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26996000: Hyperkeratosis (morphologic abnormality)


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
45144017 Hyperkeratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45145016 Keratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45148019 Excessive cornification en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45149010 Skin callus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45150010 Callosity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45151014 Keratoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45152019 Tyloma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45153012 Tylosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
757512010 Hyperkeratosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
45144017 Hyperkeratosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45144017 Hyperkeratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45145016 Keratosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45145016 Keratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45148019 Excessive cornification en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45148019 Excessive cornification en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45149010 Skin callus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45149010 Skin callus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45150010 Callosity en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45150010 Callosity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45151014 Keratoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45151014 Keratoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45152019 Tyloma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45152019 Tyloma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
45153012 Tylosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
45153012 Tylosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
757512010 Hyperkeratosis (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
757512010 Hyperkeratosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


26 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperkeratosis Is a Hyperplasia true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Palmoplantar keratoderma with leukoplakia (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Porokeratosis of Mibelli, superficial disseminated type Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Papillon-Lefèvre syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Papillon-Lefèvre syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Diffuse palmoplantar keratoderma of Thost-Unna Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary diffuse palmoplantar keratoderma Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Retention hyperkeratosis (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Retention hyperkeratosis due to neglect Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Punctate palmoplantar keratoderma (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Superficial keratosis Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Pretalar callosity (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Cutaneous horn (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Callosity on hand (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired keratoderma palmaris et plantaris Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Plantar callosity (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Follicular atrophoderma with palmoplantar hyperkeratosis (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Follicular atrophoderma with palmoplantar hyperkeratosis (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Keratosis caused by radiation Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Tar keratosis (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Keratoderma blennorrhagicum Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hidrotic ectodermal dysplasia syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Hidrotic ectodermal dysplasia syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Cole disease Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Cole disease Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Formation of an epidermal layer which lacks nuclei during normal keratinisation. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Acral keratosis Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Acral keratosis Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmoplantar keratoderma Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Neu-Laxova syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare genetic ectodermal dysplasia syndrome characterised by woolly hair (presenting at birth), palmoplantar keratoderma (developing in the first year of life) and dilated cardiomyopathy with predominant left ventricle involvement (developing in childhood) which can lead to life-threatening heart failure in childhood or adolescence. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic ectodermal dysplasia syndrome characterised by woolly hair (presenting at birth), palmoplantar keratoderma (developing in the first year of life) and dilated cardiomyopathy with predominant left ventricle involvement (developing in childhood) which can lead to life-threatening heart failure in childhood or adolescence. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Haim Munk syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare dysostosis with predominant vertebral involvement characterized by paraspinal ligament ossification (most pronounced in the lower thoracic region), osteophytosis, marginal sacroiliac joint sclerosis, and punctate hyperkeratosis on the soles and palms. Patients may be asymptomatic or present mild to moderate back pain. There have been no further descriptions in the literature since 1969. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
A rare dysostosis with predominant vertebral involvement characterized by paraspinal ligament ossification (most pronounced in the lower thoracic region), osteophytosis, marginal sacroiliac joint sclerosis, and punctate hyperkeratosis on the soles and palms. Patients may be asymptomatic or present mild to moderate back pain. There have been no further descriptions in the literature since 1969. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse palmoplantar keratoderma and acrocyanosis syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Diffuse palmoplantar keratoderma and acrocyanosis syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Palmoplantar keratoderma with deafness syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Palmoplantar keratoderma with deafness syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Palmoplantar keratoderma with clinodactyly syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Palmoplantar keratoderma with clinodactyly syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Arthrogryposis hyperkeratosis syndrome lethal form Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
Focal palmoplantar keratoderma with joint keratoses Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Diffuse palmoplantar keratoderma with painful fissures Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 7
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 8
Curly hair, acral keratoderma, caries syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 8
Curly hair, acral keratoderma, caries syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 7
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome is an inherited epidermal disorder characterised by palmoplantar keratoderma, linear hyperkeratotic papules on the flexural side of large joints (cord-like distribution around wrists, in antecubital and popliteal folds), hyperkeratotic plaques (on neck, axillae, elbows, wrists, and knees), mild ichthyosiform scaling, and sclerotic constrictions around fingers that present flexural deformities. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Wooly hair with palmoplantar keratoderma syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Wooly hair with palmoplantar keratoderma syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Striate palmoplantar keratoderma Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Striate palmoplantar keratoderma Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 8
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 7
Punctate palmoplantar keratoderma type 2 is a type of isolated, punctate, hereditary palmoplantar keratoderma characterized by multiple, asymptomatic, 1 to 2 mm-long, firm, hyperkeratotic projections (spiny keratosis) on the palms, soles and digits (typically confined to their volar and/or lateral aspects). Histopathologically, compact columnar parakeratosis over hypo- or agranular epidermis is observed. Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
Porokeratosis of Mibelli, linear unilateral type Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Palmoplantar keratoderma, spastic paralysis syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Arsenical keratosis Is a True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept)
Psoralen and long-wave ultraviolet radiation keratosis (morphologic abnormality) Is a True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept)
Rough skin (finding) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Rough skin of hands (finding) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Keratitis ichthyosis and deafness syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Lymphedematous hyperkeratosis Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Keratosis (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperkeratotic eczema of palms and soles (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Hyperkeratotic eczema of soles Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Ulerythema of cheeks Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Harlequin fetus Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperkeratotic eczema of palms Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperkeratotic fissured eczema of palms (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Hyperkeratotic eczema of palms and soles (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5

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