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"

12 matching diseasesClear search ×

Pierre Robin syndrome associated with collagen disease

Pierre Robin sequence associated with collagen disease

ORPHA:138041

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: Sucking/swallowing disorder not related with Pierre Robin syndrome

OBSOLETE: Sucking/swallowing disorder not related with Pierre Robin sequence

ORPHA:138069

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 branchial archs anomalies

Pierre Robin sequence associated with branchial archs anomalies

ORPHA:138050

Pulmonary arterial hypertension associated with another disease

PAH · PAH associated with another disease

ORPHA:275791

Pulmonary arterial hypertension associated with congenital heart disease

PAH · PAH associated with congenital heart disease

ORPHA:275803

Pulmonary arterial hypertension associated with connective tissue disease

PAH · PAH associated with connective tissue disease

ORPHA:275798

Rare disease with Pierre Robin syndrome

ORPHA:138044