Showing entry for Pfeiffer type acrocephalosyndactyly

General Disease Information
BXGD Id	BXGD018089
Disease Name	Pfeiffer type acrocephalosyndactyly
Disease CUI Id	C2931888
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:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations