Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Metal Metabolism, Inborn Errors [NCBI]

Gene


 Gene Link Information
Gain		 01
CP [NCBI] 2.87132e-05
HFE [NCBI] 2.02501e-05
ATP7A [NCBI] 1.90936e-05
SUOX [NCBI] 1.35427e-05
FXYD2 [NCBI] 1.33275e-05
COMMD1 [NCBI] 1.22954e-05
ATOX1 [NCBI] 1.19012e-05
SLC40A1 [NCBI] 1.0485e-05
ATP7B [NCBI] 8.90978e-06
TFR2 [NCBI] 8.83461e-06
CYP27A1 [NCBI] 8.40735e-06
FXN [NCBI] 7.4247e-06
SLC11A1 [NCBI] 7.11378e-06
NOS2 [NCBI] 4.39235e-06



OMIM


 OMIM Link Information
gain		 01
zinc, elevated plasma [NCBI] 0.00213636
HHC2 [NCBI] 0.000991404
menkes disease [NCBI] 0.000479668
aceruloplasminemia [NCBI] 0.000176359
COMMD1 [NCBI] 0.000161558
copper deficiency, familial benign [NCBI] 0.000136591
wilson disease [NCBI] 0.00011205
HOMG2 [NCBI] 9.27854e-05
ATP6V0E1 [NCBI] 8.31009e-05
SUOX [NCBI] 8.31009e-05
CP [NCBI] 8.14232e-05
HOMG [NCBI] 7.9483e-05
hemochromatosis, neonatal [NCBI] 7.82382e-05
molybdenum cofactor deficiency [NCBI] 7.60048e-05
cutis laxa, autosomal recessive, type i [NCBI] 7.14886e-05
cutis laxa, x-linked [NCBI] 6.86125e-05
CACNA1C [NCBI] 6.56767e-05
HEPH [NCBI] 6.26709e-05
FIH [NCBI] 6.21912e-05
HHC1 [NCBI] 6.01273e-05
NPC1 [NCBI] 5.33135e-05
NPC1 [NCBI] 5.07564e-05



Database Center for Life Science