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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
Diffuse palmoplantar keratoderma of Thost-Unna Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Enucleation of corn Direct morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Inflammatory hyperkeratotic dermatosis, chronic Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Acrokerato-elastoidosis Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Acrokerato-elastoidosis Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Palmar hyperkeratosis of yaws Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired plantar keratoderma (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Palmar callosity (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Enucleation of corn Direct morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Removal of corn sinus Direct morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Keratoderma areata Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Keratoderma with mental retardation and spastic paraplegia Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Mutilating keratoderma Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal dominant mutilating keratoderma Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
A hereditary palmoplantar keratoderma with characteristics of the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques. Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital keratoderma Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Keratoderma with pachyonychia congenita Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Keratoderma punctata Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Leukoplakia of penis Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Epidermolytic palmoplantar keratoderma of Vorner Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Excessive keratinized residual ridge mucosa (finding) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Keratoderma (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Minimal keratinized residual ridge mucosa (finding) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary diffuse palmoplantar keratoderma Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary palmoplantar keratoderma Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal hyperkeratosis Is a True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept)
Punctate palmoplantar keratoderma (disorder) 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) 2
Keratoderma with deafness Associated morphology False 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) 1
Palmar hyperkeratosis of yaws Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Plantar hyperkeratosis of yaws Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Hyperkeratosis of yaws Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Palmar callosity (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Cole disease Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Gonococcal keratosis Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Syndromic recessive X-linked ichthyosis (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept)
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
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 False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 7
Self-healing collodion baby Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
Acral self-healing collodion baby Associated morphology False 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 False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 7
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 False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 8
Haim Munk syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
Diffuse palmoplantar keratoderma and acrocyanosis syndrome Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
MEDNIK syndrome Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 5
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma 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 False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Palmoplantar keratoderma with deafness syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 7
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Palmoplantar keratoderma with clinodactyly syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
callosité causée par le fait de mordre et/ou de mâcher Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity on toe Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity between toes (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity under metatarsal head Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Senile keratoma Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Apical callus Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Foot callus Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Prayer nodule Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse callus Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Pinch callus Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity on hand (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity resulting from occupation Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity due to habit tic (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callosity caused by prosthesis and/or appliance (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Plantar callosity (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Pretalar callosity (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial painful callosities (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Callus of heel (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may include eye involvement (optic atrophy, diplopia), neuromuscular involvement (ataxia, pyramidal syndrome, gait disturbance) and sensory disorder. There have been no further descriptions in the literature since 1992. Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 7
callosité causée par le fait de mordre et/ou de mâcher Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Onychophosis (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperkeratosis of mucous membrane of mouth due to and following traumatic injury Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 6
Arsenical keratosis (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Wooly hair with palmoplantar keratoderma syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
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) 1
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
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) 2
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) 1
Curly hair, acral keratoderma, caries syndrome (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome is an ectodermal dysplasia syndrome characterised by severe generalised lamellar icthyosis at birth with alopecia, eclabium, ectropion and intellectual disability. Although similar to Sjögren-Larsson syndrome, this syndrome lacks the presence of neurologic or macular changes. There have been no further descriptions in the literature since 1987. Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 4
Curly hair, acral keratoderma, caries syndrome (disorder) Associated morphology True 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) 2
Hereditary benign acanthosis nigricans (disorder) Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Acanthosis nigricans due to type 2 diabetes mellitus Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary benign acanthosis nigricans with insulin resistance Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3
Acanthosis palmaris Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary benign acanthosis nigricans (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Drug-induced acanthosis nigricans Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired acanthosis nigricans (disorder) Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign acanthosis nigricans Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary benign acanthosis nigricans with insulin resistance Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Malignant acanthosis nigricans Associated morphology False Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 2
Leukoencephalopathy, palmoplantar keratoderma syndrome Associated morphology True Hyperkeratosis Inferred relationship Existential restriction modifier (core metadata concept) 3

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