Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

16 matching diseasesClear search ×

Methylmalonic acidemia with homocystinuria

Combined defect in adenosylcobalamin and methylcobalamin synthesis · Methylmalonic aciduria with homocystinuria

ORPHA:26

Methylmalonic acidemia with homocystinuria type cblF

CblF defect · Cobalamin F defect

ORPHA:79284

Methylmalonic acidemia with homocystinuria, type cblC

CblC defect · Cobalamin C defect

ORPHA:79282

Methylmalonic acidemia with homocystinuria, type cblD

CblD defect · Cobalamin D defect

ORPHA:79283

Methylmalonic acidemia with homocystinuria, type cblJ

CblJ defects · Cobalamin J defect

ORPHA:369955

Methylmalonic acidemia with homocystinuria, type cblX

Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX · Methylmalonic aciduria with homocystinuria, type cblX

ORPHA:369962

3-methylglutaconic aciduria

ORPHA:289902

Combined malonic and methylmalonic acidemia

CMAMMA · Combined malonic and methylmalonic aciduria

ORPHA:289504

Fatal infantile lactic acidosis with methylmalonic aciduria

ORPHA:17

Homocystinuria without methylmalonic aciduria

Functional methionine synthase deficiency · Methylcobalamin deficiency

ORPHA:622

Malonic aciduria

Malonyl-CoA decarboxylase deficiency · Malonic acidemia

ORPHA:943

Methylmalonic acidemia without homocystinuria

Methylmalonic aciduria without homocystinuria

ORPHA:293355

Methylmalonic aciduria due to transcobalamin receptor defect

Methylmalonic acidemia, TCb1R type · Methylmalonic acidemia, TCbIR type

ORPHA:280183

Mevalonic aciduria

Complete mevalonate kinase deficiency · MVA

ORPHA:29

Vitamin B12-responsive methylmalonic acidemia

Adenosylcobalamin deficiency · Vitamin B12-responsive methylmalonic aciduria

ORPHA:28

Vitamin B12-unresponsive methylmalonic acidemia

Methylmalonyl-Coenzyme A mutase deficiency · Vitamin B12-unresponsive methylmalonic aciduria

ORPHA:27