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"

4 matching diseasesClear search ×

Camptodactyly-fibrous tissue hyperplasia-skeletal anomalies syndrome

Goodman camptodactyly

ORPHA:1321

Camptobrachydactyly

ORPHA:1319

Camptodactyly of fingers

ORPHA:295016

Camptodactyly-joint contractures-facial skeletal defects syndrome

Rozin camptodactyly syndrome

ORPHA:1323