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PCCA-related propionic acidemia

MONDO:1060182

Any propionic acidemia in which the cause of the disease is a variation in PCCA gene.

Also known as: PCCA-related propionic acidemia

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Propionic acidemia (8) Inborn organic aciduria (5) Inborn disorder of amino acid metabolism (4) Disease of genetic or genomic mechanism (2) Amino acid metabolism disease (1)

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