Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3331138017 | Palmoplantar keratoderma with deafness syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3331139013 | Palmoplantar keratoderma with deafness syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3331140010 | A keratinization disorder characterized by focal or diffuse palmoplantar keratoderma. A patchy distribution is observed with accentuation on the thenar, hypothenar and the arches of the feet. The disease becomes apparent in infancy and is associated with sensorineural hearing loss that shows a variable age of onset. The disease is transmitted in an autosomal dominant manner with incomplete penetrance. Caused by heterozygous mutation in the gene encoding connexin-26 (GJB2; 121011) on chromosome 13q12. | en | Definition | Active | Case sensitive | SNOMED CT core |
3331141014 | A keratinisation disorder characterised by focal or diffuse palmoplantar keratoderma. A patchy distribution is observed with accentuation on the thenar, hypothenar and the arches of the feet. The disease becomes apparent in infancy and is associated with sensorineural hearing loss that shows a variable age of onset. The disease is transmitted in an autosomal dominant manner with incomplete penetrance. Caused by heterozygous mutation in the gene encoding connexin-26 (GJB2; 121011) on chromosome 13q12. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Palmoplantar keratoderma with deafness syndrome | Finding site | Skin structure of sole of foot | true | Inferred relationship | Some | 2 | |
Palmoplantar keratoderma with deafness syndrome | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 5 | |
Palmoplantar keratoderma with deafness syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
Palmoplantar keratoderma with deafness syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 5 | |
Palmoplantar keratoderma with deafness syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Palmoplantar keratoderma with deafness syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Is a | Sensorineural hearing loss | true | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Is a | Congenital hearing disorder | false | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Is a | Hereditary palmoplantar keratoderma | true | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Finding site | Structure of auditory system | true | Inferred relationship | Some | 3 | |
Palmoplantar keratoderma with deafness syndrome | Has definitional manifestation | Abnormal keratinisation | false | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Interprets | Hearing | true | Inferred relationship | Some | 4 | |
Palmoplantar keratoderma with deafness syndrome | Interprets | Functional observable | false | Inferred relationship | Some | ||
Palmoplantar keratoderma with deafness syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 6 | |
Palmoplantar keratoderma with deafness syndrome | Finding site | Skin structure | false | Inferred relationship | Some | 6 | |
Palmoplantar keratoderma with deafness syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 7 | |
Palmoplantar keratoderma with deafness syndrome | Finding site | Skin structure | false | Inferred relationship | Some | 7 | |
Palmoplantar keratoderma with deafness syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 6 | |
Palmoplantar keratoderma with deafness syndrome | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 7 | |
Palmoplantar keratoderma with deafness syndrome | Interprets | Keratinisation | false | Inferred relationship | Some | 2 | |
Palmoplantar keratoderma with deafness syndrome | Has interpretation | Abnormal | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set