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MeSH keywords -> Related genes, diseases (OMIM)


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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