Showing entry for Robinow syndrome, autosomal recessive

General Disease Information
BXGD Id	BXGD015038
Disease Name	Robinow syndrome, autosomal recessive
Disease CUI Id	C1849334
MeSH Codes	C16   C05   C07
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic 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