Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
98752012 | Cutis laxa, autosomal recessive | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
798295015 | Cutis laxa, autosomal recessive (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Cutis laxa, recessive, type I | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Existential restriction modifier | |
Cutis laxa, recessive, type II | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Existential restriction modifier | |
Macrocephaly, alopecia, cutis laxa, scoliosis syndrome | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Existential restriction modifier | |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Existential restriction modifier | |
Cutis laxa-corneal clouding-oligophrenia syndrome | Is a | True | Cutis laxa, autosomal recessive | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets