Hereditary hypercarotenemia and vitamin A deficiency

MONDO:0007272

Hereditary hypercarotenemia and vitamin A deficiency is an extremely rare metabolic disorder characterized clinically by skin discoloration, elevated levels of carotene and low levels of vitamin A described in fewer than 5 patients to date.

Also known as: Carotenoids, plasma level of, quantitative trait locus 1, HCVAD, hypercarotenemia and vitamin A deficiency, autosomal dominant

0 clinical trials for this condition and its sub-types, 0 tagged with Hereditary hypercarotenemia and vitamin A deficiency itself.

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↑ Disorder of vitamin and non-protein cofactor absorption and transport (10)

Sub-types of Hereditary hypercarotenemia and vitamin A deficiency

Hypercarotenemia and vitamin A deficiency, autosomal recessive 0 trials

Including sub-types (0) Tagged with Hereditary hypercarotenemia and vitamin A deficiency (0)

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