Search results for Iron

2821 hits were found for Iron

# Family MCID Name MIFTS Score
1
IRN002 Iron Metabolism Disease 58 8.720
2
IRN004 Iron-Refractory Iron Deficiency Anemia 45 8.504
3
IRN001 Iron Deficiency Anemia 59 6.079
4
c NRD032 Neurodegeneration with Brain Iron Accumulation 5 49 6.021
5
c NRD014 Neurodegeneration with Brain Iron Accumulation 4 41 5.596
6
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 58 5.504
7
P NRD007 Neurodegeneration with Brain Iron Accumulation 48 5.412
8
c NRD009 Neurodegeneration with Brain Iron Accumulation 2b 39 5.364
9
IRN008 Iron Overload in Africa 51 5.262
10
P RRH023 Rare Hereditary Hemochromatosis 41 5.233
11
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 48 4.922
12
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 26 4.897
13
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 4.742
14
c HMC034 Hemochromatosis, Type 5 34 4.668
15
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 45 4.186
16
c ANM027 Anemia, Hypochromic Microcytic, with Iron Overload 2 22 4.092
17
HMS001 Hemosiderosis 54 3.745
18
GRC001 Gracile Syndrome 38 3.506
19
MTC036 Mitochondrial Membrane Protein-Associated Neurodegeneration 22 3.500
20
MCR018 Microcytic Anemia 46 3.476
21
c HMC039 Hemochromatosis, Type 1 73 3.335
22
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 3.281
23
c ANM036 Anemia, Sideroblastic, 1 56 3.218
24
c NRD047 Neurodegeneration with Brain Iron Accumulation 7 22 3.109
25
c NRD048 Neurodegeneration with Brain Iron Accumulation 8 19 3.109
26
LYM125 Lymphedema, Cardiac Septal Defects, and Characteristic Facies 21 3.088
27
CSY002 Coasy Protein-Associated Neurodegeneration 22 2.680
28
MYP025 Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme 11 2.196
29
IRN005 Irons Bhan Syndrome 8 2.190
30
P SDR002 Siderosis 42 2.043
31
P SDR003 Sideroblastic Anemia 47 1.778
32
c HMC009 Hemochromatosis Type 2 45 1.718
33
MYP009 Myopathy with Deficiency of Iscu 12 1.608
34
MYP097 Myopathy with Lactic Acidosis, Hereditary 31 1.596
35
GNT037 Genetic Hyperferritinemia Without Iron Overload 9 1.583
36
c CNS020 Constitutional Anemia Due to Iron Metabolism Disorder 4 1.572
37
KRK002 Karak Syndrome 18 1.567
38
DSR030 Disorder of Iron Metabolism and Transport 3 1.567
39
P ZLL001 Zellweger Syndrome 56 1.560
40
OBS149 Obsolete: Hereditary Iron Overload with Neurologic Manifestation 2 1.560
41
OBS376 Obsolete: Rare Hereditary Iron Overload Disease 2 1.560
42
OBS148 Obsolete: Hereditary Iron Overload with Anemia 1 1.560
43
FRR002 Ferro-Cerebro-Cutaneous Syndrome 10 1.544
44
SLC011 Silicosiderosis 9 1.533
45
ARN001 Arena Syndrome 5 1.533
46
DFC004 Deficiency Anemia 77 1.191
47
P THL005 Thalassemia 62 0.566
48
c CHR684 Chronic Kidney Disease 68 0.345
49
P KDN018 Kidney Disease 73 0.344
50
c BTT014 Beta-Thalassemia 73 0.325
51
P LVR013 Liver Disease 71 0.285
52
NTR005 Nutritional Deficiency Disease 61 0.282
53
MYL009 Myelodysplastic Syndrome 72 0.266
54
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.253
55
P HRT032 Heart Disease 78 0.252
56
P INF037 Inflammatory Bowel Disease 57 0.245
57
P SCK005 Sickle Cell Disease 53 0.236
58
CNG034 Congestive Heart Failure 69 0.235
59
END030 End Stage Renal Failure 60 0.232
60
LVR012 Liver Cirrhosis 67 0.232
61
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.221
62
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.205
63
c HPT001 Hepatitis C 62 0.193
64
MLR004 Malaria 82 0.192
65
P DRR001 Diarrhea 55 0.190
66
P GST044 Gastritis 58 0.185
67
P RST001 Restless Legs Syndrome 54 0.185
68
P PRP029 Porphyria 58 0.185
69
FTT001 Fatty Liver Disease 63 0.181
70
HYP266 Hypoxia 58 0.177
71
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.176
72
P ALZ034 Alzheimer Disease 90 0.169
73
P CLC063 Celiac Disease 1 66 0.166
74
HLC007 Helicobacter Pylori Infection 61 0.165
75
ACR006 Aceruloplasminemia 74 0.163
76
HYP001 Hypochromic Microcytic Anemia 38 0.163
77
KRT002 Keratomalacia 47 0.161
78
P HPT023 Hepatocellular Carcinoma 99 0.161
79
SCK003 Sickle Cell Anemia 74 0.160
80
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.158
81
c ALP101 Alpha-Thalassemia 63 0.158
82
HMG005 Hemoglobinopathy 57 0.158
83
CNS004 Constipation 59 0.155
84
P PRP003 Porphyria Cutanea Tarda 66 0.155
85
P CLR023 Colorectal Cancer 100 0.154
86
P HML002 Hemolytic Anemia 64 0.149
87
ATH013 Atherosclerosis Susceptibility 68 0.146
88
P FRD012 Friedreich Ataxia 1 65 0.145
89
PCD001 Pica Disease 33 0.145
90
c VRL010 Viral Hepatitis 56 0.140
91
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.140
92
c ATR087 Atrial Standstill 1 76 0.138
93
P NRB010 Neuroblastoma 1 66 0.137
94
THR004 Thrombocytosis 52 0.136
95
P APL001 Aplastic Anemia 76 0.134
97
CHL079 Children's Interstitial Lung Disease 27 0.134
98
HYP080 Hypogonadism 51 0.133
99
ATS010 Autosomal Recessive Disease 49 0.133
100
CRH001 Crohn's Disease 75 0.131
101
HLX001 Helix Syndrome 46 0.131
102
HYP064 Hypogonadotropism 40 0.131
103
48X005 48,xyyy 37 0.131
104
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.131
105
c HPT073 Hepatitis C Virus 74 0.130
106
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.129
107
P PRK057 Parkinson Disease, Late-Onset 77 0.128
108
ALL026 Allergic Hypersensitivity Disease 65 0.128
109
P MLT020 Multiple Sclerosis 73 0.127
110
P HYP086 Hypothyroidism 70 0.127
111
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.127
112
NNL006 Non-Alcoholic Steatohepatitis 53 0.127
113
P PLY018 Polycythemia 56 0.126
114
ULC004 Ulcerative Colitis 75 0.124
115
HMT018 Hematopoietic Stem Cell Transplantation 54 0.124
116
P HPT021 Hepatitis 69 0.123
117
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.123
118
P PLM037 Pulmonary Hypertension 69 0.122
119
GRN017 Granulocytopenia 46 0.122
120
P RHM011 Rheumatoid Arthritis 82 0.121
121
BCT022 Bacterial Infectious Disease 57 0.121
122
P LTR001 Lateral Sclerosis 56 0.121
123
VTM002 Vitamin B12 Deficiency 48 0.121
124
P ART023 Arthropathy 61 0.121
125
P DYS154 Dystonia 65 0.120
126
CLT003 Colitis 63 0.119
127
CYS001 Cystic Fibrosis 84 0.118
128
HYP781 Hypoascorbemia 48 0.118
129
GST033 Gestational Diabetes 58 0.117
130
P NTR004 Neutropenia 64 0.117
131
HYP017 Hypophosphatemia 48 0.117
132
P GLM045 Glioma 64 0.115
133
P CRN300 Coronary Heart Disease 1 59 0.115
134
ERY051 Erythroleukemia, Familial 58 0.115
135
GLL048 Glial Tumor 48 0.115
136
P HNT016 Huntington Disease 72 0.114
137
P DBT009 Diabetes Mellitus 66 0.114
138
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.114
139
c JVN024 Juvenile Hereditary Hemochromatosis 32 0.114
140
P THR014 Thrombocytopenia 67 0.113
141
P CTR002 Cataract 62 0.113
142
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.113
143
AGN016 Aging 58 0.113
144
RFR010 Refractory Anemia 50 0.113
145
GLB002 Glioblastoma 74 0.112
146
c PRC016 Pre-Eclampsia 63 0.112
147
GLB015 Glioblastoma Multiforme 60 0.112
149
47X002 47,xyy 49 0.112
150
P LKM002 Leukemia 69 0.110
151
LNG099 Lung Disease 62 0.110
152
RCK004 Rickets 70 0.109
153
P RTN016 Retinal Degeneration 56 0.108
154
SPL018 Splenomegaly 48 0.108
155
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.107
156
HMP009 Haemophilus Influenzae 46 0.107
157
HRW001 Hair Whorl 36 0.107
158
HYP801 Hyperferritinemia with or Without Cataract 48 0.106
159
P BRS047 Breast Cancer 99 0.105
160
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.104
161
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.104
162
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.104
163
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.104
164
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.104
165
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.104
166
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.104
167
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.104
168
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.104
169
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.104
170
ALC007 Alcohol Dependence 68 0.103
171
CHL123 Chlamydia 60 0.103
172
ISC004 Ischemia 62 0.102
173
c ACT073 Acute Leukemia 59 0.102
174
P LYM031 Lymphocytic Leukemia 56 0.102
175
c HMC021 Hemochromatosis, Type 2a 51 0.101
176
c LKM061 Leukemia, Acute Myeloid 84 0.100
177
P MYC007 Myocardial Infarction 74 0.100
178
PLM001 Pulmonary Tuberculosis 72 0.100
179
P VSC007 Vascular Disease 65 0.100
180
ADN018 Adenoma 60 0.100
181
P INT068 Intestinal Disease 56 0.100
182
c HYP595 Hypertension, Essential 87 0.099
183
c RHB024 Rhabdomyosarcoma 2 64 0.099
184
P EXN002 Exanthem 58 0.099
185
BRN071 Brain Injury 51 0.099
186
P ART022 Arthritis 71 0.098
187
P MVM001 Movement Disease 63 0.098
188
DPH001 Diphtheria 61 0.098
189
P TRM003 Tremor 55 0.098
190
ANT018 Anthracosis 46 0.098
191
PPT005 Peptic Ulcer Disease 60 0.097
192
P PNM006 Pneumoconiosis 55 0.097
193
CYT002 Cytokine Deficiency 46 0.097
194
CRB039 Cerebrovascular Disease 71 0.096
195
P ADN016 Adenocarcinoma 65 0.096
196
P ALC033 Alcohol Use Disorder 58 0.096
197
P GST053 Gastric Cancer 85 0.095
198
P TRN020 Turner Syndrome 66 0.095
199
LSH001 Leishmaniasis 64 0.095
200
P ATR005 Atrophic Gastritis 49 0.095
201
P KLZ004 Kala-Azar 1 43 0.095
202
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.094
203
P END044 Endometriosis 63 0.094
204
GST050 Gastrointestinal System Disease 57 0.093
205
URM002 Uremia 50 0.093
206
HYP025 Hyperphosphatemia 47 0.093
207
PST092 Posttransplant Acute Limbic Encephalitis 29 0.093
208
P OST002 Osteoporosis 79 0.092
209
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.092
210
MYL005 Myelofibrosis 69 0.092
211
ATM095 Autoimmune Disease 62 0.092
212
P MYL006 Myeloid Leukemia 61 0.092
213
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.090
214
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.089
215
MCR141 Mucormycosis 48 0.089
216
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.089
217
MTH071 Methane Production 26 0.089
218
GTR002 Goiter 54 0.088
219
BNR002 Bone Resorption Disease 51 0.088
220
P PNC035 Pancreatic Cancer 86 0.087
221
DWN001 Down Syndrome 70 0.087
222
P LYM118 Lymphoma 70 0.087
223
PRT037 Pertussis 66 0.087
224
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.087
225
ALL014 Allergic Encephalomyelitis 40 0.087
226
OST011 Osteomalacia 51 0.086
227
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.086
228
WLS001 Wilson Disease 69 0.085
229
ADL002 Adult Syndrome 62 0.085
230
THR024 Thrombosis 58 0.085
231
PLG002 Plague 54 0.085
232
ATX019 Ataxia with Vitamin E Deficiency 46 0.085
233
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.085
234
P SZR006 Seizure Disorder 59 0.084
235
ANX004 Anoxia 44 0.084
236
HMC038 Hemochromatosis, Neonatal 34 0.084
237
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.082
238
DPR016 Depression 64 0.082
239
P MYP004 Myopathy 63 0.082
240
VSL002 Visual Epilepsy 58 0.082
241
DYS073 Dysphagia 52 0.082
242
DNT012 Dental Caries 52 0.082
243
P PLM085 Pulmonary Hemosiderosis 43 0.082
244
STR067 Stroke, Ischemic 82 0.081
245
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.081
246
SLC006 Silicosis 55 0.081
247
c HMC035 Hemochromatosis, Type 4 48 0.081
248
c MCR120 Microvascular Complications of Diabetes 7 48 0.081
249
MYL069 Myeloma, Multiple 85 0.080
250
P PNM007 Pneumonia 71 0.080
251
PRT036 Peritonitis 66 0.080
252
c ACT075 Acute Myocardial Infarction 59 0.080
253
ACT058 Active Peptic Ulcer Disease 55 0.080
254
ATR002 Atransferrinemia 53 0.080
255
P LNG032 Lung Cancer 99 0.079
256
ANX010 Anxiety 75 0.079
257
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.079
258
P CRN018 Coronary Artery Anomaly 67 0.079
259
c INF071 Inflammatory Bowel Disease 1 66 0.079
260
P ENC018 Encephalopathy 64 0.079
261
c HPT016 Hepatitis B 63 0.079
262
BND020 Bone Disease 60 0.079
263
c PRT132 Protoporphyria, Erythropoietic, 1 59 0.079
264
P MGL001 Megaloblastic Anemia 54 0.079
265
TLN003 Telangiectasis 53 0.079
266
P GRF003 Graft-Versus-Host Disease 71 0.078
267
P LKM062 Leukemia, Acute Lymphoblastic 68 0.078
268
HYP066 Hyperglycemia 63 0.078
269
c ACT071 Acute Kidney Failure 60 0.078
270
ART140 Arteries, Anomalies of 60 0.078
271
SPN035 Spindle Cell Sarcoma 57 0.078
272
TRM010 Traumatic Brain Injury 54 0.078
273
BRN024 Bronchitis 70 0.076
274
P MYC084 Mycobacterium Tuberculosis 1 69 0.076
275
P ATS364 Autism 68 0.076
276
SRC014 Sarcoma 67 0.076
277
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.076
278
P HMN010 Hemangioma 62 0.076
279
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.076
280
PLS007 Plasmodium Falciparum Malaria 53 0.076
281
PRN011 Pernicious Anemia 51 0.076
282
SYS003 Systolic Heart Failure 43 0.076
283
P OVR042 Ovarian Cancer 89 0.075
284
PLY001 Polycythemia Vera 70 0.075
285
BRN004 Brain Edema 57 0.075
286
DYS014 Dyspepsia 51 0.075
287
PST021 Postpartum Depression 51 0.075
288
P DDN001 Duodenal Ulcer 50 0.075
289
PLM049 Plummer Vinson Syndrome 29 0.075
290
PRP027 Peripheral Vascular Disease 72 0.074
291
P DMN001 Diamond-Blackfan Anemia 69 0.074
292
P DMN002 Dementia 68 0.074
293
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.074
294
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.074
295
P ESP024 Esophagitis 62 0.074
296
MNT002 Mental Depression 60 0.074
297
PLC008 Placenta Disease 51 0.074
298
c HYP836 Hypercholesterolemia, Familial, 1 74 0.073
299
SCH014 Schistosomiasis 57 0.073
300
c MCR113 Microvascular Complications of Diabetes 3 55 0.073
301
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.073
302
P ECL001 Eclampsia 53 0.073
303
c HMC010 Hemochromatosis, Type 3 46 0.073
304
c MCR130 Microvascular Complications of Diabetes 6 42 0.073
305
c MCR133 Microvascular Complications of Diabetes 4 42 0.073
306
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.073
307
P PRS040 Prostate Cancer 97 0.071
308
DRM006 Dermatitis 63 0.071
309
GST045 Gastroenteritis 60 0.071
310
P BRS044 Breast Adenocarcinoma 59 0.071
311
P NRP001 Neuropathy 57 0.071
312
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.071
313
GST023 Gastric Ulcer 53 0.071
314
HMG002 Hemoglobinuria 49 0.071
315
ANC001 Ancylostomiasis 39 0.071
316
P NPH012 Nephrotic Syndrome 65 0.070
317
SPN186 Spinal Cord Injury 63 0.070
318
P URT039 Urticaria 61 0.070
319
c ACT210 Acute Respiratory Distress Syndrome 59 0.070
320
P TRC086 Trichohepatoenteric Syndrome 1 57 0.070
321
GLC003 Glucose Intolerance 55 0.070
322
PNC001 Pancytopenia 54 0.070
323
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.070
324
MLT157 Multiple System Atrophy 1 71 0.069
325
c ACT068 Acute Cystitis 63 0.069
326
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.069
327
SYN007 Synovitis 55 0.069
328
P FBR031 Febrile Seizures 54 0.069
329
GRD001 Giardiasis 42 0.069
330
c HMG029 Hemoglobin Se Disease 40 0.069
331
c FNC043 Fanconi Anemia, Complementation Group E 64 0.067
332
PRT013 Portal Hypertension 61 0.067
333
PLM031 Poliomyelitis 58 0.067
334
CHL014 Cholera 58 0.067
335
PRT038 Protein-Energy Malnutrition 56 0.067
336
P CNG003 Congenital Dyserythropoietic Anemia 47 0.067
337
RBF001 Riboflavin Deficiency 46 0.067
338
ANG011 Angiodysplasia 45 0.067
339
c HMG003 Hemoglobin E Disease 43 0.067
340
SPR126 Superior Semicircular Canal Dehiscence 39 0.067
341
c RST012 Restless Legs Syndrome 1 34 0.067
342
c THR092 Thrombophilia Due to Thrombin Defect 74 0.066
343
P CNR004 Cone-Rod Dystrophy 2 72 0.066
344
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.066
345
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.066
346
P PSR002 Psoriasis 63 0.066
347
P HYP730 Hypogonadotropic Hypogonadism 54 0.066
348
P RTN018 Retinal Disease 53 0.066
349
P LCT001 Lactic Acidosis 52 0.066
350
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.066
351
ENT011 Enterocolitis 51 0.066
352
PST011 Pustulosis of Palm and Sole 51 0.066
353
DYS015 Dysentery 45 0.066
354
MCR017 Macrocytic Anemia 41 0.066
355
SCR011 Scrapie 37 0.066
356
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 21 0.066
358
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.064
359
ESP021 Esophageal Cancer 90 0.064
360
c SYS001 Systemic Lupus Erythematosus 88 0.064
361
OST012 Osteoarthritis 80 0.064
362
P RSP003 Respiratory Failure 75 0.064
363
c ATS007 Autism Spectrum Disorder 69 0.064
364
P PRD008 Periodontitis 66 0.064
365
P HYP069 Hyperparathyroidism 64 0.064
366
P VSC011 Vasculitis 64 0.064
367
P GLM007 Glomerulonephritis 58 0.064
368
P ALP008 Alopecia 58 0.064
369
CRH005 Crohn's Colitis 56 0.064
370
P HYP076 Hyperthyroidism 55 0.064
371
P RCT021 Rectum Cancer 54 0.064
372
AMN001 Amenorrhea 54 0.064
373
c LRG017 Large Intestine Cancer 53 0.064
374
BRT055 Breath-Holding Spells 29 0.064
375
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.063
376
MLN008 Melanoma 68 0.063
377
ANR007 Anorexia Nervosa 64 0.063
378
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.063
379
P BCL017 B-Cell Lymphoma 61 0.063
380
P CND004 Candidiasis 61 0.063
381
P HRD011 Hereditary Spherocytosis 59 0.063
382
P SLP005 Sleep Disorder 58 0.063
383
P HYP024 Hypoparathyroidism 56 0.063
384
HYP060 Hyperinsulinism 55 0.063
385
LYM019 Lymphosarcoma 48 0.063
386
P BNG032 Benign Mesothelioma 47 0.063
387
KWS001 Kwashiorkor 46 0.063
388
RDC006 Red Cell Aplasia 45 0.063
389
c ATM101 Autoimmune Gastritis 42 0.063
390
ANK010 Ankylostomiasis 30 0.063
391
c DLT002 Dilated Cardiomyopathy 81 0.061
392
P AMY004 Amyloidosis 71 0.061
393
c EXD008 Exudative Vitreoretinopathy 1 69 0.061
394
P ASP006 Aspergillosis 67 0.061
395
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.061
396
ORL011 Oral Cancer 62 0.061
397
TYP007 Typhoid Fever 61 0.061
398
CHL068 Cholestasis 61 0.061
399
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.061
400
PLM017 Pulmonary Alveolar Microlithiasis 54 0.061
401
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.061
402
SPS057 Spasticity 38 0.061
403
ANM001 Anemia of Prematurity 38 0.061
404
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.061
406
IMM167 Immune Deficiency Disease 79 0.060
407
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.060
408
P BLD134 Bladder Cancer 79 0.060
409
BRN028 Brain Cancer 75 0.060
410
c SPN225 Spondyloarthropathy 1 74 0.060
411
LPT014 Leptin Deficiency or Dysfunction 72 0.060
412
c MGR028 Migraine with or Without Aura 1 70 0.060
413
P LPR021 Leprosy 3 67 0.060
414
P HYP098 Hypereosinophilic Syndrome 67 0.060
415
BRR014 Barrett Esophagus 67 0.060
416
SKN016 Skin Disease 64 0.060
417
P LPS004 Lupus Erythematosus 62 0.060
418
P SNS001 Sensorineural Hearing Loss 62 0.060
419
P PLY011 Polycystic Ovary Syndrome 58 0.060
420
PYR041 Pyruvate Kinase Deficiency of Red Cells 58 0.060
421
RHM027 Rheumatic Disease 56 0.060
422
PRP030 Purpura 56 0.060
423
OCL069 Ocular Motor Apraxia 53 0.060
424
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 51 0.060
425
P PRR002 Pure Red-Cell Aplasia 47 0.060
426
GLS007 Glossitis 44 0.060
427
HNS001 Hansen's Disease 35 0.060
428
NRX001 Neuroaxonal Dystrophy 33 0.060
429
RRD056 Rare Disease in Surgical Orthopedic 29 0.060
430
NRL016 Neural Tube Defects 83 0.058
431
HMN044 Human Immunodeficiency Virus Type 1 73 0.058
432
P SRC025 Sarcoidosis 1 72 0.058
433
LYM133 Lymphoma, Hodgkin, Classic 70 0.058
434
OST159 Osteogenic Sarcoma 67 0.058
435
P PRP019 Peripheral Nervous System Disease 64 0.058
436
LPD008 Lipid Metabolism Disorder 64 0.058
437
P HDC001 Headache 59 0.058
438
P PYL005 Pyelonephritis 58 0.058
439
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.058
440
LMY002 Leiomyoma 52 0.058
441
STM007 Stomatitis 51 0.058
442
CRY005 Cryptococcosis 51 0.058
443
THR013 Thoracic Outlet Syndrome 49 0.058
444
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.058
445
DWR001 Dwarfism 45 0.058
446
c PCH010 Pachyonychia Congenita 3 43 0.058
447
CRB004 Cerebral Artery Occlusion 38 0.058
448
P ATX030 Ataxia-Telangiectasia 83 0.057
449
P LNG064 Lung Cancer Susceptibility 3 79 0.057
450
SVR004 Severe Combined Immunodeficiency 74 0.057
451
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.057
452
HYP056 Hypoglycemia 68 0.057
453
P PLM036 Pulmonary Fibrosis 66 0.057
454
IDP011 Idiopathic Interstitial Pneumonia 65 0.057
455
ANR040 Aneurysm 60 0.057
456
P INF032 Infertility 60 0.057
457
BLR008 Bilirubin Metabolic Disorder 58 0.057
458
ORL004 Oral Submucous Fibrosis 55 0.057
459
KFR001 Kufor-Rakeb Syndrome 54 0.057
460
MTB004 Metabolic Acidosis 48 0.057
461
RTN023 Retinitis 46 0.057
462
NRR001 Neuroretinitis 46 0.057
463
HRN026 Hernia, Hiatus 46 0.057
464
PHN003 Phenylketonuria 73 0.055
465
OTT002 Otitis Media 71 0.055
466
P MSC005 Muscular Dystrophy 68 0.055
467
P ATR011 Atrial Fibrillation 67 0.055
468
GST040 Gastric Adenocarcinoma 67 0.055
469
CLN015 Colon Adenocarcinoma 65 0.055
470
TXC005 Toxic Shock Syndrome 63 0.055
471
c BRN108 Branchiootic Syndrome 1 62 0.055
472
ACQ007 Acquired Immunodeficiency Syndrome 61 0.055
473
P MYC008 Myocarditis 60 0.055
474
c HPT003 Hepatitis a 60 0.055
475
P PRN023 Prion Disease 57 0.055
476
VSC003 Visceral Leishmaniasis 55 0.055
477
IMP005 Impotence 53 0.055
478
MYM001 Myoma 52 0.055
479
P HMG032 Hemoglobin H Disease 52 0.055
480
GLS018 Glass Syndrome 51 0.055
481
CND006 Candida Glabrata 33 0.055
482
PTT016 Patterson Pseudoleprechaunism Syndrome 27 0.055
483
c LKM071 Leukemia, Chronic Lymphocytic 81 0.053
484
P PHC003 Pheochromocytoma 71 0.053
485
P CRD119 Cardiac Arrest 71 0.053
486
AND002 Androgen Insensitivity Syndrome 66 0.053
487
P ANG001 Angelman Syndrome 65 0.053
488
CLR108 Colorectal Adenoma 64 0.053
489
P ANR048 Aniridia 1 64 0.053
490
P GCH001 Gaucher's Disease 63 0.053
491
P ART005 Arteriovenous Malformation 63 0.053
492
TTN003 Tetanus 62 0.053
493
ACN002 Acanthosis Nigricans 62 0.053
494
P SYP003 Syphilis 59 0.053
495
P AXN002 Axenfeld-Rieger Syndrome 58 0.053
496
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.053
497
P MTC069 Mitochondrial Disorders 57 0.053
498
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.053
499
DDN006 Duodenitis 44 0.053
500
GST020 Gastric Antral Vascular Ectasia 42 0.053
501
ATX010 Ataxia Neuropathy Spectrum 39 0.053
502
ALR002 Al-Raqad Syndrome 32 0.053
503
P ACT232 Acute Necrotizing Encephalopathy 28 0.053
504
BLD137 Blood Group--Ahonen 17 0.053
505
c FNC027 Fanconi Anemia, Complementation Group a 81 0.051
506
P MCR115 Microvascular Complications of Diabetes 5 67 0.051
507
CHG001 Chagas Disease 66 0.051
508
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.051
509
P HYP750 Hypertriglyceridemia, Familial 62 0.051
510
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.051
511
P RHN004 Rhinitis 59 0.051
512
PLS011 Plasmacytoma 57 0.051
513
HYP005 Hypokalemia 55 0.051
514
PRN019 Perinatal Necrotizing Enterocolitis 55 0.051
515
SPP010 Suppressor of Tumorigenicity 3 54 0.051
516
c ACT134 Acute Liver Failure 53 0.051
517
CHR073 Choreatic Disease 52 0.051
518
NPH018 Nephrogenic Systemic Fibrosis 51 0.051
519
c DMN023 Diamond-Blackfan Anemia 1 51 0.051
520
CNG028 Congenital Hypoplastic Anemia 46 0.051
521
SYN036 Syncope 46 0.051
522
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.051
523
HPT082 Hepatic Adenomas, Familial 40 0.051
524
c CHR682 Chronic Bilirubin Encephalopathy 36 0.051
525
c ATM060 Autoimmune Atrophic Gastritis 23 0.051
526
ARG006 Aregenerative Anemia 22 0.051
527
CHL065 Cholangiocarcinoma 68 0.050
528
P HYD006 Hydrocephalus 68 0.050
529
VRC005 Varicose Veins 61 0.050
530
P PNC044 Pancreatitis 61 0.050
531
P ADL010 Adult Respiratory Distress Syndrome 61 0.050
532
P KDN017 Kidney Cancer 60 0.050
533
TRD006 Tardive Dyskinesia 58 0.050
534
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 56 0.050
535
c CNG216 Congenital Hydrocephalus 55 0.050
536
INT079 Intrahepatic Cholangiocarcinoma 54 0.050
537
DMY004 Demyelinating Disease 54 0.050
538
c GLL024 Gallbladder Disease 1 53 0.050
539
P AST007 Astrocytoma 52 0.050
540
P THR015 Thrombophilia 51 0.050
541
ADR040 Adrenal Gland Pheochromocytoma 51 0.050
542
MTC005 Mitochondrial Metabolism Disease 50 0.050
543
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 49 0.050
544
PST048 Postural Orthostatic Tachycardia Syndrome 49 0.050
545
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.050
546
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.050
547
ENT004 Enthesopathy 46 0.050
548
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.050
549
49X002 49,xxxxy Syndrome 39 0.050
550
MCK029 Meckel Diverticulum 37 0.050
551
PPL052 Papillomatosis, Confluent and Reticulated 34 0.050
552
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.050
553
KPS004 Kaposi Sarcoma 75 0.048
554
c LKM063 Leukemia, Chronic Myeloid 74 0.048
555
P EPL164 Epilepsy 73 0.048
556
GST092 Gastroesophageal Reflux 68 0.048
557
BRK010 Burkitt Lymphoma 68 0.048
558
P MNN013 Meningitis 67 0.048
559
P HRP006 Herpes Simplex 66 0.048
560
DSS008 Disease of Mental Health 66 0.048
561
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.048
562
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.048
563
P LYM033 Lymphoproliferative Syndrome 62 0.048
564
ETN001 Eating Disorder 61 0.048
565
CTN007 Cutaneous Leishmaniasis 61 0.048
566
ART001 Arterial Tortuosity Syndrome 60 0.048
567
FBR047 Fibromyalgia 60 0.048
568
PLM033 Pulmonary Embolism 60 0.048
569
P END033 Endocarditis 58 0.048
570
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.048
571
HPT046 Hepatic Veno-Occlusive Disease 56 0.048
572
P ALP106 Alport Syndrome 1, X-Linked 55 0.048
573
MST005 Mastitis 55 0.048
574
PNG002 Pain Agnosia 52 0.048
575
CRT013 Carotid Stenosis 50 0.048
576
INT017 Intestinal Schistosomiasis 49 0.048
577
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.048
578
P OBS001 Obstructive Jaundice 49 0.048
579
RTC005 Reticulosarcoma 48 0.048
580
P HMR005 Hemorrhoid 47 0.048
581
NSS002 Neisseria Meningitidis Infection 47 0.048
582
MNN020 Meningococcal Infection 46 0.048
583
ASB001 Asbestosis 44 0.048
584
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.048
585
c CHR064 Chronic Monocytic Leukemia 43 0.048
586
ADP007 Adie Pupil 40 0.048
587
END028 Endemic Goiter 37 0.048
588
ATR073 Atrophic Glossitis 32 0.048
589
MYC088 Mycobacterium Avium Complex Infections 30 0.048
590
MNG007 Manganese Poisoning 28 0.048
591
HNM002 Hinman Syndrome 26 0.048
592
ASB003 Asbestos Intoxication 26 0.048
593
RRD019 Rare Deficiency Anemia 24 0.048
594
INS024 Insulin-Like Growth Factor I 79 0.046
595
P RTN008 Retinitis Pigmentosa 77 0.046
596
P INF038 Influenza 69 0.046
597
P ESS003 Essential Thrombocythemia 69 0.046
598
EWN003 Ewing Sarcoma 69 0.046
599
PSY004 Psychotic Disorder 68 0.046
600
c BSL007 Basal Cell Carcinoma 68 0.046
601
MYL031 Myeloproliferative Neoplasm 66 0.046
602
P MTR014 Motor Neuron Disease 66 0.046
603
CHY002 Chylomicron Retention Disease 63 0.046
604
CHR066 Chronic Fatigue Syndrome 61 0.046
605
APP008 Appendicitis 61 0.046
606
MSL001 Measles 61 0.046
607
INT002 Intermittent Claudication 60 0.046
608
CNT047 Contact Dermatitis 58 0.046
609
P FBR017 Fibrosarcoma 57 0.046
610
ANT024 Anthrax Disease 56 0.046
611
MCS002 Mucositis 56 0.046
612
LYM040 Lymphoblastic Lymphoma 54 0.046
613
P SLM003 Salmonellosis 54 0.046
614
VCC001 Vaccinia 50 0.046
615
c CNG027 Congenital Hemolytic Anemia 48 0.046
616
NRL004 Neuroleptic Malignant Syndrome 48 0.046
617
P MTH007 Methemoglobinemia 47 0.046
618
c PRM038 Primary Agammaglobulinemia 45 0.046
619
RDN001 Reading Disorder 42 0.046
620
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 41 0.046
621
CHL147 Chlamydia Pneumonia 39 0.046
622
c FML324 Familial Porphyria Cutanea Tarda 31 0.046
623
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.046
624
c ATS210 Autosomal Recessive Sideroblastic Anemia 27 0.046
625
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 23 0.046
626
AND005 Androgen Insensitivity Syndrome, Mild 20 0.046
627
NRD068 Neurodegeneration, Early-Onset, with Choreoathetoid Movements and Microcytic Anemia 17 0.046
628
P SLP006 Sleep Apnea 71 0.043
629
CRB037 Cerebral Palsy 69 0.043
630
P SYS005 Systemic Scleroderma 68 0.043
631
P NRV007 Nervous System Disease 68 0.043
632
P FLL037 Follicular Lymphoma 67 0.043
633
P PRS038 Personality Disorder 66 0.043
634
OST017 Osteomyelitis 65 0.043
635
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.043
636
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.043
637
c SCL052 Scleroderma, Familial Progressive 62 0.043
638
LKD001 Leukodystrophy 61 0.043
639
c DWL002 Dowling-Degos Disease 1 59 0.043
640
c MST023 Mesothelioma, Malignant 59 0.043
641
TRG002 Trigeminal Neuralgia 58 0.043
642
ENH001 Enhanced S-Cone Syndrome 56 0.043
643
c CHR417 Chronic Graft Versus Host Disease 56 0.043
644
P VNS003 Venous Insufficiency 55 0.043
645
INT075 Intracranial Hypertension 54 0.043
646
P CHL066 Cholangitis 53 0.043
647
c ACT135 Acute Graft Versus Host Disease 52 0.043
648
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.043
649
c SCN007 Secondary Hyperparathyroidism 52 0.043
650
P CTN015 Cutaneous T Cell Lymphoma 52 0.043
651
P MSC003 Muscular Atrophy 52 0.043
652
OVR082 Overgrowth Syndrome 51 0.043
653
P KRT007 Keratoconus 51 0.043
654
MCR004 Macroglobulinemia 50 0.043
655
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.043
656
c INV001 Invasive Aspergillosis 48 0.043
657
BHR001 Behr Syndrome 47 0.043
658
CHR074 Choriocarcinoma 47 0.043
659
HDN002 Head Injury 47 0.043
660
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 47 0.043
661
PPL021 Papilledema 46 0.043
662
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.043
663
DMP001 Dumping Syndrome 44 0.043
664
MRS001 Marasmus 39 0.043
665
BLR027 Blue Rubber Bleb Nevus 39 0.043
666
STT004 Steatorrhea 39 0.043
667
SPR066 Superficial Siderosis 38 0.043
668
HRN029 Hearing Loss, Noise-Induced 38 0.043
669
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.043
670
c LKM004 Leukemia, B-Cell, Chronic 35 0.043
671
PYR016 Pyridoxine Deficiency 31 0.043
672
c PRP091 Porphyria Cutanea Tarda, Type I 31 0.043
673
P FML340 Familial Episodic Pain Syndrome 28 0.043
674
PLS032 Plasmodium Falciparum Blood Infection Level 22 0.043
675
CRV035 Cervical Cancer 77 0.041
676
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.041
677
ART016 Aortic Aneurysm 71 0.041
678
MNT001 Mantle Cell Lymphoma 69 0.041
679
c HMP029 Hemophilia a 69 0.041
680
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.041
681
CRT072 Creutzfeldt-Jakob Disease 67 0.041
682
c MCR129 Microvascular Complications of Diabetes 1 67 0.041
683
P SKN015 Skin Carcinoma 67 0.041
684
ANG054 Angina Pectoris 66 0.041
685
c GCH015 Gaucher Disease, Type I 65 0.041
686
P ENC004 Encephalitis 64 0.041
687
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.041
688
c ATM011 Autoimmune Hepatitis 63 0.041
689
P ACR001 Aicardi-Goutieres Syndrome 63 0.041
690
VRL011 Viral Infectious Disease 62 0.041
691
TRN015 Transient Cerebral Ischemia 62 0.041
692
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.041
693
P ALP009 Alopecia Areata 61 0.041
694
P PLY014 Polycystic Kidney Disease 61 0.041
695
SQM006 Squamous Cell Carcinoma 60 0.041
696
GNG013 Gingivitis 60 0.041
697
ALC006 Alcoholic Hepatitis 60 0.041
698
P HMP007 Hemophilia 58 0.041
699
HPT022 Hepatoblastoma 58 0.041
700
BRN056 Bronchopulmonary Dysplasia 57 0.041
701
ALL010 Allergic Contact Dermatitis 56 0.041
702
APH001 Aphthous Stomatitis 56 0.041
703
P RBL001 Rubella 56 0.041
704
RHM001 Rheumatic Fever 56 0.041
705
LST001 Listeriosis 55 0.041
706
MRG003 Marginal Zone B-Cell Lymphoma 55 0.041
707
PRP016 Paraplegia 54 0.041
708
VGN023 Vaginitis 54 0.041
709
INF034 Infective Endocarditis 53 0.041
710
CHR100 Chronic Ulcer of Skin 53 0.041
711
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.041
712
ALC009 Alcoholic Liver Cirrhosis 53 0.041
713
HST011 Histoplasmosis 52 0.041
714
c FLL041 Follicular Lymphoma 1 50 0.041
715
CLC001 Calciphylaxis 49 0.041
716
CVR006 Cavernous Hemangioma 49 0.041
717
ATN005 Autonomic Dysfunction 48 0.041
718
TRC012 Trichuriasis 47 0.041
719
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.041
720
c HMG001 Hemoglobin C Disease 43 0.041
721
BBN001 Bubonic Plague 40 0.041
722
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 38 0.041
723
CTN011 Cutaneous Porphyria 36 0.041
724
PLY150 Polykaryocytosis Inducer 31 0.041
725
c BLD140 Blood Group, I System 29 0.041
726
ARG004 Argyria 28 0.041
727
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.041
728
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 27 0.041
729
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.041
730
BLD163 Blood Group, Dombrock System 24 0.041
731
PRT025 Protein-Deficiency Anemia 24 0.041
732
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.039
733
c SML038 Small Cell Cancer of the Lung 67 0.039
734
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.039
735
MSC007 Muscle Hypertrophy 65 0.039
736
P VNW001 Von Willebrand's Disease 64 0.039
737
MDD011 Mood Disorder 62 0.039
738
CRC021 Carcinosarcoma 62 0.039
739
SDD001 Sudden Infant Death Syndrome 61 0.039
740
STT001 Status Epilepticus 61 0.039
741
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.039
742
c ANM038 Anemia, Autoimmune Hemolytic 61 0.039
743
c ACT027 Acute Pancreatitis 60 0.039
744
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.039
745
c MCL013 Mucolipidosis Iv 60 0.039
746
P OPT006 Optic Nerve Disease 59 0.039
747
P UVT001 Uveitis 58 0.039
748
DSS009 Disseminated Intravascular Coagulation 58 0.039
749
INT007 Intermediate Coronary Syndrome 58 0.039
750
PRM236 Primary Biliary Cholangitis 57 0.039
751
HRY003 Hairy Cell Leukemia 57 0.039
752
CMR002 Coumarin Resistance 56 0.039
753
c SVR001 Severe Acute Respiratory Syndrome 56 0.039
754
c PRD040 Periodontitis, Chronic 56 0.039
755
P ART021 Arteriosclerosis 56 0.039
756
VRG001 Variegate Porphyria 55 0.039
757
PLC005 Placental Insufficiency 55 0.039
758
PRP082 Porphyria, Congenital Erythropoietic 55 0.039
759
P MMB011 Membranous Nephropathy 54 0.039
760
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.039
761
CST005 Castleman Disease 54 0.039
762
P ACT105 Acute Mountain Sickness 53 0.039
763
ESN011 Eisenmenger Syndrome 52 0.039
764
ILS001 Ileus 51 0.039
765
CLR109 Colorectal Adenocarcinoma 51 0.039
766
c SVR005 Severe Pre-Eclampsia 50 0.039
767
P RTN022 Retinal Vein Occlusion 50 0.039
768
P OVR046 Ovarian Cyst 50 0.039
769
MNN009 Meningoencephalitis 50 0.039
770
c CNT016 Central Retinal Vein Occlusion 48 0.039
771
P NGH001 Night Blindness 48 0.039
772
HYP068 Hyperostosis 48 0.039
773
PLC007 Placental Abruption 47 0.039
774
SLP001 Sleeping Sickness 47 0.039
775
P PRP056 Porphyria, Acute Hepatic 46 0.039
776
CHL056 Cheilitis 46 0.039
777
CCC002 Coccidiosis 46 0.039
778
HPT067 Hepatocellular Adenoma 45 0.039
779
TLR001 Tularemia 44 0.039
780
BRN032 Brain Glioma 44 0.039
781
DRG024 Drug Allergy 43 0.039
782
PRD002 Periodic Limb Movement Disorder 40 0.039
783
AMN006 Aminoaciduria 39 0.039
784
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.039
785
PST010 Pasteurellosis 37 0.039
786
NNT011 Neonatal Anemia 31 0.039
787
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.039
788
ANG061 Angular Cheilitis 25 0.039
789
P RTT002 Rett Syndrome 81 0.036
790
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.036
791
AST005 Asthma 80 0.036
792
GST019 Gastrointestinal Stromal Tumor 76 0.036
793
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.036
794
PTZ001 Peutz-Jeghers Syndrome 70 0.036
795
PNC129 Pancreatic Adenocarcinoma 69 0.036
796
P HYP061 Hypertrophic Cardiomyopathy 68 0.036
797
P ORT004 Orthostatic Intolerance 68 0.036
798
ABT001 Abetalipoproteinemia 68 0.036
799
P NSP012 Nasopharyngeal Carcinoma 67 0.036
800
c HRD010 Hereditary Spastic Paraplegia 67 0.036
801
MYC006 Mycosis Fungoides 67 0.036
802
IRR002 Irritable Bowel Syndrome 65 0.036
803
HMT002 Hematologic Cancer 64 0.036
804
GT001 Gout 63 0.036
805
P RHB003 Rhabdomyosarcoma 62 0.036
806
BRC012 Brucellosis 62 0.036
807
P ANP001 Anaplastic Large Cell Lymphoma 62 0.036
808
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.036
809
INS001 Insulinoma 60 0.036
810
LPT001 Leptospirosis 60 0.036
811
P NRM001 Neuromyelitis Optica 60 0.036
812
BRN002 Bronchiolitis 60 0.036
813
c ADL017 Adult T-Cell Leukemia 59 0.036
814
HMR039 Hemorrhage, Intracerebral 59 0.036
815
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 59 0.036
816
SZR001 Sezary's Disease 59 0.036
817
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.036
818
EMB004 Embryonal Carcinoma 57 0.036
819
VSC002 Vascular Dementia 57 0.036
820
SFT003 Soft Tissue Sarcoma 57 0.036
821
P SHR029 Short Syndrome 56 0.036
822
DFF005 Diffuse Large B-Cell Lymphoma 56 0.036
823
PPL022 Papilloma 56 0.036
824
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.036
825
P PRM006 Primary Biliary Cirrhosis 54 0.036
826
P HST010 Histiocytosis 54 0.036
827
PTT009 Pituitary Gland Disease 54 0.036
828
P ANG015 Angioedema 54 0.036
829
HMC014 Homocysteinemia 54 0.036
830
P HYP083 Hypopituitarism 53 0.036
831
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.036
832
P THY032 Thyroiditis 52 0.036
833
INT303 Intracranial Hypertension, Idiopathic 52 0.036
834
KRT009 Keratosis 52 0.036
835
P CHR345 Chronic Pain 52 0.036
836
CHR105 Choreoacanthocytosis 51 0.036
837
c ALM001 Al Amyloidosis 50 0.036
838
TRY001 Trypanosomiasis 50 0.036
839
SQM002 Squamous Cell Papilloma 49 0.036
840
P TCL004 T-Cell Leukemia 48 0.036
841
PLS025 Plasmablastic Lymphoma 48 0.036
842
GRW007 Growth Hormone Deficiency 48 0.036
843
TRC003 Trichomoniasis 46 0.036
844
FSC002 Fascioliasis 44 0.036
845
MCR011 Microinvasive Gastric Cancer 43 0.036
846
c ACQ010 Acquired Polycythemia 43 0.036
847
P GLM044 Glomerular Disease 42 0.036
848
WDH003 Woodhouse-Sakati Syndrome 38 0.036
849
c ACT004 Acute Diarrhea 38 0.036
850
c LKM005 Leukemia, T-Cell, Chronic 35 0.036
851
c PRK071 Parkinson Disease 14, Autosomal Recessive 34 0.036
852
RRS014 Rare Surgical Neurologic Disease 33 0.036
853
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.036
854
CLS052 Classic Hairy Cell Leukemia 28 0.036
855
STN013 Stenotrophomonas Maltophilia Infection 26 0.036
856
c HMC019 Hemochromatosis, Type 2b 24 0.036
857
BLD165 Blood Group, Colton System 21 0.036
858
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.036
859
TRN072 Transferrin Serum Level Quantitative Trait Locus 2 14 0.036
860
P MDL005 Medulloblastoma 78 0.034
861
P NRF023 Neurofibromatosis, Type Ii 77 0.034
862
P SCH015 Schizophrenia 76 0.034
863
END057 Endometrial Cancer 74 0.034
864
c MNN043 Meningioma, Familial 74 0.034
865
P RTN024 Retinoblastoma 74 0.034
866
P FML011 Familial Adenomatous Polyposis 73 0.034
867
P CHR012 Chronic Granulomatous Disease 69 0.034
868
CNN005 Connective Tissue Disease 68 0.034
869
CRP001 Carpal Tunnel Syndrome 68 0.034
870
P DRM053 Dermatitis, Atopic 68 0.034
871
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.034
872
c DPH024 Diaphragmatic Hernia, Congenital 66 0.034
873
MLD001 Melioidosis 66 0.034
874
P OCL013 Oculodentodigital Dysplasia 65 0.034
875
KWS002 Kawasaki Disease 65 0.034
876
FCT007 Factor Vii Deficiency 65 0.034
877
MNN042 Meningioma, Radiation-Induced 64 0.034
878
KHL003 Kohlschutter-Tonz Syndrome 63 0.034
879
HSH003 Hashimoto Thyroiditis 63 0.034
880
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.034
881
MNK001 Menkes Disease 62 0.034
882
LYM012 Lymphoplasmacytic Lymphoma 62 0.034
883
PRP083 Porphyria, Acute Intermittent 62 0.034
884
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.034
885
c PNS012 Paine Syndrome 61 0.034
886
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.034
887
P TXP001 Toxoplasmosis 61 0.034
888
IGR001 Ige Responsiveness, Atopic 61 0.034
889
P CRD132 Cardiac Conduction Defect 61 0.034
890
CHL067 Cholecystitis 60 0.034
891
c LPM012 Lipomatosis, Multiple 60 0.034
892
STF001 Stiff-Person Syndrome 60 0.034
893
P INT070 Intestinal Obstruction 60 0.034
894
ANG020 Angiosarcoma 59 0.034
895
CHR063 Chronic Mucocutaneous Candidiasis 59 0.034
896
NRN004 Neuroendocrine Tumor 59 0.034
897
ADL030 Adult-Onset Still's Disease 59 0.034
898
CYT008 Cytomegalovirus Infection 58 0.034
899
CMM005 Common Cold 57 0.034
900
CLL003 Cellulitis 56 0.034
901
ALL006 Allergic Asthma 56 0.034
902
FCL014 Focal Epilepsy 56 0.034
903
c CNT035 Central Nervous System Disease 56 0.034
904
P FTL001 Fetal Alcohol Syndrome 56 0.034
905
P PLM034 Pulmonary Emphysema 55 0.034
906
P TCD001 Tic Disorder 55 0.034
907
PRC002 Paracoccidioidomycosis 55 0.034
908
P SML001 Small Cell Carcinoma 55 0.034
909
PRS045 Prostatic Hypertrophy 55 0.034
910
PST046 Post-Transplant Lymphoproliferative Disease 55 0.034
911
P LYM025 Lymphedema 54 0.034
912
SPN051 Spondylitis 53 0.034
913
P TMP001 Temporal Lobe Epilepsy 53 0.034
914
THY030 Thyroid Gland Disease 53 0.034
915
BRN038 Bronchial Disease 53 0.034
916
LNG031 Lung Benign Neoplasm 52 0.034
917
PRS021 Prostatic Adenoma 52 0.034
918
c CHR418 Chronic Leukemia 52 0.034
919
c MLG054 Malignant Histiocytosis 51 0.034
920
HYP063 Hypersplenism 51 0.034
921
LMB062 Limb Ischemia 50 0.034
922
MNC006 Monoclonal Gammopathy of Uncertain Significance 50 0.034
923
LPR001 Lepromatous Leprosy 50 0.034
924
P DRM007 Dermatitis Herpetiformis 50 0.034
925
MLK003 Melkersson-Rosenthal Syndrome 50 0.034
926
c INF145 Infantile Liver Failure Syndrome 1 50 0.034
927
SXL003 Sexual Disorder 49 0.034
928
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.034
929
PRS129 Prostatic Hyperplasia, Benign 49 0.034
930
TST014 Testicular Cancer 49 0.034
931
RNL011 Renal Osteodystrophy 49 0.034
932
SPL004 Splenic Marginal Zone Lymphoma 48 0.034
933
HYP043 Hyperandrogenism 48 0.034
934
BNM001 Bone Marrow Cancer 48 0.034
935
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.034
936
VTM033 Vitamin K Deficiency Bleeding 47 0.034
937
PPT001 Peptic Esophagitis 47 0.034
938
CLD007 Cold Agglutinin Disease 47 0.034
939
LYM051 Lymphomatoid Granulomatosis 47 0.034
940
c LKD010 Leukodystrophy, Hypomyelinating, 2 46 0.034
941
ERY004 Erysipelas 46 0.034
942
URN003 Urinary Schistosomiasis 45 0.034
943
CYN002 Cyanosis, Transient Neonatal 45 0.034
944
ASP004 Asphyxia Neonatorum 44 0.034
945
ORL015 Oral Squamous Cell Carcinoma 44 0.034
946
SDD008 Sudden Sensorineural Hearing Loss 44 0.034
947
P PRC031 Preeclampsia/eclampsia 1 42 0.034
948
LCN001 Lice Infestation 41 0.034
949
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 41 0.034
950
CRB086 Cerebral Aneurysms 41 0.034
951
PLM005 Pleomorphic Lipoma 41 0.034
952
PRM329 Premature Aging 41 0.034
953
PRT019 Protein-Losing Enteropathy 41 0.034
954
MYF001 Myofibroma 40 0.034
955
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.034
956
SPN021 Spinal Meningioma 40 0.034
957
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 38 0.034
958
XRP001 Xerophthalmia 37 0.034
959
c DRM040 Dermatitis Herpetiformis, Familial 36 0.034
960
SPN331 Spondyloocular Syndrome 35 0.034
961
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.034
962
c HYP716 Hypermanganesemia with Dystonia 1 34 0.034
963
PYR009 Pyridoxine Deficiency Anemia 32 0.034
964
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.034
965
STT009 Sutton Disease 2 31 0.034
966
TRG019 Trigonocephaly with Short Stature and Developmental Delay 31 0.034
967
CRB009 Cerebritis 31 0.034
968
MTL002 Metal Metabolism Disorder 30 0.034
969
c INF078 Inflammatory Bowel Disease 2 29 0.034
970
KLB004 Klebsiella Infection 28 0.034
971
HDG004 Hodgkin's Granuloma 27 0.034
973
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.034
974
HVY002 Heavy Metal Poisoning 23 0.034
975
VBR003 Vibrio Vulnificus Infection 23 0.034
976
HDG006 Hodgkin's Paragranuloma 23 0.034
977
c PRK008 Parkinson Disease Type 9 21 0.034
978
MSC157 Muscular Dystrophy, Duchenne Type 70 0.031
979
P MJR001 Major Depressive Disorder 69 0.031
980
P MYS003 Myasthenia Gravis 68 0.031
981
c FML001 Familial Atrial Fibrillation 67 0.031
982
c JVN010 Juvenile Rheumatoid Arthritis 67 0.031
983
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.031
984
c ART101 Aortic Valve Disease 2 67 0.031
985
LNG039 Lung Squamous Cell Carcinoma 66 0.031
986
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.031
987
ART002 Arts Syndrome 63 0.031
988
ACT119 Acute Promyelocytic Leukemia 63 0.031
989
c WLM018 Wilms Tumor 5 63 0.031
990
P LMY004 Leiomyosarcoma 63 0.031
991
PPL049 Papillon-Lefevre Syndrome 63 0.031
992
NRM005 Neuromuscular Disease 62 0.031
993
THY029 Thyroid Carcinoma 62 0.031
994
CRD223 Cardiac Arrhythmia 61 0.031
995
INT066 Interstitial Lung Disease 61 0.031
996
c DNG003 Dengue Disease 61 0.031
997
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.031
998
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.031
999
P CYS018 Cystitis 59 0.031
1000
EYD002 Eye Disease 59 0.031
1001
P LRY044 Larynx Cancer 59 0.031
1002
c PRX059 Peroxisome Biogenesis Disorder 1a 57 0.031
1003
P SJG008 Sjogren Syndrome 57 0.031
1004
BLM002 Bulimia Nervosa 56 0.031
1005
DBT010 Diabetic Neuropathy 56 0.031
1006
P ANT006 Antiphospholipid Syndrome 56 0.031
1007
ACD008 Acid-Labile Subunit Deficiency 55 0.031
1008
BRN012 Bronchiolitis Obliterans 55 0.031
1009
END040 Endogenous Depression 55 0.031
1010
P LCH002 Lichen Planus 55 0.031
1011
SPT004 Septic Arthritis 55 0.031
1012
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.031
1013
P MTR003 Mitral Valve Stenosis 54 0.031
1014
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.031
1015
FDL002 Food Allergy 52 0.031
1016
LYS002 Lysosomal Storage Disease 52 0.031
1017
HYP074 Hypersensitivity Vasculitis 52 0.031
1018
BCT002 Bacterial Vaginosis 52 0.031
1019
P PRT096 Peritoneal Mesothelioma 52 0.031
1020
c INH020 Inherited Metabolic Disorder 51 0.031
1021
ASC010 Ascaris Lumbricoides Infection 51 0.031
1022
c FNC025 Fanconi Anemia, Complementation Group J 51 0.031
1023
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 51 0.031
1024
APR001 Apraxia 50 0.031
1025
P PLM006 Pulmonary Alveolar Proteinosis 50 0.031
1026
ILT001 Ileitis 50 0.031
1027
P SHR001 Short Bowel Syndrome 50 0.031
1028
CRD137 Cardiogenic Shock 50 0.031
1029
c MLG074 Malignant Mesenchymoma 50 0.031
1030
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.031
1031
MST002 Mast-Cell Leukemia 49 0.031
1032
BWN001 Bowen-Conradi Syndrome 49 0.031
1033
PRD004 Prediabetes Syndrome 49 0.031
1034
P FNG006 Feingold Syndrome 1 48 0.031
1035
INT051 Intussusception 48 0.031
1036
P FNC004 Fanconi Syndrome 48 0.031
1037
LGN006 Legionnaire Disease 48 0.031
1038
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.031
1039
P PLL002 Pellagra 47 0.031
1040
P MRC003 Mercury Poisoning 47 0.031
1041
LRY017 Laryngeal Disease 47 0.031
1042
P MCL001 Mucolipidosis 46 0.031
1043
c MLG068 Malignant Glioma 46 0.031
1044
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 46 0.031
1045
c FML008 Familial Retinoblastoma 46 0.031
1046
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.031
1047
AVD001 Avoidant Personality Disorder 45 0.031
1048
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.031
1049
c FTL006 Fetal Alcohol Spectrum Disorder 45 0.031
1050
BCK006 Back Pain 44 0.031
1051
MLK006 Milk Allergy 44 0.031
1052
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.031
1053
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 43 0.031
1054
PYG006 Pyogenic Granuloma 43 0.031
1055
c CHR546 Chronic Mountain Sickness 43 0.031
1056
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.031
1057
CHL109 Childhood Apraxia of Speech 43 0.031
1058
P MYG005 Myoglobinuria 43 0.031
1059
RMS001 Rem Sleep Behavior Disorder 43 0.031
1060
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.031
1061
ACT003 Acute Kidney Tubular Necrosis 42 0.031
1062
c MCR112 Microvascular Complications of Diabetes 2 42 0.031
1063
PLS016 Plasma Cell Leukemia 41 0.031
1064
TRP004 Tropical Sprue 41 0.031
1065
CLN044 Colon Adenoma 41 0.031
1066
EXC002 Exocrine Pancreatic Insufficiency 41 0.031
1067
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.031
1068
c SPH013 Spherocytosis, Type 1 39 0.031
1069
P CRB059 Cerebellar Degeneration 38 0.031
1070
SCR001 Secretory Meningioma 38 0.031
1071
CRY036 Cryptogenic Cirrhosis 38 0.031
1072
NRN002 Neuronitis 37 0.031
1073
CHR178 Chromosomal Triplication 36 0.031
1074
P AXN001 Axonal Neuropathy 36 0.031
1075
ACT216 Acute Leukemia of Ambiguous Lineage 35 0.031
1076
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 35 0.031
1077
GST039 Gastroduodenitis 34 0.031
1078
CRB132 Cerebral Sinovenous Thrombosis 33 0.031
1079
PRT094 Protoporphyria, Erythropoietic, X-Linked 33 0.031
1080
ATR003 Atrophic Rhinitis