Search results for hes1

531 hits were found for hes1

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 97 21.475
2
P MDL005 Medulloblastoma 75 17.130
3
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 14.063
4
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 12.300
5
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 10.790
6
P MTR004 Maturity-Onset Diabetes of the Young 66 8.584
7
HLX001 Helix Syndrome 47 5.979
8
P PNC035 Pancreatic Cancer 87 2.767
9
P LKM062 Leukemia, Acute Lymphoblastic 69 2.370
10
ISC004 Ischemia 61 2.314
11
P ADN016 Adenocarcinoma 63 2.293
12
P LKM002 Leukemia 65 2.263
13
OST159 Osteogenic Sarcoma 66 2.213
14
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 2.177
15
c LKM061 Leukemia, Acute Myeloid 83 2.162
16
P MYL006 Myeloid Leukemia 60 2.147
17
P CLR023 Colorectal Cancer 100 2.085
18
P GST053 Gastric Cancer 82 1.981
19
SQM006 Squamous Cell Carcinoma 59 1.907
20
P LNG032 Lung Cancer 98 1.866
21
P OVR042 Ovarian Cancer 88 1.841
22
GLL048 Glial Tumor 51 1.807
23
HYP266 Hypoxia 56 1.802
24
GLM045 Glioma 62 1.797
25
c LKM005 Leukemia, T-Cell, Chronic 33 1.755
26
GLB002 Glioblastoma 67 1.752
27
c MCR133 Microvascular Complications of Diabetes 4 41 1.662
28
c MCR113 Microvascular Complications of Diabetes 3 52 1.662
29
c MCR130 Microvascular Complications of Diabetes 6 41 1.662
30
c MCR120 Microvascular Complications of Diabetes 7 47 1.662
31
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.652
32
SPN186 Spinal Cord Injury 60 1.652
33
P RTN024 Retinoblastoma 72 1.642
34
c FNC042 Fanconi Anemia, Complementation Group D2 54 1.567
35
P PRS040 Prostate Cancer 95 1.519
36
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.478
37
HYP066 Hyperglycemia 60 1.468
38
BRN028 Brain Cancer 73 1.468
39
CHL065 Cholangiocarcinoma 57 1.448
40
INT079 Intrahepatic Cholangiocarcinoma 51 1.448
41
TRM010 Traumatic Brain Injury 50 1.427
42
BRN071 Brain Injury 50 1.427
43
c SML038 Small Cell Cancer of the Lung 68 1.417
44
P HRT032 Heart Disease 84 1.384
45
DFC004 Deficiency Anemia 74 1.361
46
P HPT023 Hepatocellular Carcinoma 95 1.349
47
c FNC027 Fanconi Anemia, Complementation Group a 80 1.336
48
OST012 Osteoarthritis 77 1.324
49
c ACT073 Acute Leukemia 59 1.298
50
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.284
51
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.270
52
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.241
53
P SPP010 Suppressor of Tumorigenicity 3 50 1.226
54
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.226
55
BLR001 Biliary Atresia 55 1.210
56
HMC014 Homocysteinemia 52 1.193
57
CLT003 Colitis 63 1.188
58
CRB004 Cerebral Artery Occlusion 45 1.177
59
HRN029 Hearing Loss, Noise-Induced 37 1.175
60
P HNT016 Huntington Disease 73 1.175
61
NRN001 Neuroendocrine Carcinoma 47 1.175
62
ADN018 Adenoma 58 1.156
63
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.133
64
ULC004 Ulcerative Colitis 74 1.133
65
P BCL017 B-Cell Lymphoma 57 1.121
66
c BRN108 Branchiootic Syndrome 1 63 1.095
67
P ALG028 Alagille Syndrome 1 73 1.072
68
END057 Endometrial Cancer 76 1.072
69
ORL015 Oral Squamous Cell Carcinoma 43 1.059
70
BNR002 Bone Resorption Disease 47 1.031
71
P MCR010 Microcephaly 59 1.031
72
STR067 Stroke, Ischemic 79 1.017
73
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 1.017
74
P NSP012 Nasopharyngeal Carcinoma 60 1.002
75
MCR013 Microphthalmia 59 1.002
76
CLB010 Coloboma of Macula 53 0.986
77
CRV035 Cervical Cancer 72 0.986
78
ADN011 Adenoid Cystic Carcinoma 68 0.986
79
THY029 Thyroid Carcinoma 55 0.970
80
c FNC029 Fanconi Anemia, Complementation Group I 55 0.954
81
CLN015 Colon Adenocarcinoma 64 0.954
82
ACT098 Acute Erythroid Leukemia 55 0.954
83
CRV002 Cervix Uteri Carcinoma in Situ 48 0.954
84
CRV045 Cervical Intraepithelial Neoplasia 38 0.954
85
P SML001 Small Cell Carcinoma 52 0.936
86
c LKM063 Leukemia, Chronic Myeloid 70 0.936
87
c PCH010 Pachyonychia Congenita 3 43 0.936
88
P VNT002 Ventricular Septal Defect 58 0.936
89
PRP030 Purpura 54 0.936
90
OVR105 Ovarian Serous Carcinoma 37 0.936
91
SPN035 Spindle Cell Sarcoma 51 0.936
92
PST011 Pustulosis of Palm and Sole 52 0.936
93
MDD011 Mood Disorder 61 0.936
94
ALL029 Allergic Disease 61 0.936
95
SRC014 Sarcoma 64 0.936
96
P PSR002 Psoriasis 63 0.936
97
CRC006 Carcinoid Syndrome 55 0.936
98
SPL018 Splenomegaly 47 0.936
99
c SYS001 Systemic Lupus Erythematosus 85 0.918
100
SRS001 Serous Cystadenocarcinoma 51 0.918
101
SVR004 Severe Combined Immunodeficiency 70 0.918
102
P DBT009 Diabetes Mellitus 67 0.918
103
P HYP098 Hypereosinophilic Syndrome 66 0.918
104
P LNG064 Lung Cancer Susceptibility 3 69 0.898
105
CLR109 Colorectal Adenocarcinoma 50 0.898
106
CRH001 Crohn's Disease 80 0.898
107
c MJR022 Major Affective Disorder 8 37 0.878
108
c MJR024 Major Affective Disorder 9 40 0.878
109
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.878
110
HMN047 Human Cytomegalovirus Infection 59 0.878
111
LPD008 Lipid Metabolism Disorder 61 0.878
112
P BPL003 Bipolar Disorder 56 0.878
113
CRB138 Core Binding Factor Acute Myeloid Leukemia 45 0.878
114
P EPL164 Epilepsy 70 0.878
115
P GST044 Gastritis 55 0.878
116
P MLN008 Melanoma 75 0.878
117
P HYP083 Hypopituitarism 51 0.878
118
FTT001 Fatty Liver Disease 61 0.878
119
P HRP006 Herpes Simplex 65 0.878
120
ART140 Arteries, Anomalies of 52 0.855
121
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.855
122
THY111 Thyroid Carcinoma, Familial Medullary 67 0.855
123
c RTN041 Retinitis Pigmentosa 11 43 0.855
124
TRN018 Transitional Cell Carcinoma 56 0.855
125
P MLT074 Multiple Endocrine Neoplasia 58 0.855
126
INV004 Invasive Bladder Transitional Cell Carcinoma 32 0.855
127
THY125 Thyroid Gland Medullary Carcinoma 48 0.855
128
EXN003 Exencephaly 30 0.855
129
c PRG020 Paragangliomas 3 39 0.831
130
DWN001 Down Syndrome 70 0.831
131
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.831
132
P LTR001 Lateral Sclerosis 57 0.831
133
HYD002 Hydronephrosis 58 0.831
134
P MYT002 Myotonic Dystrophy 51 0.831
135
P MSC003 Muscular Atrophy 52 0.831
136
NRL025 Neural Tube Closure Defect 27 0.831
137
c TYP009 Type 2 Diabetes Mellitus 91 0.804
138
c GLC092 Glaucoma, Primary Open Angle 60 0.804
139
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.804
140
LPP008 Lipoprotein Quantitative Trait Locus 65 0.804
141
ESP021 Esophageal Cancer 84 0.804
142
P OPN001 Open-Angle Glaucoma 55 0.804
143
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.774
144
BLR028 Biliary Atresia, Extrahepatic 36 0.774
145
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.774
146
c DFN352 Deafness, Autosomal Recessive 8 37 0.774
147
BLR008 Bilirubin Metabolic Disorder 57 0.774
148
NWC001 Newcastle Disease 47 0.774
149
STM007 Stomatitis 52 0.774
150
c NNS007 Nonsyndromic Deafness 36 0.774
151
ANX004 Anoxia 40 0.774
152
P PTN014 Patent Ductus Arteriosus 1 59 0.738
153
PTT001 Pituitary Hypoplasia 34 0.738
154
P RTT002 Rett Syndrome 79 0.691
155
c MCR115 Microvascular Complications of Diabetes 5 65 0.691
156
EXS001 Exostosis 49 0.578
157
P LNG021 Lung Occult Small Cell Carcinoma 20 0.543
158
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.543
159
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.543
160
MYL069 Myeloma, Multiple 76 0.543
161
CLL010 Cellular Ependymoma 58 0.517
162
BRR014 Barrett Esophagus 66 0.467
163
P NRB001 Neuroblastoma 66 0.467
164
48X005 48,xyyy 39 0.424
165
INS001 Insulinoma 59 0.376
166
P PLM036 Pulmonary Fibrosis 65 0.376
167
P ALZ034 Alzheimer Disease 87 0.358
168
ART016 Aortic Aneurysm 68 0.340
169
DGN001 Degenerative Disc Disease 48 0.340
170
ANR040 Aneurysm 60 0.340
171
P KDN018 Kidney Disease 71 0.320
172
GST092 Gastroesophageal Reflux 59 0.300
173
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.300
174
c HPT016 Hepatitis B 62 0.300
175
P RHB003 Rhabdomyosarcoma 66 0.300
176
P TRT010 Teratoma 50 0.300
177
P ART022 Arthritis 70 0.300
178
OVR094 Ovarian Epithelial Cancer 39 0.300
179
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.278
180
MYL009 Myelodysplastic Syndrome 67 0.278
181
DCT002 Ductal Carcinoma in Situ 58 0.278
182
P OST002 Osteoporosis 76 0.278
183
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.278
184
c CHR711 Chronic Asthma 41 0.278
185
CHL068 Cholestasis 61 0.278
186
P HPT021 Hepatitis 68 0.278
187
SKN019 Skin Melanoma 70 0.278
188
LNG099 Lung Disease 62 0.278
189
P INS002 in Situ Carcinoma 52 0.278
190
47X002 47,xyy 47 0.278
191
P DBT005 Diabetes Insipidus 54 0.278
192
SFT003 Soft Tissue Sarcoma 43 0.278
193
c ATS007 Autism Spectrum Disorder 71 0.253
194
P ATR011 Atrial Fibrillation 66 0.253
195
P APL001 Aplastic Anemia 72 0.253
196
RNL077 Renal Fibrosis 46 0.253
197
P LYM118 Lymphoma 66 0.253
198
c WLM013 Wilms Tumor 1 65 0.253
199
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.253
200
P FML011 Familial Adenomatous Polyposis 70 0.253
201
c CHL119 Cholangitis, Primary Sclerosing 57 0.253
202
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.253
203
P AST005 Asthma 75 0.253
204
P MYC007 Myocardial Infarction 69 0.253
205
MNN043 Meningioma, Familial 79 0.253
207
PRP009 Peripartum Cardiomyopathy 54 0.253
208
c ATR087 Atrial Standstill 1 74 0.253
209
P PNC045 Pancreatic Agenesis 42 0.253
210
KRT008 Keratopathy 46 0.253
211
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.253
212
P SCL009 Sclerosing Cholangitis 46 0.253
213
ART074 Aortic Dissection 53 0.253
214
P END044 Endometriosis 62 0.253
215
SCR001 Secretory Meningioma 40 0.253
216
P ART005 Arteriovenous Malformation 64 0.253
217
INT395 Intracranial Meningioma 47 0.253
218
HPT022 Hepatoblastoma 54 0.253
219
P LCH002 Lichen Planus 54 0.253
220
END086 End Stage Renal Disease 54 0.253
221
P CHL066 Cholangitis 51 0.253
222
ALL014 Allergic Encephalomyelitis 34 0.253
223
PTT037 Pituitary Tumors 44 0.253
224
ORL013 Oral Lichen Planus 45 0.253
225
P SCL048 Sclerosteosis 58 0.227
226
P INF037 Inflammatory Bowel Disease 53 0.227
227
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.227
228
P ATS364 Autism 72 0.227
229
NRL016 Neural Tube Defects 80 0.227
230
CRC014 Carcinoid Tumors, Intestinal 46 0.227
231
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.227
232
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.227
233
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.227
234
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.227
235
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.227
236
AGN016 Aging 53 0.227
237
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.227
238
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.227
239
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.227
240
P MJR001 Major Depressive Disorder 68 0.227
241
P MYC084 Mycobacterium Tuberculosis 1 68 0.227
242
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.227
243
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.227
244
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.227
245
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.227
246
c CWD006 Cowden Syndrome 1 78 0.227
247
c OPT053 Optic Atrophy 1 62 0.227
248
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.227
249
P GLM040 Glioma Susceptibility 1 70 0.227
250
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.227
251
P MLN069 Melanoma, Uveal 59 0.227
252
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.227
253
P BND020 Bone Disease 60 0.227
254
MLG169 Malignant Astrocytoma 57 0.227
255
CLR030 Clear Cell Renal Cell Carcinoma 53 0.227
256
OVR063 Overnutrition 42 0.227
257
c HPT001 Hepatitis C 61 0.227
258
MCP006 Mucoepidermoid Carcinoma 48 0.227
259
MNT002 Mental Depression 56 0.227
260
P CWD010 Cowden Syndrome 70 0.227
261
ORL011 Oral Cancer 60 0.227
262
DPR016 Depression 64 0.227
263
PRT251 Proteinuria, Chronic Benign 58 0.196
264
P RHM011 Rheumatoid Arthritis 81 0.196
265
P SCH015 Schizophrenia 74 0.196
266
ATH013 Atherosclerosis Susceptibility 63 0.196
267
VNH007 Von Hippel-Lindau Syndrome 72 0.196
268
P ANR048 Aniridia 1 66 0.196
269
P BLD134 Bladder Cancer 79 0.196
270
INS024 Insulin-Like Growth Factor I 77 0.196
271
c DPH024 Diaphragmatic Hernia, Congenital 63 0.196
272
KPS004 Kaposi Sarcoma 76 0.196
273
FBR012 Fabry Disease 71 0.196
274
GST019 Gastrointestinal Stromal Tumor 78 0.196
275
HJD001 Hajdu-Cheney Syndrome 62 0.196
276
BRK010 Burkitt Lymphoma 65 0.196
277
P LKM071 Leukemia, Chronic Lymphocytic 74 0.196
278
DFF005 Diffuse Large B-Cell Lymphoma 55 0.196
279
P ART021 Arteriosclerosis 53 0.196
280
c BSL007 Basal Cell Carcinoma 67 0.196
281
P HMN010 Hemangioma 61 0.196
282
CRN022 Corneal Degeneration 33 0.196
283
P ESP024 Esophagitis 60 0.196
284
MCN001 Mucinous Adenocarcinoma 49 0.196
285
P MYP004 Myopathy 67 0.196
286
APP009 Appendix Adenocarcinoma 47 0.196
287
URM002 Uremia 47 0.196
288
P HYD006 Hydrocephalus 62 0.196
289
SKN016 Skin Disease 63 0.196
290
END085 Endometrial Serous Adenocarcinoma 43 0.196
291
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.196
292
P RTN016 Retinal Degeneration 52 0.196
293
ACT250 Acute Megakaryocytic Leukemia 63 0.196
294
NRT011 Neurotrophic Keratopathy 36 0.196
295
CHR178 Chromosomal Triplication 33 0.196
296
TBR011 Tuberculous Meningitis 48 0.196
297
GLM044 Glomerular Disease 34 0.196
298
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 0.196
299
P CHR345 Chronic Pain 50 0.196
300
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 54 0.160
301
P ADM011 Adams-Oliver Syndrome 60 0.160
302
P DWL001 Dowling-Degos Disease 45 0.160
303
TNG009 Tongue Squamous Cell Carcinoma 43 0.160
304
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.160
305
OTT002 Otitis Media 70 0.160
306
c DWL002 Dowling-Degos Disease 1 58 0.160
307
LTR009 Lateral Meningocele Syndrome 53 0.160
308
TTH029 Teeth Present at Birth 20 0.160
309
MSC157 Muscular Dystrophy, Duchenne Type 78 0.160
310
MLG141 Malignant Atrophic Papulosis 35 0.160
311
ANX010 Anxiety 70 0.160
312
EWN003 Ewing Sarcoma 69 0.160
313
c THY107 Thymoma, Familial 42 0.160
314
P CRB048 Cerebral Cavernous Malformations 63 0.160
315
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.160
316
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.160
317
c HMC039 Hemochromatosis, Type 1 73 0.160
318
ACR062 Acroosteolysis 33 0.160
319
P PHC003 Pheochromocytoma 70 0.160
320
OLV002 Oliver Syndrome 41 0.160
321
MNT001 Mantle Cell Lymphoma 65 0.160
322
ADR040 Adrenal Gland Pheochromocytoma 45 0.160
323
PRP080 Peripheral Artery Disease 54 0.160
324
LMB062 Limb Ischemia 55 0.160
325
CLR108 Colorectal Adenoma 63 0.160
326
HYP060 Hyperinsulinism 53 0.160
327
P THY023 Thymoma 64 0.160
328
c ACT071 Acute Kidney Failure 60 0.160
329
ANP005 Anaplastic Astrocytoma 59 0.160
330
P BNC003 Bone Cancer 58 0.160
331
DYS018 Dysostosis 43 0.160
332
HMS001 Hemosiderosis 48 0.160
333
HRT011 Heart Septal Defect 49 0.160
334
BRN004 Brain Edema 54 0.160
335
DBL002 Double Outlet Right Ventricle 56 0.160
336
PNC034 Pancreas Disease 49 0.160
337
DFF016 Diffuse Astrocytoma 48 0.160
338
ADN009 Adenosquamous Carcinoma 49 0.160
339
ESP025 Esophagus Adenocarcinoma 37 0.160
340
HGH043 High Grade Glioma 46 0.160
341
P SKN015 Skin Carcinoma 71 0.160
342
P BRS044 Breast Adenocarcinoma 58 0.160
343
PRM236 Primary Biliary Cholangitis 62 0.160
344
OST011 Osteomalacia 52 0.160
345
GLC003 Glucose Intolerance 53 0.160
346
TNG007 Tongue Carcinoma 55 0.160
347
c PRC016 Pre-Eclampsia 64 0.160
348
PRM013 Premature Menopause 57 0.160
349
P PRS038 Personality Disorder 65 0.160
350
GST040 Gastric Adenocarcinoma 66 0.160
351
CRB039 Cerebrovascular Disease 65 0.160
352
P NRF002 Neurofibromatosis 60 0.160
353
BLR013 Biliary Tract Cancer 43 0.160
354
CYT002 Cytokine Deficiency 43 0.160
355
GBL002 Goblet Cell Carcinoid 32 0.160
356
P SPN081 Spondylocostal Dysostosis, Autosomal Recessive 47 0.160
357
c CHR684 Chronic Kidney Disease 73 0.160
358
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.160
359
PRM243 Primary Bone Cancer 22 0.160
360
TTR011 Tetraploidy 43 0.160
361
P MSC005 Muscular Dystrophy 66 0.160
362
c CHR036 Chronic Cholangitis 24 0.160
363
LMB050 Limbal Stem Cell Deficiency 51 0.160
364
P RRH023 Rare Hereditary Hemochromatosis 52 0.160
365
DWR001 Dwarfism 44 0.160
366
CRB090 Cerebral Hypoxia 42 0.160
367
MYL020 Myelomeningocele 51 0.113
368
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.113
369
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.113
370
c ALZ056 Alzheimer Disease 3 56 0.113
371
BRN032 Brain Glioma 45 0.113
372
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.113
373
c FNC024 Fanconi Anemia, Complementation Group D1 51 0.113
374
P CTN015 Cutaneous T Cell Lymphoma 48 0.113
375
ERY003 Erythema Multiforme 56 0.113
376
c ART115 Aortic Valve Disease 1 72 0.113
377
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.113
378
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.113
379
ONC005 Oncogene Bmyc 9 0.113
380
OCL008 Oculopharyngeal Muscular Dystrophy 52 0.113
381
PPL052 Papillomatosis, Confluent and Reticulated 34 0.113
382
P MJR007 Major Affective Disorder 1 42 0.113
383
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.113
384
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.113
385
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.113
386
P HRS035 Hirschsprung Disease 1 66 0.113
387
DGR001 Digeorge Syndrome 62 0.113
388
RTC012 Reticuloendotheliosis, X-Linked 35 0.113
389
P MLT020 Multiple Sclerosis 79 0.113
390
c CRB191 Cerebral Cavernous Malformations 2 45 0.113
391
c CRB094 Cerebral Cavernous Malformations 3 41 0.113
392
P BRC006 Brachydactyly 52 0.113
393
c HPT073 Hepatitis C Virus 70 0.113
394
c FNC023 Fanconi Anemia, Complementation Group N 48 0.113
395
P ACN016 Acne Inversa, Familial, 3 28 0.113
396
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.113
397
c HRM008 Hermansky-Pudlak Syndrome 5 46 0.113
398
FTL006 Fetal Alcohol Spectrum Disorder 43 0.113
399
c PNC106 Pancreatic Agenesis 1 51 0.113
400
c FNC032 Fanconi Anemia, Complementation Group B 48 0.113
401
P SPR119 Spermatogenic Failure, X-Linked, 1 36 0.113
402
ANN002 Anencephaly 57 0.113
403
P ATX030 Ataxia-Telangiectasia 80 0.113
404
c TYP008 Type 1 Diabetes Mellitus 77 0.113
405
P TTR001 Tetralogy of Fallot 69 0.113
406
PCK003 Pick Disease of Brain 70 0.113
407
MYC006 Mycosis Fungoides 64 0.113
408
MWT001 Mowat-Wilson Syndrome 57 0.113
409
P FRG001 Fragile X Syndrome 70 0.113
410
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.113
411
FRN006 Frontotemporal Dementia 68 0.113
412
P STR020 Strabismus 56 0.113
413
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.113
414
INF158 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations 30 0.113
415
c FNC028 Fanconi Anemia, Complementation Group L 46 0.113
416
c FNC025 Fanconi Anemia, Complementation Group J 52 0.113
417
JVN004 Juvenile Myelomonocytic Leukemia 66 0.113
418
c ART101 Aortic Valve Disease 2 65 0.113
419
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.113
420
SVR097 Severe Cutaneous Adverse Reaction 68 0.113
421
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 0.113
422
c DWL003 Dowling-Degos Disease 2 22 0.113
423
P DNG005 Dengue Virus 55 0.113
424
APL023 Aplasia Cutis Congenita, Nonsyndromic 46 0.113
425
c FNC043 Fanconi Anemia, Complementation Group E 62 0.113
426
P FNC044 Fanconi Anemia, Complementation Group C 56 0.113
427
CHR594 Chromosome 3q29 Deletion Syndrome 41 0.113
428
P ADL017 Adult T-Cell Leukemia 53 0.113
429
P PRM030 Permanent Neonatal Diabetes Mellitus 59 0.113
430
c ERL056 Early-Onset Parkinson's Disease 39 0.113
431
SPN221 Spina Bifida Occulta 39 0.113
432
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.113
433
c ATM099 Autoimmune Uveitis 44 0.113
434
GLL029 Gallbladder Adenoma 30 0.113
435
P LFT003 Left Ventricular Noncompaction 58 0.113
436
P SNS001 Sensorineural Hearing Loss 60 0.113
437
OST017 Osteomyelitis 63 0.113
438
SLT007 Solitary Rectal Ulcer Syndrome 16 0.113
439
THY128 Thyroid Tumor 33 0.113
440
P RSP003 Respiratory Failure 73 0.113
441
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.113
442
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.113
443
NNL006 Non-Alcoholic Steatohepatitis 54 0.113
444
PRL017 Prolymphocytic Leukemia 47 0.113
445
PRP036 Peripheral T-Cell Lymphoma 52 0.113
446
THY006 Thymus Lymphoma 27 0.113
447
HND002 Hand, Foot and Mouth Disease 50 0.113
448
PNC001 Pancytopenia 52 0.113
449
OST015 Osteochondrodysplasia 60 0.113
450
P CRN037 Craniosynostosis 67 0.113
451
MYL031 Myeloproliferative Neoplasm 66 0.113
452
P LRY044 Larynx Cancer 53 0.113
453
BRN012 Bronchiolitis Obliterans 56 0.113
454
BRS099 Breast Ductal Carcinoma 61 0.113
455
PPL022 Papilloma 53 0.113
456
P FBR017 Fibrosarcoma 55 0.113
457
RTN020 Retinal Vascular Disease 45 0.113
458
NRN004 Neuroendocrine Tumor 55 0.113
459
c ADM010 Adams-Oliver Syndrome 5 33 0.113
460
P ALC033 Alcohol Use Disorder 67 0.113
461
P ECL001 Eclampsia 52 0.113
462
LVR012 Liver Cirrhosis 62 0.113
463
URT010 Ureteral Obstruction 44 0.113
464
P PLC011 Pilocytic Astrocytoma 55 0.113
465
P CRV031 Cervical Adenocarcinoma 48 0.113
466
CRV038 Cervical Squamous Cell Carcinoma 56 0.113
467
ART017 Aortic Disease 49 0.113
468
CLR013 Clear Cell Hidradenoma 26 0.113
469
P EYD002 Eye Disease 57 0.113
470
P PRP019 Peripheral Nervous System Disease 57 0.113
471
P GLL018 Gallbladder Cancer 59 0.113
472
CNG034 Congestive Heart Failure 69 0.113
473
c INF023 Inflammatory Breast Carcinoma 48 0.113
474
AMN001 Amenorrhea 53 0.113
475
RNL025 Renal Hypoplasia 46 0.113
476
SQM002 Squamous Cell Papilloma 45 0.113
477
BRN002 Bronchiolitis 57 0.113
478
IGG001 Iga Glomerulonephritis 50 0.113
479
CNS004 Constipation 56 0.113
480
HYP005 Hypokalemia 55 0.113
481
MTH009 Mouth Disease 57 0.113
482
HDR004 Hidradenoma 37 0.113
483
INT066 Interstitial Lung Disease 60 0.113
484
PNC129 Pancreatic Adenocarcinoma 64 0.113
485
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.113
486
HMT002 Hematologic Cancer 61 0.113
487
GLS001 Gliosarcoma 63 0.113
488
CHL018 Childhood Medulloblastoma 48 0.113
489
DMY004 Demyelinating Disease 50 0.113
490
TRT001 Teratocarcinoma 41 0.113
491
ALC005 Alcoholic Pancreatitis 38 0.113
492
P PNC044 Pancreatitis 61 0.113
493
TRP005 Trophoblastic Neoplasm 38 0.113
494
PLM010 Pulmonary Edema 54 0.113
495
P LKD001 Leukodystrophy 58 0.113
496
P MNN007 Meningocele 39 0.113
497
P HYP040 Hypospadias 51 0.113
498
RCK004 Rickets 64 0.113
499
P FCL005 Focal Segmental Glomerulosclerosis 57 0.113
500
P UVT001 Uveitis 57 0.113
501
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 0.113
502
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.113
503
P THR014 Thrombocytopenia 66 0.113
504
PLP001 Pulpitis 48 0.113
505
TLN003 Telangiectasis 51 0.113
506
P RTN018 Retinal Disease 53 0.113
507
P PNC025 Panic Disorder 52 0.113
508
CHR074 Choriocarcinoma 46 0.113
509
CLF001 Cleft Lip 54 0.113
510
MCH006 Mechanical Strabismus 40 0.113
511
DBT010 Diabetic Neuropathy 54 0.113
512
P NRV007 Nervous System Disease 65 0.113
513
P LPS004 Lupus Erythematosus 61 0.113
514
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.113
515
RTN123 Retinochoroidal Coloboma 19 0.113
516
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.113
517
DFF036 Differentiated Thyroid Carcinoma 51 0.113
518
P PHC014 Phocomelia 23 0.113
519
c CRB051 Cerebral Cavernous Malformation, Familial 41 0.113
520
ART030 Aortic Arch Interruption 25 0.113
521
LWG005 Low-Grade Astrocytoma 38 0.113
522
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.113
523
TCL005 T-Cell Prolymphocytic Leukemia 48 0.113
524
MLG164 Malignant Epithelial Tumor of Ovary 24 0.113
525
ERY066 Erythema Multiforme Major 29 0.113
526
LKP003 Leukoplakia 39 0.113
527
CVR010 Cavernous Malformation 29 0.113
528
CLF004 Cleft Lip/palate 56 0.113
529
P SPN237 Spina Bifida Aperta 19 0.113
530
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.113
531
P OVR082 Overgrowth Syndrome 41 0.113
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