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	392
Biotinidase	57
Mol	34
holocarboxylase synthetase	32
Sep	26
pyruvate carboxylase	16
histone	14
BTD	13
Holocarboxylase synthetase	11
MRI	8
She	7
propionyl-CoA carboxylase	6
cholesterol esterase	6
acetyl-CoA carboxylase	6
sodium-dependent multivitamin transporter	6
pyruvate dehydrogenase	5
peroxidase	5
microsomal	5
albumin	4
H2A	4
Vanin-1	4
thymus	3
CSF	3
H2B	3
hemoglobin	3
SDS	3
MCD	3
medium-chain acyl-CoA dehydrogenase	3
K18	3
monocarboxylate transporter 1	3
glycoprotein	3
galactose-1-phosphate uridyltransferase	3
NBS	3
histone H3	3
B12	2
ATP	2
insulin	2
Boc	2
histone H2A	2
PKU	2
GPI	2
histone H4	2
methylmalonyl-CoA mutase	2
Rett syndrome	2
serum albumin	2
trypsinogen	2
axonal	2
AMP	2
Sp1	2
NHS	2
VNN2	2
K12	2
acyl-CoA dehydrogenase	2
polypeptide	2
K13	2
SLC5A6	1
casein	1
alpha-fetoprotein	1
Interferon-gamma	1
C15	1
EIF2B4	1
NOD	1
MC1	1
3-hydroxyacyl-CoA dehydrogenase	1
pantetheinase	1
kit	1
brush border	1
UTR	1
GPI-80	1
thyrotropin-releasing hormone	1
cytochrome c oxidase	1
classical)	1
nodal	1
PBS	1
mTOR	1
cryptic	1
ESI	1
TSK	1
dopa decarboxylase	1
transferrin receptor	1

Disease
Biotinidase deficiency	87
phenylketonuria	30
metabolic disorder	21
developmental delay	21
rash	18
optic atrophy	16
galactosemia	16
maple syrup urine disease	15
homocystinuria	14
congenital hypothyroidism	14
cystic fibrosis	14
congenital adrenal hyperplasia	12
dermatitis	11
Biotin deficiency	8
encephalopathy	8
mental retardation	8
cancer	8
mental retardation	8
deafness	7
sensorineural hearing loss	7
hypoglycemia	6
epilepsy	6
neuroblastoma	6
seborrheic dermatitis	6
lactic acidosis	6
sickle cell disease	6
fits	6
enzyme deficiency	6
hypothyroidism	5
Leigh syndrome	5
myelopathy	5
tyrosinemia	5
glycogen storage disease	5
tumor	5
hemoglobinopathies	4
Multiple carboxylase deficiency	4
failure to thrive	4
West	4
liver disease	4
neuropathy	4
eczema	3
NBS	3
MCD	3
stroke	3
malnutrition	3
conjunctivitis	3
SDS	3
genetic disorder	2
hepatocellular carcinoma	2
tetraplegia	2
candidiasis	2
papillary thyroid cancer	2
hyperglycemia	2
brain atrophy	2
diabetes	2
coma	2
cleft palate	2
hemiparesis	2
myopathy	2
ketosis	2
congenital disorder	2
multiple sclerosis	2
immune deficiency	2
autism	2
vitamin E deficiency	2
Phenylketonuria	2
basal ganglia disease	2
plaque	2
folate deficiency	2
Holocarboxylase synthetase deficiency	2
methylmalonic acidemia	2
propionic acidemia	2
hemophagocytic lymphohistiocytosis	2
ABL	2
glutaric aciduria	2
depression	2
Rett syndrome	2
cirrhosis	2
motor neuron disease	2
HMG-CoA lyase deficiency	2

Enzyme
biotinidase	392
pyruvate carboxylase	17
acyl-CoA dehydrogenase	9
propionyl-CoA carboxylase	7
propionyl-CoA carboxylase	6
acetyl-CoA carboxylase	6
pyruvate dehydrogenase	5
pyruvate dehydrogenase	5
peroxidase	5
pyruvate dehydrogenase	5
deaminase	3
acyl-CoA dehydrogenase	2
trypsin	2
alpha-ketoglutarate dehydrogenase	2
methylmalonyl-CoA mutase	2
methylcrotonyl-CoA carboxylase	2
pantetheinase	2
holocarboxylase-synthetase	2
cystathionine gamma-synthase	1
DOPA decarboxylase	1
uridyltransferase	1
AMPK	1
ACS	1
protein kinase	1
AMPK	1
DNA polymerase	1
AST	1
KAT	1
ceruloplasmin	1
PNGase F	1
glucose-6-phosphate dehydrogenase	1
lipoprotein lipase	1
transcarboxylase	1
alanine aminotransferase	1
lipase	1
cytochrome oxidase	1
citrate synthase	1
EC 6.3.4.10	1
caspase-3	1
3-hydroxyacyl-CoA dehydrogenase	1
aspartate aminotransferase	1
delta-aminolevulinic acid dehydratase	1
succinate dehydrogenase	1
AMP-activated protein kinase	1
3-hydroxyacyl-CoA dehydrogenase	1