Search results for Palmitic Acid

1003 hits were found for Palmitic Acid

# Family MCID Name MIFTS Score
1
FTT001 Fatty Liver Disease 61 0.351
2
P LVR013 Liver Disease 68 0.316
3
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.312
4
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.290
5
P SCH015 Schizophrenia 74 0.280
6
LPD008 Lipid Metabolism Disorder 62 0.237
7
P NRB001 Neuroblastoma 72 0.235
8
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.230
9
P CLR023 Colorectal Cancer 99 0.228
10
48X005 48,xyyy 39 0.224
11
LVR012 Liver Cirrhosis 62 0.220
12
HLX001 Helix Syndrome 47 0.215
13
NNL006 Non-Alcoholic Steatohepatitis 54 0.214
14
P KDN018 Kidney Disease 72 0.212
15
ACT119 Acute Promyelocytic Leukemia 63 0.211
16
HYP066 Hyperglycemia 61 0.210
17
HYP014 Hyperuricemia 52 0.204
18
P SZR006 Seizure Disorder 56 0.202
19
P CRN300 Coronary Heart Disease 1 63 0.198
20
c NRF023 Neurofibromatosis, Type Ii 80 0.198
21
NRL016 Neural Tube Defects 82 0.198
22
P DRR001 Diarrhea 55 0.197
23
P HYP750 Hypertriglyceridemia, Familial 62 0.191
24
VSL002 Visual Epilepsy 59 0.191
25
P BRS047 Breast Cancer 97 0.190
26
ALL026 Allergic Hypersensitivity Disease 62 0.190
27
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.189
28
ATH013 Atherosclerosis Susceptibility 65 0.187
29
DRM006 Dermatitis 61 0.185
30
c GLL024 Gallbladder Disease 1 53 0.183
31
OST012 Osteoarthritis 78 0.182
32
ISC004 Ischemia 58 0.180
33
BNR002 Bone Resorption Disease 48 0.179
34
P HPT023 Hepatocellular Carcinoma 100 0.178
35
HYP056 Hypoglycemia 66 0.177
36
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.174
37
GST092 Gastroesophageal Reflux 67 0.173
38
P VSC007 Vascular Disease 63 0.172
39
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.170
40
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.170
41
HYP060 Hyperinsulinism 54 0.170
42
LPP008 Lipoprotein Quantitative Trait Locus 62 0.167
43
CYT002 Cytokine Deficiency 42 0.167
44
P PRS040 Prostate Cancer 97 0.167
45
CLT003 Colitis 62 0.165
46
P PSR002 Psoriasis 62 0.164
47
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.164
48
P ENC018 Encephalopathy 61 0.164
49
KRT002 Keratomalacia 47 0.164
50
P LKM002 Leukemia 68 0.164
51
P INF037 Inflammatory Bowel Disease 54 0.163
52
PRT037 Pertussis 65 0.163
53
PST011 Pustulosis of Palm and Sole 52 0.163
54
P GLM045 Glioma 63 0.162
55
GLL048 Glial Tumor 45 0.160
56
c HYP836 Hypercholesterolemia, Familial, 1 73 0.158
57
PPT005 Peptic Ulcer Disease 59 0.157
58
GLB015 Glioblastoma Multiforme 75 0.156
59
c MCR120 Microvascular Complications of Diabetes 7 47 0.155
60
ATM095 Autoimmune Disease 62 0.155
61
c MCR113 Microvascular Complications of Diabetes 3 52 0.155
62
c MCR130 Microvascular Complications of Diabetes 6 41 0.155
63
c MCR133 Microvascular Complications of Diabetes 4 41 0.155
64
P BPL003 Bipolar Disorder 56 0.154
65
c MJR024 Major Affective Disorder 9 41 0.154
66
c MJR022 Major Affective Disorder 8 38 0.154
67
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.153
68
c CHR684 Chronic Kidney Disease 70 0.153
69
ART140 Arteries, Anomalies of 52 0.152
70
DFC004 Deficiency Anemia 70 0.152
71
PSY004 Psychotic Disorder 67 0.152
72
CYS001 Cystic Fibrosis 81 0.151
73
c PRC016 Pre-Eclampsia 63 0.151
74
INS001 Insulinoma 60 0.150
75
HMN044 Human Immunodeficiency Virus Type 1 71 0.149
76
P DBT009 Diabetes Mellitus 64 0.148
77
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.148
78
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.148
79
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.148
80
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.148
81
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.148
82
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.148
83
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.148
84
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.148
85
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.148
86
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.148
87
ADN018 Adenoma 59 0.146
88
P OST002 Osteoporosis 74 0.145
89
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.144
90
P ADN016 Adenocarcinoma 64 0.144
91
P MYL006 Myeloid Leukemia 60 0.143
92
HRW001 Hair Whorl 36 0.143
93
P HRT032 Heart Disease 75 0.142
94
PLM001 Pulmonary Tuberculosis 69 0.141
95
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.140
96
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.140
97
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.138
98
47X002 47,xyy 49 0.137
99
P PNC035 Pancreatic Cancer 84 0.137
100
IRN002 Iron Metabolism Disease 57 0.137
101
c HYP595 Hypertension, Essential 84 0.136
102
P NRP001 Neuropathy 56 0.135
103
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.135
104
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.134
105
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.134
106
P BND020 Bone Disease 59 0.133
107
P CRD246 Cardiovascular System Disease 57 0.133
108
P LNG032 Lung Cancer 98 0.132
109
P ALZ034 Alzheimer Disease 88 0.132
110
P DRM053 Dermatitis, Atopic 66 0.131
111
BCT022 Bacterial Infectious Disease 56 0.131
112
DPR016 Depression 63 0.131
113
P ESP024 Esophagitis 62 0.131
114
OCL069 Ocular Motor Apraxia 51 0.130
115
SKN016 Skin Disease 63 0.130
116
NTR005 Nutritional Deficiency Disease 62 0.130
117
c LKM061 Leukemia, Acute Myeloid 84 0.130
118
P ATS364 Autism 70 0.129
119
P PRD008 Periodontitis 64 0.129
120
HYP266 Hypoxia 57 0.128
121
HPT004 Hepatic Coma 45 0.128
122
GLC003 Glucose Intolerance 54 0.127
123
END086 End Stage Renal Disease 51 0.127
124
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.126
125
MYL069 Myeloma, Multiple 85 0.126
126
CRB039 Cerebrovascular Disease 67 0.126
127
P TRM003 Tremor 54 0.126
128
P MYC007 Myocardial Infarction 70 0.126
129
DWN001 Down Syndrome 70 0.126
130
CNG034 Congestive Heart Failure 69 0.126
131
P BCL017 B-Cell Lymphoma 58 0.125
132
c HPT073 Hepatitis C Virus 72 0.125
133
STR067 Stroke, Ischemic 81 0.125
134
P GST053 Gastric Cancer 83 0.125
135
PPL052 Papillomatosis, Confluent and Reticulated 33 0.125
136
SCH012 Schizoaffective Disorder 50 0.125
137
ANX004 Anoxia 40 0.124
138
P BLD134 Bladder Cancer 79 0.124
139
P HYP086 Hypothyroidism 69 0.123
140
CHL014 Cholera 59 0.123
141
STM007 Stomatitis 50 0.123
142
GST023 Gastric Ulcer 53 0.122
143
ALC007 Alcohol Dependence 66 0.122
144
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.122
145
P CHL066 Cholangitis 51 0.122
146
P ART022 Arthritis 69 0.122
147
ADL002 Adult Syndrome 70 0.121
148
c ACT071 Acute Kidney Failure 60 0.120
149
OST159 Osteogenic Sarcoma 66 0.120
150
HPT019 Hepatic Encephalopathy 60 0.120
151
P TRN020 Turner Syndrome 67 0.119
152
c RHB024 Rhabdomyosarcoma 2 67 0.119
153
P RHM011 Rheumatoid Arthritis 80 0.118
154
HYP781 Hypoascorbemia 51 0.118
155
HMC014 Homocysteinemia 53 0.118
156
P MYP004 Myopathy 70 0.118
157
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.118
159
INS024 Insulin-Like Growth Factor I 79 0.117
160
DSS008 Disease of Mental Health 58 0.117
161
CNS004 Constipation 58 0.117
162
BRN071 Brain Injury 49 0.116
163
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.116
164
c ACT075 Acute Myocardial Infarction 57 0.116
165
P MCR115 Microvascular Complications of Diabetes 5 66 0.116
166
NPH009 Nephrolithiasis 55 0.116
167
P LTR001 Lateral Sclerosis 54 0.116
168
MNT002 Mental Depression 58 0.115
169
c DWL002 Dowling-Degos Disease 1 58 0.115
170
c FNC043 Fanconi Anemia, Complementation Group E 62 0.114
171
P HRP006 Herpes Simplex 65 0.114
172
c DBT099 Diabetes Mellitus, Type I 65 0.114
173
TRM010 Traumatic Brain Injury 51 0.114
174
THR024 Thrombosis 57 0.110
175
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.110
176
ANX010 Anxiety 73 0.110
177
CRV035 Cervical Cancer 76 0.109
178
KRT009 Keratosis 51 0.109
179
c ACT027 Acute Pancreatitis 60 0.108
180
c ATS007 Autism Spectrum Disorder 67 0.108
181
BRR014 Barrett Esophagus 65 0.108
182
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.108
183
CLF027 Cleft Palate, Isolated 64 0.108
184
GST033 Gestational Diabetes 61 0.108
185
RCK004 Rickets 68 0.108
186
ADR007 Adrenoleukodystrophy 75 0.107
187
SPN186 Spinal Cord Injury 60 0.107
188
OST003 Osteonecrosis 61 0.107
189
LNG099 Lung Disease 60 0.107
190
VTM002 Vitamin B12 Deficiency 48 0.107
191
P MNN013 Meningitis 66 0.106
192
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.106
193
CHL004 Cholelithiasis 49 0.106
194
P EPL164 Epilepsy 71 0.106
195
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.105
196
EYD002 Eye Disease 58 0.105
197
P SKN015 Skin Carcinoma 66 0.105
198
P PRP019 Peripheral Nervous System Disease 58 0.105
199
SQM006 Squamous Cell Carcinoma 60 0.105
200
ADR022 Adrenomyeloneuropathy 38 0.105
201
CHL079 Children's Interstitial Lung Disease 26 0.105
202
MTH071 Methane Production 26 0.104
203
P MLN008 Melanoma 69 0.104
204
c SML038 Small Cell Cancer of the Lung 65 0.104
205
P OVR082 Overgrowth Syndrome 50 0.103
206
TXC005 Toxic Shock Syndrome 62 0.103
207
PLM033 Pulmonary Embolism 59 0.103
208
HMP009 Haemophilus Influenzae 43 0.103
209
P DMN002 Dementia 66 0.103
210
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.103
211
P MJR001 Major Depressive Disorder 68 0.103
212
P ENC004 Encephalitis 61 0.102
213
CRB004 Cerebral Artery Occlusion 45 0.102
214
c MGR028 Migraine with or Without Aura 1 67 0.102
215
P CTR002 Cataract 60 0.101
216
CHL123 Chlamydia 59 0.101
217
IMM167 Immune Deficiency Disease 78 0.101
218
CNT047 Contact Dermatitis 58 0.101
219
ATX019 Ataxia with Vitamin E Deficiency 42 0.101
220
c ACT068 Acute Cystitis 63 0.100
221
c SYS001 Systemic Lupus Erythematosus 86 0.100
222
P HPT021 Hepatitis 67 0.100
223
P FBR017 Fibrosarcoma 56 0.100
224
P MSC005 Muscular Dystrophy 66 0.100
225
MDD011 Mood Disorder 62 0.100
226
DBT010 Diabetic Neuropathy 54 0.099
227
SCH003 Schizophreniform Disorder 56 0.099
228
P PLM036 Pulmonary Fibrosis 65 0.099
229
DNT012 Dental Caries 53 0.099
230
c HPT001 Hepatitis C 62 0.099
231
P INF032 Infertility 57 0.099
232
c THR092 Thrombophilia Due to Thrombin Defect 73 0.099
233
PPL022 Papilloma 54 0.098
234
PLM010 Pulmonary Edema 54 0.098
235
P MLT020 Multiple Sclerosis 72 0.098
236
TRD006 Tardive Dyskinesia 54 0.098
237
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.098
238
P PNM007 Pneumonia 68 0.097
239
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.097
240
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.097
241
AGN016 Aging 56 0.097
242
P ART021 Arteriosclerosis 54 0.097
243
c INH020 Inherited Metabolic Disorder 47 0.097
244
P ALC033 Alcohol Use Disorder 58 0.096
245
P THR014 Thrombocytopenia 67 0.096
246
c ATR087 Atrial Standstill 1 75 0.096
247
c SVR001 Severe Acute Respiratory Syndrome 62 0.096
248
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.096
249
P EXN002 Exanthem 57 0.095
250
ALL014 Allergic Encephalomyelitis 38 0.095
251
ANG054 Angina Pectoris 66 0.095
252
SQM002 Squamous Cell Papilloma 46 0.095
253
HYP005 Hypokalemia 55 0.095
254
LPT014 Leptin Deficiency or Dysfunction 74 0.095
255
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.094
256
P HYP076 Hyperthyroidism 55 0.094
257
LYS012 Lysosomal Acid Lipase Deficiency 65 0.094
258
P ATR011 Atrial Fibrillation 66 0.094
259
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.093
260
P LPS004 Lupus Erythematosus 61 0.093
261
P RSP003 Respiratory Failure 74 0.093
262
URL001 Urolithiasis 45 0.093
263
P RHN004 Rhinitis 57 0.093
264
P ECL001 Eclampsia 50 0.093
265
P DYS154 Dystonia 65 0.093
266
BRN024 Bronchitis 68 0.093
267
MYL009 Myelodysplastic Syndrome 70 0.093
268
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.092
269
P AST007 Astrocytoma 51 0.092
270
HNS001 Hansen's Disease 34 0.092
271
c MLG068 Malignant Glioma 46 0.092
272
P LPR021 Leprosy 3 69 0.092
273
P CRD119 Cardiac Arrest 67 0.092
274
ACQ007 Acquired Immunodeficiency Syndrome 60 0.092
275
P PNC044 Pancreatitis 61 0.091
276
ENT011 Enterocolitis 51 0.091
277
P PHC003 Pheochromocytoma 71 0.090
278
CLN015 Colon Adenocarcinoma 65 0.090
279
ADR040 Adrenal Gland Pheochromocytoma 46 0.090
280
P LNG064 Lung Cancer Susceptibility 3 78 0.090
281
SRC014 Sarcoma 65 0.090
282
SPN035 Spindle Cell Sarcoma 53 0.090
283
P LYM118 Lymphoma 68 0.089
284
c HPT016 Hepatitis B 59 0.089
285
ESP021 Esophageal Cancer 90 0.089
286
P CYS018 Cystitis 59 0.089
287
MSL001 Measles 62 0.089
288
PNG002 Pain Agnosia 51 0.088
289
P INF038 Influenza 68 0.088
290
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.088
291
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.088
292
P ALP008 Alopecia 54 0.087
293
c VRL010 Viral Hepatitis 52 0.087
294
TTN003 Tetanus 65 0.087
295
P MYC084 Mycobacterium Tuberculosis 1 68 0.087
296
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.087
297
P PLY019 Polyneuropathy 56 0.086
298
HYP081 Hypolipoproteinemia 51 0.086
299
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.086
300
BRN004 Brain Edema 56 0.086
301
PRP027 Peripheral Vascular Disease 71 0.085
302
DPH001 Diphtheria 60 0.085
303
P ACT008 Actinic Keratosis 53 0.085
304
MTH009 Mouth Disease 56 0.085
305
OST115 Osteonecrosis of the Jaw 40 0.085
306
P BRS044 Breast Adenocarcinoma 59 0.084
307
P HDC001 Headache 57 0.084
308
MST005 Mastitis 53 0.084
309
AST005 Asthma 76 0.083
310
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.083
311
ALL010 Allergic Contact Dermatitis 56 0.083
312
P NPH012 Nephrotic Syndrome 60 0.083
313
P GLM040 Glioma Susceptibility 1 81 0.083
314
c PRS136 Prostate Cancer, Hereditary, 6 33 0.082
315
c PRS130 Prostate Cancer, Hereditary, 8 32 0.082
316
P RTN016 Retinal Degeneration 53 0.082
317
P MVM001 Movement Disease 63 0.082
318
P CNR004 Cone-Rod Dystrophy 2 73 0.082
319
49X006 49, Xxxxy Syndrome 41 0.082
320
P LKM062 Leukemia, Acute Lymphoblastic 69 0.081
321
ZLL002 Zollinger-Ellison Syndrome 55 0.081
322
ALL003 Allergic Rhinitis 67 0.081
323
GST045 Gastroenteritis 59 0.081
324
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.081
325
P MJR007 Major Affective Disorder 1 43 0.080
326
RYS001 Reye Syndrome 51 0.080
327
P PLY011 Polycystic Ovary Syndrome 56 0.080
328
P SBS003 Substance Abuse 55 0.080
329
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.080
330
CRV045 Cervical Intraepithelial Neoplasia 39 0.080
331
P CND004 Candidiasis 58 0.080
332
NWC001 Newcastle Disease 45 0.080
333
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.080
334
P ART023 Arthropathy 62 0.080
335
PLC008 Placenta Disease 50 0.080
336
P INT143 Interstitial Cystitis 61 0.079
337
RSC001 Rosacea 54 0.079
338
P MLN007 Male Infertility 55 0.078
339
c DRR009 Diarrhea 6 46 0.078
340
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.078
341
IRN001 Iron Deficiency Anemia 59 0.078
342
ORL011 Oral Cancer 60 0.078
343
PRN019 Perinatal Necrotizing Enterocolitis 59 0.077
344
P NSP012 Nasopharyngeal Carcinoma 66 0.077
345
SBC016 Subacute Delirium 44 0.077
346
P INT068 Intestinal Disease 53 0.077
347
LSH001 Leishmaniasis 63 0.077
348
P CHR345 Chronic Pain 44 0.077
349
P KLZ004 Kala-Azar 1 41 0.077
350
P LKM071 Leukemia, Chronic Lymphocytic 79 0.077
351
P GRF003 Graft-Versus-Host Disease 72 0.076
352
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.076
353
SCH014 Schistosomiasis 57 0.076
354
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.076
355
P HYP069 Hyperparathyroidism 63 0.076
356
P THL005 Thalassemia 60 0.076
357
P HYD006 Hydrocephalus 66 0.076
358
CYS013 Cystinuria 63 0.076
359
RTN023 Retinitis 46 0.076
360
NRR001 Neuroretinitis 42 0.076
361
LNG031 Lung Benign Neoplasm 51 0.075
362
DRY001 Dry Eye Syndrome 47 0.075
363
P PLM037 Pulmonary Hypertension 67 0.075
364
OTT002 Otitis Media 72 0.075
365
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.075
366
LYM019 Lymphosarcoma 46 0.075
367
BRN028 Brain Cancer 74 0.074
368
P SHR001 Short Bowel Syndrome 53 0.074
369
c BSL007 Basal Cell Carcinoma 68 0.074
370
PRP030 Purpura 54 0.074
371
PRT013 Portal Hypertension 59 0.074
372
P RTN008 Retinitis Pigmentosa 79 0.073
373
CLR108 Colorectal Adenoma 64 0.073
374
P HYP265 Hypotonia 43 0.073
375
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.073
376
PLS009 Plasma Cell Neoplasm 51 0.073
377
CVD001 Covid-19 44 0.073
378
KRT013 Keratolytic Winter Erythema 46 0.073
379
c MJR003 Major Affective Disorder 6 33 0.073
380
c MJR006 Major Affective Disorder 5 33 0.073
381
P PRK057 Parkinson Disease, Late-Onset 78 0.073
382
P MNC007 Monocytic Leukemia 53 0.073
383
HMS001 Hemosiderosis 54 0.073
384
c FML035 Familial Hyperlipidemia 55 0.073
385
MLR004 Malaria 81 0.073
386
c HPT003 Hepatitis a 62 0.072
387
P URT039 Urticaria 58 0.072
388
c MJR008 Major Affective Disorder 2 35 0.072
389
c MJR023 Major Affective Disorder 7 33 0.072
390
c MJR004 Major Affective Disorder 4 28 0.072
391
BLR001 Biliary Atresia 50 0.072
392
CMM005 Common Cold 57 0.072
393
BCT002 Bacterial Vaginosis 53 0.072
394
P END044 Endometriosis 63 0.071
395
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.071
396
P RRH023 Rare Hereditary Hemochromatosis 41 0.071
397
MSC007 Muscle Hypertrophy 64 0.071
398
CHR074 Choriocarcinoma 47 0.071
399
IGR001 Ige Responsiveness, Atopic 59 0.070
400
P RCT021 Rectum Cancer 52 0.070
401
P BNG032 Benign Mesothelioma 46 0.070
402
GLS018 Glass Syndrome 57 0.070
403
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.070
404
P MDL005 Medulloblastoma 77 0.070
405
MSC157 Muscular Dystrophy, Duchenne Type 72 0.070
406
TRN015 Transient Cerebral Ischemia 63 0.070
407
KRT019 Keratitis, Hereditary 65 0.069
408
BRN056 Bronchopulmonary Dysplasia 57 0.069
409
P SCK005 Sickle Cell Disease 50 0.069
410
P OPN001 Open-Angle Glaucoma 49 0.069
411
FDL002 Food Allergy 51 0.069
412
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.069
413
KRT001 Keratoconjunctivitis Sicca 49 0.069
414
KHL003 Kohlschutter-Tonz Syndrome 65 0.069
415
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.068
416
GTR002 Goiter 53 0.068
417
P CNJ013 Conjunctivitis 65 0.068
418
TYP007 Typhoid Fever 63 0.068
419
c DLT002 Dilated Cardiomyopathy 79 0.067
420
DYS073 Dysphagia 50 0.067
421
P ADL010 Adult Respiratory Distress Syndrome 65 0.067
422
GNG013 Gingivitis 59 0.067
423
ANR040 Aneurysm 59 0.067
424
CLF001 Cleft Lip 53 0.067
425
SCK003 Sickle Cell Anemia 74 0.066
426
PLM031 Poliomyelitis 64 0.066
427
END040 Endogenous Depression 55 0.066
428
c PRD040 Periodontitis, Chronic 53 0.066
429
c PRM038 Primary Agammaglobulinemia 44 0.066
430
c PNS012 Paine Syndrome 61 0.066
431
PRT038 Protein-Energy Malnutrition 54 0.066
432
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.066
433
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.065
434
PST092 Posttransplant Acute Limbic Encephalitis 29 0.065
435
NWB001 Newborn Respiratory Distress Syndrome 58 0.065
436
P PRS038 Personality Disorder 65 0.065
437
PHR003 Pharyngitis 57 0.065
438
CHL067 Cholecystitis 57 0.065
439
HDN002 Head Injury 46 0.065
440
VRC005 Varicose Veins 60 0.065
441
DYS015 Dysentery 52 0.065
442
EXN003 Exencephaly 31 0.065
443
P END033 Endocarditis 57 0.064
444
ILS001 Ileus 51 0.064
445
KRT006 Keratoconjunctivitis 53 0.064
446
P HYP061 Hypertrophic Cardiomyopathy 70 0.064
447
P SLP006 Sleep Apnea 69 0.064
448
c MCR129 Microvascular Complications of Diabetes 1 66 0.064
449
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.064
450
SKN019 Skin Melanoma 68 0.064
451
CRN030 Coronary Stenosis 50 0.064
452
PLG002 Plague 63 0.063
453
c FML001 Familial Atrial Fibrillation 65 0.063
454
CRC021 Carcinosarcoma 62 0.063
455
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.063
456
P FML011 Familial Adenomatous Polyposis 72 0.063
457
c BRN108 Branchiootic Syndrome 1 62 0.063
458
P UVT001 Uveitis 57 0.063
459
LYM133 Lymphoma, Hodgkin, Classic 69 0.063
460
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.063
461
ANR007 Anorexia Nervosa 63 0.063
462
NRT001 Neurotic Disorder 53 0.063
463
c SPN225 Spondyloarthropathy 1 73 0.062
464
KWS001 Kwashiorkor 44 0.062
465
LKP003 Leukoplakia 39 0.062
466
P RTN018 Retinal Disease 53 0.062
467
SPL018 Splenomegaly 48 0.062
468
P THY023 Thymoma 65 0.062
469
c THY107 Thymoma, Familial 52 0.062
470
P CLC063 Celiac Disease 1 66 0.062
471
P VSC011 Vasculitis 62 0.062
472
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.062
473
MXD026 Mixed Glioma 45 0.062
474
SFT003 Soft Tissue Sarcoma 56 0.061
475
PRP080 Peripheral Artery Disease 53 0.061
476
c HNT004 Huntington Disease-Like 2 50 0.061
477
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.061
478
PTT037 Pituitary Tumors 44 0.061
479
c GLC092 Glaucoma, Primary Open Angle 62 0.061
480
CRD223 Cardiac Arrhythmia 60 0.061
481
RTN017 Retinal Detachment 61 0.061
482
NSP002 Nasopharyngitis 43 0.061
483
BRK010 Burkitt Lymphoma 67 0.061
484
CRH005 Crohn's Colitis 53 0.061
485
P SLP005 Sleep Disorder 59 0.061
486
CRT015 Carotid Artery Occlusion 45 0.061
487
HYP020 Hyperprolactinemia 64 0.061
488
OST017 Osteomyelitis 64 0.060
489
P MYC008 Myocarditis 59 0.060
490
P HYP058 Hypervitaminosis a 48 0.060
491
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.060
492
P ALP009 Alopecia Areata 60 0.060
493
HYP025 Hyperphosphatemia 48 0.060
494
PST021 Postpartum Depression 50 0.059
495
PNM008 Pneumothorax 56 0.059
496
P NRV007 Nervous System Disease 66 0.059
497
SPS057 Spasticity 45 0.059
498
HND015 Hand Skill, Relative 33 0.059
499
SXL003 Sexual Disorder 47 0.059
500
GLS001 Gliosarcoma 54 0.059
501
HPT022 Hepatoblastoma 56 0.058
502
P OCL013 Oculodentodigital Dysplasia 69 0.058
503
AMN001 Amenorrhea 54 0.058
504
P ANG015 Angioedema 57 0.058
505
DMY004 Demyelinating Disease 52 0.058
506
SPN051 Spondylitis 51 0.058
507
INF009 Inflammatory Spondylopathy 31 0.058
508
TRP004 Tropical Sprue 41 0.058
509
VRL011 Viral Infectious Disease 61 0.058
510
HYD002 Hydronephrosis 60 0.057
511
MCR013 Microphthalmia 57 0.057
512
ACT084 Acute Stress Disorder 47 0.057
513
CRB037 Cerebral Palsy 69 0.057
514
PPL001 Papillary Adenoma 44 0.057
515
P NGH001 Night Blindness 48 0.057
516
PST028 Post-Traumatic Stress Disorder 58 0.056
517
RBS001 Rabies 58 0.056
518
c SVR005 Severe Pre-Eclampsia 50 0.056
519
ATN005 Autonomic Dysfunction 46 0.056
520
RDN001 Reading Disorder 40 0.056
521
P GRV001 Graves' Disease 55 0.056
522
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.056
523
FBR047 Fibromyalgia 58 0.056
524
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.056
525
VSC003 Visceral Leishmaniasis 55 0.056
526
LMY002 Leiomyoma 52 0.056
527
ART016 Aortic Aneurysm 69 0.055
528
P OLG002 Oligodendroglioma 67 0.055
529
P PTT006 Pituitary Adenoma 55 0.055
530
SLC006 Silicosis 56 0.055
531
ATN004 Autonomic Neuropathy 45 0.055
532
TNS005 Tonsillitis 57 0.055
533
MCL006 Macular Retinal Edema 55 0.054
534
YLL002 Yellow Fever 61 0.054
535
HMT002 Hematologic Cancer 62 0.054
536
P VSC018 Visceral Steatosis 33 0.054
537
XRP001 Xerophthalmia 41 0.054
538
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.054
539
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.054
540
INT002 Intermittent Claudication 61 0.053
541
c PSR017 Psoriasis 2 53 0.053
542
c PSR023 Psoriasis 1 52 0.053
543
c SCN007 Secondary Hyperparathyroidism 51 0.053
544
LNT004 Lentigines 50 0.053
545
c PSR032 Psoriasis 11 47 0.053
546
c PSR028 Psoriasis 7 42 0.053
547
c PSR018 Psoriasis 13 41 0.053
548
P MLG074 Malignant Mesenchymoma 40 0.053
549
OBS002 Obsessive-Compulsive Disorder 68 0.053
550
WST001 West Syndrome 61 0.053
551
PLC005 Placental Insufficiency 57 0.053
552
TRP009 Triple X Syndrome 42 0.053
553
FCT007 Factor Vii Deficiency 67 0.053
554
VGN023 Vaginitis 54 0.053
555
INT075 Intracranial Hypertension 53 0.053
556
PLR008 Pleurisy 50 0.053
557
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 0.052
558
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.052
559
P TRT010 Teratoma 52 0.052
560
c INF145 Infantile Liver Failure Syndrome 1 50 0.052
561
INF034 Infective Endocarditis 53 0.052
562
c EXD008 Exudative Vitreoretinopathy 1 71 0.052
563
P TBR001 Tuberous Sclerosis 70 0.052
564
STN013 Stenotrophomonas Maltophilia Infection 25 0.052
565
CYT018 Cytochrome P450 2d6 Variant 27 0.052
566
MNT001 Mantle Cell Lymphoma 69 0.052
567
P MTC069 Mitochondrial Disorders 56 0.052
568
P PNC025 Panic Disorder 53 0.052
569
c CHR682 Chronic Bilirubin Encephalopathy 39 0.052
570
CHR178 Chromosomal Triplication 35 0.052
571
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.052
572
c HMC039 Hemochromatosis, Type 1 74 0.051
573
P TXP001 Toxoplasmosis 60 0.051
574
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.051
575
c MCR112 Microvascular Complications of Diabetes 2 41 0.051
576
P FLL037 Follicular Lymphoma 67 0.051
577
CHR066 Chronic Fatigue Syndrome 61 0.051
578
P LRY044 Larynx Cancer 55 0.051
579
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.051
580
ACR007 Acromegaly 71 0.050
581
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.050
582
P OPT006 Optic Nerve Disease 60 0.050
583
NRN004 Neuroendocrine Tumor 55 0.050
584
BCK006 Back Pain 42 0.050
585
SPT004 Septic Arthritis 58 0.050
586
PRD004 Prediabetes Syndrome 47 0.050
587
EXC002 Exocrine Pancreatic Insufficiency 42 0.050
588
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.050
589
c MST023 Mesothelioma, Malignant 57 0.050
590
DFF005 Diffuse Large B-Cell Lymphoma 55 0.050
591
LYM040 Lymphoblastic Lymphoma 54 0.050
592
P BLR006 Biliary Tract Disease 47 0.050
593
DBT002 Diabetic Autonomic Neuropathy 41 0.050
594
CMR002 Coumarin Resistance 56 0.050
595
EWN003 Ewing Sarcoma 69 0.049
596
P RBL001 Rubella 59 0.049
597
PLS007 Plasmodium Falciparum Malaria 52 0.049
598
MLT157 Multiple System Atrophy 1 70 0.049
599
CHY002 Chylomicron Retention Disease 65 0.049
600
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.049
601
BRN002 Bronchiolitis 59 0.049
602
ESP002 Esophageal Varix 51 0.049
603
ASP007 Aspiration Pneumonia 48 0.049
604
FSC004 Fasciitis 50 0.049
605
P INT070 Intestinal Obstruction 58 0.049
606
P HYP726 Hypercalcemia, Infantile, 1 58 0.049
607
P BNG030 Benign Ependymoma 60 0.048
608
P SYP003 Syphilis 58 0.048
609
MCR004 Macroglobulinemia 49 0.048
610
P PRC031 Preeclampsia/eclampsia 1 38 0.048
611
NRM005 Neuromuscular Disease 64 0.048
612
APP008 Appendicitis 61 0.048
613
TND005 Tendinitis 54 0.048
614
RTN020 Retinal Vascular Disease 46 0.048
615
GNG003 Gingival Recession 44 0.048
616
HYP457 Hypertrophic Scars 42 0.048
617
GST020 Gastric Antral Vascular Ectasia 41 0.048
618
P SJG008 Sjogren Syndrome 61 0.047
619
CLL010 Cellular Ependymoma 54 0.047
620
P PTS002 Ptosis 53 0.047
621
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.047
622
PLR007 Pleural Empyema 50 0.047
623
VTM033 Vitamin K Deficiency Bleeding 48 0.047
624
LPT006 Leptin Receptor Deficiency 48 0.047
625
GST030 Gastrinoma 45 0.047
626
ASP008 Aspiration Pneumonitis 45 0.047
627
c BPL002 Bipolar I Disorder 49 0.047
628
PPL049 Papillon-Lefevre Syndrome 65 0.047
629
HYP080 Hypogonadism 50 0.047
630
c LKM070 Leukemia, Acute Monocytic 57 0.046
631
FLL008 Folliculitis 46 0.046
632
MYM001 Myoma 54 0.046
633
CLL003 Cellulitis 54 0.046
634
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.046
635
BRS051 Breast Disease 58 0.046
636
ACD008 Acid-Labile Subunit Deficiency 54 0.046
637
PRS063 Paresthesia 41 0.046
638
PRN009 Paranoid Schizophrenia 50 0.045
639
CRP001 Carpal Tunnel Syndrome 67 0.045
640
HLL004 Hellp Syndrome 54 0.045
641
CHL013 Cholecystolithiasis 37 0.045
642
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.045
643
PRT058 Pure Autonomic Failure 59 0.045
644
SYN036 Syncope 45 0.045
645
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.045
646
CRC006 Carcinoid Syndrome 55 0.045
647
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.045
648
c FLL041 Follicular Lymphoma 1 49 0.045
649
CLN045 Colonic Benign Neoplasm 46 0.045
650
CHL045 Choline Deficiency Disease 39 0.045
651
ANG049 Angioedema Induced by Ace Inhibitors 40 0.045
652
c TBR025 Tuberous Sclerosis 1 77 0.044
653
WLS001 Wilson Disease 71 0.044
654
c ALP101 Alpha-Thalassemia 62 0.044
655
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 0.044
656
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.044
657
P HMR005 Hemorrhoid 46 0.044
658
c SYS043 Systemic Lupus Erythematosus 1 38 0.044
659
APN008 Apnea, Obstructive Sleep 64 0.044
660
GST071 Gastrointestinal Carcinoma 47 0.044
661
LPD009 Lipid Storage Disease 46 0.044
662
PLL012 Pollen Allergy 46 0.044
663
ATM052 Autoimmune Disease 1 37 0.044
664
TXC020 Toxic Oil Syndrome 33 0.044
665
AYM001 Ayme-Gripp Syndrome 57 0.044
666
ACT200 Acute Monoblastic Leukemia 52 0.044
667
P PHT010 Photoparoxysmal Response 1 42 0.044
668
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.044
669
INT303 Intracranial Hypertension, Idiopathic 57 0.044
670
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.044
671
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.044
672
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.044
673
SHG001 Shigellosis 60 0.043
674
ORL005 Oral Candidiasis 56 0.043
675
OST011 Osteomalacia 52 0.043
676
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.043
677
CNT033 Central Nervous System Cancer 47 0.043
678
P HYP733 Hypercalciuria, Absorptive, 2 45 0.043
679
CRB090 Cerebral Hypoxia 44 0.043
680
TND004 Tendinopathy 43 0.043
681
P CRB088 Cerebral Atrophy 37 0.043
682
VGN020 Vaginal Disease 49 0.043
683
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.043
684
SYS003 Systolic Heart Failure 49 0.043
685
LMY014 Leiomyoma, Uterine 56 0.043
686
CLF004 Cleft Lip/palate 54 0.043
687
PRP036 Peripheral T-Cell Lymphoma 53 0.043
688
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.043
689
GNT002 Giant Cell Glioblastoma 50 0.043
690
VLV011 Vulvovaginal Candidiasis 49 0.043
691
CYN002 Cyanosis, Transient Neonatal 45 0.043
692
MYF001 Myofibroma 45 0.043
693
LWC001 Low Compliance Bladder 43 0.043
694
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.043
695
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.043
696
HMR039 Hemorrhage, Intracerebral 57 0.042
697
ALL009 Allergic Conjunctivitis 50 0.042
698
P END046 Endometritis 49 0.042
699
IRR003 Irritant Dermatitis 49 0.042
700
c XNT010 Xanthinuria, Type I 53 0.042
701
RTC005 Reticulosarcoma 47 0.042
702
c ACT004 Acute Diarrhea 39 0.042
703
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.041
704
TRC003 Trichomoniasis 53 0.041
705
THR016 Thrombophlebitis 51 0.041
706
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.041
707
VGN019 Vaginal Discharge 46 0.041
708
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.041
709
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.041
710
SPR126 Superior Semicircular Canal Dehiscence 40 0.041
711
c HMG029 Hemoglobin Se Disease 39 0.041
712
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.041
713
APH001 Aphthous Stomatitis 57 0.041
714
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.041
715
BRD004 Borderline Personality Disorder 53 0.041
716
P HYP040 Hypospadias 51 0.041
717
ART004 Aortic Atherosclerosis 47 0.041
718
P AVS003 Avascular Necrosis 42 0.041
719
CHL039 Choledocholithiasis 38 0.041
720
c PNC108 Pancreatitis, Hereditary 70 0.040
721
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.040
722
c BSL024 Basal Cell Carcinoma 1 56 0.040
723
GST049 Gastrointestinal System Cancer 49 0.040
724
c BCT013 Bacterial Pneumonia 48 0.040
725
PLS025 Plasmablastic Lymphoma 47 0.040
726
GLC036 Glucagonoma 45 0.040
727
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.040
728
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.040
729
P END047 Endophthalmitis 53 0.040
730
SMT001 Somatization Disorder 46 0.040
731
ENT001 Enterocele 39 0.040
732
RSP007 Respiratory Distress Syndrome, Infant 30 0.040
733
CNN003 Conn's Syndrome 79 0.040
734
FBR012 Fabry Disease 72 0.040
735
ACR041 Acromelic Frontonasal Dysostosis 52 0.040
736
DBT006 Diabetic Macular Edema 48 0.040
737
SKN005 Skin Atrophy 43 0.040
738
HML018 Homologous Wasting Disease 22 0.040
739
c OPT053 Optic Atrophy 1 63 0.039
740
c CNG216 Congenital Hydrocephalus 47 0.039
741
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.039
742
TBC004 Tobacco Addiction 64 0.039
743
WLD007 Waldenstroem's Macroglobulinemia 61 0.039
744
P LCT002 Lactose Intolerance 53 0.039
745
MCN017 Meconium Ileus 52 0.039
746
CRN027 Corneal Neovascularization 47 0.039
747
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.039
748
MYF002 Myofascial Pain Syndrome 42 0.039
749
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.038
750
c LTN004 Late-Onset Retinal Degeneration 59 0.038
751
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.038
752
P KRT007 Keratoconus 50 0.038
753
INT017 Intestinal Schistosomiasis 48 0.038
754
P BLD051 Blood Coagulation Disease 46 0.038
755
GRM010 Germ Cells Tumors 34 0.038
756
GNT167 Genetic Obesity 33 0.038
757
BWN001 Bowen-Conradi Syndrome 52 0.038
758
CRC014 Carcinoid Tumors, Intestinal 47 0.038
759
CRB086 Cerebral Aneurysms 40 0.038
760
ABT001 Abetalipoproteinemia 69 0.037
761
CRN036 Craniopharyngioma 65 0.037
762
FRZ001 Frozen Shoulder 53 0.037
763
NTR018 Neutrophilia, Hereditary 52 0.037
764
P BRN035 Brain Stem Glioma 52 0.037
765
HND002 Hand, Foot and Mouth Disease 51 0.037
766
c HRD202 Hereditary Lymphedema I 50 0.037
767
CLS016 Clostridium Difficile Colitis 48 0.037
768
P PRG092 Pregnancy Loss, Recurrent 1 40 0.037
769
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.037
770
PTT009 Pituitary Gland Disease 54 0.037
771
CRT016 Carotid Artery Disease 52 0.037
772
P LBR014 Leber Congenital Amaurosis 4 56 0.037
773
P ORL007 Oral Cavity Cancer 53 0.037
774
PRV004 Periventricular Leukomalacia 52 0.037
775
LYM012 Lymphoplasmacytic Lymphoma 47 0.037
776
c DRM054 Dermatitis, Atopic, 2 44 0.037
777
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.037
778
CLS047 Classic Progressive Supranuclear Palsy Syndrome 31 0.037
779
P TTR001 Tetralogy of Fallot 70 0.036
780
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.036
781
PNM010 Pneumothorax, Primary Spontaneous 60 0.036
782
P PTN014 Patent Ductus Arteriosus 1 60 0.036
783
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.036
784
CHR005 Chorioamnionitis 51 0.036
785
DRG024 Drug Allergy 42 0.036
786
STT009 Sutton Disease 2 30 0.036
787
OBS003 Obsessive-Compulsive Personality Disorder 46 0.036
788
P MTR004 Maturity-Onset Diabetes of the Young 65 0.035
789
P PLV020 Pelvic Organ Prolapse 57 0.035
790
FND002 Fundus Dystrophy 55 0.035
791
BRN045 Brunner Syndrome 55 0.035
792
APR001 Apraxia 52 0.035
793
BHR001 Behr Syndrome 51 0.035
794
ADR016 Adrenal Cortical Carcinoma 48 0.035
795
NCR007 Necrotizing Fasciitis 48 0.035
796
BRS064 Bursitis 48 0.035
797
MNN020 Meningococcal Infection 46 0.035
798
LYM051 Lymphomatoid Granulomatosis 45 0.035
799
P CRN024 Corneal Disease 44 0.035
800
MGK001 Megakaryocytic Leukemia 64 0.035
801
P FCL005 Focal Segmental Glomerulosclerosis 57 0.035
802
APH002 Aphasia 57 0.035
803
ISL001 Islet Cell Tumor 56 0.035
804
HYP063 Hypersplenism 53 0.035
805
SPS003 Spastic Diplegia 51 0.035
806
HDR003 Hidradenitis 49 0.035
807
NRN001 Neuroendocrine Carcinoma 47 0.035
808
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.035
809
CRN322 Coronavirus Infectious Disease 40 0.035
810
MCL003 Macular Holes 40 0.035
811
c PRG020 Paragangliomas 3 39 0.035
812
ADR004 Adrenal Cortical Adenocarcinoma 39 0.035
813
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.034
814
IDP011 Idiopathic Interstitial Pneumonia 59 0.034
815
ERY004 Erysipelas 49 0.034
816
CLC006 Calcinosis 48 0.034
817
BCK003 Background Diabetic Retinopathy 46 0.034
818
ANL022 Anal Fistula 46 0.034
819
c FML346 Familial Adenomatous Polyposis 1 66 0.033
820
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.033
821
P STR022 Stargardt Disease 58 0.033
822
HDR002 Hidradenitis Suppurativa 55 0.033
823
ECH003 Echinococcosis 53 0.033
824
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.033
825
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.033
826
NSS002 Neisseria Meningitidis Infection 47 0.033
827
PRP017 Periapical Periodontitis 46 0.033
828
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.033
829
CLN044 Colon Adenoma 44 0.033
830
VLV010 Vulvovaginitis 41 0.033
831
HYP344 Hyperthyroidism, Familial Gestational 39 0.033
832
CVT001 Cavitary Optic Disc Anomalies 38 0.033
833
JVN026 Jeavons Syndrome 24 0.033
834
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.033
835
MSM014 Mismatch Repair Cancer Syndrome 65 0.033
836
ADN009 Adenosquamous Carcinoma 47 0.033
837
PRL017 Prolymphocytic Leukemia 47 0.033
838
P OCY003 Oocyte Maturation Defect 1 45 0.033
839
CLL014 Cll/sll 45 0.033
840
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.033
841
P CLS010 Cluster Headache 42 0.033
842
ACT011 Acute Contagious Conjunctivitis 40 0.033
843
P DYS021 Dysautonomia 39 0.033
844
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 0.033
845
HRP008 Herpes Simiae 25 0.033
846
PNM001 Pneumocystosis 59 0.032
847
LNN001 Lennox-Gastaut Syndrome 57 0.032
848
FRY006 Fryns Microphthalmia Syndrome 52 0.032
849
P HYP730 Hypogonadotropic Hypogonadism 52 0.032
850
P AGG001 Aggressive Periodontitis 50 0.032
851
c DYS119 Dystonia 9 50 0.032
852
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.032
853
ACT055 Actinomycosis 47 0.032
854
SRT004 Serotonin Syndrome 47 0.032
855
CYS009 Cystadenoma 44 0.032
856
P EPN001 Ependymoblastoma 44 0.032
857
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.032
858
ACL001 Acalculous Cholecystitis 35 0.032
859
CRN302 Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal 34 0.032
860
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.031
861
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.031
862
c HYP740 Hyperlipoproteinemia, Type V 53 0.031
863
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.031
864
P PNB001 Pineoblastoma 50 0.031
865
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.031
866
PLY068 Polysubstance Abuse 43 0.031
867
ULC007 Ulcerative Stomatitis 39 0.031
868
CRB026 Cerebellar Astrocytoma 37 0.031
869
BNN005 Bunion 33 0.031
870
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.031
871
DMN031 Dementia, Lewy Body 65 0.030
872
P ORT004 Orthostatic Intolerance 62 0.030
873
ADR005 Adrenal Carcinoma 58 0.030
874
CRT033 Corticobasal Degeneration 57 0.030
875
ORP003 Oropharynx Cancer 55 0.030
876
P ACT105 Acute Mountain Sickness 52 0.030
877
FML037 Female Breast Cancer 52 0.030
878
c PYR010 Peyronie's Disease 50 0.030
879
c HYP739 Hyperlipoproteinemia, Type Iv 50 0.030
880
CHL018 Childhood Medulloblastoma 49 0.030
881
P SCL015 Scleritis 48 0.030
882
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.030
883
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.030
885
PNC085 Penicillin Allergy 45 0.030
886
MMM006 Mammographic Density 41 0.030
887
c MCR312 Microphthalmia, Syndromic 10 35 0.030
888
CHL057 Childhood Brain Stem Glioma 32 0.030
889
PDT014 Pediatric Ependymoma 32 0.030
890
PLN007 Plantar Fasciitis 32 0.030
891
BRN049 Brain Tumor, Childhood 29 0.030
892
CGN007 Cognitive Function 1, Social 27 0.030
893
LRY027 Laryngeal Papillomatosis 23 0.030
894
CHL009 Childhood Cerebral Astrocytoma 14 0.030
895
c SCH082 Schizophrenia 5 31 0.030
896
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.029
897
P TST021 Testicular Germ Cell Tumor 60 0.029
898
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.029
899
P SPN052 Spondyloarthropathy 54 0.029
900
PTH002 Pathological Gambling 49 0.029
901
P GND004 Gonadal Dysgenesis 48 0.029
902
PRS115 Prosthetic Joint Infection 42 0.029
903
CNT060 Central Serous Chorioretinopathy 38 0.029
904
LBR036 Leber Plus Disease 66 0.028
906
PND002 Pendred Syndrome 65 0.028
907
P SCK002 Sick Sinus Syndrome 55 0.028
908
RCT017 Rectal Disease 46 0.028
909
OBS004 Obstructive Hydrocephalus 46 0.028
910
PNC056 Pineocytoma 45 0.028
911
P BCT020 Bacteremia 2 44 0.028
912
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.028
913
PDT015 Pediatric Supratentorial Ependymoma 24 0.028
914
INT053 Intracranial Vasospasm 24 0.028
915
PDT016 Pediatric Infratentorial Ependymoma 22 0.028
916
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.027
917
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.027
918
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.027
919
ERY029 Erythermalgia, Primary 58 0.027
920
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.027
921
CHR078 Chorioretinitis 50 0.027
922
P CRN028 Corneal Ulcer 47 0.027
923
CNT017 Central Nervous System Origin Vertigo 45 0.027
924
DNT014 Dental Pulp Disease 42 0.027
925
c HYP057 Hypervitaminosis D 42 0.027
926
DNT006 Dental Pulp Necrosis 41 0.027
927
CLD014 Cole Disease 40 0.027
928
c PLM022 Pulmonary Valve Insufficiency 39 0.027
929
RTN002 Retinal Perforation 38 0.027
930
BLN010 Balanitis 37 0.027
931
TQP001 Taqi Polymorphism 32 0.027
932
DLT018 Dilution, Pigmentary 28 0.027
933
HYP213 Hypomelanotic Disorder 23 0.027
934
SDD004 Sudden Arrhythmia Death Syndrome 22 0.027
935
P USH001 Usher Syndrome 60 0.026
936
BRD001 Brody Myopathy 57 0.026
937
P AGN002 Agnosia 55 0.026
938
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.026
939
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.026
940
CHR515 Chronic Atrial and Intestinal Dysrhythmia 50 0.026
941
GYN001 Gynecomastia 49 0.026
942
P RCR004 Recurrent Respiratory Papillomatosis 49 0.026
943
GNG008 Ganglioneuroblastoma 48 0.026
944
P ATT003 Attenuated Familial Adenomatous Polyposis 48 0.026
945
MTS001 Mutism 46 0.026
946
P HRN001 Horner's Syndrome 45 0.026
947
P END039 Endodermal Sinus Tumor 44 0.026
948
PNL014 Pineal Gland Cancer 41 0.026
949
GRM004 Germinoma 40 0.026
950
CNN010 Connective Tissue Benign Neoplasm 40 0.026
951
TST018 Testicular Yolk Sac Tumor 39 0.026
952
c SCH080 Schizophrenia 3 32 0.026
953
CHL006 Childhood Oligodendroglioma 31 0.026
954
INF021 Infant Gynecomastia 31 0.026
955
P CNT036 Central Nervous System Germ Cell Tumor 28 0.026
956
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.026
957
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 0.025
958
NRL004 Neuroleptic Malignant Syndrome 56 0.025
959
c MYP132 Myopathy, Congenital 55 0.025
960
SMT003 Somatostatinoma 52 0.025
961
SMT006 Somatoform Disorder 50 0.025
962
P CRC039 Coarctation of Aorta 47 0.025
963
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.025
964
CHL012 Childhood Disintegrative Disease 44 0.025
965
SPN119 Spondylarthropathy 44 0.025
966
P INT260 Intracranial Berry Aneurysm 39 0.025
967
STR046 Stargardt Macular Degeneration 31 0.025
968
CRB054 Cerebellar Astrocytoma, Childhood 9 0.025
969
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 0.023
970
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.023
971
VLV032 Vulva Cancer 59 0.023
972
VPM001 Vipoma 50 0.023
973
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.023
974
ANS012 Anus Disease 45 0.023
975
LRY022 Laryngoonychocutaneous Syndrome 44 0.023
976
TND006 Tendinosis 42 0.023
977
MDS018 Mediastinal Cancer 41 0.023
978
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.023
979
PNC008 Pancreatic Endocrine Carcinoma 39 0.023
980
PNC016 Pancreatic Cholera 37 0.023
981
PRR004 Preretinal Fibrosis 37 0.023
982
SPP003 Suppurative Periapical Periodontitis 34 0.023
983
BLN002 Balanitis Xerotica Obliterans 29 0.023
984
MLR020 Malaria, Mild 27 0.023
985
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.023
986
LKP001 Leukoplakia of Penis 25 0.023
987
ACT133 Acetylation, Slow 23 0.023
988
P HRD012 Hereditary Elliptocytosis 51 0.021
989
P PRS049 Persistent Mullerian Duct Syndrome 50 0.021
990
P DPY001 Dupuytren Contracture 48 0.021
991
SYM002 Sympathetic Ophthalmia 47 0.021
992
RMS001 Rem Sleep Behavior Disorder 46 0.021
993
LMR001 Lemierre's Syndrome 42 0.021
994
GLC096 Galactorrhea 42 0.021
995
DDN003 Duodenum Adenocarcinoma 41 0.021
996
PHM001 Phimosis 37 0.021
997
c GLC041 Glaucoma 1, Open Angle, a 34 0.021
998
HMP003 Hemopneumothorax 33 0.021
999
c SCH081 Schizophrenia 6 31 0.021
1000
ENG004 Engraftment Syndrome 30 0.021
1001
PPM002 Ppoma 29 0.021
1002
c ADL080 Adult Acute Respiratory Distress Syndrome 26 0.021
1003
ACT206 Acitretin/etretinate Embryopathy 18 0.021
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