Search results for smad1

493 hits were found for smad1

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 97 19.338
2
P PLM037 Pulmonary Hypertension 69 17.589
3
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 13.252
4
FBR011 Fibrodysplasia Ossificans Progressiva 67 12.963
5
c PLM164 Pulmonary Hypertension, Primary, 1 80 11.485
6
BSC001 Buschke-Ollendorff Syndrome 56 11.423
7
OST014 Osteopoikilosis 41 11.423
8
MLR003 Melorheostosis 48 11.423
9
P CLD001 Cleidocranial Dysplasia 64 8.220
10
c SPN395 Spinal Muscular Atrophy, Type Ii 55 8.077
11
c SPN394 Spinal Muscular Atrophy, Type Iii 52 7.962
12
c SPN398 Spinal Muscular Atrophy, Type Iv 44 7.962
13
c MCR133 Microvascular Complications of Diabetes 4 41 4.034
14
c MCR113 Microvascular Complications of Diabetes 3 52 4.034
15
c MCR130 Microvascular Complications of Diabetes 6 41 4.034
16
c MCR120 Microvascular Complications of Diabetes 7 47 4.034
17
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.509
18
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.328
19
BNR002 Bone Resorption Disease 47 2.142
20
OST159 Osteogenic Sarcoma 66 2.045
21
TLN003 Telangiectasis 51 2.017
22
HMS001 Hemosiderosis 48 2.008
23
P RRH023 Rare Hereditary Hemochromatosis 53 2.008
24
P CLR023 Colorectal Cancer 100 1.966
25
P LYM118 Lymphoma 69 1.965
26
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.901
27
ISC004 Ischemia 61 1.884
28
P BCL017 B-Cell Lymphoma 57 1.833
29
END086 End Stage Renal Disease 54 1.823
30
P ART005 Arteriovenous Malformation 65 1.801
31
HLX001 Helix Syndrome 47 1.787
32
GLM045 Glioma 62 1.767
33
GLL048 Glial Tumor 52 1.767
34
ESP021 Esophageal Cancer 84 1.742
35
P OST002 Osteoporosis 77 1.732
36
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.732
37
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.732
38
RNL077 Renal Fibrosis 46 1.713
39
CRB004 Cerebral Artery Occlusion 46 1.691
40
P PRS040 Prostate Cancer 95 1.672
41
OST012 Osteoarthritis 77 1.664
42
c SCL052 Scleroderma, Familial Progressive 60 1.651
43
P MLN007 Male Infertility 56 1.634
44
GLB002 Glioblastoma 67 1.606
45
P GLM007 Glomerulonephritis 59 1.569
46
P SYS005 Systemic Scleroderma 73 1.556
47
SQM006 Squamous Cell Carcinoma 59 1.516
48
P PNC035 Pancreatic Cancer 86 1.483
49
c HMC039 Hemochromatosis, Type 1 73 1.470
50
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.390
51
LYM133 Lymphoma, Hodgkin, Classic 74 1.367
52
URT010 Ureteral Obstruction 45 1.365
53
DFF005 Diffuse Large B-Cell Lymphoma 55 1.352
54
P PLM036 Pulmonary Fibrosis 65 1.352
55
P BND020 Bone Disease 60 1.347
56
P FLL037 Follicular Lymphoma 73 1.339
57
HYP066 Hyperglycemia 60 1.339
58
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.318
59
HGH043 High Grade Glioma 46 1.296
60
BRN056 Bronchopulmonary Dysplasia 57 1.281
61
P LNG064 Lung Cancer Susceptibility 3 70 1.266
62
P HPT023 Hepatocellular Carcinoma 95 1.266
63
P INF032 Infertility 60 1.266
64
P PRL003 Proliferative Glomerulonephritis 43 1.249
65
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.249
66
LNG099 Lung Disease 62 1.249
67
P MCR010 Microcephaly 59 1.232
68
ATH013 Atherosclerosis Susceptibility 63 1.215
69
RNL078 Renal Dysplasia 46 1.215
70
HYP266 Hypoxia 56 1.188
71
P PLY011 Polycystic Ovary Syndrome 57 1.176
72
P ADL010 Adult Respiratory Distress Syndrome 71 1.133
73
AZS001 Azoospermia 45 1.108
74
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.108
75
PRT251 Proteinuria, Chronic Benign 58 1.090
76
IDP092 Idiopathic/heritable Pulmonary Arterial Hypertension 43 1.085
77
DFC004 Deficiency Anemia 74 1.076
78
P VSC007 Vascular Disease 62 1.062
79
IRN002 Iron Metabolism Disease 56 1.062
80
c CHR684 Chronic Kidney Disease 74 1.047
81
c ART115 Aortic Valve Disease 1 72 1.032
82
c DPH024 Diaphragmatic Hernia, Congenital 64 1.032
83
c TYP009 Type 2 Diabetes Mellitus 92 0.983
84
P ADN016 Adenocarcinoma 63 0.983
85
P DBT009 Diabetes Mellitus 67 0.983
86
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.965
87
c MCR115 Microvascular Complications of Diabetes 5 65 0.947
88
ORL015 Oral Squamous Cell Carcinoma 43 0.947
89
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.947
90
P RCT021 Rectum Cancer 54 0.947
91
P NRB001 Neuroblastoma 66 0.947
92
P AST005 Asthma 76 0.927
93
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.927
94
TND004 Tendinopathy 45 0.927
95
TND005 Tendinitis 54 0.927
96
c PCH010 Pachyonychia Congenita 3 43 0.927
97
P LNG032 Lung Cancer 98 0.927
98
P HRS035 Hirschsprung Disease 1 66 0.927
99
DGR001 Digeorge Syndrome 62 0.927
100
P INT070 Intestinal Obstruction 57 0.927
101
PLY150 Polykaryocytosis Inducer 29 0.906
102
P RSP003 Respiratory Failure 74 0.906
103
BRN004 Brain Edema 54 0.906
104
LNG039 Lung Squamous Cell Carcinoma 57 0.906
105
P OVR042 Ovarian Cancer 88 0.883
106
KPS004 Kaposi Sarcoma 76 0.883
107
RTN020 Retinal Vascular Disease 45 0.883
108
P HYP086 Hypothyroidism 69 0.883
109
DGN001 Degenerative Disc Disease 48 0.883
110
EXS001 Exostosis 49 0.859
111
NNT004 Neonatal Respiratory Failure 36 0.859
112
CNS004 Constipation 56 0.859
113
P HLP001 Holoprosencephaly 69 0.859
114
P WLL002 Weill-Marchesani Syndrome 55 0.832
115
c SML038 Small Cell Cancer of the Lung 69 0.832
116
P JVN014 Juvenile Polyposis Syndrome 65 0.832
117
P CHR345 Chronic Pain 50 0.832
118
P THL005 Thalassemia 56 0.832
119
P OVR082 Overgrowth Syndrome 42 0.832
120
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.801
121
P BRC006 Brachydactyly 52 0.801
122
c SPR119 Spermatogenic Failure, X-Linked, 1 36 0.764
123
P ISL078 Isolated Ectopia Lentis 58 0.764
124
PLM184 Pulmonary Arterial Hypertension Associated with Congenital Heart Disease 42 0.764
125
URN010 Urinary Tract Obstruction 55 0.717
126
KRT009 Keratosis 52 0.717
127
TRN018 Transitional Cell Carcinoma 56 0.717
128
P ACT008 Actinic Keratosis 54 0.717
129
P LKM062 Leukemia, Acute Lymphoblastic 69 0.680
130
MYL005 Myelofibrosis 70 0.632
131
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.630
132
P TTR001 Tetralogy of Fallot 69 0.602
133
P KDN017 Kidney Cancer 60 0.602
134
MYL069 Myeloma, Multiple 77 0.430
135
c SPN225 Spondyloarthropathy 1 70 0.430
136
SPN051 Spondylitis 51 0.430
137
INF009 Inflammatory Spondylopathy 30 0.430
138
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.398
139
P CHN012 Chondrosarcoma 56 0.398
140
P MLT074 Multiple Endocrine Neoplasia 58 0.398
141
IRN001 Iron Deficiency Anemia 58 0.381
142
P PRD008 Periodontitis 64 0.381
143
AGN016 Aging 54 0.345
144
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.345
145
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.345
146
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.345
147
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.345
148
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.345
149
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.345
150
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.345
151
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.345
152
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.345
153
CYT002 Cytokine Deficiency 43 0.345
154
P SCL048 Sclerosteosis 58 0.325
155
P LKM002 Leukemia 66 0.325
156
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 0.325
157
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.304
158
P GST053 Gastric Cancer 82 0.304
159
MSC007 Muscle Hypertrophy 64 0.304
160
P CRB045 Cerebellar Hypoplasia 40 0.304
161
SCH014 Schistosomiasis 56 0.304
162
P FBR017 Fibrosarcoma 55 0.304
163
SPN186 Spinal Cord Injury 61 0.304
164
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.282
165
P MYC007 Myocardial Infarction 69 0.282
166
FBR047 Fibromyalgia 58 0.282
167
P PRP019 Peripheral Nervous System Disease 57 0.282
168
P CRN037 Craniosynostosis 67 0.282
169
P ART023 Arthropathy 60 0.282
170
EMB004 Embryonal Carcinoma 55 0.282
171
P MYL006 Myeloid Leukemia 60 0.282
172
P SPP010 Suppressor of Tumorigenicity 3 51 0.257
173
INS024 Insulin-Like Growth Factor I 77 0.257
174
CHR005 Chorioamnionitis 50 0.257
175
P PLY014 Polycystic Kidney Disease 71 0.257
176
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.257
177
ADR040 Adrenal Gland Pheochromocytoma 45 0.257
178
ATM095 Autoimmune Disease 61 0.257
179
P PHC003 Pheochromocytoma 70 0.257
180
NRL016 Neural Tube Defects 81 0.257
181
CHR100 Chronic Ulcer of Skin 57 0.257
182
LMY002 Leiomyoma 51 0.257
183
LVR012 Liver Cirrhosis 62 0.257
184
P LTR001 Lateral Sclerosis 58 0.257
185
SLC006 Silicosis 55 0.257
186
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.257
187
c LKM061 Leukemia, Acute Myeloid 83 0.257
188
P NSP012 Nasopharyngeal Carcinoma 60 0.257
189
P MSC003 Muscular Atrophy 52 0.257
190
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.257
191
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 0.257
192
NSP003 Nasopharyngeal Disease 33 0.257
193
DWR001 Dwarfism 45 0.257
194
ADN027 Adenomyosis 59 0.230
195
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.230
196
CRV035 Cervical Cancer 72 0.230
197
BRR014 Barrett Esophagus 66 0.230
198
c PRC016 Pre-Eclampsia 64 0.230
199
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.230
200
P MLT020 Multiple Sclerosis 79 0.230
201
LMB062 Limb Ischemia 55 0.230
202
P ATR011 Atrial Fibrillation 66 0.230
203
c HPT073 Hepatitis C Virus 71 0.230
204
HRW001 Hair Whorl 35 0.230
205
c PRG021 Paragangliomas 4 38 0.230
206
c HPT001 Hepatitis C 61 0.230
207
P SKN015 Skin Carcinoma 71 0.230
208
HPT009 Hepatopulmonary Syndrome 48 0.230
209
P ALP008 Alopecia 53 0.230
210
ART140 Arteries, Anomalies of 52 0.199
211
P RTN024 Retinoblastoma 72 0.199
212
CHR103 Charge Syndrome 65 0.199
213
ARC025 Arachnoid Cysts, Intracranial 37 0.199
215
c LKM063 Leukemia, Chronic Myeloid 71 0.199
216
CRT069 Cortical Malformations, Occipital 31 0.199
217
LPP008 Lipoprotein Quantitative Trait Locus 65 0.199
218
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.199
219
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 0.199
220
INT395 Intracranial Meningioma 48 0.199
221
ALC007 Alcohol Dependence 65 0.199
222
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.199
223
P CRC039 Coarctation of Aorta 46 0.199
224
c EXS019 Exostoses, Multiple, Type I 54 0.199
225
c SPS099 Spastic Paraplegia 42, Autosomal Dominant 39 0.199
226
c PRG020 Paragangliomas 3 39 0.199
227
TRS030 Tarsal Coalition 25 0.199
228
c HMC009 Hemochromatosis Type 2 58 0.199
229
CLT003 Colitis 63 0.199
230
TTH002 Tooth Agenesis 61 0.199
231
P CYS039 Cystic Kidney Disease 52 0.199
232
CRB039 Cerebrovascular Disease 65 0.199
233
P PNC044 Pancreatitis 61 0.199
234
SVR004 Severe Combined Immunodeficiency 71 0.199
235
CHN010 Chondroma 43 0.199
236
P MLN008 Melanoma 75 0.199
237
CRT017 Cartilage Disease 52 0.199
238
KHN001 Kuhnt-Junius Degeneration 48 0.199
239
GST033 Gestational Diabetes 61 0.199
240
INT066 Interstitial Lung Disease 60 0.199
241
P KRT005 Keratoacanthoma 47 0.199
242
ART016 Aortic Aneurysm 69 0.199
243
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.199
244
MNN043 Meningioma, Familial 79 0.199
245
ANR040 Aneurysm 60 0.199
246
P GST044 Gastritis 55 0.199
247
P INS002 in Situ Carcinoma 53 0.199
248
PTT037 Pituitary Tumors 44 0.199
249
P KDN018 Kidney Disease 72 0.199
250
SCR001 Secretory Meningioma 40 0.199
251
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.199
252
P CRB059 Cerebellar Degeneration 36 0.199
253
PRT036 Peritonitis 65 0.199
254
ALL006 Allergic Asthma 56 0.199
255
GRN022 Granulosa Cell Tumor of the Ovary 34 0.199
256
c ACT075 Acute Myocardial Infarction 55 0.199
257
P ATR005 Atrophic Gastritis 50 0.199
258
ART141 Arteriovenous Malformations of the Brain 58 0.163
259
P BCK002 Beckwith-Wiedemann Syndrome 61 0.163
260
c PRD040 Periodontitis, Chronic 52 0.163
261
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 43 0.163
262
ACR008 Acrocallosal Syndrome 70 0.163
263
P PRX021 Proximal Symphalangism 50 0.163
264
OST003 Osteonecrosis 61 0.163
265
RNL025 Renal Hypoplasia 46 0.163
266
ART074 Aortic Dissection 53 0.163
267
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.163
268
HPT046 Hepatic Veno-Occlusive Disease 55 0.163
269
c ATR087 Atrial Standstill 1 74 0.163
270
BRK010 Burkitt Lymphoma 66 0.163
271
P HYP058 Hypervitaminosis a 47 0.163
272
c TYP008 Type 1 Diabetes Mellitus 77 0.163
273
c ATS007 Autism Spectrum Disorder 72 0.163
274
P FML011 Familial Adenomatous Polyposis 71 0.163
275
P ANP001 Anaplastic Large Cell Lymphoma 61 0.163
276
P DRM053 Dermatitis, Atopic 65 0.163
277
INT146 Intervertebral Disc Disease 61 0.163
278
P MCR129 Microvascular Complications of Diabetes 1 68 0.163
279
KLD003 Keloid Formation 34 0.163
280
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.163
281
c EXS020 Exostoses, Multiple, Type Ii 38 0.163
282
c NRF024 Neurofibromatosis, Type I 76 0.163
283
MCC012 Mccune-Albright Syndrome 69 0.163
284
CLF027 Cleft Palate, Isolated 64 0.163
285
CYN002 Cyanosis, Transient Neonatal 43 0.163
286
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.163
287
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.163
288
c ACT073 Acute Leukemia 59 0.163
289
PTN001 Patent Foramen Ovale 62 0.163
290
P MYP006 Myopia 55 0.163
291
c ACT027 Acute Pancreatitis 60 0.163
292
CNG034 Congestive Heart Failure 69 0.163
293
c JVN002 Juvenile Type Testicular Granulosa Cell Tumor 34 0.163
294
DNT012 Dental Caries 53 0.163
295
SYN007 Synovitis 54 0.163
296
P OST001 Osteopetrosis 70 0.163
297
P VNT002 Ventricular Septal Defect 58 0.163
298
P OTS001 Otosclerosis 49 0.163
299
PLC002 Plica Syndrome 35 0.163
300
NPH010 Nephrosclerosis 50 0.163
301
P HRT032 Heart Disease 84 0.163
302
SKN016 Skin Disease 62 0.163
303
P ECT006 Ectodermal Dysplasia 62 0.163
304
GST040 Gastric Adenocarcinoma 66 0.163
305
DRM006 Dermatitis 62 0.163
306
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.163
307
SFT003 Soft Tissue Sarcoma 57 0.163
308
BCK006 Back Pain 43 0.163
309
HRP004 Herpes Zoster 60 0.163
310
P CTR002 Cataract 59 0.163
311
P PLM025 Pulmonary Venoocclusive Disease 44 0.163
312
48X005 48,xyyy 39 0.163
313
CHC001 Chickenpox 56 0.163
314
PLC008 Placenta Disease 49 0.163
315
P MSC005 Muscular Dystrophy 66 0.163
316
KLD004 Keloid Disorder 39 0.163
317
FTT001 Fatty Liver Disease 61 0.163
318
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 0.163
319
ENC014 Enchondroma 28 0.163
320
P SCK005 Sickle Cell Disease 56 0.163
321
GLM044 Glomerular Disease 34 0.163
322
P ALZ034 Alzheimer Disease 87 0.115
323
P BLD134 Bladder Cancer 79 0.115
324
MGL003 Megalocornea 47 0.115
325
c ORF037 Orofaciodigital Syndrome I 59 0.115
326
WCK001 Wieacker-Wolff Syndrome 40 0.115
327
HLC007 Helicobacter Pylori Infection 67 0.115
328
c NPH049 Nephrotic Syndrome, Type 2 52 0.115
329
P PSD087 Pseudoxanthoma Elasticum 66 0.115
330
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.115
331
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 48 0.115
332
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 0.115
333
PLY001 Polycythemia Vera 69 0.115
334
WLF001 Wolff-Parkinson-White Syndrome 63 0.115
335
c BRN108 Branchiootic Syndrome 1 63 0.115
336
HMC014 Homocysteinemia 52 0.115
337
ANX010 Anxiety 70 0.115
338
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 53 0.115
339
KWS002 Kawasaki Disease 65 0.115
340
ADR016 Adrenal Cortical Carcinoma 61 0.115
341
P TMR010 Tumor Predisposition Syndrome 69 0.115
342
KSH004 Kashin-Beck Disease 37 0.115
343
PYR010 Peyronie's Disease 50 0.115
344
ATS010 Autosomal Recessive Disease 42 0.115
345
MNT001 Mantle Cell Lymphoma 65 0.115
346
P GRF003 Graft-Versus-Host Disease 71 0.115
347
P INF037 Inflammatory Bowel Disease 53 0.115
348
P GLP001 Geleophysic Dysplasia 46 0.115
349
CMB007 Combined Immunodeficiency 56 0.115
350
P KRT007 Keratoconus 50 0.115
351
BCT022 Bacterial Infectious Disease 56 0.115
352
GLC003 Glucose Intolerance 53 0.115
353
P WLF004 Wolfram Syndrome 61 0.115
354
TNG007 Tongue Carcinoma 55 0.115
355
NNL006 Non-Alcoholic Steatohepatitis 54 0.115
356
PRM013 Premature Menopause 57 0.115
357
c MGR028 Migraine with or Without Aura 1 64 0.115
358
c BRC079 Brachydactyly, Type A2 50 0.115
359
c BRC081 Brachydactyly, Type C 48 0.115
360
ACR043 Acromicric Dysplasia 49 0.115
361
P CLB034 Coloboma, Ocular, Autosomal Dominant 48 0.115
362
c SPN330 Spondylocostal Dysostosis 5 55 0.115
363
c WLF013 Wolfram Syndrome 1 60 0.115
364
CNT061 Conotruncal Heart Malformations 66 0.115
365
TRC118 Trichodentoosseous Syndrome 42 0.115
366
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.115
367
P CTN015 Cutaneous T Cell Lymphoma 48 0.115
368
OST006 Osteoblastoma 38 0.115
369
INT029 Interleukin-7 Receptor Alpha Deficiency 28 0.115
370
MTB004 Metabolic Acidosis 48 0.115
371
P CRD119 Cardiac Arrest 68 0.115
372
MLS013 Miles-Carpenter Syndrome 33 0.115
373
ANG020 Angiosarcoma 63 0.115
374
AMG001 Amegakaryocytic Thrombocytopenia, Congenital 55 0.115
375
c BRC052 Brachydactyly, Type B2 40 0.115
376
HYP748 Hypertelorism 46 0.115
377
c HYP836 Hypercholesterolemia, Familial, 1 73 0.115
378
P DVL012 Developmental Dysplasia of the Hip 1 45 0.115
379
P HNT016 Huntington Disease 73 0.115
380
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.115
381
LMY014 Leiomyoma, Uterine 55 0.115
382
LTR009 Lateral Meningocele Syndrome 52 0.115
383
c SYS001 Systemic Lupus Erythematosus 86 0.115
384
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.115
385
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.115
386
HYD002 Hydronephrosis 58 0.115
387
SRC014 Sarcoma 64 0.115
388
P SPN052 Spondyloarthropathy 54 0.115
389
MCR018 Microcytic Anemia 47 0.115
390
MYH012 Myhre Syndrome 43 0.115
391
P GLM040 Glioma Susceptibility 1 70 0.115
392
HND015 Hand Skill, Relative 29 0.115
393
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.115
394
IRN004 Iron-Refractory Iron Deficiency Anemia 46 0.115
395
ODN023 Odontochondrodysplasia 70 0.115
396
STP011 Stapes Ankylosis with Broad Thumbs and Toes 28 0.115
397
c SYM022 Symphalangism, Proximal, 1a 28 0.115
398
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 56 0.115
399
P ATS364 Autism 72 0.115
400
P LKM071 Leukemia, Chronic Lymphocytic 74 0.115
401
DYS018 Dysostosis 43 0.115
402
OST017 Osteomyelitis 63 0.115
403
c ERL056 Early-Onset Parkinson's Disease 39 0.115
404
ACT098 Acute Erythroid Leukemia 55 0.115
405
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.115
406
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.115
407
CRN022 Corneal Degeneration 33 0.115
408
OPS001 Opisthorchiasis 41 0.115
409
PNC001 Pancytopenia 52 0.115
410
MLG169 Malignant Astrocytoma 57 0.115
411
TRC005 Tracheal Stenosis 43 0.115
412
P END044 Endometriosis 62 0.115
413
BRN012 Bronchiolitis Obliterans 56 0.115
414
BRN002 Bronchiolitis 57 0.115
415
P HML002 Hemolytic Anemia 62 0.115
416
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.115
417
LYM027 Lymphopenia 56 0.115
418
PRP016 Paraplegia 52 0.115
419
PLM041 Pulmonary Valve Stenosis 50 0.115
420
PLC001 Placenta Accreta 44 0.115
421
P RTN018 Retinal Disease 53 0.115
422
P ALP004 Alport Syndrome 70 0.115
423
ANK001 Ankylosis 51 0.115
424
P LMY004 Leiomyosarcoma 62 0.115
425
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.115
426
P AGM001 Agammaglobulinemia 67 0.115
427
PPL022 Papilloma 53 0.115
428
c MLG084 Malignant Fibrous Histiocytoma 62 0.115
429
SQM002 Squamous Cell Papilloma 45 0.115
430
P THR014 Thrombocytopenia 66 0.115
431
ANS011 Anus Cancer 55 0.115
432
P AGG001 Aggressive Periodontitis 55 0.115
433
CYS008 Cystic Echinococcosis 57 0.115
434
ECH003 Echinococcosis 52 0.115
435
P HYD006 Hydrocephalus 63 0.115
436
P ESP024 Esophagitis 60 0.115
437
NRG002 Neurogenic Bladder 55 0.115
438
P NPH012 Nephrotic Syndrome 62 0.115
439
P RST002 Restrictive Cardiomyopathy 54 0.115
440
NNS002 Nonspecific Interstitial Pneumonia 42 0.115
441
P CNT005 Central Nervous System Lymphoma 51 0.115
442
P PTT006 Pituitary Adenoma 55 0.115
443
CHR074 Choriocarcinoma 46 0.115
444
CLN015 Colon Adenocarcinoma 64 0.115
445
SMT002 Smooth Muscle Tumor 38 0.115
446
ADR004 Adrenal Cortical Adenocarcinoma 38 0.115
447
P HRD001 Hereditary Multiple Exostoses 48 0.115
448
P AML002 Amelogenesis Imperfecta 56 0.115
449
P ART021 Arteriosclerosis 53 0.115
450
PLM029 Palmoplantar Keratosis 48 0.115
451
MSC157 Muscular Dystrophy, Duchenne Type 79 0.115
452
c SPS127 Spastic Paraplegia 6, Autosomal Dominant 48 0.115
453
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.115
454
P PLY006 Polydactyly 58 0.115
455
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.115
456
PYC001 Pycnodysostosis 55 0.115
457
P PTN014 Patent Ductus Arteriosus 1 59 0.115
458
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 0.115
459
NRM005 Neuromuscular Disease 63 0.115
460
HRT012 Heart Valve Disease 53 0.115
461
SPN035 Spindle Cell Sarcoma 51 0.115
462
SMN007 Seminoma 42 0.115
463
HYP572 Hypoganglionosis 27 0.115
464
OVR094 Ovarian Epithelial Cancer 39 0.115
465
P VSC011 Vasculitis 61 0.115
466
TRC037 Tracheobronchomalacia 23 0.115
467
XLN085 X-Linked Complicated Spastic Paraplegia Type 1 21 0.115
468
SPS057 Spasticity 43 0.115
469
P NRC002 Narcolepsy 55 0.115
470
P PLY018 Polycythemia 56 0.115
471
HRD104 Hereditary Multiple Osteochondromas 43 0.115
472
P TRC031 Trichorhinophalangeal Syndrome 37 0.115
473
TNS014 Tenosynovitis 45 0.115
474
PRM226 Primary Central Nervous System Lymphoma 47 0.115
475
c SPS041 Spastic Paraplegia 6 26 0.115
476
VNF001 Vein of Galen Aneurysm 18 0.115
477
P LPS004 Lupus Erythematosus 61 0.115
478
P HYP076 Hyperthyroidism 53 0.115
479
47X002 47,xyy 48 0.115
480
EXP004 Exophthalmos 50 0.115
481
P NRF002 Neurofibromatosis 60 0.115
482
GGN002 Gigantism 33 0.115
483
P OST028 Osteochondroma 44 0.115
484
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.115
485
FBR019 Fibromatosis 44 0.115
486
SYS071 Systemic Autoimmune Disease 35 0.115
487
HGH041 High-Grade Astrocytoma 36 0.115
488
INH023 Inherited Cancer-Predisposing Syndrome 53 0.115
489
GNR035 Generalized Juvenile Polyposis/juvenile Polyposis Coli 41 0.115
490
P LTH050 Lethal Chondrodysplasia 13 0.115
491
P VTR007 Vitreoretinopathy 45 0.115
492
ACR121 Acromelic Dysplasia 11 0.115
493
HRD218 Hereditary Stomatocytosis 31 0.115
Content
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