Methylmalonic aciduria and homocystinuria type cblD

MONDO:0010185

A form of methylmalonic acidemia with homocystinuria, an inborn error of vitamin B12 (cobalamin) metabolism characterized by variable biochemical, neurological and hematological manifestations.

Also known as: cblD defect, cobalamin D defect, cobalamin d disease, combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD, methylmalonic aciduria and homocystinuria type cblD, methylmalonic aciduria with homocystinuria, type cblD, MAHCD, cblD - cobalamin locus d

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

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Broader categories

Disease (618) Metabolic disease (215) Nutritional deficiency disease (206) Anemia (203) Hereditary disease (172) Hematologic disorder (160) Nutritional disorder (116) Inborn errors of metabolism (42) Human disease (14) Vitamin B12 deficiency (10)

Trials to join now! 35 Not yet recruiting 6 Not yet finished but already full! 10 Completed 21 Terminated 1

Can extra care after transplant help older patients live better?

Disease control Terminated

This study tested two extra care programs—supportive palliative care and clinical management of other health issues—for older or frail patients who had a donor stem cell transplant. The goal was to see if these programs could improve quality of life and survival compared to stand…

Phase: PHASE2, PHASE3 • Sponsor: Fred Hutchinson Cancer Center • Aim: Disease control

Last updated Jun 27, 2026 08:10 UTC

Methylmalonic aciduria and homocystinuria type cblD

Broader categories

Can extra care after transplant help older patients live better?