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 ]
Synonyms: allergic form of dermatitis allergic dermatitis eczematous dermatitis Atopic dermatitis eczema Besnier's prurigo atopic eczema Atopic neurodermatitis
Term information
- OMIMPS:603165 (MONDO:equivalentTo)
- EFO:0000274 (MONDO:equivalentTo)
- HP:0001047 (https://orcid.org/0000-0002-9584-9618)
- SCTID:24079001 (https://orcid.org/0000-0002-9584-9618)
- UMLS:C0011615 (MONDO:equivalentTo)
- ICD9:691 (EFO:0000274)
- DOID:3310 (MONDO:equivalentTo)
- ICD9:691.8 (EFO:0000274)
- SCTID:200775004 (https://orcid.org/0000-0002-9584-9618)
- MEDGEN:41502 (MONDO:equivalentTo)
- NCIT:C3001 (MONDO:equivalentTo)
- ICD10CM:L20 (https://orcid.org/0000-0002-9584-9618)
otar
http://purl.obolibrary.org/obo/NCIT_C3001
http://identifiers.org/snomedct/24079001
http://purl.obolibrary.org/obo/DOID_3310
http://purl.bioontology.org/ontology/ICD10CM/L20
http://linkedlifedata.com/resource/umls/id/C0011615
http://identifiers.org/medgen/41502
https://omim.org/phenotypicSeries/PS603165
http://identifiers.org/snomedct/200775004