Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
378446018 | Inherited cutis laxa | en | Synonym | Active | Case insensitive | SNOMED CT core |
645081011 | Inherited cutis laxa (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
SCARF syndrome | Is a | True | Inherited cutis laxa | Inferred relationship | Some | |
Localised congenital cutis laxa | Is a | True | Inherited cutis laxa | Inferred relationship | Some | |
Cutis laxa, x-linked | Is a | True | Inherited cutis laxa | Inferred relationship | Some | |
Cutis laxa, autosomal recessive | Is a | True | Inherited cutis laxa | Inferred relationship | Some | |
Cutis laxa, autosomal dominant | Is a | True | Inherited cutis laxa | Inferred relationship | Some | |
RIN2 syndrome | Is a | False | Inherited cutis laxa | Inferred relationship | Some | |
Neonatal cutis laxa with marfanoid phenotype | Is a | True | Inherited cutis laxa | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set