Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Palmoplantar keratoderma transgrediens |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acroerythrokeratoderma |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Progressive palmoplantar keratoderma of Greither |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Epidermolytic palmoplantar keratoderma of Vorner |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diffuse palmoplantar keratoderma of Thost-Unna |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Haim Munk syndrome |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diffuse palmoplantar keratoderma and acrocyanosis syndrome |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Palmoplantar keratoderma with clinodactyly syndrome (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Curly hair, acral keratoderma, caries syndrome (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diffuse palmoplantar keratoderma with painful fissures |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Papillon-Lefèvre syndrome |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
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. |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
KRT1-related diffuse nonepidermolytic keratoderma |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome |
Is a |
True |
Hereditary diffuse palmoplantar keratoderma |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|