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"

156 matching diseasesClear search ×

Paternal uniparental disomy of chromosome 5 syndrome

UPD(5)pat

ORPHA:96190

Paternal uniparental disomy of chromosome 6 syndrome

UPD(6)pat

ORPHA:96191

Paternal uniparental disomy of chromosome 7 syndrome

UPD(7)pat

ORPHA:96192

Paternal uniparental disomy of chromosome X syndrome

UPD(X)pat

ORPHA:261524

Polysomy of X chromosome syndrome

ORPHA:263723

Ring chromosome 1 syndrome

Ring chromosome 1 · Ring 1

ORPHA:1437

Trisomy 18p syndrome

Duplication 18p · Duplication of the short arm of chromosome 18

ORPHA:1715

Trisomy 20p syndrome

Dup(20p) · Duplication of 20p

ORPHA:261318

Trisomy 4p syndrome

Trisomy of the short arm of chromosome 4 · Duplication 4p

ORPHA:1738

Trisomy 5p syndrome

Duplication 5p · Duplication of the short arm of chromosome 5

ORPHA:1742

Trisomy 9p syndrome

Duplication 9p · Duplication of the short arm of chromosome 9

ORPHA:236

Uniparental disomy of chromosome X syndrome

UPD(X)

ORPHA:263793