Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308620010 | Punctate palmoplantar keratoderma type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308621014 | Buschke Fischer Brauer syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308622019 | Keratodermia palmoplantaris papulosa Buschke Fischer Brauer type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
927921000172118 | kératodermie palmoplantaire ponctuée type 1 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
1014201000172114 | KPPP1 - kératodermie palmoplantaire ponctuée type 1 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
877711000172117 | punctata puntvormige palmoplantaire keratodermie type 1 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
931501000172111 | syndroom van Buschke-Fischer-Brauer | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Punctate palmoplantar keratoderma type 1 (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Punctate palmoplantar keratoderma type 1 (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Punctate palmoplantar keratoderma type 1 (disorder) | Is a | Punctate palmoplantar keratoderma (disorder) | true | Inferred relationship | Some | ||
Punctate palmoplantar keratoderma type 1 (disorder) | Has definitional manifestation | Abnormal keratinization | false | Inferred relationship | Some | ||
Punctate palmoplantar keratoderma type 1 (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 3 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 4 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Interprets | Keratinization | false | Inferred relationship | Some | 1 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 2 | |
Punctate palmoplantar keratoderma type 1 (disorder) | Finding site | Skin structure of sole of foot (body structure) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set