| 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 |