Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3643799015 | KLICK syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3643800016 | Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3643801017 | Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643802012 | An inherited epidermal disorder with characteristics of 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. The disease is caused by homozygous mutation in the POMP gene. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure of palmar area of hand | false | Inferred relationship | Some | 2 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 4 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Erythrokeratodermia variabilis | false | Inferred relationship | Some | ||
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure of sole of foot | false | Inferred relationship | Some | 4 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Entire skin | true | Inferred relationship | Some | 1 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Hereditary diffuse palmoplantar keratoderma | true | Inferred relationship | Some | ||
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Rough skin of hands | true | Inferred relationship | Some | ||
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Entire skin of palmar area of hand | true | Inferred relationship | Some | 2 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Entire skin of sole of foot | true | Inferred relationship | Some | 4 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Mutilating keratoderma | false | Inferred relationship | Some | ||
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | Autosomal recessive ichthyosis | true | Inferred relationship | Some | ||
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Has interpretation | Abnormal | true | Inferred relationship | Some | 3 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Interprets | Keratinisation | true | Inferred relationship | Some | 3 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set