Showing entry for Keratoderma, Palmoplantar, Epidermolytic

General Disease Information
BXGD Id	BXGD013700
Disease Name	Keratoderma, Palmoplantar, Epidermolytic
Disease CUI Id	C1721006
MeSH Codes	C16   C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0001574
Human Phenotype Ontology Term	Abnormality of the integument
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations