DiseaseID 3946
食管闭锁
disease
NCI2016_02D:A congenital abnormality of the esophagus in which the upper esophagus ends as a blind pouch and does not connect with the lower esophagus; it is often accompanied by a tracheoesophageal fistula. Signs and sy
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Disease: 1Symptom: 3Target: 12Links: 15
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3946
- Core Entity Id
- 60219
- Source Entity Count
- 2
- Preferred Name
- Esophageal Atresia
- Name Cn
- 食管闭锁
- Name Pinyin
- Shi Guan Bi Suo
- Name En
- Esophageal Atresia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the digestive system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
- Hpo Class Name
- Abnormality of the digestive system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:A congenital abnormality of the esophagus in which the upper esophagus ends as a blind pouch and does not connect with the lower esophagus; it is often accompanied by a tracheoesophageal fistula. Signs and symptoms in a newborn with this abnormality include excessive salivation, choking, coughing, and the development of cyanosis and respiratory distress when fed.|MSH2017_2016_08_12:Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA.|HPO2016_07_04:A developmental defect resulting in complete obliteration of the lumen of the esophagus such that the esophagus ends in a blind pouch rather than connecting to the stomach. [HPO:curators]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Esophageal Atresia
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002032
Herb
HBDIS000987
Me Sh
D004933
Umls
C0014850
Icd10
Q39.0
Sym Map
SMDE08493
Do Class
DOID:7
Dis Ge Net
C0014850
Umls Sty
T019
Hpo Class
HP:0025031
Me Sh Class
C06C16
Tcmbank Disease
2086028374
Itcmdb Generated
ITX-DISEASE-A2E683E42D64
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the digestive system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the digestive system
Umls Disease Type
Congenital Abnormality
Disease Definition
NCI2016_02D:A congenital abnormality of the esophagus in which the upper esophagus ends as a blind pouch and does not connect with the lower esophagus; it is often accompanied by a tracheoesophageal fistula. Signs and symptoms in a newborn with this abnormality include excessive salivation, choking, coughing, and the development of cyanosis and respiratory distress when fed.|MSH2017_2016_08_12:Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA.|HPO2016_07_04:A developmental defect resulting in complete obliteration of the lumen of the esophagus such that the esophagus ends in a blind pouch rather than connecting to the stomach. [HPO:curators]
Me Sh Disease Class
Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Umls Semantic Type Name
Congenital Abnormality