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"

20 matching diseasesClear search ×

Classic maple syrup urine disease

Classic BCKD deficiency · Classic MSUD

ORPHA:268145

2-methylbutyryl-CoA dehydrogenase deficiency

2-methylbutyric aciduria · Developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency

ORPHA:79157

Acyl-CoA dehydrogenase 9 deficiency

ACAD9 deficiency

ORPHA:99901

Acyl-CoA dehydrogenase deficiency

ORPHA:309120

Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency

ORPHA:308410

Class I glucose-6-phosphate dehydrogenase deficiency

Class I G6PD deficiency · Severe hemolytic anemia due to G6PD deficiency

ORPHA:466026

Dimethylglycine dehydrogenase deficiency

DMG dehydrogenase deficiency · DMGDH deficiency

ORPHA:243343

Intermediate maple syrup urine disease

Intermediate BCKD deficiency · Intermediate MSUD

ORPHA:268162

Intermittent maple syrup urine disease

Intermittent BCKD deficiency · Intermittent MSUD

ORPHA:268173

Isovaleric acidemia

Isovaleric acid CoA dehydrogenase deficiency

ORPHA:33

Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency

LCHAD deficiency · LCHADD

ORPHA:5

Long chain acyl-CoA dehydrogenase deficiency

LCAD

ORPHA:99900

Maple syrup urine disease

BCKD deficiency · BCKDH deficiency

ORPHA:511

Medium chain acyl-CoA dehydrogenase deficiency

ACADM deficiency · Carnitine deficiency secondary to medium-chain acyl-CoA dehydrogenase deficiency

ORPHA:42

Oxoglutaric aciduria

Alpha-ketoglutarate dehydrogenase deficiency

ORPHA:31

Pyruvate dehydrogenase E1-alpha deficiency

PDHAD · Pyruvate decarboxylase deficiency

ORPHA:79243

Pyruvate dehydrogenase E3-binding protein deficiency

2-oxoglutarate complex deficiency · Branched chain alpha-ketoacid dehydrogenase complex deficiency

ORPHA:255182

Short chain acyl-CoA dehydrogenase deficiency

ACADS deficiency · SCAD deficiency

ORPHA:26792

Thiamine-responsive maple syrup urine disease

Thiamine-responsive BCKD deficiency · Thiamine-responsive MSUD

ORPHA:268184

Very long chain acyl-CoA dehydrogenase deficiency

VLCAD deficiency · VLCADD

ORPHA:26793