Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2008. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2690878011 | Congenital hypoplasia of fovea centralis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
2693410016 | Congenital hypoplasia of fovea centralis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2694076018 | Congenital hypoplasia of fovea | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Foveal hypoplasia with presenile cataract syndrome | Is a | True | Congenital hypoplasia of fovea centralis | Inferred relationship | Existential restriction modifier | |
Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome | Is a | True | Congenital hypoplasia of fovea centralis | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets