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 ×

Progressive symmetric erythrokeratodermia

Darier-Gottron disease · Erythrokeratodermia progressiva symmetrica

ORPHA:316

Erythrokeratoderma

ORPHA:79355

Erythrokeratoderma variabilis progressiva

ORPHA:308166

Erythrokeratodermia variabilis

EKV · Erythrokeratodermia variabilis, Mendes da Costa type

ORPHA:317

Spinocerebellar ataxia type 34

Erythrokeratodermia with ataxia · SCA34

ORPHA:1955