Achalasia
Symptom Information:
Symptom ID: | HPO:0002571 | ||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 spastic and hypermotility disorders(MedDRA:10018006) Achalasia(HPO:0002571) Gastrointestinal dyskinetic disorders(MedDRA:10017950) Achalasia(HPO:0002571) |
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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) |