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 ×

Idiopathic eosinophilic myositis

Idiopathic eosinophilia-associated myopathy

ORPHA:247724

Idiopathic acute eosinophilic pneumonia

IAEP

ORPHA:724

Idiopathic chronic eosinophilic pneumonia

Chronic eosinophilic pneumonia

ORPHA:2902

Idiopathic copper-associated cirrhosis

Non-Wilsonian hepatic copper toxicosis of infancy and childhood

ORPHA:209919

Idiopathic eosinophilic pneumonia

ORPHA:182101

Idiopathic pregnancy-associated osteoporosis

PAO · Pregnancy and lactation-associated osteoporosis

ORPHA:647823

Muscle filaminopathy

FLNC-associated myofibrillar myopathy · Filamin C-related filaminopathy

ORPHA:171445

Myalgia-eosinophilia syndrome associated with tryptophan

ORPHA:2582