Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308619016 | Punctate palmoplantar keratoderma type 1 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3308620010 | Punctate palmoplantar keratoderma type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3308621014 | Buschke Fischer Brauer syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3308622019 | Keratodermia palmoplantaris papulosa Buschke Fischer Brauer type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3308623012 | A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also present later in life. Mutations in the AAGAB gene (15q22.33-q23) have recently been identified as one of the causes. Mutations in the COL14A1 gene (8q23) have also been identified as causal in some cases in Asia that seem to have a similar phenotype | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set