achalasia, familial esophageal

Preferred Label : achalasia, familial esophageal;

MeSH synonym : familial esophageal achalasia;

Origin ID

C536011;

UMLS CUI

C1860213;

Currated CISMeF NLP mapping
- Achalasia, familial esophageal [OMIM Phenotype]
- Familial esophageal achalasia [ORDO Disease]
- Idiopathic achalasia [ORDO Disease]
MeSH term(s) associated for indexing
- esophageal achalasia [MeSH Descriptor]
ORDO relation(s)
- Familial esophageal achalasia [ORDO Disease]
- Idiopathic achalasia [ORDO Disease]
Record concept(s)
- Achalasia, familial esophageal [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Achalasia, familial esophageal [OMIM Phenotype]
- Familial esophageal achalasia [ORDO Disease]