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"

9 matching diseasesClear search ×

PAPA syndrome

FRA · Familial recurrent arthritis

ORPHA:69126

Bullous pyoderma gangrenosum

Phemphigoid pyoderma gangrenosum

ORPHA:538869

Classic pyoderma gangrenosum

Ulcerative pyoderma gangrenosum

ORPHA:538863

PAPASH syndrome

Pyogenic arthritis-pyoderma gangrenosum-acne-hidradenitis suppurativa syndrome

ORPHA:641380

PASH syndrome

Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome

ORPHA:289478

PASS syndrome

Pyoderma gangrenosum-acne-hidradenitis suppurativa-ankylosing spondylitis syndrome

ORPHA:641385

PsAPASH syndrome

Psoriatic arthritis-pyoderma gangrenosum-acne-hidradenitis suppurativa syndrome

ORPHA:641390

Pustular pyoderma gangrenosum

ORPHA:538866

Pyoderma gangrenosum

ORPHA:48104