Search results for gata4

433 hits were found for gata4

# Family MCID Name MIFTS Score
1
c ATR067 Atrioventricular Septal Defect 4 26 46.678
2
INT276 Interatrial Communication 52 39.375
3
P TTR001 Tetralogy of Fallot 69 38.188
4
P HRT032 Heart Disease 84 37.699
5
P ATR066 Atrial Septal Defect 2 41 37.437
6
c VNT028 Ventricular Septal Defect 1 28 32.609
7
TST035 Testicular Anomalies with or Without Congenital Heart Disease 20 29.676
8
P VNT002 Ventricular Septal Defect 58 21.426
9
PTN001 Patent Foramen Ovale 61 17.162
10
c FML001 Familial Atrial Fibrillation 65 17.113
11
46X012 46,xy Partial Gonadal Dysgenesis 41 16.436
12
c DLT002 Dilated Cardiomyopathy 79 16.227
13
CHR266 Chromosome 8p23.1 Deletion 25 14.874
14
P ATR010 Atrial Heart Septal Defect 58 14.801
15
HRT011 Heart Septal Defect 49 14.683
16
P ATR001 Atrioventricular Septal Defect 54 14.528
17
EMB004 Embryonal Carcinoma 55 13.948
18
ALC007 Alcohol Dependence 65 12.794
19
P MYC007 Myocardial Infarction 69 12.500
20
ATR057 Atrioventricular Block 54 11.888
21
PLM041 Pulmonary Valve Stenosis 50 11.613
22
c 46X055 46,xy Sex Reversal 3 40 11.556
23
P MCR010 Microcephaly 59 11.194
24
c CNG404 Congenital Heart Defects, Multiple Types, 4 39 10.583
25
P HYP061 Hypertrophic Cardiomyopathy 68 10.485
26
DBL002 Double Outlet Right Ventricle 56 10.438
27
P INT070 Intestinal Obstruction 57 10.383
28
P TRT010 Teratoma 50 10.357
29
RNL051 Renal Cysts and Diabetes Syndrome 58 10.213
30
P RSP003 Respiratory Failure 73 10.213
31
HYD002 Hydronephrosis 58 10.213
32
P ALC033 Alcohol Use Disorder 67 9.879
33
P HYP040 Hypospadias 51 9.807
34
c ART115 Aortic Valve Disease 1 72 9.715
35
c HYP595 Hypertension, Essential 84 9.225
36
c DPH024 Diaphragmatic Hernia, Congenital 63 9.224
37
EBS001 Ebstein Anomaly 54 9.133
38
c 46X082 46,xy Sex Reversal 52 9.133
39
LPP008 Lipoprotein Quantitative Trait Locus 65 9.072
40
ING001 Inguinal Hernia 59 8.864
41
ADR016 Adrenal Cortical Carcinoma 61 8.864
42
P END039 Endodermal Sinus Tumor 42 8.864
43
DSS008 Disease of Mental Health 74 8.605
44
P PNC045 Pancreatic Agenesis 42 8.112
45
P PTN014 Patent Ductus Arteriosus 1 59 7.970
46
HLT001 Holt-Oram Syndrome 66 7.924
47
PRT048 Partial Atrioventricular Canal 36 7.398
48
P LFT003 Left Ventricular Noncompaction 58 7.168
49
DGR001 Digeorge Syndrome 62 7.119
50
TRC062 Tricuspid Atresia 54 6.608
51
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 6.608
52
c ART101 Aortic Valve Disease 2 65 6.537
53
c 46X030 46,xy Sex Reversal 9 43 6.508
54
P HYP055 Hypoplastic Left Heart Syndrome 65 6.508
55
CRY035 Cryptorchidism, Unilateral or Bilateral 57 6.476
56
VLC001 Velocardiofacial Syndrome 57 6.388
57
JCB001 Jacobsen Syndrome 50 6.388
58
P TRC087 Tricuspid Valve Disease 48 6.388
59
RSP023 Rasopathy 54 6.388
60
NNN026 Noonan Syndrome with Multiple Lentigines 64 6.388
61
INT084 Intrinsic Cardiomyopathy 29 6.267
62
TTL012 Total Anomalous Pulmonary Venous Return 1 58 6.267
63
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 6.267
64
CHR390 Chromosome 14q11-Q22 Deletion Syndrome 36 6.267
65
HRT008 Heart Conduction Disease 45 6.267
66
MXD008 Mixed Germ Cell-Sex Cord Neoplasm 22 6.267
67
GRM005 Germ Cell Cancer 46 6.267
68
GRM001 Germ Cell and Embryonal Cancer 28 6.267
69
PTS001 Patau Syndrome 55 6.267
70
DPH021 Diaphragm Disease 43 6.267
71
P PLM040 Pulmonary Valve Disease 40 6.267
72
MLG037 Malignant Childhood Germ Cell Neoplasm 18 6.267
73
TST013 Testicular Thecoma 18 6.267
74
DXR001 Doxorubicin Induced Cardiomyopathy 32 6.267
75
P GLM040 Glioma Susceptibility 1 70 2.560
76
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.508
77
P GST053 Gastric Cancer 82 2.478
78
c ATR087 Atrial Standstill 1 74 2.461
79
P PNC035 Pancreatic Cancer 87 2.271
80
P DSR090 Disorder of Sexual Development 45 2.170
81
HLX001 Helix Syndrome 47 2.118
82
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.040
83
GLM045 Glioma 62 1.978
84
HYP066 Hyperglycemia 60 1.925
85
HPT022 Hepatoblastoma 54 1.925
86
P OVR042 Ovarian Cancer 88 1.801
87
P BRS047 Breast Cancer 97 1.759
88
MSC007 Muscle Hypertrophy 64 1.667
89
PLM070 Pulmonic Stenosis 49 1.644
90
P ATR011 Atrial Fibrillation 66 1.622
91
GLB002 Glioblastoma 67 1.610
92
CRD223 Cardiac Arrhythmia 63 1.572
93
TRC022 Tricuspid Valve Insufficiency 46 1.470
94
c VNT024 Ventricular Septal Defect 3 24 1.442
95
MCR013 Microphthalmia 59 1.442
96
CNT061 Conotruncal Heart Malformations 66 1.437
97
P SYN140 Syndrome with 46,xy Disorder of Sex Development 23 1.425
98
P ADN016 Adenocarcinoma 63 1.425
99
P INF032 Infertility 60 1.425
100
PPL052 Papillomatosis, Confluent and Reticulated 34 1.413
101
INT066 Interstitial Lung Disease 60 1.350
103
MLG169 Malignant Astrocytoma 57 1.334
104
P BCL017 B-Cell Lymphoma 57 1.334
105
P PRM030 Permanent Neonatal Diabetes Mellitus 59 1.304
106
TRT017 Teratoma, Ovarian 28 1.257
107
P LNG032 Lung Cancer 98 1.257
108
OVR109 Ovarian Germ Cell Teratoma 32 1.257
109
c GLM043 Glioma Susceptibility 9 30 1.226
110
c GLM025 Glioma Susceptibility 2 30 1.226
111
c GLM047 Glioma Susceptibility 3 32 1.226
112
MNN043 Meningioma, Familial 79 1.226
113
P OLG002 Oligodendroglioma 66 1.226
114
P SPR119 Spermatogenic Failure, X-Linked, 1 36 1.222
115
TRT001 Teratocarcinoma 41 1.222
116
DWN001 Down Syndrome 70 1.141
117
c MCR133 Microvascular Complications of Diabetes 4 41 1.141
118
c MCR113 Microvascular Complications of Diabetes 3 52 1.141
119
c MCR130 Microvascular Complications of Diabetes 6 41 1.141
120
c MCR120 Microvascular Complications of Diabetes 7 47 1.141
121
ATR088 Atrial Septal Defect 7 with or Without Atrioventricular Conduction Defects 30 1.141
122
ATR093 Atrial Heart Septal Defect 7 22 1.141
123
P PLM037 Pulmonary Hypertension 69 1.134
124
P HPT023 Hepatocellular Carcinoma 95 1.134
125
CNG034 Congestive Heart Failure 69 1.134
126
c WLM013 Wilms Tumor 1 65 1.063
127
P GND004 Gonadal Dysgenesis 46 1.063
128
c LKM061 Leukemia, Acute Myeloid 83 1.048
129
THR100 Thrombocytopenic Purpura, Autoimmune 60 1.048
130
CHL149 Childhood Acute Myeloid Leukemia 42 1.048
131
BRR014 Barrett Esophagus 66 1.048
132
PRP030 Purpura 54 1.048
133
HYP006 Hypertensive Heart Disease 48 1.048
134
GST040 Gastric Adenocarcinoma 66 1.048
135
P MYL006 Myeloid Leukemia 60 1.048
136
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.032
137
P RTN024 Retinoblastoma 72 1.032
138
P LVR013 Liver Disease 68 1.032
139
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.032
140
P CRD246 Cardiovascular System Disease 55 1.031
141
ATH013 Atherosclerosis Susceptibility 63 1.016
142
P LNG064 Lung Cancer Susceptibility 3 69 1.016
143
PNG002 Pain Agnosia 51 0.999
144
P NSP012 Nasopharyngeal Carcinoma 60 0.999
145
c ACT075 Acute Myocardial Infarction 55 0.999
146
P RHM011 Rheumatoid Arthritis 81 0.981
147
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.981
148
ATM095 Autoimmune Disease 61 0.981
149
AZS001 Azoospermia 45 0.981
150
P ART022 Arthritis 70 0.981
151
UNV002 Univentricular Heart 26 0.981
152
AGN016 Aging 53 0.963
153
P LKM062 Leukemia, Acute Lymphoblastic 69 0.963
154
HYP080 Hypogonadism 49 0.963
155
PNC013 Pancreatic Ductal Carcinoma 48 0.963
156
PLP001 Pulpitis 48 0.963
157
P CTR002 Cataract 59 0.963
158
P DBT009 Diabetes Mellitus 67 0.963
159
HGH041 High-Grade Astrocytoma 36 0.963
160
ATR055 Atrial Septal Aneurysm 23 0.963
161
SYS003 Systolic Heart Failure 49 0.943
162
DCT002 Ductal Carcinoma in Situ 58 0.922
163
P NNT058 Neonatal Diabetes 52 0.922
164
P OVR046 Ovarian Cyst 43 0.922
165
P INS002 in Situ Carcinoma 52 0.922
166
P CRD119 Cardiac Arrest 68 0.877
167
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.877
168
P LKM002 Leukemia 65 0.877
169
PNS014 Penis Agenesis 38 0.877
170
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.867
171
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.867
172
SKN022 Skin Squamous Cell Carcinoma 53 0.867
173
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.867
174
VRC005 Varicose Veins 59 0.851
175
P CRC039 Coarctation of Aorta 46 0.851
176
c VNT026 Ventricular Septal Defect 2 23 0.851
177
END057 Endometrial Cancer 76 0.851
178
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.851
179
P MLN007 Male Infertility 56 0.851
180
ART017 Aortic Disease 49 0.851
181
CHG001 Chagas Disease 65 0.851
182
HRT036 Heritable Thoracic Aortic Disease 36 0.851
183
OVR094 Ovarian Epithelial Cancer 39 0.851
184
CHR178 Chromosomal Triplication 33 0.851
185
PRM329 Premature Aging 36 0.851
186
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.823
187
WST005 West Nile Virus 55 0.823
188
DXT001 Dextrocardia 54 0.823
189
CYT002 Cytokine Deficiency 43 0.823
190
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.790
191
P PLV020 Pelvic Organ Prolapse 57 0.790
192
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.790
193
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.790
194
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.790
195
ACR022 Acardia 13 0.790
196
CRY010 Cryptophthalmos 26 0.790
197
c SML038 Small Cell Cancer of the Lung 68 0.752
198
P END044 Endometriosis 62 0.752
199
GLL048 Glial Tumor 51 0.752
200
P CLR023 Colorectal Cancer 100 0.751
201
BRR002 Barrett's Adenocarcinoma 37 0.690
202
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.582
203
P TMR010 Tumor Predisposition Syndrome 69 0.582
204
INH023 Inherited Cancer-Predisposing Syndrome 53 0.582
205
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.482
206
CLL010 Cellular Ependymoma 58 0.482
207
HYP266 Hypoxia 56 0.417
208
P PLY011 Polycystic Ovary Syndrome 57 0.381
209
c TYP008 Type 1 Diabetes Mellitus 77 0.361
210
ISC004 Ischemia 61 0.361
211
SVR004 Severe Combined Immunodeficiency 70 0.361
212
8P2002 8p23.1 Duplication Syndrome 22 0.341
213
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.341
214
SQM006 Squamous Cell Carcinoma 59 0.319
215
TLN003 Telangiectasis 51 0.319
216
ORL015 Oral Squamous Cell Carcinoma 43 0.295
217
P ATX030 Ataxia-Telangiectasia 80 0.295
218
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.295
219
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 0.295
220
ALC010 Alcoholic Cardiomyopathy 42 0.295
221
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.269
222
c DPH016 Diaphragmatic Hernia 3 24 0.269
223
GLC003 Glucose Intolerance 53 0.269
224
ART030 Aortic Arch Interruption 25 0.269
225
P CMP005 Campomelic Dysplasia 65 0.241
226
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.241
227
P BLD134 Bladder Cancer 79 0.241
228
P FBR017 Fibrosarcoma 55 0.241
229
P HYP086 Hypothyroidism 68 0.241
230
GST033 Gestational Diabetes 60 0.241
231
CMP035 Complete Atrioventricular Canal 24 0.241
232
SNG003 Single Ventricular Heart 30 0.241
233
ART140 Arteries, Anomalies of 52 0.209
234
c HYP762 Hypothyroidism, Congenital, Nongoitrous, 5 23 0.209
235
OTT002 Otitis Media 70 0.209
236
HYP784 Hypogonadism, Male 43 0.209
237
P PLY006 Polydactyly 58 0.209
238
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.209
239
c HYP517 Hypoplastic Left Heart Syndrome 2 22 0.209
240
CMB007 Combined Immunodeficiency 56 0.209
241
SMN007 Seminoma 42 0.209
242
DYS101 Dysgerminoma 43 0.209
243
OVR063 Overnutrition 42 0.209
244
HYP043 Hyperandrogenism 47 0.209
245
47X002 47,xyy 47 0.209
246
THY098 Thyroid Ectopia 31 0.209
247
P HYP265 Hypotonia 42 0.209
248
c ATR031 Atrial Septal Defect 4 30 0.170
249
HMM004 Hamamy Syndrome 39 0.170
250
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.170
251
MYL009 Myelodysplastic Syndrome 67 0.170
252
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.170
253
P INF037 Inflammatory Bowel Disease 53 0.170
254
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.170
255
P NNN008 Noonan Syndrome 1 76 0.170
256
P OST002 Osteoporosis 76 0.170
257
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.170
258
c TYP009 Type 2 Diabetes Mellitus 91 0.170
259
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.170
260
CRD132 Cardiac Conduction Defect 59 0.170
261
GST092 Gastroesophageal Reflux 59 0.170
262
INS024 Insulin-Like Growth Factor I 77 0.170
263
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.170
264
c CNG521 Congenital Heart Defects, Multiple Types, 5 23 0.170
265
P BRG001 Brugada Syndrome 69 0.170
266
c ATR056 Atrial Septal Defect 9 26 0.170
267
HRS016 Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction 26 0.170
268
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.170
269
MRF001 Marfan Syndrome 76 0.170
270
P HNT016 Huntington Disease 73 0.170
271
c HYP836 Hypercholesterolemia, Familial, 1 73 0.170
272
HRW001 Hair Whorl 35 0.170
273
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.170
274
CHD004 Chudley-Mccullough Syndrome 47 0.170
275
FRY002 Fryns Syndrome 39 0.170
276
c HMP013 Hemophagocytic Lymphohistiocytosis, Familial, 3 47 0.170
277
c SPR118 Spermatogenic Failure 1 36 0.170
278
c SVR003 Severe Congenital Neutropenia 59 0.170
279
DFF005 Diffuse Large B-Cell Lymphoma 55 0.170
280
PPL022 Papilloma 53 0.170
281
P VSC007 Vascular Disease 62 0.170
282
LPD008 Lipid Metabolism Disorder 61 0.170
283
ADN018 Adenoma 58 0.170
284
SQM002 Squamous Cell Papilloma 45 0.170
285
P LYN001 Lynch Syndrome 76 0.170
286
CLB002 Clubfoot 50 0.170
287
PRM013 Premature Menopause 57 0.170
288
P NTR004 Neutropenia 62 0.170
289
RGH001 Right Bundle Branch Block 47 0.170
290
NNS042 Nonsyndromic Disorders of Testicular Development 21 0.170
291
CLF001 Cleft Lip 54 0.170
292
SKN019 Skin Melanoma 70 0.170
293
P MYC008 Myocarditis 59 0.170
294
CRH001 Crohn's Disease 80 0.170
295
P HYP076 Hyperthyroidism 53 0.170
296
P MSC005 Muscular Dystrophy 66 0.170
297
HYD005 Hydrocele 46 0.170
298
ANX004 Anoxia 40 0.170
299
G6P001 G6pc3 Deficiency 23 0.170
300
c PSD047 Pseudo-Turner Syndrome 52 0.170
301
MNG006 Monogenic Diabetes 45 0.170
302
CRV068 Cervical Polyp 27 0.120
303
c MJR022 Major Affective Disorder 8 37 0.120
304
ACT119 Acute Promyelocytic Leukemia 62 0.120
305
P CRN038 Carney Complex Variant 63 0.120
306
c PRG020 Paragangliomas 3 39 0.120
307
P MTR004 Maturity-Onset Diabetes of the Young 66 0.120
308
SNT005 Sinoatrial Node Disease 48 0.120
309
P SCH015 Schizophrenia 74 0.120
310
P CLC063 Celiac Disease 1 65 0.120
311
DNN002 Donnai-Barrow Syndrome 55 0.120
312
MCK029 Meckel Diverticulum 38 0.120
313
P PRS040 Prostate Cancer 95 0.120
314
c RTN172 Retinitis Pigmentosa 1 45 0.120
315
NRL016 Neural Tube Defects 80 0.120
316
PLY150 Polykaryocytosis Inducer 29 0.120
317
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.120
318
P HRS035 Hirschsprung Disease 1 66 0.120
319
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.120
320
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 62 0.120
321
SPR004 Supravalvular Aortic Stenosis 57 0.120
322
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.120
323
MSC157 Muscular Dystrophy, Duchenne Type 78 0.120
324
OST159 Osteogenic Sarcoma 66 0.120
325
P PRR016 Pierre Robin Syndrome 50 0.120
326
RHB024 Rhabdomyosarcoma 2 65 0.120
327
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.120
328
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.120
329
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.120
330
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.120
331
HTR014 Heterotaxy, Visceral, 1, X-Linked 40 0.120
332
GND001 Gonadoblastoma 42 0.120
333
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.120
334
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.120
335
c MJR024 Major Affective Disorder 9 40 0.120
336
c PTN013 Patent Ductus Arteriosus 2 21 0.120
337
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.120
338
c SPR162 Spermatogenic Failure 50 42 0.120
339
OCC002 Occult Macular Dystrophy 46 0.120
340
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.120
341
P LYS001 Loeys-Dietz Syndrome 65 0.120
342
P TST021 Testicular Germ Cell Tumor 61 0.120
343
CTY001 Cat Eye Syndrome 45 0.120
344
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.120
345
TCL025 T-Cell Immunodeficiency with Thymic Aplasia 43 0.120
346
P RTN008 Retinitis Pigmentosa 79 0.120
347
c 46X049 46,xy Sex Reversal 2 51 0.120
348
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.120
349
c CNG385 Congenital Heart Defects, Multiple Types, 3 18 0.120
350
LPT014 Leptin Deficiency or Dysfunction 77 0.120
351
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 0.120
352
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.120
353
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.120
354
c HYP511 Hypogonadotropic Hypogonadism 15 with or Without Anosmia 29 0.120
355
c ATR062 Atrial Septal Defect 1 40 0.120
356
c OPT053 Optic Atrophy 1 62 0.120
357
CLF027 Cleft Palate, Isolated 64 0.120
358
ESP021 Esophageal Cancer 84 0.120
359
P LPR012 Leopard Syndrome 1 48 0.120
360
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.120
361
HMN044 Human Immunodeficiency Virus Type 1 76 0.120
362
c WLF013 Wolfram Syndrome 1 60 0.120
363
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.120
364
IMM177 Immunodeficiency 54 45 0.120
365
HRT039 Heart Defects, Congenital, and Other Congenital Anomalies 48 0.120
366
NBL001 Nablus Mask-Like Facial Syndrome 27 0.120
367
c PRM031 Primary Autosomal Recessive Microcephaly 55 0.120
368
BNR002 Bone Resorption Disease 47 0.120
369
MGC001 Megacolon 48 0.120
370
NKC002 Nk Cell Deficiency 31 0.120
371
CLR108 Colorectal Adenoma 63 0.120
372
P PRS049 Persistent Mullerian Duct Syndrome 51 0.120
373
OST015 Osteochondrodysplasia 60 0.120
374
TRN018 Transitional Cell Carcinoma 56 0.120
375
BCT002 Bacterial Vaginosis 52 0.120
376
P SCK002 Sick Sinus Syndrome 55 0.120
377
PYR003 Pyromania 27 0.120
378
P BNC003 Bone Cancer 58 0.120
379
c MLG084 Malignant Fibrous Histiocytoma 62 0.120
380
P HYP730 Hypogonadotropic Hypogonadism 57 0.120
381
HMP001 Hemopericardium 47 0.120
382
P TRN020 Turner Syndrome 67 0.120
383
P MLT074 Multiple Endocrine Neoplasia 58 0.120
384
P BPL003 Bipolar Disorder 56 0.120
385
c JVN002 Juvenile Type Testicular Granulosa Cell Tumor 34 0.120
386
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.120
387
AMN001 Amenorrhea 53 0.120
388
MTR002 Mitral Valve Insufficiency 51 0.120
389
FML063 Familial Glucocorticoid Deficiency 58 0.120
390
P END033 Endocarditis 58 0.120
391
NRR001 Neuroretinitis 42 0.120
392
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.120
393
HRT012 Heart Valve Disease 53 0.120
394
P MYP004 Myopathy 67 0.120
395
LNG039 Lung Squamous Cell Carcinoma 57 0.120
396
ANV001 Anovulation 46 0.120
397
P RHB003 Rhabdomyosarcoma 66 0.120
398
ART016 Aortic Aneurysm 68 0.120
399
CNN003 Conn's Syndrome 77 0.120
400
PLM010 Pulmonary Edema 54 0.120
401
P PRC012 Pericardial Effusion 50 0.120
402
BRD004 Borderline Personality Disorder 53 0.120
403
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.120
404
P PRS038 Personality Disorder 65 0.120
405
CMM004 Common Variable Immunodeficiency 71 0.120
406
P MLN008 Melanoma 75 0.120
407
RTN023 Retinitis 45 0.120
408
OVR059 Ovary Adenocarcinoma 49 0.120
409
BRN024 Bronchitis 67 0.120
410
ANT024 Anthrax Disease 57 0.120
411
P FBR003 Fibrous Histiocytoma 43 0.120
412
SBV001 Subvalvular Aortic Stenosis 31 0.120
413
HTR003 Heterotaxy 43 0.120
414
KLD004 Keloid Disorder 38 0.120
415
OST012 Osteoarthritis 77 0.120
416
PLY012 Polyhydramnios 46 0.120
417
DBT010 Diabetic Neuropathy 54 0.120
419
8PN001 8p Inverted Duplication/deletion Syndrome 21 0.120
420
48X005 48,xyyy 39 0.120
421
DPH010 Diaphragmatic Hernia Exomphalos Corpus Callosum Agenesis 8 0.120
422
GRM010 Germ Cells Tumors 33 0.120
423
P PLM069 Pulmonary Venous Return Anomaly 29 0.120
424
ORL011 Oral Cancer 60 0.120
425
ANR018 Anorchia 36 0.120
426
ATR018 Atrial Septal Defect Ostium Primum 22 0.120
427
BWN005 Bowing of Long Bones Congenital 15 0.120
428
P PRC019 Precocious Puberty 48 0.120
429
SFT003 Soft Tissue Sarcoma 43 0.120
430
ISL075 Isolated Pierre Robin Sequence 29 0.120
431
P RRT020 Rare Tumor 39 0.120
432
BRN071 Brain Injury 50 0.120
433
c ACT134 Acute Liver Failure 57 0.120
Content
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