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"

16 matching diseasesClear search ×

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

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

ORPHA:138069

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: Rare sucking/swallowing disorder

ORPHA:138221

OBSOLETE: Sucking/swallowing disorder associated to a chromosomal anomaly

ORPHA:138076

OBSOLETE: Sucking/swallowing disorder associated with a neuromuscular disease

ORPHA:138115

OBSOLETE: Sucking/swallowing disorder associated with an identified syndrome

ORPHA:138072

OBSOLETE: Sucking/swallowing disorder associated with basal ganglia anomalies

ORPHA:138104

OBSOLETE: Sucking/swallowing disorder associated with cerebellar anomalies

ORPHA:138112

OBSOLETE: Sucking/swallowing disorder associated with neurologic anomalies

ORPHA:138095

OBSOLETE: Sucking/swallowing disorder associated with posterior fossa anomalies

ORPHA:138109

OBSOLETE: Sucking/swallowing disorder associated with suprabulbar anomalies

ORPHA:138101

OBSOLETE: Syndrome associated with Pierre Robin syndrome

OBSOLETE: Syndrome associated with Pierre Robin sequence

ORPHA:138063

OBSOLETE: Syndromic sucking/swallowing disorder with unidentifyed syndrome

ORPHA:138080

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