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encyclopedia of Rare Disease Annotation for Precision Medicine

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	tracheoesophageal fistula

Disease ID	1828
Disease	tracheoesophageal fistula
Definition	Abnormal passage between the ESOPHAGUS and the TRACHEA, acquired or congenital, often associated with ESOPHAGEAL ATRESIA.
Synonym	esophagotracheal fistula esophagotracheal fistulas fistula tracheo-esophageal fistula tracheoesophageal fistula, esophagotracheal fistula, tracheo-esophageal fistula, tracheoesophageal fistulas tracheoesophageal fistulas, esophagotracheal fistulas, tracheoesophageal oesophago-tracheal fistula oesophagotracheal fistula tof - tracheo-oesophageal fistula tof - tracheoesophageal fistula trached-esophageal fistula tracheesophageal fistula tracheo-esophageal fistula tracheo-oesophageal fistula tracheo-oesophageal fistula (disorder) tracheoesophageal fistula (disorder) tracheoesophageal fistula [disease/finding] tracheoesophageal fistula, nos tracheoesophageal fistulas tracheoesophageal fstula
UMLS	C0040588
MeSH	D014138
SNOMED-CT	SNOMEDCT_US_2016_09_01:95435007
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:25) C0014850 \| esophageal atresia \| 101 C0014850 \| oesophageal atresia \| 14 C0040583 \| tracheal stenosis \| 4 C0014859 \| esophageal cancer \| 2 C0700639 \| hypertrophic pyloric stenosis \| 1 C0024299 \| lymphoma \| 1 C0032290 \| aspiration pneumonia \| 1 C0035229 \| respiratory insufficiency \| 1 C0019284 \| diaphragmatic hernia \| 1 C0017168 \| oesophageal reflux \| 1 C0242379 \| lung cancer \| 1 C0034194 \| pyloric stenosis \| 1 C0007137 \| squamous cell carcinoma \| 1 C0003466 \| anal atresia \| 1 C0032285 \| pneumonia \| 1 C0149925 \| small cell lung cancer \| 1 C0003125 \| anorexia nervosa \| 1 C0175703 \| tar syndrome \| 1 C0014858 \| esophageal dysmotility \| 1 C0546837 \| oesophageal cancer \| 1 C0036202 \| sarcoidosis \| 1 C0011633 \| dermatomyositis \| 1 C0019829 \| hodgkin lymphoma \| 1 C0017168 \| esophageal reflux \| 1 C0017168 \| gastroesophageal reflux \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 5125 \| PCSK5 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1828
Disease	tracheoesophageal fistula
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:35) HP:0002032 \| Esophageal atresia \| 105 HP:0002777 \| Tracheal stenosis \| 4 HP:0000077 \| Renal anomaly \| 2 HP:0002020 \| Heartburn \| 2 HP:0010450 \| Narrowing of the esophagus \| 2 HP:0004791 \| Esophagus ulcer \| 1 HP:0001518 \| Small for gestational age \| 1 HP:0000110 \| Renal dysplasia \| 1 HP:0011626 \| Scimitar anomaly \| 1 HP:0002021 \| Pyloric stenosis \| 1 HP:0002039 \| Anorexia \| 1 HP:0100790 \| Hernia \| 1 HP:0030731 \| Carcinoma \| 1 HP:0002786 \| Tracheobronchomalacia \| 1 HP:0008751 \| Laryngotracheal cleft \| 1 HP:0100682 \| Tracheal atresia \| 1 HP:0002023 \| Anal atresia \| 1 HP:0000453 \| Blockage of the rear opening of the nasal cavity \| 1 HP:0002835 \| Aspiration \| 1 HP:0002664 \| Neoplasia \| 1 HP:0004961 \| Pulmonary artery sling \| 1 HP:0012189 \| Hodgkin disease \| 1 HP:0000776 \| Diaphragmatic hernia \| 1 HP:0030707 \| Unilateral pulmonary agenesis \| 1 HP:0002860 \| Squamous cell carcinoma \| 1 HP:0010310 \| Chylothorax \| 1 HP:0030357 \| Small cell lung carcinoma \| 1 HP:0000078 \| Genital abnormalities \| 1 HP:0004894 \| Laryngotracheal stenosis \| 1 HP:0002665 \| Lymphoma \| 1 HP:0025025 \| Vestibular fistula \| 1 HP:0100594 \| Esophageal web \| 1 HP:0003198 \| Myopathic changes \| 1 HP:0012020 \| Right aortic arch \| 1 HP:0002015 \| Swallowing difficulty \| 1

Disease ID	1828
Disease	tracheoesophageal fistula
Manually Symptom	UMLS \| Name(Total Manually Symptoms:2) C0014850 \| esophageal atresia C0001168 \| obturation
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0014850 \| esophageal atresia \| 78

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	1828
Disease	tracheoesophageal fistula
Case	(Waiting for update.)

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