methylmalonic aciduria and homocystinuria type cblD https://www.malacards.org/card/methylmalonic_aciduria_and_homocystinuria_cbld_type mehtylmalonic acidemia with homocystinuria cbI d methylmalonic acidemia with homocystinuria type cblD SCTID:31220004 methylmalonic aciduria and homocystinuria type cblD homocystinuria, cblD type, variant 1, included MEDGEN:341253 Orphanet:79283 MONDO:0010185 methylmalonic aciduria, Cblh type methylmalonic aciduria, cblD type, variant 2, included combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD cblD defect GARD:0003582 MAHCD methylmalonic acidemia, Cblh type OMIM:277410 NANDO:2201108 A form of methylmalonic acidemia with homocystinuria, an inborn error of vitamin B12 (cobalamin) metabolism characterized by variable biochemical, neurological and hematological manifestations. methylmalonic aciduria with homocystinuria, type cblD DOID:0050716 UMLS:C1848552 MESH:C564743 cobalamin d disease NANDO:1200797 cobalamin D defect methylmalonic aciduria and homocystinuria methylmalonic aciduria and/or homocystinuria, cblD type Methylmalonic acidemia with homocystinuria, type cblD