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"

14 matching diseasesClear search ×

Succinyl-CoA:3-oxoacid CoA transferase deficiency

OXCT1 deficiency · SCOT deficiency

ORPHA:832

ALG1-CDG

CDG syndrome type Ik · CDG-Ik

ORPHA:79327

ALG12-CDG

CDG syndrome type Ig · CDG-Ig

ORPHA:79324

ALG2-CDG

CDG syndrome type Ii · CDG-Ii

ORPHA:79326

ALG3-CDG

CDG syndrome type Id · CDG-Id

ORPHA:79321

ALG6-CDG

CDG syndrome type Ic · CDG-Ic

ORPHA:79320

ALG8-CDG

CDG syndrome type Ih · CDG-Ih

ORPHA:79325

Beta-ketothiolase deficiency

3-ketothiolase deficiency · 3-oxothiolase deficiency

ORPHA:134

Beta-mercaptolactate cysteine disulfiduria

Ampola syndrome · MCDU

ORPHA:1035

Carnitine palmitoyl transferase 1A deficiency

CPT1A deficiency · Carnitine palmitoyl transferase IA deficiency

ORPHA:156

Gamma-glutamyl transpeptidase deficiency

Glutathionuria · Gamma-glutamyl transferase deficiency

ORPHA:33573

Lipoyl transferase 1 deficiency

ORPHA:401862

Lipoyl transferase 2 deficiency

ORPHA:447795

Transketolase deficiency

TKT deficiency · Short stature-developmental delay-congenital heart defect syndrome

ORPHA:488618