Showing entry for Xeroderma pigmentosum, variant form

General Disease Information
BXGD Id	BXGD008776
Disease Name	Xeroderma pigmentosum, variant form
Disease CUI Id	C0432328
MeSH Codes	C16   C04   C18   C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Semantic Type	Disease or Syndrome; Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations