Clinical Signs and Symptoms
ORPHA:411696 Proton-pump inhibitor-responsive esophageal eosinophilia
The phenotypic description of this disease is based on an analysis of the biomedical literature and uses the terms of the Human Phenotype Ontology (HPO). Phenotypic abnormalities are presented by order of frequency of occurrence in the patient population, then by alphabetical order inside each frequency group.
- Eosinophilic infiltration of the esophagus HP:0410151
- Esophagitis HP:0100633
Very frequent
- Abdominal pain HP:0002027
- Abnormal peristalsis HP:0030914
- Dysphagia HP:0002015
- Esophageal exudate HP:0031985
- Esophageal food impaction HP:0031984
- Esophageal furrows HP:0031858
- Feeding difficulties HP:0011968
- Feeding difficulties in infancy HP:0008872
- Food allergy HP:0500093
- Gastroesophageal reflux HP:0002020
- Increased anti-food allergen IgE antibody level HP:0410227
- Irritability HP:0000737
Frequent
- Allergic rhinitis HP:0003193
- Asthma HP:0002099
- Atopic dermatitis HP:0001047
- Chest pain HP:0100749
- Egg allergy HP:0410328
- Eosinophilic microabscess formation in the esophagus HP:0410152
- Epigastric pain HP:0410019
- Esophageal atresia HP:0002032
- Esophageal stenosis HP:0010450
- Failure to thrive HP:0001508
- Food-induced anaphylaxis HP:0500095
- Lactose intolerance HP:0004789
- Nausea HP:0002018
- Urticaria HP:0001025
- Vomiting HP:0002013
Occasional
Additional information
Further information
Specialised Social Services
Warning
The information provided is based on published scientific articles.
The information provided is estimated for the entire population of patients in routine care. Some phenotypic abnormalities reported here may occur individually with a variable temporality or severity, while others, not listed, may still be encountered. Phenotypic annotations are not yet available for all rare diseases; the annotation process is ongoing.
The information contained in Orphanet is regularly updated. It is possible that discoveries have been made since the last update and have not yet been incorporated.
Professionals are encouraged to always consult the latest scientific publications before making a decision based on the information provided. The information contained in Orphanet is not intended to replace the services of a healthcare professional. Orphanet cannot be held responsible for the deleterious, truncated or erroneous use of any information found in the Orphanet database.