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"

5 matching diseasesClear search ×

Primary condylar hyperplasia

Type 1 condylar hyperplasia

ORPHA:477781

Congenital adrenal hyperplasia

CAH

ORPHA:418

Cono-spondylar dysplasia

Short stature-kyphosis-hypoplasia of basal ilia-cone epiphyses-facial dysmorphism syndrome

ORPHA:420794

Hyperprolinemia type 1

Proline oxidase deficiency

ORPHA:419

Pontocerebellar hypoplasia type 1

Norman disease · PCH1

ORPHA:2254