Disease #01229 (HCVAD (hypercarotenemia and vitamin A deficiency, autosomal dominant (HCVAD)), OMIM:115300)

Official abbreviation HCVAD
Name hypercarotenemia and vitamin A deficiency, autosomal dominant (HCVAD)
OMIM ID 115300
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene BCMO1
Associated tissues -
Disease features autosomal dominant
Remarks -