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"

8 matching diseasesClear search ×

Sex-chromosome anomaly syndrome

Allosome anomaly

ORPHA:98155

Autosomal anomaly syndrome

ORPHA:98127

Hair anomaly

ORPHA:79363

Nail anomaly

ORPHA:79368

OBSOLETE: X chromosome anomaly

ORPHA:263711

Sex-chromosome number anomaly syndrome

Allosome number anomaly

ORPHA:98156

Sex-chromosome structural anomaly syndrome

Allosome structural anomaly

ORPHA:98157

Uhl anomaly

ORPHA:3403