DiseaseID 26654
特发性贲门失弛缓症
Idiopathic Achalasia
Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition
Relationship Network
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Disease: 1Target: 12Links: 12
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26654
- Core Entity Id
- 119222
- Source Entity Count
- 1
- Preferred Name
- Idiopathic Achalasia
- Name Cn
- 特发性贲门失弛缓症
- Name Pinyin
- Te Fa Xing Ben Men Shi Chi Huan Zheng
- Name En
- Idiopathic Achalasia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Idiopathic Achalasia
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Omim
200400
Umls
C0014848C0859976
Med Dra
10036669
Sym Map
SMDE04522
Orphanet
930
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition