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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"
Familial keratoacanthoma
Hereditary keratoacanthoma · Multiple keratoacanthoma
Muir-Torre syndrome
Multiple keratoacanthoma, Muir-Torre type
Multiple self-healing squamous epithelioma
Familial primary self-healing squamous epithelioma of the skin, Ferguson-Smith type · Ferguson-Smith disease
Generalized eruptive keratoacanthoma
GEKA · Generalized eruptive keratoacanthomas of Grzybowski
Multiple myeloma
Kahler disease · Medullary plasmacytoma