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:

OTHER ATOPIC DERMATITIS

Eczema, Atopic

Besnier's prurigo

Other atopic dermatitis and related conditions

Disseminated Neurodermatitides

Dermatitis, Atopic

Atopic Dermatitis

Atopic dermatitis

Neurodermatitis, Atopic

Neurodermatitides, Disseminated

Infantile Eczema

Atopic Neurodermatitis

atopic eczema

allergic dermatitis

Neurodermatitis, Disseminated

allergic form of dermatitis

Atopic dermatitis and related conditions (disorder)

eczematous dermatitis

Dermatitides, Atopic

Atopic neurodermatitis

Atopic Dermatitides

atopic dermatitis and related conditions

Disseminated Neurodermatitis

eczema

Eczema, Infantile

Neurodermatitides, Atopic

Atopic Neurodermatitides

allergic

This is just here as a test because I lose it

Term information

database cross reference
  • SNOMEDCT:200775004
  • MONDO:0004980
  • OMIM:603165
  • DOID:3310 (MONDO:equivalentTo)
  • ICD10:L20
  • ICD9:691 (EFO:0000274)
  • MedDRA:10003641
  • MeSH:D003876
  • ICD9:691.8 (EFO:0000274)
  • OMIM:605803
  • OMIM:147050
  • NCIT:C3001 (MONDO:equivalentTo)
  • SNOMEDCT:90823000
  • SNOMEDCT:24079001
  • OMIMPS:603165 (MONDO:equivalentTo)
exactMatch
  • http://purl.obolibrary.org/obo/DOID_3310
  • http://purl.obolibrary.org/obo/NCIT_C3001
  • https://omim.org/phenotypicSeries/PS603165
gwas trait
  • true
id
  • EFO:0000274
term editor
  • Tomasz Adamusiak
  • James Malone