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 ×

Generalized essential telangiectasia

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ORPHA:280774

Extramammary Paget disease

ORPHA:2800

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

IBMPFD · Limb-girdle muscular dystrophy with Paget disease of bone

ORPHA:52430

Juvenile Paget disease

Familial osteoectasia · Hereditary hyperphosphatasia

ORPHA:2801

Localized pagetoid reticulosis

Pagetoid reticulosis, Woringer-Kolopp type

ORPHA:178517

Paget disease of the nipple

Paget's disease of the nipple · Paget disease of the breast

ORPHA:180275

Pemphigus vegetans

ORPHA:79479

Spastic paraplegia-Paget disease of bone syndrome

ORPHA:329475

Vegetative pyoderma gangrenosum

Granulomatous pyoderma gangrenosum

ORPHA:538872