Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
798295015 | Cutis laxa, autosomal recessive (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
98752012 | Cutis laxa, autosomal recessive | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
RIN2 syndrome | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Some | |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Some | |
Cutis laxa-corneal clouding-oligophrenia syndrome | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Some | |
Cutis laxa, recessive, type I | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Some | |
Cutis laxa, recessive, type II | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set