Search results for Palmitic Acid

996 hits were found for Palmitic Acid

# Family MCID Name MIFTS Score
1
FTT001 Fatty Liver Disease 63 0.338
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.330
3
P LVR013 Liver Disease 71 0.312
4
P SCH015 Schizophrenia 76 0.285
5
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.273
6
PLM017 Pulmonary Alveolar Microlithiasis 54 0.271
7
P NRB010 Neuroblastoma 1 66 0.242
8
LPD008 Lipid Metabolism Disorder 64 0.238
9
48X005 48,xyyy 37 0.231
10
P CLR023 Colorectal Cancer 100 0.231
11
LVR012 Liver Cirrhosis 67 0.230
12
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.221
13
HLX001 Helix Syndrome 46 0.219
14
ACT119 Acute Promyelocytic Leukemia 63 0.217
15
P KDN018 Kidney Disease 73 0.215
16
HYP066 Hyperglycemia 63 0.213
17
P SZR006 Seizure Disorder 59 0.210
18
ALL026 Allergic Hypersensitivity Disease 65 0.206
19
HYP014 Hyperuricemia 52 0.204
20
NNL006 Non-Alcoholic Steatohepatitis 53 0.204
21
VSL002 Visual Epilepsy 58 0.204
22
P DRR001 Diarrhea 55 0.204
23
NRL016 Neural Tube Defects 83 0.203
24
P BRS047 Breast Cancer 99 0.198
25
P CRN300 Coronary Heart Disease 1 59 0.197
26
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.196
27
ATH013 Atherosclerosis Susceptibility 68 0.195
28
P NRF023 Neurofibromatosis, Type Ii 77 0.193
29
P HYP750 Hypertriglyceridemia, Familial 62 0.190
30
DRM006 Dermatitis 63 0.189
31
c GLL024 Gallbladder Disease 1 53 0.189
32
ISC004 Ischemia 62 0.189
33
OST012 Osteoarthritis 80 0.185
34
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.183
35
HYP056 Hypoglycemia 68 0.182
36
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.178
37
BNR002 Bone Resorption Disease 51 0.178
38
GST092 Gastroesophageal Reflux 68 0.177
39
CLT003 Colitis 63 0.176
40
P HPT023 Hepatocellular Carcinoma 99 0.176
41
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.175
42
P VSC007 Vascular Disease 65 0.174
43
HYP060 Hyperinsulinism 55 0.172
44
P ENC018 Encephalopathy 64 0.172
45
P PSR002 Psoriasis 63 0.171
46
P GLM045 Glioma 64 0.170
47
PST011 Pustulosis of Palm and Sole 51 0.169
48
P LKM002 Leukemia 69 0.169
49
PRT037 Pertussis 66 0.168
50
GLL048 Glial Tumor 48 0.168
51
P INF037 Inflammatory Bowel Disease 57 0.168
52
CYT002 Cytokine Deficiency 46 0.168
53
P PRS040 Prostate Cancer 97 0.166
54
KRT002 Keratomalacia 47 0.166
55
P CRN018 Coronary Artery Anomaly 67 0.164
56
PPT005 Peptic Ulcer Disease 60 0.163
57
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.161
58
GLB002 Glioblastoma 74 0.160
59
GLB015 Glioblastoma Multiforme 60 0.159
60
ART140 Arteries, Anomalies of 60 0.158
61
ATM095 Autoimmune Disease 62 0.158
62
DFC004 Deficiency Anemia 77 0.158
63
P BPL003 Bipolar Disorder 59 0.157
64
c HYP836 Hypercholesterolemia, Familial, 1 74 0.157
65
CYS001 Cystic Fibrosis 84 0.156
66
c MJR024 Major Affective Disorder 9 42 0.156
67
c MJR022 Major Affective Disorder 8 39 0.156
68
c MCR120 Microvascular Complications of Diabetes 7 48 0.155
69
PSY004 Psychotic Disorder 68 0.155
70
c MCR113 Microvascular Complications of Diabetes 3 55 0.155
71
c MCR130 Microvascular Complications of Diabetes 6 42 0.155
72
c MCR133 Microvascular Complications of Diabetes 4 42 0.155
73
P HRT032 Heart Disease 78 0.154
74
P DBT009 Diabetes Mellitus 66 0.154
75
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.154
76
c CHR684 Chronic Kidney Disease 68 0.153
77
HMN044 Human Immunodeficiency Virus Type 1 73 0.153
78
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.153
79
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.152
80
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.152
81
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.152
82
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.152
83
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.152
84
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.152
85
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.152
86
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.152
87
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.152
88
ADN018 Adenoma 60 0.152
89
P OST002 Osteoporosis 79 0.151
90
P ADN016 Adenocarcinoma 65 0.150
91
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.150
92
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.149
93
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.148
94
INS001 Insulinoma 60 0.147
95
P MYL006 Myeloid Leukemia 61 0.147
96
HRW001 Hair Whorl 36 0.147
97
c ACT210 Acute Respiratory Distress Syndrome 59 0.146
98
PLM001 Pulmonary Tuberculosis 72 0.146
99
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.144
100
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.144
101
c PRC016 Pre-Eclampsia 63 0.143
102
c HYP595 Hypertension, Essential 87 0.143
103
P PNC035 Pancreatic Cancer 86 0.143
104
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.142
105
47X002 47,xyy 49 0.141
106
IRN002 Iron Metabolism Disease 58 0.141
107
P LNG032 Lung Cancer 99 0.139
108
P NRP001 Neuropathy 57 0.139
109
OCL069 Ocular Motor Apraxia 53 0.137
110
CRB039 Cerebrovascular Disease 71 0.137
111
P ALZ034 Alzheimer Disease 90 0.137
112
P BLD134 Bladder Cancer 79 0.137
113
P ATS364 Autism 68 0.136
114
P ESP024 Esophagitis 62 0.136
115
HYP266 Hypoxia 58 0.135
116
DWN001 Down Syndrome 70 0.133
117
GLC003 Glucose Intolerance 55 0.133
118
P DRM053 Dermatitis, Atopic 68 0.133
119
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.133
120
P MYC007 Myocardial Infarction 74 0.133
121
HPT004 Hepatic Coma 42 0.132
122
NTR005 Nutritional Deficiency Disease 61 0.132
123
BND020 Bone Disease 60 0.132
124
SKN016 Skin Disease 64 0.131
125
c LKM061 Leukemia, Acute Myeloid 84 0.131
126
c RHB024 Rhabdomyosarcoma 2 64 0.131
127
MYL069 Myeloma, Multiple 85 0.131
128
c HPT073 Hepatitis C Virus 74 0.131
129
STR067 Stroke, Ischemic 82 0.130
130
BCT022 Bacterial Infectious Disease 57 0.130
131
P TRM003 Tremor 55 0.130
132
P GST053 Gastric Cancer 85 0.129
133
ADL002 Adult Syndrome 62 0.129
134
ANX004 Anoxia 44 0.128
135
P PRD008 Periodontitis 66 0.128
136
DPR016 Depression 64 0.128
137
CNG034 Congestive Heart Failure 69 0.128
138
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.128
139
P HYP086 Hypothyroidism 70 0.127
140
SCH012 Schizoaffective Disorder 50 0.127
141
CHL014 Cholera 58 0.127
142
P BCL017 B-Cell Lymphoma 61 0.127
143
P LYM031 Lymphocytic Leukemia 56 0.127
144
STM007 Stomatitis 51 0.127
145
ALC007 Alcohol Dependence 68 0.126
146
END030 End Stage Renal Failure 60 0.126
147
GST023 Gastric Ulcer 53 0.125
148
c ACT071 Acute Kidney Failure 60 0.125
149
P RHM011 Rheumatoid Arthritis 82 0.124
150
BRN071 Brain Injury 51 0.124
151
P TRN020 Turner Syndrome 66 0.124
152
P ART022 Arthritis 71 0.124
153
HPT019 Hepatic Encephalopathy 60 0.123
154
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.123
155
TRM010 Traumatic Brain Injury 54 0.123
156
OST159 Osteogenic Sarcoma 67 0.122
157
P MYP004 Myopathy 63 0.122
158
P CHL066 Cholangitis 53 0.121
159
PPL052 Papillomatosis, Confluent and Reticulated 34 0.121
160
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.121
161
INS024 Insulin-Like Growth Factor I 79 0.120
162
HMC014 Homocysteinemia 54 0.120
163
DSS008 Disease of Mental Health 66 0.120
164
CNS004 Constipation 59 0.120
165
HYP781 Hypoascorbemia 48 0.120
166
c ACT075 Acute Myocardial Infarction 59 0.119
167
P HRP006 Herpes Simplex 66 0.119
168
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.119
169
P LTR001 Lateral Sclerosis 56 0.118
170
P MCR115 Microvascular Complications of Diabetes 5 67 0.118
171
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.117
173
THR024 Thrombosis 58 0.116
174
c DWL002 Dowling-Degos Disease 1 59 0.115
175
P EPL164 Epilepsy 73 0.115
176
CRV035 Cervical Cancer 77 0.114
177
DYS014 Dyspepsia 51 0.113
178
BRR014 Barrett Esophagus 67 0.111
179
AGN016 Aging 58 0.111
180
SQM006 Squamous Cell Carcinoma 60 0.111
181
ADR007 Adrenoleukodystrophy 72 0.111
182
SPN186 Spinal Cord Injury 63 0.111
183
KRT009 Keratosis 52 0.111
184
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.110
185
CLF027 Cleft Palate, Isolated 67 0.110
186
LNG099 Lung Disease 62 0.110
187
c SML038 Small Cell Cancer of the Lung 67 0.110
188
VTM002 Vitamin B12 Deficiency 48 0.110
189
CHL004 Cholelithiasis 50 0.110
190
ADR022 Adrenomyeloneuropathy 39 0.109
191
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.108
192
c HPT001 Hepatitis C 62 0.108
193
P DMN002 Dementia 68 0.108
194
c MGR028 Migraine with or Without Aura 1 70 0.108
195
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.107
196
CHL079 Children's Interstitial Lung Disease 27 0.107
197
HMP009 Haemophilus Influenzae 46 0.107
198
ANX010 Anxiety 75 0.107
199
P PRP019 Peripheral Nervous System Disease 64 0.107
200
P INF032 Infertility 60 0.106
201
P ART021 Arteriosclerosis 56 0.106
202
P MLT020 Multiple Sclerosis 73 0.106
203
P SKN015 Skin Carcinoma 67 0.106
204
c ATS007 Autism Spectrum Disorder 69 0.106
205
P CTR002 Cataract 62 0.106
206
PLM033 Pulmonary Embolism 60 0.106
207
EYD002 Eye Disease 59 0.106
208
IMM167 Immune Deficiency Disease 79 0.106
209
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.105
210
P ENC004 Encephalitis 64 0.105
211
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.105
212
P MNN013 Meningitis 67 0.105
213
TXC005 Toxic Shock Syndrome 63 0.105
214
CHL123 Chlamydia 60 0.104
215
c FNC043 Fanconi Anemia, Complementation Group E 64 0.104
216
P MJR001 Major Depressive Disorder 69 0.104
217
c ACT068 Acute Cystitis 63 0.104
218
MTH071 Methane Production 26 0.104
219
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.103
220
P FBR017 Fibrosarcoma 57 0.103
221
P MSC005 Muscular Dystrophy 68 0.103
222
c SYS001 Systemic Lupus Erythematosus 88 0.103
223
CRB004 Cerebral Artery Occlusion 38 0.103
224
P HPT021 Hepatitis 69 0.103
225
RCK004 Rickets 70 0.103
226
SCH003 Schizophreniform Disorder 49 0.103
227
P EXN002 Exanthem 58 0.102
228
CNT047 Contact Dermatitis 58 0.102
229
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.102
230
SRC014 Sarcoma 67 0.102
231
SPN035 Spindle Cell Sarcoma 57 0.102
232
c ACT027 Acute Pancreatitis 60 0.102
233
OST003 Osteonecrosis 62 0.102
234
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.102
235
MDD011 Mood Disorder 62 0.101
236
MLN008 Melanoma 68 0.101
237
TRD006 Tardive Dyskinesia 58 0.101
238
P THR014 Thrombocytopenia 67 0.101
239
DBT010 Diabetic Neuropathy 56 0.101
240
PPL022 Papilloma 56 0.101
241
PLM010 Pulmonary Edema 56 0.101
242
c THR092 Thrombophilia Due to Thrombin Defect 74 0.100
243
P ALC033 Alcohol Use Disorder 58 0.100
244
c INH020 Inherited Metabolic Disorder 51 0.099
245
DNT012 Dental Caries 52 0.099
246
P PNM007 Pneumonia 71 0.099
247
OVR082 Overgrowth Syndrome 51 0.099
248
ATX019 Ataxia with Vitamin E Deficiency 46 0.099
249
P DYS154 Dystonia 65 0.099
250
ANG054 Angina Pectoris 66 0.098
251
HYP005 Hypokalemia 55 0.098
252
P HYP076 Hyperthyroidism 55 0.098
253
P LPS004 Lupus Erythematosus 62 0.098
254
P ATR011 Atrial Fibrillation 67 0.097
255
ALL014 Allergic Encephalomyelitis 40 0.097
256
SQM002 Squamous Cell Papilloma 49 0.097
257
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.097
258
LPT014 Leptin Deficiency or Dysfunction 72 0.097
259
LYS012 Lysosomal Acid Lipase Deficiency 63 0.097
260
c LRG017 Large Intestine Cancer 53 0.097
261
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.096
262
P CRD119 Cardiac Arrest 71 0.096
263
MYL009 Myelodysplastic Syndrome 72 0.096
264
P INF038 Influenza 69 0.096
265
HNS001 Hansen's Disease 35 0.096
266
P PNC044 Pancreatitis 61 0.096
267
P LPR021 Leprosy 3 67 0.095
268
c ATR087 Atrial Standstill 1 76 0.095
269
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.095
270
P RSP003 Respiratory Failure 75 0.095
271
CLN015 Colon Adenocarcinoma 65 0.095
272
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.095
273
BRN024 Bronchitis 70 0.095
274
P AST007 Astrocytoma 52 0.095
275
c MLG068 Malignant Glioma 46 0.095
276
P ECL001 Eclampsia 53 0.094
277
ACQ007 Acquired Immunodeficiency Syndrome 61 0.094
278
P RHN004 Rhinitis 59 0.094
279
P LYM118 Lymphoma 70 0.094
280
MLR004 Malaria 82 0.093
281
c HPT016 Hepatitis B 63 0.092
282
ESP021 Esophageal Cancer 90 0.092
283
P CYS018 Cystitis 59 0.092
284
ENT011 Enterocolitis 51 0.091
285
PNG002 Pain Agnosia 52 0.091
286
c VRL010 Viral Hepatitis 56 0.091
287
MSL001 Measles 61 0.090
288
P MYC084 Mycobacterium Tuberculosis 1 69 0.090
289
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.090
290
GST033 Gestational Diabetes 58 0.090
291
TTN003 Tetanus 62 0.089
292
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.089
293
P PLM036 Pulmonary Fibrosis 66 0.089
294
IDP011 Idiopathic Interstitial Pneumonia 65 0.089
295
P HDC001 Headache 59 0.089
296
P ALP008 Alopecia 58 0.089
297
P PLY019 Polyneuropathy 55 0.088
298
PRP027 Peripheral Vascular Disease 72 0.088
299
DPH001 Diphtheria 61 0.088
300
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.087
301
P ACT008 Actinic Keratosis 50 0.087
302
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.087
303
AST005 Asthma 80 0.087
304
MTH009 Mouth Disease 56 0.086
305
OST115 Osteonecrosis of the Jaw 40 0.086
306
P NPH012 Nephrotic Syndrome 65 0.086
307
ALL010 Allergic Contact Dermatitis 56 0.085
308
P MVM001 Movement Disease 63 0.085
309
MST005 Mastitis 55 0.085
310
49X002 49,xxxxy Syndrome 39 0.085
311
ZLL002 Zollinger-Ellison Syndrome 54 0.084
312
P CNR004 Cone-Rod Dystrophy 2 72 0.084
313
P LKM062 Leukemia, Acute Lymphoblastic 68 0.084
314
P BRS044 Breast Adenocarcinoma 59 0.084
315
P SBS003 Substance Abuse 56 0.084
316
P LNG064 Lung Cancer Susceptibility 3 79 0.084
317
c PRS136 Prostate Cancer, Hereditary, 6 34 0.084
318
c PRS130 Prostate Cancer, Hereditary, 8 33 0.084
319
ALL003 Allergic Rhinitis 69 0.084
320
P RTN016 Retinal Degeneration 56 0.084
321
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.083
322
P MJR007 Major Affective Disorder 1 44 0.083
323
RYS001 Reye Syndrome 49 0.083
324
GST045 Gastroenteritis 60 0.082
325
P CHR345 Chronic Pain 52 0.082
326
STT004 Steatorrhea 39 0.082
327
NWC001 Newcastle Disease 45 0.082
328
HYP081 Hypolipoproteinemia 51 0.082
329
P INT143 Interstitial Cystitis 62 0.081
330
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.081
331
CRV045 Cervical Intraepithelial Neoplasia 41 0.081
332
P ART023 Arthropathy 61 0.081
333
BRN004 Brain Edema 57 0.081
334
IRN001 Iron Deficiency Anemia 59 0.080
335
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.080
336
P PLM037 Pulmonary Hypertension 69 0.080
337
P PLY011 Polycystic Ovary Syndrome 58 0.080
338
c LKM071 Leukemia, Chronic Lymphocytic 81 0.080
339
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.080
340
ORL011 Oral Cancer 62 0.080
341
RSC001 Rosacea 55 0.080
342
LNG031 Lung Benign Neoplasm 52 0.080
343
P NSP012 Nasopharyngeal Carcinoma 67 0.079
344
SBC016 Subacute Delirium 43 0.079
345
P HYD006 Hydrocephalus 68 0.078
346
c CNG216 Congenital Hydrocephalus 55 0.078
347
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.078
348
P INS002 in Situ Carcinoma 55 0.078
349
RTN023 Retinitis 46 0.078
350
NRR001 Neuroretinitis 46 0.078
351
P HYP069 Hyperparathyroidism 64 0.078
352
OTT002 Otitis Media 71 0.078
353
CYS013 Cystinuria 66 0.078
354
LSH001 Leishmaniasis 64 0.078
355
P KLZ004 Kala-Azar 1 43 0.078
356
P INT068 Intestinal Disease 56 0.078
357
PRN019 Perinatal Necrotizing Enterocolitis 55 0.078
358
LYM019 Lymphosarcoma 48 0.077
359
c LKM004 Leukemia, B-Cell, Chronic 35 0.077
360
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.077
361
P GRF003 Graft-Versus-Host Disease 71 0.077
362
c PNS012 Paine Syndrome 61 0.077
363
SCH014 Schistosomiasis 57 0.077
364
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.077
365
P THL005 Thalassemia 62 0.077
366
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.076
367
P SHR001 Short Bowel Syndrome 50 0.076
368
PRT013 Portal Hypertension 61 0.076
369
P RTN008 Retinitis Pigmentosa 77 0.076
370
P PRK057 Parkinson Disease, Late-Onset 77 0.076
371
BRN028 Brain Cancer 75 0.076
372
CLR108 Colorectal Adenoma 64 0.076
373
PRP030 Purpura 56 0.076
374
RRS014 Rare Surgical Neurologic Disease 33 0.076
375
DRY001 Dry Eye Syndrome 50 0.076
376
c BSL007 Basal Cell Carcinoma 68 0.075
377
c FML035 Familial Hyperlipidemia 56 0.075
378
CMM005 Common Cold 57 0.075
379
c HPT003 Hepatitis a 60 0.075
380
P HYP265 Hypotonia 43 0.075
381
c MJR003 Major Affective Disorder 6 34 0.075
382
c MJR006 Major Affective Disorder 5 34 0.075
383
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.074
384
HMS001 Hemosiderosis 54 0.074
385
P URT039 Urticaria 61 0.074
386
P END033 Endocarditis 58 0.074
387
c MJR008 Major Affective Disorder 2 35 0.074
388
c MJR023 Major Affective Disorder 7 34 0.074
389
c MJR004 Major Affective Disorder 4 29 0.074
390
P CND004 Candidiasis 61 0.074
391
BLR001 Biliary Atresia 51 0.074
392
CHR074 Choriocarcinoma 47 0.073
393
P BNG032 Benign Mesothelioma 47 0.073
394
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.073
395
P RCT021 Rectum Cancer 54 0.073
396
TRN015 Transient Cerebral Ischemia 62 0.073
397
IGR001 Ige Responsiveness, Atopic 61 0.073
398
GLS018 Glass Syndrome 51 0.073
399
MSC007 Muscle Hypertrophy 65 0.072
400
P RRH023 Rare Hereditary Hemochromatosis 41 0.072
401
MSC157 Muscular Dystrophy, Duchenne Type 70 0.072
402
P END044 Endometriosis 63 0.072
403
KHL003 Kohlschutter-Tonz Syndrome 63 0.072
404
BCT002 Bacterial Vaginosis 52 0.072
405
P MLN007 Male Infertility 57 0.072
406
c SVR001 Severe Acute Respiratory Syndrome 56 0.072
407
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.071
408
P OPN001 Open-Angle Glaucoma 50 0.071
409
P MDL005 Medulloblastoma 78 0.071
410
GTR002 Goiter 54 0.071
411
P SCK005 Sickle Cell Disease 53 0.071
412
FDL002 Food Allergy 52 0.071
413
KRT019 Keratitis, Hereditary 69 0.070
414
PLC008 Placenta Disease 51 0.070
415
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.070
416
P GLM040 Glioma Susceptibility 1 68 0.070
417
P CNJ013 Conjunctivitis 67 0.070
418
END040 Endogenous Depression 55 0.070
419
DYS073 Dysphagia 52 0.070
420
KRT001 Keratoconjunctivitis Sicca 53 0.070
421
TYP007 Typhoid Fever 61 0.070
422
PLM031 Poliomyelitis 58 0.069
423
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.069
424
GNG013 Gingivitis 60 0.068
425
PRT038 Protein-Energy Malnutrition 56 0.068
426
CHL067 Cholecystitis 60 0.068
427
SCK003 Sickle Cell Anemia 74 0.067
428
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.067
429
PHR003 Pharyngitis 56 0.067
430
DYS015 Dysentery 45 0.067
431
c PRM038 Primary Agammaglobulinemia 45 0.067
432
c CHR064 Chronic Monocytic Leukemia 43 0.067
433
LYM133 Lymphoma, Hodgkin, Classic 70 0.067
434
EXN003 Exencephaly 32 0.067
435
P PRS038 Personality Disorder 66 0.067
436
VRC005 Varicose Veins 61 0.067
437
PST092 Posttransplant Acute Limbic Encephalitis 29 0.067
438
NRT001 Neurotic Disorder 53 0.066
439
BRN056 Bronchopulmonary Dysplasia 57 0.066
440
c FML001 Familial Atrial Fibrillation 67 0.066
441
KRT006 Keratoconjunctivitis 53 0.066
442
c PRD040 Periodontitis, Chronic 56 0.066
443
CRC021 Carcinosarcoma 62 0.066
444
KRT013 Keratolytic Winter Erythema 45 0.066
445
NWB001 Newborn Respiratory Distress Syndrome 58 0.065
446
PLG002 Plague 54 0.065
447
P SLP006 Sleep Apnea 71 0.065
448
P HYP061 Hypertrophic Cardiomyopathy 68 0.065
449
BRK010 Burkitt Lymphoma 68 0.065
450
CRN030 Coronary Stenosis 49 0.065
451
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 36 0.065
452
KWS001 Kwashiorkor 46 0.065
453
MXD026 Mixed Glioma 36 0.065
454
SKN019 Skin Melanoma 68 0.065
455
P FML011 Familial Adenomatous Polyposis 73 0.065
456
c MCR129 Microvascular Complications of Diabetes 1 67 0.065
457
P UVT001 Uveitis 58 0.065
458
LKP003 Leukoplakia 40 0.064
459
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.064
460
P THY023 Thymoma 64 0.064
461
c THY107 Thymoma, Familial 55 0.064
462
ANR007 Anorexia Nervosa 64 0.064
463
P VSC011 Vasculitis 64 0.064
464
c BRN108 Branchiootic Syndrome 1 62 0.064
465
HMT018 Hematopoietic Stem Cell Transplantation 54 0.064
466
SPL018 Splenomegaly 48 0.064
467
c HNT004 Huntington Disease-Like 2 48 0.064
468
c SPN225 Spondyloarthropathy 1 74 0.063
469
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.063
470
CRH005 Crohn's Colitis 56 0.063
471
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.063
472
PTT037 Pituitary Tumors 47 0.063
473
c GLC092 Glaucoma, Primary Open Angle 63 0.063
474
ANR040 Aneurysm 60 0.063
475
PRP080 Peripheral Artery Disease 51 0.063
476
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.063
477
SFT003 Soft Tissue Sarcoma 57 0.062
478
P RTN018 Retinal Disease 53 0.062
479
HYP020 Hyperprolactinemia 62 0.062
480
P SLP005 Sleep Disorder 58 0.062
481
P MNC007 Monocytic Leukemia 52 0.062
482
CRT015 Carotid Artery Occlusion 44 0.062
483
RRD056 Rare Disease in Surgical Orthopedic 29 0.062
484
OST017 Osteomyelitis 65 0.062
485
P MYC008 Myocarditis 60 0.062
486
P CLC063 Celiac Disease 1 66 0.062
487
RTN017 Retinal Detachment 62 0.062
488
P ADL010 Adult Respiratory Distress Syndrome 61 0.062
489
CLF001 Cleft Lip 53 0.062
490
P HYP058 Hypervitaminosis a 45 0.061
491
NSP002 Nasopharyngitis 41 0.061
492
P OCL013 Oculodentodigital Dysplasia 65 0.061
493
PNM008 Pneumothorax 56 0.061
494
PST021 Postpartum Depression 51 0.061
495
P ALP009 Alopecia Areata 61 0.061
496
GLS001 Gliosarcoma 56 0.061
497
SPS057 Spasticity 38 0.061
498
SXL003 Sexual Disorder 49 0.061
499
AMN001 Amenorrhea 54 0.061
500
HPT022 Hepatoblastoma 58 0.060
501
P NRV007 Nervous System Disease 68 0.060
502
ILS001 Ileus 51 0.060
503
P ANG015 Angioedema 54 0.060
504
HYD002 Hydronephrosis 58 0.059
505
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.059
506
TRP004 Tropical Sprue 41 0.059
507
DMY004 Demyelinating Disease 54 0.059
508
SPN051 Spondylitis 53 0.058
509
INF009 Inflammatory Spondylopathy 29 0.058
510
TRP009 Triple X Syndrome 42 0.058
511
MCR013 Microphthalmia 62 0.058
512
P GRV001 Graves' Disease 57 0.058
513
P OLG002 Oligodendroglioma 67 0.058
514
ATN005 Autonomic Dysfunction 48 0.058
515
CRB037 Cerebral Palsy 69 0.057
516
RBS001 Rabies 57 0.057
517
TNS005 Tonsillitis 58 0.057
518
ATN004 Autonomic Neuropathy 43 0.057
519
RDN001 Reading Disorder 42 0.057
520
SLC006 Silicosis 55 0.057
521
P PTT006 Pituitary Adenoma 53 0.057
522
PPL001 Papillary Adenoma 42 0.057
523
c SVR005 Severe Pre-Eclampsia 50 0.056
524
ACT084 Acute Stress Disorder 42 0.056
525
YLL002 Yellow Fever 58 0.056
526
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 55 0.056
527
c PSR017 Psoriasis 2 55 0.056
528
c PSR023 Psoriasis 1 50 0.056
529
c PSR028 Psoriasis 7 40 0.056
530
c PSR018 Psoriasis 13 40 0.056
531
c PSR032 Psoriasis 11 40 0.056
532
VRL011 Viral Infectious Disease 62 0.056
533
VSC003 Visceral Leishmaniasis 55 0.056
534
PST028 Post-Traumatic Stress Disorder 60 0.056
535
MCL006 Macular Retinal Edema 52 0.056
536
CRD223 Cardiac Arrhythmia 61 0.055
537
INT002 Intermittent Claudication 60 0.055
538
P VSC018 Visceral Steatosis 34 0.055
539
LMY002 Leiomyoma 52 0.055
540
LNT004 Lentigines 47 0.055
541
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.055
542
P NGH001 Night Blindness 48 0.055
543
XRP001 Xerophthalmia 37 0.055
544
FCT007 Factor Vii Deficiency 65 0.055
545
FBR047 Fibromyalgia 60 0.055
546
c SCN007 Secondary Hyperparathyroidism 52 0.055
547
P TRT010 Teratoma 52 0.055
548
CHR178 Chromosomal Triplication 36 0.055
549
CYT018 Cytochrome P450 2d6 Variant 28 0.055
550
WST001 West Syndrome 61 0.055
551
MNT001 Mantle Cell Lymphoma 69 0.054
552
INT075 Intracranial Hypertension 54 0.054
553
OBS002 Obsessive-Compulsive Disorder 69 0.054
554
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.054
555
VGN023 Vaginitis 54 0.054
556
PLR008 Pleurisy 50 0.054
557
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.054
558
PLC005 Placental Insufficiency 55 0.054
559
P PNC025 Panic Disorder 53 0.054
560
c INF145 Infantile Liver Failure Syndrome 1 50 0.054
561
c MLG074 Malignant Mesenchymoma 50 0.054
562
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 62 0.054
563
c HMC039 Hemochromatosis, Type 1 73 0.053
564
P FLL037 Follicular Lymphoma 67 0.053
565
c EXD008 Exudative Vitreoretinopathy 1 69 0.053
566
P LRY044 Larynx Cancer 59 0.053
567
HYP025 Hyperphosphatemia 47 0.053
568
BCK006 Back Pain 44 0.053
569
STN013 Stenotrophomonas Maltophilia Infection 26 0.053
570
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.053
571
CMR002 Coumarin Resistance 56 0.053
572
CHR066 Chronic Fatigue Syndrome 61 0.053
573
P TXP001 Toxoplasmosis 61 0.053
574
P TBR001 Tuberous Sclerosis 72 0.052
575
ACR007 Acromegaly 70 0.052
576
c MST023 Mesothelioma, Malignant 59 0.052
577
P MTC069 Mitochondrial Disorders 57 0.052
578
SPT004 Septic Arthritis 55 0.052
579
c MCR112 Microvascular Complications of Diabetes 2 42 0.052
580
EXC002 Exocrine Pancreatic Insufficiency 41 0.052
581
LYM040 Lymphoblastic Lymphoma 54 0.052
582
c CHR682 Chronic Bilirubin Encephalopathy 36 0.052
583
c NGH026 Night Blindness, Congenital Stationary, Type 1a 46 0.052
584
MLT157 Multiple System Atrophy 1 71 0.051
585
EWN003 Ewing Sarcoma 69 0.051
586
HMT002 Hematologic Cancer 64 0.051
587
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.051
588
DFF005 Diffuse Large B-Cell Lymphoma 56 0.051
589
IMM064 Immunodeficiency, Common Variable, 10 51 0.051
590
PLS007 Plasmodium Falciparum Malaria 53 0.051
591
P INT070 Intestinal Obstruction 60 0.051
592
NRN004 Neuroendocrine Tumor 59 0.051
593
PRD004 Prediabetes Syndrome 49 0.051
594
NRM005 Neuromuscular Disease 62 0.051
595
P HYP726 Hypercalcemia, Infantile, 1 58 0.051
596
P RBL001 Rubella 56 0.051
597
MCR004 Macroglobulinemia 50 0.051
598
RTC005 Reticulosarcoma 48 0.051
599
ASP007 Aspiration Pneumonia 46 0.051
600
FSC004 Fasciitis 47 0.050
601
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 37 0.050
602
CHY002 Chylomicron Retention Disease 63 0.050
603
P EPN002 Ependymoma 61 0.050
604
DBT002 Diabetic Autonomic Neuropathy 45 0.050
605
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.050
606
ESP002 Esophageal Varix 49 0.050
607
P BLR006 Biliary Tract Disease 49 0.050
608
TND005 Tendinitis 45 0.050
609
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.049
610
APP008 Appendicitis 61 0.049
611
BRN002 Bronchiolitis 60 0.049
612
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.049
613
c BNG030 Benign Ependymoma 48 0.049
614
GST020 Gastric Antral Vascular Ectasia 42 0.049
615
P PTS002 Ptosis 53 0.049
616
LPT006 Leptin Receptor Deficiency 47 0.049
617
ASP008 Aspiration Pneumonitis 41 0.049
618
P SYP003 Syphilis 59 0.049
619
P SJG008 Sjogren Syndrome 57 0.049
620
GST030 Gastrinoma 43 0.049
621
P PRC031 Preeclampsia/eclampsia 1 42 0.049
622
c LKM070 Leukemia, Acute Monocytic 55 0.048
623
CLL003 Cellulitis 56 0.048
624
CLN045 Colonic Benign Neoplasm 52 0.048
625
VTM033 Vitamin K Deficiency Bleeding 47 0.048
626
HYP457 Hypertrophic Scars 44 0.048
627
BRS051 Breast Disease 59 0.048
628
P PRV006 Pervasive Developmental Disorder 58 0.048
629
HYP080 Hypogonadism 51 0.048
630
c FLL041 Follicular Lymphoma 1 50 0.048
631
PLR007 Pleural Empyema 44 0.048
632
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.048
633
c BPL002 Bipolar I Disorder 48 0.048
634
PPL049 Papillon-Lefevre Syndrome 63 0.047
635
RTN020 Retinal Vascular Disease 49 0.047
636
PRS063 Paresthesia 46 0.047
637
HYP064 Hypogonadotropism 40 0.047
638
CHL013 Cholecystolithiasis 37 0.047
639
CRP001 Carpal Tunnel Syndrome 68 0.047
640
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.047
641
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.047
642
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.047
643
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.047
644
PRN009 Paranoid Schizophrenia 47 0.047
645
ACD008 Acid-Labile Subunit Deficiency 55 0.046
646
GNG003 Gingival Recession 43 0.046
647
GST071 Gastrointestinal Carcinoma 42 0.046
648
PRT058 Pure Autonomic Failure 60 0.046
649
ACT200 Acute Monoblastic Leukemia 56 0.046
650
SYN036 Syncope 46 0.046
651
APN008 Apnea, Obstructive Sleep 64 0.046
652
P HMR005 Hemorrhoid 47 0.046
653
PLL012 Pollen Allergy 46 0.046
654
c SYS043 Systemic Lupus Erythematosus 1 39 0.046
655
c ALP101 Alpha-Thalassemia 63 0.045
656
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.045
657
CRC006 Carcinoid Syndrome 55 0.045
658
P NRV006 Nervous System Cancer 55 0.045
659
PRP036 Peripheral T-Cell Lymphoma 53 0.045
660
INT303 Intracranial Hypertension, Idiopathic 52 0.045
661
MYM001 Myoma 52 0.045
662
TXC020 Toxic Oil Syndrome 34 0.045
663
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.045
664
HMR039 Hemorrhage, Intracerebral 59 0.045
665
MTC027 Mitochondrial Trifunctional Protein Deficiency 55 0.045
666
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.045
667
NRL018 Neural Tube Defects, Folate-Sensitive 50 0.045
668
LPD009 Lipid Storage Disease 49 0.045
669
P HYP733 Hypercalciuria, Absorptive, 2 45 0.045
670
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.045
671
P PHT010 Photoparoxysmal Response 1 39 0.045
672
FLL008 Folliculitis 46 0.045
673
WLS001 Wilson Disease 69 0.045
674
c MCL013 Mucolipidosis Iv 60 0.045
675
SHG001 Shigellosis 54 0.045
676
INF034 Infective Endocarditis 53 0.045
677
GNT002 Giant Cell Glioblastoma 52 0.045
678
OST011 Osteomalacia 51 0.045
679
c CNT033 Central Nervous System Cancer 51 0.045
680
CRB090 Cerebral Hypoxia 45 0.045
681
CHL045 Choline Deficiency Disease 39 0.045
682
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.045
683
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.044
684
SYS003 Systolic Heart Failure 43 0.044
685
c TBR025 Tuberous Sclerosis 1 74 0.044
686
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.044
687
PLS025 Plasmablastic Lymphoma 48 0.044
688
CYN002 Cyanosis, Transient Neonatal 45 0.044
689
P CRB088 Cerebral Atrophy 43 0.044
690
c XNT010 Xanthinuria, Type I 51 0.044
691
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.044
692
IRR003 Irritant Dermatitis 46 0.044
693
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.044
694
TND004 Tendinopathy 44 0.044
695
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.044
696
ATM052 Autoimmune Disease 1 38 0.044
697
ALL009 Allergic Conjunctivitis 50 0.043
698
RSP007 Respiratory Distress Syndrome, Infant 31 0.043
699
ORL005 Oral Candidiasis 56 0.043
700
GST049 Gastrointestinal System Cancer 49 0.043
701
LWC001 Low Compliance Bladder 45 0.043
702
P AVS003 Avascular Necrosis 43 0.043
703
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 37 0.043
704
SMT001 Somatization Disorder 45 0.042
705
ENT001 Enterocele 44 0.042
706
c PNC108 Pancreatitis, Hereditary 70 0.042
707
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.042
708
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.042
709
LMY014 Leiomyoma, Uterine 57 0.042
710
ACR041 Acromelic Frontonasal Dysostosis 50 0.042
711
THR016 Thrombophlebitis 50 0.042
712
P END046 Endometritis 49 0.042
713
ART004 Aortic Atherosclerosis 47 0.042
714
DBT006 Diabetic Macular Edema 46 0.042
715
c ACT004 Acute Diarrhea 38 0.042
716
VGN019 Vaginal Discharge 35 0.042
717
P HYP040 Hypospadias 54 0.041
718
BRD004 Borderline Personality Disorder 51 0.041
719
c BCT013 Bacterial Pneumonia 49 0.041
720
RNL011 Renal Osteodystrophy 49 0.041
721
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.041
722
TRC003 Trichomoniasis 46 0.041
723
SKN005 Skin Atrophy 41 0.041
724
GRM010 Germ Cells Tumors 35 0.041
725
P END047 Endophthalmitis 50 0.041
726
VGN020 Vaginal Disease 45 0.041
727
LYM012 Lymphoplasmacytic Lymphoma 62 0.041
728
APH001 Aphthous Stomatitis 56 0.041
729
STP011 Stapes Ankylosis with Broad Thumbs and Toes 50 0.041
730
GLC036 Glucagonoma 45 0.041
731
c HMG029 Hemoglobin Se Disease 40 0.041
732
SPR126 Superior Semicircular Canal Dehiscence 39 0.041
733
PLY068 Polysubstance Abuse 44 0.041
734
P LCT002 Lactose Intolerance 51 0.040
735
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.040
736
VLV011 Vulvovaginal Candidiasis 50 0.040
737
P BLD051 Blood Coagulation Disease 48 0.040
738
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.040
739
MYF001 Myofibroma 40 0.040
740
CHL039 Choledocholithiasis 37 0.040
741
P BRN035 Brain Stem Glioma 51 0.040
742
c LTN004 Late-Onset Retinal Degeneration 49 0.040
743
CRC014 Carcinoid Tumors, Intestinal 49 0.040
744
CRN027 Corneal Neovascularization 48 0.040
745
c BSL024 Basal Cell Carcinoma 1 47 0.040
746
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.039
747
CRN036 Craniopharyngioma 65 0.039
748
NTR018 Neutrophilia, Hereditary 53 0.039
749
FRZ001 Frozen Shoulder 53 0.039
750
OPT003 Opiate Dependence 50 0.039
751
INT017 Intestinal Schistosomiasis 49 0.039
752
c DRM054 Dermatitis, Atopic, 2 45 0.039
753
MYF002 Myofascial Pain Syndrome 39 0.039
754
FBR012 Fabry Disease 68 0.039
755
ABT001 Abetalipoproteinemia 68 0.039
756
P PTN014 Patent Ductus Arteriosus 1 60 0.039
757
P ORL007 Oral Cavity Cancer 57 0.039
758
c LBR014 Leber Congenital Amaurosis 4 55 0.039
759
P KRT007 Keratoconus 51 0.039
760
PRV004 Periventricular Leukomalacia 50 0.039
761
CLS016 Clostridium Difficile Colitis 48 0.039
762
LYM051 Lymphomatoid Granulomatosis 47 0.039
763
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.039
764
CRB086 Cerebral Aneurysms 41 0.039
765
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.039
766
OBS003 Obsessive-Compulsive Personality Disorder 42 0.038
767
P LYM025 Lymphedema 54 0.038
768
BWN001 Bowen-Conradi Syndrome 49 0.038
769
EWN002 Ewing's Family of Tumors 48 0.038
770
CLC006 Calcinosis 48 0.038
771
P PRG092 Pregnancy Loss, Recurrent 1 40 0.038
772
PNM010 Pneumothorax, Primary Spontaneous 60 0.037
773
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 58 0.037
774
SPS003 Spastic Diplegia 53 0.037
775
NRN001 Neuroendocrine Carcinoma 48 0.037
776
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 48 0.037
777
BHR001 Behr Syndrome 47 0.037
778
CRT016 Carotid Artery Disease 53 0.037
779
P TTR001 Tetralogy of Fallot 70 0.037
780
P PLV020 Pelvic Organ Prolapse 61 0.037
781
BRN045 Brunner Syndrome 57 0.037
782
APH002 Aphasia 56 0.037
783
HND002 Hand, Foot and Mouth Disease 52 0.037
784
APR001 Apraxia 50 0.037
785
HDR003 Hidradenitis 48 0.037
786
NCR007 Necrotizing Fasciitis 47 0.037
787
BRS064 Bursitis 42 0.037
788
MNN028 Mononeuropathy of the Median Nerve, Mild 41 0.037
789
CLS047 Classic Progressive Supranuclear Palsy Syndrome 30 0.037
790
ANL022 Anal Fistula 47 0.036
791
MGK001 Megakaryocytic Leukemia 65 0.036
792
P FCL005 Focal Segmental Glomerulosclerosis 63 0.036
793
FND002 Fundus Dystrophy 52 0.036
794
CHR005 Chorioamnionitis 51 0.036
795
HYP063 Hypersplenism 51 0.036
796
ERY004 Erysipelas 46 0.036
797
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.036
798
LCH009 Lichen Sclerosus 39 0.036
799
c PRG020 Paragangliomas 3 36 0.036
800
JVN026 Jeavons Syndrome 24 0.036
801
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.035
802
HDR002 Hidradenitis Suppurativa 58 0.035
803
ADR016 Adrenal Cortical Carcinoma 51 0.035
804
PRP017 Periapical Periodontitis 43 0.035
805
P CRN024 Corneal Disease 42 0.035
806
ACL001 Acalculous Cholecystitis 35 0.035
807
STT009 Sutton Disease 2 31 0.035
808
PTT009 Pituitary Gland Disease 54 0.035
809
c FML346 Familial Adenomatous Polyposis 1 71 0.034
810
P STR022 Stargardt Disease 59 0.034
811
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 58 0.034
812
ECH003 Echinococcosis 54 0.034
813
SRT004 Serotonin Syndrome 48 0.034
814
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.034
815
PRL017 Prolymphocytic Leukemia 45 0.034
816
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.034
817
CLL014 Cll/sll 44 0.034
818
ADR004 Adrenal Cortical Adenocarcinoma 44 0.034
819
VLV010 Vulvovaginitis 42 0.034
820
CLN044 Colon Adenoma 41 0.034
821
SPR008 Supratentorial Primitive Neuroectodermal Tumor 39 0.034
822
CVT001 Cavitary Optic Disc Anomalies 39 0.034
823
ACT011 Acute Contagious Conjunctivitis 35 0.034
824
MSM014 Mismatch Repair Cancer Syndrome 65 0.034
825
P TST021 Testicular Germ Cell Tumor 63 0.034
826
PNM001 Pneumocystosis 53 0.034
827
ADN009 Adenosquamous Carcinoma 50 0.034
828
MTY001 Mutyh-Associated Polyposis 48 0.034
829
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.034
830
P OCY003 Oocyte Maturation Defect 1 44 0.034
831
MCL003 Macular Holes 44 0.034
832
CYS009 Cystadenoma 43 0.034
833
P DYS021 Dysautonomia 41 0.034
834
BCK003 Background Diabetic Retinopathy 37 0.034
835
CRB026 Cerebellar Astrocytoma 31 0.034
836
MYP139 Myopathy, Proximal, and Ophthalmoplegia 56 0.034
837
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.033
838
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 58 0.033
839
LNN001 Lennox-Gastaut Syndrome 56 0.033
840
ORP003 Oropharynx Cancer 55 0.033
841
P HYP730 Hypogonadotropic Hypogonadism 54 0.033
842
P SPN052 Spondyloarthropathy 54 0.033
843
OPD006 Opioid Addiction 49 0.033
844
PNC119 Pancreatic Neuroendocrine Tumor 48 0.033
845
AYM001 Ayme-Gripp Syndrome 45 0.033
846
c DYS119 Dystonia 9 45 0.033
847
P CLS010 Cluster Headache 44 0.033
848
BNN005 Bunion 34 0.033
849
CRN302 Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal 32 0.033
850
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 28 0.033
851
CHL057 Childhood Brain Stem Glioma 19 0.033
852
CHL009 Childhood Cerebral Astrocytoma 15 0.033
853
NRL004 Neuroleptic Malignant Syndrome 48 0.032
854
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.032
855
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.032
856
FRY006 Fryns Microphthalmia Syndrome 55 0.032
857
c HYP740 Hyperlipoproteinemia, Type V 53 0.032
858
P PNB001 Pineoblastoma 52 0.032
859
P AGG001 Aggressive Periodontitis 50 0.032
860
P SCL015 Scleritis 49 0.032
861
P GND004 Gonadal Dysgenesis 47 0.032
862
CHL018 Childhood Medulloblastoma 46 0.032
864
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.032
865
RCT017 Rectal Disease 39 0.032
866
HYP189 Hypoadrenalism 39 0.032
867
PDT014 Pediatric Ependymoma 33 0.032
868
EMB015 Embryonal Tumor with Multilayered Rosettes 29 0.032
869
CGN007 Cognitive Function 1, Social 28 0.032
870
P ORT004 Orthostatic Intolerance 68 0.031
871
DMN031 Dementia, Lewy Body 66 0.031
872
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.031
873
ADR005 Adrenal Carcinoma 58 0.031
874
CRT033 Corticobasal Degeneration 55 0.031
875
P ACT105 Acute Mountain Sickness 53 0.031
876
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.031
877
FML037 Female Breast Cancer 52 0.031
878
c HYP739 Hyperlipoproteinemia, Type Iv 50 0.031
879
ISL001 Islet Cell Tumor 47 0.031
880
P BCT020 Bacteremia 2 45 0.031
881
PNC085 Penicillin Allergy 44 0.031
882
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.031
883
PRS115 Prosthetic Joint Infection 43 0.031
884
MMM006 Mammographic Density 43 0.031
885
c MCR312 Microphthalmia, Syndromic 10 34 0.031
886
BRN049 Brain Tumor, Childhood 30 0.031
887
LRY027 Laryngeal Papillomatosis 24 0.031
888
P MLN066 Melanoma, Cutaneous Malignant 1 69 0.030
889
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.030
890
P SCK002 Sick Sinus Syndrome 56 0.030
891
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.030
892
c PYR010 Peyronie's Disease 51 0.030
893
PTH002 Pathological Gambling 48 0.030
894
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.030
895
ULC007 Ulcerative Stomatitis 41 0.030
896
CNT060 Central Serous Chorioretinopathy 41 0.030
897
HRN003 Heroin Dependence 41 0.030
898
CNT017 Central Nervous System Origin Vertigo 38 0.030
899
PLN007 Plantar Fasciitis 32 0.030
900
PDT015 Pediatric Supratentorial Ependymoma 31 0.030
901
PDT016 Pediatric Infratentorial Ependymoma 29 0.030
902
SDD004 Sudden Arrhythmia Death Syndrome 23 0.030
903
P LBR001 Leber Congenital Amaurosis 67 0.029
905
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.029
906
P AGN002 Agnosia 56 0.029
907
P CRN028 Corneal Ulcer 49 0.029
908
CLD014 Cole Disease 41 0.029
909
OBS004 Obstructive Hydrocephalus 39 0.029
910
c JVN024 Juvenile Hereditary Hemochromatosis 32 0.029
911
INT053 Intracranial Vasospasm 32 0.029
912
CHL006 Childhood Oligodendroglioma 31 0.029
913
VNT037 Ventral Hernia 31 0.029
914
DLT018 Dilution, Pigmentary 28 0.029
915
P CNT036 Central Nervous System Germ Cell Tumor 28 0.029
916
HYP213 Hypomelanotic Disorder 25 0.029
917
THY020 Thyroid Hyalinizing Trabecular Adenoma 23 0.029
918
c SCH082 Schizophrenia 5 40 0.028
919
PNC012 Punctate Epithelial Keratoconjunctivitis 30 0.028
920
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.028
921
ERY029 Erythermalgia, Primary 58 0.028
922
P HRN001 Horner's Syndrome 46 0.028
923
GRM004 Germinoma 45 0.028
924
P END039 Endodermal Sinus Tumor 44 0.028
925
CNN010 Connective Tissue Benign Neoplasm 44 0.028
926
CHR078 Chorioretinitis 43 0.028
927
c HYP057 Hypervitaminosis D 41 0.028
928
TST018 Testicular Yolk Sac Tumor 39 0.028
929
DNT014 Dental Pulp Disease 38 0.028
930
DNT006 Dental Pulp Necrosis 37 0.028
931
LCH016 Lichen Sclerosus Et Atrophicus 36 0.028
932
c PLM022 Pulmonary Valve Insufficiency 35 0.028
933
BLN010 Balanitis 34 0.028
934
TQP001 Taqi Polymorphism 34 0.028
935
RTN002 Retinal Perforation 33 0.028
936
c RTN181 Retinitis Pigmentosa 2, X-Linked 16 0.028
937
P USH001 Usher Syndrome 58 0.027
938
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.027
939
SMT006 Somatoform Disorder 51 0.027
940
PST048 Postural Orthostatic Tachycardia Syndrome 49 0.027
941
ATT003 Attenuated Familial Adenomatous Polyposis 48 0.027
942
RCR004 Recurrent Respiratory Papillomatosis 48 0.027
943
GNG008 Ganglioneuroblastoma 47 0.027
944
SYM002 Sympathetic Ophthalmia 46 0.027
945
PNC056 Pineocytoma 46 0.027
946
MTS001 Mutism 43 0.027
947
CHL012 Childhood Disintegrative Disease 41 0.027
948
P INT260 Intracranial Berry Aneurysm 38 0.027
949
ANS012 Anus Disease 37 0.027
950
CHN040 Choanal Atresia and Lymphedema 36 0.027
951
CRB054 Cerebellar Astrocytoma, Childhood 9 0.027
952
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 60 0.025
953
VTM028 Vitamin E, Familial Isolated Deficiency of 57 0.025
954
c MYP132 Myopathy, Congenital 55 0.025
955
BRD001 Brody Myopathy 55 0.025
956
SMT003 Somatostatinoma 49 0.025
957
SPN119 Spondylarthropathy 45 0.025
958
MDS018 Mediastinal Cancer 40 0.025
959
AMP007 Amphetamine Abuse 39 0.025
960
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 38 0.025
961
c SCH080 Schizophrenia 3 34 0.025
962
STR046 Stargardt Macular Degeneration 32 0.025
963
CHR288 Chronic Recurrent Multifocal Osteomyelitis 58 0.024
964
VLV032 Vulva Cancer 53 0.024
965
VPM001 Vipoma 47 0.024
966
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.024
967
LRY022 Laryngoonychocutaneous Syndrome 45 0.024
968
P CNT037 Central Nervous System Germinoma 43 0.024
969
RMS001 Rem Sleep Behavior Disorder 43 0.024
970
TND006 Tendinosis 42 0.024
971
PNL014 Pineal Gland Cancer 40 0.024
972
BLN002 Balanitis Xerotica Obliterans 38 0.024
973
PNC008 Pancreatic Endocrine Carcinoma 36 0.024
974
PRR004 Preretinal Fibrosis 36 0.024
975
SPP003 Suppurative Periapical Periodontitis 34 0.024
976
MXD032 Mixed Germ Cell Tumor 32 0.024
977
WDH001 Wdha Syndrome 32 0.024
978
PPM002 Ppoma 28 0.024
979
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 27 0.024
980
MLR020 Malaria, Mild 27 0.024
981
MXD025 Mixed Germ Cell Cancer 26 0.024
982
ACT133 Acetylation, Slow 23 0.024
983
LKP001 Leukoplakia of Penis 19 0.024
984
CHL046 Childhood Central Nervous System Mixed Germ Cell Tumor 11 0.024
985
CHL027 Childhood Central Nervous System Germinoma 11 0.024
986
P PRS049 Persistent Mullerian Duct Syndrome 53 0.022
987
P HRD012 Hereditary Elliptocytosis 50 0.022
988
P DPY001 Dupuytren Contracture 48 0.022
989
c PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 45 0.022
990
GLC096 Galactorrhea 44 0.022
991
PHM001 Phimosis 39 0.022
992
c GLC041 Glaucoma 1, Open Angle, a 33 0.022
993
ENG004 Engraftment Syndrome 30 0.022
994
HMP003 Hemopneumothorax 29 0.022
995
c SCH081 Schizophrenia 6 27 0.022
996
ACT206 Acitretin/etretinate Embryopathy 16 0.022
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