Showing entry for Thyroid hemiagenesis

General Disease Information
BXGD Id	BXGD021141
Disease Name	Thyroid hemiagenesis
Disease CUI Id	C4023190
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	HP:0000818
Human Phenotype Ontology Term	Abnormality of the endocrine system
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations