Biomaterial Database

[Investigations on constitution and heredity in atopic dermatitis (neurodermatitis)]. 1951

A G KOCHS

UI	MeSH Term	Description	Entries
D009450	Neurodermatitis	An extremely variable eczematous skin disease that is presumed to be a response to prolonged vigorous scratching, rubbing, or pinching to relieve intense pruritus. It varies in intensity, severity, course, and morphologic expression in different individuals. Neurodermatitis is believed by some to be psychogenic. The circumscribed or localized form is often referred to as lichen simplex chronicus.	Lichen Simplex Chronicus,Neurodermatitis, Circumscribed,Neurodermatitis, Localized,Circumscribed Neurodermatitides,Circumscribed Neurodermatitis,Localized Neurodermatitides,Localized Neurodermatitis,Neurodermatitides,Neurodermatitides, Circumscribed,Neurodermatitides, Localized
D003872	Dermatitis	Any inflammation of the skin.	Dermatitides
D003876	Dermatitis, Atopic	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.	Eczema, Atopic,Eczema, Infantile,Neurodermatitis, Atopic,Neurodermatitis, Disseminated,Atopic Dermatitis,Atopic Eczema,Atopic Neurodermatitis,Disseminated Neurodermatitis,Infantile Eczema
D004485	Eczema	A dermatitis characterized by a spongiotic tissue reaction pattern occurring as a reaction to many endogenous and exogenous agents.	Dermatitis, Eczematous,Eczematous Dermatitis
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D040941	Heredity	The transmission of traits encoded in GENES from parent to offspring.