A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. [ MESH : D003876 ]
Term information
- ICD9:691.8 (EFO:0000274)
- DOID:3310 (MONDO:equivalentTo)
- ICD9:691 (EFO:0000274)
- EFO:0000274 (MONDO:equivalentTo)
- NCIT:C3001 (MONDO:equivalentTo)
- OMIMPS:603165 (MONDO:equivalentTo)
- http://purl.obolibrary.org/obo/mondo/patterns/allergic_form_of_disease.yaml
- A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema.
- http://purl.obolibrary.org/obo/NCIT_C3001
- https://omim.org/phenotypicSeries/PS603165
- http://purl.obolibrary.org/obo/DOID_3310
- atopic eczema
- allergic dermatitis
- eczema
- Atopic neurodermatitis
- allergic
- eczematous dermatitis
- Atopic dermatitis
- allergic form of dermatitis
- Besnier's prurigo
- MONDO:0004980
- http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml