Multiple carboxylase deficiency
MONDO:0015454Multiple carboxylase deficiency (MCD) is a term used to describe inborn errors of biotin metabolism characterized by reduced activities of biotin-dependent enzymes resulting in a wide spectrum of symptoms, including feeding difficulty, breathing difficulties, lethargy, seizures, skin rash, alopecia, and developmental delay.
Also known as: MCD, multiple carboxylase deficiency
4 clinical trials for this condition and its sub-types.
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Broader categories
Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Human disease
(15)
Inborn disorder of amino acid metabolism
(6)
Inborn organic aciduria
(5)
Carbohydrate metabolism disease
(4)
Amino acid metabolism disease
(2)
Disease of genetic or genomic mechanism
(2)