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"

6 matching diseasesClear search ×

Familial visceral myopathy

Familial hollow visceral myopathy · Hereditary hollow visceral myopathy

ORPHA:2604

GNE myopathy

DMRV · Distal myopathy with rimmed vacuoles

ORPHA:602

Hereditary cerebral amyloid angiopathy

HCHWA · Hereditary cerebral hemorrhage with amyloidosis

ORPHA:85458

Hereditary inclusion body myopathy type 4

HIBM4

ORPHA:324381

Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome

HIBM3 · Hereditary inclusion body myopathy type 3

ORPHA:79091

Neuroferritinopathy

Adult basal ganglia disease · Ferritin-related neurodegeneration

ORPHA:157846