DiseaseID 11606
特发性贲门失弛缓症
disease
SNOMEDCT_US_2016_09_01:Characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter relaxation in response to deglutition. A rare disease with no gender predilection, the peak incidence occ
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Disease: 1Symptom: 1Target: 4Links: 5
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 11606
- Core Entity Id
- 69010
- Source Entity Count
- 1
- Preferred Name
- Idiopathic Achalasia of Esophagus
- 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 of Esophagus
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Digestive System Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Digestive System Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- SNOMEDCT_US_2016_09_01:Characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter relaxation in response to deglutition. A rare disease with no gender predilection, the peak incidence occurs between 30 and 60 years of age. Although the precise etiology is unknown, it is often thought to be either autoimmune, viral immune, or neurodegenerative. Some familial cases have been reported, but the rarity of familial occurrence does not support the hypothesis that genetic inheritance is a significant etiologic factor.|SNOMEDCT_US_2016_09_01:Characterised by loss of oesophageal peristalsis and insufficient lower oesophageal sphincter relaxation in response to deglutition. A rare disease with no gender predilection, the peak incidence occurs between 30 and 60 years of age. Although the precise aetiology is unknown, it is often thought to be either autoimmune, viral immune, or neurodegenerative. Some familial cases have been reported, but the rarity of familial occurrence does not support the hypothesis that genetic inheritance is a significant aetiologic factor.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Idiopathic Achalasia of Esophagus
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS012149
Sym Map
SMDE09756
Dis Ge Net
C0859976
Umls Sty
T047
Me Sh Class
C06
Tcmbank Disease
8671
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
SNOMEDCT_US_2016_09_01:Characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter relaxation in response to deglutition. A rare disease with no gender predilection, the peak incidence occurs between 30 and 60 years of age. Although the precise etiology is unknown, it is often thought to be either autoimmune, viral immune, or neurodegenerative. Some familial cases have been reported, but the rarity of familial occurrence does not support the hypothesis that genetic inheritance is a significant etiologic factor.|SNOMEDCT_US_2016_09_01:Characterised by loss of oesophageal peristalsis and insufficient lower oesophageal sphincter relaxation in response to deglutition. A rare disease with no gender predilection, the peak incidence occurs between 30 and 60 years of age. Although the precise aetiology is unknown, it is often thought to be either autoimmune, viral immune, or neurodegenerative. Some familial cases have been reported, but the rarity of familial occurrence does not support the hypothesis that genetic inheritance is a significant aetiologic factor.
Me Sh Disease Class
Digestive System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Digestive System Diseases
Umls Semantic Type Name
Disease or Syndrome