adisease

Showing entry for Hippocampal atrophy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD022694
Disease Name	Hippocampal atrophy
Disease CUI Id	C4315130
MeSH Codes
Disease Class Name
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0000707
Human Phenotype Ontology Term	Abnormality of the nervous system
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
O00341	BXGT003913	Excitatory amino acid transporter 5	6512	reviewed	Transporter
P39060	BXGT010088	Collagen alpha-1(XVIII) chain	80781	reviewed
P52803	BXGT010958	Ephrin-A5	1946	reviewed	Signaling
Q96PY6	BXGT019712	Serine/threonine-protein kinase Nek1	4750	reviewed	Kinase

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}