Showing entry for Congenital Hypothyroidism

General Disease Information
BXGD Id	BXGD000661
Disease Name	Congenital Hypothyroidism
Disease CUI Id	C0010308
MeSH Codes	C16   C05   C19
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; 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	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations