adisease

Showing entry for Ornithine carbamoyltransferase deficiency

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005977
Disease Name	Ornithine carbamoyltransferase deficiency
Disease CUI Id	C0268542
MeSH Codes	C16 C18 C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:0014667 DOID:630
Disease Ontology Class Name	disease of metabolism; genetic disease
Disorder Network	disorder-protein-compound-food associations

The disease-related target proteins

Proteins

Uniport Id	BXGT Id	Protein Name	Gene	Status	Protein Class
Uniport Id	BXGT Id	Protein name	Gene	Status	Protein class
P00156	BXGT005469	Cytochrome b	4519	reviewed
P00480	BXGT005551	Ornithine carbamoyltransferase, mitochondrial	5009	reviewed
P08686	BXGT006813	Steroid 21-hydroxylase	1589	reviewed
P08709	BXGT006818	Coagulation factor VII	2155	reviewed	Enzyme
P15104	BXGT008081	Glutamine synthetase	2752	reviewed	Enzyme
P24298	BXGT008960	Alanine aminotransferase 1	2875	reviewed	Enzyme
P31327	BXGT009523	Carbamoyl-phosphate synthase [ammonia], mitochondrial	1373	reviewed	Enzyme
Q16874	BXGT013685	Cytochrome P450 21-hydroxylase	1589	unreviewed
Q92834	BXGT019381	X-linked retinitis pigmentosa GTPase regulator	6103	reviewed
Q9Y619	BXGT022316	Mitochondrial ornithine transporter 1	10166	reviewed	Transporter

The disease-related compounds

Compounds

BXGC Id	Compound Name	Structure	Molecular Weight	Number of targets^{?Number of times compound connecting the disease , higher numbers indicate the compound is more associated with the disease}

The disease-related foods

Foods

BXGF Id	Food Name	Scientific Name	Food Group	Number of compounds in food^{?Number of compounds in food that connecting disease, higher numbers indicate the more compounds in food are more associated with the dusease}