Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3757278012 | Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3757279016 | Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3757280018 | Atypical dentin dysplasia due to SMOC2 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3757281019 | Dentin dysplasia type 1 with microdontia and shape anomalies | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Finding site | Dentin structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Is a | Digestive system hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Associated morphology | Dysplasia | true | Inferred relationship | Existential restriction modifier | 1 | |
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Is a | Dentin dysplasia | true | Inferred relationship | Existential restriction modifier | ||
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency | Is a | Developmental hereditary disorder | false | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets