Showing entry for ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT

General Disease Information
BXGD Id	BXGD016567
Disease Name	ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
Disease CUI Id	C1876214
MeSH Codes	C16   C18   C11   C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations