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 ×

Huntington disease-like 3

HDL3

ORPHA:157946

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

ALSP · Autosomal dominant leukoencephalopathy with neuroaxonal spheroids

ORPHA:313808

Huntington disease-like 1

Early-onset prion disease with prominent psychiatric features · HDL1

ORPHA:157941

Huntington disease-like 2

HDL2

ORPHA:98934