Search results for Serine

1531 hits were found for Serine

# Family MCID Name MIFTS Score
1
c HYP794 Hyperoxaluria, Primary, Type I 63 4.794
2
SRN001 Serine Deficiency 24 3.541
3
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 3.536
4
DSR076 Disorder of Serine or Glycine Metabolism 3 2.409
5
SRN004 Serine Biosynthesis Pathway Deficiency, Infantile/juvenile Form 1 2.409
6
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.331
7
c HPT073 Hepatitis C Virus 72 0.217
8
c HPT001 Hepatitis C 62 0.163
9
P SCH015 Schizophrenia 74 0.151
10
P BRS047 Breast Cancer 97 0.137
11
HLX001 Helix Syndrome 47 0.136
12
P CLR023 Colorectal Cancer 99 0.127
13
P NRB001 Neuroblastoma 72 0.124
14
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.123
15
P GLM045 Glioma 63 0.120
16
P PRS040 Prostate Cancer 97 0.119
17
VCC001 Vaccinia 49 0.119
18
GLL048 Glial Tumor 45 0.117
19
P OVR042 Ovarian Cancer 88 0.116
20
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.111
21
P LTR001 Lateral Sclerosis 54 0.111
22
P ALZ034 Alzheimer Disease 88 0.108
23
TLN003 Telangiectasis 52 0.108
24
P ADN016 Adenocarcinoma 64 0.107
25
P ATX030 Ataxia-Telangiectasia 82 0.105
26
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.104
27
P MCR010 Microcephaly 59 0.104
28
P RTN024 Retinoblastoma 73 0.102
29
SQM006 Squamous Cell Carcinoma 60 0.102
30
c FML008 Familial Retinoblastoma 53 0.100
31
P HPT023 Hepatocellular Carcinoma 100 0.099
32
HMN044 Human Immunodeficiency Virus Type 1 71 0.097
33
PHS021 Phosphoglycerate Dehydrogenase Deficiency 47 0.097
34
P PNC035 Pancreatic Cancer 84 0.095
35
GLB015 Glioblastoma Multiforme 75 0.095
36
P NRP001 Neuropathy 56 0.095
37
CYS001 Cystic Fibrosis 81 0.093
38
P LKM002 Leukemia 68 0.093
39
P LNG032 Lung Cancer 98 0.092
40
P PRK057 Parkinson Disease, Late-Onset 78 0.092
41
LSH001 Leishmaniasis 63 0.092
42
P KLZ004 Kala-Azar 1 41 0.092
43
P DNG005 Dengue Virus 59 0.090
44
SKN016 Skin Disease 63 0.088
45
P HRD021 Hereditary Sensory Neuropathy 48 0.088
46
CYT002 Cytokine Deficiency 42 0.088
47
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.086
48
P GST053 Gastric Cancer 83 0.086
49
ATM095 Autoimmune Disease 62 0.086
50
P MYL006 Myeloid Leukemia 60 0.086
51
BCT022 Bacterial Infectious Disease 56 0.084
52
P PRD008 Periodontitis 64 0.082
53
c SVR001 Severe Acute Respiratory Syndrome 62 0.082
54
PPL052 Papillomatosis, Confluent and Reticulated 33 0.082
55
FTT001 Fatty Liver Disease 61 0.080
56
LNG099 Lung Disease 60 0.080
57
IMM167 Immune Deficiency Disease 78 0.078
58
LVR012 Liver Cirrhosis 62 0.078
59
P DRR001 Diarrhea 55 0.078
60
HMP009 Haemophilus Influenzae 43 0.078
61
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.078
62
P MLN008 Melanoma 69 0.076
63
P LYM118 Lymphoma 68 0.076
64
c ACT027 Acute Pancreatitis 60 0.076
65
ATN004 Autonomic Neuropathy 45 0.076
66
c PCH010 Pachyonychia Congenita 3 44 0.076
67
PHS023 Phosphoserine Aminotransferase Deficiency 42 0.076
68
SVR004 Severe Combined Immunodeficiency 73 0.073
69
PTZ001 Peutz-Jeghers Syndrome 70 0.073
70
PSY004 Psychotic Disorder 67 0.073
71
PRT037 Pertussis 65 0.073
72
P BCL017 B-Cell Lymphoma 58 0.073
73
P FBR017 Fibrosarcoma 56 0.073
74
SCH012 Schizoaffective Disorder 50 0.073
75
47X002 47,xyy 49 0.073
77
c LKM061 Leukemia, Acute Myeloid 84 0.071
78
P BLD134 Bladder Cancer 79 0.071
79
P VSC007 Vascular Disease 63 0.071
80
SCH003 Schizophreniform Disorder 56 0.071
81
HYP060 Hyperinsulinism 54 0.071
82
48X005 48,xyyy 39 0.071
83
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.071
84
DFC004 Deficiency Anemia 70 0.069
85
P LVR013 Liver Disease 68 0.069
86
NTH001 Netherton Syndrome 60 0.069
87
IRN002 Iron Metabolism Disease 57 0.069
88
HYP266 Hypoxia 57 0.069
89
P SZR006 Seizure Disorder 56 0.069
90
BRN071 Brain Injury 49 0.069
91
P DRM053 Dermatitis, Atopic 66 0.066
92
P HRP006 Herpes Simplex 65 0.066
93
P PSR002 Psoriasis 62 0.066
94
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.066
95
P PNC044 Pancreatitis 61 0.066
96
VSL002 Visual Epilepsy 59 0.066
97
ISC004 Ischemia 58 0.066
98
P PRP019 Peripheral Nervous System Disease 58 0.066
99
P INF037 Inflammatory Bowel Disease 54 0.066
100
SNS003 Sensory Peripheral Neuropathy 54 0.066
101
P NLX004 Neu-Laxova Syndrome 1 52 0.066
102
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.066
103
INS024 Insulin-Like Growth Factor I 79 0.063
104
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.063
105
P KDN018 Kidney Disease 72 0.063
106
P PHC003 Pheochromocytoma 71 0.063
107
c PNC108 Pancreatitis, Hereditary 70 0.063
108
P LKM062 Leukemia, Acute Lymphoblastic 69 0.063
109
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.063
110
OST159 Osteogenic Sarcoma 66 0.063
111
P MTR014 Motor Neuron Disease 65 0.063
112
INF034 Infective Endocarditis 53 0.063
113
HMC014 Homocysteinemia 53 0.063
114
c MCR113 Microvascular Complications of Diabetes 3 52 0.063
115
c MCR120 Microvascular Complications of Diabetes 7 47 0.063
116
ADR040 Adrenal Gland Pheochromocytoma 46 0.063
117
c MCR130 Microvascular Complications of Diabetes 6 41 0.063
118
c MCR133 Microvascular Complications of Diabetes 4 41 0.063
119
ESP021 Esophageal Cancer 90 0.061
120
BRT054 Brittle Bone Disorder 72 0.061
121
ADN018 Adenoma 59 0.061
122
DSS009 Disseminated Intravascular Coagulation 57 0.061
123
P END033 Endocarditis 57 0.061
124
AMB001 Amebiasis 55 0.061
125
VSC003 Visceral Leishmaniasis 55 0.061
126
RSC001 Rosacea 54 0.061
127
PST011 Pustulosis of Palm and Sole 52 0.061
128
CRB004 Cerebral Artery Occlusion 45 0.061
129
ORL015 Oral Squamous Cell Carcinoma 43 0.061
130
c HRD201 Hereditary Sensory and Autonomic Neuropathy Type 1 41 0.061
131
c SYS001 Systemic Lupus Erythematosus 86 0.058
132
MLR004 Malaria 81 0.058
133
TXC005 Toxic Shock Syndrome 62 0.058
134
P ENC018 Encephalopathy 61 0.058
135
CHC001 Chickenpox 60 0.058
136
c HRD002 Hereditary Angioedema 60 0.058
137
c ACT073 Acute Leukemia 58 0.058
138
P GLM007 Glomerulonephritis 57 0.058
139
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.058
140
P CHR345 Chronic Pain 44 0.058
141
c NRP033 Neuropathy, Hereditary Sensory and Autonomic, Type Ia 44 0.058
142
MST004 Mast Cell Neoplasm 42 0.058
143
EXT007 Extracutaneous Mastocytoma 38 0.058
144
PHS022 Phosphoserine Phosphatase Deficiency 36 0.058
145
MYL069 Myeloma, Multiple 85 0.055
146
P LKM071 Leukemia, Chronic Lymphocytic 79 0.055
147
CRV035 Cervical Cancer 76 0.055
148
P HNT016 Huntington Disease 72 0.055
149
P PLM037 Pulmonary Hypertension 67 0.055
150
c RHB024 Rhabdomyosarcoma 2 67 0.055
151
P DMN002 Dementia 66 0.055
152
P MCR115 Microvascular Complications of Diabetes 5 66 0.055
153
ATH013 Atherosclerosis Susceptibility 65 0.055
154
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.055
155
c ACT068 Acute Cystitis 63 0.055
156
CLT003 Colitis 62 0.055
157
c BRN108 Branchiootic Syndrome 1 62 0.055
158
ALL026 Allergic Hypersensitivity Disease 62 0.055
159
HYP066 Hyperglycemia 61 0.055
160
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.055
161
CHL014 Cholera 59 0.055
162
CHL123 Chlamydia 59 0.055
163
P ANG015 Angioedema 57 0.055
164
NNL006 Non-Alcoholic Steatohepatitis 54 0.055
165
P HMP007 Hemophilia 51 0.055
166
KRT009 Keratosis 51 0.055
167
STM007 Stomatitis 50 0.055
168
LYM009 Lymphocytic Choriomeningitis 47 0.055
169
CWP001 Cowpox 46 0.055
170
STN013 Stenotrophomonas Maltophilia Infection 25 0.055
171
OST012 Osteoarthritis 78 0.052
172
P LNG064 Lung Cancer Susceptibility 3 78 0.052
173
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.052
174
ULC004 Ulcerative Colitis 73 0.052
175
P GRF003 Graft-Versus-Host Disease 72 0.052
176
DWN001 Down Syndrome 70 0.052
177
EWN003 Ewing Sarcoma 69 0.052
178
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.052
179
P MSC005 Muscular Dystrophy 66 0.052
180
P NSP012 Nasopharyngeal Carcinoma 66 0.052
181
P PLM036 Pulmonary Fibrosis 65 0.052
182
PPL049 Papillon-Lefevre Syndrome 65 0.052
183
c PRC016 Pre-Eclampsia 63 0.052
184
DPR016 Depression 63 0.052
185
LPD008 Lipid Metabolism Disorder 62 0.052
186
P PRM002 Primary Hyperoxaluria 62 0.052
187
CTN007 Cutaneous Leishmaniasis 62 0.052
188
INS001 Insulinoma 60 0.052
189
c HPT016 Hepatitis B 59 0.052
190
PST028 Post-Traumatic Stress Disorder 58 0.052
191
SCH014 Schistosomiasis 57 0.052
192
P BPL003 Bipolar Disorder 56 0.052
193
TRM010 Traumatic Brain Injury 51 0.052
194
ATS010 Autosomal Recessive Disease 48 0.052
195
ACT084 Acute Stress Disorder 47 0.052
196
CVD001 Covid-19 44 0.052
197
c MJR024 Major Affective Disorder 9 41 0.052
198
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.052
199
c MJR022 Major Affective Disorder 8 38 0.052
200
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.048
201
AST005 Asthma 76 0.048
202
P HRT032 Heart Disease 75 0.048
203
END057 Endometrial Cancer 74 0.048
204
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.048
205
ANX010 Anxiety 73 0.048
206
c CHR684 Chronic Kidney Disease 70 0.048
207
P INF038 Influenza 68 0.048
208
MLD001 Melioidosis 68 0.048
209
PNC129 Pancreatic Adenocarcinoma 68 0.048
210
BRK010 Burkitt Lymphoma 67 0.048
211
c SML038 Small Cell Cancer of the Lung 65 0.048
212
KRT019 Keratitis, Hereditary 65 0.048
213
SRC014 Sarcoma 65 0.048
214
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.048
215
CLN015 Colon Adenocarcinoma 65 0.048
216
c HPT003 Hepatitis a 62 0.048
217
P VSC011 Vasculitis 62 0.048
218
MDD011 Mood Disorder 62 0.048
219
DRM006 Dermatitis 61 0.048
220
YLL002 Yellow Fever 61 0.048
221
P ENC004 Encephalitis 61 0.048
222
THY029 Thyroid Carcinoma 59 0.048
223
IRN001 Iron Deficiency Anemia 59 0.048
224
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.048
225
ALL006 Allergic Asthma 56 0.048
226
ERY051 Erythroleukemia, Familial 56 0.048
227
P MLN007 Male Infertility 55 0.048
228
P PLM034 Pulmonary Emphysema 55 0.048
229
WST005 West Nile Virus 54 0.048
230
c PRD040 Periodontitis, Chronic 53 0.048
231
SCB001 Scabies 50 0.048
232
NTR046 Neutrophil Migration 50 0.048
233
RNL077 Renal Fibrosis 47 0.048
234
c NRP040 Neuropathy, Hereditary Sensory and Autonomic, Type Ic 42 0.048
235
c CHR020 Chronic Interstitial Cystitis 37 0.048
236
c FNC027 Fanconi Anemia, Complementation Group a 81 0.045
237
P RHM011 Rheumatoid Arthritis 80 0.045
238
c NRF023 Neurofibromatosis, Type Ii 80 0.045
239
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.045
240
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.045
241
CRH001 Crohn's Disease 74 0.045
242
P MYC007 Myocardial Infarction 70 0.045
243
P ASP006 Aspergillosis 69 0.045
244
P PNM007 Pneumonia 68 0.045
245
P SKN015 Skin Carcinoma 66 0.045
246
P MNN013 Meningitis 66 0.045
247
KHL003 Kohlschutter-Tonz Syndrome 65 0.045
248
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.045
249
LYM017 Lyme Disease 64 0.045
250
INT002 Intermittent Claudication 61 0.045
251
c ACT071 Acute Kidney Failure 60 0.045
252
P BRS044 Breast Adenocarcinoma 59 0.045
253
BRN002 Bronchiolitis 59 0.045
254
P ANP001 Anaplastic Large Cell Lymphoma 58 0.045
255
ANT024 Anthrax Disease 58 0.045
256
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.045
257
DSS008 Disease of Mental Health 58 0.045
258
MNT002 Mental Depression 58 0.045
259
MCR013 Microphthalmia 57 0.045
260
P RHN004 Rhinitis 57 0.045
261
P CRD246 Cardiovascular System Disease 57 0.045
262
P PLY019 Polyneuropathy 56 0.045
263
AGN016 Aging 56 0.045
264
P ANT006 Antiphospholipid Syndrome 55 0.045
265
GLC003 Glucose Intolerance 54 0.045
266
P RTN016 Retinal Degeneration 53 0.045
267
SPN035 Spindle Cell Sarcoma 53 0.045
268
TRY001 Trypanosomiasis 50 0.045
269
VLV047 Volvulus of Midgut 49 0.045
270
BNR002 Bone Resorption Disease 48 0.045
271
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.045
272
TRT001 Teratocarcinoma 45 0.045
273
ALL014 Allergic Encephalomyelitis 38 0.045
274
HRW001 Hair Whorl 36 0.045
275
PLY150 Polykaryocytosis Inducer 31 0.045
276
ARG004 Argyria 27 0.045
277
MSP001 Masp2 Deficiency 25 0.045
278
c HYP595 Hypertension, Essential 84 0.041
279
STR067 Stroke, Ischemic 81 0.041
280
c HYP836 Hypercholesterolemia, Familial, 1 73 0.041
281
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.041
282
P FML011 Familial Adenomatous Polyposis 72 0.041
283
P AMY004 Amyloidosis 70 0.041
284
CNG034 Congestive Heart Failure 69 0.041
285
PLM001 Pulmonary Tuberculosis 69 0.041
286
P LPR021 Leprosy 3 69 0.041
287
P HPT021 Hepatitis 67 0.041
288
ALL003 Allergic Rhinitis 67 0.041
289
c HMP029 Hemophilia a 67 0.041
290
ALC007 Alcohol Dependence 66 0.041
291
CHG001 Chagas Disease 66 0.041
292
P NRV007 Nervous System Disease 66 0.041
293
P LPS002 Liposarcoma 65 0.041
294
IRR002 Irritable Bowel Syndrome 65 0.041
295
P ADL010 Adult Respiratory Distress Syndrome 65 0.041
296
P THY023 Thymoma 65 0.041
297
PRT036 Peritonitis 64 0.041
298
P NTR004 Neutropenia 63 0.041
299
c WLM018 Wilms Tumor 5 61 0.041
300
SPN186 Spinal Cord Injury 60 0.041
301
STT001 Status Epilepticus 60 0.041
302
c DNG003 Dengue Disease 59 0.041
303
GST045 Gastroenteritis 59 0.041
304
P INF032 Infertility 57 0.041
305
P HDC001 Headache 57 0.041
306
THR024 Thrombosis 57 0.041
307
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.041
308
CHR177 Chromophobe Renal Cell Carcinoma 57 0.041
309
P PLY011 Polycystic Ovary Syndrome 56 0.041
310
EMB004 Embryonal Carcinoma 56 0.041
311
BRN004 Brain Edema 56 0.041
312
HYP005 Hypokalemia 55 0.041
313
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.041
314
SLP001 Sleeping Sickness 54 0.041
315
TRC023 Trichinosis 53 0.041
316
P RNL017 Renal Oncocytoma 53 0.041
317
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.041
318
c VRL010 Viral Hepatitis 52 0.041
319
P MSC003 Muscular Atrophy 52 0.041
320
c THY107 Thymoma, Familial 52 0.041
321
CLR109 Colorectal Adenocarcinoma 51 0.041
322
ENT011 Enterocolitis 51 0.041
323
P TMP001 Temporal Lobe Epilepsy 50 0.041
324
URM002 Uremia 49 0.041
325
c NRP041 Neuropathy, Hereditary Sensory, Type Ie 47 0.041
326
CHR074 Choriocarcinoma 47 0.041
327
LYM019 Lymphosarcoma 46 0.041
328
TST014 Testicular Cancer 46 0.041
329
ACT003 Acute Kidney Tubular Necrosis 45 0.041
330
SPS057 Spasticity 45 0.041
331
DWR001 Dwarfism 44 0.041
332
OVR094 Ovarian Epithelial Cancer 38 0.041
333
HNS001 Hansen's Disease 34 0.041
334
c LKM005 Leukemia, T-Cell, Chronic 34 0.041
335
GRN004 Granulomatous Amebic Encephalitis 30 0.041
336
TCK004 Tick Infestation 28 0.041
337
P GLM040 Glioma Susceptibility 1 81 0.037
338
c DLT002 Dilated Cardiomyopathy 79 0.037
339
KPS004 Kaposi Sarcoma 75 0.037
340
P RSP003 Respiratory Failure 74 0.037
341
P EPL164 Epilepsy 71 0.037
342
MLT157 Multiple System Atrophy 1 70 0.037
343
ADL002 Adult Syndrome 70 0.037
344
P TBR001 Tuberous Sclerosis 70 0.037
345
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.037
346
P ART022 Arthritis 69 0.037
347
LYM133 Lymphoma, Hodgkin, Classic 69 0.037
348
P SYS005 Systemic Scleroderma 68 0.037
349
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
350
CHL065 Cholangiocarcinoma 68 0.037
351
P FRN006 Frontotemporal Dementia 68 0.037
352
BLM001 Bloom Syndrome 67 0.037
353
P HYP098 Hypereosinophilic Syndrome 67 0.037
354
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.037
355
HYP056 Hypoglycemia 66 0.037
356
TTN003 Tetanus 65 0.037
357
MRK001 Merkel Cell Carcinoma 65 0.037
358
CLR108 Colorectal Adenoma 64 0.037
359
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.037
360
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.037
361
P HML002 Hemolytic Anemia 63 0.037
362
PLG002 Plague 63 0.037
363
ACT119 Acute Promyelocytic Leukemia 63 0.037
364
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.037
365
GLY010 Glycine Encephalopathy 62 0.037
366
P LPS004 Lupus Erythematosus 61 0.037
367
P NPH012 Nephrotic Syndrome 60 0.037
368
DPH001 Diphtheria 60 0.037
369
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.037
370
CRD223 Cardiac Arrhythmia 60 0.037
371
ACQ007 Acquired Immunodeficiency Syndrome 60 0.037
372
DNG002 Dengue Hemorrhagic Fever 60 0.037
373
P CTR002 Cataract 60 0.037
374
ANT009 Antithrombin Iii Deficiency 59 0.037
375
P BRN022 Bronchiectasis 59 0.037
376
AVN001 Avian Influenza 59 0.037
377
P GLL022 Guillain-Barre Syndrome 59 0.037
378
ANR040 Aneurysm 59 0.037
379
RBS001 Rabies 58 0.037
380
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.037
381
P EHL001 Ehlers-Danlos Syndrome 58 0.037
382
P CND004 Candidiasis 58 0.037
383
c ACT075 Acute Myocardial Infarction 57 0.037
384
P PLY018 Polycythemia 56 0.037
385
P GST044 Gastritis 56 0.037
386
HPT022 Hepatoblastoma 56 0.037
387
DFF005 Diffuse Large B-Cell Lymphoma 55 0.037
388
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.037
389
AMN003 Amnestic Disorder 54 0.037
390
P ALP008 Alopecia 54 0.037
391
PRS045 Prostatic Hypertrophy 53 0.037
392
P HMC002 Homocystinuria 53 0.037
393
P HML001 Hemolytic-Uremic Syndrome 53 0.037
394
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.037
395
OCL069 Ocular Motor Apraxia 51 0.037
396
PRS021 Prostatic Adenoma 51 0.037
397
INT079 Intrahepatic Cholangiocarcinoma 51 0.037
398
END086 End Stage Renal Disease 51 0.037
399
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.037
400
P CRN025 Corneal Dystrophy 49 0.037
401
c HPT015 Hepatitis D 49 0.037
402
c INV001 Invasive Aspergillosis 49 0.037
403
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.037
404
c NLX003 Neu-Laxova Syndrome 2 47 0.037
405
P BLD051 Blood Coagulation Disease 46 0.037
406
RTN023 Retinitis 46 0.037
407
c SCH079 Schizophrenia 1 46 0.037
408
GRW007 Growth Hormone Deficiency 46 0.037
409
URT010 Ureteral Obstruction 45 0.037
410
P PSD003 Pseudohypoaldosteronism 44 0.037
411
MDD018 Middle East Respiratory Syndrome 43 0.037
412
NRR001 Neuroretinitis 42 0.037
413
RTT001 Ritter's Disease 41 0.037
414
RDN001 Reading Disorder 40 0.037
415
DGL002 D-Glyceric Aciduria 39 0.037
416
SCR011 Scrapie 39 0.037
417
AMN006 Aminoaciduria 38 0.037
418
c DFN352 Deafness, Autosomal Recessive 8 38 0.037
419
P CRB188 Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy 38 0.037
420
CRB009 Cerebritis 37 0.037
421
BLB005 Beaulieu-Boycott-Innes Syndrome 37 0.037
422
CND006 Candida Glabrata 32 0.037
423
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.037
424
ACN019 Acanthamoeba Keratitis 31 0.037
425
P EST010 Esterase B 14 0.037
426
P RTN008 Retinitis Pigmentosa 79 0.032
427
GST019 Gastrointestinal Stromal Tumor 78 0.032
428
c TBR025 Tuberous Sclerosis 1 77 0.032
429
ADR007 Adrenoleukodystrophy 75 0.032
430
BRN028 Brain Cancer 74 0.032
431
P OST002 Osteoporosis 74 0.032
432
c THR092 Thrombophilia Due to Thrombin Defect 73 0.032
433
P MLT020 Multiple Sclerosis 72 0.032
434
PRP027 Peripheral Vascular Disease 71 0.032
435
P ATS364 Autism 70 0.032
436
GST040 Gastric Adenocarcinoma 70 0.032
437
MYL009 Myelodysplastic Syndrome 70 0.032
438
PLY001 Polycythemia Vera 69 0.032
439
c HMP004 Hemophilia B 68 0.032
440
P MJR001 Major Depressive Disorder 68 0.032
441
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.032
442
c ATS007 Autism Spectrum Disorder 67 0.032
443
c MGR028 Migraine with or Without Aura 1 67 0.032
444
P CLC063 Celiac Disease 1 66 0.032
445
P LNG028 Long Qt Syndrome 66 0.032
446
GLL008 Gilles De La Tourette Syndrome 66 0.032
447
c MCR129 Microvascular Complications of Diabetes 1 66 0.032
448
P ATR011 Atrial Fibrillation 66 0.032
449
MYL031 Myeloproliferative Neoplasm 66 0.032
450
c MCL013 Mucolipidosis Iv 66 0.032
451
PRP001 Propionic Acidemia 65 0.032
452
GRN037 Granulomatosis with Polyangiitis 65 0.032
453
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.032
454
MSC007 Muscle Hypertrophy 64 0.032
455
P RHB003 Rhabdomyosarcoma 63 0.032
456
c MLG084 Malignant Fibrous Histiocytoma 63 0.032
457
P CRN300 Coronary Heart Disease 1 63 0.032
458
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.032
459
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.032
460
HMT002 Hematologic Cancer 62 0.032
461
c FNC043 Fanconi Anemia, Complementation Group E 62 0.032
462
P PLY014 Polycystic Kidney Disease 62 0.032
463
P ART023 Arthropathy 62 0.032
464
BRS099 Breast Ductal Carcinoma 62 0.032
465
NRM019 Neuraminidase Deficiency 62 0.032
466
MSL001 Measles 62 0.032
467
NTR005 Nutritional Deficiency Disease 62 0.032
468
ALC006 Alcoholic Hepatitis 61 0.032
469
VRL011 Viral Infectious Disease 61 0.032
470
P SCL018 Scoliosis 60 0.032
471
INT066 Interstitial Lung Disease 60 0.032
472
ACN002 Acanthosis Nigricans 60 0.032
473
RHM001 Rheumatic Fever 60 0.032
474
ORL011 Oral Cancer 60 0.032
475
P THL005 Thalassemia 60 0.032
476
PLM033 Pulmonary Embolism 59 0.032
477
P ALC033 Alcohol Use Disorder 58 0.032
478
P URT039 Urticaria 58 0.032
479
NWB001 Newborn Respiratory Distress Syndrome 58 0.032
480
EYD002 Eye Disease 58 0.032
481
CRV038 Cervical Squamous Cell Carcinoma 58 0.032
482
CNS004 Constipation 58 0.032
483
c DWL002 Dowling-Degos Disease 1 58 0.032
484
LYM027 Lymphopenia 58 0.032
485
P GLL018 Gallbladder Cancer 57 0.032
486
P FNC044 Fanconi Anemia, Complementation Group C 57 0.032
487
GLS018 Glass Syndrome 57 0.032
488
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.032
489
CHK001 Chikungunya 57 0.032
490
P OST122 Osteogenesis Imperfecta, Type Iii 57 0.032
491
VSC002 Vascular Dementia 57 0.032
492
HMR039 Hemorrhage, Intracerebral 57 0.032
493
P PYL005 Pyelonephritis 56 0.032
494
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.032
495
TCK001 Tick-Borne Encephalitis 56 0.032
496
TRN018 Transitional Cell Carcinoma 56 0.032
497
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.032
498
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.032
499
P NRF002 Neurofibromatosis 56 0.032
500
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 56 0.032
501
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.032
502
GLC012 Galactosialidosis 55 0.032
503
NPH009 Nephrolithiasis 55 0.032
504
CHR100 Chronic Ulcer of Skin 55 0.032
505
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 55 0.032
506
HRY003 Hairy Cell Leukemia 55 0.032
507
SYN007 Synovitis 54 0.032
508
PYD001 Pyoderma Gangrenosum 54 0.032
509
CRT017 Cartilage Disease 54 0.032
510
P ICH004 Ichthyosis 54 0.032
511
P TRM003 Tremor 54 0.032
512
P LCH002 Lichen Planus 53 0.032
513
P TCD001 Tic Disorder 53 0.032
514
RHM028 Rheumatic Heart Disease 53 0.032
515
GSG001 Gas Gangrene 53 0.032
516
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.032
517
DYS015 Dysentery 52 0.032
518
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.032
519
THR004 Thrombocytosis 51 0.032
520
P SPP010 Suppressor of Tumorigenicity 3 51 0.032
521
FDL002 Food Allergy 51 0.032
522
LNG031 Lung Benign Neoplasm 51 0.032
523
P PRC012 Pericardial Effusion 51 0.032
524
CRT013 Carotid Stenosis 50 0.032
525
P SCK005 Sickle Cell Disease 50 0.032
526
PYD002 Pyoderma 50 0.032
527
P MYT002 Myotonic Dystrophy 49 0.032
528
P ART018 Aortic Valve Insufficiency 49 0.032
529
PRS129 Prostatic Hyperplasia, Benign 49 0.032
530
INT078 Intracranial Thrombosis 49 0.032
531
c OST121 Osteogenesis Imperfecta, Type Iv 48 0.032
532
HMP001 Hemopericardium 48 0.032
533
VTM002 Vitamin B12 Deficiency 48 0.032
534
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.032
535
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.032
536
MCR018 Microcytic Anemia 47 0.032
537
c INH020 Inherited Metabolic Disorder 47 0.032
538
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.032
539
ATN005 Autonomic Dysfunction 46 0.032
540
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.032
541
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.032
542
HDN002 Head Injury 46 0.032
543
c DRR009 Diarrhea 6 46 0.032
544
c MLG068 Malignant Glioma 46 0.032
545
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.032
546
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.032
547
CRT015 Carotid Artery Occlusion 45 0.032
548
PTT037 Pituitary Tumors 44 0.032
549
PRT011 Protein C Deficiency 44 0.032
550
TNG009 Tongue Squamous Cell Carcinoma 44 0.032
551
OVR063 Overnutrition 44 0.032
552
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.032
553
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.032
554
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.032
555
P HYP265 Hypotonia 43 0.032
556
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.032
557
c MCR112 Microvascular Complications of Diabetes 2 41 0.032
558
CRN322 Coronavirus Infectious Disease 40 0.032
559
HYP264 Hypertonia 38 0.032
560
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.032
561
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.032
562
c MCR211 Microphthalmia, Isolated 6 37 0.032
563
PLC002 Plica Syndrome 36 0.032
564
LCH001 Leech Infestation 35 0.032
565
CHR178 Chromosomal Triplication 35 0.032
566
PRM329 Premature Aging 35 0.032
567
PYR009 Pyridoxine Deficiency Anemia 34 0.032
568
c SCH081 Schizophrenia 6 31 0.032
569
SPS190 Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly 29 0.032
570
HYP346 Hypotrichosis and Recurrent Skin Vesicles 28 0.032
571
CHL079 Children's Interstitial Lung Disease 26 0.032
572
MST020 Mast Cell Activation Syndrome 26 0.032
573
c EPL249 Epileptic Encephalopathy, Early Infantile, 82 23 0.032
574
MYC021 Mycobacterium Xenopi 20 0.032
575
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.032
576
NRL016 Neural Tube Defects 82 0.026
577
CNN003 Conn's Syndrome 79 0.026
578
c ART115 Aortic Valve Disease 1 75 0.026
579
SCK003 Sickle Cell Anemia 74 0.026
580
c MNN043 Meningioma, Familial 74 0.026
581
P CNR004 Cone-Rod Dystrophy 2 73 0.026
582
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.026
583
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.026
584
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.026
585
c LKM063 Leukemia, Chronic Myeloid 72 0.026
586
ACR007 Acromegaly 71 0.026
587
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.026
588
MYL005 Myelofibrosis 70 0.026
589
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.026
590
P HYP061 Hypertrophic Cardiomyopathy 70 0.026
591
CRB037 Cerebral Palsy 69 0.026
592
P OCL013 Oculodentodigital Dysplasia 69 0.026
593
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.026
594
ART016 Aortic Aneurysm 69 0.026
595
MST024 Mastocytosis, Cutaneous 69 0.026
596
MNT001 Mantle Cell Lymphoma 69 0.026
597
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.026
598
SKN019 Skin Melanoma 68 0.026
599
P ESS003 Essential Thrombocythemia 68 0.026
600
BRN024 Bronchitis 68 0.026
601
c INF071 Inflammatory Bowel Disease 1 67 0.026
602
FCT007 Factor Vii Deficiency 67 0.026
603
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.026
604
CRB039 Cerebrovascular Disease 67 0.026
605
P FLL037 Follicular Lymphoma 67 0.026
606
P TRN020 Turner Syndrome 67 0.026
607
MYC006 Mycosis Fungoides 66 0.026
608
ANG054 Angina Pectoris 66 0.026
609
c FML021 Familial Hypercholesterolemia 66 0.026
610
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.026
612
AND002 Androgen Insensitivity Syndrome 66 0.026
613
P HYD006 Hydrocephalus 66 0.026
614
LNG039 Lung Squamous Cell Carcinoma 66 0.026
615
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.026
616
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.026
617
BRR014 Barrett Esophagus 65 0.026
618
c ART101 Aortic Valve Disease 2 65 0.026
619
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.026
620
c WLM013 Wilms Tumor 1 65 0.026
621
P CTS001 Cutis Laxa 65 0.026
622
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 65 0.026
623
c DBT099 Diabetes Mellitus, Type I 65 0.026
624
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.026
625
P DBT009 Diabetes Mellitus 64 0.026
626
NRM005 Neuromuscular Disease 64 0.026
627
OST017 Osteomyelitis 64 0.026
628
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.026
629
P ANR048 Aniridia 1 63 0.026
630
TRN015 Transient Cerebral Ischemia 63 0.026
631
ANR007 Anorexia Nervosa 63 0.026
632
c GLC092 Glaucoma, Primary Open Angle 62 0.026
633
c ALP101 Alpha-Thalassemia 62 0.026
634
P ECT006 Ectodermal Dysplasia 62 0.026
635
c LCL006 Localized Scleroderma 62 0.026
636
P SPN046 Spinal Muscular Atrophy 62 0.026
637
LPP008 Lipoprotein Quantitative Trait Locus 62 0.026
638
P HYP750 Hypertriglyceridemia, Familial 62 0.026
639
P ESP024 Esophagitis 62 0.026
640
P TRC086 Trichohepatoenteric Syndrome 1 62 0.026
641
P ORT004 Orthostatic Intolerance 62 0.026
642
P ACR001 Aicardi-Goutieres Syndrome 62 0.026
643
MNN042 Meningioma, Radiation-Induced 62 0.026
644
CRC021 Carcinosarcoma 62 0.026
645
CHL068 Cholestasis 61 0.026
646
P HYP097 Hyperekplexia 61 0.026
647
c SCL052 Scleroderma, Familial Progressive 61 0.026
648
ALV005 Alveolar Soft Part Sarcoma 61 0.026
649
RCT015 Reactive Arthritis 61 0.026
650
GST033 Gestational Diabetes 61 0.026
651
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.026
652
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.026
653
P KDN017 Kidney Cancer 60 0.026
654
PTN001 Patent Foramen Ovale 60 0.026
655
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.026
656
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.026
657
HPT019 Hepatic Encephalopathy 60 0.026
658
P ALP009 Alopecia Areata 60 0.026
659
VRC005 Varicose Veins 60 0.026
660
P CHR285 Chronic Myelomonocytic Leukemia 60 0.026
661
VGN017 Vaginal Cancer 60 0.026
662
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.026
663
P BRN019 Bernard-Soulier Syndrome 60 0.026
664
P OPT006 Optic Nerve Disease 60 0.026
665
SPP011 Suppression of Tumorigenicity 12 59 0.026
666
P MYC008 Myocarditis 59 0.026
667
P AXN002 Axenfeld-Rieger Syndrome 59 0.026
668
PRT013 Portal Hypertension 59 0.026
669
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.026
670
IDP011 Idiopathic Interstitial Pneumonia 59 0.026
671
P LKD001 Leukodystrophy 59 0.026
672
IGR001 Ige Responsiveness, Atopic 59 0.026
673
PRT058 Pure Autonomic Failure 59 0.026
674
PRN019 Perinatal Necrotizing Enterocolitis 59 0.026
675
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.026
676
c LTN004 Late-Onset Retinal Degeneration 59 0.026
677
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.026
678
VLV032 Vulva Cancer 59 0.026
679
PPT005 Peptic Ulcer Disease 59 0.026
680
CCC001 Coccidioidomycosis 58 0.026
681
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.026
682
CNT047 Contact Dermatitis 58 0.026
683
P MTR012 Mitral Valve Disease 58 0.026
684
P BNC003 Bone Cancer 58 0.026
685
P EXN002 Exanthem 57 0.026
686
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.026
687
BLR008 Bilirubin Metabolic Disorder 57 0.026
688
LYS003 Lysinuric Protein Intolerance 57 0.026
689
c LKM070 Leukemia, Acute Monocytic 57 0.026
690
JPN002 Japanese Encephalitis 57 0.026
691
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.026
692
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.026
693
P CHN012 Chondrosarcoma 56 0.026
694
LST001 Listeriosis 56 0.026
695
HPT046 Hepatic Veno-Occlusive Disease 56 0.026
696
P MLT074 Multiple Endocrine Neoplasia 56 0.026
697
PLS011 Plasmacytoma 56 0.026
698
EXF001 Exfoliation Syndrome 56 0.026
699
c ESS001 Essential Tremor 56 0.026
700
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.026
701
SFT003 Soft Tissue Sarcoma 56 0.026
702
SBC001 Subacute Sclerosing Panencephalitis 56 0.026
703
ORL005 Oral Candidiasis 56 0.026
704
c GRV008 Graves Disease 1 56 0.026
705
MCS002 Mucositis 56 0.026
706
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 55 0.026
707
BRN012 Bronchiolitis Obliterans 55 0.026
708
c PRG126 Progressive Familial Heart Block 55 0.026
709
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.026
710
LMB062 Limb Ischemia 55 0.026
711
c BCT007 Bacterial Meningitis 55 0.026
712
ACT058 Active Peptic Ulcer Disease 55 0.026
713
P SBS003 Substance Abuse 55 0.026
714
FLR002 Filariasis 55 0.026
715
P VNS003 Venous Insufficiency 55 0.026
716
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.026
717
FCT004 Factor Xii Deficiency 55 0.026
718
CHR101 Char Syndrome 55 0.026
719
INT007 Intermediate Coronary Syndrome 55 0.026
720
TRD006 Tardive Dyskinesia 54 0.026
721
P PMP001 Pemphigus 54 0.026
722
THR013 Thoracic Outlet Syndrome 54 0.026
723
PLM010 Pulmonary Edema 54 0.026
724
ANL018 Analbuminemia 54 0.026
725
P ART021 Arteriosclerosis 54 0.026
726
HMS001 Hemosiderosis 54 0.026
727
LYM040 Lymphoblastic Lymphoma 54 0.026
728
SPN008 Spondyloepiphyseal Dysplasia Congenita 54 0.026
729
PRC002 Paracoccidioidomycosis 54 0.026
730
c SPN294 Spinocerebellar Ataxia 1 53 0.026
731
CLR030 Clear Cell Renal Cell Carcinoma 53 0.026
732
CRY001 Cryptogenic Organizing Pneumonia 53 0.026
733
HRT012 Heart Valve Disease 53 0.026
734
P MNC007 Monocytic Leukemia 53 0.026
735
CRH005 Crohn's Colitis 53 0.026
736
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.026
737
MST005 Mastitis 53 0.026
738
P SHR001 Short Bowel Syndrome 53 0.026
739
P HMR003 Hemorrhagic Disease 53 0.026
740
HYP063 Hypersplenism 53 0.026
741
PLT004 Platelet Glycoprotein Iv Deficiency 53 0.026
742
INT075 Intracranial Hypertension 53 0.026
743
P ACT008 Actinic Keratosis 53 0.026
744
GST023 Gastric Ulcer 53 0.026
745
P RTN022 Retinal Vein Occlusion 53 0.026
746
PRP080 Peripheral Artery Disease 53 0.026
747
c GLL024 Gallbladder Disease 1 53 0.026
748
c CNT035 Central Nervous System Disease 52 0.026
749
P ATN002 Autonomic Nervous System Disease 52 0.026
750
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.026
751
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.026
752
DMY004 Demyelinating Disease 52 0.026
753
c ACH041 Achondrogenesis, Type Ii 52 0.026
754
IMP005 Impotence 52 0.026
755
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.026
756
CRT016 Carotid Artery Disease 52 0.026
757
P CNG436 Congenital Disorder of Deglycosylation 52 0.026
758
LGN006 Legionnaire Disease 52 0.026
759
PPT001 Peptic Esophagitis 52 0.026
760
ACT200 Acute Monoblastic Leukemia 52 0.026
761
ART074 Aortic Dissection 52 0.026
762
P OVR049 Ovarian Disease 52 0.026
763
NTR018 Neutrophilia, Hereditary 52 0.026
764
c ACT135 Acute Graft Versus Host Disease 52 0.026
765
c VRL005 Viral Pneumonia 52 0.026
766
SPS003 Spastic Diplegia 51 0.026
768
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.026
769
FCT001 Factor Viii Deficiency 51 0.026
770
PLS009 Plasma Cell Neoplasm 51 0.026
771
THR016 Thrombophlebitis 51 0.026
772
CYS014 Cystadenocarcinoma 51 0.026
773
ESP002 Esophageal Varix 51 0.026
774
CCC002 Coccidiosis 51 0.026
775
P THR015 Thrombophilia 51 0.026
776
P PST095 Post-Thrombotic Syndrome 51 0.026
777
P AST007 Astrocytoma 51 0.026
778
TLR001 Tularemia 51 0.026
779
BHR001 Behr Syndrome 51 0.026
780
SKN013 Skin Benign Neoplasm 51 0.026
781
RLP003 Relapsing Fever 51 0.026
782
HYP781 Hypoascorbemia 51 0.026
783
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 51 0.026
784
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.026
785
HYP081 Hypolipoproteinemia 51 0.026
786
P MMB011 Membranous Nephropathy 50 0.026
787
c PRM012 Primary Polycythemia 50 0.026
788
SPN021 Spinal Meningioma 50 0.026
789
P ECL001 Eclampsia 50 0.026
790
RSP006 Respiratory System Disease 50 0.026
791
HPT014 Hepatorenal Syndrome 50 0.026
792
CRN030 Coronary Stenosis 50 0.026
793
c INF145 Infantile Liver Failure Syndrome 1 50 0.026
794
PRT018 Portal Vein Thrombosis 50 0.026
795
P ACH011 Achondrogenesis 50 0.026
796
MTB004 Metabolic Acidosis 50 0.026
797
P MTH008 Methylmalonic Acidemia 50 0.026
798
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.026
799
PRT129 Prothrombin Deficiency, Congenital 50 0.026
800
c CHR418 Chronic Leukemia 49 0.026
801
c THR090 Thrombocythemia 1 49 0.026
802
c CHR431 Chronic Venous Insufficiency 49 0.026
803
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.026
804
LFT001 Left Bundle Branch Hemiblock 49 0.026
805
CCN002 Cocaine Abuse 49 0.026
806
P OPN001 Open-Angle Glaucoma 49 0.026
807
ACT029 Acute Interstitial Pneumonia 49 0.026
808
P CMP008 Compartment Syndrome 49 0.026
809
HYP043 Hyperandrogenism 48 0.026
810
CCN001 Cocaine Dependence 48 0.026
811
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.026
812
CLC006 Calcinosis 48 0.026
813
INT067 Interstitial Nephritis 48 0.026
814
SPL018 Splenomegaly 48 0.026
815
IGG001 Iga Glomerulonephritis 48 0.026
816
DGN001 Degenerative Disc Disease 48 0.026
817
CHL147 Chlamydia Pneumonia 48 0.026
818
c MTR002 Mitral Valve Insufficiency 48 0.026
819
INT010 Intracranial Embolism 48 0.026
820
ADN009 Adenosquamous Carcinoma 47 0.026
821
DRG003 Drug Dependence 47 0.026
822
CRD001 Cardiac Tamponade 47 0.026
823
P CLL015 Collagen Disease 47 0.026
824
KHN001 Kuhnt-Junius Degeneration 47 0.026
825
IRN004 Iron-Refractory Iron Deficiency Anemia 47 0.026
826
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.026
827
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.026
828
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.026
829
NDL013 Nodular Regenerative Hyperplasia 47 0.026
830
CMP002 Campylobacteriosis 46 0.026
831
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 0.026
832
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.026
833
ALB002 Albinism 46 0.026
834
DDN010 Duodenum Cancer 46 0.026
835
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.026
836
MNT046 Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia 46 0.026
837
P BNG032 Benign Mesothelioma 46 0.026
838
GST010 Gestational Trophoblastic Neoplasm 46 0.026
839
3MC003 3mc Syndrome 46 0.026
840
OBS037 Obesity-Hypoventilation Syndrome 46 0.026
841
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.026
842
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.026
843
KTL001 Keutel Syndrome 45 0.026
844
CYN002 Cyanosis, Transient Neonatal 45 0.026
845
HPT004 Hepatic Coma 45 0.026
846
NWC001 Newcastle Disease 45 0.026
847
IMM136 Immune System Disease 45 0.026
848
SWN001 Swine Influenza 45 0.026
849
BRN032 Brain Glioma 45 0.026
850
ADR012 Adrenal Gland Disease 45 0.026
851
OVR112 Ovarian Germ Cell Cancer 45 0.026
852
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.026
854
CRB008 Cerebral Atherosclerosis 44 0.026
855
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.026
856
c ORT011 Orthostatic Hypotension 1 44 0.026
857
P BCT020 Bacteremia 2 44 0.026
858
c SPR086 Spermatogenic Failure 3 44 0.026
859
FBR054 Fibroma 44 0.026
860
IDP033 Idiopathic Edema 44 0.026
861
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.026
862
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 43 0.026
863
BNM001 Bone Marrow Cancer 43 0.026
864
PLY068 Polysubstance Abuse 43 0.026
865
DNG001 Dengue Shock Syndrome 43 0.026
866
P MJR007 Major Affective Disorder 1 43 0.026
867
TRP009 Triple X Syndrome 42 0.026
868
BNS003 Binswanger's Disease 42 0.026
869
PNM013 Pneumococcal Meningitis 42 0.026
870
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 42 0.026
871
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.026
872
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.026
873
IDP070 Idiopathic Scoliosis 42 0.026
874
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.026
875
GST020 Gastric Antral Vascular Ectasia 41 0.026
876
49X006 49, Xxxxy Syndrome 41 0.026
877
DFF003 Diffuse Scleroderma 41 0.026
878
EST007 Estrogen Resistance 41 0.026
879
PRS063 Paresthesia 41 0.026
880
P RRH023 Rare Hereditary Hemochromatosis 41 0.026
881
LRG008 Large Granular Lymphocyte Leukemia 41 0.026
882
SCR001 Secretory Meningioma 41 0.026
883
P MLG074 Malignant Mesenchymoma 40 0.026
884
c PRK090 Parkinson Disease 3, Autosomal Dominant 40 0.026
885
ANX004 Anoxia 40 0.026
886
HPR006 Heparin Cofactor Ii Deficiency 40 0.026
887
PRT012 Prothrombin Deficiency 40 0.026
888
SPR126 Superior Semicircular Canal Dehiscence 40 0.026
889
ANG049 Angioedema Induced by Ace Inhibitors 40 0.026
890
CLP006 Clopidogrel Resistance 40 0.026
891
PLY100 Polyploidy 40 0.026
892
UTR043 Uterine Sarcoma 39 0.026
893
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.026
894
TRN012 Transient Global Amnesia 39 0.026
895
AMN002 Amino Acid Metabolic Disorder 39 0.026
896
CRN020 Coronary Restenosis 39 0.026
897
P FML340 Familial Episodic Pain Syndrome 39 0.026
898
c PLM022 Pulmonary Valve Insufficiency 39 0.026
899
c HMG029 Hemoglobin Se Disease 39 0.026
900
NRD004 Neurodegeneration Due to Cerebral Folate Transport Deficiency 39 0.026
901
c CHR682 Chronic Bilirubin Encephalopathy 39 0.026
902
c SYS043 Systemic Lupus Erythematosus 1 38 0.026
903
HYP041 Hypochondrogenesis 37 0.026
904
SYS071 Systemic Autoimmune Disease 37 0.026
905
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.026
906
ACT056 Acute Cor Pulmonale 36 0.026
907
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.026
908
TCK003 Tick-Borne Relapsing Fever 35 0.026
909
c NNS007 Nonsyndromic Deafness 35 0.026
910
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.026
911
ATX010 Ataxia Neuropathy Spectrum 34 0.026
912
GRM010 Germ Cells Tumors 34 0.026
913
OVR060 Ovary Epithelial Cancer 34 0.026
914
3MC002 3mc Syndrome 1 33 0.026
915
PHS018 Phosphorylase Kinase Deficiency 33 0.026
916
BNN005 Bunion 33 0.026
917
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.026
918
ALR002 Al-Raqad Syndrome 33 0.026
919
ACT064 Acute Necrotizing Encephalitis 33 0.026
920
c PRS136 Prostate Cancer, Hereditary, 6 33 0.026
921
HND015 Hand Skill, Relative 33 0.026
922
c PRS130 Prostate Cancer, Hereditary, 8 32 0.026
923
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.026
924
P LTT001 Lattice Corneal Dystrophy 31 0.026
925
SNG003 Single Ventricular Heart 30 0.026
926
RSP007 Respiratory Distress Syndrome, Infant 30 0.026
927
PRK005 Prekallikrein Deficiency 29 0.026
928
INT076 Intracranial Sinus Thrombosis 29 0.026
929
ISC001 Ischemic Neuropathy 29 0.026
930
CRD220 Cardiac Valvular Defect, Developmental 29 0.026
931
MYC019 Mycobacterium Marinum 29 0.026
932
c ATR092 Atrial Fibrillation, Familial, 15 28 0.026
933
ENM001 Enamel Caries 28 0.026
934
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.026
935
PRR019 Perioral Myoclonia with Absences 27 0.026
936
CYT018 Cytochrome P450 2d6 Variant 27 0.026
937
MYT019 May-Thurner Syndrome 27 0.026
938
P PLM069 Pulmonary Venous Return Anomaly 26 0.026
939
MLG164 Malignant Epithelial Tumor of Ovary 26 0.026
940
FTL073 Fetal Anticonvulsant Syndrome 26 0.026
941
ATR055 Atrial Septal Aneurysm 25 0.026
942
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.026
943
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.026
944
NRM022 Neurometabolic Disease 25 0.026
945
JVN026 Jeavons Syndrome 24 0.026
946
BLD163 Blood Group, Dombrock System 24 0.026
947
PLM104 Palmoplantar Keratoderma, Nagashima Type 23 0.026
948
INT074 Intracranial Arteriosclerosis 23 0.026
949
ATR024 Atrial Fibrillation and Stroke 22 0.026
950
HML018 Homologous Wasting Disease 22 0.026
951
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.026
952
c BRN144 Bronchiectasis 2 21 0.026
953
BLD165 Blood Group, Colton System 20 0.026
954
AMB007 Amoebic Keratitis 20 0.026
955
BLD137 Blood Group--Ahonen 16 0.026
957
HTR025 Htra1 Disorder 12 0.026
958
SRP007 Serpinopathy 11 0.026
959
SYN164 Syndromic Congenital Sodium Diarrhea 8 0.026
960
P RTT002 Rett Syndrome 80 0.018
961
PFF001 Pfeiffer Syndrome 79 0.018
962
P LYN001 Lynch Syndrome 77 0.018
963
P MDL005 Medulloblastoma 77 0.018
964
c NRF024 Neurofibromatosis, Type I 77 0.018
965
P NNN008 Noonan Syndrome 1 76 0.018
966
c ATR087 Atrial Standstill 1 75 0.018
967
P NJM001 Nijmegen Breakage Syndrome 74 0.018
968
VNH007 Von Hippel-Lindau Syndrome 73 0.018
969
c SPN225 Spondyloarthropathy 1 73 0.018
970
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.018
971
MSC157 Muscular Dystrophy, Duchenne Type 72 0.018
972
OTT002 Otitis Media 72 0.018
973
AGM019 Agammaglobulinemia, X-Linked 71 0.018
974
c EXD008 Exudative Vitreoretinopathy 1 71 0.018
975
WLS001 Wilson Disease 71 0.018
976
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.018
977
P MTC003 Metachromatic Leukodystrophy 70 0.018
978
P CRD224 Cardiofaciocutaneous Syndrome 1 70 0.018
979
P OST001 Osteopetrosis 70 0.018
980
P FRG001 Fragile X Syndrome 70 0.018
981
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.018
982
P MYP004 Myopathy 70 0.018
983
WRN001 Werner Syndrome 69 0.018
984
P PRM011 Primary Ciliary Dyskinesia 69 0.018
985
P TYS001 Tay-Sachs Disease 69 0.018
986
P HYP086 Hypothyroidism 69 0.018
987
P ANG001 Angelman Syndrome 69 0.018
988
c BSL007 Basal Cell Carcinoma 68 0.018
989
CST001 Costello Syndrome 68 0.018
990
PCK003 Pick Disease of Brain 68 0.018
991
P ALP004 Alport Syndrome 68 0.018
992
RCK004 Rickets 68 0.018
993
HYL004 Hyaline Fibromatosis Syndrome 67 0.018
994
GST092 Gastroesophageal Reflux 67 0.018
995
c HYP768 Hyperlipoproteinemia, Type I 67 0.018
996
P CRD119 Cardiac Arrest 67 0.018
997
P CRB048 Cerebral Cavernous Malformations 67 0.018
998
OMN001 Omenn Syndrome 67 0.018
999
FLL027 Fallopian Tube Carcinoma 67 0.018
1000
P BLD062 Bile Duct Cancer 67 0.018
1001
CRP001 Carpal Tunnel Syndrome 67 0.018
1002
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.018
1003
MYX005 Myxoid Liposarcoma 66 0.018
1004
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.018
1005
LBR036 Leber Plus Disease 66 0.018
1006
P CCK001 Cockayne Syndrome 66 0.018
1007
P AGM001 Agammaglobulinemia 65 0.018
1008
DMN031 Dementia, Lewy Body 65 0.018
1009
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.018
1010
P CLD001 Cleidocranial Dysplasia 65 0.018
1011
P PRS038 Personality Disorder 65 0.018
1012
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 0.018
1013
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.018
1014
LYS012 Lysosomal Acid Lipase Deficiency 65 0.018
1015
P CHR071 Charcot-Marie-Tooth Disease 65 0.018
1016
MNK001 Menkes Disease 64 0.018
1017
NRF007 Neurofibroma 64 0.018
1018
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.018
1019
CLF027 Cleft Palate, Isolated 64 0.018
1020
P MST009 Mastocytosis 64 0.018
1021
c JVN010 Juvenile Rheumatoid Arthritis 64 0.018
1022
GT001 Gout 64 0.018
1023
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.018
1024
MGK001 Megakaryocytic Leukemia 64 0.018
1025
HYP020 Hyperprolactinemia 64 0.018
1026
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.018
1027
c DPH024 Diaphragmatic Hernia, Congenital 63 0.018
1028
CYS013 Cystinuria 63 0.018
1029
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.018
1030
TYP007 Typhoid Fever 63 0.018
1031
P HYP069 Hyperparathyroidism 63 0.018
1032
END041 Endometrial Adenocarcinoma 63 0.018
1033
P MVM001 Movement Disease 63 0.018
1034
P END044 Endometriosis 63 0.018
1035
c OPT053 Optic Atrophy 1 63 0.018
1036
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.018
1037
P MCH002 Machado-Joseph Disease 62 0.018
1038
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.018
1039
c ANM038 Anemia, Autoimmune Hemolytic 62 0.018
1040
ASP002 Aspartylglucosaminuria 62 0.018
1041
P PRP029 Porphyria 62 0.018
1042
P DRM010 Dermatomyositis 61 0.018
1043
PSR001 Psoriatic Arthritis 61 0.018
1044
P HYP035 Hypophosphatasia 61 0.018
1045
WST001 West Syndrome 61 0.018
1046
CNV004 Canavan Disease 61 0.018
1047
CHR066 Chronic Fatigue Syndrome 61 0.018
1048
RTN017 Retinal Detachment 61 0.018
1049
APP008 Appendicitis 61 0.018
1050
P HMN010 Hemangioma 61 0.018
1051
NRL005 Neurilemmoma 60 0.018
1052
SHG001 Shigellosis 60 0.018
1053
SZR001 Sezary's Disease 60 0.018
1054
CFF002 Coffin-Lowry Syndrome 60 0.018
1055
TRG002 Trigeminal Neuralgia 60 0.018
1056
P TXP001 Toxoplasmosis 60 0.018
1057
P BNG030 Benign Ependymoma 60 0.018
1058
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.018
1059
c ORF037 Orofaciodigital Syndrome I 60 0.018
1060
c LYN004 Lynch Syndrome I 60 0.018
1061
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 0.018
1062
P SNS001 Sensorineural Hearing Loss 60 0.018
1063
P EMR001 Emery-Dreifuss Muscular Dystrophy 60 0.018
1064
HYD002 Hydronephrosis 60 0.018
1065
ETN001 Eating Disorder 60 0.018
1066
P GLY013 Glycogen Storage Disease 60 0.018
1067
P HRD011 Hereditary Spherocytosis 60 0.018
1068
FCT002 Factor Xi Deficiency 60 0.018
1069
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.018
1070
P BND020 Bone Disease 59 0.018
1071
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 59 0.018
1072
UTR024 Uterine Carcinosarcoma 59 0.018
1073
P SLP005 Sleep Disorder 59 0.018
1074
P PRD006 Prader-Willi Syndrome 59 0.018
1075
P LYM033 Lymphoproliferative Syndrome 59 0.018
1076
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.018
1077
P MLN069