Showing entry for Autosomal dominant optic atrophy plus syndrome

General Disease Information
BXGD Id	BXGD022366
Disease Name	Autosomal dominant optic atrophy plus syndrome
Disease CUI Id	C4275164
MeSH Codes	C23   C18   C11   C05   C10   C14
Disease Class Name	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular 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