Tracheoesophageal fistula

Symptom Information:

Symptom ID: HPO:0002575
Synonyms:
Tracheoesophageal Fistula [Orphanet:26140]
Tracheoesophageal fistula (disorder) [Orphanet:26140]
Tracheoesophageal fistula [OMIM:Tracheoesophageal fistula]
Tracheo-esophageal fistula/esophageal atresia/stenosis [Orphanet:26140]
Tracheo-oesophageal fistula [HPO:0002575]
Tracheo-oesophageal fistula [Orphanet:26140]
Tracheo-oesophageal fistula [MedDRA:10044310]
Congenital tracheo-oesophageal fistula [MedDRA:10044310]
Trached-esophageal fistula [MedDRA:10044310]
Tracheo-oesophageal fistula NOS [MedDRA:10044310]
Tracheoesophageal fistula [MedDRA:10044310]
Congenital tracheo-esophageal fistula [MedDRA:10044310]
Tracheo-esophageal fistula [MedDRA:10044310]
Quality:
Cross references:
Orphanet:26140 "Tracheo-esophageal fistula/esophageal atresia/stenosis" [Orphanet:26140]
OMIM: "Tracheoesophageal fistula" [OMIM:Tracheoesophageal fistula]
UMLS:C0040588 "Tracheoesophageal Fistula" [Orphanet:26140]
Is a (Direct Parents):
HPO         Abnormality of the trachea
Orphanet Esophageal atresia
MedDRA Tracheal disorders (excl infections and neoplasms)
HPO         Abnormality of the esophagus
Orphanet Esophageal anomaly
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of the upper respiratory tract(HPO:0002087)
                Abnormality of the tracheobronchial system(HPO:0005607)
                   Abnormality of the trachea(HPO:0002778)
                      Tracheoesophageal fistula(HPO:0002575)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of the esophagus(HPO:0002031)
                   Tracheoesophageal fistula(HPO:0002575)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Upper respiratory tract disorders (excl infections)(MedDRA:10046304)
       Tracheal disorders (excl infections and neoplasms)(MedDRA:10044288)
          Tracheoesophageal fistula(HPO:0002575)
Database Frequency: 54 / 7739
Resource:

All diseases associated with this symptom:

17q12 microduplication syndrome (Orphanet:261272)
46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
Acro-renal-mandibular syndrome (Orphanet:958)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Bilateral renal agenesis (Orphanet:1848)
CHARGE syndrome (Orphanet:138)
Chronic granulomatous disease (Orphanet:379)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital hypothyroidism (Orphanet:442)
Diabetic embryopathy (Orphanet:1926)
Dyskeratosis congenita (Orphanet:1775)
Dysmorphism - multiple structural anomalies (Orphanet:1780)
Dystrophic epidermolysis bullosa (Orphanet:303)
Esophageal atresia (Orphanet:1199)
FANCONI ANEMIA, COMPLEMENTATION GROUP B (OMIM:300514)
FANCONI ANEMIA, COMPLEMENTATION GROUP L (OMIM:614083)
FEINGOLD SYNDROME 1 (OMIM:164280)
Fanconi anemia (Orphanet:84)
Feingold syndrome (Orphanet:1305)
Generalized dominant dystrophic epidermolysis bullosa (Orphanet:231568)
Goldenhar syndrome (Orphanet:374)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome (Orphanet:293864)
Infantile myofibromatosis (Orphanet:2591)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Kindler syndrome (Orphanet:2908)
LOC syndrome (Orphanet:2407)
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia (Orphanet:2005)
Lyell syndrome (Orphanet:537)
Methimazole embryofetopathy (Orphanet:1923)
Microgastria - limb reduction defect (Orphanet:2538)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Odontomatosis - aortae esophagus stenosis (Orphanet:2724)
Opitz G/BBB syndrome (Orphanet:2745)
Pallister-Hall syndrome (Orphanet:672)
Pericardial and diaphragmatic defect (Orphanet:2847)
Phocomelia, Schinzel type (Orphanet:2879)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Schisis association (Orphanet:63862)
Scleroderma (Orphanet:801)
Septo-optic dysplasia (Orphanet:3157)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Sirenomelia (Orphanet:3169)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Tracheo-esophageal fistula - hypospadias (Orphanet:2042)
Treacher-Collins syndrome (Orphanet:861)
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS (OMIM:314390)
VACTERL with hydrocephalus (Orphanet:3412)
VACTERL/VATER association (Orphanet:887)
Williams syndrome (Orphanet:904)