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"

7 matching diseasesClear search ×

Pierre Robin syndrome associated with branchial archs anomalies

Pierre Robin sequence associated with branchial archs anomalies

ORPHA:138050

Isolated Pierre Robin sequence

PRS

ORPHA:718

OBSOLETE: Pierre Robin syndrome associated with miscellaneous anomalies

OBSOLETE: Pierre Robin sequence associated with miscellaneous anomalies

ORPHA:138066

OBSOLETE: Syndrome associated with Pierre Robin syndrome

OBSOLETE: Syndrome associated with Pierre Robin sequence

ORPHA:138063

Pierre Robin syndrome associated with a chromosomal anomaly

Pierre Robin sequence associated with a chromosomal anomaly

ORPHA:138047

Pierre Robin syndrome associated with bone disease

Pierre Robin sequence associated with bone disease

ORPHA:138055

Pierre Robin syndrome associated with collagen disease

Pierre Robin sequence associated with collagen disease

ORPHA:138041