Hypertrophic 34 1.250
285
HYP060 Hyperinsulinism 53 1.242
286
P NPH012 Nephrotic Syndrome 61 1.242
287
c ACT135 Acute Graft Versus Host Disease 51 1.240
288
P TXP001 Toxoplasmosis 59 1.239
289
INS024 Insulin-Like Growth Factor I 77 1.233
290
DNG003 Dengue Disease 65 1.233
291
ILS001 Ileus 49 1.233
292
P HYP098 Hypereosinophilic Syndrome 66 1.231
293
HRD090 Harderoporphyria 25 1.227
294
CHL014 Cholera 62 1.225
295
P THR014 Thrombocytopenia 66 1.225
296
TRY001 Trypanosomiasis 50 1.224
297
P MSC005 Muscular Dystrophy 66 1.224
298
XLN067 X-Linked Protoporphyria 19 1.220
299
P ART022 Arthritis 70 1.215
300
ADN018 Adenoma 58 1.211
301
P OLG002 Oligodendroglioma 66 1.207
302
PST011 Pustulosis of Palm and Sole 52 1.207
303
CHL065 Cholangiocarcinoma 57 1.206
304
INT079 Intrahepatic Cholangiocarcinoma 51 1.206
305
CTN007 Cutaneous Leishmaniasis 61 1.206
306
GLB001 Gilbert Syndrome 53 1.203
307
ART002 Arts Syndrome 66 1.196
308
c OPT053 Optic Atrophy 1 62 1.194
309
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 1.180
310
ACQ007 Acquired Immunodeficiency Syndrome 58 1.173
311
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.172
312
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.172
313
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.172
314
ANT039 Antisynthetase Syndrome 55 1.172
315
TLN003 Telangiectasis 51 1.167
316
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.165
317
P SKN015 Skin Carcinoma 71 1.165
318
P ATX030 Ataxia-Telangiectasia 80 1.156
319
P MYC008 Myocarditis 59 1.156
320
BRN002 Bronchiolitis 57 1.153
321
c HMG003 Hemoglobin E Disease 41 1.149
322
c ACT068 Acute Cystitis 60 1.141
323
CRY005 Cryptococcosis 61 1.141
324
P END033 Endocarditis 58 1.136
325
c SVR005 Severe Pre-Eclampsia 49 1.134
326
ACT017 Acute Chest Syndrome 50 1.132
327
FLR002 Filariasis 55 1.132
328
YLL002 Yellow Fever 61 1.132
329
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.124
330
OCL069 Ocular Motor Apraxia 57 1.124
331
ANG054 Angina Pectoris 65 1.124
332
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.124
333
P RCT021 Rectum Cancer 54 1.124
334
P HYP076 Hyperthyroidism 53 1.124
335
c PCH010 Pachyonychia Congenita 3 43 1.123
336
P OBS001 Obstructive Jaundice 49 1.123
337
BRN012 Bronchiolitis Obliterans 56 1.120
338
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.111
339
P BNG032 Benign Mesothelioma 53 1.111
340
P KDN017 Kidney Cancer 60 1.111
341
CNS004 Constipation 56 1.109
342
P RTN024 Retinoblastoma 72 1.106
343
FLR001 Filarial Elephantiasis 59 1.106
344
P PLM034 Pulmonary Emphysema 58 1.098
345
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.097
346
THR123 Thrombotic Microangiopathy 40 1.097
347
GSG001 Gas Gangrene 52 1.087
348
c ACT073 Acute Leukemia 59 1.085
349
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 1.078
350
P GST044 Gastritis 55 1.078
351
P MNC007 Monocytic Leukemia 48 1.078
352
CLN015 Colon Adenocarcinoma 64 1.071
353
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.071
354
MSC157 Muscular Dystrophy, Duchenne Type 78 1.068
355
P MLT020 Multiple Sclerosis 79 1.068
356
DRM006 Dermatitis 61 1.068
357
HPT009 Hepatopulmonary Syndrome 48 1.068
358
SBC016 Subacute Delirium 42 1.068
359
CRH001 Crohn's Disease 80 1.068
360
P SDR002 Siderosis 42 1.066
361
HPT019 Hepatic Encephalopathy 59 1.058
362
HPT004 Hepatic Coma 43 1.058
363
c THR092 Thrombophilia Due to Thrombin Defect 74 1.056
364
PRP030 Purpura 54 1.056
365
CHN002 Chancroid 36 1.051
366
RFR010 Refractory Anemia 49 1.051
367
OST159 Osteogenic Sarcoma 66 1.047
368
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.047
369
MCL057 Macular Dystrophy with Central Cone Involvement 28 1.047
370
c TYP008 Type 1 Diabetes Mellitus 77 1.036
371
PLG002 Plague 58 1.036
372
INT007 Intermediate Coronary Syndrome 53 1.036
373
P MLN008 Melanoma 75 1.025
374
KWS002 Kawasaki Disease 65 1.024
375
P MYP004 Myopathy 67 1.020
376
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 1.013
377
P AMY004 Amyloidosis 69 1.013
378
PLM001 Pulmonary Tuberculosis 69 1.006
379
c ANM038 Anemia, Autoimmune Hemolytic 63 1.001
380
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 1.001
381
LYM019 Lymphosarcoma 46 1.001
382
GST050 Gastrointestinal System Disease 55 1.001
383
P MTH007 Methemoglobinemia 46 0.999
384
P HRM021 Hair Morphology 2 21 0.989
385
P BRS044 Breast Adenocarcinoma 58 0.989
386
P ENC004 Encephalitis 61 0.989
387
BTN004 Biotin Deficiency 44 0.985
388
CNG034 Congestive Heart Failure 69 0.985
389
P MTC069 Mitochondrial Disorders 57 0.985
390
NTR005 Nutritional Deficiency Disease 60 0.983
391
P NTR004 Neutropenia 62 0.976
392
VSC002 Vascular Dementia 59 0.976
393
c SYS001 Systemic Lupus Erythematosus 85 0.967
394
MDD018 Middle East Respiratory Syndrome 44 0.967
395
PRS129 Prostatic Hyperplasia, Benign 48 0.962
396
PRS021 Prostatic Adenoma 43 0.962
397
P ART023 Arthropathy 59 0.962
398
PRS045 Prostatic Hypertrophy 53 0.962
399
HPT022 Hepatoblastoma 54 0.962
400
P RTN018 Retinal Disease 53 0.958
401
P FRD001 Friedreich Ataxia 62 0.954
402
c GLL024 Gallbladder Disease 1 53 0.948
403
P RTN016 Retinal Degeneration 52 0.948
404
NRL016 Neural Tube Defects 80 0.947
405
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.947
406
ANT042 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis 37 0.947
407
MNN043 Meningioma, Familial 79 0.947
408
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.947
409
BRC012 Brucellosis 66 0.947
410
SCR001 Secretory Meningioma 40 0.947
411
INT395 Intracranial Meningioma 47 0.947
412
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.947
413
PRQ002 Paraquat Poisoning 28 0.947
414
P HYD006 Hydrocephalus 62 0.938
415
P MDL005 Medulloblastoma 75 0.932
416
c SCL052 Scleroderma, Familial Progressive 60 0.932
417
WLL004 Wallerian Degeneration 38 0.932
418
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.928
419
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.928
420
TST044 Testicular Torsion 45 0.928
421
CLR109 Colorectal Adenocarcinoma 50 0.928
422
ANT078 Antipyrine Metabolism 24 0.918
423
P UVT001 Uveitis 57 0.915
424
VRL011 Viral Infectious Disease 60 0.915
425
CYT014 Cytochrome P450 Oxidoreductase Deficiency 35 0.915
426
P ALP008 Alopecia 53 0.915
427
P FML011 Familial Adenomatous Polyposis 70 0.907
428
FWL003 Fowler Urethral Sphincter Dysfunction Syndrome 22 0.907
429
GST045 Gastroenteritis 58 0.907
430
P URN019 Urinary Tract Infection 48 0.907
431
AML001 Amelanotic Melanoma 37 0.907
432
SPR066 Superficial Siderosis 42 0.907
433
OST017 Osteomyelitis 63 0.905
434
P CLL015 Collagen Disease 47 0.900
435
SLC006 Silicosis 55 0.897
436
ENT004 Enthesopathy 51 0.897
437
PLM033 Pulmonary Embolism 58 0.897
438
HGH043 High Grade Glioma 46 0.896
439
HYP056 Hypoglycemia 65 0.896
440
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.884
441
P FBR017 Fibrosarcoma 55 0.884
442
P RHB003 Rhabdomyosarcoma 66 0.877
443
MCR225 Macrophage Activation Syndrome 45 0.877
444
IGG001 Iga Glomerulonephritis 50 0.872
445
HYP005 Hypokalemia 55 0.872
446
P LYM118 Lymphoma 66 0.859
447
DGR001 Digeorge Syndrome 62 0.859
448
VLV047 Volvulus of Midgut 55 0.859
449
P ESP024 Esophagitis 60 0.859
450
MST005 Mastitis 52 0.859
451
P INF032 Infertility 60 0.859
452
PRP007 Priapism 46 0.859
453
P HMP007 Hemophilia 52 0.859
454
AZS001 Azoospermia 45 0.854
455
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.854
456
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.846
457
c TYR012 Tyrosinemia, Type I 61 0.846
458
P MMB011 Membranous Nephropathy 50 0.846
459
HMN044 Human Immunodeficiency Virus Type 1 76 0.846
460
OBS082 Obstructive Nephropathy 41 0.846
461
P EYD002 Eye Disease 57 0.846
462
c HPT016 Hepatitis B 62 0.846
463
c DLT002 Dilated Cardiomyopathy 79 0.846
464
ATN005 Autonomic Dysfunction 45 0.846
465
P OVR042 Ovarian Cancer 88 0.842
466
GTL001 Gitelman Syndrome 65 0.832
467
PRP027 Peripheral Vascular Disease 71 0.832
468
P LKM062 Leukemia, Acute Lymphoblastic 69 0.832
469
END057 Endometrial Cancer 76 0.832
470
MYC013 Mycobacterium Abscessus 42 0.832
471
PRM329 Premature Aging 36 0.832
472
c ALP101 Alpha-Thalassemia 62 0.825
473
ESN009 Eosinophil Peroxidase Deficiency 29 0.818
474
ONC002 Onchocerciasis 50 0.818
475
P PLY041 Polymyositis 58 0.818
476
PHR003 Pharyngitis 57 0.818
477
P THR015 Thrombophilia 51 0.818
478
CLN044 Colon Adenoma 44 0.818
479
P PLY011 Polycystic Ovary Syndrome 57 0.818
480
SPT005 Spotted Fever 49 0.818
481
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.818
482
c LKM005 Leukemia, T-Cell, Chronic 33 0.818
483
CYN002 Cyanosis, Transient Neonatal 43 0.817
484
P HYP086 Hypothyroidism 68 0.808
485
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.802
486
P HMN010 Hemangioma 61 0.802
487
P BRB001 Beriberi 44 0.802
488
CVD001 Covid-19 59 0.802
489
CRB086 Cerebral Aneurysms 40 0.802
490
c ERY016 Erythropoietic Protoporphyria, Autosomal Recessive 19 0.789
491
FCT001 Factor Viii Deficiency 61 0.785
492
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 25 0.785
493
c HMP029 Hemophilia a 69 0.785
494
MTC087 Mitochondrial Complex Iii Deficiency, Nuclear Type 4 31 0.785
495
CHL123 Chlamydia 58 0.785
496
c JVN010 Juvenile Rheumatoid Arthritis 52 0.785
497
RGH009 Right Atrial Isomerism 57 0.773
498
ATN011 Autoinflammation with Infantile Enterocolitis 46 0.773
499
TXC002 Toxic Encephalopathy 51 0.773
500
PRN011 Pernicious Anemia 52 0.767
501
MLD001 Melioidosis 67 0.767
502
c MST023 Mesothelioma, Malignant 56 0.767
503
DFF005 Diffuse Large B-Cell Lymphoma 55 0.767
504
CNT047 Contact Dermatitis 56 0.767
505
RCK002 Rocky Mountain Spotted Fever 34 0.767
506
PLC005 Placental Insufficiency 55 0.767
507
SNS003 Sensory Peripheral Neuropathy 51 0.767
508
CMM005 Common Cold 55 0.767
509
ORL004 Oral Submucous Fibrosis 56 0.767
510
DGN001 Degenerative Disc Disease 48 0.767
511
PPT005 Peptic Ulcer Disease 58 0.767
512
LWF001 Low-Flow Priapism 16 0.767
513
P FBR031 Febrile Seizures 52 0.767
514
P SCH015 Schizophrenia 74 0.759
515
P PLY019 Polyneuropathy 52 0.759
516
c HPT003 Hepatitis a 63 0.756
517
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.749
518
IRN004 Iron-Refractory Iron Deficiency Anemia 46 0.749
519
CRT015 Carotid Artery Occlusion 45 0.749
520
P ATR011 Atrial Fibrillation 66 0.747
521
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.747
522
INT030 Intracranial Aneurysm 55 0.747
523
PPL022 Papilloma 53 0.747
524
CNN005 Connective Tissue Disease 66 0.747
525
SQM002 Squamous Cell Papilloma 45 0.747
526
SYN007 Synovitis 54 0.747
527
MCP006 Mucoepidermoid Carcinoma 48 0.747
528
PLC002 Plica Syndrome 35 0.747
529
ALC006 Alcoholic Hepatitis 61 0.747
530
HNC001 Henoch-Schoenlein Purpura 56 0.747
531
DNG002 Dengue Hemorrhagic Fever 59 0.747
532
GT001 Gout 63 0.747
533
FST010 Fasting Hypoglycemia 33 0.747
534
THY029 Thyroid Carcinoma 55 0.747
535
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.738
536
P CYS018 Cystitis 58 0.738
537
STT001 Status Epilepticus 58 0.738
538
NRM005 Neuromuscular Disease 62 0.738
539
P CTR002 Cataract 59 0.738
540
c HMG029 Hemoglobin Se Disease 41 0.738
541
CTS002 Cat-Scratch Disease 42 0.727
542
P FNC004 Fanconi Syndrome 60 0.727
543
CND006 Candida Glabrata 29 0.727
544
P NSP012 Nasopharyngeal Carcinoma 60 0.724
545
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.724
546
LPT014 Leptin Deficiency or Dysfunction 77 0.724
547
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.724
548
CLR030 Clear Cell Renal Cell Carcinoma 53 0.724
549
HYD002 Hydronephrosis 58 0.724
550
MYC005 Myocardial Stunning 45 0.724
551
ACT119 Acute Promyelocytic Leukemia 62 0.715
552
P BND020 Bone Disease 60 0.715
553
CLR108 Colorectal Adenoma 63 0.715
554
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.703
555
BCT021 Bacterial Sepsis 43 0.703
556
PST010 Pasteurellosis 38 0.703
557
CRY003 Cryptosporidiosis 55 0.703
558
BRN024 Bronchitis 67 0.703
559
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.703
560
P HRS035 Hirschsprung Disease 1 66 0.697
561
c SPN225 Spondyloarthropathy 1 70 0.697
562
SPP011 Suppression of Tumorigenicity 12 61 0.697
563
GST019 Gastrointestinal Stromal Tumor 78 0.697
564
P BLD062 Bile Duct Cancer 69 0.697
565
MST004 Mast Cell Neoplasm 41 0.697
566
SPN051 Spondylitis 51 0.697
567
EXT007 Extracutaneous Mastocytoma 38 0.697
568
INF009 Inflammatory Spondylopathy 30 0.697
569
P ESN008 Eosinophilic Pneumonia 50 0.697
570
P MTR012 Mitral Valve Disease 57 0.697
571
PLM035 Pulmonary Eosinophilia 49 0.697
572
c BSL007 Basal Cell Carcinoma 67 0.690
573
TCK004 Tick Infestation 29 0.690
574
ADL030 Adult-Onset Still's Disease 59 0.690
575
c ATS210 Autosomal Recessive Sideroblastic Anemia 31 0.690
576
CRB090 Cerebral Hypoxia 42 0.690
577
VRC005 Varicose Veins 59 0.677
578
CRV035 Cervical Cancer 72 0.677
579
HMN047 Human Cytomegalovirus Infection 59 0.677
580
P VNT002 Ventricular Septal Defect 58 0.677
581
VCC001 Vaccinia 49 0.677
582
CHR546 Chronic Mountain Sickness 43 0.677
583
MLT001 Multiple Chemical Sensitivity 38 0.677
584
HPT014 Hepatorenal Syndrome 49 0.677
585
P TRM003 Tremor 50 0.677
586
P LKM071 Leukemia, Chronic Lymphocytic 74 0.663
587
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.663
588
TST015 Testicular Disease 42 0.663
589
KHN001 Kuhnt-Junius Degeneration 48 0.663
590
HMG009 Hemoglobin Zurich 21 0.663
591
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.662
592
CRN020 Coronary Restenosis 39 0.662
593
GNG013 Gingivitis 59 0.662
594
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.649
595
P PHT010 Photoparoxysmal Response 1 46 0.649
596
HRT037 Heart and Brain Malformation Syndrome 32 0.649
597
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 35 0.649
598
P SPP010 Suppressor of Tumorigenicity 3 50 0.649
599
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.649
600
c THY056 Thyroid Dyshormonogenesis 3 32 0.649
601
RBF001 Riboflavin Deficiency 49 0.649
602
TLR001 Tularemia 56 0.649
603
MNN009 Meningoencephalitis 47 0.649
604
BBN001 Bubonic Plague 40 0.649
605
P FCL005 Focal Segmental Glomerulosclerosis 57 0.649
606
P DMN002 Dementia 65 0.649
607
MST020 Mast Cell Activation Syndrome 27 0.649
608
BCL011 Bacillary Angiomatosis 29 0.633
609
RTN017 Retinal Detachment 60 0.633
610
CRD132 Cardiac Conduction Defect 59 0.633
611
c BRN108 Branchiootic Syndrome 1 63 0.633
612
c HNT010 Huntington Disease-Like 1 54 0.633
613
SBC001 Subacute Sclerosing Panencephalitis 53 0.633
614
MTC209 Mitochondrial Complex Iv Deficiency, Nuclear Type 6 24 0.633
615
HMN004 Hemangioma of Liver 34 0.633
616
c HMG001 Hemoglobin C Disease 41 0.633
617
P SYS005 Systemic Scleroderma 73 0.633
618
GTR002 Goiter 52 0.633
619
PPT001 Peptic Esophagitis 51 0.633
620
PLR008 Pleurisy 49 0.633
621
P LCT001 Lactic Acidosis 50 0.633
622
P AXN001 Axonal Neuropathy 33 0.633
623
P BRN022 Bronchiectasis 59 0.633
624
P HRP006 Herpes Simplex 65 0.633
625
ANG037 Angiomatosis 31 0.633
626
MNG007 Manganese Poisoning 28 0.633
627
END072 Endotheliitis 36 0.632
628
c MJR022 Major Affective Disorder 8 37 0.617
629
P APL001 Aplastic Anemia 72 0.617
630
FBR099 Fibromuscular Dysplasia, Arterial 23 0.617
631
P RST001 Restless Legs Syndrome 52 0.617
632
c MJR024 Major Affective Disorder 9 40 0.617
633
P EXN002 Exanthem 58 0.617
634
PLY001 Polycythemia Vera 69 0.617
635
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 0.617
636
HYP781 Hypoascorbemia 52 0.617
637
FRN006 Frontotemporal Dementia 68 0.617
639
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 30 0.617
640
c DMN023 Diamond-Blackfan Anemia 1 68 0.617
641
IGR001 Ige Responsiveness, Atopic 58 0.617
642
P MYG005 Myoglobinuria 40 0.617
643
P INC035 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 3 26 0.617
644
ESP002 Esophageal Varix 51 0.617
645
P HMR003 Hemorrhagic Disease 59 0.617
646
NRT004 Neuritis 53 0.617
647
P PYL005 Pyelonephritis 56 0.617
648
ATR003 Atrophic Rhinitis 40 0.617
649
ELP001 Elephantiasis 43 0.617
650
P BPL003 Bipolar Disorder 56 0.617
651
P INT068 Intestinal Disease 53 0.617
652
P CND004 Candidiasis 57 0.617
653
BTT017 Beta-Thalassemia Major 54 0.617
654
INS001 Insulinoma 59 0.617
655
INT060 Intestinal Atresia 40 0.617
656
PRM013 Premature Menopause 57 0.617
657
OCL006 Ocular Hypertension 53 0.617
658
P MSC003 Muscular Atrophy 52 0.617
659
P NRV007 Nervous System Disease 65 0.617
660
P INS002 in Situ Carcinoma 52 0.617
661
HVY002 Heavy Metal Poisoning 22 0.617
662
P MRC003 Mercury Poisoning 48 0.617
663
GLM044 Glomerular Disease 34 0.617
664
c RNG015 Ring Chromosome 2 22 0.617
665
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.598
666
c PRG020 Paragangliomas 3 39 0.598
667
c WLM013 Wilms Tumor 1 65 0.598
668
LYM133 Lymphoma, Hodgkin, Classic 69 0.598
669
P MCR129 Microvascular Complications of Diabetes 1 67 0.598
670
c MCR112 Microvascular Complications of Diabetes 2 42 0.598
671
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 67 0.598
672
P HYP750 Hypertriglyceridemia, Familial 61 0.598
673
HRN029 Hearing Loss, Noise-Induced 37 0.598
674
INT051 Intussusception 53 0.598
675
P PLG001 Pelger-Huet Anomaly 51 0.598
676
HLC007 Helicobacter Pylori Infection 67 0.598
677
P PLY014 Polycystic Kidney Disease 71 0.598
678
P HYP069 Hyperparathyroidism 62 0.598
679
VLV010 Vulvovaginitis 42 0.598
680
c CNT035 Central Nervous System Disease 53 0.598
681
LYM027 Lymphopenia 56 0.598
682
c MLG069 Malignant Hypertension 46 0.598
683
SCR011 Scrapie 39 0.598
684
BWN006 Bowen's Disease 32 0.598
685
KDN013 Kidney Hypertrophy 33 0.598
686
OVR094 Ovarian Epithelial Cancer 39 0.598
687
PCH007 Pouchitis 42 0.598
688
INF034 Infective Endocarditis 53 0.578
689
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.578
690
BSM002 Bosma Arhinia Microphthalmia Syndrome 44 0.578
691
MSC007 Muscle Hypertrophy 64 0.578
692
c PNC106 Pancreatic Agenesis 1 51 0.578
693
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.578
694
MTH071 Methane Production 24 0.578
695
HYP856 Hypothyroidism, Central, with Testicular Enlargement 38 0.578
696
c ART101 Aortic Valve Disease 2 65 0.578
698
c THR071 Thrombocytopenia 1 48 0.578
699
ADN027 Adenomyosis 59 0.578
700
P ADL017 Adult T-Cell Leukemia 53 0.578
701
TRN004 Trench Fever 28 0.578
702
PNC001 Pancytopenia 52 0.578
703
P MLN007 Male Infertility 56 0.578
704
c HRD026 Hereditary Ataxia 46 0.578
705
END011 Endometriosis of Ovary 40 0.578
706
MSN003 Mesenteric Vascular Occlusion 24 0.578
707
INT020 Intravenous Leiomyomatosis 35 0.578
708
LMY003 Leiomyomatosis 43 0.578
709
PNC034 Pancreas Disease 49 0.578
710
PRM236 Primary Biliary Cholangitis 62 0.578
711
P LKD001 Leukodystrophy 58 0.578
712
AMN003 Amnestic Disorder 53 0.578
713
c PRM005 Primary Hyperparathyroidism 59 0.578
714
P FML340 Familial Episodic Pain Syndrome 50 0.578
715
HLL004 Hellp Syndrome 53 0.578
716
ACH005 Achalasia 54 0.578
717
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.578
718
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.578
719
IDP093 Idiopathic Gastroparesis 28 0.578
720
HST016 Histiocytic Sarcoma 38 0.578
721
LKP003 Leukoplakia 39 0.578
722
FTL004 Fetal Erythroblastosis 33 0.576
723
P ALP009 Alopecia Areata 59 0.576
724
ISC015 Ischemic Colitis 43 0.555
725
c FNC027 Fanconi Anemia, Complementation Group a 80 0.555
726
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.555
727
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.555
728
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.555
729
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.555
730
P MYM013 Moyamoya Disease 1 59 0.555
731
BDD001 Budd-Chiari Syndrome 62 0.555
732
c LKM070 Leukemia, Acute Monocytic 56 0.555
733
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 55 0.555
734
c LNG109 Lung Cancer Susceptibility 1 26 0.555
735
P SLM003 Salmonellosis 54 0.555
736
CMB007 Combined Immunodeficiency 56 0.555
737
PNM005 Pneumonic Plague 46 0.555
738
TTH006 Tooth Disease 51 0.555
739
LNG091 Lung Mucoepidermoid Carcinoma 32 0.555
740
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.555
741
P ANT006 Antiphospholipid Syndrome 55 0.555
742
GST010 Gestational Trophoblastic Neoplasm 52 0.555
743
ALL010 Allergic Contact Dermatitis 55 0.555
744
P CHR071 Charcot-Marie-Tooth Disease 64 0.555
745
ALC009 Alcoholic Liver Cirrhosis 54 0.555
746
GST040 Gastric Adenocarcinoma 66 0.555
747
c LCL006 Localized Scleroderma 64 0.555
748
MYP009 Myopathy with Deficiency of Iscu 12 0.555
749
ACT200 Acute Monoblastic Leukemia 40 0.555
750
BBS001 Babesiosis 48 0.555
751
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.555
753
ATY012 Atypical Mycobacteriosis, Familial 34 0.555
754
WRM004 Warm Antibody Hemolytic Anemia 19 0.555
755
c HRD088 Hereditary Neuropathies 34 0.555
756
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.547
757
P FNG006 Feingold Syndrome 1 61 0.547
758
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.547
759
P HMN038 Human Coronavirus Sensitivity 30 0.547
760
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.547
761
HMR039 Hemorrhage, Intracerebral 57 0.547
762
ADL002 Adult Syndrome 69 0.547
763
APN008 Apnea, Obstructive Sleep 66 0.547
764
c BLD140 Blood Group, I System 47 0.547
765
SPR126 Superior Semicircular Canal Dehiscence 41 0.547
766
HMT002 Hematologic Cancer 61 0.547
767
CHR682 Chronic Bilirubin Encephalopathy 37 0.547
768
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 39 0.528
769
P CTN015 Cutaneous T Cell Lymphoma 48 0.528
770
PNG002 Pain Agnosia 51 0.528
771
TCK001 Tick-Borne Encephalitis 58 0.528
772
HNZ004 Heinz Body Anemias 40 0.528
773
PHS021 Phosphoglycerate Dehydrogenase Deficiency 46 0.528
774
AGM019 Agammaglobulinemia, X-Linked 71 0.528
775
c THY107 Thymoma, Familial 42 0.528
776
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.528
777
CHR005 Chorioamnionitis 50 0.528
778
ZKF001 Zika Fever 51 0.528
779
NDL001 Nodular Malignant Melanoma 44 0.528
780
OST003 Osteonecrosis 60 0.528
781
TCL003 T Cell Deficiency 44 0.528
782
PRM003 Premature Ejaculation 44 0.528
783
P TMP001 Temporal Lobe Epilepsy 49 0.528
784
P THY023 Thymoma 64 0.528
785
PRS036 Parasitic Protozoa Infectious Disease 44 0.528
786
NNS002 Nonspecific Interstitial Pneumonia 42 0.528
787
CRT016 Carotid Artery Disease 52 0.528
788
P BNC003 Bone Cancer 58 0.528
789
TRC003 Trichomoniasis 53 0.528
790
BRN014 Bronchopneumonia 52 0.528
791
HMP001 Hemopericardium 47 0.528
792
c LRG001 Large Cell Carcinoma 48 0.528
793
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.528
794
P MTR014 Motor Neuron Disease 65 0.528
795
RTR008 Root Resorption 44 0.528
796
ART004 Aortic Atherosclerosis 46 0.528
797
P AGM001 Agammaglobulinemia 67 0.528
798
c FML015 Familial Nephrotic Syndrome 48 0.528
799
ART006 Arthus Reaction 40 0.528
800
LST001 Listeriosis 59 0.528
801
P PRC012 Pericardial Effusion 50 0.528
802
TXC004 Toxic Diffuse Goiter 24 0.528
803
JPN002 Japanese Encephalitis 61 0.528
804
TNG007 Tongue Carcinoma 55 0.528
805
PYL006 Pyloric Stenosis 48 0.528
806
P KRT007 Keratoconus 49 0.528
807
P OVR046 Ovarian Cyst 43 0.528
808
SZR001 Sezary's Disease 60 0.528
809
CRD016 Cardiac Rupture 34 0.528
810
P FML187 Familial Hypertension 34 0.528
811
c ATM075 Autoimmune Encephalitis 39 0.528
812
CRR012 Cirrhotic Cardiomyopathy 22 0.528
813
SPS019 Spastic Paraparesis 38 0.528
814
HMM004 Hamamy Syndrome 39 0.493
815
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.493
816
DNG001 Dengue Shock Syndrome 40 0.493
817
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.493
818
c ART115 Aortic Valve Disease 1 72 0.493
819
ALK013 Alkaptonuria 58 0.493
820
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.493
821
PNM010 Pneumothorax, Primary Spontaneous 58 0.493
822
STR033 Storm Syndrome 28 0.493
823
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 0.493
824
RHB024 Rhabdomyosarcoma 2 65 0.493
825
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.493
826
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.493
827
BRG013 Buerger Disease 56 0.493
828
c DPH024 Diaphragmatic Hernia, Congenital 63 0.493
829
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.493
830
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.493
831
P INT099 Intrahepatic Cholestasis of Pregnancy 61 0.493
832
SLD003 Sialadenitis 47 0.493
833
INT067 Interstitial Nephritis 46 0.493
834
PNM008 Pneumothorax 54 0.493
835
OLG022 Oligoasthenoteratozoospermia 36 0.493
836
SBP001 Subependymal Giant Cell Astrocytoma 45 0.493
837
OVR063 Overnutrition 42 0.493
838
LYM017 Lyme Disease 63 0.493
839
P MTR003 Mitral Valve Stenosis 53 0.493
840
AVN001 Avian Influenza 61 0.493
841
RTR001 Retrograde Amnesia 41 0.493
842
c ESS001 Essential Tremor 56 0.493
843
HRT012 Heart Valve Disease 53 0.493
844
LNG039 Lung Squamous Cell Carcinoma 57 0.493
845
PLR007 Pleural Empyema 50 0.493
846
P TRT010 Teratoma 50 0.493
847
CRN030 Coronary Stenosis 50 0.493
848
END062 Endometrial Hyperplasia 47 0.493
849
BTT018 Beta-Thalassemia Intermedia 31 0.493
850
OLG001 Oligospermia 45 0.493
851
P HYP009 Hypertrophic Pyloric Stenosis 41 0.493
852
VRC001 Varicocele 48 0.493
853
c PST005 Posterior Uveitis 54 0.493
854
MXD005 Mixed Connective Tissue Disease 57 0.493
855
SPT004 Septic Arthritis 58 0.493
856
ART010 Arteriolosclerosis 37 0.493
857
ART012 Aortitis 41 0.493
858
BNT001 Banti's Syndrome 21 0.493
859
LSS003 Lassa Fever 49 0.493
860
SKN019 Skin Melanoma 70 0.493
861
TRC020 Tracheitis 43 0.493
862
CMP064 Complement Component 3 Deficiency 34 0.493
863
P HMR005 Hemorrhoid 49 0.493
864
BRK012 Broken Heart Syndrome 42 0.493
865
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 54 0.493
866
OPD006 Opioid Addiction 48 0.493
867
IRR002 Irritable Bowel Syndrome 64 0.493
868
RFR003 Refractive Error 41 0.493
869
c AMY009 Amyloidosis Aa 47 0.493
870
PLY100 Polyploidy 36 0.493
871
SRF006 Surfactant Dysfunction 33 0.493
872
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 38 0.493
873
RFR009 Refractory Cytopenia with Multilineage Dysplasia 30 0.493
874
VRL017 Viral Hemorrhagic Fever 35 0.493
875
MYL013 Myeloperoxidase Deficiency 44 0.467
876
P INT260 Intracranial Berry Aneurysm 40 0.408
877
TBC004 Tobacco Addiction 63 0.408
878
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.408
879
c PRG019 Paragangliomas 2 30 0.408
880
CVR006 Cavernous Hemangioma 51 0.408
881
TRC022 Tricuspid Valve Insufficiency 46 0.408
882
P HYP024 Hypoparathyroidism 55 0.408
883
EXP004 Exophthalmos 50 0.408
884
UNS001 Unstable Hemoglobin Disease 7 0.408
885
PST046 Post-Transplant Lymphoproliferative Disease 53 0.408
886
c DWL002 Dowling-Degos Disease 1 58 0.400
887
RCK004 Rickets 64 0.391
888
CYT018 Cytochrome P450 2d6 Variant 26 0.391
889
P HYP077 Hypertrichosis 48 0.381
890
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.372
891
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.372
892
c ERY064 Erythrocytosis, Familial, 6 30 0.362
893
HRW001 Hair Whorl 35 0.352
894
GST023 Gastric Ulcer 52 0.341
895
ARG004 Argyria 26 0.341
896
PLY150 Polykaryocytosis Inducer 29 0.330
897
ATN004 Autonomic Neuropathy 42 0.330
898
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.319
899
P OST002 Osteoporosis 76 0.319
900
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.319
901
MTC005 Mitochondrial Metabolism Disease 44 0.319
902
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.295
903
c EXD008 Exudative Vitreoretinopathy 1 71 0.295
904
KRT009 Keratosis 52 0.295
905
PYR009 Pyridoxine Deficiency Anemia 35 0.295
906
c FML324 Familial Porphyria Cutanea Tarda 29 0.295
907
P ACN011 Acne 55 0.283
908
MTB004 Metabolic Acidosis 48 0.270
909
ANX010 Anxiety 70 0.270
910
MYL005 Myelofibrosis 70 0.270
911
P ASP006 Aspergillosis 71 0.270
912
TTN003 Tetanus 64 0.270
913
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 39 0.270
914
CRB011 Cerebrotendinous Xanthomatosis 64 0.256
915
c PRP091 Porphyria Cutanea Tarda, Type I 30 0.256
916
XNT003 Xanthomatosis 48 0.256
917
ADR051 Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency 43 0.256
918
HMR023 Hemorrhagic Cystitis 43 0.256
919
BRR014 Barrett Esophagus 66 0.256
920
CRC021 Carcinosarcoma 62 0.256
921
DMY004 Demyelinating Disease 50 0.256
922
HNS001 Hansen's Disease 32 0.256
924
CLF051 Cleft Larynx, Posterior 27 0.241
925
c PRM032 Primary Congenital Glaucoma 40 0.241
926
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.241
927
P LPR021 Leprosy 3 71 0.241
928
P VTM036 Vitamin D-Dependent Rickets 40 0.241
929
c HMC009 Hemochromatosis Type 2 58 0.241
930
STR008 Strongyloidiasis 52 0.241
931
CHL004 Cholelithiasis 48 0.241
932
CLS034 Clostridium Septicum Infection 13 0.241
933
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 0.241
934
SPR032 Superficial Siderosis of the Central Nervous System 23 0.241
935
c MGR028 Migraine with or Without Aura 1 63 0.226
936
HYP765 Hyperbilirubinemia, Shunt, Primary 17 0.226
937
c CNG006 Congenital Hypothyroidism 63 0.226
938
DBN001 Dubin-Johnson Syndrome 58 0.226
939
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.226
940
THR051 Thrombocytopenia with Beta-Thalassemia, X-Linked 44 0.226
941
P ANP001 Anaplastic Large Cell Lymphoma 59 0.226
942
LPT001 Leptospirosis 65 0.226
943
MGL001 Megaloblastic Anemia 59 0.226
944
P GLL022 Guillain-Barre Syndrome 59 0.226
945
P DRM010 Dermatomyositis 61 0.226
946
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.226
947
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.209
948
ALC007 Alcohol Dependence 65 0.209
949
VTM002 Vitamin B12 Deficiency 48 0.209
950
PHN003 Phenylketonuria 76 0.209
951
PSD014 Pseudopseudohypoparathyroidism 54 0.209
952
P DRR001 Diarrhea 55 0.209
953
PRP016 Paraplegia 52 0.209