Methylmalonic aciduria, cblB type

MONDO:0009614

An autosomal recessive form of methylmalonic aciduria, caused by mutation(s) in the MMAB gene, encoding cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial.

Also known as: methylmalonic acidemia cblB type, methylmalonic acidemia, cblB type, methylmalonic aciduria, cblB type, methylmalonic aciduria, vitamin B12-responsive, cblB type, vitamin B12-responsive methylmalonic acidemia type cblB, vitamin B12-responsive methylmalonic aciduria, type cblB, methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type

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

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