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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

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Keratinization Is a Skin function false Inferred relationship Some
Keratinization Is a Skin growth true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Bowenoid actinic keratosis Interprets False Keratinization Inferred relationship Some 2
Inverted follicular keratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Acquired palmoplantar keratoderma (disorder) Interprets False Keratinization Inferred relationship Some 2
Hyperkeratosis Interprets False Keratinization Inferred relationship Some 1
Primary seborrhea Interprets False Keratinization Inferred relationship Some 1
Diffuse palmoplantar keratoderma of Thost-Unna (disorder) Interprets False Keratinization Inferred relationship Some 2
Keratosis rubra pilaris (disorder) Interprets True Keratinization Inferred relationship Some 1
Keratosis pilaris atrophicans (disorder) Interprets True Keratinization Inferred relationship Some 2
Porokeratosis (disorder) Interprets True Keratinization Inferred relationship Some 1
Acrokeratosis verruciformis of Hopf (disorder) Interprets True Keratinization Inferred relationship Some 1
Hereditary diffuse palmoplantar keratoderma (disorder) Interprets False Keratinization Inferred relationship Some 2
Xerosis due to atopic dermatitis (disorder) Interprets False Keratinization Inferred relationship Some 1
Nail dystrophy due to pityriasis rubra pilaris (disorder) Interprets True Keratinization Inferred relationship Some 1
Follicular hyperkeratosis Interprets False Keratinization Inferred relationship Some 2
Acanthosis nigricans of oral mucous membranes (disorder) Interprets True Keratinization Inferred relationship Some 1
Retention hyperkeratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Retention hyperkeratosis due to neglect Interprets False Keratinization Inferred relationship Some 1
Desquamation of skin following febrile illness (disorder) Interprets True Keratinization Inferred relationship Some 1
Drug-induced desquamation of skin (disorder) Interprets True Keratinization Inferred relationship Some 1
Desquamation secondary to acute systemic illness (disorder) Interprets True Keratinization Inferred relationship Some 1
Acanthosis nigricans (disorder) Interprets True Keratinization Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) Interprets False Keratinization Inferred relationship Some 1
Punctate palmoplantar keratoderma (disorder) Interprets False Keratinization Inferred relationship Some 2
Lichenoid actinic keratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Acantholytic actinic keratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Atrophic actinic keratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Proliferative actinic keratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Multiple actinic keratoses (disorder) Interprets False Keratinization Inferred relationship Some 1
Multiple actinic keratoses involving scalp (disorder) Interprets False Keratinization Inferred relationship Some 2
Multiple actinic keratoses involving face (disorder) Interprets False Keratinization Inferred relationship Some 2
Multiple actinic keratoses involving forehead and temples (disorder) Interprets False Keratinization Inferred relationship Some 1
Multiple actinic keratoses involving hands (disorder) Interprets False Keratinization Inferred relationship Some 2
Multiple actinic keratoses involving lower limbs (disorder) Interprets False Keratinization Inferred relationship Some 2
Diffuse actinic hyperkeratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu (disorder) Interprets False Keratinization Inferred relationship Some 2
Pachyonychia congenita type II of Jackson-Lawler (disorder) Interprets False Keratinization Inferred relationship Some 2
Pachyonychia congenita type III of Schafer-Brunauer (disorder) Interprets False Keratinization Inferred relationship Some 2
Actinic keratosis of eyelid (disorder) Interprets False Keratinization Inferred relationship Some 2
Pigmented actinic keratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Hyperkeratotic actinic keratosis Interprets False Keratinization Inferred relationship Some 1
Acral keratosis Interprets False Keratinization Inferred relationship Some 2
Severe achondrolasia with developmental delay and acanthosis nigricans Interprets False Keratinization Inferred relationship Some 4
Xeroderma of lower eyelid Interprets False Keratinization Inferred relationship Some 1
Xeroderma of upper eyelid Interprets False Keratinization Inferred relationship Some 1
Crouzon syndrome with acanthosis nigricans (disorder) Interprets True Keratinization Inferred relationship Some 1
Congenital reticular ichthyosiform erythroderma (disorder) Interprets True Keratinization Inferred relationship Some 1
Palmoplantar keratoderma Interprets False Keratinization Inferred relationship Some 1
Keratoderma Interprets False Keratinization Inferred relationship Some 1
Orthokeratosis Interprets False Keratinization Inferred relationship Some 1
Cole disease Interprets False Keratinization Inferred relationship Some 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) Interprets False Keratinization Inferred relationship Some 1
Punctate palmoplantar keratoderma type 1 (disorder) Interprets False Keratinization Inferred relationship Some 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) Interprets False Keratinization Inferred relationship Some 1
Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Generalized peeling skin syndrome (disorder) Interprets True Keratinization Inferred relationship Some 1
Lelis syndrome Interprets True Keratinization Inferred relationship Some 1
Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome Interprets False Keratinization Inferred relationship Some 1
Curly hair, acral keratoderma, caries syndrome (disorder) Interprets False Keratinization Inferred relationship Some 4
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Wooly hair with palmoplantar keratoderma syndrome Interprets False Keratinization Inferred relationship Some 3
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome Interprets False Keratinization Inferred relationship Some 7
Striate palmoplantar keratoderma (disorder) Interprets False Keratinization Inferred relationship Some 2
Focal palmoplantar and gingival keratoderma Interprets False Keratinization Inferred relationship Some 3
Arsenical keratosis (disorder) Interprets False Keratinization Inferred relationship Some 4
Superficial keratosis Interprets False Keratinization Inferred relationship Some 2
Punctate palmoplantar keratoderma type 2 (disorder) Interprets False Keratinization Inferred relationship Some 2
Tar keratosis (disorder) Interprets False Keratinization Inferred relationship Some 1
Palmoplantar keratoderma with deafness syndrome (disorder) Interprets False Keratinization Inferred relationship Some 2
Congenital keratoderma Interprets True Keratinization Inferred relationship Some 2
Disseminated superficial porokeratosis Interprets True Keratinization Inferred relationship Some 2
Ulerythema ophryogenes (disorder) Interprets True Keratinization Inferred relationship Some 3
Keratosis caused by radiation Interprets False Keratinization Inferred relationship Some 1
Arthrogryposis hyperkeratosis syndrome lethal form (disorder) Interprets False Keratinization Inferred relationship Some 3
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) Interprets False Keratinization Inferred relationship Some 3
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder) Interprets True Keratinization Inferred relationship Some 4
Palmoplantar keratoderma with clinodactyly syndrome (disorder) Interprets False Keratinization Inferred relationship Some 3
Palmoplantar keratoderma Nagashima type (disorder) Interprets False Keratinization Inferred relationship Some 2
Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder) Interprets False Keratinization Inferred relationship Some 4
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder) Interprets True Keratinization Inferred relationship Some 2
Linear porokeratosis Interprets True Keratinization Inferred relationship Some 2
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Diffuse palmoplantar keratoderma and acrocyanosis syndrome (disorder) Interprets False Keratinization Inferred relationship Some 2
Xeroderma pigmentosum and Cockayne syndrome complex (disorder) Interprets False Keratinization Inferred relationship Some 3
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) Interprets False Keratinization Inferred relationship Some 2
Keratosis follicularis, dwarfism, cerebral atrophy syndrome Interprets True Keratinization Inferred relationship Some 3
Spinocerebellar ataxia type 34 (disorder) Interprets True Keratinization Inferred relationship Some 2
Acral peeling skin syndrome Interprets True Keratinization Inferred relationship Some 2
Van den Bosch syndrome (disorder) Interprets False Keratinization Inferred relationship Some 4
Ankylosing vertebral hyperostosis with tylosis syndrome (disorder) Interprets False Keratinization Inferred relationship Some 2
Cutaneous horn (disorder) Interprets False Keratinization Inferred relationship Some 1
Hereditary skin peeling syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome Interprets False Keratinization Inferred relationship Some 7
Porokeratosis plantaris palmaris et disseminata (disorder) Interprets True Keratinization Inferred relationship Some 3
Naxos disease Interprets False Keratinization Inferred relationship Some 3
Hyperkeratosis of mucous membrane of mouth due to and following traumatic injury (disorder) Interprets False Keratinization Inferred relationship Some 2
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder) Interprets False Keratinization Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) Interprets True Keratinization Inferred relationship Some 2
Haim Munk syndrome (disorder) Interprets False Keratinization Inferred relationship Some 3
Trichodysplasia xeroderma syndrome (disorder) Interprets False Keratinization Inferred relationship Some 3
XTE syndrome Interprets False Keratinization Inferred relationship Some 2
Classical juvenile pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 3

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