Search results for Iron

2999 hits were found for Iron

# Family MCID Name MIFTS Score
1
IRN002 Iron Metabolism Disease 57 8.638
2
IRN004 Iron-Refractory Iron Deficiency Anemia 47 8.607
3
c NRD032 Neurodegeneration with Brain Iron Accumulation 5 51 6.096
4
IRN001 Iron Deficiency Anemia 59 6.049
5
c NRD014 Neurodegeneration with Brain Iron Accumulation 4 45 5.668
6
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 5.568
7
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 5.464
8
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 51 5.450
9
c NRD009 Neurodegeneration with Brain Iron Accumulation 2b 41 5.435
10
IRN008 Iron Overload in Africa 51 5.322
11
P RRH023 Rare Hereditary Hemochromatosis 41 5.171
12
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 4.797
13
c HMC034 Hemochromatosis, Type 5 42 4.737
14
GRC001 Gracile Syndrome 47 4.732
15
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 18 4.446
16
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 52 4.240
17
c ANM027 Anemia, Hypochromic Microcytic, with Iron Overload 2 23 4.144
18
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 3.997
19
HMS001 Hemosiderosis 54 3.660
20
MTC036 Mitochondrial Membrane Protein-Associated Neurodegeneration 25 3.549
21
MCR018 Microcytic Anemia 47 3.505
22
c HMC039 Hemochromatosis, Type 1 74 3.298
23
c ANM036 Anemia, Sideroblastic, 1 57 3.252
24
c NRD047 Neurodegeneration with Brain Iron Accumulation 7 23 3.155
25
c NRD048 Neurodegeneration with Brain Iron Accumulation 8 21 3.155
26
LYM125 Lymphedema, Cardiac Septal Defects, and Characteristic Facies 22 3.128
27
MYP025 Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme 11 2.223
28
IRN005 Irons Bhan Syndrome 7 2.218
29
P SDR002 Siderosis 44 2.033
30
P SDR003 Sideroblastic Anemia 49 1.785
31
c HMC009 Hemochromatosis Type 2 50 1.774
32
MYP009 Myopathy with Deficiency of Iscu 12 1.624
33
MYP097 Myopathy with Lactic Acidosis, Hereditary 31 1.613
34
GNT037 Genetic Hyperferritinemia Without Iron Overload 11 1.600
35
c CNS020 Constitutional Anemia Due to Iron Metabolism Disorder 4 1.590
36
KRK002 Karak Syndrome 17 1.585
37
DSR030 Disorder of Iron Metabolism and Transport 3 1.585
38
P ZLL001 Zellweger Syndrome 57 1.579
39
FRR002 Ferro-Cerebro-Cutaneous Syndrome 10 1.564
40
SLC011 Silicosiderosis 9 1.553
41
ARN001 Arena Syndrome 5 1.553
42
DFC004 Deficiency Anemia 70 1.127
43
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.879
44
P THL005 Thalassemia 60 0.540
45
P KDN018 Kidney Disease 72 0.325
46
c CHR684 Chronic Kidney Disease 70 0.324
47
c BTT014 Beta-Thalassemia 74 0.312
48
P LVR013 Liver Disease 68 0.268
49
NTR005 Nutritional Deficiency Disease 62 0.268
50
MYL009 Myelodysplastic Syndrome 70 0.254
51
P HRT032 Heart Disease 75 0.245
52
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.245
53
CNG034 Congestive Heart Failure 69 0.235
54
P INF037 Inflammatory Bowel Disease 54 0.234
55
P SCK005 Sickle Cell Disease 50 0.222
56
LVR012 Liver Cirrhosis 62 0.218
57
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.207
58
END086 End Stage Renal Disease 51 0.202
59
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.188
60
P RST001 Restless Legs Syndrome 54 0.181
61
c HPT001 Hepatitis C 62 0.180
62
P DRR001 Diarrhea 55 0.179
63
MLR004 Malaria 81 0.178
64
P PRP029 Porphyria 62 0.177
65
P GST044 Gastritis 56 0.176
66
FTT001 Fatty Liver Disease 61 0.173
67
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.165
68
HYP266 Hypoxia 57 0.165
69
P ALZ034 Alzheimer Disease 88 0.160
70
HYP001 Hypochromic Microcytic Anemia 38 0.157
71
P CLC063 Celiac Disease 1 66 0.155
72
HLC007 Helicobacter Pylori Infection 59 0.155
73
KRT002 Keratomalacia 47 0.154
74
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.154
75
HMG005 Hemoglobinopathy 56 0.153
76
SCK003 Sickle Cell Anemia 74 0.152
77
c ALP101 Alpha-Thalassemia 62 0.151
78
CNS004 Constipation 58 0.151
79
ACR006 Aceruloplasminemia 65 0.150
80
P HPT023 Hepatocellular Carcinoma 100 0.148
81
P PRP003 Porphyria Cutanea Tarda 67 0.147
82
P HML002 Hemolytic Anemia 63 0.141
83
P CLR023 Colorectal Cancer 99 0.139
84
RCK004 Rickets 68 0.139
85
P FRD001 Friedreich Ataxia 64 0.138
86
PCD001 Pica Disease 41 0.137
87
ATH013 Atherosclerosis Susceptibility 65 0.136
88
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.134
89
c VRL010 Viral Hepatitis 52 0.132
90
P NRB001 Neuroblastoma 72 0.131
91
THR004 Thrombocytosis 51 0.131
92
CHL079 Children's Interstitial Lung Disease 26 0.128
93
c ATR087 Atrial Standstill 1 75 0.128
94
ATS010 Autosomal Recessive Disease 48 0.128
95
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.126
96
NNL006 Non-Alcoholic Steatohepatitis 54 0.126
97
HYP080 Hypogonadism 50 0.126
98
HLX001 Helix Syndrome 47 0.126
99
P APL001 Aplastic Anemia 74 0.126
101
CRH001 Crohn's Disease 74 0.124
102
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.122
103
P PRK057 Parkinson Disease, Late-Onset 78 0.121
104
P MLT020 Multiple Sclerosis 72 0.120
105
ALL026 Allergic Hypersensitivity Disease 62 0.120
106
c HPT073 Hepatitis C Virus 72 0.120
107
P HPT021 Hepatitis 67 0.120
108
P PLY018 Polycythemia 56 0.120
109
HYP017 Hypophosphatemia 50 0.120
110
P PLM037 Pulmonary Hypertension 67 0.118
111
P LTR001 Lateral Sclerosis 54 0.118
112
48X005 48,xyyy 39 0.118
113
P DYS154 Dystonia 65 0.118
114
P HYP086 Hypothyroidism 69 0.117
115
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.117
116
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.117
117
BCT022 Bacterial Infectious Disease 56 0.116
118
ULC004 Ulcerative Colitis 73 0.115
119
GRN017 Granulocytopenia 44 0.115
120
P ART023 Arthropathy 62 0.115
121
GST033 Gestational Diabetes 61 0.115
122
VTM002 Vitamin B12 Deficiency 48 0.115
123
HYP781 Hypoascorbemia 51 0.111
124
CYS001 Cystic Fibrosis 81 0.110
125
GLB015 Glioblastoma Multiforme 75 0.110
126
P GLM045 Glioma 63 0.110
127
P NTR004 Neutropenia 63 0.110
128
CLT003 Colitis 62 0.110
129
GLL048 Glial Tumor 45 0.110
130
P CRN300 Coronary Heart Disease 1 63 0.110
131
HRW001 Hair Whorl 36 0.109
132
P HNT016 Huntington Disease 72 0.108
133
c PRC016 Pre-Eclampsia 63 0.108
134
ERY051 Erythroleukemia, Familial 56 0.108
135
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.108
136
P DBT009 Diabetes Mellitus 64 0.107
137
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.107
138
P CTR002 Cataract 60 0.107
140
P THR014 Thrombocytopenia 67 0.106
141
RFR010 Refractory Anemia 48 0.106
142
LNG099 Lung Disease 60 0.105
143
AGN016 Aging 56 0.105
144
P LKM002 Leukemia 68 0.104
145
SPL018 Splenomegaly 48 0.103
146
HYP801 Hyperferritinemia with or Without Cataract 53 0.103
147
P RTN016 Retinal Degeneration 53 0.103
148
P RHM011 Rheumatoid Arthritis 80 0.102
149
c DRR009 Diarrhea 6 46 0.102
150
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.101
151
HMP009 Haemophilus Influenzae 43 0.101
152
47X002 47,xyy 49 0.100
153
CHL123 Chlamydia 59 0.098
154
c ACT073 Acute Leukemia 58 0.098
155
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.098
156
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.098
157
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.098
158
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.098
159
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.098
160
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.098
161
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.098
162
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.098
163
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.098
164
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.098
165
P BRS047 Breast Cancer 97 0.096
166
c LKM061 Leukemia, Acute Myeloid 84 0.096
167
ALC007 Alcohol Dependence 66 0.096
168
P MVM001 Movement Disease 63 0.095
169
c HMC021 Hemochromatosis, Type 2a 51 0.095
170
CYT002 Cytokine Deficiency 42 0.095
171
c HYP595 Hypertension, Essential 84 0.094
172
ATM095 Autoimmune Disease 62 0.094
173
ISC004 Ischemia 58 0.094
174
BRN071 Brain Injury 49 0.094
175
PLM001 Pulmonary Tuberculosis 69 0.093
176
ADN018 Adenoma 59 0.093
177
P EXN002 Exanthem 57 0.093
178
MTH071 Methane Production 26 0.093
179
P MYC007 Myocardial Infarction 70 0.092
180
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.092
181
P ADN016 Adenocarcinoma 64 0.092
182
P VSC007 Vascular Disease 63 0.092
183
HYP025 Hyperphosphatemia 48 0.092
184
LSH001 Leishmaniasis 63 0.092
185
DPH001 Diphtheria 60 0.092
186
PPT005 Peptic Ulcer Disease 59 0.092
187
P PNM006 Pneumoconiosis 56 0.092
188
ANT018 Anthracosis 48 0.092
189
P KLZ004 Kala-Azar 1 41 0.092
190
c RHB024 Rhabdomyosarcoma 2 67 0.091
191
P TRM003 Tremor 54 0.091
192
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.090
193
P ALC033 Alcohol Use Disorder 58 0.090
194
GST050 Gastrointestinal System Disease 56 0.090
195
PST092 Posttransplant Acute Limbic Encephalitis 29 0.090
196
P GST053 Gastric Cancer 83 0.089
197
P ART022 Arthritis 69 0.089
198
P END044 Endometriosis 63 0.089
199
P ATR005 Atrophic Gastritis 50 0.089
200
MYL005 Myelofibrosis 70 0.088
201
P TRN020 Turner Syndrome 67 0.088
202
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.088
203
P INT068 Intestinal Disease 53 0.088
204
P OST002 Osteoporosis 74 0.087
205
OST011 Osteomalacia 52 0.087
206
c HMC035 Hemochromatosis, Type 4 51 0.087
207
URM002 Uremia 49 0.087
208
BNR002 Bone Resorption Disease 48 0.087
209
P MYL006 Myeloid Leukemia 60 0.086
210
ATX019 Ataxia with Vitamin E Deficiency 42 0.085
211
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.084
212
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.084
213
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.083
214
MCR141 Mucormycosis 56 0.083
215
GTR002 Goiter 53 0.083
216
P PNC035 Pancreatic Cancer 84 0.082
217
ADL002 Adult Syndrome 70 0.082
218
ALL014 Allergic Encephalomyelitis 38 0.082
219
PRT037 Pertussis 65 0.081
220
THR024 Thrombosis 57 0.081
221
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.080
222
PLG002 Plague 63 0.080
223
P SZR006 Seizure Disorder 56 0.080
224
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.079
225
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.079
226
WLS001 Wilson Disease 71 0.079
227
LPP008 Lipoprotein Quantitative Trait Locus 62 0.079
228
VSL002 Visual Epilepsy 59 0.079
229
ART140 Arteries, Anomalies of 52 0.079
230
ANX004 Anoxia 40 0.079
231
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.079
232
P LYM118 Lymphoma 68 0.078
233
DNT012 Dental Caries 53 0.078
234
DYS073 Dysphagia 50 0.078
235
HMC038 Hemochromatosis, Neonatal 35 0.078
236
MYL069 Myeloma, Multiple 85 0.077
237
STR067 Stroke, Ischemic 81 0.077
238
ANX010 Anxiety 73 0.077
239
P MYP004 Myopathy 70 0.077
240
P PNM007 Pneumonia 68 0.077
241
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.077
242
ATR002 Atransferrinemia 50 0.077
243
P PLM085 Pulmonary Hemosiderosis 44 0.077
244
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.077
245
P LNG032 Lung Cancer 98 0.076
246
P LKM062 Leukemia, Acute Lymphoblastic 69 0.076
247
c INF071 Inflammatory Bowel Disease 1 67 0.076
248
DPR016 Depression 63 0.076
249
SLC006 Silicosis 56 0.076
250
SYS003 Systolic Heart Failure 49 0.076
251
P OVR042 Ovarian Cancer 88 0.075
252
PRT036 Peritonitis 64 0.075
253
HYP066 Hyperglycemia 61 0.075
254
c ACT071 Acute Kidney Failure 60 0.075
255
P BND020 Bone Disease 59 0.075
256
TLN003 Telangiectasis 52 0.075
257
c MCR120 Microvascular Complications of Diabetes 7 47 0.075
258
P GRF003 Graft-Versus-Host Disease 72 0.074
259
DWN001 Down Syndrome 70 0.074
260
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.074
261
P ENC018 Encephalopathy 61 0.074
262
c HPT016 Hepatitis B 59 0.074
263
c ACT075 Acute Myocardial Infarction 57 0.074
264
ACT058 Active Peptic Ulcer Disease 55 0.074
265
PRN011 Pernicious Anemia 53 0.074
266
PLY001 Polycythemia Vera 69 0.073
267
P MYC084 Mycobacterium Tuberculosis 1 68 0.073
268
BRN024 Bronchitis 68 0.073
269
SRC014 Sarcoma 65 0.073
270
P HMN010 Hemangioma 61 0.073
271
SPN035 Spindle Cell Sarcoma 53 0.073
272
PLS007 Plasmodium Falciparum Malaria 52 0.073
273
MGL001 Megaloblastic Anemia 51 0.073
274
c HMC010 Hemochromatosis, Type 3 50 0.073
275
P ATS364 Autism 70 0.071
276
CRB039 Cerebrovascular Disease 67 0.071
277
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.071
278
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.071
279
BRN004 Brain Edema 56 0.071
280
TRM010 Traumatic Brain Injury 51 0.071
281
P ECL001 Eclampsia 50 0.071
282
PST021 Postpartum Depression 50 0.071
283
P DMN002 Dementia 66 0.070
284
P ESP024 Esophagitis 62 0.070
285
P DDN001 Duodenal Ulcer 52 0.070
286
PLC008 Placenta Disease 50 0.070
287
PLM049 Plummer Vinson Syndrome 30 0.070
288
c HYP836 Hypercholesterolemia, Familial, 1 73 0.069
289
P DMN001 Diamond-Blackfan Anemia 69 0.069
290
P SLP005 Sleep Disorder 59 0.069
291
P BRS044 Breast Adenocarcinoma 59 0.069
292
GST045 Gastroenteritis 59 0.069
293
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.069
294
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.069
295
MLT157 Multiple System Atrophy 1 70 0.068
296
P TRC086 Trichohepatoenteric Syndrome 1 62 0.068
297
DRM006 Dermatitis 61 0.068
298
CHL014 Cholera 59 0.068
299
MNT002 Mental Depression 58 0.068
300
SCH014 Schistosomiasis 57 0.068
301
P NRP001 Neuropathy 56 0.068
302
P FBR031 Febrile Seizures 53 0.068
303
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.068
304
c RST012 Restless Legs Syndrome 1 34 0.068
305
OST159 Osteogenic Sarcoma 66 0.067
306
c ACT068 Acute Cystitis 63 0.067
307
P URT039 Urticaria 58 0.067
308
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 57 0.067
309
GLC003 Glucose Intolerance 54 0.067
310
GST023 Gastric Ulcer 53 0.067
311
c MCR113 Microvascular Complications of Diabetes 3 52 0.067
312
HMG002 Hemoglobinuria 50 0.067
313
P CNG003 Congenital Dyserythropoietic Anemia 49 0.067
314
ANC001 Ancylostomiasis 43 0.067
315
c MCR130 Microvascular Complications of Diabetes 6 41 0.067
316
c MCR133 Microvascular Complications of Diabetes 4 41 0.067
317
PRP027 Peripheral Vascular Disease 71 0.065
318
c MGR028 Migraine with or Without Aura 1 67 0.065
319
PLM031 Poliomyelitis 64 0.065
320
P NPH012 Nephrotic Syndrome 60 0.065
321
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.065
322
SYN007 Synovitis 54 0.065
323
PNC001 Pancytopenia 54 0.065
324
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.065
325
c THR092 Thrombophilia Due to Thrombin Defect 73 0.064
326
P PRD008 Periodontitis 64 0.064
327
PRT013 Portal Hypertension 59 0.064
328
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.064
329
GRD001 Giardiasis 45 0.064
330
MCR017 Macrocytic Anemia 44 0.064
331
c HMG029 Hemoglobin Se Disease 39 0.064
332
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 37 0.064
333
PLC002 Plica Syndrome 36 0.064
334
BRT055 Breath-Holding Spells 30 0.064
335
P PRS040 Prostate Cancer 97 0.063
336
OST012 Osteoarthritis 78 0.063
337
c ATS007 Autism Spectrum Disorder 67 0.063
338
c FNC043 Fanconi Anemia, Complementation Group E 62 0.063
339
P PLY011 Polycystic Ovary Syndrome 56 0.063
340
PRT038 Protein-Energy Malnutrition 54 0.063
341
CRH005 Crohn's Colitis 53 0.063
342
P RTN018 Retinal Disease 53 0.063
343
ENT011 Enterocolitis 51 0.063
344
RBF001 Riboflavin Deficiency 49 0.063
345
c HMG003 Hemoglobin E Disease 45 0.063
346
ANG011 Angiodysplasia 43 0.063
347
SPR126 Superior Semicircular Canal Dehiscence 40 0.063
348
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.063
349
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.062
350
P RSP003 Respiratory Failure 74 0.062
351
P CNR004 Cone-Rod Dystrophy 2 73 0.062
352
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.062
353
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.062
354
P HYP069 Hyperparathyroidism 63 0.062
355
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.062
356
P BCL017 B-Cell Lymphoma 58 0.062
357
P CND004 Candidiasis 58 0.062
358
P CRD246 Cardiovascular System Disease 57 0.062
359
HYP060 Hyperinsulinism 54 0.062
360
P ALP008 Alopecia 54 0.062
361
P HYP730 Hypogonadotropic Hypogonadism 52 0.062
362
P RCT021 Rectum Cancer 52 0.062
363
DYS015 Dysentery 52 0.062
364
P LCT001 Lactic Acidosis 51 0.062
365
P BNG032 Benign Mesothelioma 46 0.062
366
SCR011 Scrapie 39 0.062
368
ESP021 Esophageal Cancer 90 0.060
369
c SYS001 Systemic Lupus Erythematosus 86 0.060
370
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.060
371
BRN028 Brain Cancer 74 0.060
372
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.060
373
LPD008 Lipid Metabolism Disorder 62 0.060
374
SPN186 Spinal Cord Injury 60 0.060
375
KFR001 Kufor-Rakeb Syndrome 60 0.060
376
P GLM007 Glomerulonephritis 57 0.060
377
P HYP076 Hyperthyroidism 55 0.060
378
AMN001 Amenorrhea 54 0.060
379
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.060
380
c DLT002 Dilated Cardiomyopathy 79 0.059
381
c SPN225 Spondyloarthropathy 1 73 0.059
382
P AMY004 Amyloidosis 70 0.059
383
P ASP006 Aspergillosis 69 0.059
384
TYP007 Typhoid Fever 63 0.059
385
ANR007 Anorexia Nervosa 63 0.059
386
P PSR002 Psoriasis 62 0.059
387
P VSC011 Vasculitis 62 0.059
388
ORL011 Oral Cancer 60 0.059
389
P HRD011 Hereditary Spherocytosis 60 0.059
390
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.059
391
P HYP024 Hypoparathyroidism 56 0.059
392
PRP030 Purpura 54 0.059
393
PST011 Pustulosis of Palm and Sole 52 0.059
394
GLS007 Glossitis 47 0.059
395
KWS001 Kwashiorkor 44 0.059
396
c ATM101 Autoimmune Gastritis 43 0.059
397
RDC006 Red Cell Aplasia 43 0.059
399
HMN044 Human Immunodeficiency Virus Type 1 71 0.057
400
c EXD008 Exudative Vitreoretinopathy 1 71 0.057
401
P MLN008 Melanoma 69 0.057
402
P HYP098 Hypereosinophilic Syndrome 67 0.057
403
P PLM036 Pulmonary Fibrosis 65 0.057
404
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.057
405
CHL068 Cholestasis 61 0.057
406
P LPS004 Lupus Erythematosus 61 0.057
407
P SNS001 Sensorineural Hearing Loss 60 0.057
408
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.057
409
CRY005 Cryptococcosis 58 0.057
410
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.057
411
LMY002 Leiomyoma 52 0.057
412
LYM019 Lymphosarcoma 46 0.057
413
CND006 Candida Glabrata 32 0.057
414
ANM001 Anemia of Prematurity 31 0.057
415
P BLD134 Bladder Cancer 79 0.056
416
LPT014 Leptin Deficiency or Dysfunction 74 0.056
417
P SRC025 Sarcoidosis 1 70 0.056
418
LYM133 Lymphoma, Hodgkin, Classic 69 0.056
419
P LPR021 Leprosy 3 69 0.056
420
BRR014 Barrett Esophagus 65 0.056
421
SKN016 Skin Disease 63 0.056
422
GLS018 Glass Syndrome 57 0.056
423
P HDC001 Headache 57 0.056
424
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.056
425
SPS057 Spasticity 45 0.056
426
HNS001 Hansen's Disease 34 0.056
427
NRL016 Neural Tube Defects 82 0.054
428
IMM167 Immune Deficiency Disease 78 0.054
429
SVR004 Severe Combined Immunodeficiency 73 0.054
430
c SVR001 Severe Acute Respiratory Syndrome 62 0.054
431
ACQ007 Acquired Immunodeficiency Syndrome 60 0.054
432
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.054
433
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.054
434
ANR040 Aneurysm 59 0.054
435
P PRP019 Peripheral Nervous System Disease 58 0.054
436
P INF032 Infertility 57 0.054
437
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.054
438
THR013 Thoracic Outlet Syndrome 54 0.054
439
OCL069 Ocular Motor Apraxia 51 0.054
440
STM007 Stomatitis 50 0.054
441
P PRR002 Pure Red-Cell Aplasia 47 0.054
442
CRB004 Cerebral Artery Occlusion 45 0.054
443
c PCH010 Pachyonychia Congenita 3 44 0.054
444
DWR001 Dwarfism 44 0.054
445
NRX001 Neuroaxonal Dystrophy 35 0.054
446
P ATX030 Ataxia-Telangiectasia 82 0.053
447
P LKM071 Leukemia, Chronic Lymphocytic 79 0.053
448
P LNG064 Lung Cancer Susceptibility 3 78 0.053
449
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.053
450
OTT002 Otitis Media 72 0.053
451
P ANG001 Angelman Syndrome 69 0.053
452
P MSC005 Muscular Dystrophy 66 0.053
453
HYP056 Hypoglycemia 66 0.053
454
P ART005 Arteriovenous Malformation 65 0.053
455
P ADL010 Adult Respiratory Distress Syndrome 65 0.053
456
CLN015 Colon Adenocarcinoma 65 0.053
457
P MYC008 Myocarditis 59 0.053
458
BLR008 Bilirubin Metabolic Disorder 57 0.053
459
P PYL005 Pyelonephritis 56 0.053
460
HYP005 Hypokalemia 55 0.053
461
ORL004 Oral Submucous Fibrosis 55 0.053
462
VSC003 Visceral Leishmaniasis 55 0.053
463
MYM001 Myoma 54 0.053
464
MTB004 Metabolic Acidosis 50 0.053
465
HRN026 Hernia, Hiatus 47 0.053
466
RTN023 Retinitis 46 0.053
467
NRR001 Neuroretinitis 42 0.053
468
GST020 Gastric Antral Vascular Ectasia 41 0.053
469
49X006 49, Xxxxy Syndrome 41 0.053
470
PHN003 Phenylketonuria 75 0.051
471
P PHC003 Pheochromocytoma 71 0.051
472
GST040 Gastric Adenocarcinoma 70 0.051
473
AND002 Androgen Insensitivity Syndrome 66 0.051
474
TTN003 Tetanus 65 0.051
475
c HPT003 Hepatitis a 62 0.051
476
c BRN108 Branchiootic Syndrome 1 62 0.051
477
TXC005 Toxic Shock Syndrome 62 0.051
478
P AXN002 Axenfeld-Rieger Syndrome 59 0.051
479
P SYP003 Syphilis 58 0.051
480
P ANP001 Anaplastic Large Cell Lymphoma 58 0.051
481
P PRN023 Prion Disease 57 0.051
482
CHR105 Choreoacanthocytosis 57 0.051
483
c ACT134 Acute Liver Failure 56 0.051
484
P MTC069 Mitochondrial Disorders 56 0.051
485
CHR073 Choreatic Disease 52 0.051
486
IMP005 Impotence 52 0.051
487
DDN006 Duodenitis 49 0.051
488
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.051
489
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 46 0.051
490
ALR002 Al-Raqad Syndrome 33 0.051
491
PTT016 Patterson Pseudoleprechaunism Syndrome 28 0.051
492
c FNC027 Fanconi Anemia, Complementation Group a 81 0.050
493
c LKM063 Leukemia, Chronic Myeloid 72 0.050
494
CHL065 Cholangiocarcinoma 68 0.050
495
P ATR011 Atrial Fibrillation 66 0.050
496
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.050
497
CLR108 Colorectal Adenoma 64 0.050
498
P GCH001 Gaucher's Disease 63 0.050
499
P ANR048 Aniridia 1 63 0.050
500
ACN002 Acanthosis Nigricans 60 0.050
501
PRN019 Perinatal Necrotizing Enterocolitis 59 0.050
502
P RHN004 Rhinitis 57 0.050
503
P HMG032 Hemoglobin H Disease 52 0.050
504
P SPP010 Suppressor of Tumorigenicity 3 51 0.050
505
P AST007 Astrocytoma 51 0.050
506
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.050
507
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.050
508
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.050
509
ATX010 Ataxia Neuropathy Spectrum 34 0.050
510
PPL052 Papillomatosis, Confluent and Reticulated 33 0.050
511
ACT064 Acute Necrotizing Encephalitis 33 0.050
512
BLD137 Blood Group--Ahonen 16 0.050
513
P EPL164 Epilepsy 71 0.048
514
P CRD119 Cardiac Arrest 67 0.048
515
CHG001 Chagas Disease 66 0.048
516
P HYD006 Hydrocephalus 66 0.048
517
KHL003 Kohlschutter-Tonz Syndrome 65 0.048
518
P HYP750 Hypertriglyceridemia, Familial 62 0.048
519
INT002 Intermittent Claudication 61 0.048
520
c DMN023 Diamond-Blackfan Anemia 1 53 0.048
521
DMY004 Demyelinating Disease 52 0.048
522
P THR015 Thrombophilia 51 0.048
523
NPH018 Nephrogenic Systemic Fibrosis 50 0.048
524
ENT004 Enthesopathy 49 0.048
525
SYN036 Syncope 45 0.048
526
c CHR682 Chronic Bilirubin Encephalopathy 39 0.048
527
ARG006 Aregenerative Anemia 27 0.048
528
c ATM060 Autoimmune Atrophic Gastritis 22 0.048
529
BRK010 Burkitt Lymphoma 67 0.046
530
PSY004 Psychotic Disorder 67 0.046
531
P MCR115 Microvascular Complications of Diabetes 5 66 0.046
532
P MNN013 Meningitis 66 0.046
533
MYL031 Myeloproliferative Neoplasm 66 0.046
534
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.046
535
CTN007 Cutaneous Leishmaniasis 62 0.046
536
MSL001 Measles 62 0.046
537
CHR066 Chronic Fatigue Syndrome 61 0.046
538
P PNC044 Pancreatitis 61 0.046
539
P KDN017 Kidney Cancer 60 0.046
540
VRC005 Varicose Veins 60 0.046
541
P LYM033 Lymphoproliferative Syndrome 59 0.046
542
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.046
543
P END033 Endocarditis 57 0.046
544
HPT046 Hepatic Veno-Occlusive Disease 56 0.046
545
PLS011 Plasmacytoma 56 0.046
546
TRD006 Tardive Dyskinesia 54 0.046
547
MST005 Mastitis 53 0.046
548
c GLL024 Gallbladder Disease 1 53 0.046
549
PLS009 Plasma Cell Neoplasm 51 0.046
550
INT079 Intrahepatic Cholangiocarcinoma 51 0.046
551
P OVR082 Overgrowth Syndrome 50 0.046
552
P OBS001 Obstructive Jaundice 50 0.046
553
MTC005 Mitochondrial Metabolism Disease 49 0.046
554
ADR040 Adrenal Gland Pheochromocytoma 46 0.046
555
P HMR005 Hemorrhoid 46 0.046
556
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.046
557
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.046
558
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.046
559
MCK029 Meckel Diverticulum 38 0.046
560
END028 Endemic Goiter 37 0.046
561
ATR073 Atrophic Glossitis 31 0.046
562
KPS004 Kaposi Sarcoma 75 0.044
563
P SLP006 Sleep Apnea 69 0.044
564
P INF038 Influenza 68 0.044
565
P ESS003 Essential Thrombocythemia 68 0.044
566
GST092 Gastroesophageal Reflux 67 0.044
567
ART001 Arterial Tortuosity Syndrome 66 0.044
568
c ART101 Aortic Valve Disease 2 65 0.044
569
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.044
570
OST017 Osteomyelitis 64 0.044
571
P LKD001 Leukodystrophy 59 0.044
572
PLM033 Pulmonary Embolism 59 0.044
573
FBR047 Fibromyalgia 58 0.044
574
CNT047 Contact Dermatitis 58 0.044
575
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.044
576
P ALP106 Alport Syndrome 1, X-Linked 55 0.044
577
P SLM003 Salmonellosis 55 0.044
578
LYM040 Lymphoblastic Lymphoma 54 0.044
579
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 52 0.044
580
PNG002 Pain Agnosia 51 0.044
581
CRT013 Carotid Stenosis 50 0.044
582
INT017 Intestinal Schistosomiasis 48 0.044
583
CHL147 Chlamydia Pneumonia 48 0.044
584
ASB001 Asbestosis 47 0.044
585
NSS002 Neisseria Meningitidis Infection 47 0.044
586
MNN020 Meningococcal Infection 46 0.044
587
HPT082 Hepatic Adenomas, Familial 44 0.044
588
CVD001 Covid-19 44 0.044
589
P FML340 Familial Episodic Pain Syndrome 39 0.044
590
ADP007 Adie Pupil 39 0.044
591
MNG007 Manganese Poisoning 29 0.044
592
MYC088 Mycobacterium Avium Complex Infections 29 0.044
593
HNM002 Hinman Syndrome 27 0.044
594
ASB003 Asbestos Intoxication 26 0.044
595
RRD019 Rare Deficiency Anemia 23 0.044
596
P RTN008 Retinitis Pigmentosa 79 0.043
597
INS024 Insulin-Like Growth Factor I 79 0.043
598
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.043
599
CRV035 Cervical Cancer 76 0.043
600
CRB037 Cerebral Palsy 69 0.043
601
EWN003 Ewing Sarcoma 69 0.043
602
MNT001 Mantle Cell Lymphoma 69 0.043
603
c BSL007 Basal Cell Carcinoma 68 0.043
604
P FLL037 Follicular Lymphoma 67 0.043
605
ANG054 Angina Pectoris 66 0.043
606
P MTR014 Motor Neuron Disease 65 0.043
607
P HRP006 Herpes Simplex 65 0.043
608
CHY002 Chylomicron Retention Disease 65 0.043
609
P PRS038 Personality Disorder 65 0.043
610
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.043
611
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.043
612
ALC006 Alcoholic Hepatitis 61 0.043
613
APP008 Appendicitis 61 0.043
614
ETN001 Eating Disorder 60 0.043
615
ANT024 Anthrax Disease 58 0.043
616
DSS008 Disease of Mental Health 58 0.043
617
c DWL002 Dowling-Degos Disease 1 58 0.043
618
c MST023 Mesothelioma, Malignant 57 0.043
619
P FBR017 Fibrosarcoma 56 0.043
620
LST001 Listeriosis 56 0.043
621
NRL004 Neuroleptic Malignant Syndrome 56 0.043
622
MCS002 Mucositis 56 0.043
623
CHR100 Chronic Ulcer of Skin 55 0.043
624
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.043
625
INT075 Intracranial Hypertension 53 0.043
626
P MSC003 Muscular Atrophy 52 0.043
627
P ACT105 Acute Mountain Sickness 52 0.043
628
c ACT135 Acute Graft Versus Host Disease 52 0.043
629
c SCN007 Secondary Hyperparathyroidism 51 0.043
630
c INF145 Infantile Liver Failure Syndrome 1 50 0.043
631
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 49 0.043
632
MCR004 Macroglobulinemia 49 0.043
633
VCC001 Vaccinia 49 0.043
634
c PRM038 Primary Agammaglobulinemia 44 0.043
635
RDN001 Reading Disorder 40 0.043
636
c FML324 Familial Porphyria Cutanea Tarda 31 0.043
638
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.043
639
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 25 0.043
640
NRD068 Neurodegeneration, Early-Onset, with Choreoathetoid Movements and Microcytic Anemia 21 0.043
641
AND005 Androgen Insensitivity Syndrome, Mild 19 0.043
642
ART016 Aortic Aneurysm 69 0.041
643
P SYS005 Systemic Scleroderma 68 0.041
644
BRC012 Brucellosis 64 0.041
645
c ATM011 Autoimmune Hepatitis 63 0.041
646
c SCL052 Scleroderma, Familial Progressive 61 0.041
647
TRG002 Trigeminal Neuralgia 60 0.041
648
P RBL001 Rubella 59 0.041
649
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.041
650
c CHR417 Chronic Graft Versus Host Disease 57 0.041
651
ALL010 Allergic Contact Dermatitis 56 0.041
652
PRP082 Porphyria, Congenital Erythropoietic 56 0.041
653
P VNS003 Venous Insufficiency 55 0.041
654
VGN023 Vaginitis 54 0.041
655
INF034 Infective Endocarditis 53 0.041
656
FNG017 Fungal Infectious Disease 53 0.041
657
ALC009 Alcoholic Liver Cirrhosis 53 0.041
658
PRP016 Paraplegia 52 0.041
659
MRG003 Marginal Zone B-Cell Lymphoma 52 0.041
660
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 51 0.041
661
BHR001 Behr Syndrome 51 0.041
662
P CHL066 Cholangitis 51 0.041
663
P KRT007 Keratoconus 50 0.041
664
c CNG027 Congenital Hemolytic Anemia 50 0.041
665
c CHR418 Chronic Leukemia 49 0.041
666
PPL021 Papilledema 49 0.041
667
c FLL041 Follicular Lymphoma 1 49 0.041
668
MNN009 Meningoencephalitis 49 0.041
669
P CTN015 Cutaneous T Cell Lymphoma 49 0.041
670
c INV001 Invasive Aspergillosis 49 0.041
671
P NGH001 Night Blindness 48 0.041
672
RTC005 Reticulosarcoma 47 0.041
673
CHR074 Choriocarcinoma 47 0.041
674
HDN002 Head Injury 46 0.041
675
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.041
676
DMP001 Dumping Syndrome 44 0.041
677
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.041
678
MRS001 Marasmus 42 0.041
679
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.041
680
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.041
681
BLR027 Blue Rubber Bleb Nevus 40 0.041
682
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.041
683
HRN029 Hearing Loss, Noise-Induced 37 0.041
684
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.041
685
PLY150 Polykaryocytosis Inducer 31 0.041
686
PYR016 Pyridoxine Deficiency 30 0.041
687
c PRP091 Porphyria Cutanea Tarda, Type I 29 0.041
688
PLS032 Plasmodium Falciparum Blood Infection Level 22 0.041
689
c GCH015 Gaucher Disease, Type I 70 0.038
690
CRT072 Creutzfeldt-Jakob Disease 70 0.038
691
c HMP029 Hemophilia a 67 0.038
692
P SKN015 Skin Carcinoma 66 0.038
693
c MCR129 Microvascular Complications of Diabetes 1 66 0.038
694
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.038
695
c DBT099 Diabetes Mellitus, Type I 65 0.038
696
MSC007 Muscle Hypertrophy 64 0.038
697
TRN015 Transient Cerebral Ischemia 63 0.038
698
HMT002 Hematologic Cancer 62 0.038
699
P PLY014 Polycystic Kidney Disease 62 0.038
700
c ANM038 Anemia, Autoimmune Hemolytic 62 0.038
701
P ACR001 Aicardi-Goutieres Syndrome 62 0.038
702
VRL011 Viral Infectious Disease 61 0.038
703
P ALP009 Alopecia Areata 60 0.038
704
RHM001 Rheumatic Fever 60 0.038
705
GNG013 Gingivitis 59 0.038
706
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.038
707
BRN056 Bronchopulmonary Dysplasia 57 0.038
708
APH001 Aphthous Stomatitis 57 0.038
709
VSC002 Vascular Dementia 57 0.038
710
PLC005 Placental Insufficiency 57 0.038
711
HPT022 Hepatoblastoma 56 0.038
712
HST011 Histoplasmosis 55 0.038
713
LMB062 Limb Ischemia 55 0.038
714
ESN011 Eisenmenger Syndrome 55 0.038
715
INT007 Intermediate Coronary Syndrome 55 0.038
716
HRY003 Hairy Cell Leukemia 55 0.038
717
P ART021 Arteriosclerosis 54 0.038
718
c CNT016 Central Retinal Vein Occlusion 53 0.038
719
c PRD040 Periodontitis, Chronic 53 0.038
720
HMC014 Homocysteinemia 53 0.038
721
P RTN022 Retinal Vein Occlusion 53 0.038
722
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.038
723
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.038
724
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.038
725
P HMP007 Hemophilia 51 0.038
726
CLR109 Colorectal Adenocarcinoma 51 0.038
727
CLC001 Calciphylaxis 51 0.038
728
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 51 0.038
729
CVR006 Cavernous Hemangioma 49 0.038
730
c PRK071 Parkinson Disease 14, Autosomal Recessive 48 0.038
731
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.038
732
ATN005 Autonomic Dysfunction 46 0.038
733
P MTH007 Methemoglobinemia 46 0.038
734
TRC012 Trichuriasis 45 0.038
735
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.038
736
BBN001 Bubonic Plague 41 0.038
737
ORM002 Oromandibular Dystonia 39 0.038
738
SPR066 Superficial Siderosis 39 0.038
739
CTN011 Cutaneous Porphyria 38 0.038
740
c HMC019 Hemochromatosis, Type 2b 36 0.038
741
c BLD140 Blood Group, I System 32 0.038
742
ARG004 Argyria 27 0.038
743
PRT025 Protein-Deficiency Anemia 27 0.038
744
c ATS210 Autosomal Recessive Sideroblastic Anemia 26 0.038
745
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.038
746
STN013 Stenotrophomonas Maltophilia Infection 25 0.038
747
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.038
748
BLD163 Blood Group, Dombrock System 24 0.038
749
P MDL005 Medulloblastoma 77 0.036
750
AST005 Asthma 76 0.036
751
c MNN043 Meningioma, Familial 74 0.036
752
MYC006 Mycosis Fungoides 66 0.036
753
LPT001 Leptospirosis 66 0.036
754
P NSP012 Nasopharyngeal Carcinoma 66 0.036
755
c HRD010 Hereditary Spastic Paraplegia 66 0.036
756
P NRV007 Nervous System Disease 66 0.036
757
c MCL013 Mucolipidosis Iv 66 0.036
758
c SML038 Small Cell Cancer of the Lung 65 0.036
759
P VNW001 Von Willebrand's Disease 65 0.036
760
GT001 Gout 64 0.036
761
c MLG084 Malignant Fibrous Histiocytoma 63 0.036
762
MNN042 Meningioma, Radiation-Induced 62 0.036
763
CRC021 Carcinosarcoma 62 0.036
764
MDD011 Mood Disorder 62 0.036
765
P PRM006 Primary Biliary Cirrhosis 62 0.036
766
NRM001 Neuromyelitis Optica 61 0.036
767
P ENC004 Encephalitis 61 0.036
768
SDD001 Sudden Infant Death Syndrome 61 0.036
769
SZR001 Sezary's Disease 60 0.036
770
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.036
771
c ACT027 Acute Pancreatitis 60 0.036
772
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.036
773
SQM006 Squamous Cell Carcinoma 60 0.036
774
STT001 Status Epilepticus 60 0.036
775
P OPT006 Optic Nerve Disease 60 0.036
776
P UVT001 Uveitis 57 0.036
777
CST005 Castleman Disease 57 0.036
778
DSS009 Disseminated Intravascular Coagulation 57 0.036
779
P ADL017 Adult T-Cell Leukemia 56 0.036
780
CMR002 Coumarin Resistance 56 0.036
781
VRG001 Variegate Porphyria 56 0.036
782
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.036
783
SLP001 Sleeping Sickness 54 0.036
784
PST046 Post-Transplant Lymphoproliferative Disease 53 0.036
785
TRC003 Trichomoniasis 53 0.036
786
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.036
787
ILS001 Ileus 51 0.036
788
CCC002 Coccidiosis 51 0.036
789
TLR001 Tularemia 51 0.036
790
c ALM001 Al Amyloidosis 50 0.036
791
P MMB011 Membranous Nephropathy 50 0.036
792
SPN021 Spinal Meningioma 50 0.036
793
c SVR005 Severe Pre-Eclampsia 50 0.036
794
HYP068 Hyperostosis 48 0.036
795
CHL056 Cheilitis 48 0.036
796
PLC007 Placental Abruption 48 0.036
797
P PRP056 Porphyria, Acute Hepatic 48 0.036
798
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.036
799
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.036
800
PLS025 Plasmablastic Lymphoma 47 0.036
801
P OVR046 Ovarian Cyst 47 0.036
802
BRN032 Brain Glioma 45 0.036
803
MYF001 Myofibroma 45 0.036
804
HPT067 Hepatocellular Adenoma 44 0.036
805
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.036
806
MDD018 Middle East Respiratory Syndrome 43 0.036
807
DRG024 Drug Allergy 42 0.036
808
c HMG001 Hemoglobin C Disease 40 0.036
809
c SPS130 Spastic Paraplegia 43, Autosomal Recessive 39 0.036
810
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.036
811
AMN006 Aminoaciduria 38 0.036
812
c LKM005 Leukemia, T-Cell, Chronic 34 0.036
813
PST010 Pasteurellosis 34 0.036
814
NNT011 Neonatal Anemia 34 0.036
815
PRD002 Periodic Limb Movement Disorder 33 0.036
816
FLC001 Folic Acid Deficiency Anemia 32 0.036
817
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.036
818
ANG061 Angular Cheilitis 26 0.036
819
P RTT002 Rett Syndrome 80 0.034
820
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.034
821
GST019 Gastrointestinal Stromal Tumor 78 0.034
822
END057 Endometrial Cancer 74 0.034
823
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.034
824
P RTN024 Retinoblastoma 73 0.034
825
PTZ001 Peutz-Jeghers Syndrome 70 0.034
826
P HYP061 Hypertrophic Cardiomyopathy 70 0.034
827
ABT001 Abetalipoproteinemia 69 0.034
828
P OCL013 Oculodentodigital Dysplasia 69 0.034
829
OBS002 Obsessive-Compulsive Disorder 68 0.034
830
PNC129 Pancreatic Adenocarcinoma 68 0.034
831
FCT007 Factor Vii Deficiency 67 0.034
832
P DRM053 Dermatitis, Atopic 66 0.034
833
IRR002 Irritable Bowel Syndrome 65 0.034
834
MNK001 Menkes Disease 64 0.034
835
P RHB003 Rhabdomyosarcoma 63 0.034
836
P SHR029 Short Syndrome 63 0.034
837
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.034
838
P ORT004 Orthostatic Intolerance 62 0.034
839
c PNS012 Paine Syndrome 61 0.034
840
WLD007 Waldenstroem's Macroglobulinemia 61 0.034
841
P TXP001 Toxoplasmosis 60 0.034
842
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.034
843
INS001 Insulinoma 60 0.034
844
IGR001 Ige Responsiveness, Atopic 59 0.034
845
BRN002 Bronchiolitis 59 0.034
846
HMR039 Hemorrhage, Intracerebral 57 0.034
847
INT303 Intracranial Hypertension, Idiopathic 57 0.034
848
P ANG015 Angioedema 57 0.034
849
EMB004 Embryonal Carcinoma 56 0.034
850
DFF005 Diffuse Large B-Cell Lymphoma 55 0.034
851
FCL014 Focal Epilepsy 54 0.034
852
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.034
853
PPL022 Papilloma 54 0.034
854
PTT009 Pituitary Gland Disease 54 0.034
855
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.034
856
P TCD001 Tic Disorder 53 0.034
857
P HYP083 Hypopituitarism 53 0.034
858
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.034
859
P THY032 Thyroiditis 52 0.034
860
SPN051 Spondylitis 51 0.034
861
KRT009 Keratosis 51 0.034
862
SPL004 Splenic Marginal Zone Lymphoma 51 0.034
863
TRY001 Trypanosomiasis 50 0.034
864
ERY004 Erysipelas 49 0.034
865
HST010 Histiocytosis 48 0.034
866
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.034
867
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.034
868
ASP004 Asphyxia Neonatorum 46 0.034
869
RTN020 Retinal Vascular Disease 46 0.034
870
c ACQ010 Acquired Polycythemia 46 0.034
871
GRW007 Growth Hormone Deficiency 46 0.034
872
SQM002 Squamous Cell Papilloma 46 0.034
873
c MLG068 Malignant Glioma 46 0.034
874
CYN002 Cyanosis, Transient Neonatal 45 0.034
875
P CHR345 Chronic Pain 44 0.034
876
MCR011 Microinvasive Gastric Cancer 43 0.034
877
ORL015 Oral Squamous Cell Carcinoma 43 0.034
878
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.034
879
FSC002 Fascioliasis 42 0.034
880
SCR001 Secretory Meningioma 41 0.034
881
CRB086 Cerebral Aneurysms 40 0.034
882
c ACT004 Acute Diarrhea 39 0.034
883
GLM044 Glomerular Disease 37 0.034
884
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.034
885
c HYP716 Hypermanganesemia with Dystonia 1 35 0.034
886
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.034
887
c CHR064 Chronic Monocytic Leukemia 33 0.034
888
MTL002 Metal Metabolism Disorder 30 0.034
889
HVY002 Heavy Metal Poisoning 22 0.034
890
BLD165 Blood Group, Colton System 20 0.034
891
TRN072 Transferrin Serum Level Quantitative Trait Locus 2 16 0.034
892
c NRF023 Neurofibromatosis, Type Ii 80 0.031
893
P SCH015 Schizophrenia 74 0.031
894
MSC157 Muscular Dystrophy, Duchenne Type 72 0.031
895
P FML011 Familial Adenomatous Polyposis 72 0.031
896
CNN005 Connective Tissue Disease 68 0.031
897
MLD001 Melioidosis 68 0.031
898
P CHR012 Chronic Granulomatous Disease 67 0.031
899
CRP001 Carpal Tunnel Syndrome 67 0.031
900
KWS002 Kawasaki Disease 65 0.031
901
ANG020 Angiosarcoma 64 0.031
902
CLF027 Cleft Palate, Isolated 64 0.031
903
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.031
904
PRP083 Porphyria, Acute Intermittent 64 0.031
905
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.031
906
c DPH024 Diaphragmatic Hernia, Congenital 63 0.031
907
CHR063 Chronic Mucocutaneous Candidiasis 63 0.031
908
HYD038 Hydrops Fetalis, Nonimmune 62 0.031
909
HSH003 Hashimoto Thyroiditis 62 0.031
910
c LPM012 Lipomatosis, Multiple 60 0.031
911
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.031
912
STF001 Stiff-Person Syndrome 60 0.031
913
P INT070 Intestinal Obstruction 58 0.031
914
CRD132 Cardiac Conduction Defect 58 0.031
915
ADL030 Adult-Onset Still's Disease 58 0.031
916
EYD002 Eye Disease 58 0.031
917
CHL067 Cholecystitis 57 0.031
918
CMM005 Common Cold 57 0.031
919
P FTL001 Fetal Alcohol Syndrome 57 0.031
920
CYT008 Cytomegalovirus Infection 57 0.031
921
ALL006 Allergic Asthma 56 0.031
922
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 0.031
923
BRN012 Bronchiolitis Obliterans 55 0.031
924
NPH009 Nephrolithiasis 55 0.031
925
P PLM034 Pulmonary Emphysema 55 0.031
926
P ANT006 Antiphospholipid Syndrome 55 0.031
927
P DRM007 Dermatitis Herpetiformis 55 0.031
928
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 54 0.031
929
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.031
930
PRC013 Pericarditis 54 0.031
931
PRC002 Paracoccidioidomycosis 54 0.031
932
CLL003 Cellulitis 54 0.031
933
PRS045 Prostatic Hypertrophy 53 0.031
934
BCT002 Bacterial Vaginosis 53 0.031
935
BRN038 Bronchial Disease 53 0.031
936
HYP063 Hypersplenism 53 0.031
937
c FML008 Familial Retinoblastoma 53 0.031
938
c CNT035 Central Nervous System Disease 52 0.031
939
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.031
940
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.031
941
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.031
942
P SML001 Small Cell Carcinoma 52 0.031
943
THY030 Thyroid Gland Disease 52 0.031
944
PPT001 Peptic Esophagitis 52 0.031
945
c FNC025 Fanconi Anemia, Complementation Group J 52 0.031
946
PRS021 Prostatic Adenoma 51 0.031
947
ALK024 Alkuraya-Kucinskas Syndrome 51 0.031
948
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.031
949
c HRD202 Hereditary Lymphedema I 50 0.031
950
ASC010 Ascaris Lumbricoides Infection 50 0.031
951
P TMP001 Temporal Lobe Epilepsy 50 0.031
952
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.031
953
LPR001 Lepromatous Leprosy 50 0.031
954
RNL011 Renal Osteodystrophy 50 0.031
955
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.031
956
P MST002 Mast-Cell Leukemia 49 0.031
957
PRS129 Prostatic Hyperplasia, Benign 49 0.031
958
HYP043 Hyperandrogenism 48 0.031
959
VTM033 Vitamin K Deficiency Bleeding 48 0.031
960
SXL003 Sexual Disorder 47 0.031
961
LYM012 Lymphoplasmacytic Lymphoma 47 0.031
962
TST014 Testicular Cancer 46 0.031
963
URN003 Urinary Schistosomiasis 46 0.031
964
MLK003 Melkersson-Rosenthal Syndrome 45 0.031
965
PRT019 Protein-Losing Enteropathy 45 0.031
966
LYM051 Lymphomatoid Granulomatosis 45 0.031
967
CLD007 Cold Agglutinin Disease 45 0.031
968
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.031
969
SDD008 Sudden Sensorineural Hearing Loss 43 0.031
970
BCK006 Back Pain 42 0.031
971
LCN001 Lice Infestation 42 0.031
972
XRP001 Xerophthalmia 41 0.031
973
PLM005 Pleomorphic Lipoma 40 0.031
974
WDH003 Woodhouse-Sakati Syndrome 40 0.031
975
c ERL056 Early-Onset Parkinson's Disease 39 0.031
976
HYP344 Hyperthyroidism, Familial Gestational 39 0.031
977
P PRC031 Preeclampsia/eclampsia 1 38 0.031
978
CRB009 Cerebritis 37 0.031
979
SPN331 Spondyloocular Syndrome 36 0.031
980
P AXN001 Axonal Neuropathy 36 0.031
981
c DRM040 Dermatitis Herpetiformis, Familial 35 0.031
982
PRM329 Premature Aging 35 0.031
983
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.031
984
PYR009 Pyridoxine Deficiency Anemia 34 0.031
985
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 0.031
986
NRN002 Neuronitis 32 0.031
987
PRT094 Protoporphyria, Erythropoietic, X-Linked 31 0.031
988
STT009 Sutton Disease 2 30 0.031
989
MTY003 Mutyh Polyposis 30 0.031
990
c INF078 Inflammatory Bowel Disease 2 29 0.031
991
CLS052 Classic Hairy Cell Leukemia 27 0.031
992
HDG004 Hodgkin's Granuloma 23 0.031
993
HDG006 Hodgkin's Paragranuloma 22 0.031
994
VBR003 Vibrio Vulnificus Infection 22 0.031
995
PST047 Post-Traumatic Epilepsy 22 0.031
996
P TTR001 Tetralogy of Fallot 70 0.029
997
c PNC108 Pancreatitis, Hereditary 70 0.029
998
MST024 Mastocytosis, Cutaneous 69 0.029
999
SKN019 Skin Melanoma 68 0.029
1000
P MYS003 Myasthenia Gravis 68 0.029
1001
P MJR001 Major Depressive Disorder 68 0.029
1002
P FRN006 Frontotemporal Dementia 68 0.029
1003
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.029
1004
ALL003 Allergic Rhinitis 67 0.029
1005
LNG039 Lung Squamous Cell Carcinoma 66 0.029
1006
c FML001 Familial Atrial Fibrillation 65 0.029
1007
PPL049 Papillon-Lefevre Syndrome 65 0.029
1008
MSM014 Mismatch Repair Cancer Syndrome 65 0.029
1009
PND002 Pendred Syndrome 65 0.029
1010
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.029
1011
NRM005 Neuromuscular Disease 64 0.029
1012
c JVN010 Juvenile Rheumatoid Arthritis 64 0.029
1013
ART002 Arts Syndrome 64 0.029
1014
LYM017 Lyme Disease 64 0.029
1015
P DST002 Distal Arthrogryposis 63 0.029
1016
ACT119 Acute Promyelocytic Leukemia 63 0.029
1017
P LMY004 Leiomyosarcoma 63 0.029
1018
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.029
1019
c DYS056 Dystonia 12 62 0.029
1020
YLL002 Yellow Fever 61 0.029
1021
c WLM018 Wilms Tumor 5 61 0.029
1022
P SJG008 Sjogren Syndrome 61 0.029
1023
INT066 Interstitial Lung Disease 60 0.029
1024
CRD223 Cardiac Arrhythmia 60 0.029
1025
ING001 Inguinal Hernia 60 0.029
1026
P GLY013 Glycogen Storage Disease 60 0.029
1027
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.029
1028
THY029 Thyroid Carcinoma 59 0.029
1029
P CYS018 Cystitis 59 0.029
1030
SPT004 Septic Arthritis 58 0.029
1031
NWB001 Newborn Respiratory Distress Syndrome 58 0.029
1032
P BNC003 Bone Cancer 58 0.029
1033
BLM002 Bulimia Nervosa 57 0.029
1034
AYM001 Ayme-Gripp Syndrome 57 0.029
1035
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 0.029
1036
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.029
1037
SFT003 Soft Tissue Sarcoma 56 0.029
1038
P NRF002 Neurofibromatosis 56 0.029
1039
FLR002 Filariasis 55 0.029
1040
END040 Endogenous Depression 55 0.029
1041
P LRY044 Larynx Cancer 55 0.029
1042
GLS001 Gliosarcoma 54 0.029
1043
ACD008 Acid-Labile Subunit Deficiency 54 0.029
1044
DBT010 Diabetic Neuropathy 54 0.029
1045
P LCH002 Lichen Planus 53 0.029
1046
PLS016 Plasma Cell Leukemia 53 0.029
1047
KRT006 Keratoconjunctivitis 53 0.029
1048
P MNC007 Monocytic Leukemia 53 0.029
1049
P PLM006 Pulmonary Alveolar Proteinosis 53 0.029
1050
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.029
1051
P SHR001 Short Bowel Syndrome 53 0.029
1052
INT051 Intussusception 53 0.029
1053
PRP080 Peripheral Artery Disease 53 0.029
1054
LYS002 Lysosomal Storage Disease 52 0.029
1055
BWN001 Bowen-Conradi Syndrome 52 0.029
1056
LGN006 Legionnaire Disease 52 0.029
1057
APR001 Apraxia 52 0.029
1058
TRC010 Trichotillomania 51 0.029
1059
AVD001 Avoidant Personality Disorder 51 0.029
1060
FDL002 Food Allergy 51 0.029
1061
LNG031 Lung Benign Neoplasm 51 0.029
1062
P PRC012 Pericardial Effusion 51 0.029
1063
HYP074 Hypersensitivity Vasculitis 51 0.029
1064
CHR005 Chorioamnionitis 51 0.029
1065
P FNC004 Fanconi Syndrome 50 0.029
1066
P PRT096 Peritoneal Mesothelioma 50 0.029
1067
P MTR003 Mitral Valve Stenosis 50 0.029
1068
FSC004 Fasciitis 50 0.029
1069
ILT001 Ileitis 50 0.029
1070
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.029
1071
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 50 0.029
1072
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.029
1073
PTT059 Pettigrew Syndrome 49 0.029
1074
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.029
1075
P MCL001 Mucolipidosis 48 0.029
1076
HMP001 Hemopericardium 48 0.029
1077
MLK006 Milk Allergy 48 0.029
1078
P MRC003 Mercury Poisoning 48 0.029
1079
PRL017 Prolymphocytic Leukemia 47 0.029
1080
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 47 0.029
1081
ABD017