Showing entry for Hypocalcemia, Autosomal Dominant, with Bartter Syndrome

General Disease Information
BXGD Id	BXGD013863
Disease Name	Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Disease CUI Id	C1832612
MeSH Codes	C18   C13   C12   C19
Disease Class Name	Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; 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