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MeSH keywords -> Related genes, diseases (OMIM)


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01 Life Expectancy [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
hereditary motor and sensory neuropathy, type iic [NCBI] 0.000942438
gapo syndrome [NCBI] 0.000942438
PARK3 [NCBI] 0.000799687
aneurysm, intracranial berry, 1 [NCBI] 0.00067303
alport syndrome, autosomal dominant [NCBI] 0.000653591
longevity [NCBI] 0.000160324
KLK3 [NCBI] 0.000141255
MFS [NCBI] 0.000110615
CF [NCBI] 0.000105914
craniofacial dysostosis with diaphyseal hyperplasia [NCBI] 0.000103332
hyperalphalipoproteinemia [NCBI] 8.74792e-05
d-bifunctional protein deficiency [NCBI] 7.11277e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 5.78454e-05
RECQL2 [NCBI] 5.45198e-05
sandhoff disease [NCBI] 5.11569e-05
DYT1 [NCBI] 4.62271e-05
sickle cell anemia [NCBI] 4.45706e-05
menkes disease [NCBI] 3.85525e-05
glycogen storage disease ii [NCBI] 3.85525e-05
MSRA [NCBI] 3.74174e-05
WRN [NCBI] 3.51962e-05
XRCC4 [NCBI] 3.37234e-05
danubian endemic familial nephropathy [NCBI] 3.36244e-05
WHS [NCBI] 3.23828e-05
SGCD [NCBI] 2.98356e-05
CCS [NCBI] 2.93786e-05
BTD [NCBI] 2.89545e-05
CRC [NCBI] 2.79394e-05
HSR [NCBI] 2.58446e-05
PMS2 [NCBI] 2.538e-05
PWS [NCBI] 2.28651e-05
AMACR [NCBI] 2.23167e-05
HD [NCBI] 2.1941e-05
COL3A1 [NCBI] 2.15711e-05
NOS3 [NCBI] 2.03165e-05
APOA1 [NCBI] 1.89789e-05
APOE [NCBI] 1.84893e-05
RA [NCBI] 1.77769e-05
ATM [NCBI] 1.63821e-05
CEACAM5 [NCBI] 1.56314e-05
CVID [NCBI] 1.49249e-05
APC [NCBI] 1.18679e-05
NF1 [NCBI] 1.184e-05
SOD1 [NCBI] 1.16961e-05
TP53 [NCBI] 1.16155e-05
polycystic kidneys [NCBI] 1.13231e-05
SLC6A4 [NCBI] 1.06338e-05
CFTR [NCBI] 1.03319e-05
CAT [NCBI] 1.03015e-05
LPL [NCBI] 9.91083e-06
SOD2 [NCBI] 7.62784e-06
PTHLH [NCBI] 6.66855e-06
FRAP1 [NCBI] 6.4821e-06
HBB [NCBI] 5.6084e-06
APOB [NCBI] 5.39674e-06
lymphoma, non-hodgkin, familial [NCBI] 3.03825e-06
SLE [NCBI] 2.90234e-06
PD [NCBI] 1.56558e-06
BDNF [NCBI] 8.27574e-07
PCNA [NCBI] 3.14198e-07
AD [NCBI] 1.79767e-07
PRL [NCBI] 2.37518e-09



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