Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Bowenoid actinic keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Inverted follicular keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Acquired palmoplantar keratoderma |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Hyperkeratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Primary seborrhea |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Diffuse palmoplantar keratoderma of Thost-Unna |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Keratosis rubra pilaris |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Keratosis pilaris atrophicans |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Porokeratosis |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Acrokeratosis verruciformis of Hopf |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary diffuse palmoplantar keratoderma |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Xerosis due to atopic dermatitis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Nail dystrophy due to pityriasis rubra pilaris |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Follicular hyperkeratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Acanthosis nigricans of oral mucous membranes |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Retention hyperkeratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Retention hyperkeratosis due to neglect |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Desquamation of skin following febrile illness |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Drug-induced desquamation of skin |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Desquamation secondary to acute systemic illness |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Acanthosis nigricans |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Xeroderma in genetic syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Punctate palmoplantar keratoderma |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Lichenoid actinic keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Acantholytic actinic keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Atrophic actinic keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Proliferative actinic keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Multiple actinic keratoses |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Multiple actinic keratoses involving scalp |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Multiple actinic keratoses involving face |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Multiple actinic keratoses involving forehead and temples |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Multiple actinic keratoses involving hands |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Multiple actinic keratoses involving lower limbs |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Diffuse actinic hyperkeratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Pachyonychia congenita type II of Jackson-Lawler |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Pachyonychia congenita type III of Schafer-Brunauer |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Actinic keratosis of eyelid |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Pigmented actinic keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Hyperkeratotic actinic keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Acral keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Severe achondrolasia with developmental delay and acanthosis nigricans |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
4 |
Xeroderma of lower eyelid |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Xeroderma of upper eyelid |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Crouzon syndrome with acanthosis nigricans |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital reticular ichthyosiform erythroderma |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Palmoplantar keratoderma |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Keratoderma |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Orthokeratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Punctate palmoplantar keratoderma type 1 |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary palmoplantar keratoderma Gamborg Nielsen type |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Generalized peeling skin syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Ectodermal dysplasia with acanthosis nigricans syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Curly hair, acral keratoderma, caries syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
4 |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Wooly hair with palmoplantar keratoderma syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
7 |
Striate palmoplantar keratoderma |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Focal palmoplantar and gingival keratoderma |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Arsenical keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
4 |
Superficial keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Punctate palmoplantar keratoderma type 2 |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Tar keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Palmoplantar keratoderma with deafness syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital keratoderma |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Disseminated superficial porokeratosis |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Ulerythema ophryogenes |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Radiation-induced keratosis |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Arthrogryposis hyperkeratosis syndrome lethal form |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
4 |
Palmoplantar keratoderma with clinodactyly syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Palmoplantar keratoderma Nagashima type |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant palmoplantar keratoderma and congenital alopecia |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
4 |
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Linear porokeratosis |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Diffuse palmoplantar keratoderma and acrocyanosis syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Xeroderma pigmentosum and Cockayne syndrome complex |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Spinocerebellar ataxia type 34 |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Acral peeling skin syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Van den Bosch syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
4 |
Ankylosing vertebral hyperostosis with tylosis syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Cutaneous horn |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary skin peeling syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
7 |
Porokeratosis plantaris palmaris et disseminata |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Hyperkeratosis of mucous membrane of mouth due to and following traumatic injury |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Keratoderma hereditarium mutilans with ichthyosis syndrome |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Haim Munk syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Trichodysplasia xeroderma syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |
Xeroderma, talipes and enamel defect syndrome |
Interprets |
False |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
2 |
Classical juvenile pityriasis rubra pilaris |
Interprets |
True |
Keratinization, function |
Inferred relationship |
Existential restriction modifier |
3 |