adisease

Showing entry for Embryonal nuclear cataract (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD003890
Disease Name	Embryonal nuclear cataract (disorder)
Disease CUI Id	C0158551
MeSH Codes	C16 C11
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
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
P02792	BXGT005966	Ferritin light chain	2512	reviewed	Storage
Q9ULV5	BXGT024442	Heat shock factor protein 4	3299	reviewed	Transcription factor
P07315	BXGT026109	Gamma-crystallin C	1420	reviewed
P07320	BXGT026150	Gamma-crystallin D	1421	reviewed
P02489	BXGT026168	Alpha-crystallin A chain	1409	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}