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"

8 matching diseasesClear search ×

Peeling skin syndrome type A

Generalized peeling skin syndrome type A · Non-inflammatory generalized peeling skin syndrome type A.

ORPHA:263548

Acral peeling skin syndrome

Acral PSS · Peeling skin syndrome 2

ORPHA:263534

Generalized epilepsy-paroxysmal dyskinesia syndrome

GEPD

ORPHA:79137

Generalized peeling skin syndrome

Generalized PSS · Generalized deciduous skin

ORPHA:263543

OBSOLETE: Peeling skin syndrome type C

OBSOLETE: Generalized deciduous skin type C · OBSOLETE: Generalized peeling skin syndrome type C

ORPHA:263558

Parana hard skin syndrome

Hard skin syndrome, Parana type

ORPHA:2812

Peeling skin syndrome

Deciduous skin · Familial continuous skin peeling syndrome

ORPHA:817

Peeling skin syndrome type B

Generalized peeling skin syndrome type B · Inflammatory peeling skin syndrome

ORPHA:263553