Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 98752012 | Cutis laxa, autosomal recessive | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 798295015 | Cutis laxa, autosomal recessive (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5990121000172110 | cutis laxa, forme autosomique récessive | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 5288881000172115 | autosomaal recessieve cutis laxa | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 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 | |
| Macrocephaly, alopecia, cutis laxa, scoliosis syndrome (disorder) | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Some | |
| Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (disorder) | 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 |
This concept is not in any reference sets