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"

3 matching diseasesClear search ×

Familial clubfoot due to 5q31 microdeletion

Hereditary clubfoot due to 5q31 microdeletion

ORPHA:293144

Familial clubfoot due to 17q23.1q23.2 microduplication

Hereditary clubfoot due to 17q23.1-q23.2 microduplication

ORPHA:238578

Familial clubfoot due to PITX1 point mutation

Hereditary clubfoot due to PITX1 point mutation

ORPHA:293150