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44138005: Keratinization, function (observable entity)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1203192014 Keratinization, function (observable entity) en Fully specified name Active Case insensitive SNOMED CT core
2670991015 Keratinization, function en Synonym Active Case insensitive SNOMED CT core
493794013 Keratinisation en Synonym Active Case insensitive SNOMED CT core
73613019 Keratinization en Synonym Active Case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

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

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