EC:3.5.1.12 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.5.1.12 (biotinidase)
392 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
biotinidase	16.3
Biotinidase	16.0
holocarboxylase synthetase	14.3
VNN2	13.4
sodium-dependent multivitamin transporter	13.3
BTD	13.2
Holocarboxylase synthetase	13.2
Thyroid stimulating hormone receptor	13.0
EIF2B4	12.7
L12a	12.5
SLC5A6	12.2
GSD IX	12.0
Vanin-1	11.9
SMVT	11.7
GPI-80	11.4
propionyl-CoA carboxylase	10.6
very-long-chain acyl-CoA dehydrogenase	10.5
SLC19A3	10.2
PTMA	10.1
MSUD	10.1
pantetheinase	10.1
galactose-1-phosphate uridyltransferase	10.1
PCCB	10.0
NARP	9.9
pyruvate carboxylase	9.8
liver glycogen phosphorylase	9.7
SPINK5	9.6
monocarboxylate transporter 1	9.6
cholesterol esterase	9.5
medium-chain acyl-CoA dehydrogenase	9.4
K23	9.4
B(0)AT1	9.3
ACC2	9.2
beta-ketothiolase	9.1
LHON	9.0
MCD	8.6
K13	8.5
short-chain acyl-CoA dehydrogenase	8.5
aminoacylase	8.4
long-chain acyl-CoA dehydrogenase	8.4

Disease
Biotinidase deficiency	16.1
Multiple carboxylase deficiency	15.5
Holocarboxylase synthetase deficiency	14.3
Other metabolic disorders	14.0
Biotin deficiency	13.3
trichoptilosis	13.3
Organic acidemias	13.0
HMG-CoA lyase deficiency	13.0
Trichorrhexis nodosa	12.7
glycinuria	12.3
GSD IX	12.2
Vertebral anomalies	11.6
Staphylococcus aureus meningitis	11.4
Thiamine-responsive megaloblastic anemia	11.0
basal ganglia disease	11.0
Peroxisomal disorders	10.8
Hers	10.7
galactosemia	10.6
maple syrup urine disease	10.3
homocystinuria	10.2
disorders of amino acid metabolism	10.0
Medulla	9.8
HND	9.7
phenylketonuria	9.6
Ohtahara syndrome	9.5
brittle hair	9.5
hypermethioninemia	9.4
Coffin-Siris syndrome	9.4
tyrosinemia	9.4
optic atrophy	9.2
blepharoconjunctivitis	9.1
congenital hypothyroidism	9.1
MCAD deficiency	9.1
PC deficiency	9.0
hyperargininemia	8.9
glutaric aciduria	8.9
Inborn errors of metabolism	8.7
MCD	8.6
Norrie disease	8.6
congenital adrenal hyperplasia	8.6

Enzyme
biotinidase	16.3
holocarboxylase-synthetase	15.7
EC 6.3.4.10	15.3
methylcrotonyl-CoA carboxylase	10.8
propionyl-CoA carboxylase	10.7
pantetheinase	10.5
propionyl-CoA carboxylase	10.5
pyruvate carboxylase	9.8
transcarboxylase	9.5
acyl-CoA dehydrogenase	9.0
cystathionine gamma-synthase	8.8
methylmalonyl-CoA mutase	8.7
uridyltransferase	8.6
acyl-CoA dehydrogenase	7.7
acetyl-CoA carboxylase	7.4
alpha-ketoglutarate dehydrogenase	7.0
3-hydroxyacyl-CoA dehydrogenase	6.9
3-hydroxyacyl-CoA dehydrogenase	6.9
pyruvate dehydrogenase	6.9
pyruvate dehydrogenase	6.9
KAT	6.5
delta-aminolevulinic acid dehydratase	6.5
DOPA decarboxylase	6.3
pyruvate dehydrogenase	6.2
PNGase F	5.7
deaminase	5.6
citrate synthase	4.2
ceruloplasmin	4.0
AST	3.7
AMPK	3.7
lipoprotein lipase	3.5
glucose-6-phosphate dehydrogenase	3.4
succinate dehydrogenase	3.3
cytochrome oxidase	3.2
AMPK	2.7
AMP-activated protein kinase	2.6
peroxidase	2.6
DNA polymerase	2.3
lipase	2.1
trypsin	1.9