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 |