skip navigation links
National Cancer Institute
Enterprise Vocabulary Services
Box
NCIm Version: 201808 (Browser Version 2.9, using LexEVS 6.5.1)
SearchBox Top
SearchBox Bottom
Dermatitis, Atopic (CUI C0011615) Suggest changes to this concept
Add to Cart

Terms & Properties

Concept Unique Identifier (CUI): C0011615

Semantic Type: Disease or Syndrome

HPO Definition: A chronic inflammatory genetically determined disease of the skin manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. [HPO:probinson]

CSP Definition: chronic inflammatory skin disorder in individuals with a hereditary predisposition to a lowered threshold to pruritus; characterized by extreme itching, leading to scratching and rubbing that result in typical lesions of eczema.

MSH Definition: 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.

Synonyms & Abbreviations: (see Synonym Details)
AD - Atopic dermatitis
allergic dermatitis
allergic eczema
ATOD
Atopic Dermatitides
Atopic dermatitis (disorder)
Atopic dermatitis, chronic
Atopic dermatitis, unspecified
atopic dermatitis
Atopic eczema
Atopic Neurodermatitides
Atopic neurodermatitis (disorder)
Atopic neurodermatitis
Dermatitides, Atopic
DERMATITIS ALLERGIC
DERMATITIS ATOPIC
Dermatitis, Atopic [Disease/Finding]
DERMATITIS, ATOPIC
Disseminated Neurodermatitides
Disseminated Neurodermatitis
Eczema allergic
ECZEMA ATOPIC
Eczema, allergic
ECZEMA, ATOPIC
Neurodermatitides, Atopic
Neurodermatitides, Disseminated
Neurodermatitis, Atopic
NEURODERMATITIS, DISSEMINATED

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN a type of immediate hypersensitivity MSH
AQL BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000017005 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
CTV3ID M111. SNOMEDCT_US
CTV3ID M117. SNOMEDCT_US
DC 1 MSH
DEFINITION_STATUS_ID 900000000000073002 SNOMEDCT_US
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DID 2716-6917 CSP
DID 2716-6989 CSP
DX 19660101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
EFFECTIVE_TIME 20060131 SNOMEDCT_US
GENELOCUS ,3,q,2,1, OMIM
GENESYMBOL ATOD1 OMIM
HPO_COMMENT In infants, atopic dermatitis is known as infantile eczema. HPO
IAN DEFAULT ICD10
MDA 19990101 MSH
MESH_DEFINITION 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. NDFRT
MESH_DUI D003876 NDFRT
MESH_NAME Dermatitis, Atopic NDFRT
MESH_UI M0006050 NDFRT
MIMTYPE 5 OMIM
MIMTYPEMEANING Mendelian phenotype or locus, molecular basis unknown. OMIM
MIMTYPEVALUE perc OMIM
MMR 20150618 MSH
MN C16.320.850.210 MSH
MN C17.800.174.193 MSH
MN C17.800.815.193 MSH
MN C17.800.827.210 MSH
MN C20.543.480.343 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000000943 NDFRT
ORDER_NO 14032 ICD10CM
ORDER_NO 14035 ICD10CM
ORDER_NO 14040 ICD10CM
PRIMARY_PATH 10012434$10012435$10014982$10040785$Dermatitis allergic$Dermatitis and eczema$Epidermal and dermal conditions$Skin and subcutaneous tissue disorders MDR
PRIMARY_PATH 10012438$10012435$10014982$10040785$Dermatitis atopic$Dermatitis and eczema$Epidermal and dermal conditions$Skin and subcutaneous tissue disorders MDR
PRIMARY_SOC 10040785 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 20.0 MDR
PT_IN_VERSION 20.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RXAUI 3145893 RXNORM
RXAUI 3145894 RXNORM
RXAUI 3153192 RXNORM
RXAUI 3206096 RXNORM
RXAUI 3206098 RXNORM
RXCUI 1022124 RXNORM
SID HP:0007533 HPO
SID HP:0007564 HPO
SMQ_TERM_ADDVERSION 16.0 MDR
SMQ_TERM_ADDVERSION 19.0 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_CAT B MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 16.0 MDR
SMQ_TERM_LMVERSION 19.0 MDR
SMQ_TERM_SCOPE 1 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 200773006 NDFRT
SNOMED_CID 200775004 NDFRT
SNOMED_CID 24079001 NDFRT
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS L20.8 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS L20.9 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~L20.8 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~L20.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS L20.81 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS L20.9 | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~L20.81 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~L20.9 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~M111. SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~M117. SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T011526 MSH
TERMUI T011527 MSH
TERMUI T011528 MSH
TERMUI T011529 MSH
TH NLM (1966) MSH
TH OMIM (2013) MSH
TH UNK (19XX) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0011615

Mainbox Bottom