Search results for Citrulline

1172 hits were found for Citrulline

# Family MCID Name MIFTS Score
1
P RHM011 Rheumatoid Arthritis 82 38.610
2
P ART022 Arthritis 71 30.841
3
CTR172 Citrullinemia, Classic 65 20.640
4
CTR030 Citrulline Transport Defect 9 18.733
5
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 16.340
6
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 13.011
7
URC002 Urea Cycle Disorder 51 12.785
8
ATM095 Autoimmune Disease 61 12.301
9
P PRD008 Periodontitis 64 10.855
10
P SHR001 Short Bowel Syndrome 53 9.677
11
PLC002 Plica Syndrome 35 9.550
12
SYN007 Synovitis 55 9.550
13
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 8.808
14
P PLM037 Pulmonary Hypertension 72 8.759
15
LNG099 Lung Disease 62 8.286
16
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 7.883
17
PSR001 Psoriatic Arthritis 62 7.750
18
c JVN010 Juvenile Rheumatoid Arthritis 66 7.736
19
ENT004 Enthesopathy 51 7.701
20
INT066 Interstitial Lung Disease 60 6.623
21
CNN005 Connective Tissue Disease 67 6.204
22
CRH001 Crohn's Disease 80 6.083
23
SPN051 Spondylitis 51 6.053
24
INF009 Inflammatory Spondylopathy 30 6.053
25
c SPN225 Spondyloarthropathy 1 70 5.982
26
PPL052 Papillomatosis, Confluent and Reticulated 34 5.973
27
P LPS004 Lupus Erythematosus 61 5.680
28
P VSC007 Vascular Disease 63 5.649
29
c SYS001 Systemic Lupus Erythematosus 87 5.589
30
P SCK005 Sickle Cell Disease 56 5.469
31
PLM129 Pulmonary Disease, Chronic Obstructive 74 5.469
32
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 5.466
33
ENT011 Enterocolitis 55 5.379
34
48X005 48,xyyy 39 5.363
35
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 5.332
36
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 5.281
37
LYS003 Lysinuric Protein Intolerance 57 5.238
38
P ART023 Arthropathy 61 5.237
39
MCS002 Mucositis 56 5.196
40
PRN019 Perinatal Necrotizing Enterocolitis 60 5.152
41
TXC005 Toxic Shock Syndrome 62 5.081
42
c SCL052 Scleroderma, Familial Progressive 61 5.034
43
ISC004 Ischemia 61 4.962
44
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 4.933
45
HYP266 Hypoxia 57 4.932
46
P INT068 Intestinal Disease 53 4.922
47
P MLT020 Multiple Sclerosis 79 4.835
48
c PRC016 Pre-Eclampsia 65 4.771
49
P MSC005 Muscular Dystrophy 67 4.745
50
P CLC063 Celiac Disease 1 66 4.662
51
P HRT032 Heart Disease 81 4.647
52
SYS071 Systemic Autoimmune Disease 35 4.502
53
IMP005 Impotence 52 4.471
54
P LCT001 Lactic Acidosis 51 4.436
55
P VSC011 Vasculitis 61 4.429
56
47X002 47,xyy 48 4.405
57
CYT002 Cytokine Deficiency 43 4.377
58
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 4.352
59
P ADL010 Adult Respiratory Distress Syndrome 71 4.340
60
P LVR013 Liver Disease 69 4.304
61
P PRN023 Prion Disease 60 4.257
62
P MTC069 Mitochondrial Disorders 57 4.237
63
FTT001 Fatty Liver Disease 62 4.204
64
ULC004 Ulcerative Colitis 74 4.199
65
BRN056 Bronchopulmonary Dysplasia 56 4.175
66
c PRD040 Periodontitis, Chronic 52 4.165
67
ARG002 Argininosuccinic Aciduria 61 4.118
68
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.075
69
P INF037 Inflammatory Bowel Disease 53 4.070
70
ATH013 Atherosclerosis Susceptibility 63 4.043
71
P SPN052 Spondyloarthropathy 55 4.002
72
ALL014 Allergic Encephalomyelitis 34 3.908
73
P PLY041 Polymyositis 59 3.858
74
MTC004 Mitochondrial Encephalomyopathy 42 3.842
75
CHL068 Cholestasis 61 3.836
76
ART140 Arteries, Anomalies of 53 3.829
77
P PLM036 Pulmonary Fibrosis 66 3.827
78
SCK003 Sickle Cell Anemia 74 3.822
79
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.807
80
DFC004 Deficiency Anemia 74 3.745
81
AGN016 Aging 54 3.728
82
c TYP009 Type 2 Diabetes Mellitus 92 3.657
83
P SJG008 Sjogren Syndrome 61 3.655
84
MSC157 Muscular Dystrophy, Duchenne Type 79 3.650
85
c CHR684 Chronic Kidney Disease 69 3.634
86
c HYP595 Hypertension, Essential 85 3.598
87
P DRR001 Diarrhea 55 3.570
88
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.564
89
ANT039 Antisynthetase Syndrome 55 3.530
90
P CRN300 Coronary Heart Disease 1 73 3.523
91
SCR011 Scrapie 39 3.505
92
OCL069 Ocular Motor Apraxia 57 3.503
93
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.451
94
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.451
95
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.451
96
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 3.451
97
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.451
98
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 3.451
99
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.451
100
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 3.451
101
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.451
102
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.451
103
P ALZ034 Alzheimer Disease 87 3.450
104
P ENC018 Encephalopathy 62 3.450
105
ACT228 Acute Radiation Syndrome 30 3.439
106
MTC005 Mitochondrial Metabolism Disease 45 3.394
107
P SYS005 Systemic Scleroderma 74 3.376
108
PLN005 Palindromic Rheumatism 43 3.372
109
PRP027 Peripheral Vascular Disease 71 3.361
110
P MYP004 Myopathy 67 3.343
111
P DBT009 Diabetes Mellitus 67 3.339
112
c HPT001 Hepatitis C 62 3.252
113
CRT072 Creutzfeldt-Jakob Disease 68 3.200
114
RCT015 Reactive Arthritis 61 3.183
115
CRH005 Crohn's Colitis 53 3.173
116
c ACT027 Acute Pancreatitis 60 3.166
117
DMY004 Demyelinating Disease 50 3.166
118
P GRF003 Graft-Versus-Host Disease 71 3.149
119
ATS010 Autosomal Recessive Disease 42 3.132
120
P PSR002 Psoriasis 63 3.091
121
PST011 Pustulosis of Palm and Sole 52 3.091
122
LPP008 Lipoprotein Quantitative Trait Locus 65 3.088
123
c ATM011 Autoimmune Hepatitis 63 3.080
124
PLM134 Pulmonary Fibrosis, Idiopathic 76 3.071
125
BNR002 Bone Resorption Disease 47 3.071
126
P BRN022 Bronchiectasis 60 3.071
127
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 3.036
128
P MSC003 Muscular Atrophy 52 3.010
129
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.989
130
P NTR004 Neutropenia 63 2.986
131
P PNC044 Pancreatitis 61 2.986
132
TTN003 Tetanus 65 2.973
133
P TMP003 Temporal Arteritis 69 2.934
134
MSC152 Muscular Dystrophy, Becker Type 69 2.927
135
P AST005 Asthma 76 2.924
136
PRP080 Peripheral Artery Disease 54 2.900
137
P MYS005 Myositis 56 2.898
138
P ECL001 Eclampsia 52 2.892
139
CLT003 Colitis 63 2.861
140
TNS014 Tenosynovitis 46 2.860
141
c HYP836 Hypercholesterolemia, Familial, 1 73 2.851
142
FLT011 Felty Syndrome 52 2.843
143
BRC012 Brucellosis 66 2.823
144
P DRM010 Dermatomyositis 61 2.819
145
HPT004 Hepatic Coma 43 2.761
146
RYS001 Reye Syndrome 49 2.753
147
LVR012 Liver Cirrhosis 63 2.735
148
c ACT135 Acute Graft Versus Host Disease 51 2.708
149
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 50 2.698
150
NCT003 N-Acetylglutamate Synthase Deficiency 43 2.661
151
ARG007 Argininemia 58 2.660
152
URM002 Uremia 47 2.658
153
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.651
154
BCT022 Bacterial Infectious Disease 56 2.621
155
PRT038 Protein-Energy Malnutrition 53 2.616
156
HYP066 Hyperglycemia 61 2.585
157
HPT019 Hepatic Encephalopathy 59 2.566
158
c HPT073 Hepatitis C Virus 71 2.563
159
P KLZ004 Kala-Azar 1 41 2.559
160
LSH001 Leishmaniasis 64 2.559
161
END086 End Stage Renal Disease 52 2.541
162
P RSP003 Respiratory Failure 74 2.522
163
c TYP008 Type 1 Diabetes Mellitus 70 2.512
164
OST012 Osteoarthritis 77 2.512
165
ORN004 Ornithinemia 13 2.497
166
SPN119 Spondylarthropathy 38 2.494
167
ESN011 Eisenmenger Syndrome 47 2.480
168
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 39 2.471
169
P GLM007 Glomerulonephritis 60 2.471
170
ORT008 Orotic Aciduria 57 2.462
171
LPD008 Lipid Metabolism Disorder 62 2.462
172
P FML018 Familial Mediterranean Fever 73 2.437
173
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.431
174
c MGR028 Migraine with or Without Aura 1 64 2.431
175
P LTR001 Lateral Sclerosis 58 2.431
176
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.425
177
CRB039 Cerebrovascular Disease 66 2.391
178
c CHR464 Chronic Intestinal Failure 24 2.368
179
PRT251 Proteinuria, Chronic Benign 57 2.353
180
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.351
181
PPL022 Papilloma 53 2.349
182
SQM002 Squamous Cell Papilloma 46 2.349
183
P MYC008 Myocarditis 59 2.349
184
PLM031 Poliomyelitis 63 2.326
185
PRT013 Portal Hypertension 59 2.315
186
GT001 Gout 64 2.307
187
MTB004 Metabolic Acidosis 48 2.276
188
MLR004 Malaria 80 2.276
189
SKN016 Skin Disease 63 2.274
190
MXD005 Mixed Connective Tissue Disease 57 2.274
191
P TRN020 Turner Syndrome 67 2.269
192
TBL029 Tubulin, Beta 28 2.263
193
P KDN018 Kidney Disease 72 2.263
194
P ADN016 Adenocarcinoma 63 2.263
195
VSC003 Visceral Leishmaniasis 55 2.246
196
P PRP019 Peripheral Nervous System Disease 58 2.246
197
PRM236 Primary Biliary Cholangitis 60 2.224
198
c HPT016 Hepatitis B 62 2.219
199
BRN002 Bronchiolitis 57 2.173
200
ANX004 Anoxia 40 2.172
201
TRM010 Traumatic Brain Injury 51 2.172
202
HYP060 Hyperinsulinism 54 2.172
203
SPL018 Splenomegaly 49 2.172
204
ANC002 Anca-Associated Vasculitis 44 2.172
205
PYR037 Pyruvate Carboxylase Deficiency 45 2.171
206
P CLR023 Colorectal Cancer 100 2.154
207
P TRM003 Tremor 48 2.154
208
CNG034 Congestive Heart Failure 69 2.154
209
ADL002 Adult Syndrome 70 2.143
210
THR024 Thrombosis 56 2.128
211
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.124
212
c MCR130 Microvascular Complications of Diabetes 6 41 2.124
213
c MCR120 Microvascular Complications of Diabetes 7 47 2.124
214
CLR109 Colorectal Adenocarcinoma 50 2.124
215
c MCR113 Microvascular Complications of Diabetes 3 52 2.124
216
c MCR133 Microvascular Complications of Diabetes 4 41 2.124
217
SCH014 Schistosomiasis 56 2.124
218
BRN004 Brain Edema 54 2.111
219
c DLT002 Dilated Cardiomyopathy 78 2.111
220
c INH020 Inherited Metabolic Disorder 48 2.094
221
RCK004 Rickets 68 2.075
222
P MNN013 Meningitis 65 2.075
223
P HPT021 Hepatitis 69 2.072
224
OST159 Osteogenic Sarcoma 66 2.068
225
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.068
226
P ANT006 Antiphospholipid Syndrome 55 2.068
227
DPR016 Depression 65 2.068
228
CVD001 Covid-19 57 2.066
229
LGH007 Leigh Syndrome 70 2.046
230
SPR126 Superior Semicircular Canal Dehiscence 41 2.026
231
c HMG029 Hemoglobin Se Disease 40 2.026
232
c ACT071 Acute Kidney Failure 60 2.023
233
c RNG008 Ring Chromosome 13 30 2.023
234
c LKM061 Leukemia, Acute Myeloid 83 2.023
235
PRT037 Pertussis 65 2.023
236
SVR004 Severe Combined Immunodeficiency 72 2.023
237
BRN071 Brain Injury 50 2.023
238
P ATR001 Atrioventricular Septal Defect 55 1.979
239
P VNT002 Ventricular Septal Defect 58 1.979
240
HRT011 Heart Septal Defect 49 1.979
241
END057 Endometrial Cancer 72 1.976
242
RHM033 Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis 19 1.976
243
GLM045 Glioma 63 1.976
244
HLX001 Helix Syndrome 48 1.970
245
GNG013 Gingivitis 59 1.970
246
P NRP001 Neuropathy 60 1.945
247
P LPR021 Leprosy 3 71 1.939
248
HNS001 Hansen's Disease 32 1.939
249
ALL006 Allergic Asthma 56 1.929
250
GLL048 Glial Tumor 52 1.929
251
P CRD119 Cardiac Arrest 67 1.929
252
HSH003 Hashimoto Thyroiditis 60 1.915
253
P PNC035 Pancreatic Cancer 86 1.879
254
P MLN008 Melanoma 76 1.879
255
CLN019 Colonic Disease 47 1.879
256
SPN035 Spindle Cell Sarcoma 54 1.857
257
TNS005 Tonsillitis 57 1.857
258
SRC014 Sarcoma 65 1.857
259
P CRD246 Cardiovascular System Disease 56 1.854
260
c ACT134 Acute Liver Failure 59 1.828
261
P OST002 Osteoporosis 76 1.828
262
P EXN002 Exanthem 58 1.828
263
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.828
264
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.828
265
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 1.828
266
P OPN001 Open-Angle Glaucoma 55 1.828
267
P HDC001 Headache 57 1.828
268
DWN001 Down Syndrome 70 1.815
269
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 1.804
270
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.796
271
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 47 1.796
272
PLM001 Pulmonary Tuberculosis 69 1.796
273
BNN003 Bone Inflammation Disease 48 1.796
274
ANK001 Ankylosis 51 1.796
275
MCR088 Microscopic Polyangiitis 51 1.796
276
P LNG032 Lung Cancer 98 1.775
277
CLF027 Cleft Palate, Isolated 64 1.775
278
c SML038 Small Cell Cancer of the Lung 69 1.775
279
c GLC092 Glaucoma, Primary Open Angle 62 1.775
280
CLF001 Cleft Lip 53 1.775
281
FBR047 Fibromyalgia 58 1.775
282
CMB007 Combined Immunodeficiency 57 1.775
283
PRP030 Purpura 54 1.775
284
ACT017 Acute Chest Syndrome 50 1.765
285
INT002 Intermittent Claudication 61 1.759
286
ACR041 Acromelic Frontonasal Dysostosis 53 1.755
287
NWB001 Newborn Respiratory Distress Syndrome 56 1.755
288
CYS013 Cystinuria 66 1.750
289
P AGG001 Aggressive Periodontitis 55 1.738
290
P CTR002 Cataract 60 1.731
291
c THR092 Thrombophilia Due to Thrombin Defect 74 1.719
292
P ORF002 Orofacial Cleft 43 1.719
293
P PRS040 Prostate Cancer 95 1.719
294
P HPT023 Hepatocellular Carcinoma 96 1.719
295
P MYC007 Myocardial Infarction 70 1.719
296
CLF056 Cleft Lip with or Without Cleft Palate 42 1.719
297
P INT070 Intestinal Obstruction 57 1.719
298
P DMN002 Dementia 66 1.719
299
P UVT001 Uveitis 57 1.719
300
RYN005 Raynaud Phenomenon 45 1.719
301
P PNM007 Pneumonia 67 1.686
302
SVR001 Severe Acute Respiratory Syndrome 67 1.665
303
IMM166 Immunodeficiency 27a 60 1.662
304
ISL109 Isolated Cleft Lip 33 1.661
305
P LYM118 Lymphoma 67 1.661
306
P SRC025 Sarcoidosis 1 71 1.661
307
ESP021 Esophageal Cancer 83 1.661
308
URT010 Ureteral Obstruction 45 1.661
309
ORF053 Orofacial Clefting Syndrome 31 1.661
310
INS001 Insulinoma 59 1.661
311
ADN018 Adenoma 59 1.661
312
ALL029 Allergic Disease 59 1.661
313
HGH043 High Grade Glioma 45 1.661
314
NNS002 Nonspecific Interstitial Pneumonia 42 1.661
315
GST045 Gastroenteritis 58 1.661
316
P HYP265 Hypotonia 42 1.661
317
c RNG015 Ring Chromosome 2 22 1.661
318
c JVN061 Juvenile Arthritis 56 1.658
319
LYM133 Lymphoma, Hodgkin, Classic 74 1.600
320
SPN186 Spinal Cord Injury 61 1.600
321
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.600
322
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.600
323
MYL069 Myeloma, Multiple 77 1.600
324
P THY032 Thyroiditis 57 1.600
325
P MTR014 Motor Neuron Disease 65 1.600
326
P BNG032 Benign Mesothelioma 53 1.600
327
VSC002 Vascular Dementia 60 1.600
328
END072 Endotheliitis 36 1.590
329
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.590
330
NNL006 Non-Alcoholic Steatohepatitis 54 1.588
331
IMM167 Immune Deficiency Disease 78 1.588
332
CHC001 Chickenpox 57 1.588
333
c VRL010 Viral Hepatitis 53 1.588
334
CRT015 Carotid Artery Occlusion 45 1.588
335
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.569
336
LYM017 Lyme Disease 62 1.569
337
STR067 Stroke, Ischemic 80 1.551
338
PRT036 Peritonitis 65 1.551
339
STT001 Status Epilepticus 59 1.551
340
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.536
341
ANR007 Anorexia Nervosa 60 1.536
342
P MYC084 Mycobacterium Tuberculosis 1 68 1.536
343
PLY150 Polykaryocytosis Inducer 29 1.536
344
DSS032 Disease by Infectious Agent 55 1.536
345
LNG091 Lung Mucoepidermoid Carcinoma 32 1.536
346
OBS082 Obstructive Nephropathy 41 1.536
347
MCP006 Mucoepidermoid Carcinoma 48 1.536
348
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.536
349
CHG001 Chagas Disease 66 1.536
350
P HYD006 Hydrocephalus 61 1.536
351
HML018 Homologous Wasting Disease 21 1.536
352
P HNT016 Huntington Disease 73 1.505
353
P HYP086 Hypothyroidism 69 1.505
354
GST033 Gestational Diabetes 61 1.505
355
c PRM038 Primary Agammaglobulinemia 47 1.488
356
c SPS158 Spastic Paraplegia 9a, Autosomal Dominant 44 1.485
357
P BLD134 Bladder Cancer 79 1.467
358
SMT004 Smith-Lemli-Opitz Syndrome 70 1.467
359
c ATR087 Atrial Standstill 1 74 1.467
360
c CLC042 Celiac Disease 9 14 1.467
361
P MPL001 Maple Syrup Urine Disease 70 1.467
362
PHN003 Phenylketonuria 76 1.467
363
P BCL017 B-Cell Lymphoma 59 1.467
364
P ACN011 Acne 57 1.467
365
TLN003 Telangiectasis 51 1.467
366
SYS003 Systolic Heart Failure 49 1.467
367
P MYC033 Myoclonus 47 1.467
368
HMP009 Haemophilus Influenzae 41 1.467
369
c MCR115 Microvascular Complications of Diabetes 5 65 1.457
370
AND005 Androgen Insensitivity Syndrome, Mild 21 1.433
371
P DYS154 Dystonia 64 1.419
372
c MTC200 Mitochondrial Dna Depletion Syndrome 17 20 1.413
373
CRB004 Cerebral Artery Occlusion 45 1.407
374
RFR013 Refractory Celiac Disease 33 1.393
375
P HYP111 Hyperprolinemia 45 1.393
376
SXL003 Sexual Disorder 49 1.393
377
HLC007 Helicobacter Pylori Infection 67 1.393
378
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.393
379
P ASP006 Aspergillosis 72 1.393
380
GYR004 Gyrate Atrophy of Choroid and Retina 58 1.393
381
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 1.393
382
GLC003 Glucose Intolerance 54 1.393
383
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.393
384
P MYG005 Myoglobinuria 40 1.393
385
P TRT010 Teratoma 51 1.393
386
MRP001 Morphine Dependence 42 1.393
387
CRY004 Cryoglobulinemia 48 1.393
388
GST023 Gastric Ulcer 52 1.393
389
TLR001 Tularemia 56 1.393
390
RHM014 Rheumatoid Vasculitis 37 1.393
391
P CLS010 Cluster Headache 42 1.393
392
c MYT029 Myotonia Congenita, Autosomal Recessive 40 1.391
393
END021 Endomyocardial Fibrosis 56 1.391
394
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.376
395
P SZR006 Seizure Disorder 70 1.356
396
INS024 Insulin-Like Growth Factor I 78 1.356
397
CYS001 Cystic Fibrosis 78 1.356
398
ART016 Aortic Aneurysm 68 1.356
399
PMP006 Pemphigus Vulgaris, Familial 58 1.319
400
P PMP001 Pemphigus 55 1.319
401
P RBL001 Rubella 58 1.319
402
P EYD002 Eye Disease 57 1.319
403
GST009 Gastroschisis 53 1.313
404
SMT017 Somatomammotropinoma 17 1.313
405
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.313
406
P LKM071 Leukemia, Chronic Lymphocytic 75 1.313
407
P PRK057 Parkinson Disease, Late-Onset 80 1.313
408
HYP780 Hypoadrenocorticism, Familial 61 1.313
410
DST006 Diastolic Heart Failure 45 1.313
411
P ENC004 Encephalitis 61 1.313
412
ABD010 Abdominal Wall Defect 39 1.313
413
BNS003 Binswanger's Disease 41 1.313
414
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.303
415
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.303
416
P HYP750 Hypertriglyceridemia, Familial 62 1.303
417
CHR100 Chronic Ulcer of Skin 57 1.248
418
HYP056 Hypoglycemia 65 1.248
419
NTR005 Nutritional Deficiency Disease 61 1.235
420
INT276 Interatrial Communication 51 1.227
421
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.227
422
P ATR010 Atrial Heart Septal Defect 58 1.227
423
KPS004 Kaposi Sarcoma 77 1.224
424
ARG004 Argyria 26 1.224
426
XLN228 X-Linked Recessive Disease 24 1.224
427
P CHL066 Cholangitis 52 1.224
428
c HMG001 Hemoglobin C Disease 41 1.224
429
UND007 Undifferentiated Connective Tissue Disease 28 1.224
430
P CHR345 Chronic Pain 50 1.224
431
RMT001 Remitting Seronegative Symmetrical Synovitis with Pitting Edema 17 1.224
432
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 32 1.205
433
SPS057 Spasticity 42 1.190
434
HMC014 Homocysteinemia 52 1.190
435
P END033 Endocarditis 58 1.190
436
PLM033 Pulmonary Embolism 58 1.190
437
P DRM053 Dermatitis, Atopic 65 1.128
438
P MJR001 Major Depressive Disorder 68 1.128
439
CHL067 Cholecystitis 60 1.128
440
MNT002 Mental Depression 57 1.128
441
ILS001 Ileus 50 1.128
442
DYS064 Dystonia 3, Torsion, X-Linked 45 1.123
443
c MST023 Mesothelioma, Malignant 56 1.123
444
c SYS045 Systemic Lupus Erythematosus 14 13 1.123
445
KRT019 Keratitis, Hereditary 66 1.123
446
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 53 1.123
447
MLT157 Multiple System Atrophy 1 69 1.123
448
P CRY007 Cryoglobulinemia, Familial Mixed 49 1.123
449
P PRK039 Parkinsonism 55 1.123
450
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 19 1.123
451
P HYP098 Hypereosinophilic Syndrome 66 1.123
452
P CYS018 Cystitis 59 1.123
453
P RTN016 Retinal Degeneration 52 1.123
454
BRN012 Bronchiolitis Obliterans 56 1.123
455
HYP068 Hyperostosis 47 1.123
456
MNN009 Meningoencephalitis 48 1.123
457
SPT004 Septic Arthritis 58 1.123
458
MLT016 Multicentric Reticulohistiocytosis 39 1.123
459
c SVR005 Severe Pre-Eclampsia 50 1.123
460
HRP004 Herpes Zoster 61 1.123
461
KDN013 Kidney Hypertrophy 34 1.123
462
P OVR042 Ovarian Cancer 88 1.064
463
P BRS047 Breast Cancer 98 1.064
464
P ANP001 Anaplastic Large Cell Lymphoma 61 1.064
465
P URN019 Urinary Tract Infection 49 1.064
466
P LKM062 Leukemia, Acute Lymphoblastic 69 1.064
467
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.064
468
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.064
469
P AMY004 Amyloidosis 70 1.064
470
LRN003 Learning Disability 49 1.064
471
RHM036 Rheumatoid Arthritis Interstitial Lung Disease 31 1.064
472
P PLM006 Pulmonary Alveolar Proteinosis 53 1.064
473
BLR001 Biliary Atresia 55 1.064
474
PST106 Post-Cardiac Arrest Syndrome 31 1.064
475
P KDN017 Kidney Cancer 61 1.064
476
SBC016 Subacute Delirium 43 1.064
477
c SCN046 Secondary Short Bowel Syndrome 14 1.036
478
PHS029 Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic 26 1.036
479
GST050 Gastrointestinal System Disease 55 1.028
480
DSR072 Disorder of Energy Metabolism 10 1.013
481
P PRC031 Preeclampsia/eclampsia 1 43 1.013
482
c HYP724 Hyperlipoproteinemia, Type Iii 67 1.013
483
AGG012 Aggressive Nk-Cell Leukemia 46 1.013
484
PST020 Postpoliomyelitis Syndrome 43 1.013
485
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.013
486
P MYS003 Myasthenia Gravis 68 1.004
487
OTT002 Otitis Media 71 1.004
488
CHR005 Chorioamnionitis 50 1.004
489
P FML011 Familial Adenomatous Polyposis 71 1.004
490
CHK001 Chikungunya 60 1.004
491
PMP004 Pemphigus Foliaceus 43 1.004
492
TQP001 Taqi Polymorphism 29 1.004
493
CVT001 Cavitary Optic Disc Anomalies 37 1.004
494
HYD003 Hydrarthrosis 30 1.004
495
P RHB003 Rhabdomyosarcoma 66 1.004
496
INT182 Intermittent Hydrarthrosis 17 1.004
497
IGG001 Iga Glomerulonephritis 50 1.004
498
BRD005 Borderline Leprosy 28 1.004
499
RFL002 Reflex Epilepsy 41 1.004
500
SPP004 Suppurative Cholangitis 23 1.004
501
IDP011 Idiopathic Interstitial Pneumonia 59 1.004
502
LPR001 Lepromatous Leprosy 49 1.004
503
TBR006 Tuberculoid Leprosy 43 1.004
504
P OBS001 Obstructive Jaundice 48 1.004
505
P SCL015 Scleritis 48 1.004
506
PST046 Post-Transplant Lymphoproliferative Disease 53 1.004
507
P PHC003 Pheochromocytoma 69 0.995
508
ADR040 Adrenal Gland Pheochromocytoma 46 0.995
509
GLB002 Glioblastoma 67 0.995
510
PRP016 Paraplegia 52 0.995
511
P LKM002 Leukemia 67 0.995
512
c ACT068 Acute Cystitis 61 0.995
513
P MCR010 Microcephaly 60 0.995
514
P CTS001 Cutis Laxa 65 0.995
515
P ACT105 Acute Mountain Sickness 52 0.995
516
P OVR082 Overgrowth Syndrome 49 0.921
517
INF034 Infective Endocarditis 54 0.921
518
MLD018 Mild Cognitive Impairment 48 0.921
519
VRC005 Varicose Veins 60 0.921
520
P NRB001 Neuroblastoma 66 0.921
521
P HRP006 Herpes Simplex 65 0.921
522
P HML002 Hemolytic Anemia 62 0.921
523
P ALP008 Alopecia 54 0.921
524
P THR014 Thrombocytopenia 66 0.921
525
BLR008 Bilirubin Metabolic Disorder 57 0.921
526
CHL014 Cholera 62 0.921
527
ESP002 Esophageal Varix 51 0.921
528
DSS009 Disseminated Intravascular Coagulation 57 0.921
529
c FML021 Familial Hypercholesterolemia 72 0.921
530
P PLY019 Polyneuropathy 52 0.921
531
ADL030 Adult-Onset Still's Disease 59 0.921
532
IRN002 Iron Metabolism Disease 57 0.921
533
CRB037 Cerebral Palsy 67 0.921
534
AMN006 Aminoaciduria 37 0.921
535
c HMC039 Hemochromatosis, Type 1 73 0.848
536
RST023 Resting Heart Rate, Variation in 40 0.848
537
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.848
538
c RTN047 Retinitis Pigmentosa 18 46 0.848
539
DFF005 Diffuse Large B-Cell Lymphoma 54 0.848
540
CRS005 Crest Syndrome 36 0.848
541
c SPN226 Spondyloarthropathy 2 15 0.848
542
c SYS046 Systemic Lupus Erythematosus 3 18 0.848
543
ALV005 Alveolar Soft Part Sarcoma 61 0.848
544
c PSR033 Psoriasis 12 26 0.848
545
ORB013 Orbital Disease 42 0.848
546
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 0.848
547
P EPL164 Epilepsy 68 0.848
548
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.848
549
EXT034 Extrinsic Allergic Alveolitis 57 0.848
550
c ACT004 Acute Diarrhea 40 0.848
551
CRY001 Cryptogenic Organizing Pneumonia 54 0.848
552
FRZ001 Frozen Shoulder 55 0.848
553
EXS001 Exostosis 49 0.848
554
BRS064 Bursitis 51 0.848
555
SCL011 Sclerosing Keratitis 24 0.848
556
CLC006 Calcinosis 47 0.848
557
P MRC003 Mercury Poisoning 49 0.848
558
RTB001 Rat Bite Fever 26 0.848
559
CHR178 Chromosomal Triplication 34 0.848
560
P RTN008 Retinitis Pigmentosa 80 0.841
561
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 47 0.841
562
RTN017 Retinal Detachment 60 0.841
563
MRF001 Marfan Syndrome 76 0.841
564
P MCR129 Microvascular Complications of Diabetes 1 68 0.841
565
P GST053 Gastric Cancer 83 0.841
566
P GLC113 Galactosemia I 66 0.841
567
P GLM040 Glioma Susceptibility 1 71 0.841
568
HRW001 Hair Whorl 35 0.841
569
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.841
570
ORG002 Organic Acidemia 44 0.841
571
NRR001 Neuroretinitis 42 0.841
572
c ACT075 Acute Myocardial Infarction 56 0.841
573
RTN023 Retinitis 46 0.841
574
P HMC002 Homocystinuria 53 0.841
575
P MYL006 Myeloid Leukemia 61 0.841
576
P MTH008 Methylmalonic Acidemia 52 0.841
577
P BRS044 Breast Adenocarcinoma 58 0.841
578
APP008 Appendicitis 62 0.841
579
MLG079 Malignant Pleural Mesothelioma 42 0.841
580
c MCR112 Microvascular Complications of Diabetes 2 42 0.841
581
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.841
582
P GRV001 Graves' Disease 55 0.841
583
DNT012 Dental Caries 53 0.841
584
PYL006 Pyloric Stenosis 48 0.841
585
MLG169 Malignant Astrocytoma 57 0.841
586
HNC001 Henoch-Schoenlein Purpura 54 0.841
587
P RHN004 Rhinitis 57 0.841
588
THY030 Thyroid Gland Disease 50 0.841
589
P INF032 Infertility 57 0.841
590
P HYP076 Hyperthyroidism 53 0.841
591
P ART021 Arteriosclerosis 54 0.841
592
PLG002 Plague 58 0.841
593
PLM010 Pulmonary Edema 55 0.841
594
KRT001 Keratoconjunctivitis Sicca 50 0.841
595
c MTC014 Mitochondrial Dna Deletion Syndromes 16 0.841
596
THR123 Thrombotic Microangiopathy 40 0.752
597
c SPR086 Spermatogenic Failure 3 46 0.752
598
HYP003 Hypermethioninemia 51 0.752
599
MSC007 Muscle Hypertrophy 64 0.752
600
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.752
601
P CRP001 Carpal Tunnel Syndrome 66 0.752
602
c CTR129 Cataract 31, Multiple Types 36 0.752
603
c SPS159 Spastic Paraplegia 9b, Autosomal Recessive 40 0.752
604
P TYR004 Tyrosinemia 50 0.752
605
PRP007 Priapism 47 0.752
606
PRC013 Pericarditis 53 0.752
607
P GST044 Gastritis 55 0.752
608
ACT049 Acute Disseminated Encephalomyelitis 48 0.752
609
PRP009 Peripartum Cardiomyopathy 55 0.752
610
CRN017 Coronary Thrombosis 46 0.752
611
ASP003 Aseptic Meningitis 50 0.752
612
DYS015 Dysentery 50 0.752
613
PNC001 Pancytopenia 53 0.752
614
ALC006 Alcoholic Hepatitis 61 0.752
615
CNS004 Constipation 56 0.752
616
P HMN010 Hemangioma 62 0.752
617
P NPH012 Nephrotic Syndrome 60 0.752
618
c HRD010 Hereditary Spastic Paraplegia 66 0.752
619
CLN015 Colon Adenocarcinoma 65 0.752
620
HMP001 Hemopericardium 47 0.752
621
CRD001 Cardiac Tamponade 43 0.752
622
P PRC012 Pericardial Effusion 50 0.752
623
ALC005 Alcoholic Pancreatitis 38 0.752
624
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.752
625
SFT003 Soft Tissue Sarcoma 57 0.752
626
BCK006 Back Pain 47 0.752
627
ANR040 Aneurysm 61 0.752
628
c DVL105 Developmental and Epileptic Encephalopathy 82 23 0.733
629
c BLD140 Blood Group, I System 46 0.702
630
CHY002 Chylomicron Retention Disease 64 0.702
631
c INF071 Inflammatory Bowel Disease 1 65 0.702
632
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.702
633
P ATS364 Autism 69 0.652
634
DFF031 Diffuse Alveolar Hemorrhage 31 0.652
635
c SPS042 Spastic Paraplegia 9 21 0.652
636
STN013 Stenotrophomonas Maltophilia Infection 26 0.652
637
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.652
638
PRS127 Pearson Marrow-Pancreas Syndrome 52 0.652
639
P SCH015 Schizophrenia 74 0.652
640
c EXD008 Exudative Vitreoretinopathy 1 71 0.652
641
ALC007 Alcohol Dependence 66 0.652
642
3HY001 3-Hydroxyisobutyric Aciduria 26 0.652
643
P HYP769 Hyperlysinemia, Type I 42 0.652
644
HMN044 Human Immunodeficiency Virus Type 1 78 0.652
645
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.652
646
ANG054 Angina Pectoris 66 0.652
647
P ADL017 Adult T-Cell Leukemia 56 0.652
648
WST001 West Syndrome 59 0.652
649
c CHR711 Chronic Asthma 41 0.652
650
P FTL001 Fetal Alcohol Syndrome 55 0.652
651
KRN002 Kearns-Sayre Syndrome 63 0.652
652
c BRN108 Branchiootic Syndrome 1 62 0.652
654
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.652
655
c CTS041 Cutis Laxa, Autosomal Dominant 3 45 0.652
656
PRT082 Preterm Premature Rupture of the Membranes 57 0.652
657
THY029 Thyroid Carcinoma 51 0.652
658
CWP001 Cowpox 45 0.652
659
CMP010 Complex Regional Pain Syndrome 60 0.652
660
P PLY017 Polyarteritis Nodosa 60 0.652
661
P RNV001 Renovascular Hypertension 49 0.652
662
P CHR012 Chronic Granulomatous Disease 69 0.652
663
VCC001 Vaccinia 47 0.652
664
P CND004 Candidiasis 58 0.652
665
P AGN002 Agnosia 54 0.652
666
PPT005 Peptic Ulcer Disease 58 0.652
667
LYM027 Lymphopenia 56 0.652
668
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.652
669
XRP001 Xerophthalmia 41 0.652
670
PLR008 Pleurisy 50 0.652
671
HMS001 Hemosiderosis 48 0.652
672
P MLN007 Male Infertility 56 0.652
673
ACR007 Acromegaly 70 0.652
674
RTN020 Retinal Vascular Disease 46 0.652
675
NNT012 Neonatal Jaundice 53 0.652
676
URT001 Urethritis 53 0.652
677
IRN001 Iron Deficiency Anemia 58 0.652
678
MST005 Mastitis 53 0.652
679
P FNC004 Fanconi Syndrome 60 0.652
680
BRN024 Bronchitis 67 0.652
681
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.652
682
P CRV039 Cervicitis 52 0.652
683
PLS007 Plasmodium Falciparum Malaria 52 0.652
684
PNN001 Panniculitis 52 0.652
685
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.652
686
P HYP009 Hypertrophic Pyloric Stenosis 41 0.652
687
HDR002 Hidradenitis Suppurativa 54 0.652
688
HDR003 Hidradenitis 50 0.652
689
SQM006 Squamous Cell Carcinoma 60 0.652
690
ISL099 Isolated Methylmalonic Acidemia 36 0.652
691
NRF007 Neurofibroma 64 0.652
692
IRR002 Irritable Bowel Syndrome 65 0.652
693
c LKM005 Leukemia, T-Cell, Chronic 34 0.652
694
P FML187 Familial Hypertension 34 0.652
695
SNG003 Single Ventricular Heart 30 0.532
696
GRW007 Growth Hormone Deficiency 46 0.532
697
ADR022 Adrenomyeloneuropathy 39 0.532
698
P AVS003 Avascular Necrosis 41 0.532
699
SPS019 Spastic Paraparesis 38 0.532
700
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.532
701
FRN006 Frontotemporal Dementia 68 0.532
702
ADR007 Adrenoleukodystrophy 73 0.532
703
c THY107 Thymoma, Familial 42 0.532
704
CRD132 Cardiac Conduction Defect 60 0.532
705
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 56 0.532
706
ALL003 Allergic Rhinitis 67 0.532
707
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.532
708
c PSR029 Psoriasis 9 24 0.532
709
ANX010 Anxiety 70 0.532
710
c PNC108 Pancreatitis, Hereditary 69 0.532
711
BRK010 Burkitt Lymphoma 66 0.532
712
P ATX030 Ataxia-Telangiectasia 80 0.532
713
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.532
714
FDB001 Foodborne Botulism 55 0.532
715
P MLT008 Multinodular Goiter 42 0.532
717
c MJR022 Major Affective Disorder 8 38 0.532
718
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 0.532
719
LMB062 Limb Ischemia 55 0.532
720
TND005 Tendinitis 54 0.532
721
PYR010 Peyronie's Disease 50 0.532
722
P ERY036 Erythema Nodosum 49 0.532
723
c ATS007 Autism Spectrum Disorder 72 0.532
724
P PLY014 Polycystic Kidney Disease 69 0.532
725
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.532
726
APH002 Aphasia 56 0.532
727
ILT001 Ileitis 48 0.532
728
HPT046 Hepatic Veno-Occlusive Disease 62 0.532
729
c ATM022 Autoimmune Myocarditis 36 0.532
730
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.532
731
NRL016 Neural Tube Defects 81 0.532
732
c DPH024 Diaphragmatic Hernia, Congenital 64 0.532
733
PRP001 Propionic Acidemia 65 0.532
734
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.532
735
c MJR024 Major Affective Disorder 9 41 0.532
736
c CHL119 Cholangitis, Primary Sclerosing 58 0.532
737
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.532
738
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.532
739
P SPP010 Suppressor of Tumorigenicity 3 51 0.532
740
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.532
741
P STR020 Strabismus 56 0.532
742
P UNC017 Uncombable Hair Syndrome 1 32 0.532
743
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.532
744
P CRC039 Coarctation of Aorta 46 0.532
745
DNB001 Danubian Endemic Familial Nephropathy 41 0.532
746
MYL057 Myelopathy, Htlv-1-Associated 38 0.532
747
HND015 Hand Skill, Relative 30 0.532
748
P HRS035 Hirschsprung Disease 1 66 0.532
750
PLM124 Pulmonary Hypertension, Neonatal 20 0.532
751
OST017 Osteomyelitis 63 0.532
752
P PLY188 Polyendocrinopathy 31 0.532
753
PMP014 Pemphigoid 51 0.532
754
P MYP006 Myopia 56 0.532
755
P LCH002 Lichen Planus 54 0.532
756
INT075 Intracranial Hypertension 53 0.532
757
ACH005 Achalasia 55 0.532
758
MCH006 Mechanical Strabismus 40 0.532
759
KRT006 Keratoconjunctivitis 53 0.532
760
P MTC133 Mitochondrial Myopathy 50 0.532
761
DBT010 Diabetic Neuropathy 54 0.532
762
P RRH023 Rare Hereditary Hemochromatosis 54 0.532
763
P ALC033 Alcohol Use Disorder 61 0.532
764
P PTT006 Pituitary Adenoma 55 0.532
765
P BPL003 Bipolar Disorder 56 0.532
766
P FBR017 Fibrosarcoma 56 0.532
767
P MST009 Mastocytosis 64 0.532
768
PNM008 Pneumothorax 54 0.532
769
CRV038 Cervical Squamous Cell Carcinoma 58 0.532
770
P SYP003 Syphilis 59 0.532
771
HRT012 Heart Valve Disease 53 0.532
772
P NLD001 Nail Disease 51 0.532
773
c VRL007 Viral Encephalitis 50 0.532
774
P INF038 Influenza 68 0.532
775
BLL006 Bullous Pemphigoid 61 0.532
776
P MMB011 Membranous Nephropathy 50 0.532
777
P CRN024 Corneal Disease 44 0.532
778
NSP002 Nasopharyngitis 45 0.532
779
c ATM104 Autoimmune Vasculitis 37 0.532
780
INT060 Intestinal Atresia 41 0.532
781
P HYP061 Hypertrophic Cardiomyopathy 69 0.532
782
GTR002 Goiter 53 0.532
783
TRN015 Transient Cerebral Ischemia 63 0.532
784
P PST095 Post-Thrombotic Syndrome 51 0.532
785
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.532
786
P SCL009 Sclerosing Cholangitis 48 0.532
787
NRT004 Neuritis 53 0.532
788
HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.532
789
KRT009 Keratosis 53 0.532
790
GLS001 Gliosarcoma 64 0.532
791
PPL018 Papillary Adenocarcinoma 44 0.532
792
P INT143 Interstitial Cystitis 60 0.532
793
PRS036 Parasitic Protozoa Infectious Disease 44 0.532
794
HPT014 Hepatorenal Syndrome 49 0.532
795
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.532
796
P BND020 Bone Disease 59 0.532
797
PLP001 Pulpitis 48 0.532
798
CHL123 Chlamydia 58 0.532
799
P CHN059 Chondrocalcinosis 52 0.532
800
c VRL005 Viral Pneumonia 53 0.532
801
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.532
802
OST016 Osteochondrosis 52 0.532
803
BRS099 Breast Ductal Carcinoma 61 0.532
804
CYS009 Cystadenoma 43 0.532
805
ACR005 Acrodermatitis 38 0.532
806
P THY023 Thymoma 64 0.532
807
c CNT035 Central Nervous System Disease 54 0.532
808
MDD011 Mood Disorder 62 0.532
809
DRM006 Dermatitis 62 0.532
810
TRP002 Tropical Spastic Paraparesis 49 0.532
811
TYP007 Typhoid Fever 64 0.532
812
P GND004 Gonadal Dysgenesis 47 0.532
813
EXC002 Exocrine Pancreatic Insufficiency 42 0.532
814
FML035 Familial Hyperlipidemia 55 0.532
815
MGC001 Megacolon 48 0.532
816
AMN003 Amnestic Disorder 54 0.532
817
QDR001 Quadriplegia 50 0.532
818
HYP014 Hyperuricemia 51 0.532
819
HYP080 Hypogonadism 50 0.532
820
HST011 Histoplasmosis 55 0.532
821
PST028 Post-Traumatic Stress Disorder 59 0.532
822
NCR007 Necrotizing Fasciitis 49 0.532
823
HYP141 Hyperphenylalaninemia 42 0.532
824
P INS002 in Situ Carcinoma 53 0.532
825
FSC004 Fasciitis 49 0.532
826
P TXP001 Toxoplasmosis 60 0.532
827
STM007 Stomatitis 54 0.532
828
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.532
829
MST020 Mast Cell Activation Syndrome 28 0.532
830
TRC096 Trichothiodystrophy 55 0.532
831
HDN002 Head Injury 44 0.532
832
MCR225 Macrophage Activation Syndrome 45 0.532
833
c ATM075 Autoimmune Encephalitis 40 0.532
834
ENT007 Enteropathica 25 0.532
835
P NRV007 Nervous System Disease 67 0.532
836
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.532
837
MTT004 Metatarsus Adductus 17 0.532
838
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.496
839
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.496
840
P ANR048 Aniridia 1 64 0.496
841
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.496
842
c DRR009 Diarrhea 6 45 0.496
843
TRP004 Tropical Sprue 39 0.496
844
ENT001 Enterocele 42 0.496
845
P CMP008 Compartment Syndrome 50 0.496
846
P CLL015 Collagen Disease 48 0.496
847
RSP007 Respiratory Distress Syndrome, Infant 40 0.496
848
DDN006 Duodenitis 50 0.496
849
c ATS392 Autosomal Recessive Cutis Laxa Type Iii 48 0.472
850
GRN020 Granulomatous Hypophysitis 14 0.472
851
DMN042 Diaminopentanuria 14 0.376
852
RNL024 Renal Glucosuria 60 0.376
853
CLF004 Cleft Lip/palate 57 0.376
854
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.376
855
PCH007 Pouchitis 42 0.376
856
P NNT042 Neonatal Lupus Erythematosus 37 0.376
857
ERY014 Erythrokeratoderma 26 0.376
858
MTR087 Maternal Uniparental Disomy 28 0.376
859
P HRD217 Hereditary Optic Neuropathy 36 0.376
860
GRN033 Granulomatous Mastitis 32 0.376
861
c INH030 Inherited Retinal Disorder 28 0.376
862
SMT007 Smith-Fineman-Myers Syndrome 32 0.376
863
THP001 Thiopurine S Methyltranferase Deficiency 20 0.376
864
P THL005 Thalassemia 56 0.376
865
SDD008 Sudden Sensorineural Hearing Loss 41 0.376
866
CNG491 Congenital Portosystemic Shunt 17 0.376
867
PFF001 Pfeiffer Syndrome 77 0.376
868
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.376
869
P NSP012 Nasopharyngeal Carcinoma 61 0.376
870
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 0.376
871
FMR004 Fumarase Deficiency 50 0.376
872
c DRM040 Dermatitis Herpetiformis, Familial 35 0.376
873
BRT054 Brittle Bone Disorder 74 0.376
874
LPM012 Lipomatosis, Multiple 60 0.376
875
P MCR364 Macrodactyly 40 0.376
876
PRL019 Prolidase Deficiency 50 0.376
877
CRD002 Cri-Du-Chat Syndrome 49 0.376
878
EPD002 Epidermolytic Hyperkeratosis 56 0.376
879
GST092 Gastroesophageal Reflux 61 0.376
880
VLV047 Volvulus of Midgut 52 0.376
881
P PTY003 Pityriasis Rubra Pilaris 57 0.376
882
PRG071 Progressive Pseudorheumatoid Dysplasia 45 0.376
883
c FNC027 Fanconi Anemia, Complementation Group a 81 0.376
884
ISV001 Isovaleric Acidemia 54 0.376
885
HYP001 Hypochromic Microcytic Anemia 37 0.376
886
FTL006 Fetal Alcohol Spectrum Disorder 43 0.376
887
MNT001 Mantle Cell Lymphoma 67 0.376
888
MYL009 Myelodysplastic Syndrome 67 0.376
889
BTN004 Biotin Deficiency 45 0.376
890
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.376
891
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.376
892
KSH004 Kashin-Beck Disease 38 0.376
894
ART074 Aortic Dissection 53 0.376
895
C1N001 C1 Inhibitor Deficiency 43 0.376
896
APR001 Apraxia 52 0.376
897
P ATR011 Atrial Fibrillation 66 0.376
898
RSP021 Respiratory Allergy 41 0.376
899
P LYM033 Lymphoproliferative Syndrome 59 0.376
900
INT072 Intestinal Pseudo-Obstruction 62 0.376
901
HYP025 Hyperphosphatemia 48 0.376
902
P BRC006 Brachydactyly 51 0.376
903
LMB024 Limbic Encephalitis 43 0.376
904
c RTN041 Retinitis Pigmentosa 11 42 0.376
905
P FNC044 Fanconi Anemia, Complementation Group C 56 0.376
906
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.376
907
GLT014 Glutathionuria 37 0.376
908
GDP001 Goodpasture Syndrome 55 0.376
909
TRD006 Tardive Dyskinesia 53 0.376
910
c GRV008 Graves Disease 1 54 0.376
911
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.376
912
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.376
913
c CHR320 Chiari Malformation Type I 46 0.376
914
ICH001 Ichthyosis Vulgaris 53 0.376
915
SPN019 Spondylolisthesis 52 0.376
916
P PRD006 Prader-Willi Syndrome 61 0.376
917
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.376
918
LGH019 Light Fixation Seizure Syndrome 27 0.376
919
LNG108 Langerhans Cell Histiocytosis 58 0.376
920
BLD063 Bile Duct Cysts 42 0.376
921
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 0.376
922
AKL001 Au-Kline Syndrome 39 0.376
923
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.376
924
EWN003 Ewing Sarcoma 70 0.376
925
TMP012 Temple Syndrome 38 0.376
926
ACT119 Acute Promyelocytic Leukemia 62 0.376
927
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 31 0.376
928
c SYS040 Systemic Lupus Erythematosus 10 22 0.376
929
SCC002 Saccharopinuria 26 0.376
930
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.376
931
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.376
932
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.376
933
P HRT035 Heart Block, Congenital 43 0.376
934
c PLM167 Pulmonary Venoocclusive Disease 2, Autosomal Recessive 38 0.376
935
P HYP058 Hypervitaminosis a 47 0.376
936
INT303 Intracranial Hypertension, Idiopathic 56 0.376
937
LRN002 Laron Syndrome 63 0.376
938
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.376
939
P PLM085 Pulmonary Hemosiderosis 44 0.376
940
P MJR007 Major Affective Disorder 1 42 0.376
941
INC002 Inclusion Body Myositis 57 0.376
942
CMP040 Complement Component 4, Partial Deficiency of 34 0.376
943
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.376
944
DMN031 Dementia, Lewy Body 65 0.376
945
DYS053 Dystelephalangy 14 0.376
946
P PYR039 Peyronie Disease 39 0.376
947
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 40 0.376
948
c SYS069 Systemic Lupus Erythematosus 6 21 0.376
949