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"

11 matching diseasesClear search ×

Isolated tracheoesophageal fistula

H-type tracheoesophageal fistula

ORPHA:454750

Esophageal atresia

CEA · Congenital esophageal atresia

ORPHA:1199

Feingold syndrome type 1

Brunner-Winter syndrome type 1 · Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1

ORPHA:391641

Feingold syndrome type 2

Brachydactyly-short stature-microcephaly syndrome · Brunner-Winter syndrome type 2

ORPHA:391646

Laryngotracheoesophageal cleft type 0

Laryngo-tracheo-esophageal cleft type 0 · LTEC0

ORPHA:280205

Laryngotracheoesophageal cleft type 1

Laryngo-tracheo-esophageal cleft type 1 · LTEC I

ORPHA:93938

Laryngotracheoesophageal cleft type 2

Laryngo-tracheo-esophageal cleft type 2 · LTEC II

ORPHA:93939

Laryngotracheoesophageal cleft type 3

Laryngo-tracheo-esophageal cleft type 3 · LTEC III

ORPHA:93940

Laryngotracheoesophageal cleft type 4

Laryngo-tracheo-esophageal cleft type 4 · LTEC IV

ORPHA:93941

OBSOLETE: Blaichman syndrome

OBSOLETE: Tracheo-esophageal fistula-symphalangism syndrome

ORPHA:1250

OBSOLETE: Tracheo-esophageal fistula-hypospadias syndrome

ORPHA:2042