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"

3 matching diseasesClear search ×

Autosomal recessive carpotarsal osteolysis

Hereditary multicentric osteolysis

ORPHA:2775

Multicentric carpo-tarsal osteolysis with or without nephropathy

Idiopathic multicentric osteolysis with or without nephropathy

ORPHA:2774

Multicentric osteolysis-nodulosis-arthropathy spectrum

MONA spectrum

ORPHA:371428