Showing entry for Skin Diseases, Genetic



                               
General Disease Information
BXGD IdBXGD002677
Disease NameSkin Diseases, Genetic
Disease CUI IdC0037277
MeSH Codes C16   C17  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue 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