Showing entry for Congenital absence of parathyroid gland

General Disease Information
BXGD Id	BXGD012451
Disease Name	Congenital absence of parathyroid gland
Disease CUI Id	C1321907
MeSH Codes	C16   C19
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
Semantic Type	Congenital Abnormality
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