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Results 1 - 6 of 6 for Methylmalonic aciduria homocystinuria
  1. ... methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria methylmalonic aciduria and homocystinuria type D protein, mitochondrial methylmalonic aciduria and homocystinuria ...
  2. ... methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria methylmalonic aciduria and homocystinuria type C protein Tests of MMACHC PubMed METABOLISM ...
  3. ... as mutations) have been identified in people with methylmalonic acidemia with homocystinuria, cblX type, which is one form of a ... imbalances leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. Neurological and developmental problems are especially severe in ...
  4. ... mutations) in the PRDX1 gene are involved in methylmalonic acidemia with homocystinuria, epi-cblC type (shortened to epi-cblC), which ... molecules leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. Research suggests that PRDX1 gene variants may also ...
  5. ... the ABCD4 gene have been found to cause methylmalonic acidemia with homocystinuria, cblJ type, which is one form of a ... imbalances leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. More About This Health Condition 69 kDa peroxisomal ...
  6. ... the LMBRD1 gene have been found to cause methylmalonic acidemia with homocystinuria, cblF type, which is one form of a ... imbalances leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. More About This Health Condition bA810I22.1 C6orf209 ...