Esophageal stenosis
Symptom Information:
Symptom ID: | HPO:0010450 | ||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||||||||||||||||||
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) Esophageal stenosis(HPO:0010450) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal stenosis and obstruction(MedDRA:10018008) Oesophageal stenosis and obstruction(MedDRA:10030196) Esophageal stenosis(HPO:0010450) |
||||||||||||||||||||||||||||||||||||||||||
Database Frequency: | 7 / 7739 | ||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microduplication syndrome | (Orphanet:261272) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 | (OMIM:615190) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |