MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Telangiectasis
[NCBI]
Gene
Gene
Link
Information
Gain
01
CTD
[NCBI]
0.000817003
TELAB1
[NCBI]
0.000401057
VEGFA
[NCBI]
5.33103e-05
ACVRL1
[NCBI]
3.02425e-05
ENG
[NCBI]
2.29852e-05
ANGPT1
[NCBI]
1.76805e-05
GRIPAP1
[NCBI]
1.55515e-05
EEA1
[NCBI]
1.36358e-05
ANGPTL2
[NCBI]
1.32901e-05
SOX18
[NCBI]
1.23502e-05
ALMS1
[NCBI]
1.05252e-05
HSPA4
[NCBI]
9.99305e-06
KLF5
[NCBI]
9.99305e-06
GSTA1
[NCBI]
9.35188e-06
NDP
[NCBI]
8.91064e-06
RPGR
[NCBI]
8.08002e-06
BMPR2
[NCBI]
7.61233e-06
OSM
[NCBI]
6.44366e-06
TGFBR1
[NCBI]
6.04434e-06
HNF1A
[NCBI]
5.99994e-06
NOS3
[NCBI]
3.84334e-06
CD68
[NCBI]
3.8363e-06
AFP
[NCBI]
2.97523e-06
MS
[NCBI]
1.05887e-06
OMIM
OMIM
Link
Information
gain
01
telangiectasia, hereditary benign
[NCBI]
0.00395781
CMTC
[NCBI]
0.00321093
scleroderma, familial progressive
[NCBI]
0.00304547
BLM
[NCBI]
0.0011738
megalencephaly-cutis marmorata telangiectatica congenita
[NCBI]
0.000792892
angioma serpiginosum, x-linked
[NCBI]
0.000758187
nevus flammeus of nape of neck
[NCBI]
0.000623113
coats disease
[NCBI]
0.000559446
malignant atrophic papulosis
[NCBI]
0.000552346
sclerotylosis
[NCBI]
0.000526328
nevi flammei, familial multiple
[NCBI]
0.000526328
immune defect due to absence of thymus
[NCBI]
0.000484704
FSHMD1A
[NCBI]
0.000459504
MYMY1
[NCBI]
0.000425256
angioma serpiginosum, autosomal dominant
[NCBI]
0.00040665
AOS
[NCBI]
0.000249058
HHT
[NCBI]
0.000245962
kabuki syndrome
[NCBI]
0.000209323
glomerulonephritis with sparse hair and telangiectases
[NCBI]
0.000178324
SLE
[NCBI]
0.000133998
epilepsy-telangiectasia
[NCBI]
0.000111529
hypotrichosis-lymphedema-telangiectasia syndrome
[NCBI]
0.000111529
FDH
[NCBI]
9.13082e-05
velofacioskeletal syndrome
[NCBI]
8.90732e-05
skeletal dysplasia with telangiectases and mesodermal dysgenesis of the iris
[NCBI]
8.90732e-05
SOX18
[NCBI]
8.09985e-05
EEA1
[NCBI]
6.99095e-05
ramon syndrome
[NCBI]
6.7789e-05
achondroplasia, so-called, and severe combined immunodeficiency
[NCBI]
6.50911e-05
KLF5
[NCBI]
6.48204e-05
AT
[NCBI]
6.34343e-05
PBC
[NCBI]
6.2784e-05
FLT4
[NCBI]
5.89764e-05
complement component 7 deficiency
[NCBI]
5.73734e-05
white sponge nevus of cannon
[NCBI]
5.73734e-05
ATS
[NCBI]
5.45784e-05
NDP
[NCBI]
4.93785e-05
ENG
[NCBI]
4.8835e-05
KFSD
[NCBI]
4.83203e-05
ORW2
[NCBI]
4.59334e-05
RPGR
[NCBI]
4.495e-05
EVR1
[NCBI]
4.32334e-05
RP3
[NCBI]
4.04136e-05
von willebrand disease
[NCBI]
3.70453e-05
RTS
[NCBI]
3.11233e-05
MUC1
[NCBI]
1.95758e-05
FA
[NCBI]
1.6677e-05
VEGF
[NCBI]
1.14648e-05
AFP
[NCBI]
9.36101e-06
RP
[NCBI]
9.00194e-07
Database Center for Life Science