Showing entry for Autosomal recessive ocular albinism

General Disease Information
BXGD Id	BXGD005967
Disease Name	Autosomal recessive ocular albinism
Disease CUI Id	C0268503
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	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations