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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hydroxylysine [NCBI]

Gene


 Gene Link Information
Gain		 01
PLOD1 [NCBI] 5.55038e-06
PLOD3 [NCBI] 2.72765e-06
COL4A1 [NCBI] 2.25321e-06
LOX [NCBI] 2.17499e-06
CD44 [NCBI] 1.83018e-06
ACP5 [NCBI] 1.5499e-06
BMP2 [NCBI] 1.46242e-06



OMIM


 OMIM Link Information
gain		 01
ehlers-danlos syndrome, type vib [NCBI] 0.00194777
proteus syndrome [NCBI] 0.00178344
ehlers-danlos syndrome, type vi [NCBI] 0.000758227
osteogenesis imperfecta, type i [NCBI] 0.000185325
epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase [NCBI] 0.000162803
MFS [NCBI] 0.00013807
PLOD1 [NCBI] 0.000122529
d-2-@hydroxyglutaric aciduria [NCBI] 0.00011807
sulfocysteinuria [NCBI] 0.000114103
ehlers-danlos syndrome, type i [NCBI] 0.000112353
osteogenesis imperfecta, type iia [NCBI] 9.3118e-05
C1QA [NCBI] 3.82295e-05
COL6A1 [NCBI] 3.20182e-05
LOX [NCBI] 2.73966e-05
COL1A1 [NCBI] 2.53555e-05
ACP5 [NCBI] 1.6393e-05
CF [NCBI] 8.01594e-12



Database Center for Life Science