Search results for Threonine

2583 hits were found for Threonine

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.169
2
HLX001 Helix Syndrome 47 3.927
3
TLN003 Telangiectasis 51 3.504
4
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.502
5
P ATX030 Ataxia-Telangiectasia 80 3.440
6
P RTN024 Retinoblastoma 72 2.879
7
P MYC084 Mycobacterium Tuberculosis 1 68 2.820
8
PTZ001 Peutz-Jeghers Syndrome 69 2.792
9
P PNC035 Pancreatic Cancer 87 2.787
10
P LNG032 Lung Cancer 98 2.654
11
AGN016 Aging 53 2.628
12
GLM045 Glioma 62 2.613
13
GLL048 Glial Tumor 51 2.598
14
P NRB001 Neuroblastoma 66 2.569
15
P OVR042 Ovarian Cancer 88 2.552
16
c HYP595 Hypertension, Essential 84 2.454
17
SQM006 Squamous Cell Carcinoma 59 2.450
18
P CLR023 Colorectal Cancer 100 2.445
19
VCC001 Vaccinia 49 2.415
20
P GST053 Gastric Cancer 82 2.334
21
CYT002 Cytokine Deficiency 43 2.330
22
FTT001 Fatty Liver Disease 61 2.321
23
HMN044 Human Immunodeficiency Virus Type 1 76 2.308
24
c TRC125 Trichothiodystrophy 7, Nonphotosensitive 19 2.294
25
c LKM061 Leukemia, Acute Myeloid 83 2.136
26
P LTR001 Lateral Sclerosis 57 2.105
27
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.102
28
P BRS047 Breast Cancer 97 2.100
29
CLT003 Colitis 63 2.072
30
P ALZ034 Alzheimer Disease 87 2.034
31
ULC004 Ulcerative Colitis 74 2.020
32
HYP266 Hypoxia 56 2.012
33
CRH001 Crohn's Disease 80 2.004
34
GLB002 Glioblastoma 67 1.986
35
P HRP006 Herpes Simplex 65 1.981
36
OST159 Osteogenic Sarcoma 66 1.924
37
48X005 48,xyyy 39 1.919
38
47X002 47,xyy 47 1.915
39
PPL052 Papillomatosis, Confluent and Reticulated 34 1.852
40
HYP005 Hypokalemia 55 1.831
41
P ADN016 Adenocarcinoma 63 1.830
42
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 50 1.819
43
P PRS040 Prostate Cancer 95 1.816
44
P MYL006 Myeloid Leukemia 60 1.812
45
IMM167 Immune Deficiency Disease 76 1.811
46
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 57 1.802
47
P HPT021 Hepatitis 68 1.797
48
ORL015 Oral Squamous Cell Carcinoma 43 1.780
49
P MLN008 Melanoma 75 1.745
50
P PHC003 Pheochromocytoma 70 1.737
51
P LKM002 Leukemia 65 1.733
52
c DPH024 Diaphragmatic Hernia, Congenital 63 1.726
53
ADR040 Adrenal Gland Pheochromocytoma 45 1.700
54
ISC004 Ischemia 61 1.666
55
P BCL017 B-Cell Lymphoma 57 1.659
56
c HPT073 Hepatitis C Virus 70 1.657
57
PRT037 Pertussis 49 1.647
58
CRH005 Crohn's Colitis 53 1.644
59
P HPT023 Hepatocellular Carcinoma 95 1.639
60
P LNG064 Lung Cancer Susceptibility 3 69 1.631
61
c PCH010 Pachyonychia Congenita 3 43 1.625
62
P GLM040 Glioma Susceptibility 1 70 1.621
63
INS024 Insulin-Like Growth Factor I 77 1.615
64
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.596
65
ALL029 Allergic Disease 61 1.567
66
STM007 Stomatitis 52 1.522
67
SPN035 Spindle Cell Sarcoma 51 1.498
68
SRC014 Sarcoma 64 1.498
69
HYP066 Hyperglycemia 60 1.494
70
P BLD134 Bladder Cancer 79 1.491
71
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.481
72
P LKM071 Leukemia, Chronic Lymphocytic 74 1.477
73
c MJR022 Major Affective Disorder 8 37 1.476
74
c MJR024 Major Affective Disorder 9 40 1.476
75
P BPL003 Bipolar Disorder 56 1.476
76
P INF038 Influenza 68 1.474
77
SPS057 Spasticity 43 1.467
78
SVR004 Severe Combined Immunodeficiency 70 1.466
79
c SML038 Small Cell Cancer of the Lung 68 1.464
80
THY029 Thyroid Carcinoma 55 1.461
81
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.440
82
P MYT002 Myotonic Dystrophy 51 1.436
83
c INF071 Inflammatory Bowel Disease 1 65 1.434
84
INS001 Insulinoma 59 1.419
85
P RTN016 Retinal Degeneration 52 1.412
86
P PLY019 Polyneuropathy 52 1.408
87
P LYM118 Lymphoma 66 1.405
88
FRN006 Frontotemporal Dementia 68 1.400
89
P ENC018 Encephalopathy 62 1.399
90
MLR004 Malaria 77 1.397
91
END057 Endometrial Cancer 76 1.391
92
P KDN017 Kidney Cancer 60 1.386
93
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.381
94
HYP060 Hyperinsulinism 53 1.376
95
ANT024 Anthrax Disease 57 1.364
96
P TMR010 Tumor Predisposition Syndrome 69 1.352
97
INH023 Inherited Cancer-Predisposing Syndrome 53 1.352
98
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 1.346
99
P PRK057 Parkinson Disease, Late-Onset 79 1.336
100
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.333
101
P AMY004 Amyloidosis 69 1.333
102
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.331
103
c HPT001 Hepatitis C 61 1.326
104
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.321
105
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.321
106
P HNT016 Huntington Disease 73 1.310
107
P GLM007 Glomerulonephritis 59 1.309
108
NTR005 Nutritional Deficiency Disease 60 1.304
109
CHL014 Cholera 62 1.270
110
NWC001 Newcastle Disease 47 1.254
111
P FBR017 Fibrosarcoma 55 1.251
112
GLC003 Glucose Intolerance 53 1.239
113
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.233
114
P PRR016 Pierre Robin Syndrome 50 1.229
115
c MCR133 Microvascular Complications of Diabetes 4 41 1.223
116
c MCR113 Microvascular Complications of Diabetes 3 52 1.223
117
c MCR130 Microvascular Complications of Diabetes 6 41 1.223
118
c MCR120 Microvascular Complications of Diabetes 7 47 1.223
119
TRT001 Teratocarcinoma 41 1.218
120
c HYP836 Hypercholesterolemia, Familial, 1 73 1.206
121
P LVR013 Liver Disease 68 1.206
122
P ACN011 Acne 55 1.199
123
c LKM063 Leukemia, Chronic Myeloid 70 1.188
124
EMB004 Embryonal Carcinoma 55 1.185
125
PYD002 Pyoderma 49 1.177
126
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.172
127
NRN004 Neuroendocrine Tumor 55 1.170
128
c HPT003 Hepatitis a 63 1.170
129
P KLZ004 Kala-Azar 1 41 1.170
130
LSH001 Leishmaniasis 63 1.170
131
MSL001 Measles 61 1.170
132
VSC002 Vascular Dementia 59 1.162
133
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.156
134
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.155
135
P OTS014 Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant 52 1.155
136
ADL002 Adult Syndrome 69 1.155
137
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 52 1.155
138
ENT001 Enterocele 42 1.155
139
ISL075 Isolated Pierre Robin Sequence 29 1.155
140
PYD001 Pyoderma Gangrenosum 53 1.154
141
CCC002 Coccidiosis 50 1.154
142
THR118 Threoninemia 14 1.146
143
MLG169 Malignant Astrocytoma 57 1.133
144
c HPT016 Hepatitis B 62 1.133
145
P LKM062 Leukemia, Acute Lymphoblastic 69 1.129
146
P INF037 Inflammatory Bowel Disease 53 1.128
147
P NSP012 Nasopharyngeal Carcinoma 60 1.116
148
BCT022 Bacterial Infectious Disease 55 1.116
149
MLD018 Mild Cognitive Impairment 48 1.112
150
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.110
151
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.110
152
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.110
153
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.110
154
P PLM037 Pulmonary Hypertension 69 1.110
155
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.110
156
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.110
157
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.110
158
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.110
159
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.110
160
BNR002 Bone Resorption Disease 47 1.110
161
P MLT074 Multiple Endocrine Neoplasia 58 1.110
162
PRT251 Proteinuria, Chronic Benign 58 1.097
163
DWN001 Down Syndrome 70 1.094
164
P HYP750 Hypertriglyceridemia, Familial 61 1.094
165
ACT098 Acute Erythroid Leukemia 55 1.085
166
CHL065 Cholangiocarcinoma 57 1.078
167
INT079 Intrahepatic Cholangiocarcinoma 51 1.078
168
P NRP001 Neuropathy 59 1.071
169
P RTN008 Retinitis Pigmentosa 79 1.058
170
DFF005 Diffuse Large B-Cell Lymphoma 55 1.058
171
TXC005 Toxic Shock Syndrome 61 1.058
172
P ESP024 Esophagitis 60 1.052
173
RBS001 Rabies 57 1.052
174
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.051
175
P SKN015 Skin Carcinoma 71 1.045
176
NRR001 Neuroretinitis 42 1.044
177
c ACT073 Acute Leukemia 59 1.044
178
RTN023 Retinitis 45 1.044
179
P MLN007 Male Infertility 56 1.037
180
P CTR002 Cataract 59 1.037
181
CDK006 Cdkl5 Deficiency Disorder 30 1.030
182
TRM010 Traumatic Brain Injury 50 1.029
183
STT001 Status Epilepticus 58 1.029
184
MYL069 Myeloma, Multiple 76 1.027
185
P EPL164 Epilepsy 70 1.022
186
c INH020 Inherited Metabolic Disorder 47 1.014
187
URM002 Uremia 47 0.998
188
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.995
189
ILT001 Ileitis 49 0.990
190
CHG001 Chagas Disease 65 0.973
191
SLP001 Sleeping Sickness 56 0.973
192
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 0.969
193
P PSD003 Pseudohypoaldosteronism 45 0.969
194
PTT037 Pituitary Tumors 44 0.964
195
P FML011 Familial Adenomatous Polyposis 70 0.958
196
c THY107 Thymoma, Familial 42 0.958
197
P THY023 Thymoma 64 0.958
198
P VSC007 Vascular Disease 62 0.958
199
CHL123 Chlamydia 58 0.955
200
ARG004 Argyria 26 0.955
201
P DMN002 Dementia 65 0.946
202
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.946
203
P LNG028 Long Qt Syndrome 63 0.946
204
P HRT032 Heart Disease 84 0.946
205
P MCR010 Microcephaly 59 0.946
206
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.936
207
TRY001 Trypanosomiasis 50 0.936
208
CNG034 Congestive Heart Failure 69 0.936
209
SCH014 Schistosomiasis 56 0.936
210
DWR001 Dwarfism 44 0.936
211
P PLM036 Pulmonary Fibrosis 65 0.929
212
c TYP008 Type 1 Diabetes Mellitus 77 0.926
213
TNP004 Tn Polyagglutination Syndrome 42 0.925
214
P MSC003 Muscular Atrophy 52 0.921
215
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.915
216
CRD223 Cardiac Arrhythmia 63 0.915
217
ESP021 Esophageal Cancer 84 0.905
218
ADN018 Adenoma 58 0.905
219
ALC007 Alcohol Dependence 65 0.904
220
c DLT002 Dilated Cardiomyopathy 79 0.898
221
HYP524 Hypoinsulinemic Hypoglycemia with Hemihypertrophy 24 0.895
222
MTH040 Methylmalonyl-Coa Epimerase Deficiency 27 0.895
223
LST001 Listeriosis 59 0.893
224
P ATR011 Atrial Fibrillation 66 0.881
225
P GLL018 Gallbladder Cancer 59 0.881
226
ACQ007 Acquired Immunodeficiency Syndrome 58 0.881
227
CHL045 Choline Deficiency Disease 39 0.880
228
CHC001 Chickenpox 56 0.879
229
ARG007 Argininemia 58 0.873
230
MTC115 Mitochondrial Myopathy, Lethal, Infantile 22 0.873
231
c TYP009 Type 2 Diabetes Mellitus 91 0.872
232
THY111 Thyroid Carcinoma, Familial Medullary 67 0.872
233
P PRK039 Parkinsonism 55 0.872
234
c AMY094 Amyotrophic Lateral Sclerosis 5, Juvenile 31 0.868
235
KRT009 Keratosis 52 0.868
236
BRK010 Burkitt Lymphoma 65 0.865
237
CRV035 Cervical Cancer 72 0.865
238
ALL014 Allergic Encephalomyelitis 34 0.865
239
RNL077 Renal Fibrosis 46 0.858
240
P KDN018 Kidney Disease 71 0.858
241
THY125 Thyroid Gland Medullary Carcinoma 48 0.858
242
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.855
243
PRM329 Premature Aging 36 0.855
244
c ATS007 Autism Spectrum Disorder 71 0.851
245
SPN186 Spinal Cord Injury 60 0.851
246
P SCH015 Schizophrenia 74 0.844
247
c BRN108 Branchiootic Syndrome 1 63 0.844
248
ORL011 Oral Cancer 60 0.844
249
MYL009 Myelodysplastic Syndrome 67 0.838
250
SKN016 Skin Disease 63 0.837
251
CYS001 Cystic Fibrosis 77 0.829
252
P SPP010 Suppressor of Tumorigenicity 3 50 0.829
253
P ADL010 Adult Respiratory Distress Syndrome 70 0.829
254
EPD002 Epidermolytic Hyperkeratosis 55 0.824
255
HGH043 High Grade Glioma 46 0.822
256
HMP009 Haemophilus Influenzae 41 0.821
257
HYP056 Hypoglycemia 65 0.821
258
CNG503 Congenital Heart Defects and Ectodermal Dysplasia 21 0.821
259
PHS018 Phosphorylase Kinase Deficiency 37 0.821
260
HPT004 Hepatic Coma 43 0.814
261
P OPT006 Optic Nerve Disease 57 0.814
262
P PYL005 Pyelonephritis 56 0.807
263
P CHR012 Chronic Granulomatous Disease 69 0.807
264
MYC019 Mycobacterium Marinum 29 0.807
265
DFC004 Deficiency Anemia 74 0.806
266
c SYS001 Systemic Lupus Erythematosus 85 0.806
267
CHR074 Choriocarcinoma 46 0.806
268
P OVR082 Overgrowth Syndrome 41 0.806
269
P NRF002 Neurofibromatosis 60 0.797
270
P PRP019 Peripheral Nervous System Disease 57 0.789
271
P GST044 Gastritis 55 0.789
272
PNC129 Pancreatic Adenocarcinoma 64 0.789
273
P ENC004 Encephalitis 61 0.789
274
P LPS004 Lupus Erythematosus 61 0.789
275
PLY100 Polyploidy 36 0.789
276
SFT003 Soft Tissue Sarcoma 43 0.788
277
CRT015 Carotid Artery Occlusion 45 0.787
278
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 37 0.787
279
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.780
280
HMC014 Homocysteinemia 52 0.780
281
ENT011 Enterocolitis 55 0.780
282
P WSK001 Wiskott-Aldrich Syndrome 72 0.780
283
NNL006 Non-Alcoholic Steatohepatitis 54 0.780
284
PRM013 Premature Menopause 57 0.780
285
PRN019 Perinatal Necrotizing Enterocolitis 60 0.780
286
CHR178 Chromosomal Triplication 33 0.780
288
OST012 Osteoarthritis 77 0.779
289
DMY004 Demyelinating Disease 50 0.771
290
GST033 Gestational Diabetes 60 0.771
291
OVR094 Ovarian Epithelial Cancer 39 0.771
292
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.762
293
LYM133 Lymphoma, Hodgkin, Classic 69 0.762
294
AVN001 Avian Influenza 61 0.762
295
P MLT020 Multiple Sclerosis 79 0.753
296
P BRS044 Breast Adenocarcinoma 58 0.753
297
P PRN023 Prion Disease 60 0.753
298
P PSR002 Psoriasis 63 0.753
299
P ATS364 Autism 72 0.743
300
P RTT002 Rett Syndrome 79 0.743
301
c PSD092 Pseudohypoaldosteronism, Type Iie 48 0.743
302
DPH001 Diphtheria 59 0.743
303
P CND004 Candidiasis 57 0.743
304
PST011 Pustulosis of Palm and Sole 52 0.743
305
END041 Endometrial Adenocarcinoma 63 0.743
306
P HML002 Hemolytic Anemia 62 0.743
307
P HMP007 Hemophilia 52 0.743
308
P THL005 Thalassemia 56 0.743
309
P TRM003 Tremor 50 0.743
310
P HMC002 Homocystinuria 52 0.737
311
P JVN014 Juvenile Polyposis Syndrome 65 0.733
312
VRL011 Viral Infectious Disease 60 0.733
313
SPL018 Splenomegaly 47 0.733
314
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 0.732
315
INT067 Interstitial Nephritis 46 0.732
316
EKR001 Eukaryotic Translation Elongation Factor 1 Alpha-1-Like 14 10 0.723
317
EWN003 Ewing Sarcoma 69 0.723
319
LBR036 Leber Plus Disease 67 0.723
320
CLN015 Colon Adenocarcinoma 64 0.723
321
P TMP001 Temporal Lobe Epilepsy 49 0.723
322
GST045 Gastroenteritis 58 0.723
323
GTR002 Goiter 52 0.723
324
P HRD217 Hereditary Optic Neuropathy 36 0.723
325
P ANR048 Aniridia 1 66 0.717
326
c HMP004 Hemophilia B 68 0.712
327
P HYD006 Hydrocephalus 62 0.712
328
YLL002 Yellow Fever 61 0.712
329
SPS019 Spastic Paraparesis 38 0.712
330
HPT019 Hepatic Encephalopathy 59 0.705
331
c GLC092 Glaucoma, Primary Open Angle 60 0.700
332
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.700
333
CMB007 Combined Immunodeficiency 56 0.700
334
P FLL037 Follicular Lymphoma 66 0.700
335
IMP005 Impotence 52 0.700
336
c FML021 Familial Hypercholesterolemia 71 0.700
337
MCR013 Microphthalmia 59 0.700
338
P OPN001 Open-Angle Glaucoma 55 0.700
339
PLG002 Plague 58 0.700
340
c NRF024 Neurofibromatosis, Type I 76 0.692
341
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.692
342
c SCH079 Schizophrenia 1 44 0.688
343
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.688
344
WST001 West Syndrome 64 0.688
345
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.688
346
P AST005 Asthma 75 0.688
347
CRT072 Creutzfeldt-Jakob Disease 67 0.688
348
P ANP001 Anaplastic Large Cell Lymphoma 59 0.688
349
P PLY041 Polymyositis 58 0.688
350
P DYS154 Dystonia 64 0.688
351
HYP141 Hyperphenylalaninemia 42 0.688
352
P CTN015 Cutaneous T Cell Lymphoma 48 0.675
353
VTM002 Vitamin B12 Deficiency 48 0.675
354
P MYS005 Myositis 55 0.675
355
CLF027 Cleft Palate, Isolated 64 0.675
356
HLC007 Helicobacter Pylori Infection 67 0.675
357
P RCT021 Rectum Cancer 54 0.675
358
TRN018 Transitional Cell Carcinoma 56 0.675
359
P VNW001 Von Willebrand's Disease 64 0.675
360
LNG031 Lung Benign Neoplasm 51 0.675
361
RHB024 Rhabdomyosarcoma 2 65 0.664
362
JVN004 Juvenile Myelomonocytic Leukemia 66 0.664
363
c DWL002 Dowling-Degos Disease 1 58 0.662
364
c BTT014 Beta-Thalassemia 72 0.662
365
P ICH004 Ichthyosis 56 0.662
366
DRM006 Dermatitis 61 0.662
367
LNG039 Lung Squamous Cell Carcinoma 57 0.662
368
P TXP001 Toxoplasmosis 59 0.662
369
PNK001 Pink1 Type of Young-Onset Parkinson Disease 8 0.662
370
c RNG015 Ring Chromosome 2 22 0.662
371
HMT002 Hematologic Cancer 61 0.648
372
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.647
373
P NJM001 Nijmegen Breakage Syndrome 75 0.647
374
TTH006 Tooth Disease 51 0.647
375
P EPD016 Epidermolysis Bullosa 53 0.647
376
P BRD002 Bardet-Biedl Syndrome 66 0.647
377
P EPD003 Epidermolysis Bullosa Simplex 56 0.647
378
MST004 Mast Cell Neoplasm 41 0.647
379
P INT068 Intestinal Disease 53 0.647
380
EXT007 Extracutaneous Mastocytoma 38 0.647
381
P CHR071 Charcot-Marie-Tooth Disease 64 0.647
382
RCK004 Rickets 64 0.647
383
ATN021 Autoinflammatory Syndrome 30 0.647
384
GLY010 Glycine Encephalopathy 57 0.643
385
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.631
386
P DRM053 Dermatitis, Atopic 65 0.631
387
FBR012 Fabry Disease 71 0.631
388
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.631
389
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 46 0.631
390
HMN047 Human Cytomegalovirus Infection 59 0.631
391
HMS001 Hemosiderosis 48 0.631
392
P BLD062 Bile Duct Cancer 69 0.631
393
INF021 Infant Gynecomastia 30 0.631
394
TST014 Testicular Cancer 51 0.631
395
GYN001 Gynecomastia 48 0.631
396
P HRD011 Hereditary Spherocytosis 63 0.631
397
BRS051 Breast Disease 58 0.631
398
P TRC031 Trichorhinophalangeal Syndrome 37 0.631
399
P CHL066 Cholangitis 51 0.631
400
GNR035 Generalized Juvenile Polyposis/juvenile Polyposis Coli 43 0.631
401
CLP005 Ciliopathy 40 0.631
402
P APL001 Aplastic Anemia 72 0.614
403
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.614
404
c RTN066 Retinitis Pigmentosa 4 42 0.614
405
c CHL119 Cholangitis, Primary Sclerosing 57 0.614
406
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.614
408
ORT008 Orotic Aciduria 56 0.614
409
c RTN041 Retinitis Pigmentosa 11 43 0.614
410
DSS009 Disseminated Intravascular Coagulation 56 0.614
411
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.614
412
c HPT015 Hepatitis D 49 0.614
413
BRS099 Breast Ductal Carcinoma 61 0.614
414
CRV038 Cervical Squamous Cell Carcinoma 56 0.614
415
P SCL009 Sclerosing Cholangitis 46 0.614
416
P CRV039 Cervicitis 52 0.614
417
LYM009 Lymphocytic Choriomeningitis 46 0.614
418
P TYR004 Tyrosinemia 49 0.614
419
P RRH023 Rare Hereditary Hemochromatosis 52 0.614
420
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.610
421
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.610
422
PST028 Post-Traumatic Stress Disorder 58 0.610
423
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.610
425
P TBR001 Tuberous Sclerosis 69 0.598
426
P OMP004 Omphalocele 47 0.594
427
BRN032 Brain Glioma 45 0.594
428
VLC001 Velocardiofacial Syndrome 57 0.594
429
DMN031 Dementia, Lewy Body 65 0.594
430
c PLY103 Polydactyly, Postaxial, Type A5 16 0.594
431
GTL001 Gitelman Syndrome 65 0.594
432
c DVL029 Developmental and Epileptic Encephalopathy 2 47 0.594
433
ANT042 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis 37 0.594
434
P PLT029 Platelet Groups--Ko System 15 0.594
435
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.594
436
KNZ001 Kanzaki Disease 37 0.594
437
AML029 Ameloblastoma 46 0.594
438
P MMP001 Mumps 56 0.594
439
BRR014 Barrett Esophagus 66 0.594
440
URT001 Urethritis 52 0.594
441
KWS001 Kwashiorkor 44 0.594
442
P RHN004 Rhinitis 56 0.594
443
LSS003 Lassa Fever 49 0.594
444
c FML191 Familial Long Qt Syndrome 54 0.594
445
EXN003 Exencephaly 30 0.594
446
PHS022 Phosphoserine Phosphatase Deficiency 37 0.589
447
P PRM002 Primary Hyperoxaluria 65 0.589
448
LPM012 Lipomatosis, Multiple 59 0.570
449
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.570
450
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.570
451
c LNG047 Long Qt Syndrome 2 59 0.570
452
INH001 Inhalation Anthrax 42 0.570
453
c SPH017 Spherocytosis, Type 5 46 0.570
454
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.570
455
STL007 Steel Syndrome 42 0.570
456
c ACR088 Aicardi-Goutieres Syndrome 3 39 0.570
458
c PRM031 Primary Autosomal Recessive Microcephaly 55 0.570
459
c PRM212 Primary Microcephaly 40 0.570
460
PLM005 Pleomorphic Lipoma 39 0.570
461
LMB024 Limbic Encephalitis 43 0.570
462
P RNV001 Renovascular Hypertension 48 0.570
463
TRC003 Trichomoniasis 53 0.570
464
CHL067 Cholecystitis 59 0.570
465
c VRL010 Viral Hepatitis 52 0.570
466
ANG016 Angiokeratoma 37 0.570
467
ADN009 Adenosquamous Carcinoma 49 0.570
468
TCK004 Tick Infestation 29 0.570
469
CRP002 Croup 42 0.570
470
LRR002 Lrrk2 Parkinson Disease 10 0.570
471
TTR005 Tetrahydrobiopterin Deficiency 49 0.570
472
PRN068 Paraneoplastic Limbic Encephalitis 21 0.570
473
MYC005 Myocardial Stunning 45 0.570
474
AMY005 Amyloid Neuropathy 31 0.570
475
P RSS029 Resistance to Thyroid Hormone Due to a Mutation in Thyroid Hormone Receptor Alpha 16 0.570
476
MYC015 Mycobacterium Fortuitum 28 0.570
477
TRP014 Triploidy 38 0.570
478
MLD001 Melioidosis 67 0.568
479
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.556
480
LWG006 Low Grade Glioma 41 0.556
481
P CHR285 Chronic Myelomonocytic Leukemia 59 0.556
482
PRS047 Prostatitis 57 0.556
483
MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.556
484
ACT084 Acute Stress Disorder 53 0.556
485
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.556
486
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.555
487
c TBR025 Tuberous Sclerosis 1 84 0.540
488
c RTN056 Retinitis Pigmentosa 28 39 0.540
489
c PRM108 Primary Progressive Multiple Sclerosis 51 0.540
490
PLS030 Plasminogen Deficiency, Type I 52 0.540
491
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.540
492
c RTN150 Retinitis Pigmentosa 10 44 0.540
493
c ORF037 Orofaciodigital Syndrome I 59 0.540
494
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.540
495
c PNC094 Pancreatic Cancer 1 28 0.540
496
c MNT158 Mental Retardation, Autosomal Dominant 22 32 0.540
497
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 35 0.540
498
ICH002 Ichthyosis Bullosa of Siemens 42 0.540
499
c CHR711 Chronic Asthma 41 0.540
500
P PRT026 Parotitis 42 0.540
501
ACL001 Acalculous Cholecystitis 34 0.540
502
c BRD016 Bardet-Biedl Syndrome 4 44 0.540
503
P MYP006 Myopia 55 0.540
504
CLC001 Calciphylaxis 50 0.540
505
P ORF001 Orofaciodigital Syndrome 50 0.540
506
P NPH005 Nephronophthisis 59 0.540
507
SCT002 Scotoma 42 0.540
508
P PRM011 Primary Ciliary Dyskinesia 68 0.540
510
STS002 Situs Inversus 44 0.540
511
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.540
512
TTR021 Tetrasomy 21 23 0.540
513
TXC011 Toxocariasis 46 0.540
514
P GNR008 Generalized Resistance to Thyroid Hormone 23 0.540
515
CYN003 Cyanide Poisoning 22 0.540
516
DMN026 Dementia Pugilistica 27 0.540
517
CLR033 Color Vision Deficiency 41 0.540
518
DNG003 Dengue Disease 65 0.530
519
ATM095 Autoimmune Disease 61 0.519
520
PHS023 Phosphoserine Aminotransferase Deficiency 41 0.515
521
CRB137 Cerebral Creatine Deficiency Syndrome 31 0.515
522
DMT001 Dimethylglycine Dehydrogenase Deficiency 27 0.515
523
HYP003 Hypermethioninemia 51 0.515
524
CYS019 Cystathioninuria 46 0.515
525
P NLX004 Neu-Laxova Syndrome 1 55 0.515
526
PHS021 Phosphoglycerate Dehydrogenase Deficiency 46 0.515
527
c GLY057 Glycogen Storage Disease X 34 0.515
528
DGL002 D-Glyceric Aciduria 40 0.515
529
CRB150 Cerebral Creatine Deficiency Syndrome 2 54 0.515
530
DNG002 Dengue Hemorrhagic Fever 59 0.507
531
P MSC005 Muscular Dystrophy 66 0.503
532
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.492
533
OST062 Osteoarthritis with Mild Chondrodysplasia 46 0.482
534
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 0.482
535
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.482
536
c PRS130 Prostate Cancer, Hereditary, 8 32 0.482
537
c OVR114 Ovarian Cancer 1 60 0.482
538
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.482
539
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.482
540
c BLD140 Blood Group, I System 47 0.482
541
IMM162 Immunoglobulin E Concentration, Serum 28 0.482
542
HYL004 Hyaline Fibromatosis Syndrome 67 0.482
543
c PRS136 Prostate Cancer, Hereditary, 6 33 0.482
544
GLS018 Glass Syndrome 60 0.482
545
CLN045 Colonic Benign Neoplasm 48 0.482
546
END035 Endocrine Gland Cancer 42 0.482
547
INT253 Intestinal Benign Neoplasm 46 0.482
548
P MLG074 Malignant Mesenchymoma 40 0.482
549
PLX002 Plexiform Neurofibroma 44 0.482
550
MXD026 Mixed Glioma 45 0.482
551
P PRP021 Peripheral Nervous System Neoplasm 39 0.482
552
PLS009 Plasma Cell Neoplasm 64 0.482
553
NRF003 Neurofibrosarcoma 43 0.482
554
NRF007 Neurofibroma 63 0.482
555
c PRM038 Primary Agammaglobulinemia 47 0.482
556
END072 Endotheliitis 36 0.482
557
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.482
558
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.482
559
AND005 Androgen Insensitivity Syndrome, Mild 21 0.482
560
CHR682 Chronic Bilirubin Encephalopathy 37 0.482
561
c WLM018 Wilms Tumor 5 53 0.476
562
P RNL017 Renal Oncocytoma 54 0.476
563
CRB004 Cerebral Artery Occlusion 45 0.469
564
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.469
565
KRT010 Kartagener Syndrome 49 0.465
566
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.465
567
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 0.465
568
OBN001 Ouabain Resistance 15 0.465
569
PYL012 Pyloric Atresia 29 0.465
570
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.465
571
P ENC054 Encephalopathy, Neonatal Severe, Due to Mecp2 Mutations 35 0.465
572
c MCR320 Microcephaly 17, Primary, Autosomal Recessive 42 0.465
573
BLB005 Beaulieu-Boycott-Innes Syndrome 41 0.465
574
NST002 Nestor-Guillermo Progeria Syndrome 35 0.465
575
DYS198 Dystonia, Focal, Task-Specific 31 0.465
576
P CNT005 Central Nervous System Lymphoma 51 0.465
577
CHR286 Chronic Neutrophilic Leukemia 42 0.465
578
NPH009 Nephrolithiasis 54 0.465
579
P CMM008 Communicating Hydrocephalus 44 0.465
580
NDL007 Nodular Goiter 48 0.465
581
P FML340 Familial Episodic Pain Syndrome 50 0.465
582
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 38 0.465
583
PRM226 Primary Central Nervous System Lymphoma 47 0.465
584
KRT006 Keratoconjunctivitis 53 0.465
585
KPS004 Kaposi Sarcoma 76 0.463
586
LPD008 Lipid Metabolism Disorder 61 0.463
587
ATH013 Atherosclerosis Susceptibility 63 0.451
588
P ART022 Arthritis 70 0.451
589
CLR108 Colorectal Adenoma 63 0.450
590
c ATR087 Atrial Standstill 1 74 0.439
591
c LKM005 Leukemia, T-Cell, Chronic 33 0.439
592
ATS010 Autosomal Recessive Disease 42 0.426
593
BRN071 Brain Injury 50 0.426
594
P EXN002 Exanthem 58 0.420
595
ANX004 Anoxia 40 0.420
596
SKN019 Skin Melanoma 70 0.413
597
CHR020 Chronic Interstitial Cystitis 36 0.402
598
HPT070 Hepatosplenic T-Cell Lymphoma 35 0.402
599
LVR012 Liver Cirrhosis 62 0.400
600
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.400
601
P PLY011 Polycystic Ovary Syndrome 57 0.393
602
P RHM011 Rheumatoid Arthritis 81 0.386
603
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.386
604
P RHB003 Rhabdomyosarcoma 66 0.386
605
P MYP004 Myopathy 67 0.378
606
P PNC044 Pancreatitis 61 0.378
607
P NTR004 Neutropenia 62 0.378
608
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.371
609
P MYC007 Myocardial Infarction 69 0.371
610
P DRR001 Diarrhea 55 0.371
611
P INF032 Infertility 60 0.371
612
MSC007 Muscle Hypertrophy 64 0.364
613
c MCR115 Microvascular Complications of Diabetes 5 65 0.364
614
CHL068 Cholestasis 61 0.364
615
BRN024 Bronchitis 67 0.364
616
LNG099 Lung Disease 62 0.356
617
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.348
618
P MDL005 Medulloblastoma 75 0.348
619
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.348
620
P PLY014 Polycystic Kidney Disease 71 0.348
621
P HYP086 Hypothyroidism 68 0.348
622
NRM005 Neuromuscular Disease 62 0.348
623
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.340
624
MTB004 Metabolic Acidosis 48 0.340
625
MNT001 Mantle Cell Lymphoma 65 0.340
626
P HYP061 Hypertrophic Cardiomyopathy 68 0.340
627
P HYP076 Hyperthyroidism 53 0.340
628
P HYP265 Hypotonia 42 0.340
629
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.332
630
c PRC016 Pre-Eclampsia 64 0.332
631
PLY150 Polykaryocytosis Inducer 29 0.323
632
MDD011 Mood Disorder 61 0.323
633
P DBT009 Diabetes Mellitus 67 0.323
634
P SZR006 Seizure Disorder 69 0.323
635
P DNG005 Dengue Virus 55 0.315
636
P MTR014 Motor Neuron Disease 65 0.315
637
c CHR684 Chronic Kidney Disease 73 0.315
638
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.306
639
PRS129 Prostatic Hyperplasia, Benign 48 0.306
640
CLR030 Clear Cell Renal Cell Carcinoma 53 0.306
641
PRS045 Prostatic Hypertrophy 53 0.306
642
MCK005 Mckusick-Kaufman Syndrome 61 0.297
643
CFF002 Coffin-Lowry Syndrome 59 0.297
644
DSS032 Disease by Infectious Agent 55 0.297
645
CRN264 Craniosynostosis with Fibular Aplasia 29 0.297
646
HRW001 Hair Whorl 35 0.297
647
BRN004 Brain Edema 54 0.297
648
SVR001 Severe Acute Respiratory Syndrome 68 0.297
649
PRS021 Prostatic Adenoma 43 0.297
650
c ACT027 Acute Pancreatitis 60 0.297
651
ALL006 Allergic Asthma 55 0.297
652
P PRD008 Periodontitis 63 0.297
653
STR067 Stroke, Ischemic 79 0.287
654
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.287
655
P CRB048 Cerebral Cavernous Malformations 63 0.287
656
GST019 Gastrointestinal Stromal Tumor 78 0.287
657
P GRF003 Graft-Versus-Host Disease 71 0.287
658
P MTH008 Methylmalonic Acidemia 52 0.287
659
MNT002 Mental Depression 56 0.287
660
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.287
661
GST040 Gastric Adenocarcinoma 66 0.287
662
c NRB010 Neuroblastoma 1 59 0.284
663
c ART120 Arthrogryposis, Distal, Type 3 50 0.278
664
PHN003 Phenylketonuria 76 0.278
665
P MJR001 Major Depressive Disorder 68 0.278
666
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 0.278
667
P END044 Endometriosis 62 0.278
668
AZS001 Azoospermia 45 0.278
669
P INS002 in Situ Carcinoma 52 0.278
670
CVR010 Cavernous Malformation 29 0.278
671
DPR016 Depression 64 0.278
672
ART140 Arteries, Anomalies of 52 0.268
673
OCL069 Ocular Motor Apraxia 57 0.268
674
c FNC027 Fanconi Anemia, Complementation Group a 80 0.268
675
LPP008 Lipoprotein Quantitative Trait Locus 65 0.268
676
PPL022 Papilloma 53 0.268
677
PRP016 Paraplegia 52 0.268
678
SQM002 Squamous Cell Papilloma 45 0.268
679
PLM010 Pulmonary Edema 54 0.268
680
P THY032 Thyroiditis 56 0.268
681
P DBT005 Diabetes Insipidus 54 0.268
682
c WLM013 Wilms Tumor 1 65 0.257
683
P NNN008 Noonan Syndrome 1 76 0.257
684
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.257
685
MSC157 Muscular Dystrophy, Duchenne Type 78 0.257
686
P BRC006 Brachydactyly 52 0.257
687
MRF001 Marfan Syndrome 76 0.257
688
INT051 Intussusception 53 0.257
689
P ADL017 Adult T-Cell Leukemia 53 0.257
690
CLR109 Colorectal Adenocarcinoma 50 0.257
691
P AML002 Amelogenesis Imperfecta 56 0.257
692
P EYD002 Eye Disease 57 0.257
693
BRC012 Brucellosis 66 0.257
694
INT066 Interstitial Lung Disease 60 0.257
695
PRT038 Protein-Energy Malnutrition 53 0.257
696
BRN028 Brain Cancer 73 0.257
697
HPT022 Hepatoblastoma 54 0.257
698
P OVR046 Ovarian Cyst 43 0.257
699
P ALP008 Alopecia 53 0.257
700
c PSD047 Pseudo-Turner Syndrome 52 0.257
701
c ACT134 Acute Liver Failure 57 0.257
702
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.246
703
PRP001 Propionic Acidemia 65 0.246
704
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.246
705
NRL016 Neural Tube Defects 80 0.246
706
P FML018 Familial Mediterranean Fever 73 0.246
707
c CRB094 Cerebral Cavernous Malformations 3 41 0.246
708
P BND020 Bone Disease 60 0.246
709
P BNG032 Benign Mesothelioma 53 0.246
710
P ECL001 Eclampsia 52 0.246
711
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.246
712
TTN003 Tetanus 64 0.246
713
P THR014 Thrombocytopenia 66 0.246
714
CND006 Candida Glabrata 29 0.246
716
MYT011 Myotonia 37 0.246
717
ACT119 Acute Promyelocytic Leukemia 62 0.235
718
P CRN300 Coronary Heart Disease 1 73 0.235
719
c MGR028 Migraine with or Without Aura 1 63 0.235
720
MYX004 Myxedema 43 0.235
721
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.235
722
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.235
723
c ERL056 Early-Onset Parkinson's Disease 39 0.235
724
OST017 Osteomyelitis 63 0.235
725
MDD018 Middle East Respiratory Syndrome 44 0.235
726
P GRV001 Graves' Disease 54 0.235
727
SCR011 Scrapie 39 0.235
728
P LCT001 Lactic Acidosis 50 0.235
729
CRB039 Cerebrovascular Disease 65 0.235
730
ISL099 Isolated Methylmalonic Acidemia 35 0.235
731
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.235
732
END086 End Stage Renal Disease 54 0.235
733
P MTC069 Mitochondrial Disorders 57 0.235
734
P SCL018 Scoliosis 57 0.223
735
CTR172 Citrullinemia, Classic 64 0.223
736
P LYS001 Loeys-Dietz Syndrome 65 0.223
737
KRT019 Keratitis, Hereditary 66 0.223
738
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.223
739
P ASP006 Aspergillosis 71 0.223
740
c OPT053 Optic Atrophy 1 62 0.223
741
WST005 West Nile Virus 55 0.223
742
P SNS001 Sensorineural Hearing Loss 60 0.223
743
P NPH012 Nephrotic Syndrome 61 0.223
744
OST015 Osteochondrodysplasia 60 0.223
745
OVR063 Overnutrition 42 0.223
746
RSP023 Rasopathy 54 0.223
747
CNS004 Constipation 56 0.223
748
P SYS005 Systemic Scleroderma 73 0.223
749
MTH009 Mouth Disease 57 0.223
750
MTC004 Mitochondrial Encephalomyopathy 42 0.223
751
PRT036 Peritonitis 65 0.223
752
P MNC007 Monocytic Leukemia 48 0.223
753
P HYP098 Hypereosinophilic Syndrome 66 0.223
754
c ACT135 Acute Graft Versus Host Disease 51 0.223
755
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.210
756
P OST002 Osteoporosis 76 0.210
757
AND002 Androgen Insensitivity Syndrome 63 0.210
758
c CNG006 Congenital Hypothyroidism 63 0.210
759
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.210
760
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.210
761
CYS013 Cystinuria 66 0.210
762
c LFR007 Li-Fraumeni Syndrome 2 45 0.210
763
P LFR001 Li-Fraumeni Syndrome 73 0.210
764
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 0.210
765
PPL002 Papillary Carcinoma 46 0.210
766
HYP014 Hyperuricemia 51 0.210
767
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.210
768
URT010 Ureteral Obstruction 44 0.210
769
P PLC011 Pilocytic Astrocytoma 55 0.210
770
LYM027 Lymphopenia 56 0.210
771
SYN007 Synovitis 54 0.210
772
CRC021 Carcinosarcoma 62 0.210
773
P LYN001 Lynch Syndrome 76 0.210
774
PLC002 Plica Syndrome 35 0.210
775
PRT013 Portal Hypertension 59 0.210
776
c HRD002 Hereditary Angioedema 61 0.210
777
GT001 Gout 63 0.210
778
P CWD010 Cowden Syndrome 70 0.210
779
MMM001 Mammary Paget's Disease 53 0.210
780
P MYC008 Myocarditis 59 0.210
781
DBT010 Diabetic Neuropathy 54 0.210
782
P FML187 Familial Hypertension 34 0.210
783
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 70 0.210
784
P MYC033 Myoclonus 46 0.210
785
P PRD021 Periodic Paralysis 42 0.210
786
WTH001 Withdrawal Disorder 47 0.196
787
PSR001 Psoriatic Arthritis 61 0.196
788
APH002 Aphasia 55 0.196
789
P FML023 Familial Hemiplegic Migraine 53 0.196
790
P MLN066 Melanoma, Cutaneous Malignant 1 65 0.196
791
c SCL052 Scleroderma, Familial Progressive 60 0.196
792
AND020 Androgen Insensitivity, Partial 54 0.196
793
c ANG068 Angioedema, Hereditary, Type I 58 0.196
794
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.196
795
P TST021 Testicular Germ Cell Tumor 61 0.196
796
DNY001 Denys-Drash Syndrome 57 0.196
797
P CHN012 Chondrosarcoma 56 0.196
798
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.196
799
P MTC003 Metachromatic Leukodystrophy 71 0.196
800
P FRG001 Fragile X Syndrome 70 0.196
801
TBL029 Tubulin, Beta 28 0.196
802
P HMN032 Human Herpesvirus 8 47 0.196
803
HJD001 Hajdu-Cheney Syndrome 62 0.196
804
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 0.196
805
OBS082 Obstructive Nephropathy 41 0.196
806
P LYM033 Lymphoproliferative Syndrome 59 0.196
807
INV001 Invasive Aspergillosis 48 0.196
808
THR024 Thrombosis 56 0.196
809
c BSL007 Basal Cell Carcinoma 67 0.196
810
HRY003 Hairy Cell Leukemia 53 0.196
811
HRT011 Heart Septal Defect 49 0.196
812
PSD009 Pseudohermaphroditism 46 0.196
813
SBP001 Subependymal Giant Cell Astrocytoma 45 0.196
814
IGG001 Iga Glomerulonephritis 50 0.196
815
P TRT010 Teratoma 50 0.196
816
ATN004 Autonomic Neuropathy 42 0.196
817
P LKD001 Leukodystrophy 58 0.196
818
P CRD246 Cardiovascular System Disease 55 0.196
819
LRN003 Learning Disability 49 0.196
820
ETN001 Eating Disorder 59 0.196
821
P SCK005 Sickle Cell Disease 56 0.196
822
GLM044 Glomerular Disease 34 0.196
823
P CHR345 Chronic Pain 50 0.196
824
DCT002 Ductal Carcinoma in Situ 58 0.182
825
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.182
826
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.182
827
CRD132 Cardiac Conduction Defect 59 0.182
828
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.182
829
P GLC113 Galactosemia I 65 0.182
830
c HYP731 Hyperaldosteronism, Familial, Type I 59 0.182
831
FRS002 Frasier Syndrome 54 0.182
832
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.182
833
P PLY006 Polydactyly 58 0.182
834
c CRB191 Cerebral Cavernous Malformations 2 45 0.182
835
SRC027 Sarcoma, Synovial 58 0.182
836
P LSS002 Lissencephaly 52 0.182
837
PLY001 Polycythemia Vera 69 0.182
838
PCK003 Pick Disease of Brain 70 0.182
839
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.182
840
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.182
841
c GRV008 Graves Disease 1 54 0.182
842
c THR092 Thrombophilia Due to Thrombin Defect 74 0.182
843
c CWD006 Cowden Syndrome 1 78 0.182
844
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.182
845
MLT157 Multiple System Atrophy 1 69 0.182
846
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.182
847
P RSP003 Respiratory Failure 73 0.182
848
PHR003 Pharyngitis 57 0.182
849
P ART021 Arteriosclerosis 53 0.182
850
HYP068 Hyperostosis 47 0.182
851
P KRT005 Keratoacanthoma 47 0.182
852
BLR008 Bilirubin Metabolic Disorder 57 0.182
853
P HMN010 Hemangioma 61 0.182
854
c ACT071 Acute Kidney Failure 60 0.182
855
HYP029 Hyperthyroxinemia 32 0.182
856
CCC001 Coccidioidomycosis 57 0.182
857
P ALC033 Alcohol Use Disorder 67 0.182
858
URN010 Urinary Tract Obstruction 55 0.182
859
CNN005 Connective Tissue Disease 66 0.182
860
IRN002 Iron Metabolism Disease 56 0.182
861
TYP007 Typhoid Fever 63 0.182
862
P NRM002 Normal Pressure Hydrocephalus 49 0.182
863
HYP043 Hyperandrogenism 47 0.182
864
P HYP040 Hypospadias 51 0.182
865
LMY002 Leiomyoma 51 0.182
866
CMP034 Complete Androgen Insensitivity Syndrome 55 0.182
867
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.182
868
AMN006 Aminoaciduria 37 0.182
869
BRN056 Bronchopulmonary Dysplasia 57 0.182
870
P PLY018 Polycythemia 56 0.182
871
FBR019 Fibromatosis 44 0.182
872
ANR040 Aneurysm 60 0.182
873
IRR002 Irritable Bowel Syndrome 64 0.182
874
CRB090 Cerebral Hypoxia 42 0.182
875
PST092 Posttransplant Acute Limbic Encephalitis 29 0.182
876
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.166
877
P CRN038 Carney Complex Variant 63 0.166
878
P MTR004 Maturity-Onset Diabetes of the Young 66 0.166
879
P HRD021 Hereditary Sensory Neuropathy 48 0.166
880
RVL002 Ruvalcaba Syndrome 42 0.166
881
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.166
882
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.166
883
c MYT021 Myotonic Dystrophy 1 67 0.166
884
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 61 0.166
885
P CLD001 Cleidocranial Dysplasia 64 0.166
886
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 0.166
887
c SPN225 Spondyloarthropathy 1 70 0.166
888
SPP011 Suppression of Tumorigenicity 12 61 0.166
889
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.166
890
HYP017 Hypophosphatemia 49 0.166
891
APP015 Apparent Mineralocorticoid Excess 57 0.166
892
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.166
893
BLM001 Bloom Syndrome 65 0.166
894
MYL005 Myelofibrosis 70 0.166
896
MNN043 Meningioma, Familial 79 0.166
897
c LSS005 Lissencephaly 1 57 0.166
898
HRN029 Hearing Loss, Noise-Induced 37 0.166
899
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 60 0.166
900
c SVR003 Severe Congenital Neutropenia 59 0.166
901
CHK001 Chikungunya 60 0.166
902
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.166
903
LMB062 Limb Ischemia 55 0.166
904
PRL017 Prolymphocytic Leukemia 47 0.166
905
P PRS049 Persistent Mullerian Duct Syndrome 51 0.166
906
P CRN037 Craniosynostosis 67 0.166
907
c HRD010 Hereditary Spastic Paraplegia 65 0.166
908
RTN020 Retinal Vascular Disease 45 0.166
909
P BNC003 Bone Cancer 58 0.166
910
P PLM006 Pulmonary Alveolar Proteinosis 53 0.166
911
OVR105 Ovarian Serous Carcinoma 37 0.166
912
GLC106 Glucocorticoid Resistance, Generalized 47 0.166
913
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.166
914
P CRV031 Cervical Adenocarcinoma 48 0.166
915
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.166
916
P EMB005 Embryonal Rhabdomyosarcoma 53 0.166
917
SPN051 Spondylitis 51 0.166
918
P PNM007 Pneumonia 64 0.166
919
TRN015 Transient Cerebral Ischemia 62 0.166
920
BLR001 Biliary Atresia 55 0.166
921
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.166
922
HMG005 Hemoglobinopathy 55 0.166
923
SCR001 Secretory Meningioma 40 0.166
924
c ESS001 Essential Tremor 56 0.166
925
THY030 Thyroid Gland Disease 50 0.166
926
PLC005 Placental Insufficiency 55 0.166
927
THY124 Thyroid Gland Papillary Carcinoma 38 0.166
928
P ART023 Arthropathy 59 0.166
929
ART016 Aortic Aneurysm 68 0.166
930
PLS011 Plasmacytoma 56 0.166
931
P ART005 Arteriovenous Malformation 64 0.166
932
DSM004 Desmoid Tumor 65 0.166
933
TNG007 Tongue Carcinoma 55 0.166
934
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 0.166
935
INT395 Intracranial Meningioma 47 0.166
936
ECH003 Echinococcosis 52 0.166
937
PLS007 Plasmodium Falciparum Malaria 52 0.166
938
P GND004 Gonadal Dysgenesis 46 0.166
939
OLG001 Oligospermia 45 0.166
940
P KRT007 Keratoconus 49 0.166
941
P DRM010 Dermatomyositis 61 0.166
942
INF009 Inflammatory Spondylopathy 30 0.166
943
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42