Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 3643799015 | KLICK syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 3643800016 | Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 3643801017 | Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Mutilating keratoderma | false | Inferred relationship | Existential restriction modifier | ||
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Autosomal recessive ichthyosis | true | Inferred relationship | Existential restriction modifier | ||
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Has interpretation | Abnormal | true | Inferred relationship | Existential restriction modifier | 3 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Interprets | Keratinization, function | true | Inferred relationship | Existential restriction modifier | 3 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 2 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Developmental anomaly | false | Inferred relationship | Existential restriction modifier | 1 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure | false | Inferred relationship | Existential restriction modifier | 2 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Existential restriction modifier | 2 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure | false | Inferred relationship | Existential restriction modifier | 1 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Existential restriction modifier | 1 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure of palmar area of hand | false | Inferred relationship | Existential restriction modifier | 2 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Existential restriction modifier | 4 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Erythrokeratodermia variabilis | false | Inferred relationship | Existential restriction modifier | ||
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure of sole of foot | false | Inferred relationship | Existential restriction modifier | 4 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Entire skin | true | Inferred relationship | Existential restriction modifier | 1 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Hereditary diffuse palmoplantar keratoderma | true | Inferred relationship | Existential restriction modifier | ||
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Rough skin of hands | true | Inferred relationship | Existential restriction modifier | ||
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Entire skin of palmar area of hand | true | Inferred relationship | Existential restriction modifier | 2 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Entire skin of sole of foot | true | Inferred relationship | Existential restriction modifier | 4 | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets