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"

4 matching diseasesClear search ×

Aicardi-Goutières syndrome

Encephalopathy with basal ganglia calcification · Encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid

ORPHA:51

Bilateral striopallidodentate calcinosis

BSPDC · Cerebrovascular ferrocalcinosis

ORPHA:1980

Leukoencephalopathy with calcifications and cysts

Labrune syndrome · LCC

ORPHA:542310

Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome

Severe neurodegenerative syndrome due to BSCL2 deficiency · Celia encephalopathy

ORPHA:363400