adisease

Showing entry for Hyperferritinemia, hereditary, with congenital cataracts

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD013900
Disease Name	Hyperferritinemia, hereditary, with congenital cataracts
Disease CUI Id	C1833213
MeSH Codes	C18 C11
Disease Class Name	Nutritional and Metabolic Diseases; Eye Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630
Disease Ontology Class Name	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
P00450	BXGT005544	Ceruloplasmin	1356	reviewed	Enzyme
P02792	BXGT005966	Ferritin light chain	2512	reviewed	Storage
P21399	BXGT008646	Cytoplasmic aconitate hydratase	48	reviewed	Enzyme
P50747	BXGT010817	Biotin--protein ligase	3141	reviewed	Enzyme
P81172	BXGT011935	Hepcidin	57817	reviewed
P99999	BXGT012235	Cytochrome c	54205	reviewed

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}