Showing entry for Robinow Syndrome, Autosomal Dominant

General Disease Information
BXGD Id	BXGD023306
Disease Name	Robinow Syndrome, Autosomal Dominant
Disease CUI Id	C4551476
MeSH Codes	C16   C13   C05   C12   C19
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Endocrine System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:225
Disease Ontology Class Name	genetic disease; syndrome
Disorder Network	disorder-protein-compound-food associations