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 |
| 378446018 | Inherited cutis laxa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 645081011 | Inherited cutis laxa (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| SCARF syndrome | est un(e) (attribut) | True | Inherited cutis laxa | Inferred relationship | Some | |
| Localized congenital cutis laxa (disorder) | est un(e) (attribut) | True | Inherited cutis laxa | Inferred relationship | Some | |
| Cutis laxa, x-linked (disorder) | est un(e) (attribut) | True | Inherited cutis laxa | Inferred relationship | Some | |
| Cutis laxa, autosomal recessive (disorder) | est un(e) (attribut) | True | Inherited cutis laxa | Inferred relationship | Some | |
| Cutis laxa, autosomal dominant | est un(e) (attribut) | True | Inherited cutis laxa | Inferred relationship | Some | |
| Macrocephaly, alopecia, cutis laxa, scoliosis syndrome (disorder) | est un(e) (attribut) | False | Inherited cutis laxa | Inferred relationship | Some | |
| Neonatal cutis laxa with marfanoid phenotype | est un(e) (attribut) | True | Inherited cutis laxa | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR