Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Menkes Kinky Hair Syndrome	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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