Search results for Citric acid

1101 hits were found for Citric acid

# Family MCID Name MIFTS Score
1
TRC120 Tricarboxylic Acid Cycle, Defect of 16 3.928
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.283
3
P LVR013 Liver Disease 68 0.278
4
FTT001 Fatty Liver Disease 61 0.249
5
P KDN018 Kidney Disease 70 0.227
6
LVR012 Liver Cirrhosis 63 0.217
7
MTB004 Metabolic Acidosis 50 0.216
8
HLX001 Helix Syndrome 47 0.214
9
P CLR023 Colorectal Cancer 98 0.213
10
ACT119 Acute Promyelocytic Leukemia 63 0.212
11
48X005 48,xyyy 39 0.211
12
HYP014 Hyperuricemia 51 0.209
13
P SZR006 Seizure Disorder 58 0.205
14
NRL016 Neural Tube Defects 82 0.204
15
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.204
16
VSL002 Visual Epilepsy 58 0.199
17
P DRR001 Diarrhea 57 0.194
18
LPD008 Lipid Metabolism Disorder 62 0.192
19
P NRF023 Neurofibromatosis, Type Ii 76 0.191
20
GST092 Gastroesophageal Reflux 65 0.190
21
BNR002 Bone Resorption Disease 48 0.189
22
OST012 Osteoarthritis 78 0.187
23
ISC004 Ischemia 60 0.186
24
GT001 Gout 63 0.179
25
HYP066 Hyperglycemia 61 0.178
26
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.177
27
ALL026 Allergic Hypersensitivity Disease 64 0.175
28
CLT003 Colitis 62 0.173
29
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.173
30
ATH013 Atherosclerosis Susceptibility 66 0.171
31
P GLM045 Glioma 63 0.169
32
P HYP750 Hypertriglyceridemia, Familial 61 0.169
33
P PRS040 Prostate Cancer 97 0.168
34
c CHR684 Chronic Kidney Disease 66 0.168
35
HYP056 Hypoglycemia 66 0.167
36
DRM006 Dermatitis 61 0.167
37
GLL048 Glial Tumor 45 0.167
38
P INF037 Inflammatory Bowel Disease 56 0.166
39
RCK004 Rickets 69 0.161
40
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.160
41
P HPT023 Hepatocellular Carcinoma 100 0.160
42
P ENC018 Encephalopathy 61 0.159
43
P LKM002 Leukemia 66 0.158
44
ULC004 Ulcerative Colitis 73 0.158
45
c HYP836 Hypercholesterolemia, Familial, 1 72 0.157
46
NNL006 Non-Alcoholic Steatohepatitis 51 0.156
47
PPT005 Peptic Ulcer Disease 58 0.156
48
c GLL024 Gallbladder Disease 1 52 0.156
49
DFC004 Deficiency Anemia 75 0.156
50
P PRD008 Periodontitis 62 0.154
51
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.154
52
P GST044 Gastritis 55 0.153
53
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.153
54
PRT037 Pertussis 65 0.153
55
P VSC007 Vascular Disease 63 0.151
56
IRN002 Iron Metabolism Disease 57 0.151
57
P OST002 Osteoporosis 73 0.151
58
P PSR002 Psoriasis 62 0.150
59
GLB015 Glioblastoma Multiforme 75 0.149
60
PST011 Pustulosis of Palm and Sole 52 0.149
61
P ADN016 Adenocarcinoma 64 0.148
62
P CRN018 Coronary Artery Anomaly 63 0.148
63
HRW001 Hair Whorl 36 0.148
64
CYS001 Cystic Fibrosis 80 0.146
65
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.145
66
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.145
67
ATM095 Autoimmune Disease 61 0.143
68
HMN044 Human Immunodeficiency Virus Type 1 71 0.142
69
P ESP024 Esophagitis 62 0.142
70
HYP060 Hyperinsulinism 54 0.140
71
P BND020 Bone Disease 59 0.140
72
P DBT009 Diabetes Mellitus 64 0.140
73
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.138
74
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.138
75
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.138
76
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.138
77
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.138
78
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.138
79
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.138
80
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.138
81
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.138
82
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.138
83
HYP266 Hypoxia 56 0.138
84
P BPL003 Bipolar Disorder 56 0.138
85
c PRC016 Pre-Eclampsia 63 0.138
86
c MJR024 Major Affective Disorder 9 41 0.137
87
c MJR022 Major Affective Disorder 8 38 0.137
88
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.137
89
ART140 Arteries, Anomalies of 53 0.137
90
OCL069 Ocular Motor Apraxia 51 0.137
91
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.137
92
P OVR042 Ovarian Cancer 89 0.136
93
P MYL006 Myeloid Leukemia 60 0.135
94
P PNC035 Pancreatic Cancer 84 0.135
95
ADN018 Adenoma 58 0.135
96
P NRP001 Neuropathy 56 0.134
97
47X002 47,xyy 49 0.134
98
HYP781 Hypoascorbemia 50 0.133
99
HPT004 Hepatic Coma 43 0.133
100
P CRD246 Cardiovascular System Disease 56 0.133
101
P DRM053 Dermatitis, Atopic 66 0.131
102
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.130
103
c HYP595 Hypertension, Essential 84 0.129
104
CYT002 Cytokine Deficiency 44 0.129
105
P BLD134 Bladder Cancer 78 0.129
106
DPR016 Depression 63 0.129
107
P ALZ034 Alzheimer Disease 88 0.128
108
CRB039 Cerebrovascular Disease 69 0.128
109
DWN001 Down Syndrome 70 0.127
110
END030 End Stage Renal Failure 58 0.127
111
P LNG032 Lung Cancer 97 0.127
112
c LKM061 Leukemia, Acute Myeloid 83 0.127
113
GST023 Gastric Ulcer 53 0.126
114
HLC007 Helicobacter Pylori Infection 59 0.126
115
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.125
116
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.125
117
MYL069 Myeloma, Multiple 85 0.124
118
NTR005 Nutritional Deficiency Disease 61 0.124
119
HPT019 Hepatic Encephalopathy 60 0.124
120
P CHL066 Cholangitis 50 0.123
121
P MYC007 Myocardial Infarction 70 0.123
122
c HPT073 Hepatitis C Virus 70 0.123
123
P ATS364 Autism 65 0.122
124
HMC014 Homocysteinemia 53 0.121
125
P MYP004 Myopathy 64 0.121
126
CHL014 Cholera 55 0.121
127
URT049 Urate Oxidase, Pseudogene 25 0.121
128
INS024 Insulin-Like Growth Factor I 79 0.121
129
CRH001 Crohn's Disease 74 0.121
130
P LYM031 Lymphocytic Leukemia 55 0.121
131
ADL002 Adult Syndrome 69 0.120
132
BCT022 Bacterial Infectious Disease 56 0.120
133
MNT002 Mental Depression 57 0.119
134
P HRP006 Herpes Simplex 65 0.119
135
P GST053 Gastric Cancer 83 0.118
136
CNG034 Congestive Heart Failure 70 0.118
137
c ACT071 Acute Kidney Failure 59 0.118
138
STM007 Stomatitis 49 0.117
139
VTM002 Vitamin B12 Deficiency 48 0.117
140
P ART022 Arthritis 70 0.117
141
c MCR120 Microvascular Complications of Diabetes 7 47 0.117
142
GLC003 Glucose Intolerance 54 0.117
143
c MCR113 Microvascular Complications of Diabetes 3 52 0.117
144
P NTR004 Neutropenia 63 0.116
145
PPL052 Papillomatosis, Confluent and Reticulated 34 0.116
146
SKN016 Skin Disease 63 0.116
147
c RHB024 Rhabdomyosarcoma 2 65 0.116
148
c MCR130 Microvascular Complications of Diabetes 6 41 0.116
149
c MCR133 Microvascular Complications of Diabetes 4 41 0.116
150
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.115
151
BRN071 Brain Injury 49 0.115
152
ALC007 Alcohol Dependence 66 0.115
153
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.114
154
P RHM011 Rheumatoid Arthritis 80 0.114
155
URM002 Uremia 49 0.114
156
P LCT001 Lactic Acidosis 51 0.114
157
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.114
158
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.114
159
P TRN020 Turner Syndrome 65 0.114
160
CRV035 Cervical Cancer 76 0.114
161
c ACT075 Acute Myocardial Infarction 56 0.114
162
STR067 Stroke, Ischemic 80 0.113
163
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.113
164
P LTR001 Lateral Sclerosis 53 0.113
165
ATX019 Ataxia with Vitamin E Deficiency 48 0.112
166
P CTR002 Cataract 60 0.112
167
P HYP086 Hypothyroidism 68 0.112
168
SPN186 Spinal Cord Injury 60 0.112
169
ADR007 Adrenoleukodystrophy 74 0.111
170
CHL123 Chlamydia 59 0.111
171
TRM010 Traumatic Brain Injury 53 0.111
172
c ATS007 Autism Spectrum Disorder 67 0.110
173
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.110
174
PLM010 Pulmonary Edema 55 0.108
175
BRN024 Bronchitis 68 0.107
176
c MGR028 Migraine with or Without Aura 1 69 0.107
177
THR024 Thrombosis 56 0.106
178
P THR014 Thrombocytopenia 68 0.106
179
AGN016 Aging 56 0.106
180
MTH071 Methane Production 26 0.106
181
PLM033 Pulmonary Embolism 59 0.106
182
THY029 Thyroid Carcinoma 59 0.105
183
HYP005 Hypokalemia 55 0.105
184
P HYP069 Hyperparathyroidism 62 0.105
185
c ACT068 Acute Cystitis 63 0.104
186
MTH009 Mouth Disease 56 0.104
187
c ACT027 Acute Pancreatitis 59 0.103
188
c SYS001 Systemic Lupus Erythematosus 86 0.103
189
P MSC005 Muscular Dystrophy 66 0.103
190
SRC014 Sarcoma 65 0.102
191
SPN035 Spindle Cell Sarcoma 51 0.102
192
P SCH015 Schizophrenia 75 0.102
193
c THR092 Thrombophilia Due to Thrombin Defect 73 0.102
194
VCC001 Vaccinia 49 0.102
195
P PRP019 Peripheral Nervous System Disease 57 0.102
196
ANX004 Anoxia 42 0.102
197
P OVR082 Overgrowth Syndrome 50 0.100
198
GST033 Gestational Diabetes 57 0.099
199
c INH020 Inherited Metabolic Disorder 46 0.099
200
MLN008 Melanoma 69 0.099
201
P LYM118 Lymphoma 68 0.098
202
P MNN013 Meningitis 65 0.098
203
P BCL017 B-Cell Lymphoma 58 0.098
204
IMM167 Immune Deficiency Disease 78 0.098
205
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.098
206
P PRP029 Porphyria 62 0.098
207
ESP021 Esophageal Cancer 90 0.098
208
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.097
209
P HYP076 Hyperthyroidism 55 0.097
210
P RNL007 Renal Tubular Acidosis 50 0.097
211
c SML038 Small Cell Cancer of the Lung 65 0.097
212
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.097
213
P LPS004 Lupus Erythematosus 61 0.096
214
P RSP003 Respiratory Failure 74 0.096
215
MYL009 Myelodysplastic Syndrome 70 0.096
216
PPT001 Peptic Esophagitis 51 0.096
217
P INF032 Infertility 57 0.096
218
P ALP008 Alopecia 56 0.096
219
P RHN004 Rhinitis 57 0.095
220
P HPT021 Hepatitis 67 0.095
221
P MSC003 Muscular Atrophy 52 0.095
222
c MLG068 Malignant Glioma 45 0.095
223
PRS045 Prostatic Hypertrophy 52 0.095
224
P AST007 Astrocytoma 50 0.095
225
c HPT001 Hepatitis C 63 0.095
226
MDD011 Mood Disorder 62 0.095
227
P PNC044 Pancreatitis 61 0.095
228
DBT010 Diabetic Neuropathy 55 0.095
229
DNT012 Dental Caries 51 0.095
230
P PNM007 Pneumonia 68 0.095
231
P MLT020 Multiple Sclerosis 72 0.095
232
PPL022 Papilloma 54 0.095
233
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.095
234
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.094
235
RHM027 Rheumatic Disease 56 0.094
236
TXC005 Toxic Shock Syndrome 61 0.094
238
PRP027 Peripheral Vascular Disease 71 0.093
239
CHL004 Cholelithiasis 49 0.093
240
P HDC001 Headache 57 0.093
241
DYS073 Dysphagia 50 0.093
242
AST005 Asthma 77 0.093
243
P PHC003 Pheochromocytoma 71 0.093
244
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.092
245
P MCR115 Microvascular Complications of Diabetes 5 66 0.092
246
ADR040 Adrenal Gland Pheochromocytoma 46 0.092
247
P CYS018 Cystitis 59 0.092
248
P TRM003 Tremor 53 0.092
249
KRT002 Keratomalacia 48 0.092
250
P BRS044 Breast Adenocarcinoma 59 0.092
251
c ACT073 Acute Leukemia 58 0.092
252
ANG054 Angina Pectoris 66 0.091
253
ANX010 Anxiety 72 0.091
254
P INF038 Influenza 68 0.091
255
P ATR011 Atrial Fibrillation 66 0.091
256
SQM002 Squamous Cell Papilloma 42 0.091
257
PNG002 Pain Agnosia 51 0.091
258
GST050 Gastrointestinal System Disease 56 0.091
259
P FBR017 Fibrosarcoma 56 0.091
260
CNS004 Constipation 57 0.090
261
MCS002 Mucositis 55 0.090
262
TTN003 Tetanus 64 0.089
263
HNS001 Hansen's Disease 34 0.089
264
P LPR021 Leprosy 3 67 0.088
265
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.088
266
P ART023 Arthropathy 62 0.088
267
P CRD119 Cardiac Arrest 67 0.088
268
P PLY019 Polyneuropathy 56 0.088
269
P ALC033 Alcohol Use Disorder 58 0.088
270
ACQ007 Acquired Immunodeficiency Syndrome 60 0.087
271
CHL079 Children's Interstitial Lung Disease 27 0.087
272
P EXN002 Exanthem 57 0.086
273
HMS001 Hemosiderosis 54 0.086
274
PRS021 Prostatic Adenoma 51 0.086
275
c HPT016 Hepatitis B 59 0.085
276
c LRG017 Large Intestine Cancer 47 0.085
277
P CNR004 Cone-Rod Dystrophy 2 71 0.085
278
P LKM062 Leukemia, Acute Lymphoblastic 68 0.085
279
ALL003 Allergic Rhinitis 67 0.084
280
c PRS136 Prostate Cancer, Hereditary, 6 33 0.084
281
c PRS130 Prostate Cancer, Hereditary, 8 32 0.084
282
c FNC043 Fanconi Anemia, Complementation Group E 62 0.084
283
P RRH023 Rare Hereditary Hemochromatosis 41 0.084
284
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.084
285
IRR002 Irritable Bowel Syndrome 63 0.084
286
GST045 Gastroenteritis 59 0.083
287
PRS129 Prostatic Hyperplasia, Benign 49 0.083
288
ENM002 Enamel Erosion 27 0.083
289
c ACT134 Acute Liver Failure 51 0.083
290
ENT004 Enthesopathy 48 0.083
291
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.082
292
P DMN002 Dementia 67 0.082
293
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.082
294
P HYP265 Hypotonia 42 0.082
295
LPT014 Leptin Deficiency or Dysfunction 73 0.081
296
MLR004 Malaria 80 0.081
297
IRN001 Iron Deficiency Anemia 58 0.081
298
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.080
299
c ATR087 Atrial Standstill 1 74 0.080
300
INT007 Intermediate Coronary Syndrome 55 0.080
301
P MLN007 Male Infertility 56 0.080
302
EYD002 Eye Disease 58 0.080
303
P CHR345 Chronic Pain 50 0.080
304
P ATR005 Atrophic Gastritis 50 0.080
305
ENT011 Enterocolitis 50 0.080
306
MMM001 Mammary Paget's Disease 53 0.080
307
P BNG032 Benign Mesothelioma 45 0.080
308
c LKM071 Leukemia, Chronic Lymphocytic 79 0.079
309
PRS047 Prostatitis 56 0.079
310
P PLM037 Pulmonary Hypertension 68 0.079
311
P PYL005 Pyelonephritis 56 0.079
312
ATS010 Autosomal Recessive Disease 48 0.079
313
GNG003 Gingival Recession 44 0.079
314
P GLM040 Glioma Susceptibility 1 81 0.079
315
P MGL001 Megaloblastic Anemia 55 0.079
316
MST005 Mastitis 53 0.079
317
P AMY004 Amyloidosis 70 0.078
318
RTN023 Retinitis 46 0.078
319
NRR001 Neuroretinitis 43 0.078
320
CYS013 Cystinuria 62 0.078
321
OTT002 Otitis Media 71 0.077
322
LYM019 Lymphosarcoma 47 0.077
323
P THL005 Thalassemia 60 0.077
324
PRT013 Portal Hypertension 60 0.076
325
END057 Endometrial Cancer 74 0.076
326
BRN028 Brain Cancer 73 0.076
327
P RTN008 Retinitis Pigmentosa 77 0.076
328
PRP030 Purpura 55 0.076
329
PLY150 Polykaryocytosis Inducer 31 0.076
330
P PRK057 Parkinson Disease, Late-Onset 76 0.076
331
c LKM063 Leukemia, Chronic Myeloid 71 0.076
332
PLS009 Plasma Cell Neoplasm 51 0.076
333
PRT038 Protein-Energy Malnutrition 54 0.075
334
P CND004 Candidiasis 57 0.075
335
MSL001 Measles 61 0.074
336
P URT039 Urticaria 58 0.074
337
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.074
338
P PLY014 Polycystic Kidney Disease 59 0.074
339
c PRD040 Periodontitis, Chronic 54 0.073
340
P END044 Endometriosis 62 0.073
341
P TCL004 T-Cell Leukemia 47 0.073
342
P RCT021 Rectum Cancer 53 0.073
343
P SYS005 Systemic Scleroderma 70 0.072
344
P SLP006 Sleep Apnea 69 0.072
345
P MDL005 Medulloblastoma 77 0.072
346
TRN015 Transient Cerebral Ischemia 62 0.072
347
SCH014 Schistosomiasis 56 0.072
348
ERY051 Erythroleukemia, Familial 56 0.072
349
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.071
350
PRN019 Perinatal Necrotizing Enterocolitis 54 0.071
351
LNG031 Lung Benign Neoplasm 50 0.071
352
PSY004 Psychotic Disorder 67 0.071
353
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.071
354
P KDN017 Kidney Cancer 61 0.071
355
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.071
356
P INT068 Intestinal Disease 52 0.071
357
P GRF003 Graft-Versus-Host Disease 71 0.070
358
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.070
359
ASP007 Aspiration Pneumonia 48 0.070
360
P CNJ013 Conjunctivitis 65 0.070
361
DSS009 Disseminated Intravascular Coagulation 57 0.070
362
PRP001 Propionic Acidemia 66 0.070
363
P INT143 Interstitial Cystitis 61 0.069
364
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.069
365
LYS002 Lysosomal Storage Disease 52 0.069
366
END040 Endogenous Depression 54 0.069
367
RRS014 Rare Surgical Neurologic Disease 32 0.069
368
ANT024 Anthrax Disease 58 0.069
369
PNC129 Pancreatic Adenocarcinoma 67 0.068
370
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.068
371
PLM031 Poliomyelitis 57 0.068
372
CMM005 Common Cold 56 0.068
373
ALL006 Allergic Asthma 56 0.068
374
c FML035 Familial Hyperlipidemia 55 0.068
375
c PRM038 Primary Agammaglobulinemia 43 0.068
376
c PRM005 Primary Hyperparathyroidism 58 0.068
377
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.067
378
SBC016 Subacute Delirium 44 0.067
379
P SCL018 Scoliosis 60 0.067
380
c CHR064 Chronic Monocytic Leukemia 34 0.067
381
DYS015 Dysentery 50 0.067
382
HRY003 Hairy Cell Leukemia 55 0.067
383
ILS001 Ileus 51 0.067
384
GST040 Gastric Adenocarcinoma 70 0.067
385
c SCL052 Scleroderma, Familial Progressive 62 0.067
386
PST092 Posttransplant Acute Limbic Encephalitis 29 0.067
387
CHR100 Chronic Ulcer of Skin 53 0.066
388
P HYD006 Hydrocephalus 65 0.066
389
P ADL010 Adult Respiratory Distress Syndrome 63 0.066
390
MSC007 Muscle Hypertrophy 63 0.066
391
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.065
392
BLR002 Bile Reflux 39 0.065
393
CHR178 Chromosomal Triplication 35 0.065
394
LYM133 Lymphoma, Hodgkin, Classic 69 0.065
395
c MCR129 Microvascular Complications of Diabetes 1 66 0.065
396
NRT001 Neurotic Disorder 52 0.065
397
MSC157 Muscular Dystrophy, Duchenne Type 71 0.065
398
P SRC025 Sarcoidosis 1 70 0.065
399
c BRN108 Branchiootic Syndrome 1 61 0.065
400
PLG002 Plague 57 0.065
401
P HMP007 Hemophilia 51 0.065
402
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.064
403
P UVT001 Uveitis 57 0.064
404
MXD026 Mixed Glioma 45 0.064
405
KPS004 Kaposi Sarcoma 75 0.064
406
PLC008 Placenta Disease 49 0.064
407
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.064
408
P MYC033 Myoclonus 46 0.064
409
ADG002 Audiogenic Seizures 26 0.064
410
P RTN018 Retinal Disease 52 0.063
411
SPL018 Splenomegaly 48 0.063
412
P THY023 Thymoma 65 0.063
413
c THY107 Thymoma, Familial 54 0.063
414
RTR008 Root Resorption 45 0.063
415
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.062
416
SFT003 Soft Tissue Sarcoma 56 0.062
417
P MJR007 Major Affective Disorder 1 43 0.062
418
CRT017 Cartilage Disease 54 0.061
419
OVR094 Ovarian Epithelial Cancer 38 0.061
420
P SLM003 Salmonellosis 54 0.061
421
P ALP009 Alopecia Areata 60 0.061
422
PST021 Postpartum Depression 50 0.061
423
P NRV007 Nervous System Disease 66 0.061
424
SPS057 Spasticity 41 0.061
425
GLS001 Gliosarcoma 54 0.060
426
P FNC004 Fanconi Syndrome 50 0.060
427
DRY001 Dry Eye Syndrome 47 0.060
428
HND015 Hand Skill, Relative 33 0.060
429
P MYS003 Myasthenia Gravis 68 0.060
430
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.060
431
ASP008 Aspiration Pneumonitis 42 0.060
432
c HYP272 Hypercholesterolemia, Familial, 3 43 0.060
433
HYD002 Hydronephrosis 59 0.059
434
HVY002 Heavy Metal Poisoning 22 0.059
435
PLS011 Plasmacytoma 56 0.059
436
KRT006 Keratoconjunctivitis 53 0.059
437
HYP017 Hypophosphatemia 49 0.059
438
c FML001 Familial Atrial Fibrillation 66 0.059
439
ACR007 Acromegaly 71 0.059
440
CRB037 Cerebral Palsy 68 0.058
441
CRC021 Carcinosarcoma 61 0.058
442
KRT013 Keratolytic Winter Erythema 46 0.058
443
MSC190 Muscular Disease 51 0.058
444
c BTT014 Beta-Thalassemia 72 0.058
445
c MJR003 Major Affective Disorder 6 33 0.058
446
c MJR006 Major Affective Disorder 5 33 0.058
447
SKN019 Skin Melanoma 67 0.058
448
c BCT007 Bacterial Meningitis 55 0.058
449
P BRB001 Beriberi 44 0.058
450
49X006 49, Xxxxy Syndrome 41 0.058
451
BRT054 Brittle Bone Disorder 70 0.057
452
P OLG002 Oligodendroglioma 67 0.057
453
P MVM001 Movement Disease 61 0.057
454
FBR047 Fibromyalgia 59 0.057
455
ATN004 Autonomic Neuropathy 44 0.057
456
LKP003 Leukoplakia 39 0.057
457
AZS001 Azoospermia 50 0.057
458
DBT002 Diabetic Autonomic Neuropathy 41 0.057
459
P MTR014 Motor Neuron Disease 64 0.057
460
RBS001 Rabies 58 0.057
461
c MJR008 Major Affective Disorder 2 34 0.057
462
c MJR023 Major Affective Disorder 7 33 0.057
463
c MJR004 Major Affective Disorder 4 28 0.057
464
P PTT006 Pituitary Adenoma 54 0.057
465
c SVR005 Severe Pre-Eclampsia 49 0.057
466
P INT070 Intestinal Obstruction 58 0.057
467
P ATX030 Ataxia-Telangiectasia 83 0.056
468
CNN005 Connective Tissue Disease 66 0.056
469
GRD007 Grade Iii Astrocytoma 59 0.056
470
c ADL017 Adult T-Cell Leukemia 57 0.056
471
P PLY018 Polycythemia 55 0.056
472
P SBS003 Substance Abuse 54 0.056
473
GLS018 Glass Syndrome 53 0.056
474
ART016 Aortic Aneurysm 68 0.056
475
VRL011 Viral Infectious Disease 61 0.056
476
YLL002 Yellow Fever 60 0.056
477
c PSR017 Psoriasis 2 52 0.056
478
c PSR023 Psoriasis 1 49 0.056
479
c PSR028 Psoriasis 7 39 0.056
480
c PSR032 Psoriasis 11 38 0.056
481
c PSR018 Psoriasis 13 38 0.056
482
P SJG008 Sjogren Syndrome 56 0.055
483
P SLP005 Sleep Disorder 59 0.055
484
P MNC007 Monocytic Leukemia 54 0.055
485
SLP001 Sleeping Sickness 48 0.055
486
P VSC018 Visceral Steatosis 33 0.055
487
P PRM002 Primary Hyperoxaluria 62 0.055
488
FCT007 Factor Vii Deficiency 66 0.055
489
c SCN007 Secondary Hyperparathyroidism 50 0.055
490
PLC005 Placental Insufficiency 57 0.054
491
c ACT135 Acute Graft Versus Host Disease 51 0.054
492
MYC006 Mycosis Fungoides 66 0.054
493
BRN056 Bronchopulmonary Dysplasia 57 0.054
494
P NRC002 Narcolepsy 51 0.054
495
KRT001 Keratoconjunctivitis Sicca 50 0.054
496
MNT001 Mantle Cell Lymphoma 66 0.053
497
P PNC025 Panic Disorder 53 0.053
498
ACT003 Acute Kidney Tubular Necrosis 45 0.053
499
c MLG074 Malignant Mesenchymoma 39 0.053
500
ACN002 Acanthosis Nigricans 60 0.053
501
P FLL037 Follicular Lymphoma 66 0.053
502
CHR066 Chronic Fatigue Syndrome 61 0.053
503
HYP025 Hyperphosphatemia 47 0.053
504
BCK006 Back Pain 42 0.053
505
c EXD008 Exudative Vitreoretinopathy 1 69 0.052
506
HMG005 Hemoglobinopathy 55 0.052
507
PTH003 Pathologic Nystagmus 51 0.052
508
c MCR112 Microvascular Complications of Diabetes 2 41 0.052
509
APN008 Apnea, Obstructive Sleep 65 0.052
510
P OPT006 Optic Nerve Disease 57 0.052
511
c CHR682 Chronic Bilirubin Encephalopathy 38 0.052
512
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.052
513
P ASP006 Aspergillosis 66 0.052
514
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.052
515
c MST023 Mesothelioma, Malignant 57 0.052
516
P MTC069 Mitochondrial Disorders 56 0.052
517
LYM040 Lymphoblastic Lymphoma 54 0.052
518
PRD004 Prediabetes Syndrome 47 0.052
519
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.051
520
HMT002 Hematologic Cancer 62 0.051
521
c CNT035 Central Nervous System Disease 54 0.051
522
PLC007 Placental Abruption 48 0.051
523
INT067 Interstitial Nephritis 46 0.051
524
RDN001 Reading Disorder 40 0.051
525
MLT157 Multiple System Atrophy 1 70 0.051
526
THY122 Thyroid Gland Cancer 58 0.051
527
PYL006 Pyloric Stenosis 48 0.051
528
P BLR006 Biliary Tract Disease 46 0.051
529
P HYP726 Hypercalcemia, Infantile, 1 57 0.050
530
TND005 Tendinitis 52 0.050
531
ACT084 Acute Stress Disorder 48 0.050
532
PPL001 Papillary Adenoma 45 0.050
533
ANK001 Ankylosis 52 0.050
534
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.050
535
BRN002 Bronchiolitis 59 0.050
536
PST028 Post-Traumatic Stress Disorder 58 0.050
537
P PLM034 Pulmonary Emphysema 56 0.050
538
FCT001 Factor Viii Deficiency 55 0.050
539
MCR004 Macroglobulinemia 50 0.050
540
NPH003 Nephrocalcinosis 51 0.050
541
FSC004 Fasciitis 50 0.050
542
c JVN010 Juvenile Rheumatoid Arthritis 67 0.050
543
c DPH024 Diaphragmatic Hernia, Congenital 64 0.050
544
P BNG030 Benign Ependymoma 60 0.050
545
P VNT002 Ventricular Septal Defect 60 0.050
546
P MYS005 Myositis 56 0.050
547
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.050
548
TXC002 Toxic Encephalopathy 52 0.050
549
THR004 Thrombocytosis 51 0.050
550
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.050
551
BCT004 Bacteriuria 48 0.050
552
RFR010 Refractory Anemia 48 0.050
553
CYS010 Cystinosis 60 0.049
554
P SYP003 Syphilis 59 0.049
555
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.049
556
HRT011 Heart Septal Defect 50 0.049
557
THY111 Thyroid Carcinoma, Familial Medullary 67 0.049
558
c HMP029 Hemophilia a 65 0.049
559
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.049
560
THR013 Thoracic Outlet Syndrome 53 0.049
561
CLL010 Cellular Ependymoma 53 0.049
562
LPT006 Leptin Receptor Deficiency 47 0.049
563
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.049
564
P OCL013 Oculodentodigital Dysplasia 69 0.048
565
WST001 West Syndrome 60 0.048
566
PNM008 Pneumothorax 56 0.048
567
c OVR114 Ovarian Cancer 1 38 0.048
568
IDP073 Idiopathic Hypercalciuria 43 0.048
569
MYL031 Myeloproliferative Neoplasm 65 0.048
570
NWB001 Newborn Respiratory Distress Syndrome 58 0.048
571
AMN001 Amenorrhea 54 0.048
572
LRN003 Learning Disability 49 0.048
573
VTM033 Vitamin K Deficiency Bleeding 48 0.048
574
P RNL015 Renal Hypertension 48 0.048
575
CHL013 Cholecystolithiasis 37 0.048
576
MCN017 Meconium Ileus 52 0.048
577
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.047
578
P CHR285 Chronic Myelomonocytic Leukemia 59 0.047
579
P PRV006 Pervasive Developmental Disorder 57 0.047
580
LMB062 Limb Ischemia 55 0.047
581
P HMR003 Hemorrhagic Disease 52 0.047
582
HYP080 Hypogonadism 50 0.047
583
PLR007 Pleural Empyema 49 0.047
584
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.047
585
PRS063 Paresthesia 43 0.047
586
P VNW001 Von Willebrand's Disease 64 0.047
587
KHL003 Kohlschutter-Tonz Syndrome 64 0.047
588
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.047
589
TRP009 Triple X Syndrome 42 0.047
590
HYP064 Hypogonadotropism 40 0.047
591
MLC004 Mulchandani-Bhoj-Conlin Syndrome 32 0.047
592
MYL005 Myelofibrosis 67 0.047
593
CRP001 Carpal Tunnel Syndrome 67 0.047
594
PPL049 Papillon-Lefevre Syndrome 63 0.047
595
URN010 Urinary Tract Obstruction 57 0.047
596
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.047
597
THY125 Thyroid Gland Medullary Carcinoma 51 0.047
598
c FLL041 Follicular Lymphoma 1 49 0.047
599
P SBR004 Seborrheic Dermatitis 45 0.047
600
ORL012 Oral Leukoplakia 39 0.047
601
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.047
602
c PRG106 Progressive Muscular Dystrophy 33 0.047
603
INC002 Inclusion Body Myositis 64 0.046
604
P GLL022 Guillain-Barre Syndrome 59 0.046
605
HLL004 Hellp Syndrome 53 0.046
606
HYP043 Hyperandrogenism 48 0.046
607
PLY001 Polycythemia Vera 69 0.046
608
P DRM010 Dermatomyositis 61 0.046
609
GST071 Gastrointestinal Carcinoma 45 0.046
610
FRZ001 Frozen Shoulder 53 0.045
611
P SPR086 Spermatogenic Failure 3 44 0.045
612
BRS099 Breast Ductal Carcinoma 62 0.045
613
CLN019 Colonic Disease 46 0.045
614
c SYS043 Systemic Lupus Erythematosus 1 38 0.045
615
c MCL013 Mucolipidosis Iv 64 0.045
616
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.045
617
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.045
618
P NRV006 Nervous System Cancer 48 0.045
619
TND004 Tendinopathy 44 0.045
620
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.045
621
c ALP101 Alpha-Thalassemia 62 0.044
622
DCT002 Ductal Carcinoma in Situ 59 0.044
623
CMR002 Coumarin Resistance 56 0.044
624
GNT002 Giant Cell Glioblastoma 52 0.044
625
BRN009 Burning Mouth Syndrome 49 0.044
626
P HYP733 Hypercalciuria, Absorptive, 2 46 0.044
627
LWC001 Low Compliance Bladder 42 0.044
628
ATM052 Autoimmune Disease 1 37 0.044
629
P APL001 Aplastic Anemia 74 0.044
630
HMR039 Hemorrhage, Intracerebral 57 0.044
631
P DBT005 Diabetes Insipidus 55 0.044
632
PLS007 Plasmodium Falciparum Malaria 52 0.044
633
c CNT033 Central Nervous System Cancer 46 0.044
634
CYN002 Cyanosis, Transient Neonatal 45 0.044
635
P DST107 Distal Renal Tubular Acidosis 41 0.044
636
P ANT006 Antiphospholipid Syndrome 54 0.043
637
ALL009 Allergic Conjunctivitis 50 0.043
638
c XNT010 Xanthinuria, Type I 50 0.043
639
P RNV001 Renovascular Hypertension 49 0.043
640
BRS064 Bursitis 47 0.043
641
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.043
642
ART002 Arts Syndrome 63 0.043
643
SZR001 Sezary's Disease 60 0.043
644
GST037 Gastroparesis 53 0.043
645
HRT012 Heart Valve Disease 53 0.043
646
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.043
647
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.043
648
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.043
649
c PNC108 Pancreatitis, Hereditary 69 0.042
650
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.042
651
ORL005 Oral Candidiasis 56 0.042
652
PLS025 Plasmablastic Lymphoma 47 0.042
653
ASP004 Asphyxia Neonatorum 45 0.042
654
MYF001 Myofibroma 42 0.042
655
P AVS003 Avascular Necrosis 42 0.042
656
HRN029 Hearing Loss, Noise-Induced 37 0.042
657
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.042
658
P MLG056 Malignant Hyperthermia 67 0.042
659
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.042
660
GST049 Gastrointestinal System Cancer 49 0.042
661
OLG001 Oligospermia 45 0.042
662
BNM001 Bone Marrow Cancer 43 0.042
663
GST020 Gastric Antral Vascular Ectasia 41 0.042
664
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.042
665
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.041
666
c ART101 Aortic Valve Disease 2 63 0.041
667
DGR001 Digeorge Syndrome 63 0.041
668
ANG005 Anogenital Venereal Wart 56 0.041
669
HMP005 Hemiplegia 54 0.041
670
P CYS039 Cystic Kidney Disease 54 0.041
671
ACR041 Acromelic Frontonasal Dysostosis 52 0.041
672
P HYP040 Hypospadias 51 0.041
673
c CHR418 Chronic Leukemia 50 0.041
674
VRC001 Varicocele 49 0.041
675
ECT026 Ectopic Pregnancy 49 0.041
676
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.041
677
CLS052 Classic Hairy Cell Leukemia 27 0.041
678
CYT018 Cytochrome P450 2d6 Variant 27 0.041
679
MYC005 Myocardial Stunning 46 0.041
680
CNN003 Conn's Syndrome 79 0.041
681
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.041
682
LYM012 Lymphoplasmacytic Lymphoma 61 0.041
683
CMP010 Complex Regional Pain Syndrome 58 0.041
684
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.041
685
c LKM070 Leukemia, Acute Monocytic 53 0.041
686
SXL003 Sexual Disorder 48 0.041
687
P OVR046 Ovarian Cyst 45 0.041
688
MYF002 Myofascial Pain Syndrome 42 0.041
689
GRM010 Germ Cells Tumors 34 0.041
690
GST019 Gastrointestinal Stromal Tumor 76 0.040
691
P HYP024 Hypoparathyroidism 55 0.040
692
RYN005 Raynaud Phenomenon 46 0.040
693
PRM003 Premature Ejaculation 44 0.040
694
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.040
695
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.040
696
HML018 Homologous Wasting Disease 22 0.040
697
EXT034 Extrinsic Allergic Alveolitis 58 0.040
698
SWL001 Swallowing Disorders 38 0.040
699
P ATR010 Atrial Heart Septal Defect 60 0.039
700
APH001 Aphthous Stomatitis 57 0.039
701
c LTN004 Late-Onset Retinal Degeneration 52 0.039
702
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.039
703
IRD001 Iridocyclitis 50 0.039
704
CRN027 Corneal Neovascularization 47 0.039
705
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.039
706
P BLD051 Blood Coagulation Disease 46 0.039
707
THR035 Thrombasthenia 41 0.039
708
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.039
709
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.039
710
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.039
711
PRT058 Pure Autonomic Failure 59 0.039
712
MRG003 Marginal Zone B-Cell Lymphoma 53 0.039
713
P BRN035 Brain Stem Glioma 51 0.039
714
URT001 Urethritis 48 0.039
715
INT017 Intestinal Schistosomiasis 47 0.039
716
MND023 Mend Syndrome 43 0.039
717
ALG001 Algoneurodystrophy 39 0.039
718
PSD088 Pseudobulbar Affect 36 0.039
719
TTH007 Tooth Erosion 31 0.039
720
MST024 Mastocytosis, Cutaneous 67 0.038
721
P ESS003 Essential Thrombocythemia 67 0.038
722
HYP020 Hyperprolactinemia 64 0.038
723
c LCL006 Localized Scleroderma 62 0.038
724
P PTN014 Patent Ductus Arteriosus 1 60 0.038
725
P MLN069 Melanoma, Uveal 58 0.038
726
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.038
727
GNR004 Generalized Anxiety Disorder 56 0.038
728
FLR002 Filariasis 55 0.038
729
ACT200 Acute Monoblastic Leukemia 55 0.038
730
P VNS003 Venous Insufficiency 55 0.038
731
c LBR014 Leber Congenital Amaurosis 4 53 0.038
732
NTR018 Neutrophilia, Hereditary 52 0.038
733
PRV004 Periventricular Leukomalacia 51 0.038
734
BLD053 Blood Platelet Disease 51 0.038
735
OPT003 Opiate Dependence 50 0.038
736
P MGR001 Migraine Without Aura 48 0.038
737
c DRM054 Dermatitis, Atopic, 2 45 0.038
738
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.038
739
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.038
740
GLN010 Glanzmann Thrombasthenia 66 0.038
741
HYD038 Hydrops Fetalis, Nonimmune 61 0.038
742
c CHR417 Chronic Graft Versus Host Disease 56 0.038
743
c ACT020 Acute T Cell Leukemia 53 0.038
744
RFL001 Reflex Sympathetic Dystrophy 53 0.038
745
BRN038 Bronchial Disease 53 0.038
746
P LYM025 Lymphedema 53 0.038
747
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.038
748
BWN001 Bowen-Conradi Syndrome 51 0.038
749
c ALM001 Al Amyloidosis 50 0.038
750
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.038
751
RDC002 Radiculopathy 48 0.038
752
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.038
753
SPP008 Suppurative Otitis Media 45 0.038
754
LYM051 Lymphomatoid Granulomatosis 45 0.038
755
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.038
756
P PRG092 Pregnancy Loss, Recurrent 1 40 0.038
757
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.038
758
c BCT006 Bacterial Conjunctivitis 33 0.038
759
P ACT105 Acute Mountain Sickness 52 0.037
760
P TTR001 Tetralogy of Fallot 69 0.037
761
P LYM033 Lymphoproliferative Syndrome 60 0.037
762
P PLV020 Pelvic Organ Prolapse 59 0.037
763
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.037
764
SYS003 Systolic Heart Failure 50 0.037
765
GST010 Gestational Trophoblastic Neoplasm 46 0.037
766
P HYP263 Hypersomnia 41 0.037
767
CRN020 Coronary Restenosis 39 0.037
768
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.037
769
PNM010 Pneumothorax, Primary Spontaneous 60 0.036
770
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.036
771
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.036
772
CYS014 Cystadenocarcinoma 51 0.036
773
SPS003 Spastic Diplegia 50 0.036
774
c INF023 Inflammatory Breast Carcinoma 49 0.036
775
ATY042 Atypical Chronic Myeloid Leukemia 49 0.036
776
NCR007 Necrotizing Fasciitis 49 0.036
777
END062 Endometrial Hyperplasia 48 0.036
778
CLC006 Calcinosis 48 0.036
779
INT054 Intraocular Lymphoma 48 0.036
780
P HMN032 Human Herpesvirus 8 46 0.036
781
AND014 Androgenic Alopecia 44 0.036
782
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.036
783
DFF003 Diffuse Scleroderma 42 0.036
784
FLL027 Fallopian Tube Carcinoma 67 0.036
785
MGK001 Megakaryocytic Leukemia 64 0.036
786
P ANP001 Anaplastic Large Cell Lymphoma 61 0.036
787
P FCL005 Focal Segmental Glomerulosclerosis 58 0.036
788
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.036
789
HMT008 Hematuria, Benign Familial 53 0.036
790
CYS036 Cystinosis, Nephropathic 51 0.036
791
ADR016 Adrenal Cortical Carcinoma 48 0.036
792
MDS022 Mediastinitis 47 0.036
793
ANP009 Anaplastic Oligodendroglioma 43 0.036
794
DFF037 Diffuse Intrinsic Pontine Glioma 42 0.036
795
c HMP004 Hemophilia B 67 0.035
796
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.035
797
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.035
798
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.035
799
SRC027 Sarcoma, Synovial 56 0.035
800
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.035
801
OLG003 Oligohydramnios 52 0.035
802
c PRM012 Primary Polycythemia 52 0.035
803
FLR001 Filarial Elephantiasis 50 0.035
804
c CNG216 Congenital Hydrocephalus 50 0.035
805
P ALP061 Alopecia, Androgenetic, 1 49 0.035
806
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.035
807
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.035
808
FBR019 Fibromatosis 44 0.035
809
IDP033 Idiopathic Edema 43 0.035
810
PYR037 Pyruvate Carboxylase Deficiency 43 0.035
811
P CRN024 Corneal Disease 43 0.035
812
ENT001 Enterocele 39 0.035
813
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.035
814
ADR004 Adrenal Cortical Adenocarcinoma 38 0.035
815
RSP007 Respiratory Distress Syndrome, Infant 30 0.035
816
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 40 0.034
817
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.034
818
OCL022 Ocular Melanoma 53 0.034
819
P OVR049 Ovarian Disease 53 0.034
820
SRS001 Serous Cystadenocarcinoma 52 0.034
821
P MGR003 Migraine with Aura 50 0.034
822
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.034
823
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.034
824
SRT004 Serotonin Syndrome 46 0.034
825
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.034
826
PRP017 Periapical Periodontitis 46 0.034
827
APP009 Appendix Adenocarcinoma 44 0.034
828
PST053 Postherpetic Neuralgia 42 0.034
829
FMR004 Fumarase Deficiency 41 0.034
830
FNC002 Functional Diarrhea 39 0.034
831
c CHR097 Chronic Purulent Otitis Media 32 0.034
832
CYT004 Cytomegalic Inclusion Disease 31 0.034
833
MLG164 Malignant Epithelial Tumor of Ovary 26 0.034
834
P URF003 Urofacial Syndrome 1 57 0.033
835
AND020 Androgen Insensitivity, Partial 55 0.033
836
MCN007 Meconium Aspiration Syndrome 52 0.033
837
AMB001 Amebiasis 49 0.033
838
URN009 Urinary System Disease 48 0.033
839
ACT098 Acute Erythroid Leukemia 48 0.033
840
DYS009 Dysthymic Disorder 48 0.033
841
PRL017 Prolymphocytic Leukemia 47 0.033
842
c PRM093 Premature Ovarian Failure 7 47 0.033
843
P OCY003 Oocyte Maturation Defect 1 45 0.033
844
CLL014 Cll/sll 45 0.033
845
P END084 Endocrine System Disease 44 0.033
846
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.033
847
CLP006 Clopidogrel Resistance 40 0.033
848
ACT011 Acute Contagious Conjunctivitis 40 0.033
849
P PRG002 Progesterone-Receptor Positive Breast Cancer 34 0.033
850
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.033
851
MNR012 Meniere Disease 57 0.033
852
PST046 Post-Transplant Lymphoproliferative Disease 53 0.033
853
P HYP730 Hypogonadotropic Hypogonadism 53 0.033
854
FBR008 Fibrillary Astrocytoma 50 0.033
855
CHL018 Childhood Medulloblastoma 49 0.033
856
c CHR431 Chronic Venous Insufficiency 49 0.033
857
c DYS119 Dystonia 9 49 0.033
858
c THR090 Thrombocythemia 1 49 0.033
859
PLS016 Plasma Cell Leukemia 46 0.033
860
AYM001 Ayme-Gripp Syndrome 46 0.033
861
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.033
862
c SRC023 Sarcoidosis 2 43 0.033
863
INH001 Inhalation Anthrax 40 0.033
864
CRB026 Cerebellar Astrocytoma 35 0.033
865
BNN005 Bunion 33 0.033
866
KLB004 Klebsiella Infection 27 0.033
867
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 57 0.032
868
JVN009 Juvenile Pilocytic Astrocytoma 55 0.032
869
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.032
870
SPL004 Splenic Marginal Zone Lymphoma 51 0.032
871
c MLG054 Malignant Histiocytosis 50 0.032
872
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.032
873
OPD006 Opioid Addiction 48 0.032
874
MGC001 Megacolon 46 0.032
875
ORC001 Orchitis 45 0.032
876
LTH001 Lethal Midline Granuloma 43 0.032
877
LRG008 Large Granular Lymphocyte Leukemia 41 0.032
878
URM005 Uremic Pruritus 39 0.032
879
THR123 Thrombotic Microangiopathy 38 0.032
880
HYP189 Hypoadrenalism 37 0.032
881
P HYP120 Hypoaldosteronism 37 0.032
882
c ADL096 Adult Hepatocellular Carcinoma 35 0.032
883
c ADL008 Adult Oligodendroglioma 35 0.032
884
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.032
885
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.032
886
GLB024 Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor 31 0.032
887
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 31 0.032
888
CHL057 Childhood Brain Stem Glioma 29 0.032
889
P OVR096 Overlap Myositis 27 0.032
890
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.032
891
CHL009 Childhood Cerebral Astrocytoma 14 0.032
892
PST037 Pasteurella Multocida Infection 14 0.032
893
P NJM001 Nijmegen Breakage Syndrome 72 0.031
894
AFB002 Afibrinogenemia, Congenital 65 0.031
895
DSM004 Desmoid Tumor 64 0.031
896
MSC152 Muscular Dystrophy, Becker Type 63 0.031
897
OVR029 Ovarian Hyperstimulation Syndrome 63 0.031
898
MXD005 Mixed Connective Tissue Disease 59 0.031
899
ADR005 Adrenal Carcinoma 58 0.031
900
P MTR012 Mitral Valve Disease 57 0.031
901
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.031
902
FML037 Female Breast Cancer 52 0.031
903
ACT017 Acute Chest Syndrome 50 0.031
904
c PYR010 Peyronie's Disease 50 0.031
905
NPH018 Nephrogenic Systemic Fibrosis 50 0.031
906
P MST002 Mast-Cell Leukemia 48 0.031
907
OPD001 Opioid Abuse 45 0.031
908
PLR022 Pleural Disease 44 0.031
909
PNC085 Penicillin Allergy 44 0.031
910
SPN040 Spinal Cancer 44 0.031
911
DSC009 Discoid Lupus Erythematosus 42 0.031
912
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 38 0.031
913
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.031
914
PDT014 Pediatric Ependymoma 32 0.031
915
RFR002 Refractory Hairy Cell Leukemia 32 0.031
916
PLN007 Plantar Fasciitis 31 0.031
917
BRN049 Brain Tumor, Childhood 29 0.031
918
FTL073 Fetal Anticonvulsant Syndrome 26 0.031
919
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.030
920
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 55 0.030
921
VLC001 Velocardiofacial Syndrome 54 0.030
922
ONC002 Onchocerciasis 51 0.030
923
PRS034 Parasitic Helminthiasis Infectious Disease 49 0.030
924
ART017 Aortic Disease 49 0.030
925
RYN001 Raynaud Disease 49 0.030
926
END021 Endomyocardial Fibrosis 48 0.030
927
SBP001 Subependymal Giant Cell Astrocytoma 48 0.030
928
P CLR019 Color Blindness 48 0.030
929
HPR003 Heparin-Induced Thrombocytopenia 47 0.030
930
ANP006 Anaplastic Ependymoma 46 0.030
931
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.030
932
PRT035 Peritoneum Cancer 44 0.030
933
DST006 Diastolic Heart Failure 44 0.030
934
PLM020 Pleomorphic Xanthoastrocytoma 43 0.030
935
DNT014 Dental Pulp Disease 43 0.030
936
DNT006 Dental Pulp Necrosis 40 0.030
937
EMB002 Embryoma 38 0.030
938
GGN002 Gigantism 34 0.030
939
FNT004 Fainting 31 0.030
940
SNG003 Single Ventricular Heart 30 0.030
941
SCN001 Secondary Hyperparathyroidism of Renal Origin 28 0.030
942
SLC024 Slc4a1-Associated Distal Renal Tubular Acidosis 19 0.030
943
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.029
944
CNT061 Conotruncal Heart Malformations 63 0.029
945
PRM126 Primary Peritoneal Carcinoma 62 0.029
946
HYP780 Hypoadrenocorticism, Familial 62 0.029
947
P PNL012 Penile Cancer 56 0.029
948
LBL001 Lobular Neoplasia 56 0.029
949
VTM027 Vitamin D-Dependent Rickets, Type 2a 55 0.029
950
LYM022 Lymphangioma 53 0.029
951
P PRT096 Peritoneal Mesothelioma 50 0.029
952
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.029
953
EXT010 Extramedullary Plasmacytoma 45 0.029
954
URN003 Urinary Schistosomiasis 44 0.029
955
P BCT020 Bacteremia 2 44 0.029
956
CNT017 Central Nervous System Origin Vertigo 44 0.029
957
BSL008 Basal Ganglia Disease 43 0.029
958
CHR286 Chronic Neutrophilic Leukemia 41 0.029
959
EPC002 Epicondylitis 41 0.029
960
MLL002 Miller Fisher Syndrome 40 0.029
961
c ACT036 Acute Cholangitis 35 0.029
962
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.029
963
P RRL003 Rare Lymphatic Malformation 31 0.029
964
PRD003 Periodontosis 26 0.029
965
PDT015 Pediatric Supratentorial Ependymoma 24 0.029
966
PDT016 Pediatric Infratentorial Ependymoma 22 0.029
967
c ADL093 Adult Acute Monocytic Leukemia 20 0.029
968
DNT002 Dentine Erosion 17 0.029
969
P PRM011 Primary Ciliary Dyskinesia 69 0.028
970
KND001 Kindler Syndrome 63 0.028
971
P PTT014 Pitt-Hopkins Syndrome 60 0.028
972
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.028
973
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.028
974
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.028
975
BRG013 Buerger Disease 57 0.028
976
PTN001 Patent Foramen Ovale 56 0.028
977
c INT064 Intermediate Uveitis 55 0.028
978
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.028
979
INT051 Intussusception 53 0.028
980
PRS030 Persistent Fetal Circulation Syndrome 52 0.028
981
DSM003 Desmoid Disease, Hereditary 50 0.028
982
CHR563 Chronic Eosinophilic Leukemia 48 0.028
983
PRS012 Pars Planitis 48 0.028
984
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.028
985
PRT019 Protein-Losing Enteropathy 46 0.028
986
FNC007 Functioning Pituitary Adenoma 44 0.028
987
c MLG064 Malignant Ependymoma 41 0.028
988
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.028
989
UTR043 Uterine Sarcoma 40 0.028
990
c PLM022 Pulmonary Valve Insufficiency 40 0.028
991
NDL024 Nodal Marginal Zone Lymphoma 39 0.028
992
MLD002 Mild Pre-Eclampsia 36 0.028
993
CHL006 Childhood Oligodendroglioma 35 0.028
994
SLT001 Solitary Osseous Plasmacytoma 31 0.028
995
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.026
996
P HYP055 Hypoplastic Left Heart Syndrome 62 0.026
997
P ATR001 Atrioventricular Septal Defect 55 0.026
998
ESN011 Eisenmenger Syndrome 54 0.026
999
FCT004 Factor Xii Deficiency 54 0.026
1000
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.026
1001
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 51 0.026
1002
SCT005 Scott Syndrome 48 0.026
1003
MCR018 Microcytic Anemia 47 0.026
1004
SBP004 Subependymoma 46 0.026
1005
MYX001 Myxopapillary Ependymoma 45 0.026
1006
c ADL023 Adult Medulloblastoma 44 0.026
1007
PLM021 Pilomyxoid Astrocytoma 43 0.026
1008
c ORT011 Orthostatic Hypotension 1 43 0.026
1009
OVR112 Ovarian Germ Cell Cancer 43 0.026
1010
P LTH003 Lethal Congenital Contracture Syndrome 42 0.026
1011
c PST022 Posterior Uveal Melanoma 41 0.026
1012
ESP025 Esophagus Adenocarcinoma 40 0.026
1013
HYP784 Hypogonadism, Male 39 0.026
1014
CHN040 Choanal Atresia and Lymphedema 36 0.026
1015
P DNT007 Dentin Sensitivity 35 0.026
1016
IDP031 Idiopathic Hypersomnia 32 0.026
1017
MLG163 Malignant Tumor of Penis 29 0.026
1018
UNV002 Univentricular Heart 28 0.026
1019
CRT064 Corticosterone Methyloxidase Deficiency 25 0.026
1020
MNS002 Mini Stroke 19 0.026
1021
c MLG023 Malignant Adult Ependymoma 15 0.026
1022
c GST103 Gastric Cancer, Hereditary Diffuse 64 0.025
1023
P DYS193 Dystonia 11, Myoclonic 56 0.025
1024
P LYM024 Lymphatic System Disease 48 0.025
1025
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 47 0.025
1026
c TRC022 Tricuspid Valve Insufficiency 45 0.025
1027
URT014 Ureterolithiasis 42 0.025
1028
ELP001 Elephantiasis 40 0.025
1029
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 39 0.025
1030
GND003 Gonadal Disease 38 0.025
1031
BRN048 Brain Stem Cancer 37 0.025
1032
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 34 0.025
1033
BRT055 Breath-Holding Spells 30 0.025
1034
c END071 Endometriosis 1 23 0.025
1035
NRR002 Norrie Disease 63 0.023
1036
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 60 0.023
1037
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 59 0.023
1038
c CLR131 Ciliary Dyskinesia, Primary, 1 58 0.023
1039
PMS001 Poems Syndrome 58 0.023
1040
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.023
1041
GDP001 Goodpasture Syndrome 55 0.023
1042
CLL002 Collecting Duct Carcinoma 54 0.023
1043
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.023
1044
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.023
1045
IRN004 Iron-Refractory Iron Deficiency Anemia 47 0.023
1046
TRC012 Trichuriasis 44 0.023
1047
INT276 Interatrial Communication 42 0.023
1048
PPL007 Papillary Serous Adenocarcinoma 41 0.023
1049
P GRW001 Growth Hormone Secreting Pituitary Adenoma 41 0.023
1050
PHS001 Phosphorus Metabolism Disease 40 0.023
1051
MCC013 Mucocutaneous Ulceration, Chronic 39 0.023
1052
TXC001 Toxic Megacolon 39 0.023
1053
PRT009 Parotid Gland Cancer 36 0.023
1054
IND016 Indolent B-Cell Non-Hodgkin Lymphoma 36 0.023
1055
MSC012 Muscular Dystrophy, Duchenne and Becker Type 34 0.023
1056
IDP093 Idiopathic Gastroparesis 30 0.023
1057
c ALC016 Alcohol Sensitivity, Acute 29 0.023
1058
c ORT012 Orthostatic Hypotension 2 27 0.023
1059
NRG006 Neurogenic Thoracic Outlet Syndrome 27 0.023
1060
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.023
1061
RDT005 Radiation Induced Cancer 25 0.023
1062
ENC002 Eunuchism 25 0.023
1063
c CTR110 Cataract 26, Multiple Types 23 0.023
1064
CHR208 Chromosome 17p Deletion 23 0.023
1065
OST024 Osteoporosis-Pseudoglioma Syndrome 60 0.021
1066
PLM070 Pulmonic Stenosis 57 0.021
1067
HYP458 Hyper Ige Syndrome 54 0.021
1068
TRC062 Tricuspid Atresia 52 0.021
1069
P CLB034 Coloboma, Ocular, Autosomal Dominant 49 0.021
1070
PLM041 Pulmonary Valve Stenosis 49 0.021
1071
P HYP828 Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant 48 0.021
1072
FBR032 Fibromuscular Dysplasia 48 0.021
1073
PRP007 Priapism 48 0.021
1074
LMT001 Limited Scleroderma 47 0.021
1075
END080 Endometrial Disease 45 0.021
1076
c HYP847 Hyper Ige Recurrent Infection Syndrome 1 44 0.021
1077
MLT073