Achalasia

Symptom Information:

Symptom ID: HPO:0002571
Synonyms:
Achalasia of esophagus (disorder) [Orphanet:26200]
Achalasia (finding) [Orphanet:26200]
Achalasia [Orphanet:26200]
Esophageal Achalasia [Orphanet:26200]
Achalasia [OMIM:Achalasia]
Megaesophagus/cardiospasm/congenital dilation of the esophagus/achalasia [Orphanet:26200]
Oesophageal achalasia [HPO:0002571]
Oesophageal achalasia [Orphanet:26200]
Cardiospasm [Orphanet:26200]
Oesophageal achalasia [MedDRA:10030136]
Achalasia [MedDRA:10030136]
Achalasia cardiae [MedDRA:10030136]
Achalasia esophageal [MedDRA:10030136]
Oesophagus achalasia of [MedDRA:10030136]
Primary achalasia [MedDRA:10030136]
Megaesophagus [MedDRA:10030136]
Esophageal achalasia [MedDRA:10030136]
Esophagus achalasia of [MedDRA:10030136]
Achalasia oesophageal [MedDRA:10030136]
Megaoesophagus [MedDRA:10030136]
Cardiospasm [MedDRA:10007645]
Achalasia and cardiospasm [MedDRA:10007645]
Esophageal achalasia [OMIM:Esophageal achalasia]
Megaoesophagus [MedDRA:10056100]
Megaesophagus [Orphanet:26200]
Megaesophagus (disorder) [Orphanet:26200]
Quality:
Cross references:
Orphanet:26200 "Megaesophagus/cardiospasm/congenital dilation of the esophagus/achalasia" [Orphanet:26200]
OMIM: "Achalasia" [OMIM:Achalasia]
OMIM: "Esophageal achalasia" [OMIM:Esophageal achalasia]
UMLS:C0014848 "Achalasia" [HPO:0002571]
UMLS:C1321756 "Achalasia" [Orphanet:26200]
UMLS:C0014848 "Esophageal Achalasia" [Orphanet:26200]
UMLS:C0025164 "Megaesophagus" [Orphanet:26200]
Is a (Direct Parents):
HPO         Abnormality of the esophagus
MedDRA Gastrointestinal spastic and hypermotility disorders
Orphanet Esophageal anomaly
MedDRA Gastrointestinal dyskinetic disorders
HPO         Gastrointestinal dysmotility
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of the esophagus(HPO:0002031)
                   Achalasia(HPO:0002571)
                Gastrointestinal dysmotility(HPO:0002579)
                   Achalasia(HPO:0002571)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal motility and defaecation conditions(MedDRA:10017977)
       Gastrointestinal dyskinetic disorders(MedDRA:10017950)
          Achalasia(HPO:0002571)
       Gastrointestinal spastic and hypermotility disorders(MedDRA:10018006)
          Achalasia(HPO:0002571)
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME (OMIM:231550)
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
Achalasia - microcephaly (Orphanet:929)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Deafness - vitiligo - achalasia (Orphanet:3239)
Developmental malformations - deafness - dystonia (Orphanet:79107)
Dihydropteridine reductase deficiency (Orphanet:226)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Dyskeratosis congenita (Orphanet:1775)
Familial esophageal achalasia (Orphanet:99723)
Familial leiomyomatosis (Orphanet:523)
Galloway-Mowat syndrome (Orphanet:2065)
Idiopathic achalasia (Orphanet:930)
Intellectual deficit - alacrima - achalasia (Orphanet:289483)
MOYAMOYA DISEASE 6 WITH ACHALASIA (OMIM:615750)
Peripheral motor neuropathy - dysautonomia (Orphanet:2400)
Posterior column ataxia - retinitis pigmentosa (Orphanet:88628)
Tetrasomy 18p (Orphanet:3307)
Triple A syndrome (Orphanet:869)