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Search results for foxc2

238 hits were found for foxc2

# Family MCID Name MIFTS Score
1
LYM029 Lymphedema-Distichiasis Syndrome 52 60.243
2
DST033 Distichiasis 35 26.908
3
P DBT009 Diabetes Mellitus 67 17.997
4
P PTS002 Ptosis 52 16.643
5
c TYP009 Type 2 Diabetes Mellitus 92 16.478
6
CLF027 Cleft Palate, Isolated 64 16.183
7
c HRD202 Hereditary Lymphedema I 49 16.141
8
VRC005 Varicose Veins 60 15.384
9
c HRD007 Hereditary Lymphedema 34 15.060
10
P PRM327 Primary Lymphedema 36 14.745
11
P HRT032 Heart Disease 81 13.633
12
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 12.476
13
INT323 Intraocular Pressure Quantitative Trait Locus 64 12.226
14
P HYP087 Hypotrichosis 42 11.933
15
FLR002 Filariasis 55 11.819
16
YLL001 Yellow Nail Syndrome 42 11.449
17
P HYP055 Hypoplastic Left Heart Syndrome 65 10.946
18
KLP010 Klippel-Trenaunay-Weber Syndrome 59 10.777
19
c CNG439 Congenital Lymphedema 30 10.326
20
CLF037 Cleft Lip/palate-Ectodermal Dysplasia Syndrome 50 10.023
21
c LYM145 Lymphatic Malformation 5 48 9.449
22
c HRD206 Hereditary Lymphedema Ii 30 9.352
23
P TTR001 Tetralogy of Fallot 69 8.997
24
CYS002 Cystic Lymphangioma 45 8.445
25
HYP139 Hypotrichosis-Lymphedema-Telangiectasia Syndrome 45 7.841
26
P ANT088 Anterior Segment Dysgenesis 55 7.620
27
CHY005 Chylothorax, Congenital 37 7.620
28
P ORF002 Orofacial Cleft 43 7.087
29
HNN001 Hennekam Syndrome 53 7.087
30
P AXN002 Axenfeld-Rieger Syndrome 63 7.087
31
P BRS047 Breast Cancer 98 6.260
32
OST159 Osteogenic Sarcoma 66 5.016
33
SQM006 Squamous Cell Carcinoma 60 4.637
34
P OVR042 Ovarian Cancer 88 4.622
35
P CLR023 Colorectal Cancer 100 4.580
36
P LNG032 Lung Cancer 98 4.200
37
c SML038 Small Cell Cancer of the Lung 69 4.176
38
HLX001 Helix Syndrome 48 4.155
39
ESP021 Esophageal Cancer 83 4.062
40
P HPT023 Hepatocellular Carcinoma 96 3.917
41
P MLN008 Melanoma 76 3.820
42
P PRS040 Prostate Cancer 95 3.765
43
CNT061 Conotruncal Heart Malformations 66 3.765
44
CRV035 Cervical Cancer 73 3.466
45
P VSC007 Vascular Disease 63 3.308
46
ARC025 Arachnoid Cysts, Intracranial 37 3.116
47
GLL048 Glial Tumor 52 3.047
48
P VNT002 Ventricular Septal Defect 58 2.849
49
P NSP012 Nasopharyngeal Carcinoma 61 2.701
50
HYD038 Hydrops Fetalis, Nonimmune 59 2.701
51
PRT251 Proteinuria, Chronic Benign 57 2.701
52
P GST053 Gastric Cancer 83 2.701
53
P HYD006 Hydrocephalus 61 2.701
54
ATH013 Atherosclerosis Susceptibility 63 2.669
55
CRV002 Cervix Uteri Carcinoma in Situ 47 2.669
56
CRV045 Cervical Intraepithelial Neoplasia 39 2.669
57
OVR094 Ovarian Epithelial Cancer 39 2.622
58
P CRN300 Coronary Heart Disease 1 73 2.599
59
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.599
60
TNG009 Tongue Squamous Cell Carcinoma 43 2.526
61
P RSP003 Respiratory Failure 74 2.454
62
P ECT005 Ectropion 41 2.454
63
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.451
64
CRN027 Corneal Neovascularization 47 2.451
65
HYD002 Hydronephrosis 58 2.451
66
DGN001 Degenerative Disc Disease 49 2.372
67
c BSL007 Basal Cell Carcinoma 68 2.372
68
VSC006 Vascular Cancer 46 2.372
69
LYM035 Lymphangiectasis 30 2.372
70
ORL015 Oral Squamous Cell Carcinoma 43 2.362
71
P VNS003 Venous Insufficiency 55 2.362
72
P STR020 Strabismus 56 2.352
73
MCH006 Mechanical Strabismus 40 2.352
74
PRS129 Prostatic Hyperplasia, Benign 49 2.290
75
P MYS005 Myositis 56 2.290
76
P BCL017 B-Cell Lymphoma 59 2.290
77
PRS021 Prostatic Adenoma 43 2.290
78
PRS045 Prostatic Hypertrophy 53 2.290
79
MYS001 Myositis Ossificans 44 2.290
80
P HYP750 Hypertriglyceridemia, Familial 62 2.265
81
P SCL018 Scoliosis 57 2.238
82
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.112
83
P PLM037 Pulmonary Hypertension 72 2.112
84
c MCR130 Microvascular Complications of Diabetes 6 41 2.112
85
c MCR120 Microvascular Complications of Diabetes 7 47 2.112
86
GLC003 Glucose Intolerance 54 2.112
87
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.112
88
c MCR113 Microvascular Complications of Diabetes 3 52 2.112
89
c MCR133 Microvascular Complications of Diabetes 4 41 2.112
90
ART030 Aortic Arch Interruption 25 2.112
91
P PNC035 Pancreatic Cancer 86 2.110
92
ISL075 Isolated Pierre Robin Sequence 29 2.046
93
GLB002 Glioblastoma 67 2.015
94
P AVS003 Avascular Necrosis 41 1.922
95
HYP060 Hyperinsulinism 54 1.920
96
c LYM144 Lymphatic Malformation 1 47 1.910
97
TLN003 Telangiectasis 51 1.910
98
P GLL018 Gallbladder Cancer 53 1.910
99
c CNG513 Congenital Ptosis 42 1.910
100
CHL065 Cholangiocarcinoma 58 1.847
101
INT079 Intrahepatic Cholangiocarcinoma 51 1.847
102
c NPH049 Nephrotic Syndrome, Type 2 51 1.796
103
CLT003 Colitis 63 1.796
104
P RTN024 Retinoblastoma 73 1.796
105
IMM039 Immune Hydrops Fetalis 33 1.796
106
P TRN020 Turner Syndrome 67 1.796
107
FLR001 Filarial Elephantiasis 59 1.796
108
LPD008 Lipid Metabolism Disorder 62 1.796
109
P GND004 Gonadal Dysgenesis 47 1.796
110
CHR074 Choriocarcinoma 46 1.686
111
c NPH055 Nephrotic Syndrome, Type 1 52 1.670
112
P ADN016 Adenocarcinoma 63 1.670
113
HMP001 Hemopericardium 47 1.670
114
P PRC012 Pericardial Effusion 50 1.670
115
END057 Endometrial Cancer 72 1.600
116
P SPP010 Suppressor of Tumorigenicity 3 51 1.600
117
HYP266 Hypoxia 57 1.600
118
GLM045 Glioma 63 1.600
119
c CNG596 Congenital Ectropion 16 1.527
120
DWN001 Down Syndrome 70 1.527
121
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.527
122
P CTR002 Cataract 60 1.527
123
ALT003 Alternating Exotropia 33 1.527
124
EXT022 Exotropia 42 1.527
125
P ART005 Arteriovenous Malformation 65 1.527
126
CHR178 Chromosomal Triplication 34 1.527
127
END041 Endometrial Adenocarcinoma 64 1.508
128
c WLM013 Wilms Tumor 1 66 1.411
129
CLF004 Cleft Lip/palate 57 1.358
130
P PRR016 Pierre Robin Syndrome 50 1.358
131
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 1.358
132
ANK020 Ankyloglossia with or Without Tooth Anomalies 46 1.358
133
P MYP006 Myopia 56 1.358
134
CLF001 Cleft Lip 53 1.358
135
FTT001 Fatty Liver Disease 62 1.358
136
GST040 Gastric Adenocarcinoma 67 1.358
137
c CNG216 Congenital Hydrocephalus 53 1.358
138
c DPH024 Diaphragmatic Hernia, Congenital 64 1.306
139
c PRC016 Pre-Eclampsia 65 1.306
140
LVR012 Liver Cirrhosis 63 1.306
141
GLM012 Glomuvenous Malformations 37 1.192
142
CLR030 Clear Cell Renal Cell Carcinoma 54 1.192
143
P SCL048 Sclerosteosis 58 1.192
144
KRT009 Keratosis 53 1.137
145
SYN031 Synovial Chondromatosis 41 1.066
146
c VSC019 Vesicoureteral Reflux 1 57 1.066
147
HYP223 Hypoplastic Right Heart Syndrome 32 1.066
148
OST003 Osteonecrosis 61 1.066
149
P MCR010 Microcephaly 60 1.066
150
c ERL012 Early-Onset Glaucoma 24 1.066
151
ASC009 Ascites, Chylous 32 0.924
152
CHR431 Chronic Venous Insufficiency 48 0.924
153
P RHB003 Rhabdomyosarcoma 66 0.924
154
HMT002 Hematologic Cancer 61 0.924
155
GST033 Gestational Diabetes 61 0.924
156
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.754
157
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.754
158
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.754
159
c THR092 Thrombophilia Due to Thrombin Defect 74 0.754
160
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.754
161
THR024 Thrombosis 56 0.754
162
P SML001 Small Cell Carcinoma 52 0.754
163
HYP652 Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome 34 0.754
164
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.754
165
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.754
166
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.754
167
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.754
168
DGR001 Digeorge Syndrome 62 0.754
169
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.754
170
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.754
171
NRN001 Neuroendocrine Carcinoma 47 0.754
172
CLL003 Cellulitis 53 0.754
173
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.754
174
P CNJ013 Conjunctivitis 66 0.754
175
SVR004 Severe Combined Immunodeficiency 72 0.754
176
PLM033 Pulmonary Embolism 58 0.754
177
c HMC039 Hemochromatosis, Type 1 73 0.533
178
P PRS124 Presynaptic Congenital Myasthenic Syndromes 36 0.533
179
c ART115 Aortic Valve Disease 1 74 0.533
180
P BLD134 Bladder Cancer 79 0.533
181
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.533
182
CTS003 Coats Disease 53 0.533
183
AGN016 Aging 54 0.533
184
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.533
185
c OPT053 Optic Atrophy 1 62 0.533
186
P SYN075 Syngnathia 43 0.533
187
P MLT020 Multiple Sclerosis 79 0.533
188
MYL009 Myelodysplastic Syndrome 67 0.533
189
KRN002 Kearns-Sayre Syndrome 63 0.533
190
c LKM061 Leukemia, Acute Myeloid 83 0.533
191
P CRB048 Cerebral Cavernous Malformations 63 0.533
192
P PRT008 Proteus Syndrome 63 0.533
193
LYM094 Lymphedema, Primary, with Myelodysplasia 39 0.533
194
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.533
195
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.533
196
MYL069 Myeloma, Multiple 77 0.533
197
LYM122 Lymphangiectasia, Pulmonary, Congenital 28 0.533
198
VTR016 Vater/vacterl Association 49 0.533
199
c TBR025 Tuberous Sclerosis 1 84 0.533
200
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.533
201
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.533
202
P MDL005 Medulloblastoma 75 0.533
203
MBS002 Moebius Syndrome 54 0.533
204
c HGH035 High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 3 8 0.533
205
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.533
206
BLP004 Blepharophimosis 36 0.533
207
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.533
208
P FBR003 Fibrous Histiocytoma 43 0.533
209
P MYP004 Myopathy 67 0.533
210
OCL006 Ocular Hypertension 53 0.533
211
ULC004 Ulcerative Colitis 74 0.533
212
P ALP009 Alopecia Areata 59 0.533
213
P ALP008 Alopecia 54 0.533
214
47X002 47,xyy 48 0.533
215
HYP066 Hyperglycemia 61 0.533
216
P PLM036 Pulmonary Fibrosis 66 0.533
217
P CNG001 Congenital Myasthenic Syndrome 68 0.533
218
RCK004 Rickets 68 0.533
219
P LNG064 Lung Cancer Susceptibility 3 70 0.533
220
P MLN007 Male Infertility 56 0.533
221
VRC001 Varicocele 48 0.533
222
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.533
223
c MLG084 Malignant Fibrous Histiocytoma 62 0.533
224
CLN015 Colon Adenocarcinoma 65 0.533
225
P TBR001 Tuberous Sclerosis 69 0.533
226
P PLY011 Polycystic Ovary Syndrome 57 0.533
227
ESP020 Esophageal Atresia 60 0.533
228
MCR013 Microphthalmia 60 0.533
229
P KDN017 Kidney Cancer 61 0.533
230
VCT001 Vacterl Association 47 0.533
231
LGP001 Lagophthalmos 30 0.533
232
PRS030 Persistent Fetal Circulation Syndrome 49 0.533
233
P MYT002 Myotonic Dystrophy 51 0.533
234
P NRF002 Neurofibromatosis 57 0.533
235
HYP056 Hypoglycemia 65 0.533
236
ORL011 Oral Cancer 60 0.533
237
CHR159 Charlie M Syndrome 21 0.533
238
LPD014 Lipodermatosclerosis 37 0.533
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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