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Methylmalonic Acidemias with Homocystinuria The genetic causes of methylmalonic acidemias with homocystinuria are due to defects in the methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria gene (MMACHC), the methylmalonic aciduria and homocystinuria, cblD type gene (MMADHC), LMBR1 domain containing 1 gene (LMBRD1

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A result that is slightly low/high may not be of medical significance, as this test often varies from day to day and from person to person