Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Neu-Laxova syndrome |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
4 |
Rough skin (finding) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Rough skin of hands |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) |
Interprets |
False |
Keratinization |
Inferred relationship |
Some |
3 |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) |
Interprets |
False |
Keratinization |
Inferred relationship |
Some |
4 |
Hypotrichosis with keratosis pilaris and lentiginosis |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
3 |
Xeroderma of left eyelid |
Interprets |
False |
Keratinization |
Inferred relationship |
Some |
4 |
Xeroderma of right eyelid (disorder) |
Interprets |
False |
Keratinization |
Inferred relationship |
Some |
4 |
Xeroderma of right upper eyelid |
Interprets |
False |
Keratinization |
Inferred relationship |
Some |
3 |
Xeroderma of left upper eyelid |
Interprets |
False |
Keratinization |
Inferred relationship |
Some |
3 |
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
1 |
Harlequin fetus |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
4 |
Autosomal recessive epidermolytic ichthyosis (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Cutis gyrata syndrome of Beare and Stevenson |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
3 |
Systematised linear porokeratosis |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Pityriasis rubra pilaris due to human immunodeficiency virus infection (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
3 |
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
6 |
Erythrokeratodermia cardiomyopathy syndrome |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
4 |
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
3 |
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
3 |
Peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads syndrome (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
5 |
Generalized inflammatory peeling skin syndrome |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
4 |
Generalized non-inflammatory peeling skin syndrome |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
3 |
Ichthyosis hystrix gravior (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Juvenile pityriasis rubra pilaris (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Acquired ichthyosis due to paraneoplastic syndrome (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Adult pityriasis rubra pilaris |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Terra firma-forme dermatosis (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
2 |
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) |
Interprets |
True |
Keratinization |
Inferred relationship |
Some |
3 |