Showing entry for Carnitine deficiency

General Disease Information
BXGD Id	BXGD011733
Disease Name	Carnitine deficiency
Disease CUI Id	C1142132
MeSH Codes
Disease Class Name
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0001939   HP:0025354
Human Phenotype Ontology Term	Abnormality of metabolism/homeostasis; Abnormal cellular phenotype
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations