Showing entry for Epidermolytic palmoplantar keratoderma of Vorner



                               
General Disease Information
BXGD IdBXGD007602
Disease NameEpidermolytic palmoplantar keratoderma of Vorner
Disease CUI IdC0343110
MeSH Codes C16   C17  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic TypeCongenital Abnormality
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