Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5066409018 | Familial congenital nasolacrimal duct obstruction (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5066410011 | Familial congenital nasolacrimal duct obstruction | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5066411010 | A rare genetic otorhinolaryngological malformation with characteristics of congenital impatency of the nasolacrimal drainage system in various members of a family. Presentation is not specific and may include a uni or bilateral medial canthal mass, dacryocystitis, nasal obstruction, periorbital cellulitis and epiphora. Dacryocystocele and lacrimal puncta agenesis may be associated. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5609561000052114 | familjär medfödd obstruktion av nästårgång | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial congenital nasolacrimal duct obstruction (disorder) | Is a | Familial disease | true | Inferred relationship | Some | ||
Familial congenital nasolacrimal duct obstruction (disorder) | Is a | Congenital nasolacrimal duct obstruction | true | Inferred relationship | Some | ||
Familial congenital nasolacrimal duct obstruction (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Familial congenital nasolacrimal duct obstruction (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Familial congenital nasolacrimal duct obstruction (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Familial congenital nasolacrimal duct obstruction (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Familial congenital nasolacrimal duct obstruction (disorder) | Finding site | Nasolacrimal duct structure | true | Inferred relationship | Some | 1 | |
Familial congenital nasolacrimal duct obstruction (disorder) | Associated morphology | Obstruction | true | Inferred relationship | Some | 1 | |
Familial congenital nasolacrimal duct obstruction (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets