238643009: Skin peeling disorder (disorder)
Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core
Descriptions:
Expanded Value Set
Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Recurrent focal palmar peeling |
Is a |
True |
Skin peeling disorder |
Inferred relationship |
Some |
|
Desquamation of skin following febrile illness (disorder) |
Is a |
True |
Skin peeling disorder |
Inferred relationship |
Some |
|
Drug-induced desquamation of skin (disorder) |
Is a |
True |
Skin peeling disorder |
Inferred relationship |
Some |
|
Desquamation secondary to acute systemic illness (disorder) |
Is a |
True |
Skin peeling disorder |
Inferred relationship |
Some |
|
Acral peeling skin syndrome |
Is a |
False |
Skin peeling disorder |
Inferred relationship |
Some |
|
Psoriasis of scalp (disorder) |
Is a |
False |
Skin peeling disorder |
Inferred relationship |
Some |
|
A form of peeling skin syndrome characterized by a generalized distribution. It comprises two sub-types: the non-inflammatory (PSS type A) and the inflammatory (PSS type B) form. PSS type A is characterized by generalized white scaling with superficial non-inflammatory peeling of the skin, while PSS type B is characterized by superficial patchy peeling of the entire skin with underlying erythroderma, pruritus, and atopy. |
Is a |
False |
Skin peeling disorder |
Inferred relationship |
Some |
|
A group of rare autosomal recessive forms of ichthyosis clinically characterized by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution for generalized PSS type A (noninflammatory) or B (inflammatory). |
Is a |
True |
Skin peeling disorder |
Inferred relationship |
Some |
|
A rare genetic skin disease characterized by generalized skin peeling or superficial blisters without scarring, leukonychia, acral punctate keratoses coalescing into focal keratoderma on the weight-bearing areas, painful angular cheilitis, and knuckle pads with multiple hyperkeratotic micropapules. The skin appears dry and scaly with superficial exfoliation and underlying erythema. Histopathologic examination of affected skin areas is not specific and shows hyperkeratosis, acanthosis, and occasional intraepidermal clefting with irregular acantholysis. |
Is a |
True |
Skin peeling disorder |
Inferred relationship |
Some |
|
Pityriasis rubra pilaris |
Is a |
True |
Skin peeling disorder |
Inferred relationship |
Some |
|
This concept is not in any reference sets
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