Showing entry for Tyrosine Transaminase Deficiency Disease

General Disease Information
BXGD Id	BXGD005961
Disease Name	Tyrosine Transaminase Deficiency Disease
Disease CUI Id	C0268487
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