adisease

Showing entry for Infantile Neuroaxonal Dystrophy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD006092
Disease Name	Infantile Neuroaxonal Dystrophy
Disease CUI Id	C0270724
MeSH Codes	C10
Disease Class Name	Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
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
P04054	BXGT006136	Phospholipase A2	5319	reviewed	Enzyme
P17050	BXGT008277	Alpha-N-acetylgalactosaminidase	4668	reviewed
P37840	BXGT010015	Alpha-synuclein	6622	reviewed	Transporter
P47712	BXGT010577	Cytosolic phospholipase A2	5321	reviewed	Enzyme
P63104	BXGT011499	14-3-3 protein zeta/delta	7534	reviewed	Chaperone
Q8TE04	BXGT018818	Pantothenate kinase 1	53354	reviewed	Kinase
Q9BZ23	BXGT020194	Pantothenate kinase 2, mitochondrial	80025	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}