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Methylmalonic acidemia with homocystinuria, type cblX

MONDO:0010657

Also known as: combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX, methylmalonic aciduria and homocysteinemia, cblx type, X-linked recessive, methylmalonic aciduria with homocystinuria, type cblX, intellectual disability, X-linked 3, mental retardation, X-linked 3, methylmalonic acidemia and HOMOCYSTEINEMIA, cblX type, methylmalonic acidemia and homocysteinemia type cblX

21 clinical trials for this condition and its sub-types, 0 tagged with Methylmalonic acidemia with homocystinuria, type cblX itself.

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