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"

5 matching diseasesClear search ×

Sex-chromosome number anomaly syndrome

Allosome number anomaly

ORPHA:98156

Sex-chromosome anomaly syndrome

Allosome anomaly

ORPHA:98155

Sex-chromosome structural anomaly syndrome

Allosome structural anomaly

ORPHA:98157

X chromosome number anomaly syndrome

ORPHA:263714

Y chromosome number anomaly syndrome

ORPHA:263746