PedAM

Pediatric Disease Annotations & Medicines


	tracheoesophageal fistula

Disease ID	1148
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:17) C0014850 \| esophageal atresia \| 80 C0014850 \| oesophageal atresia \| 8 C0040583 \| tracheal stenosis \| 3 C0007137 \| squamous cell carcinoma \| 1 C0242379 \| lung cancer \| 1 C0019284 \| diaphragmatic hernia \| 1 C0041296 \| tuberculosis \| 1 C0019829 \| hodgkin lymphoma \| 1 C0003125 \| anorexia nervosa \| 1 C0017168 \| gastroesophageal reflux \| 1 C0024299 \| lymphoma \| 1 C0175703 \| tar syndrome \| 1 C0017168 \| esophageal reflux \| 1 C0003466 \| anal atresia \| 1 C0011633 \| dermatomyositis \| 1 C0017168 \| oesophageal reflux \| 1 C0149925 \| small cell lung cancer \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) PCSK5 \| 5125 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1148
Disease	tracheoesophageal fistula
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:25) HP:0002032 \| Esophageal atresia \| 80 HP:0002777 \| Tracheal stenosis \| 3 HP:0002020 \| Heartburn \| 2 HP:0010450 \| Narrowing of the esophagus \| 2 HP:0002023 \| Anal atresia \| 1 HP:0000453 \| Blockage of the rear opening of the nasal cavity \| 1 HP:0000776 \| Diaphragmatic hernia \| 1 HP:0004894 \| Laryngotracheal stenosis \| 1 HP:0008751 \| Laryngotracheal cleft \| 1 HP:0004791 \| Esophagus ulcer \| 1 HP:0000078 \| Genital abnormalities \| 1 HP:0002664 \| Neoplasia \| 1 HP:0012020 \| Right aortic arch \| 1 HP:0012189 \| Hodgkin disease \| 1 HP:0030707 \| Unilateral pulmonary agenesis \| 1 HP:0002039 \| Anorexia \| 1 HP:0002786 \| Tracheobronchomalacia \| 1 HP:0100790 \| Hernia \| 1 HP:0000077 \| Renal anomaly \| 1 HP:0002665 \| Lymphoma \| 1 HP:0030731 \| Carcinoma \| 1 HP:0030357 \| Small cell lung carcinoma \| 1 HP:0011626 \| Scimitar anomaly \| 1 HP:0002860 \| Squamous cell carcinoma \| 1 HP:0025025 \| Vestibular fistula \| 1

Disease ID	1148
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 \| 80

Manually Genotype(Total Text Mining 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.)

Chemical(Total Drugs:0)
(Waiting for update.)

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

Web
Analytics