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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
73614013 Keratinization, NOS en Synonym (core metadata concept) Inactive 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 Inactive 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 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
Classical juvenile pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 3
Circumscribed juvenile pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 3
Atypical juvenile pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 3
Keratoderma blennorrhagicum (disorder) Interprets False Keratinization Inferred relationship Some 3
Hereditary benign acanthosis nigricans Interprets False Keratinization Inferred relationship Some 4
Acquired plantar keratoderma (disorder) Interprets False Keratinization Inferred relationship Some 3
Acquired keratoderma (disorder) Interprets False Keratinization Inferred relationship Some 3
Hereditary benign acanthosis nigricans with insulin resistance Interprets False Keratinization Inferred relationship Some 4
Pityriasis rubra (Hebra) Interprets True Keratinization Inferred relationship Some 3
Hereditary acantholytic dermatosis Interprets True Keratinization Inferred relationship Some 3
Darier disease Interprets True Keratinization Inferred relationship Some 3
Pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 3
Nail dystrophy due to Darier's disease (disorder) Interprets True Keratinization Inferred relationship Some 4
Acquired palmoplantar keratosis Interprets False Keratinization Inferred relationship Some 2
Acquired keratosis pilaris Interprets True Keratinization Inferred relationship Some 3
Trichodysplasia spinulosa caused by Polyomavirus (disorder) Interprets False Keratinization Inferred relationship Some 3
Classical adult pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 3
Atypical adult pityriasis rubra pilaris Interprets True Keratinization Inferred relationship Some 3
Acquired disorder of keratinization (disorder) Interprets True Keratinization Inferred relationship Some 2
Drug-induced ichthyosiform reaction Interprets True Keratinization Inferred relationship Some 3
Focal acral hyperkeratosis (disorder) Interprets False Keratinization Inferred relationship Some 2
Acral Darier's disease (disorder) Interprets True Keratinization Inferred relationship Some 3
Palmar pitting due to Darier disease Interprets True Keratinization Inferred relationship Some 3
Acrokeratosis verruciformis of Darier disease (disorder) Interprets True Keratinization Inferred relationship Some 3
Flexural Darier's disease (disorder) Interprets True Keratinization Inferred relationship Some 3
Hypertrophic Darier's disease (disorder) Interprets True Keratinization Inferred relationship Some 3
Linear/nevoid/zosteriform Darier's disease (disorder) Interprets True Keratinization Inferred relationship Some 3
Acquired ichthyosis Interprets True Keratinization Inferred relationship Some 1
Acrokeratosis paraneoplastica of Bazex Interprets False Keratinization Inferred relationship Some 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Interprets True Keratinization Inferred relationship Some 1
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) Interprets False Keratinization Inferred relationship Some 1
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome Interprets True Keratinization Inferred relationship Some 1
Leukokeratosis of skin Interprets True Keratinization Inferred relationship Some 2
Leukokeratosis (disorder) Interprets True Keratinization Inferred relationship Some 1
Diffuse palmoplantar keratoderma with painful fissures Interprets True Keratinization Inferred relationship Some 2
Skin fragility, wooly hair, palmoplantar keratoderma syndrome (disorder) Interprets True Keratinization Inferred relationship Some 4
Focal palmoplantar keratoderma with joint keratoses (disorder) Interprets True Keratinization Inferred relationship Some 2
Ichthyosis hystrix Interprets True Keratinization Inferred relationship Some 2
Severe ichthyoses Interprets True Keratinization Inferred relationship Some 2
Ichthyosis, oral and digital anomalies syndrome Interprets True Keratinization Inferred relationship Some 4
Atypical ichthyosis vulgaris with hypogonadism Interprets True Keratinization Inferred relationship Some 2
Congenital ichthyosis with hypotrichosis syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Autosomal recessive ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Acral self-healing collodion baby (disorder) Interprets True Keratinization Inferred relationship Some 2
Keratitis ichthyosis and deafness syndrome (disorder) Interprets True Keratinization Inferred relationship Some 2
Syndromic recessive X-linked ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Autosomal recessive exfoliative ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Ichthyosis linearis circumflexa Interprets True Keratinization Inferred relationship Some 2
Ichthyosis hystrix gravior of Rheydt Interprets False Keratinization Inferred relationship Some 2
Congenital non bullous ichthyosiform erythroderma Interprets True Keratinization Inferred relationship Some 2
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) Interprets True Keratinization Inferred relationship Some 4
Cutaneous syndrome with ichthyosis Interprets True Keratinization Inferred relationship Some 2
Bathing suit ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Limb reduction-ichthyosis syndrome Interprets True Keratinization Inferred relationship Some 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Interprets True Keratinization Inferred relationship Some 2
Hystrix ichthyosis with deafness Interprets False Keratinization Inferred relationship Some 2
Ichthyosis, cerebellar degeneration and hepatosplenomegaly (disorder) Interprets True Keratinization Inferred relationship Some 2
Ichthyosis bullosa of Siemens Interprets True Keratinization Inferred relationship Some 2
Non-bullous ichthyosiform erythroderma Interprets False Keratinization Inferred relationship Some 2
Sjögren-Larsson syndrome (disorder) Interprets True Keratinization Inferred relationship Some 2
Erythrodermic lamellar ichthyosis Interprets True Keratinization Inferred relationship Some 2
Ichthyosis cheek eyebrow syndrome (disorder) Interprets True Keratinization Inferred relationship Some 3
Congenital cataract ichthyosis syndrome Interprets True Keratinization Inferred relationship Some 3
Ichthyosis vulgaris Interprets True Keratinization Inferred relationship Some 2
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome Interprets True Keratinization Inferred relationship Some 4
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome Interprets True Keratinization Inferred relationship Some 3
Congenital ichthyosis of skin Interprets True Keratinization Inferred relationship Some 2
Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome Interprets True Keratinization Inferred relationship Some 4
Autosomal dominant ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Annular epidermolytic ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Lamellar ichthyosis (limited type) (disorder) Interprets True Keratinization Inferred relationship Some 2
Senter syndrome Interprets True Keratinization Inferred relationship Some 3
Ichthyosis hystrix of Curth-Macklin Interprets True Keratinization Inferred relationship Some 2
Ichthyosis Interprets False Keratinization Inferred relationship Some 2
Porcupine man Interprets False Keratinization Inferred relationship Some 2
Lamellar ichthyosis AND trichorrhexis invaginata syndrome Interprets False Keratinization Inferred relationship Some 2
Keratinopathic ichthyosis (disorder) Interprets True Keratinization Inferred relationship Some 2
Autosomal dominant ichthyosis vulgaris Interprets True Keratinization Inferred relationship Some 2
X-linked ichthyosis with steryl-sulfatase deficiency Interprets True Keratinization Inferred relationship Some 2
Localised bullous ichthyosiform erythroderma Interprets True Keratinization Inferred relationship Some 2
Ichthyosis prematurity syndrome Interprets True Keratinization Inferred relationship Some 2
Autosomal dominant lamellar ichthyosis Interprets True Keratinization Inferred relationship Some 2
Ichthyosis follicularis with alopecia and photophobia (IFAP) Interprets True Keratinization Inferred relationship Some 2
Self-healing collodion baby (disorder) Interprets True Keratinization Inferred relationship Some 2
Lamellar ichthyosis Interprets True Keratinization Inferred relationship Some 2
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) Interprets True Keratinization Inferred relationship Some 4
Ichthyosis congenita with biliary atresia Interprets True Keratinization Inferred relationship Some 3
Non-erythrodermic lamellar ichthyosis Interprets True Keratinization Inferred relationship Some 2
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome Interprets True Keratinization Inferred relationship Some 4
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome Interprets True Keratinization Inferred relationship Some 5
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) Interprets True Keratinization Inferred relationship Some 2
Harlequin ichthyosis Interprets True Keratinization Inferred relationship Some 4
Netherton syndrome Interprets True Keratinization Inferred relationship Some 3
Hypotrichosis and deafness syndrome Interprets True Keratinization Inferred relationship Some 3
Ichthyosis hystrix Bäfverstedt type (disorder) Interprets True Keratinization Inferred relationship Some 3
Bullous ichthyosiform erythroderma Interprets True Keratinization Inferred relationship Some 3
Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering Interprets True Keratinization Inferred relationship Some 2
Rud's syndrome Interprets True Keratinization Inferred relationship Some 3
Hyperkeratotic eczema of palms and soles Interprets False Keratinization Inferred relationship Some 5
Hyperkeratotic eczema of soles Interprets False Keratinization Inferred relationship Some 3
Neu-Laxova syndrome Interprets True Keratinization Inferred relationship Some 4

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