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MIM:115300 - HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL DOMINANT; HCVAD
Xenbase Genes: bco1
Human Disease Resource: MIM
MONDO:0007272 - hereditary hypercarotenemia and vitamin A deficiency |
Disease Ontology (DO):
DOID:9969 - carotenemia |
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MONDO:0007272 - hereditary hypercarotenemia and vitamin A deficiency |
DOID:9969 - carotenemia |