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44138005: Keratinization, function (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
73613019 Keratinization en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
493794013 Keratinisation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1203192014 Keratinization, function (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2670991015 Keratinization, function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
73613019 Keratinization en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
73613019 Keratinization en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
493794013 Keratinisation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
493794013 Keratinisation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
781231017 Keratinization (function) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1203192014 Keratinization, function (observable entity) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1203192014 Keratinization, function (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2670991015 Keratinization, function en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2670991015 Keratinization, function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Keratinisation Is a Skin function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
Keratinisation Is a Skin growth true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Bowenoid actinic keratosis Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Inverted follicular keratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired keratoderma palmaris et plantaris Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
hyperkératose Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary seborrhea Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Diffuse palmoplantar keratoderma of Thost-Unna Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Keratosis rubra pilaris Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Keratosis pilaris atrophicans (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Porokeratosis (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Acrokeratosis verruciformis of Hopf (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary diffuse palmoplantar keratoderma Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Xerosis due to atopic dermatitis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Nail dystrophy due to pityriasis rubra pilaris (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Follicular hyperkeratosis Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Acanthosis nigricans of oral mucous membranes (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Retention hyperkeratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Retention hyperkeratosis due to neglect Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Desquamation of skin following febrile illness (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Drug-induced desquamation of skin (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Desquamation secondary to acute systemic illness Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Acanthosis nigricans (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma in genetic syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Punctate palmoplantar keratoderma (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Lichenoid actinic keratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Acantholytic actinic keratosis Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic actinic keratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Proliferative actinic keratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple actinic keratoses (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple actinic keratoses involving scalp Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple actinic keratoses involving face (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple actinic keratoses involving forehead and temples (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple actinic keratoses involving hands (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple actinic keratoses involving lower limbs (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse actinic hyperkeratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Pachyonychia congenita type II of Jackson-Lawler Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Pachyonychia congenita type III of Schafer-Brunauer Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Actinic keratosis of eyelid Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Pigmented actinic keratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperkeratotic actinic keratosis Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Acral keratosis Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Severe achondrolasia with developmental delay and acanthosis nigricans Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 4
Xeroderma of lower eyelid Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma of upper eyelid Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Crouzon syndrome with acanthosis nigricans (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital reticular ichthyosiform erythroderma Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar keratoderma Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Keratoderma (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Formation of an epidermal layer which lacks nuclei during normal keratinisation. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Cole disease Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Generalized peeling skin syndrome (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Lelis syndrome Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic ectodermal dysplasia syndrome characterised by woolly hair (presenting at birth), palmoplantar keratoderma (developing in the first year of life) and dilated cardiomyopathy with predominant left ventricle involvement (developing in childhood) which can lead to life-threatening heart failure in childhood or adolescence. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Curly hair, acral keratoderma, caries syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 4
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome is an inherited epidermal disorder characterised by palmoplantar keratoderma, linear hyperkeratotic papules on the flexural side of large joints (cord-like distribution around wrists, in antecubital and popliteal folds), hyperkeratotic plaques (on neck, axillae, elbows, wrists, and knees), mild ichthyosiform scaling, and sclerotic constrictions around fingers that present flexural deformities. Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Wooly hair with palmoplantar keratoderma syndrome Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 7
Striate palmoplantar keratoderma Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Focal palmoplantar and gingival keratoderma (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Arsenical keratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 4
Superficial keratosis Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Punctate palmoplantar keratoderma type 2 is a type of isolated, punctate, hereditary palmoplantar keratoderma characterized by multiple, asymptomatic, 1 to 2 mm-long, firm, hyperkeratotic projections (spiny keratosis) on the palms, soles and digits (typically confined to their volar and/or lateral aspects). Histopathologically, compact columnar parakeratosis over hypo- or agranular epidermis is observed. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Tar keratosis (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar keratoderma with deafness syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital keratoderma Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Disseminated superficial porokeratosis (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Ulerythema ophryogenes (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Keratosis caused by radiation Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Arthrogryposis hyperkeratosis syndrome lethal form Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 4
Palmoplantar keratoderma with clinodactyly syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 4
MEDNIK syndrome Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Linear porokeratosis (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Diffuse palmoplantar keratoderma and acrocyanosis syndrome Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) together with the systemic and neurological features of Cockayne syndrome. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Keratosis follicularis, dwarfism, cerebral atrophy syndrome (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
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. Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Acral peeling skin syndrome Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Van den Bosch syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare dysostosis with predominant vertebral involvement characterized by paraspinal ligament ossification (most pronounced in the lower thoracic region), osteophytosis, marginal sacroiliac joint sclerosis, and punctate hyperkeratosis on the soles and palms. Patients may be asymptomatic or present mild to moderate back pain. There have been no further descriptions in the literature since 1969. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Cutaneous horn (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary skin peeling syndrome (disorder) Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 7
Porokeratosis plantaris palmaris et disseminata Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperkeratosis of mucous membrane of mouth due to and following traumatic injury Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder) Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Haim Munk syndrome Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
Trichodysplasia-xeroderma syndrome is an extremely rare, syndromic hair shaft anomaly characterized by sparse, coarse, brittle, excessively dry and slow-growing scalp hair, sparse axillary and pubic hair, sparse or absent eyelashes and eyebrows and dry skin. Hair shaft analysis shows pili torti, longitudinal splitting, grooves, peeling and scaling. There have been no further descriptions in the literature since 1987. Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3
XTE syndrome Interprets False Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 2
Classical juvenile pityriasis rubra pilaris Interprets True Keratinisation Inferred relationship Existential restriction modifier (core metadata concept) 3

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