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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:

Id Description Lang Type Status Case? Module
357682017 Skin peeling disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
627551019 Skin peeling disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1868131000195114 disturbo da peeling cutaneo it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6491891000241115 desquamation de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6491901000241119 desquamation cutanée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


21 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Skin peeling disorder Is a Papular, squamous and granulomatous eruptions of skin false Inferred relationship Some
Skin peeling disorder Finding site Skin structure false Inferred relationship Some 1
Skin peeling disorder Associated morphology Eruption false Inferred relationship Some 1
Skin peeling disorder Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Skin peeling disorder Is a Eruption false Inferred relationship Some
Skin peeling disorder Is a Acquired disorder of keratinization (disorder) false Inferred relationship Some
Skin peeling disorder Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Skin peeling disorder Finding site Skin structure false Inferred relationship Some 1
Skin peeling disorder Associated morphology Eruption false Inferred relationship Some 1
Skin peeling disorder Finding site Skin structure true Inferred relationship Some 2
Skin peeling disorder Is a Disorder of keratinisation true Inferred relationship Some
Skin peeling disorder Is a Skin lesion true Inferred relationship Some
Skin peeling disorder Associated morphology Exfoliative lesion (morphologic abnormality) true Inferred relationship Some 2
Skin peeling disorder Has interpretation Abnormal true Inferred relationship Some 1
Skin peeling disorder Interprets Keratinization true Inferred relationship Some 1
Skin peeling disorder Is a Keratosis false Inferred relationship Some

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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