Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire skin of plantar surface of foot and toe |
Is a |
False |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hereditary diffuse palmoplantar keratoderma |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Palmoplantar keratoderma transgrediens |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acroerythrokeratoderma |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Progressive palmoplantar keratoderma of Greither |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Epidermolytic palmoplantar keratoderma of Vorner |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diffuse palmoplantar keratoderma of Thost-Unna |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Haim Munk syndrome |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Diffuse palmoplantar keratoderma and acrocyanosis syndrome |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Palmoplantar keratoderma with clinodactyly syndrome (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Diffuse palmoplantar keratoderma with painful fissures |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Curly hair, acral keratoderma, caries syndrome (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Papillon-Lefèvre syndrome |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
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. |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
KRT1-related diffuse nonepidermolytic keratoderma |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome |
Finding site |
True |
Entire skin of sole of foot |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |