Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3333781016 | PTEN hamartoma tumor syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3333782011 | PTEN hamartoma tumor syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3333783018 | PTEN hamartoma tumour syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3644901010 | A term defining a group of clinically heterogeneous disorders united by a germline PTEN mutation and the involvement of derivatives of all 3 germ cell layers, manifesting with hamartomas, overgrowth and neoplasia. Disease onset depends on the specific disorder. The most important component seen in this group are malignancies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 979041000172117 | PHTS - PTEN hamartoma tumor syndrome | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| 1008541000172118 | syndrome tumoral hamartomateux lié à PTEN | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 923431000172116 | PHTS - phosphatase and tensin homolog hamartoomtumor-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| 991561000172118 | PTEN-hamartoomtumorsyndroom | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cowden syndrome | Is a | True | PTEN hamartoma tumor syndrome (disorder) | Inferred relationship | Some | |
| Bannayan syndrome | Is a | True | PTEN hamartoma tumor syndrome (disorder) | Inferred relationship | Some | |
| Proteus like syndrome (disorder) | Is a | True | PTEN hamartoma tumor syndrome (disorder) | Inferred relationship | Some | |
| Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | Is a | True | PTEN hamartoma tumor syndrome (disorder) | Inferred relationship | Some |
This concept is not in any reference sets