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 ×

Uniparental disomy of chromosome X syndrome

UPD(X)

ORPHA:263793

Maternal uniparental disomy of chromosome X syndrome

UPD(X)mat

ORPHA:261519

Paternal uniparental disomy of chromosome X syndrome

UPD(X)pat

ORPHA:261524