adisease

Showing entry for Hereditary Coproporphyria

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD003950
Disease Name	Hereditary Coproporphyria
Disease CUI Id	C0162531
MeSH Codes	C16 C06 C18 C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue 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
P02760	BXGT005948	Protein AMBP	259	reviewed
P07477	BXGT006629	Trypsin-1	5644	reviewed	Enzyme
P13196	BXGT007886	5-aminolevulinate synthase, nonspecific, mitochondrial	211	reviewed	Enzyme
P29350	BXGT009335	Tyrosine-protein phosphatase non-receptor type 6	5777	reviewed
P36551	BXGT009927	Oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial	1371	reviewed	Enzyme
P50336	BXGT010791	Protoporphyrinogen oxidase	5498	reviewed
Q16665	BXGT013653	Hypoxia-inducible factor 1-alpha	3091	reviewed	Transcription factor
Q5JAM2	BXGT015430	5-aminolevulinate synthase	211	unreviewed

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}