Showing entry for Acrocephalopolysyndactyly type 2



                               
General Disease Information
BXGD IdBXGD012055
Disease NameAcrocephalopolysyndactyly type 2
Disease CUI IdC1275078
MeSH Codes C16   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations