adisease

Showing entry for Dominant hereditary optic atrophy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD023328
Disease Name	Dominant hereditary optic atrophy
Disease CUI Id	C4551508
MeSH Codes	C16 C11 C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
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
O60313	BXGT004871	Dynamin-like 120 kDa protein, mitochondrial	4976	reviewed	Enzyme modulator
P11308	BXGT007684	Transcriptional regulator ERG	2078	reviewed	Transcription factor
Q13336	BXGT013343	Urea transporter 1	6563	reviewed	Transporter
O95140	BXGT024482	Mitofusin-2	9927	reviewed	Enzyme
Q04837	BXGT025484	Single-stranded DNA-binding protein, mitochondrial	6742	reviewed	Nucleic acid binding

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}