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Results 1 - 10 of 10 for Methylmalonic acidemia
  1. MMUT gene 
    ... MMUT gene have been identified in people with methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, ... and tissues, causing the signs and symptoms of methylmalonic acidemia.Mutations that prevent the production of any functional ...
    https://medlineplus.gov/genetics/gene/mmut - Genetics
  2. MMAA gene 
    ... the MMAA gene have been found to cause methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, ... leads to the serious medical problems associated with methylmalonic acidemia. Studies suggest that without the activity of this ...
    https://medlineplus.gov/genetics/gene/mmaa - Genetics
  3. MMAB gene 
    ... the MMAB gene have been found to cause methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, ... and tissues, causing the signs and symptoms of methylmalonic acidemia. More About This Health Condition ATP:Cob(I) ...
    https://medlineplus.gov/genetics/gene/mmab - Genetics
  4. MMADHC gene 
    ... the MMADHC gene have been found to cause methylmalonic acidemia, a condition characterized by feeding difficulties, life-threatening ... and tissues, causing the signs and symptoms of methylmalonic acidemia. More About This Health Condition Variants in the ...
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  5. MCEE gene 
    ... the MCEE gene have been found to cause methylmalonic acidemia, a condition characterized by feeding difficulties, developmental delay, ... enzyme with little or no function. People with methylmalonic acidemia caused by mutations in the MCEE gene typically ...
    https://medlineplus.gov/genetics/gene/mcee - Genetics
  6. HCFC1 gene 
    ... as mutations) have been identified in people with methylmalonic acidemia with homocystinuria, cblX type, which is one form ... imbalances leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. Neurological and developmental problems are especially ...
    https://medlineplus.gov/genetics/gene/hcfc1 - Genetics
  7. PRDX1 gene 
    ... mutations) in the PRDX1 gene are involved in methylmalonic acidemia with homocystinuria, epi-cblC type (shortened to epi- ... molecules leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. Research suggests that PRDX1 gene variants ...
    https://medlineplus.gov/genetics/gene/prdx1 - Genetics
  8. MMACHC gene 
    ... known as mutations) have been found to cause methylmalonic acidemia with homocystinuria, cblC type, the most common form ... imbalances leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. More About This Health Condition cblC ...
    https://medlineplus.gov/genetics/gene/mmachc - Genetics
  9. ABCD4 gene 
    ... the ABCD4 gene have been found to cause methylmalonic acidemia with homocystinuria, cblJ type, which is one form ... imbalances leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. More About This Health Condition 69 ...
    https://medlineplus.gov/genetics/gene/abcd4 - Genetics
  10. LMBRD1 gene 
    ... the LMBRD1 gene have been found to cause methylmalonic acidemia with homocystinuria, cblF type, which is one form ... imbalances leads to the signs and symptoms of methylmalonic acidemia with homocystinuria. More About This Health Condition bA810I22. ...
    https://medlineplus.gov/genetics/gene/lmbrd1 - Genetics