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"

156 matching diseasesClear search ×

Succinyl-CoA:3-oxoacid CoA transferase deficiency

OXCT1 deficiency · SCOT deficiency

ORPHA:832

Susceptibility to viral and mycobacterial infections due to STAT1 deficiency

STAT1 deficiency · Predisposition to severe viral infection due to STAT1 deficiency

ORPHA:391311

Syndrome with combined immunodeficiency

ORPHA:331217

Transcobalamin I deficiency

Haptocorrin deficiency · TCI deficiency

ORPHA:2967

Transketolase deficiency

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

ORPHA:488618

Transverse limb deficiency-hemangioma syndrome

ORPHA:2486

Tyrosinemia type 1

FAH deficiency · Fumarylacetoacetase deficiency

ORPHA:882

X-linked agammaglobulinemia

BTK-deficiency · Bruton type agammaglobulinemia

ORPHA:47

X-linked creatine transporter deficiency

Creatine transporter deficiency · SLC6A8 deficiency

ORPHA:52503

X-linked hyper-IgM syndrome

HIGM1 · Hyper-IgM syndrome due to CD40 ligand deficiency

ORPHA:101088

X-linked lymphoproliferative disease due to XIAP deficiency

X-linked lymphoproliferative syndrome type 2 · XLP2

ORPHA:538934

Xanthinuria type I

XDH deficiency · XO deficiency

ORPHA:93601