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01 Progeria [NCBI]

Gene


 Gene Link Information
Gain		 01
LMNA [NCBI] 0.000579606
ZMPSTE24 [NCBI] 0.000190355
WRN [NCBI] 3.50084e-05
B4GALT7 [NCBI] 2.65966e-05
LAMA1 [NCBI] 2.56625e-05
ERCC4 [NCBI] 1.4405e-05
PRELP [NCBI] 1.32889e-05
PCGF6 [NCBI] 1.23906e-05
PRPF19 [NCBI] 1.13736e-05
SYNE2 [NCBI] 1.13736e-05
ATR [NCBI] 1.02112e-05
B4GALT1 [NCBI] 1.00886e-05
MEOX2 [NCBI] 1.00886e-05
PCGF2 [NCBI] 9.76069e-06
PCBP1 [NCBI] 9.61762e-06
ANK3 [NCBI] 9.36301e-06
IGF1 [NCBI] 9.35309e-06
NR1H2 [NCBI] 8.94528e-06
ACAN [NCBI] 8.03365e-06
FOXM1 [NCBI] 7.87798e-06
HIP1 [NCBI] 7.40477e-06
UBE2I [NCBI] 7.36763e-06
G6PD [NCBI] 7.21054e-06
LOX [NCBI] 7.16034e-06
ELK1 [NCBI] 6.91827e-06
ING1 [NCBI] 6.41052e-06
CLN3 [NCBI] 5.65062e-06
XPA [NCBI] 4.81311e-06
SOD2 [NCBI] 4.74256e-06
FGF23 [NCBI] 4.36118e-06
PDGFA [NCBI] 4.17238e-06
PRNP [NCBI] 3.93223e-06
H2AFX [NCBI] 3.78594e-06
ERCC2 [NCBI] 3.77329e-06
EGF [NCBI] 2.34257e-06
TGFB1 [NCBI] 1.23051e-06
TP53 [NCBI] 9.96785e-07
CDKN1A [NCBI] 6.02795e-07



OMIM


 OMIM Link Information
gain		 01
progeroid syndrome, neonatal [NCBI] 0.0120565
HGPS [NCBI] 0.00800876
cutis laxa, corneal clouding, and mental retardation [NCBI] 0.00232891
LMNA [NCBI] 0.00154378
MADA [NCBI] 0.000524907
gapo syndrome [NCBI] 0.000512719
GO [NCBI] 0.000493306
acrodysostosis [NCBI] 0.000493306
acrogeria, gottron type [NCBI] 0.000292623
ehlers-danlos syndrome, progeroid form [NCBI] 0.000274555
donohue syndrome [NCBI] 0.000255893
ZMPSTE24 [NCBI] 0.000200494
B4GALT7 [NCBI] 0.000165055
EDMD2 [NCBI] 0.000110949
bird-headed dwarfism, montreal type [NCBI] 0.000109532
premature aging syndrome, penttinen type [NCBI] 0.000109532
premature aging syndrome, okamoto type [NCBI] 0.000109532
xfe progeroid syndrome [NCBI] 0.000109532
growth factors, combined defect of [NCBI] 8.70777e-05
CSA [NCBI] 8.21181e-05
EDMD3 [NCBI] 7.86143e-05
WRN [NCBI] 6.9455e-05
progeroid short stature with pigmented nevi [NCBI] 6.90475e-05
cutis gyrata syndrome of beare and stevenson [NCBI] 6.90475e-05
congenital disorder of glycosylation, type i/iix [NCBI] 6.31066e-05
aging [NCBI] 6.08016e-05
FKHL16 [NCBI] 6.0037e-05
CDG2A [NCBI] 5.87887e-05
lenz-majewski hyperostotic dwarfism [NCBI] 5.70026e-05
CDG1B [NCBI] 5.70026e-05
hydrops-ectopic calcification-moth-eaten skeletal dysplasia [NCBI] 5.70026e-05
LGMD1B [NCBI] 5.2607e-05
ERCC4 [NCBI] 5.2444e-05
ERCC1 [NCBI] 4.73736e-05
crouzon syndrome [NCBI] 4.55272e-05
cutis laxa, autosomal recessive, type i [NCBI] 4.47351e-05
LBR [NCBI] 4.34898e-05
TCOF1 [NCBI] 4.2003e-05
EMD [NCBI] 4.2003e-05
PHA [NCBI] 4.12904e-05
EKV [NCBI] 3.79773e-05
FPLD2 [NCBI] 3.70169e-05
LOX [NCBI] 3.67782e-05
anemia, sideroblastic, x-linked [NCBI] 3.65119e-05
ODDD [NCBI] 3.61144e-05
CMD1A [NCBI] 3.297e-05
CDG1A [NCBI] 3.13001e-05
WS1 [NCBI] 2.79415e-05
TCOF [NCBI] 2.65214e-05
G6PD [NCBI] 2.40397e-05
GHRH [NCBI] 1.9268e-05
SOD2 [NCBI] 1.44198e-05
BCNS [NCBI] 1.32133e-05
BWS [NCBI] 5.99897e-06
AT [NCBI] 5.52628e-06
EGF [NCBI] 3.83853e-08



Database Center for Life Science