Showing entry for Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive

General Disease Information
BXGD Id	BXGD017215
Disease Name	Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive
Disease CUI Id	C2673612
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
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations