Showing entry for 3-methylcrotonyl CoA carboxylase 1 deficiency

General Disease Information
BXGD Id	BXGD006001
Disease Name	3-methylcrotonyl CoA carboxylase 1 deficiency
Disease CUI Id	C0268600
MeSH Codes	C16   C18   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:0014667   DOID:630   DOID:7
Disease Ontology Class Name	disease of metabolism; genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations