Showing entry for Hyperthyroxinemia, Familial Dysalbuminemic

General Disease Information
BXGD Id	BXGD007439
Disease Name	Hyperthyroxinemia, Familial Dysalbuminemic
Disease CUI Id	C0342185
MeSH Codes	C16   C19
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine 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