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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
Neu-Laxova syndrome Interprets True Keratinization Inferred relationship Some 4
Rough skin (finding) Interprets True Keratinization Inferred relationship Some 2
Rough skin of hands Interprets True Keratinization Inferred relationship Some 2
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) Interprets False Keratinization Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) Interprets False Keratinization Inferred relationship Some 4
Hypotrichosis with keratosis pilaris and lentiginosis Interprets True Keratinization Inferred relationship Some 3
Xeroderma of left eyelid Interprets False Keratinization Inferred relationship Some 4
Xeroderma of right eyelid (disorder) Interprets False Keratinization Inferred relationship Some 4
Xeroderma of right upper eyelid Interprets False Keratinization Inferred relationship Some 3
Xeroderma of left upper eyelid Interprets False Keratinization Inferred relationship Some 3
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Interprets True Keratinization Inferred relationship Some 1
Harlequin fetus Interprets True Keratinization Inferred relationship Some 4
Autosomal recessive epidermolytic ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Cutis gyrata syndrome of Beare and Stevenson Interprets True Keratinization Inferred relationship Some 3
Systematised linear porokeratosis Interprets True Keratinization Inferred relationship Some 2
Pityriasis rubra pilaris due to human immunodeficiency virus infection (disorder) Interprets True Keratinization Inferred relationship Some 3
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) Interprets True Keratinization Inferred relationship Some 6
Erythrokeratodermia cardiomyopathy syndrome Interprets True Keratinization Inferred relationship Some 4
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads syndrome (disorder) Interprets True Keratinization Inferred relationship Some 5
Generalized inflammatory peeling skin syndrome Interprets True Keratinization Inferred relationship Some 4
Generalized non-inflammatory peeling skin syndrome Interprets True Keratinization Inferred relationship Some 3
Ichthyosis hystrix gravior (disorder) Interprets True Keratinization Inferred relationship Some 2
Juvenile pityriasis rubra pilaris (disorder) Interprets True Keratinization Inferred relationship Some 2
Acquired ichthyosis due to paraneoplastic syndrome (disorder) Interprets True Keratinization Inferred relationship Some 2
Adult pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 2
Terra firma-forme dermatosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3

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