Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4696579011 | Hyaline fibromatosis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
4696580014 | Hyaline fibromatosis syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4696582018 | A rare genetic disease characterised by infantile or childhood onset of abnormal growth of hyalinised fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhoea, increased susceptibility to infections, and severe failure to thrive. | en | Definition | Active | Case sensitive | SNOMED CT core |
4696583011 | A rare genetic disease characterized by infantile or childhood onset of abnormal growth of hyalinized fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhea, increased susceptibility to infections, and severe failure to thrive. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Juvenile hyaline fibromatosis | Is a | True | Hyaline fibromatosis syndrome | Inferred relationship | Some | |
Infantile systemic hyalinosis | Is a | True | Hyaline fibromatosis syndrome | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Musculoskeletal finding reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set