Tracheoesophageal fistula
Symptom Information:
Symptom ID: | HPO:0002575 | |||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |