Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
357982019 | Juvenile hyaline fibromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
357983012 | Puretic syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
357984018 | Systemic hyalinosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
4696609018 | Murray Puretic Drescher syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
627799017 | Juvenile hyaline fibromatosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4696770013 | A rare hyaline fibromatosis syndrome with characteristics of papulo-nodular skin lesions (especially around the head and neck), soft tissue masses, gingival hypertrophy, joint contractures and osteolytic bone lesions in variable degrees. Joint contractures may cripple patients and delay normal motor development if occurring in infancy. Severe gingival hyperplasia can interfere with eating and delay dentition. Histopathology analysis of involved tissues reveals cords of spindle-shaped cells embedded in an amorphous, hyaline material. | 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
Musculoskeletal finding reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set