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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
73614013 Keratinization, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
781231017 Keratinization (function) en Fully specified name Inactive Initial character 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
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome Interprets False Keratinisation Inferred relationship Some 1
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome Interprets True Keratinisation Inferred relationship Some 1
Leukokeratosis of skin Interprets True Keratinisation Inferred relationship Some 2
Leukokeratosis Interprets True Keratinisation Inferred relationship Some 1
Diffuse palmoplantar keratoderma with painful fissures Interprets True Keratinisation Inferred relationship Some 2
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome Interprets True Keratinisation Inferred relationship Some 4
Focal palmoplantar keratoderma with joint keratoses Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis hystrix Interprets True Keratinisation Inferred relationship Some 2
Severe ichthyoses Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis, oral and digital anomalies syndrome Interprets True Keratinisation Inferred relationship Some 4
Atypical ichthyosis vulgaris with hypogonadism Interprets True Keratinisation Inferred relationship Some 2
Congenital ichthyosis with hypotrichosis syndrome Interprets True Keratinisation Inferred relationship Some 3
Autosomal recessive ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Acral self-healing collodion baby Interprets True Keratinisation Inferred relationship Some 2
Keratitis ichthyosis and deafness syndrome Interprets True Keratinisation Inferred relationship Some 2
Syndromic recessive X-linked ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Autosomal recessive exfoliative ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis linearis circumflexa Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis hystrix gravior of Rheydt Interprets False Keratinisation Inferred relationship Some 2
Congenital non bullous ichthyosiform erythroderma Interprets True Keratinisation Inferred relationship Some 2
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome Interprets True Keratinisation Inferred relationship Some 4
Cutaneous syndrome with ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Bathing suit ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Limb reduction-ichthyosis syndrome Interprets True Keratinisation Inferred relationship Some 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome Interprets True Keratinisation Inferred relationship Some 2
Hystrix ichthyosis with deafness Interprets False Keratinisation Inferred relationship Some 2
Ichthyosis, cerebellar degeneration and hepatosplenomegaly Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis bullosa of Siemens Interprets True Keratinisation Inferred relationship Some 2
Non-bullous ichthyosiform erythroderma Interprets False Keratinisation Inferred relationship Some 2
Sjögren-Larsson syndrome Interprets True Keratinisation Inferred relationship Some 2
Erythrodermic lamellar ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis cheek eyebrow syndrome Interprets True Keratinisation Inferred relationship Some 3
Congenital cataract ichthyosis syndrome Interprets True Keratinisation Inferred relationship Some 3
Ichthyosis vulgaris Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome Interprets True Keratinisation Inferred relationship Some 4
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome Interprets True Keratinisation Inferred relationship Some 3
Congenital ichthyosis of skin Interprets True Keratinisation Inferred relationship Some 2
Osteosclerosis, ichthyosis, premature ovarian failure syndrome Interprets True Keratinisation Inferred relationship Some 4
Autosomal dominant ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Annular epidermolytic ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Lamellar ichthyosis (limited type) Interprets True Keratinisation Inferred relationship Some 2
Senter syndrome Interprets True Keratinisation Inferred relationship Some 3
Ichthyosis hystrix of Curth-Macklin Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis Interprets False Keratinisation Inferred relationship Some 2
Porcupine man Interprets False Keratinisation Inferred relationship Some 2
Lamellar ichthyosis AND trichorrhexis invaginata syndrome Interprets True Keratinisation Inferred relationship Some 2
Keratinopathic ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Autosomal dominant ichthyosis vulgaris Interprets True Keratinisation Inferred relationship Some 2
X-linked ichthyosis with steryl-sulfatase deficiency Interprets True Keratinisation Inferred relationship Some 2
Localised bullous ichthyosiform erythroderma Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis prematurity syndrome Interprets True Keratinisation Inferred relationship Some 2
Autosomal dominant lamellar ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis follicularis with alopecia and photophobia (IFAP) Interprets True Keratinisation Inferred relationship Some 2
Self-healing collodion baby Interprets True Keratinisation Inferred relationship Some 2
Lamellar ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome Interprets True Keratinisation Inferred relationship Some 4
Ichthyosis congenita with biliary atresia Interprets True Keratinisation Inferred relationship Some 3
Non-erythrodermic lamellar ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome Interprets True Keratinisation Inferred relationship Some 4
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome Interprets True Keratinisation Inferred relationship Some 5
Palmoplantar keratoderma, spastic paralysis syndrome Interprets True Keratinisation Inferred relationship Some 2
Harlequin ichthyosis Interprets True Keratinisation Inferred relationship Some 4
Netherton's syndrome Interprets True Keratinisation Inferred relationship Some 3
Hypotrichosis and deafness syndrome Interprets True Keratinisation Inferred relationship Some 3
Maleformatio ectodermalis generalisata of Bafverstedt Interprets True Keratinisation Inferred relationship Some 3
Bullous ichthyosiform erythroderma Interprets True Keratinisation Inferred relationship Some 3
Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering Interprets True Keratinisation Inferred relationship Some 2
Rud's syndrome Interprets True Keratinisation Inferred relationship Some 3
Hyperkeratotic eczema of hands and feet Interprets False Keratinisation Inferred relationship Some 5
Hyperkeratotic eczema of soles Interprets False Keratinisation Inferred relationship Some 3
Neu-Laxova syndrome Interprets True Keratinisation Inferred relationship Some 4
Rough skin Interprets True Keratinisation Inferred relationship Some 2
Rough skin of hands Interprets True Keratinisation Inferred relationship Some 2
Keratoderma hereditarium mutilans with ichthyosis syndrome Interprets False Keratinisation Inferred relationship Some 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Interprets False Keratinisation Inferred relationship Some 4
Hypotrichosis with keratosis pilaris and lentiginosis Interprets True Keratinisation Inferred relationship Some 3
Xeroderma of left eyelid Interprets False Keratinisation Inferred relationship Some 4
Xeroderma of right eyelid Interprets False Keratinisation Inferred relationship Some 4
Xeroderma of right upper eyelid Interprets False Keratinisation Inferred relationship Some 3
Xeroderma of left upper eyelid Interprets False Keratinisation Inferred relationship Some 3
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome Interprets True Keratinisation Inferred relationship Some 1
Harlequin fetus Interprets True Keratinisation Inferred relationship Some 4
Autosomal recessive epidermolytic ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Cutis gyrata syndrome of Beare and Stevenson Interprets True Keratinisation Inferred relationship Some 3
Systematised linear porokeratosis Interprets True Keratinisation Inferred relationship Some 2
Pityriasis rubra pilaris due to human immunodeficiency virus infection Interprets True Keratinisation Inferred relationship Some 3
Lichenoid keratosis Interprets False Keratinisation Inferred relationship Some 686841737
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome Interprets True Keratinisation Inferred relationship Some 6
Erythrokeratodermia cardiomyopathy syndrome Interprets True Keratinisation Inferred relationship Some 4
Congenital ichthyosis, microcephalus, tetraplegia syndrome Interprets True Keratinisation Inferred relationship Some 3
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome Interprets True Keratinisation Inferred relationship Some 3
PLACK syndrome Interprets True Keratinisation Inferred relationship Some 5
Generalised inflammatory peeling skin syndrome Interprets True Keratinisation Inferred relationship Some 4
Generalised non-inflammatory peeling skin syndrome Interprets True Keratinisation Inferred relationship Some 3
Ichthyosis hystrix gravior Interprets True Keratinisation Inferred relationship Some 2
Juvenile pityriasis rubra pilaris Interprets True Keratinisation Inferred relationship Some 2
Acquired paraneoplastic ichthyosis Interprets True Keratinisation Inferred relationship Some 2
Adult pityriasis rubra pilaris Interprets True Keratinisation Inferred relationship Some 2
Terra firma-forme dermatosis Interprets True Keratinisation Inferred relationship Some 2
O/E - rough skin Interprets False Keratinisation Inferred relationship Some 1
Abnormal keratinisation of hair follicle Interprets True Keratinisation Inferred relationship Some 1

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Reference Sets

Observable entity foundation reference set

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