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 ×

Isolated femoral agenesis/hypoplasia

Isolated congenital femoral deficiency · Isolated congenital short femur

ORPHA:1987

Autosomal recessive severe congenital neutropenia due to CSF3R deficiency

ORPHA:420702

Multiple benign circumferential skin creases on limbs

CCSF · Congenital circumferential skin folds

ORPHA:2505