FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

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
6990271000241111 hyperkératose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

26 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperkeratosis Is a Hyperplasia true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hyperkeratotic eczema of palms and soles Associated morphology True Hyperkeratosis Inferred relationship Some 5
Progressive palmoplantar keratoderma of Greither Associated morphology True Hyperkeratosis Inferred relationship Some 3
Progressive palmoplantar keratoderma of Greither Associated morphology True Hyperkeratosis Inferred relationship Some 4
Progressive palmoplantar keratoderma of Greither Associated morphology True Hyperkeratosis Inferred relationship Some 5
Palmoplantar keratoderma transgrediens Associated morphology True Hyperkeratosis Inferred relationship Some 3
Palmoplantar keratoderma transgrediens Associated morphology True Hyperkeratosis Inferred relationship Some 4
Acroerythrokeratoderma (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 3
Acroerythrokeratoderma (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 4
Autosomal recessive epidermolytic ichthyosis (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 1
Hyperkeratosis of vulva Associated morphology True Hyperkeratosis Inferred relationship Some 1
A hereditary palmoplantar keratoderma with characteristics of the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques. Associated morphology True Hyperkeratosis Inferred relationship Some 1
Pachyonychia congenita syndrome Associated morphology True Hyperkeratosis Inferred relationship Some 2
Pachyonychia congenita syndrome Associated morphology True Hyperkeratosis Inferred relationship Some 4
Pachyonychia congenita type II of Jackson-Lawler (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 2
Pachyonychia congenita type II of Jackson-Lawler (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 4
Pachyonychia congenita type III of Schafer-Brunauer (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 2
Pachyonychia congenita type III of Schafer-Brunauer (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 4
A form of peeling skin syndrome characterized by a generalized distribution. It comprises two sub-types: the non-inflammatory (PSS type A) and the inflammatory (PSS type B) form. PSS type A is characterized by generalized white scaling with superficial non-inflammatory peeling of the skin, while PSS type B is characterized by superficial patchy peeling of the entire skin with underlying erythroderma, pruritus, and atopy. Associated morphology True Hyperkeratosis Inferred relationship Some 3
A group of rare autosomal recessive forms of ichthyosis clinically characterized by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution for generalized PSS type A (noninflammatory) or B (inflammatory). Associated morphology True Hyperkeratosis Inferred relationship Some 1
Acral peeling skin syndrome Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare skin disease characterized by transient wrinkling of the skin, edema, formation of whitish papules, pruritus, burning sensation, or pain, on the palms and/or soles in response to contact with water. Duration of exposure and water temperature affect the rate of development and intensity of the lesions. The condition is more common in females than in males and frequently occurs in patients with cystic fibrosis. Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare skin disease characterized by transient wrinkling of the skin, edema, formation of whitish papules, pruritus, burning sensation, or pain, on the palms and/or soles in response to contact with water. Duration of exposure and water temperature affect the rate of development and intensity of the lesions. The condition is more common in females than in males and frequently occurs in patients with cystic fibrosis. Associated morphology True Hyperkeratosis Inferred relationship Some 2
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 6
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 8
Hyperkeratosis of female perineum Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare autosomal ichthyosis syndrome with prominent neurologic signs characterized by the association of congenital ichthyosis with severe developmental delay, microcephaly, spastic tetraplegia, sensorineural hearing impairment, athetosis, and myoclonus. Marked epileptic discharges with occurrence of tonic spasms have also been reported. Cerebral MRI shows diffuse cortical atrophy. There have been no further descriptions in the literature since 1995. Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare autosomal ichthyosis syndrome with prominent neurologic signs characterized by the association of congenital ichthyosis with global developmental delay, intellectual disability, infantile-onset seizures, and spastic tetraplegia. Brain imaging may show delayed myelination and cerebral atrophy. Marked intrafamilial variability has been reported. Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare genetic disease characterised by abnormalities in renal ion transport, ectodermal gland homeostasis, and epidermal integrity, resulting in generalised hypohidrosis, heat intolerance, salt-losing nephropathy, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, and xerostomia. Development of nephrolithiasis and severe enamel wear have also been described. Laboratory findings include hypermagnesaemia, hypokalaemia, hypercalcaemia, and hypocalciuria. Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare, genetic, isolated diffuse palmoplantar keratoderma characterized by diffuse, mild to thick, finely demarcated hyperkeratosis of palms and soles. Additional clinical findings include knuckle pad-like keratoses on fingers, hyperkeratosis of umbilicus and areolae, diffuse dry skin, hyperhidrosis, hangnails and frequent fungal infections. Histological examination of lesions reveals orthokeratotic hyperkeratosis, acanthosis, hypergranulosis, and mild lymphocyte infiltrations in the upper dermis with no evidence of epidermolysis. Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare, genetic, isolated diffuse palmoplantar keratoderma characterized by diffuse, mild to thick, finely demarcated hyperkeratosis of palms and soles. Additional clinical findings include knuckle pad-like keratoses on fingers, hyperkeratosis of umbilicus and areolae, diffuse dry skin, hyperhidrosis, hangnails and frequent fungal infections. Histological examination of lesions reveals orthokeratotic hyperkeratosis, acanthosis, hypergranulosis, and mild lymphocyte infiltrations in the upper dermis with no evidence of epidermolysis. Associated morphology True Hyperkeratosis Inferred relationship Some 2
A rare, genetic, autosomal dominant hereditary axonal motor and sensory neuropathy disorder characterized by childhood-onset palmoplantar keratoderma associated with motor and sensory polyneuropathy manifesting with late-onset, predominantly distal, lower limb muscle weakness and atrophy (later associating mild proximal weakness and upper limb involvement), moderate sensory impairment (hypoesthesia with stocking-glove distribution), and normal or near-normal nerve conduction velocities. Additional variable manifestations include impaired vibratory sensation, reduced tendon reflexes, paresthesia, pain, talipes equinovarus, pes cavus, and nail dystrophy. Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare, genetic, autosomal dominant hereditary axonal motor and sensory neuropathy disorder characterized by childhood-onset palmoplantar keratoderma associated with motor and sensory polyneuropathy manifesting with late-onset, predominantly distal, lower limb muscle weakness and atrophy (later associating mild proximal weakness and upper limb involvement), moderate sensory impairment (hypoesthesia with stocking-glove distribution), and normal or near-normal nerve conduction velocities. Additional variable manifestations include impaired vibratory sensation, reduced tendon reflexes, paresthesia, pain, talipes equinovarus, pes cavus, and nail dystrophy. Associated morphology True Hyperkeratosis Inferred relationship Some 2
A rare genetic skin disease characterised by infantile onset of diffuse alopecia, abnormal skin pigmentation (hypo- and hyperpigmented macules of the trunk and face and areas of reticular hypo- and hyperpigmentation of the extremities), palmoplantar keratoderma, and nail dystrophy. Patients develop recurrent spinocellular carcinomas later in life. Brittle teeth resulting in early loss of dentition have also been described. Associated morphology True Hyperkeratosis Inferred relationship Some 2
A rare genetic skin disease characterised by infantile onset of diffuse alopecia, abnormal skin pigmentation (hypo- and hyperpigmented macules of the trunk and face and areas of reticular hypo- and hyperpigmentation of the extremities), palmoplantar keratoderma, and nail dystrophy. Patients develop recurrent spinocellular carcinomas later in life. Brittle teeth resulting in early loss of dentition have also been described. Associated morphology True Hyperkeratosis Inferred relationship Some 3
A rare epidermal disease characterized by the association of punctate acrokeratoderma with a pigmentary disorder. Patients present skin-colored keratotic papules on the hands and feet and pronounced hyperkeratosis of the palms and soles. Freckle-like pigmentation on the dorsal surfaces of the hands and feet is also reported. Histological examination reveals no fragmentation of dermal elastic tissue. There have been no further descriptions in the literature since 1993. Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare epidermal disease characterized by the association of punctate acrokeratoderma with a pigmentary disorder. Patients present skin-colored keratotic papules on the hands and feet and pronounced hyperkeratosis of the palms and soles. Freckle-like pigmentation on the dorsal surfaces of the hands and feet is also reported. Histological examination reveals no fragmentation of dermal elastic tissue. There have been no further descriptions in the literature since 1993. Associated morphology True Hyperkeratosis Inferred relationship Some 2
Callus of forefoot Associated morphology True Hyperkeratosis Inferred relationship Some 1
Generalized inflammatory peeling skin syndrome Associated morphology True Hyperkeratosis Inferred relationship Some 1
Generalized non-inflammatory peeling skin syndrome Associated morphology True Hyperkeratosis Inferred relationship Some 1
Hyperkeratosis of hindfoot (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 1
Ichthyosis hystrix gravior (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 1
Acquired ichthyosis due to paraneoplastic syndrome (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 1
Drug-induced ichthyosiform reaction Associated morphology True Hyperkeratosis Inferred relationship Some 2
Thermal keratosis Associated morphology True Hyperkeratosis Inferred relationship Some 1
Talar callosity Associated morphology True Hyperkeratosis Inferred relationship Some 1
Keratosis following radiotherapy (disorder) Associated morphology True Hyperkeratosis Inferred relationship Some 1
A rare ectodermal dysplasia syndrome characterized by hypotrichosis, tooth enamel hypoplasia, hypoplastic nails, palmoplantar keratoderma, hyperhidrosis on hands, face, and scalp, bilateral partial cutaneous syndactyly, and dysmorphic facial features with large prominent ear pinnae, pointed nose, and thin upper lips. Association of cardiomegaly has also been reported. Associated morphology True Hyperkeratosis Inferred relationship Some 2
A rare ectodermal dysplasia syndrome characterized by hypotrichosis, tooth enamel hypoplasia, hypoplastic nails, palmoplantar keratoderma, hyperhidrosis on hands, face, and scalp, bilateral partial cutaneous syndactyly, and dysmorphic facial features with large prominent ear pinnae, pointed nose, and thin upper lips. Association of cardiomegaly has also been reported. Associated morphology True Hyperkeratosis Inferred relationship Some 3
Lichen planus-like keratosis (morphologic abnormality) Is a True Hyperkeratosis Inferred relationship Some
Solar lentigo Is a True Hyperkeratosis Inferred relationship Some
Debridement of callus (procedure) Direct morphology True Hyperkeratosis Inferred relationship Some 1
Malignant acanthosis nigricans Associated morphology True Hyperkeratosis Inferred relationship Some 1
Keratosis of middle ear Associated morphology True Hyperkeratosis Inferred relationship Some 1
Schöpf-Schulz-Passarge syndrome Associated morphology True Hyperkeratosis Inferred relationship Some 2
Schöpf-Schulz-Passarge syndrome Associated morphology True Hyperkeratosis Inferred relationship Some 3

Start Previous Page 6 of 6

This concept is not in any reference sets

Back to Start