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Up to: Vitamin B12 deficiency · Disorder of vitamin and non-protein cofactor absorption and transport · Inborn vitamin metabolic disorder

Inborn disorder of cobalamin metabolism and transport

An inherited metabolic disease affecting cobalamin (vitamin B12) intestinal absorption, transport in the blood, uptake by peripheral cells or cellular metabolism.

1 trial tagged with this condition →

Methylmalonic aciduria and homocystinuria 1 trial · 3 incl. sub-types Sub-types →
Homocystinuria without methylmalonic aciduria 0 trials · 2 incl. sub-types Sub-types →
Methylmalonic aciduria and/or homocystinuria, cblD type 0 trials · 2 incl. sub-types Sub-types →
Vitamin B12-responsive methylmalonic acidemia 0 trials · 2 incl. sub-types Sub-types →
Hereditary intrinsic factor deficiency 1 trial Sub-types →
Transcobalamin II deficiency 1 trial
Imerslund-Grasbeck syndrome 0 trials Sub-types →
Methylmalonic acidemia due to transcobalamin receptor defect 0 trials
Transcobalamin I deficiency 0 trials