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MeSH keywords -> Related genes, diseases (OMIM)


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01 Menkes Kinky Hair Syndrome [NCBI]


Gene


Gene Link Information
Gain
01
ATP7A [NCBI] 0.00180464
ATOX1 [NCBI] 6.90334e-05
ATP7B [NCBI] 6.01198e-05
PDZD11 [NCBI] 1.49698e-05
MTL4 [NCBI] 1.49698e-05
PAM [NCBI] 1.36642e-05
COX17 [NCBI] 1.03291e-05
GOLGA4 [NCBI] 1.03291e-05
COMMD1 [NCBI] 8.55066e-06
MT2A [NCBI] 7.6984e-06
SCO2 [NCBI] 7.6984e-06
PRKD1 [NCBI] 6.60081e-06
TYR [NCBI] 5.08636e-06
NOS1 [NCBI] 3.57796e-06
PLN [NCBI] 2.9772e-06
APOB [NCBI] 2.31135e-06
SOD1 [NCBI] 1.51184e-06
TH [NCBI] 1.3562e-06
GFAP [NCBI] 6.57435e-07
APOE [NCBI] 4.02957e-07
CASP3 [NCBI] 3.13131e-07




OMIM


OMIM Link Information
gain
01
menkes disease [NCBI] 0.00777141
ATP7A [NCBI] 0.00271336
cutis laxa, x-linked [NCBI] 0.00156837
ATP7B [NCBI] 0.000246828
wilson disease [NCBI] 0.000238093
MT1A [NCBI] 0.000177385
hair defect with photosensitivity and mental retardation [NCBI] 0.000113012
PAM [NCBI] 9.10453e-05
PDZD11 [NCBI] 7.91621e-05
MT2A [NCBI] 5.68123e-05
ATOX1 [NCBI] 5.68123e-05
GAN1 [NCBI] 4.53136e-05
ehlers-danlos syndrome, type i [NCBI] 3.86093e-05
GLB1 [NCBI] 3.44275e-05
PGK1 [NCBI] 3.33199e-05
TYR [NCBI] 2.75795e-05
osteogenesis imperfecta, type i [NCBI] 2.61506e-05
MFS [NCBI] 1.10005e-05
APOB [NCBI] 8.17332e-06
TH [NCBI] 2.49948e-06
APOE [NCBI] 6.35292e-07
GFAP [NCBI] 3.37867e-07




Database Center for Life Science