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 ×

Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome

Stevens-Johnson/toxic epidermal necrolysis overlap syndrome · SJS/TEN overlap syndrome

ORPHA:506784

Johnson neuroectodermal syndrome

Alopecia-anosmia-deafness-hypogonadism syndrome · Johnson-McMillin syndrome

ORPHA:2316

Stevens-Johnson syndrome

Dermatostomatitis, Stevens Johnson type

ORPHA:36426

Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum

SJS-TEN · Epidermal necrolysis

ORPHA:95455

Toxic epidermal necrolysis

Lyell syndrome

ORPHA:537