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"

20 matching diseasesClear search ×

OBSOLETE: Syndrome associated with Pierre Robin syndrome

OBSOLETE: Syndrome associated with Pierre Robin sequence

ORPHA:138063

Catel-Manzke syndrome

Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome · Index finger anomaly-Pierre Robin syndrome

ORPHA:1388

Isolated Pierre Robin sequence

PRS

ORPHA:718

OBSOLETE: ATR-X-related syndrome

ORPHA:263355

OBSOLETE: Dysmorphic syndrome associated with bone anomaly

ORPHA:93472

OBSOLETE: Ectodermal malformation syndrome associated with ocular features

ORPHA:98709

OBSOLETE: Pierre Robin syndrome associated with miscellaneous anomalies

OBSOLETE: Pierre Robin sequence associated with miscellaneous anomalies

ORPHA:138066

OBSOLETE: Sequence or association

ORPHA:139006

OBSOLETE: Sucking/swallowing disorder associated with an identified syndrome

ORPHA:138072

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 a congenital cardiopathy

ORPHA:98732

OBSOLETE: Syndromic ichthyosis associated with ocular features

ORPHA:98699

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

Pierre Robin syndrome associated with collagen disease

Pierre Robin sequence associated with collagen disease

ORPHA:138041

Pierre Robin syndrome-faciodigital anomaly syndrome

Chitayat-Meunier-Hodgkinson syndrome · Pierre Robin sequence-faciodigital anomaly syndrome

ORPHA:2888

Rare disease with Pierre Robin syndrome

ORPHA:138044

Robin sequence-oligodactyly syndrome

Pierre Robin sequence-oligodactyly syndrome

ORPHA:3104

Weissenbacher-Zweymuller syndrome

Pierre Robin sequence-fetal chondrodysplasia syndrome · Pierre Robin syndrome-fetal chondrodysplasia syndrome

ORPHA:3450