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69707008: Abnormal keratinization (finding)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
115798015 Abnormal keratinization en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
501362016 Abnormal keratinisation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
809682011 Abnormal keratinization (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
70911000077112 kératinisation anormale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

173 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Abnormal keratinization Is a Skin finding false Inferred relationship Some
Abnormal keratinization Interprets Keratinization false Inferred relationship Some 1
Abnormal keratinization Finding site Structure of skin region false Inferred relationship Some
Abnormal keratinization Finding site Nail structure false Inferred relationship Some
Abnormal keratinization Finding site Hair structure false Inferred relationship Some
Abnormal keratinization Finding site Hair structure (body structure) false Inferred relationship Some
Abnormal keratinization Finding site Skin structure false Inferred relationship Some
Abnormal keratinization Is a Integumentary system finding true Inferred relationship Some
Abnormal keratinization Finding site Structure of integumentary system (body structure) true Inferred relationship Some 2
Abnormal keratinization Has interpretation Abnormal false Inferred relationship Some 1
Abnormal keratinization Interprets Keratinization true Inferred relationship Some 1
Abnormal keratinization Has interpretation Abnormal true Inferred relationship Some 1
Abnormal keratinization Is a Functional finding true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Psoriasis of penis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Psoriasis of perianal skin (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Generalized psoriasis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Photoaggravated psoriasis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Psoriasis of scalp margin (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Psoriasis of face (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Non-pustular psoriasis of hands (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Hypertrophic palmar psoriasis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Hypertrophic palmoplantar psoriasis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Non-pustular psoriasis of hands and feet (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Drug-exacerbated psoriasis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acute generalized pustular psoriasis de novo (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acute generalized pustular flare of preexisting plaque psoriasis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Childhood pustular psoriasis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Early onset psoriasis type 1 (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Onset of psoriasis in infancy (<1 year) (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Onset of psoriasis in childhood (1-10 years) (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Onset of psoriasis in adolescence (10-20 years) (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Onset of psoriasis in early adulthood (20-40 years) (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Late onset psoriasis type 2 (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Familial psoriasis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Familial psoriasis with affected first degree relative (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Familial psoriasis without affected first degree relative (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Nail dystrophy due to pityriasis rubra pilaris (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Follicular hyperkeratosis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acanthosis nigricans of oral mucous membranes (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Retention hyperkeratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Retention hyperkeratosis due to neglect Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Desquamation of skin following febrile illness (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Drug-induced desquamation of skin (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Desquamation secondary to acute systemic illness (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acanthosis nigricans (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Xeroderma in genetic syndrome (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Punctate palmoplantar keratoderma (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Arsenical keratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Flexural Darier's disease (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Hypertrophic Darier's disease (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Linear/nevoid/zosteriform Darier's disease (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acral Darier's disease (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Palmar pitting due to Darier disease Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Nail dystrophy due to Darier's disease (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Nail dystrophy due to benign familial pemphigus (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Keratoderma with deafness Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Pachyonychia congenita type II of Jackson-Lawler (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Pachyonychia congenita type III of Schafer-Brunauer (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Iritis with psoriatic arthritis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acropustulosis of infancy Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Keratosis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Bowenoid actinic keratosis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Keratoderma blennorrhagicum (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acrokeratosis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
[X]Keratoderma in diseases classified elsewhere Has definitional manifestation False Abnormal keratinization Inferred relationship Some
[X]Hypertrophic disorder of skin, unspecified Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Congenital ichthyosiform erythroderma Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Ichthyosiform erythroderma Has definitional manifestation False Abnormal keratinization Inferred relationship Some
On examination - rough skin Is a False Abnormal keratinization Inferred relationship Some
impétigo herpétiforme Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Actinic keratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Hypertrophic solar keratosis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Lichenoid actinic keratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acantholytic actinic keratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Atrophic actinic keratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Proliferative actinic keratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Multiple actinic keratoses (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Multiple actinic keratoses involving scalp (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Multiple actinic keratoses involving face (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Multiple actinic keratoses involving forehead and temples (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Multiple actinic keratoses involving hands (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Multiple actinic keratoses involving lower limbs (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Diffuse actinic hyperkeratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Actinic keratosis of eyelid (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Pigmented actinic keratosis (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Hyperkeratotic actinic keratosis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acquired keratosis pilaris Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Slightly pigmented smooth or warty papules that are flesh colored and found on the upper surface of hands and feet. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Arthritis mutilans Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Severe achondrolasia with developmental delay and acanthosis nigricans Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Xeroderma of lower eyelid Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Xeroderma of upper eyelid Has definitional manifestation False Abnormal keratinization Inferred relationship Some
A distinct form of Crouzon disease associated with acanthosis nigricans caused by a specific mutation (p.Ala391Glu) in the transmembrane domain of FGFR3. The disease is transmitted in an autosomal dominant manner with variable penetrance. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Congenital reticular ichthyosiform erythroderma (disorder) Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Keratoderma Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Formation of an epidermal layer which lacks nuclei during normal keratinization. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Palmoplantar keratoderma Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Acral peeling skin syndrome Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Psoriatic arthritis mutilans Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Cole disease Has definitional manifestation False Abnormal keratinization Inferred relationship Some
A rare hypersensitivity reaction with characteristics of the rapid development of numerous, nonfollicular, sterile, pinhead-sized pustules on an erythematous base, predominantly occurring on the trunk, intertriginous and flexural areas, with rare, mostly oral, mucosal involvement. Fever, peripheral blood leukocytosis, and mild eosinophilia are accompanying features. Systemic involvement, with hepatic, renal or pulmonary dysfunction, occasionally occurs. Onset usually occurs 1-12 days after administration of the causal medication and is most frequently associated with beta‐lactam antibiotics, macrolides (including pristinamycin and clindamycin), diltiazem, terbinafine, (hydroxy‐)chloroquine but many other medications have also been implicated. Histology reveals spongiform, subcorneal and/or intraepidermal, pustules but this pattern is not specific (same in pustular psoriasis). Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Psoriatic arthritis Has definitional manifestation False Abnormal keratinization Inferred relationship Some
A rare arrhythmogenic right ventricular cardiomyopathy (ARVC) and a cutaneous phenotype, characterized by peculiar wooly hair and palmoplantar keratoderma. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
A rare diffuse, mutilating, hereditary palmoplantar keratoderma characterized by severe, honeycomb-pattern palmoplantar keratosis and pseudoainhum of the digits leading to autoamputation, associated with mild to moderate congenital sensorineural hearing loss. Additional features include stellate keratosis on the extensor surfaces of the fingers, feet, elbows and knees. Alopecia, onychogryphosis, nail dystrophy or clubbing, spastic paraplegia and myopathy may also be associated. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Hereditary palmoplantar keratoderma, Gamborg-Nielsen type is characterized by the presence of diffuse palmoplantar keratoderma without associated symptoms. The syndrome has been described in multiple families from the northernmost county of Sweden (Norrbotten). The palmoplantar keratoderma found in the Gamborg-Nielsen type disease is milder than that found in Mal de Meleda but more severe than that found in Thost-Unna palmoplantar keratoderma. Transmission is autosomal recessive. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
A rare genetic disease which is a rare form of porokeratosis occurring mainly in adolescence and characterized by small pruritic or painful keratotic papules that first appear on the palms and soles, and may gradually spread to other body zones. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
A rare isolated diffuse palmoplantar keratoderma characterized by diffuse, homogeneous, mild to thick, brown-to-yellowish palmoplantar hyperkeratosis (sometimes spreading over the dorsal aspect of fingers). Skin biopsy shows non-epidermolytic changes. There are no changes in hair, teeth or nails, and no syndromic involvement of other organs. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
This syndrome is characterized by the association of acanthosis nigricans, insulin resistance, severe muscle cramps and acral hypertrophy. Has definitional manifestation False Abnormal keratinization 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. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by congenital alopecia and palmoplantar hyperkeratosis. It is usually associated with cataracts, progressive sclerodactyly and pseudo-ainhum. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
An autosomal dominant cerebellar ataxia type I that is characterized by papulosquamous, ichthyosiform plaques on the limbs appearing shortly after birth and later manifestations including progressive ataxia, dysarthria, nystagmus and decreased reflexes. Has definitional manifestation False Abnormal keratinization Inferred relationship Some
Lelis syndrome is characterized by the association of ectodermal dysplasia (hypotrichosis and hypohidrosis) with acanthosis nigricans. Has definitional manifestation False Abnormal keratinization Inferred relationship Some

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