UMLS:C0022716 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0022716 (Menkes)
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Human Gene/Protein
NSFL1	14.9
ATP7A protein	14.2
MNK	13.9
golgin, RAB6-interacting	13.9
ATP7A	13.9
MNK2	13.7
AP1B1	13.3
lipocalin-interacting membrane receptor	13.3
PGAM3	13.3
WND	13.2
MNK1	12.7
ATOX1	12.6
Copper-transporting ATPase	12.6
Ras and Rab interactor 2	12.3
COX19	12.1
EIF4F	12.1
ATPase 7B	12.1
IBM2	12.1
MC1	12.0
CTL3	11.9
cation transporting ATPase	11.7
ATP7B	11.7
COG7	11.6
Wilson disease	11.6
AP19	11.1
hCTR2	11.1
sterolin	11.0
IGF2AS	10.9
COMMD1	10.8
procollagen I N-proteinase	10.8
copper transport protein	10.8
UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	10.8
nexilin	10.6
GNE	10.5
MURR1	10.5
N-acetylmannosamine kinase	10.5
TAL-H	10.5
Amine oxidase	10.4
X-linked recessive	10.3
Glutaredoxin-1	10.3

Disease
Hair disease	14.9
EDS VIIB	14.9
Menkes	14.9
Ehlers-Danlos syndrome type IX	14.9
SMAX3	14.9
disorders of copper metabolism	13.8
Pili torti	13.2
Disorders of pigmentation	12.9
Pollitt syndrome	12.9
Swayback	12.9
trichoptilosis	11.9
Sliding hiatal hernia	11.9
PARK5	11.6
Bladder diverticula	11.5
Trichorrhexis nodosa	11.3
QSM	11.3
cerebral degeneration	11.2
Cytotoxic edema	11.1
trichorrhexis	10.3
Copper deficiency	10.1
OHS	10.0
Ehlers-Danlos syndrome type VII	10.0
Aortic root dilatation	10.0
Wilson's disease	9.9
Kennedy syndrome	9.6
acrodermatitis enteropathica	9.6
sialic acid storage disease	9.6
cutis laxa	9.3
EDS IV	9.3
Gastric polyps	9.3
lipoprotein disorder	9.2
EDS VI	9.0
battered child syndrome	9.0
ARP1	8.7
pediatric disorder	8.7
disorders of amino acid metabolism	8.6
Pelizaeus-Merzbacher	8.6
Bazex syndrome	8.6
Netherton syndrome	8.5
CRD1	8.5

Enzyme
N-acetylmannosamine kinase	11.1
AtHMA4	10.4
UDP-N-acetylglucosamine 2-epimerase	10.2
N-acetylglucosamine kinase	9.6
N-acetylglucosamine 2-epimerase	9.6
ceruloplasmin	9.2
lysyl oxidase	9.1
CCS1	8.5
CCS	8.5
sulfhydryl oxidase	7.0
lysyl hydroxylase	6.9
CNPase	6.8
dopamine beta-hydroxylase	6.7
ATPase	6.6
type III procollagen	6.4
PAM	6.3
mannosidase II	6.3
biotinidase	6.3
transaldolase	6.2
cytochrome oxidase	6.2
sulfite oxidase	6.1
sulfite oxidase	6.0
argininosuccinate synthetase	5.5
PGM	5.4
ascorbate oxidase	5.3
tyrosinase	5.2
phenol oxidase	5.1
ALDH	5.1
prolyl hydroxylase	5.1
calcium pump	4.9
ECH	4.8
phosphoglycerate kinase	4.8
uricase	4.6
Thy1	4.6
diamine oxidase	4.6
dihydropyrimidine dehydrogenase	4.6
heme oxygenase	4.4
phenylalanine hydroxylase	4.4
gamma-glutamylcysteine synthetase	4.4
Mg2+-ATPase	4.3