Showing entry for Redundant skin



                               
General Disease Information
BXGD IdBXGD009560
Disease NameRedundant skin
Disease CUI IdC0581342
MeSH Codes C16   C17  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic TypePathologic Function
Human Phenotype Ontology Id HP:0001574  
Human Phenotype Ontology TermAbnormality of the integument
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations