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707209001: Keratoderma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3029052013 Keratoderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3029197018 Keratoderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5455641000241118 kératodermie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

376 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Keratoderma Is a Disorder of keratinisation false Inferred relationship Some
Keratoderma Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Keratoderma Associated morphology Hyperkeratosis true Inferred relationship Some 2
Keratoderma Finding site Skin structure true Inferred relationship Some 2
Keratoderma Is a Disorder of skin (disorder) true Inferred relationship Some
Keratoderma Has interpretation Abnormal false Inferred relationship Some 1
Keratoderma Interprets Keratinization false Inferred relationship Some 1
Keratoderma Is a Ichthyosis false Inferred relationship Some
Keratoderma Is a Keratosis true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital keratoderma Is a True Keratoderma Inferred relationship Some
Palmoplantar keratoderma Is a True Keratoderma Inferred relationship Some
Acquired keratoderma (disorder) Is a True Keratoderma Inferred relationship Some
A rare punctate palmoplantar keratoderma characterized by multiple small, round to oval or rhomboid, yellowish, hyperkeratotic papules and plaques most commonly localized to the palms of the hands and soles of the feet, potentially extending to the dorsum of the hands and feet in severe cases. Histopathological analysis shows hyperkeratosis, epidermal hypertrophy, and fragmentation and rarefaction of elastic fibers. The condition can be sporadic or familial. Is a True Keratoderma Inferred relationship Some
Actinic keratosis (disorder) Is a False Keratoderma Inferred relationship Some
Callosity Is a True Keratoderma Inferred relationship Some
Lymphedematous keratoderma Is a False Keratoderma Inferred relationship Some
Vitamin A-responsive dermatosis Is a True Keratoderma Inferred relationship Some
Benign acanthosis nigricans Is a True Keratoderma Inferred relationship Some
Multiple minute digitate hyperkeratosis of Goldstein Is a True Keratoderma Inferred relationship Some
Pityriasis rotunda Is a True Keratoderma Inferred relationship Some
Winer's dilated pore Is a True Keratoderma Inferred relationship Some
Onchocercal lichenification Is a True Keratoderma Inferred relationship Some
Leukoplakia of penis Is a True Keratoderma Inferred relationship Some
Retention hyperkeratosis (disorder) Is a True Keratoderma Inferred relationship Some
Seborrhoeic keratosis Is a True Keratoderma Inferred relationship Some
Tar keratosis (disorder) Is a True Keratoderma Inferred relationship Some
Keratoderma blennorrhagicum (disorder) Is a True Keratoderma Inferred relationship Some
Haber's syndrome Is a False Keratoderma Inferred relationship Some
Hyperkeratosis of yaws (disorder) Is a True Keratoderma Inferred relationship Some
Gonococcal keratosis Is a True Keratoderma Inferred relationship Some
Slightly pigmented smooth or warty papules that are flesh colored and found on the upper surface of hands and feet. Is a True Keratoderma Inferred relationship Some
Leukokeratosis of skin Is a True Keratoderma Inferred relationship Some
Hyperkeratosis of pinta Is a True Keratoderma Inferred relationship Some
A rare arthrogryposis syndrome characterized by the association of multiple congenital joint contractures (of the large joints, fingers and toes) and hyperkeratosis (i.e. thick, scaling and fissured skin), with death occurring in early infancy. There have been no further reports in the literature since 1993. Is a True Keratoderma Inferred relationship Some
Onychophosis Is a True Keratoderma Inferred relationship Some
Inflammatory hyperkeratotic dermatosis Is a True Keratoderma Inferred relationship Some
Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex (disorder) Is a True Keratoderma Inferred relationship Some
Ichthyosis Is a True Keratoderma Inferred relationship Some
Follicular keratosis Is a True Keratoderma Inferred relationship Some
Cutaneous horn (disorder) Is a True Keratoderma Inferred relationship Some
Keratosis caused by radiation Is a True Keratoderma Inferred relationship Some
Keratoderma climactericum Is a True Keratoderma Inferred relationship Some
Lymphoedematous hyperkeratosis Is a True Keratoderma Inferred relationship Some
Senile gluteal dermatosis (disorder) Is a True Keratoderma Inferred relationship Some
Virus-associated trichodysplasia spinulosa is a rare infectious skin disease characterized by the development of follicular papules with keratin spicules in various parts of the body, predominantly in the face (e.g. nose, eyebrows, auricles), that is due to polyomavirus infection in immunocompromized patients. Is a True Keratoderma Inferred relationship Some
Drug-induced ichthyosiform reaction Is a True Keratoderma Inferred relationship Some
Thermal keratosis Is a True Keratoderma Inferred relationship Some
Subungual hyperkeratosis Is a True Keratoderma Inferred relationship Some
Lichenoid actinic keratosis (disorder) Is a False Keratoderma Inferred relationship Some
Solar lentigo Is a False Keratoderma Inferred relationship Some
Acanthosis palmaris Is a True Keratoderma Inferred relationship Some
Malignant acanthosis nigricans Is a True Keratoderma Inferred relationship Some

Reference Sets

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