Showing entry for Hallermann's Syndrome

General Disease Information
BXGD Id	BXGD001198
Disease Name	Hallermann's Syndrome
Disease CUI Id	C0018522
MeSH Codes	C16   C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:225
Disease Ontology Class Name	syndrome
Disorder Network	disorder-protein-compound-food associations