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 ×

Kindler epidermolysis bullosa

Kindler syndrome · Poikiloderma of Kindler

ORPHA:2908

OBSOLETE: Hereditary acrokeratotic poikiloderma of Kindler-Weary

ORPHA:306539

Hereditary poikiloderma

ORPHA:222628

Rothmund-Thomson syndrome

Poikiloderma of Rothmund-Thomson · RTS

ORPHA:2909