Search results for heme

1626 hits were found for heme

# Family MCID Name MIFTS Score
1
HMX003 Heme Oxygenase 1 Deficiency 27 35.176
2
P PRP029 Porphyria 60 31.001
3
c PRT132 Protoporphyria, Erythropoietic, 1 61 22.503
4
IRN002 Iron Metabolism Disease 57 18.045
5
HLX001 Helix Syndrome 48 15.846
6
DFC004 Deficiency Anemia 74 15.439
7
P ATS324 Autosomal Erythropoietic Protoporphyria 24 12.649
8
BLR008 Bilirubin Metabolic Disorder 57 12.546
9
P SCK005 Sickle Cell Disease 56 12.385
10
ISC004 Ischemia 61 11.899
11
PRP083 Porphyria, Acute Intermittent 65 11.803
12
P RRH023 Rare Hereditary Hemochromatosis 54 11.088
13
HYP266 Hypoxia 57 10.957
14
ACT098 Acute Erythroid Leukemia 55 10.682
15
HMS001 Hemosiderosis 48 10.515
16
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 10.170
17
IRN001 Iron Deficiency Anemia 58 9.954
18
ACT078 Acute Porphyria 49 9.661
19
MLR004 Malaria 80 9.392
20
P HML002 Hemolytic Anemia 62 9.283
21
HMP009 Haemophilus Influenzae 41 9.162
22
c ACT071 Acute Kidney Failure 60 8.532
23
P SDR003 Sideroblastic Anemia 51 8.449
24
VRG001 Variegate Porphyria 56 8.375
25
P THL005 Thalassemia 56 8.270
26
PRP082 Porphyria, Congenital Erythropoietic 56 8.237
27
c PRC016 Pre-Eclampsia 65 8.031
28
P MYC084 Mycobacterium Tuberculosis 1 68 7.947
29
P PRP003 Porphyria Cutanea Tarda 66 7.589
30
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 7.585
31
ATH013 Atherosclerosis Susceptibility 63 7.332
32
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 7.248
33
P PLM037 Pulmonary Hypertension 72 7.099
34
P VSC007 Vascular Disease 63 6.961
35
P PRD008 Periodontitis 64 6.922
36
P ALZ034 Alzheimer Disease 87 6.882
37
HYP066 Hyperglycemia 61 6.690
38
CHG001 Chagas Disease 66 6.281
39
BRN071 Brain Injury 50 6.242
40
RPD005 Rapidly Involuting Congenital Hemangioma 46 6.198
41
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 6.189
42
P NRB001 Neuroblastoma 66 6.043
43
CPR004 Coproporphyria, Hereditary 57 6.027
44
NNT012 Neonatal Jaundice 53 6.024
45
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.013
46
HMG005 Hemoglobinopathy 56 5.970
47
P CRD246 Cardiovascular System Disease 56 5.958
48
P ADL010 Adult Respiratory Distress Syndrome 71 5.938
49
CLT003 Colitis 63 5.821
50
PRT251 Proteinuria, Chronic Benign 57 5.821
51
48X005 48,xyyy 39 5.782
52
P LVR013 Liver Disease 69 5.707
53
CRB004 Cerebral Artery Occlusion 45 5.692
54
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 5.623
55
c TYP009 Type 2 Diabetes Mellitus 92 5.582
56
SCK003 Sickle Cell Anemia 74 5.513
57
c HMC039 Hemochromatosis, Type 1 73 5.487
58
FTT001 Fatty Liver Disease 62 5.468
59
BCT022 Bacterial Infectious Disease 56 5.459
61
CYT002 Cytokine Deficiency 43 5.331
62
P KDN018 Kidney Disease 72 5.250
63
47X002 47,xyy 48 5.232
64
P BCL017 B-Cell Lymphoma 59 5.107
65
P MYC007 Myocardial Infarction 70 5.092
66
P KLZ004 Kala-Azar 1 41 5.033
67
LSH001 Leishmaniasis 64 5.033
68
c PRD040 Periodontitis, Chronic 52 4.983
69
AGN016 Aging 54 4.972
70
TRM010 Traumatic Brain Injury 51 4.911
71
BRN004 Brain Edema 54 4.824
72
c ACT027 Acute Pancreatitis 60 4.812
73
LNG099 Lung Disease 62 4.806
74
CHL068 Cholestasis 61 4.787
75
c BTT014 Beta-Thalassemia 72 4.772
76
ANT024 Anthrax Disease 58 4.728
77
P PRK057 Parkinson Disease, Late-Onset 80 4.726
78
P CRN300 Coronary Heart Disease 1 73 4.658
79
CTN011 Cutaneous Porphyria 45 4.651
80
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.622
81
PRT037 Pertussis 65 4.615
82
RNL077 Renal Fibrosis 46 4.586
83
P PLM036 Pulmonary Fibrosis 66 4.563
84
LPP008 Lipoprotein Quantitative Trait Locus 65 4.533
85
c MCR130 Microvascular Complications of Diabetes 6 41 4.493
86
c MCR120 Microvascular Complications of Diabetes 7 47 4.493
87
c MCR113 Microvascular Complications of Diabetes 3 52 4.493
88
c MCR133 Microvascular Complications of Diabetes 4 41 4.493
89
SPN186 Spinal Cord Injury 61 4.487
90
LVR012 Liver Cirrhosis 63 4.417
91
MCR018 Microcytic Anemia 47 4.412
92
MYL009 Myelodysplastic Syndrome 67 4.405
93
P DBT009 Diabetes Mellitus 67 4.398
94
c ACT134 Acute Liver Failure 59 4.372
95
P PNC044 Pancreatitis 61 4.370
96
PRT013 Portal Hypertension 59 4.367
97
TXC005 Toxic Shock Syndrome 62 4.315
98
HMG002 Hemoglobinuria 50 4.310
99
PPL052 Papillomatosis, Confluent and Reticulated 34 4.294
100
NNL006 Non-Alcoholic Steatohepatitis 54 4.280
101
ALL014 Allergic Encephalomyelitis 34 4.242
102
OTT002 Otitis Media 71 4.231
103
HYP001 Hypochromic Microcytic Anemia 37 4.231
104
c ANM036 Anemia, Sideroblastic, 1 56 4.196
105
P PHC003 Pheochromocytoma 69 4.184
106
ADR040 Adrenal Gland Pheochromocytoma 46 4.184
107
P INF037 Inflammatory Bowel Disease 53 4.173
108
ANX004 Anoxia 40 4.110
109
c PLM164 Pulmonary Hypertension, Primary, 1 76 4.062
110
GLL048 Glial Tumor 52 4.001
111
PLM010 Pulmonary Edema 55 4.001
112
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.973
113
GLM045 Glioma 63 3.957
114
P MYL006 Myeloid Leukemia 61 3.947
115
c BRS111 Breast-Ovarian Cancer, Familial 2 53 3.919
116
GLB002 Glioblastoma 67 3.894
117
c ACT075 Acute Myocardial Infarction 56 3.885
118
P DMN001 Diamond-Blackfan Anemia 71 3.872
119
ART140 Arteries, Anomalies of 53 3.865
120
c CHR684 Chronic Kidney Disease 69 3.860
121
c HPT001 Hepatitis C 62 3.835
122
P LNG064 Lung Cancer Susceptibility 3 70 3.815
123
ART016 Aortic Aneurysm 68 3.811
124
PRT036 Peritonitis 65 3.795
125
THR024 Thrombosis 56 3.730
126
P LTR001 Lateral Sclerosis 58 3.656
127
c AMY091 Amyotrophic Lateral Sclerosis 1 88 3.614
128
P NRP001 Neuropathy 60 3.603
129
P END044 Endometriosis 62 3.583
130
LMB062 Limb Ischemia 55 3.576
131
c ATR087 Atrial Standstill 1 74 3.572
132
c LKM063 Leukemia, Chronic Myeloid 71 3.544
133
MLD018 Mild Cognitive Impairment 48 3.542
134
c INH020 Inherited Metabolic Disorder 48 3.537
136
SPL018 Splenomegaly 49 3.494
137
ACT003 Acute Kidney Tubular Necrosis 46 3.473
138
P TYR004 Tyrosinemia 50 3.473
139
P HML001 Hemolytic-Uremic Syndrome 52 3.447
140
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 3.441
141
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.440
142
P DNG005 Dengue Virus 56 3.425
143
P HMC002 Homocystinuria 53 3.423
144
IMP005 Impotence 52 3.423
145
SKN016 Skin Disease 63 3.398
146
P HRT032 Heart Disease 81 3.396
147
P ECL001 Eclampsia 52 3.386
148
P ART021 Arteriosclerosis 54 3.386
149
GST033 Gestational Diabetes 61 3.378
150
LGH007 Leigh Syndrome 70 3.373
151
c HYP836 Hypercholesterolemia, Familial, 1 73 3.359
152
PST036 Posterior Column Ataxia with Retinitis Pigmentosa 38 3.357
153
ATS010 Autosomal Recessive Disease 42 3.355
154
URT010 Ureteral Obstruction 45 3.347
155
DSS032 Disease by Infectious Agent 55 3.343
156
P LKM002 Leukemia 67 3.342
157
c LKM061 Leukemia, Acute Myeloid 83 3.332
158
DPH001 Diphtheria 59 3.321
159
BNR002 Bone Resorption Disease 47 3.317
160
P PNC035 Pancreatic Cancer 86 3.275
161
GST037 Gastroparesis 52 3.267
162
P ENC018 Encephalopathy 62 3.265
163
c MCR115 Microvascular Complications of Diabetes 5 65 3.262
164
P PRP019 Peripheral Nervous System Disease 58 3.258
165
c HPT073 Hepatitis C Virus 71 3.255
166
HRM022 Hair Morphology 1 11 3.242
167
ULC004 Ulcerative Colitis 74 3.242
168
ENT011 Enterocolitis 55 3.209
169
P BLD134 Bladder Cancer 79 3.205
170
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.177
171
XLN067 X-Linked Protoporphyria 19 3.158
172
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.148
173
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.148
174
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.148
175
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 3.148
176
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 3.148
177
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.148
178
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 3.148
179
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.148
180
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.148
181
P RSP003 Respiratory Failure 74 3.148
182
P SLP006 Sleep Apnea 69 3.135
183
ANR040 Aneurysm 61 3.130
184
P PLY018 Polycythemia 56 3.128
185
P KRN004 Kernicterus 46 3.101
186
PLS007 Plasmodium Falciparum Malaria 52 3.101
187
HLT001 Holt-Oram Syndrome 66 3.089
188
c SML038 Small Cell Cancer of the Lung 69 3.073
189
STR067 Stroke, Ischemic 80 3.064
190
CRB039 Cerebrovascular Disease 66 3.064
191
SQM006 Squamous Cell Carcinoma 60 3.058
192
ATM095 Autoimmune Disease 61 3.047
193
BRN056 Bronchopulmonary Dysplasia 56 3.044
194
P HPT023 Hepatocellular Carcinoma 96 3.039
195
END086 End Stage Renal Disease 52 3.022
196
DYS015 Dysentery 50 3.020
197
URM002 Uremia 47 3.014
198
P GLM007 Glomerulonephritis 60 3.001
199
c HYP595 Hypertension, Essential 85 2.998
200
P RHN004 Rhinitis 57 2.995
201
CYS001 Cystic Fibrosis 78 2.992
202
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 2.970
203
SVR004 Severe Combined Immunodeficiency 72 2.963
204
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.952
205
c VRL010 Viral Hepatitis 53 2.933
206
P GST053 Gastric Cancer 83 2.921
207
P AST005 Asthma 76 2.911
208
P PRK039 Parkinsonism 55 2.906
209
P CHR012 Chronic Granulomatous Disease 69 2.896
210
PST092 Posttransplant Acute Limbic Encephalitis 28 2.896
211
P DRM053 Dermatitis, Atopic 65 2.894
212
PST040 Posterior Column Ataxia 23 2.876
213
SLP001 Sleeping Sickness 56 2.876
214
MCR017 Macrocytic Anemia 44 2.869
215
ALL006 Allergic Asthma 56 2.863
216
P HYP061 Hypertrophic Cardiomyopathy 69 2.846
217
ORL015 Oral Squamous Cell Carcinoma 43 2.829
218
P VSC011 Vasculitis 61 2.823
219
P END033 Endocarditis 58 2.819
220
P THR014 Thrombocytopenia 66 2.814
221
P TXP001 Toxoplasmosis 60 2.814
222
VSC003 Visceral Leishmaniasis 55 2.810
223
SVR001 Severe Acute Respiratory Syndrome 67 2.809
224
LPD008 Lipid Metabolism Disorder 62 2.809
225
CHL014 Cholera 62 2.786
226
P SZR006 Seizure Disorder 70 2.785
227
P HNT016 Huntington Disease 73 2.785
228
ORL011 Oral Cancer 60 2.781
229
NRR001 Neuroretinitis 42 2.780
230
RTN023 Retinitis 46 2.780
231
P MTH007 Methemoglobinemia 46 2.777
232
KPS004 Kaposi Sarcoma 77 2.776
233
P HPT021 Hepatitis 69 2.775
234
ADN018 Adenoma 59 2.758
235
P PRS040 Prostate Cancer 95 2.758
236
ESP021 Esophageal Cancer 83 2.758
237
ALL029 Allergic Disease 59 2.754
238
P CLR023 Colorectal Cancer 100 2.753
239
RTN003 Retinal Ischemia 49 2.753
240
P RTN008 Retinitis Pigmentosa 80 2.750
241
P ADN016 Adenocarcinoma 63 2.750
242
P LNG032 Lung Cancer 98 2.743
243
RDC006 Red Cell Aplasia 44 2.743
244
P RHM011 Rheumatoid Arthritis 82 2.743
245
P GLM040 Glioma Susceptibility 1 71 2.743
246
MLG169 Malignant Astrocytoma 57 2.743
247
PLC008 Placenta Disease 49 2.743
248
MYL069 Myeloma, Multiple 77 2.719
249
CNS004 Constipation 56 2.712
250
PRN019 Perinatal Necrotizing Enterocolitis 60 2.707
251
P ANR048 Aniridia 1 64 2.706
252
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 52 2.693
253
DSS009 Disseminated Intravascular Coagulation 57 2.689
254
HMC014 Homocysteinemia 52 2.689
255
ART002 Arts Syndrome 66 2.671
256
GLB001 Gilbert Syndrome 53 2.671
257
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.657
258
SCH014 Schistosomiasis 56 2.657
259
MCR013 Microphthalmia 60 2.657
260
P INF038 Influenza 68 2.653
261
P RNV001 Renovascular Hypertension 49 2.639
262
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 2.625
263
P PRR002 Pure Red-Cell Aplasia 47 2.622
264
P CHR345 Chronic Pain 50 2.622
265
P PNM007 Pneumonia 67 2.603
266
P FRD001 Friedreich Ataxia 61 2.597
267
THR016 Thrombophlebitis 50 2.593
268
P PRP056 Porphyria, Acute Hepatic 49 2.590
269
OST012 Osteoarthritis 77 2.587
270
ACQ007 Acquired Immunodeficiency Syndrome 59 2.579
271
ALL003 Allergic Rhinitis 67 2.570
272
P GRF003 Graft-Versus-Host Disease 71 2.564
273
c CRD219 Cardiomyopathy, Infantile Hypertrophic 34 2.559
274
MTC150 Mitochondrial Complex V Deficiency, Mitochondrial Type 1 29 2.559
275
P SKN015 Skin Carcinoma 71 2.548
276
P SDR002 Siderosis 43 2.541
277
PRP080 Peripheral Artery Disease 54 2.528
278
P NPH012 Nephrotic Syndrome 60 2.525
279
SPN035 Spindle Cell Sarcoma 54 2.516
280
SRC014 Sarcoma 65 2.516
281
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.516
282
INT066 Interstitial Lung Disease 60 2.500
283
INS024 Insulin-Like Growth Factor I 78 2.491
284
ILS001 Ileus 50 2.491
285
DNG003 Dengue Disease 65 2.491
286
c HMG003 Hemoglobin E Disease 42 2.483
287
RFR010 Refractory Anemia 49 2.481
288
CHN002 Chancroid 36 2.481
289
GLC003 Glucose Intolerance 54 2.479
290
TRY001 Trypanosomiasis 50 2.456
291
AMN017 Aminolevulinic Acid Dehydratase Deficiency Porphyria 8 2.452
292
CRY005 Cryptococcosis 60 2.450
293
c ACT068 Acute Cystitis 61 2.450
294
CNG034 Congestive Heart Failure 69 2.450
295
YLL002 Yellow Fever 61 2.416
296
FLR002 Filariasis 55 2.416
297
ACT017 Acute Chest Syndrome 50 2.416
298
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 2.408
299
P CRD119 Cardiac Arrest 67 2.403
300
OST017 Osteomyelitis 63 2.402
301
CHL065 Cholangiocarcinoma 58 2.383
302
CTN007 Cutaneous Leishmaniasis 62 2.383
303
P MSC005 Muscular Dystrophy 67 2.383
304
INT079 Intrahepatic Cholangiocarcinoma 51 2.383
305
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.382
306
ANG054 Angina Pectoris 66 2.382
307
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.382
308
OCL069 Ocular Motor Apraxia 57 2.382
309
P HYP076 Hyperthyroidism 53 2.382
310
P RCT021 Rectum Cancer 54 2.382
311
DBT010 Diabetic Neuropathy 54 2.363
312
TRN015 Transient Cerebral Ischemia 63 2.363
313
P BRS047 Breast Cancer 98 2.354
314
P NTR004 Neutropenia 63 2.346
315
P ART022 Arthritis 71 2.345
316
P PSR002 Psoriasis 63 2.324
317
CHR074 Choriocarcinoma 46 2.322
318
THR004 Thrombocytosis 53 2.322
319
P MYP004 Myopathy 67 2.320
320
P MLT020 Multiple Sclerosis 79 2.310
321
P RTN024 Retinoblastoma 73 2.310
322
FLR001 Filarial Elephantiasis 59 2.310
323
P CRG003 Crigler-Najjar Syndrome, Type I 63 2.274
324
THR123 Thrombotic Microangiopathy 40 2.273
325
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.273
326
P LPS004 Lupus Erythematosus 61 2.273
327
GSG001 Gas Gangrene 52 2.236
328
TLN003 Telangiectasis 51 2.226
329
BTN004 Biotin Deficiency 45 2.217
330
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 2.197
331
P MNC007 Monocytic Leukemia 47 2.197
332
P HYP098 Hypereosinophilic Syndrome 66 2.192
333
P ATX030 Ataxia-Telangiectasia 80 2.184
334
P MLN008 Melanoma 76 2.184
335
P MYC008 Myocarditis 59 2.184
336
CRH001 Crohn's Disease 80 2.157
337
HPT009 Hepatopulmonary Syndrome 48 2.157
338
P GST044 Gastritis 55 2.157
339
DRM006 Dermatitis 62 2.157
340
SBC016 Subacute Delirium 43 2.157
341
P OVR042 Ovarian Cancer 88 2.151
342
PST011 Pustulosis of Palm and Sole 52 2.145
343
MDD018 Middle East Respiratory Syndrome 44 2.144
344
P MTC069 Mitochondrial Disorders 57 2.144
345
CVD001 Covid-19 57 2.140
346
MSC157 Muscular Dystrophy, Duchenne Type 79 2.116
347
P RTN018 Retinal Disease 53 2.106
348
c PRT135 Protoporphyria, Erythropoietic, 2 17 2.105
349
P OLG002 Oligodendroglioma 66 2.097
350
HYP060 Hyperinsulinism 54 2.097
351
c SVR005 Severe Pre-Eclampsia 50 2.095
352
MCL057 Macular Dystrophy with Central Cone Involvement 28 2.074
353
OST159 Osteogenic Sarcoma 66 2.074
354
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 2.074
355
HPT004 Hepatic Coma 43 2.074
356
HPT019 Hepatic Encephalopathy 59 2.074
357
c GLL024 Gallbladder Disease 1 52 2.067
358
c PCH010 Pachyonychia Congenita 3 43 2.049
359
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.049
360
P OBS001 Obstructive Jaundice 48 2.049
361
c ALP101 Alpha-Thalassemia 62 2.048
362
CYN002 Cyanosis, Transient Neonatal 43 2.048
363
c TYP008 Type 1 Diabetes Mellitus 70 2.031
364
IMM167 Immune Deficiency Disease 78 2.031
365
INT007 Intermediate Coronary Syndrome 54 2.031
366
PLG002 Plague 58 2.031
367
P HYD006 Hydrocephalus 61 2.028
368
P HYP086 Hypothyroidism 69 2.012
369
P KDN017 Kidney Cancer 61 2.000
370
P BNG032 Benign Mesothelioma 53 2.000
371
c OPT053 Optic Atrophy 1 62 1.993
372
CNT057 Central Centrifugal Cicatricial Alopecia 36 1.987
373
TST044 Testicular Torsion 45 1.987
374
CLR109 Colorectal Adenocarcinoma 50 1.987
375
c ACT135 Acute Graft Versus Host Disease 51 1.966
376
P PLM034 Pulmonary Emphysema 58 1.950
377
P ENC004 Encephalitis 61 1.950
378
ANT078 Antipyrine Metabolism 23 1.945
379
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 1.939
380
P AMY004 Amyloidosis 70 1.939
381
P FML011 Familial Adenomatous Polyposis 71 1.901
382
P URN019 Urinary Tract Infection 49 1.901
383
FWL003 Fowler Urethral Sphincter Dysfunction Syndrome 22 1.901
384
SPR066 Superficial Siderosis 38 1.901
385
AML001 Amelanotic Melanoma 37 1.901
386
GST045 Gastroenteritis 58 1.901
387
c ERY016 Erythropoietic Protoporphyria, Autosomal Recessive 19 1.898
388
c ACT073 Acute Leukemia 58 1.897
389
c ANM038 Anemia, Autoimmune Hemolytic 64 1.891
390
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 27 1.891
391
P INF032 Infertility 57 1.891
392
GST050 Gastrointestinal System Disease 55 1.891
393
LYM019 Lymphosarcoma 46 1.891
394
BRN002 Bronchiolitis 57 1.879
395
MYL013 Myeloperoxidase Deficiency 44 1.873
396
PRT094 Protoporphyria, Erythropoietic, X-Linked 27 1.860
397
P RTN016 Retinal Degeneration 52 1.859
398
HGH043 High Grade Glioma 45 1.856
399
HYP056 Hypoglycemia 65 1.856
400
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.842
401
CLN015 Colon Adenocarcinoma 65 1.842
402
P HRM021 Hair Morphology 2 20 1.841
403
P BRS044 Breast Adenocarcinoma 58 1.841
404
c HPT016 Hepatitis B 62 1.841
405
P SCH015 Schizophrenia 74 1.818
406
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.810
407
HRD090 Harderoporphyria 24 1.800
408
VSC002 Vascular Dementia 60 1.788
409
c THR092 Thrombophilia Due to Thrombin Defect 74 1.783
410
PRP030 Purpura 54 1.783
411
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.776
412
CRT015 Carotid Artery Occlusion 45 1.776
413
P PLY019 Polyneuropathy 52 1.776
414
IGG001 Iga Glomerulonephritis 50 1.761
415
P FBR017 Fibrosarcoma 56 1.761
416
HYP005 Hypokalemia 55 1.761
417
BRN012 Bronchiolitis Obliterans 56 1.750
418
PRS129 Prostatic Hyperplasia, Benign 49 1.732
419
HPT022 Hepatoblastoma 54 1.732
420
P ART023 Arthropathy 61 1.732
421
PRS021 Prostatic Adenoma 43 1.732
422
PRS045 Prostatic Hypertrophy 53 1.732
423
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.732
424
IRN004 Iron-Refractory Iron Deficiency Anemia 46 1.732
425
P CYS018 Cystitis 59 1.732
426
P CTR002 Cataract 60 1.732
427
STT001 Status Epilepticus 59 1.732
428
VLV047 Volvulus of Midgut 52 1.711
429
DGR001 Digeorge Syndrome 62 1.711
430
PRP007 Priapism 47 1.711
431
P ESP024 Esophagitis 60 1.711
432
MST005 Mastitis 53 1.711
433
P HMP007 Hemophilia 52 1.711
434
NRM005 Neuromuscular Disease 63 1.687
435
P FNC004 Fanconi Syndrome 60 1.687
436
CTS002 Cat-Scratch Disease 42 1.687
437
PRQ002 Paraquat Poisoning 28 1.674
438
NRL016 Neural Tube Defects 81 1.674
439
MNN043 Meningioma, Familial 79 1.674
440
SCR001 Secretory Meningioma 40 1.674
441
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.674
442
BRC012 Brucellosis 66 1.674
443
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.674
444
SPN021 Spinal Meningioma 50 1.674
445
P TRN020 Turner Syndrome 67 1.664
446
HMN044 Human Immunodeficiency Virus Type 1 78 1.658
447
c TYR012 Tyrosinemia, Type I 61 1.658
448
OBS082 Obstructive Nephropathy 41 1.658
449
P MMB011 Membranous Nephropathy 50 1.658
450
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.658
451
c DLT002 Dilated Cardiomyopathy 78 1.658
452
ATN005 Autonomic Dysfunction 46 1.658
453
KWS002 Kawasaki Disease 65 1.653
454
CLR108 Colorectal Adenoma 64 1.641
455
ACT119 Acute Promyelocytic Leukemia 62 1.641
456
P BND020 Bone Disease 59 1.641
457
CND006 Candida Glabrata 30 1.641
458
NTR005 Nutritional Deficiency Disease 61 1.612
459
c SCL052 Scleroderma, Familial Progressive 61 1.611
460
P MDL005 Medulloblastoma 75 1.611
461
WLL004 Wallerian Degeneration 38 1.611
462
c DWL002 Dowling-Degos Disease 1 58 1.604
463
PRP027 Peripheral Vascular Disease 71 1.603
464
P LKM062 Leukemia, Acute Lymphoblastic 69 1.603
465
PRM329 Premature Aging 36 1.603
466
P FCL005 Focal Segmental Glomerulosclerosis 57 1.603
467
P EYD002 Eye Disease 57 1.603
468
MYC013 Mycobacterium Abscessus 42 1.603
469
c SYS001 Systemic Lupus Erythematosus 87 1.592
470
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.592
471
CRY003 Cryptosporidiosis 56 1.592
472
PST010 Pasteurellosis 39 1.592
473
BRN024 Bronchitis 67 1.592
474
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.592
475
PLM001 Pulmonary Tuberculosis 69 1.581
476
CYT018 Cytochrome P450 2d6 Variant 26 1.567
477
VRL011 Viral Infectious Disease 61 1.544
478
P ALP008 Alopecia 54 1.544
479
P UVT001 Uveitis 57 1.544
480
CYT014 Cytochrome P450 Oxidoreductase Deficiency 34 1.544
481
END057 Endometrial Cancer 72 1.544
482
P PLY041 Polymyositis 59 1.544
483
CLN044 Colon Adenoma 44 1.544
484
ONC002 Onchocerciasis 51 1.544
485
SPT005 Spotted Fever 49 1.544
486
P PLY011 Polycystic Ovary Syndrome 57 1.544
487
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.544
488
PHR003 Pharyngitis 58 1.544
489
P THR015 Thrombophilia 51 1.544
490
c LKM005 Leukemia, T-Cell, Chronic 34 1.544
491
CRV035 Cervical Cancer 73 1.542
492
c BSL007 Basal Cell Carcinoma 68 1.542
493
ADL030 Adult-Onset Still's Disease 59 1.542
494
CRB090 Cerebral Hypoxia 42 1.542
495
CRN048 Craniofacial-Deafness-Hand Syndrome 52 1.490
496
HMN047 Human Cytomegalovirus Infection 57 1.489
497
P LYM118 Lymphoma 67 1.489
498
VRC005 Varicose Veins 60 1.489
499
MLT001 Multiple Chemical Sensitivity 39 1.489
500
P TRM003 Tremor 48 1.489
501
c ATS210 Autosomal Recessive Sideroblastic Anemia 29 1.489
502
P VNT002 Ventricular Septal Defect 58 1.489
503
VCC001 Vaccinia 47 1.489
504
TCK004 Tick Infestation 30 1.489
505
CHR546 Chronic Mountain Sickness 43 1.489
506
HPT014 Hepatorenal Syndrome 49 1.489
507
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.482
508
P HMN010 Hemangioma 62 1.482
509
P BRB001 Beriberi 44 1.482
510
CRB086 Cerebral Aneurysms 40 1.482
511
SLC006 Silicosis 56 1.471
512
ENT004 Enthesopathy 51 1.471
513
PLM033 Pulmonary Embolism 58 1.471
514
c ERY064 Erythrocytosis, Familial, 6 30 1.450
515
P HYP077 Hypertrichosis 46 1.450
516
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.434
517
P LKM071 Leukemia, Chronic Lymphocytic 75 1.434
518
TST015 Testicular Disease 42 1.434
519
KHN001 Kuhnt-Junius Degeneration 48 1.434
520
HMG009 Hemoglobin Zurich 21 1.434
521
FCT001 Factor Viii Deficiency 60 1.414
522
MTC087 Mitochondrial Complex Iii Deficiency, Nuclear Type 4 32 1.414
523
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 25 1.414
524
c HMP029 Hemophilia a 68 1.414
525
CHL123 Chlamydia 58 1.414
526
c JVN010 Juvenile Rheumatoid Arthritis 66 1.414
527
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 1.410
528
HRW001 Hair Whorl 35 1.410
529
RCK004 Rickets 68 1.410
530
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.403
531
P RHB003 Rhabdomyosarcoma 66 1.390
532
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.375
533
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 1.375
534
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 35 1.375
535
c THY056 Thyroid Dyshormonogenesis 3 31 1.375
536
HRT037 Heart and Brain Malformation Syndrome 31 1.375
537
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.375
538
P SPP010 Suppressor of Tumorigenicity 3 51 1.375
539
GTL001 Gitelman Syndrome 65 1.375
540
P PHT010 Photoparoxysmal Response 1 46 1.375
541
RBF001 Riboflavin Deficiency 49 1.375
542
P DMN002 Dementia 66 1.375
543
BBN001 Bubonic Plague 40 1.375
544
MNN009 Meningoencephalitis 48 1.375
545
TLR001 Tularemia 56 1.375
546
MST020 Mast Cell Activation Syndrome 28 1.375
547
ARG004 Argyria 26 1.368
548
LWF001 Low-Flow Priapism 16 1.342
549
PRN011 Pernicious Anemia 53 1.342
550
c MST023 Mesothelioma, Malignant 56 1.342
551
DFF005 Diffuse Large B-Cell Lymphoma 54 1.342
552
RCK002 Rocky Mountain Spotted Fever 34 1.342
553
MLD001 Melioidosis 67 1.342
554
DGN001 Degenerative Disc Disease 49 1.342
555
PLC005 Placental Insufficiency 56 1.342
556
PPT005 Peptic Ulcer Disease 58 1.342
557
CMM005 Common Cold 56 1.342
558
SNS003 Sensory Peripheral Neuropathy 52 1.342
559
ORL004 Oral Submucous Fibrosis 56 1.342
560
CNT047 Contact Dermatitis 57 1.342
561
P FBR031 Febrile Seizures 52 1.342
562
PLY150 Polykaryocytosis Inducer 29 1.324
563
GST023 Gastric Ulcer 52 1.324
564
CRD132 Cardiac Conduction Defect 60 1.313
565
RTN017 Retinal Detachment 60 1.313
566
c HNT010 Huntington Disease-Like 1 55 1.313
567
MTC209 Mitochondrial Complex Iv Deficiency, Nuclear Type 6 24 1.313
568
SBC001 Subacute Sclerosing Panencephalitis 53 1.313
569
BCL011 Bacillary Angiomatosis 30 1.313
570
P HRP006 Herpes Simplex 65 1.313
571
MNG007 Manganese Poisoning 28 1.313
572
P LCT001 Lactic Acidosis 51 1.313
573
P SYS005 Systemic Scleroderma 74 1.313
574
PLR008 Pleurisy 50 1.313
575
GTR002 Goiter 53 1.313
576
HMN004 Hemangioma of Liver 35 1.313
577
c HMG001 Hemoglobin C Disease 41 1.313
578
PPT001 Peptic Esophagitis 52 1.313
579
P BRN022 Bronchiectasis 60 1.313
580
ANG037 Angiomatosis 30 1.313
581
c HPT003 Hepatitis a 63 1.313
582
c HMG029 Hemoglobin Se Disease 40 1.313
583
AZS001 Azoospermia 45 1.299
584
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.299
585
MTC005 Mitochondrial Metabolism Disease 45 1.279
586
ATN004 Autonomic Neuropathy 42 1.279
587
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.261
588
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 1.261
589
MCP006 Mucoepidermoid Carcinoma 48 1.261
590
CNN005 Connective Tissue Disease 67 1.261
591
GT001 Gout 64 1.261
592
PLC002 Plica Syndrome 35 1.261
593
DNG002 Dengue Hemorrhagic Fever 60 1.261
594
ALC006 Alcoholic Hepatitis 61 1.261
595
PPL022 Papilloma 53 1.261
596
SQM002 Squamous Cell Papilloma 46 1.261
597
INT030 Intracranial Aneurysm 55 1.261
598
HNC001 Henoch-Schoenlein Purpura 54 1.261
599
SYN007 Synovitis 55 1.261
600
MCR225 Macrophage Activation Syndrome 45 1.261
601
FST010 Fasting Hypoglycemia 33 1.261
602
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 1.245
603
GLM044 Glomerular Disease 35 1.245
604
FRN006 Frontotemporal Dementia 68 1.245
605
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 1.245
606
HYP781 Hypoascorbemia 52 1.245
607
P APL001 Aplastic Anemia 73 1.245
608
P RST001 Restless Legs Syndrome 52 1.245
609
P EXN002 Exanthem 58 1.245
610
c MJR022 Major Affective Disorder 8 38 1.245
611
IGR001 Ige Responsiveness, Atopic 59 1.245
612
c MJR024 Major Affective Disorder 9 41 1.245
613
PLY001 Polycythemia Vera 69 1.245
614
c DMN023 Diamond-Blackfan Anemia 1 66 1.245
615
P INC035 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 3 27 1.245
616
GRN051 Granulomatous Disease, Chronic, X-Linked 57 1.245
617
P MSC003 Muscular Atrophy 52 1.245
618
ELP001 Elephantiasis 44 1.245
619
OCL006 Ocular Hypertension 53 1.245
620
P BPL003 Bipolar Disorder 56 1.245
621
P CND004 Candidiasis 58 1.245
622
INS001 Insulinoma 59 1.245
624
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 31 1.245
625
INT060 Intestinal Atresia 41 1.245
626
NRT004 Neuritis 53 1.245
627
P HMR003 Hemorrhagic Disease 59 1.245
628
P MYG005 Myoglobinuria 40 1.245
629
P PYL005 Pyelonephritis 57 1.245
630
PRM013 Premature Menopause 58 1.245
631
ESP002 Esophageal Varix 51 1.245
632
ATR003 Atrophic Rhinitis 40 1.245
633
P INT068 Intestinal Disease 53 1.245
634
P AXN001 Axonal Neuropathy 35 1.245
635
P INS002 in Situ Carcinoma 53 1.245
636
P MRC003 Mercury Poisoning 49 1.245
637
c RNG015 Ring Chromosome 2 22 1.245
638
HVY002 Heavy Metal Poisoning 22 1.245
639
P NRV007 Nervous System Disease 67 1.245
640
P OST002 Osteoporosis 76 1.233
641
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.233
642
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.233
643
PYR009 Pyridoxine Deficiency Anemia 35 1.184
644
KRT009 Keratosis 53 1.184
645
c FML324 Familial Porphyria Cutanea Tarda 29 1.184
646
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.176
647
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.176
648
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.176
649
PCH007 Pouchitis 42 1.173
650
P PLY014 Polycystic Kidney Disease 69 1.173
651
HLC007 Helicobacter Pylori Infection 67 1.173
652
c BRN108 Branchiootic Syndrome 1 62 1.173
653
P MCR129 Microvascular Complications of Diabetes 1 68 1.173
654
HRN029 Hearing Loss, Noise-Induced 37 1.173
655
c WLM013 Wilms Tumor 1 66 1.173
656
P HYP750 Hypertriglyceridemia, Familial 62 1.173
657
INT051 Intussusception 52 1.173
658
P PLG001 Pelger-Huet Anomaly 52 1.173
659
SCR011 Scrapie 39 1.173
660
LYM027 Lymphopenia 56 1.173
661
c MCR112 Microvascular Complications of Diabetes 2 42 1.173
662
P HYP069 Hyperparathyroidism 62 1.173
663
c MLG069 Malignant Hypertension 46 1.173
664
c CNT035 Central Nervous System Disease 54 1.173
665
VLV010 Vulvovaginitis 42 1.173
666
KDN013 Kidney Hypertrophy 34 1.173
667
BWN006 Bowen's Disease 32 1.173
668
OVR094 Ovarian Epithelial Cancer 39 1.173
669
P NSP012 Nasopharyngeal Carcinoma 61 1.169
670
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.169
671
LPT014 Leptin Deficiency or Dysfunction 78 1.169
672
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.169
673
CLR030 Clear Cell Renal Cell Carcinoma 54 1.169
674
HYD002 Hydronephrosis 58 1.169
675
MYC005 Myocardial Stunning 46 1.169
676
P CLL015 Collagen Disease 48 1.158
677
c EXD008 Exudative Vitreoretinopathy 1 71 1.134
678
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.134
679
HST016 Histiocytic Sarcoma 39 1.092
680
MTH071 Methane Production 25 1.092
681
HYP856 Hypothyroidism, Central, with Testicular Enlargement 37 1.092
682
c THR071 Thrombocytopenia 1 48 1.092
683
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 1.092
684
P ADL017 Adult T-Cell Leukemia 56 1.092
685
MSC007 Muscle Hypertrophy 64 1.092
686
INF034 Infective Endocarditis 54 1.092
687
BSM002 Bosma Arhinia Microphthalmia Syndrome 44 1.092
688
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 1.092
689
c ART101 Aortic Valve Disease 2 66 1.092
690
c PNC106 Pancreatic Agenesis 1 51 1.092
692
c HRD026 Hereditary Ataxia 47 1.092
693
P LKD001 Leukodystrophy 59 1.092
694
IDP093 Idiopathic Gastroparesis 28 1.092
695
P FML340 Familial Episodic Pain Syndrome 50 1.092
696
ACH005 Achalasia 55 1.092
697
P MLN007 Male Infertility 56 1.092
698
PNC001 Pancytopenia 53 1.092
699
PRM236 Primary Biliary Cholangitis 60 1.092
700
c PRM005 Primary Hyperparathyroidism 59 1.092
701
END011 Endometriosis of Ovary 39 1.092
702
LMY003 Leiomyomatosis 44 1.092
703
INT020 Intravenous Leiomyomatosis 36 1.092
704
PNC034 Pancreas Disease 50 1.092
705
MSN003 Mesenteric Vascular Occlusion 24 1.092
706
AMN003 Amnestic Disorder 54 1.092
707
TRN004 Trench Fever 29 1.092
708
HLL004 Hellp Syndrome 53 1.092
709
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 1.092
710
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 1.092
711
LKP003 Leukoplakia 39 1.092
712
ANX010 Anxiety 70 1.081
713
MTB004 Metabolic Acidosis 48 1.081
714
P ASP006 Aspergillosis 72 1.081
715
MYL005 Myelofibrosis 71 1.081
716
TTN003 Tetanus 65 1.081
717
ESN009 Eosinophil Peroxidase Deficiency 29 1.074
718
SPP011 Suppression of Tumorigenicity 12 61 1.061
719
c SPN225 Spondyloarthropathy 1 70 1.061
720
P HRS035 Hirschsprung Disease 1 66 1.061
721
EXT007 Extracutaneous Mastocytoma 38 1.061
722
P BLD062 Bile Duct Cancer 67 1.061
723
MST004 Mast Cell Neoplasm 42 1.061
724
P ESN008 Eosinophilic Pneumonia 50 1.061
725
SPN051 Spondylitis 51 1.061
726
INF009 Inflammatory Spondylopathy 30 1.061
727
P MTR012 Mitral Valve Disease 57 1.061
728
PLM035 Pulmonary Eosinophilia 49 1.061
729
XNT003 Xanthomatosis 49 1.026
730
HMR023 Hemorrhagic Cystitis 43 1.026
731
BRR014 Barrett Esophagus 66 1.026
732
CRB011 Cerebrotendinous Xanthomatosis 65 1.026
733
c PRP091 Porphyria Cutanea Tarda, Type I 30 1.026
734
CRC021 Carcinosarcoma 64 1.026
736
P ACN011 Acne 57 1.026
737
DMY004 Demyelinating Disease 50 1.026
738
HNS001 Hansen's Disease 32 1.026
739
WRM004 Warm Antibody Hemolytic Anemia 19 1.000
740
P MYM013 Moyamoya Disease 1 59 1.000
741
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 1.000
742
BDD001 Budd-Chiari Syndrome 62 1.000
743
c LKM070 Leukemia, Acute Monocytic 56 1.000
744
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 1.000
745
c FNC027 Fanconi Anemia, Complementation Group a 81 1.000
746
ISC015 Ischemic Colitis 43 1.000
747
P ATR011 Atrial Fibrillation 66 1.000
748
P SLM003 Salmonellosis 54 1.000
749
BTT017 Beta-Thalassemia Major 51 1.000
750
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 1.000
751
c LNG109 Lung Cancer Susceptibility 1 26 1.000
752
c HYD046 Hydatidiform Mole, Recurrent, 1 59 1.000
753
LNG091 Lung Mucoepidermoid Carcinoma 32 1.000
754
THY029 Thyroid Carcinoma 51 1.000
755
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 1.000
756
GST010 Gestational Trophoblastic Neoplasm 52 1.000
757
P ANT006 Antiphospholipid Syndrome 55 1.000
758
ALL010 Allergic Contact Dermatitis 56 1.000
759
GST040 Gastric Adenocarcinoma 67 1.000
760
c LCL006 Localized Scleroderma 65 1.000
761
CMB007 Combined Immunodeficiency 57 1.000
762
PNM005 Pneumonic Plague 47 1.000
763
P CHR071 Charcot-Marie-Tooth Disease 64 1.000
764
ALC009 Alcoholic Liver Cirrhosis 54 1.000
765
TTH006 Tooth Disease 51 1.000
766
BBS001 Babesiosis 49 1.000
767
MYP009 Myopathy with Deficiency of Iscu 12 1.000
768
ACT200 Acute Monoblastic Leukemia 41 1.000
770
c HRD088 Hereditary Neuropathies 33 1.000
771
ATY012 Atypical Mycobacteriosis, Familial 32 1.000
772
SPR032 Superficial Siderosis of the Central Nervous System 23 0.967
773
P LPR021 Leprosy 3 71 0.967
774
c PRM032 Primary Congenital Glaucoma 41 0.967
775
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.967
776
CLF051 Cleft Larynx, Posterior 27 0.967
777
c HMC009 Hemochromatosis Type 2 53 0.967
778
CHL004 Cholelithiasis 49 0.967
779
STR008 Strongyloidiasis 52 0.967
780
P DRR001 Diarrhea 55 0.967
781
CHR466 Chronic Thromboembolic Pulmonary Hypertension 48 0.967
782
CLS034 Clostridium Septicum Infection 13 0.967
783
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.919
784
CRN020 Coronary Restenosis 39 0.919
785
GNG013 Gingivitis 59 0.919
786
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.905
787
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.905
788
P ANP001 Anaplastic Large Cell Lymphoma 61 0.905
789
c CNG006 Congenital Hypothyroidism 63 0.905
790
THR051 Thrombocytopenia with Beta-Thalassemia, X-Linked 44 0.905
791
HYP765 Hyperbilirubinemia, Shunt, Primary 17 0.905
792
DBN001 Dubin-Johnson Syndrome 57 0.905
793
P DRM010 Dermatomyositis 61 0.905
794
MGL001 Megaloblastic Anemia 58 0.905
795
LPT001 Leptospirosis 66 0.905
796
SPS019 Spastic Paraparesis 38 0.892
797
ADN027 Adenomyosis 57 0.892
798
AGM019 Agammaglobulinemia, X-Linked 72 0.892
799
c THY107 Thymoma, Familial 42 0.892
800
PHS021 Phosphoglycerate Dehydrogenase Deficiency 47 0.892
801
CHR005 Chorioamnionitis 50 0.892
802
P CTN015 Cutaneous T Cell Lymphoma 48 0.892
803
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 39 0.892
804
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.892
805
HNZ004 Heinz Body Anemias 40 0.892
806
PNG002 Pain Agnosia 51 0.892
807
CRR012 Cirrhotic Cardiomyopathy 22 0.892
808
TNG007 Tongue Carcinoma 52 0.892
809
ZKF001 Zika Fever 52 0.892
810
c LRG001 Large Cell Carcinoma 48 0.892
811
SZR001 Sezary's Disease 60 0.892
812
TRC003 Trichomoniasis 53 0.892
813
P KRT007 Keratoconus 50 0.892
814
TCK001 Tick-Borne Encephalitis 59 0.892
815
NDL001 Nodular Malignant Melanoma 45 0.892
816
OST003 Osteonecrosis 61 0.892
817
BRN014 Bronchopneumonia 53 0.892
818
PRM003 Premature Ejaculation 44 0.892
819
PYL006 Pyloric Stenosis 48 0.892
820
RTR008 Root Resorption 44 0.892
821
P AGM001 Agammaglobulinemia 68 0.892
822
PRS036 Parasitic Protozoa Infectious Disease 44 0.892
823
NNS002 Nonspecific Interstitial Pneumonia 42 0.892
824
TXC004 Toxic Diffuse Goiter 23 0.892
825
HMP001 Hemopericardium 47 0.892
826
JPN002 Japanese Encephalitis 61 0.892
827
TCL003 T Cell Deficiency 44 0.892
828
P PRC012 Pericardial Effusion 50 0.892
829
ART004 Aortic Atherosclerosis 47 0.892
830
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 0.892
831
P OVR046 Ovarian Cyst 46 0.892
832
c FML015 Familial Nephrotic Syndrome 48 0.892
833
P THY023 Thymoma 64 0.892
834
P MTR014 Motor Neuron Disease 65 0.892
835
P TMP001 Temporal Lobe Epilepsy 49 0.892
836
CRT016 Carotid Artery Disease 52 0.892
837
LST001 Listeriosis 59 0.892
838
ART006 Arthus Reaction 40 0.892
839
P BNC003 Bone Cancer 58 0.892
840
CRD016 Cardiac Rupture 34 0.892
841
P FML187 Familial Hypertension 34 0.892
842
c ATM075 Autoimmune Encephalitis 40 0.892
843
END072 Endotheliitis 36 0.890
844
ALC007 Alcohol Dependence 66 0.837
845
c MGR028 Migraine with or Without Aura 1 64 0.837
846
VTM002 Vitamin B12 Deficiency 48 0.837
847
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.837
848
PSD014 Pseudopseudohypoparathyroidism 54 0.837
849
ADR051 Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency 42 0.837
850
P EPL164 Epilepsy 68 0.837
851
P OPT006 Optic Nerve Disease 58 0.837
852
PRP016 Paraplegia 52 0.837
853
BRN028 Brain Cancer 74 0.837
854
P GRV001 Graves' Disease 55 0.837
855
P GLL022 Guillain-Barre Syndrome 60 0.837
856
GLS001 Gliosarcoma 64 0.837
857
P PRN023 Prion Disease 60 0.837
858
HMR002 Hemarthrosis 44 0.837
859
P HRD011 Hereditary Spherocytosis 64 0.837
860
RGH009 Right Atrial Isomerism 57 0.767
861
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.767
862
TXC002 Toxic Encephalopathy 52 0.767
863
P ATS364 Autism 69 0.764
864
c GLC097 Glaucoma 3, Primary Congenital, a 57 0.764
865
STN013 Stenotrophomonas Maltophilia Infection 26 0.764
866
FCL073 Facial Hypertrichosis 15 0.764
867
CHR100 Chronic Ulcer of Skin 57 0.764
868
c ATS007 Autism Spectrum Disorder 72 0.764
869
WLS001 Wilson Disease 70 0.764
870
c HNT011 Huntington Disease-Like 3 34 0.764
871
ARM001 Aromatase Deficiency 54 0.764
872
DWN001 Down Syndrome 70 0.764
873
PHN003 Phenylketonuria 76 0.764
874
P ALC033 Alcohol Use Disorder 61 0.764
875
c ERY065 Erythrocytosis, Familial, 7 35 0.764
876
c FML297 Familial Thyroid Dyshormonogenesis 47 0.764
877
P SLF001 Sulfhemoglobinemia 23 0.764
878
PRT038 Protein-Energy Malnutrition 53 0.764
879
c HMG004 Hemoglobin D Disease 33 0.764
880
QDR001 Quadriplegia 50 0.764
881
PLS006 Plasmodium Vivax Malaria 51 0.764
882
ALB002 Albinism 47 0.764
883
LSS003 Lassa Fever 49 0.750
884
PLY100 Polyploidy 36 0.750
885
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 39 0.750
886
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 52 0.750
887
c ART115 Aortic Valve Disease 1 74 0.750
888
ALK013 Alkaptonuria 59 0.750
889
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.750
890
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.750
891
BRG013 Buerger Disease 57 0.750
892
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.750
893
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.750
894
END062 Endometrial Hyperplasia 48 0.750
895
OLG022 Oligoasthenoteratozoospermia 36 0.750
896
BTT018 Beta-Thalassemia Intermedia 31 0.750
897
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 22 0.750
898
c DPH024 Diaphragmatic Hernia, Congenital 64 0.750
899
HMM004 Hamamy Syndrome 39 0.750
900
RHB024 Rhabdomyosarcoma 2 67 0.750
901
STR033 Storm Syndrome 27 0.750
902
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.750
903
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 0.750
904
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.750
905
PNM010 Pneumothorax, Primary Spontaneous 58 0.750
906
INT067 Interstitial Nephritis 46 0.750
907
RFR009 Refractory Cytopenia with Multilineage Dysplasia 30 0.750
908
c PST005 Posterior Uveitis 54 0.750
909
TRC020 Tracheitis 43 0.750
910
AVN001 Avian Influenza 61 0.750
911
ART010 Arteriolosclerosis 37 0.750
912
ART012 Aortitis 42 0.750
913
CRN030 Coronary Stenosis 50 0.750
914
SKN019 Skin Melanoma 71 0.750
915
P HMR005 Hemorrhoid 49 0.750
916
PNM008 Pneumothorax 54 0.750
917
PLR007 Pleural Empyema 51 0.750
918
HRT012 Heart Valve Disease 53 0.750
919
LNG039 Lung Squamous Cell Carcinoma 57 0.750
920
OVR063 Overnutrition 42 0.750
921
CMP064 Complement Component 3 Deficiency 35 0.750
922
RTR001 Retrograde Amnesia 41 0.750
923
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.750
924
DNG001 Dengue Shock Syndrome 40 0.750
925
SLD003 Sialadenitis 48 0.750
926
VRC001 Varicocele 48 0.750
927
P INT099 Intrahepatic Cholestasis of Pregnancy 62 0.750
928
LYM017 Lyme Disease 62 0.750
929
SBP001 Subependymal Giant Cell Astrocytoma 46 0.750
930
c ESS001 Essential Tremor 57 0.750
931
SPT004 Septic Arthritis 58 0.750
932
P TRT010 Teratoma 51 0.750
933
MXD005 Mixed Connective Tissue Disease 57 0.750
934
OLG001 Oligospermia 45 0.750
935
P HYP009 Hypertrophic Pyloric Stenosis 41 0.750
936
P MTR003 Mitral Valve Stenosis 53 0.750
937
RFR003 Refractive Error 41 0.750
938
IRR002 Irritable Bowel Syndrome 65 0.750
939
VRL017 Viral Hemorrhagic Fever 36 0.750
940
SRF006 Surfactant Dysfunction 33 0.750
941
OPD006 Opioid Addiction 48 0.750
942
BRK012 Broken Heart Syndrome 42 0.750
943
c AMY009 Amyloidosis Aa 47 0.750
944
BNT001 Banti's Syndrome 21 0.750
945
LYM133 Lymphoma, Hodgkin, Classic 74 0.684
946
DMN026 Dementia Pugilistica 27 0.684
947
c ACQ047 Acquired Methemoglobinemia 30 0.684
948
CYN003 Cyanide Poisoning 22 0.684
949
CHR471 Chronic Hepatic Porphyria 15 0.684
950
TYR015 Tyrosinosis 20 0.684
951
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.684
952
c HMC010 Hemochromatosis, Type 3 49 0.684
953
GST092 Gastroesophageal Reflux 61 0.684
954
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis