Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5403615011 | An exceedingly rare association characterized by cleft lip and progressive retinopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403616012 | An exceedingly rare association characterised by cleft lip and progressive retinopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3464561015 | Cleft lip retinopathy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3464562010 | Cleft lip retinopathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3464563017 | Ausems Wittebol Post Hennekam syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Is a | Cleft lip | true | Inferred relationship | Some | ||
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Is a | Autosomal recessive retinitis pigmentosa | true | Inferred relationship | Some | ||
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Is a | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Associated morphology | dysgenese | false | Inferred relationship | Some | 3 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Finding site | Structure of internal part of mouth | false | Inferred relationship | Some | 3 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Associated morphology | Dystrophy | false | Inferred relationship | Some | 4 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Finding site | Retinal structure | false | Inferred relationship | Some | 4 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Associated morphology | Developmental failure of fusion (morphologic abnormality) | false | Inferred relationship | Some | 5 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Finding site | Lip structure | false | Inferred relationship | Some | 5 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Finding site | Lip structure | true | Inferred relationship | Some | 1 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Associated morphology | Developmental failure of fusion (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Is a | Congenital anomaly of retina | true | Inferred relationship | Some | ||
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Finding site | Retinal structure | true | Inferred relationship | Some | 2 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Associated morphology | Dystrophy | true | Inferred relationship | Some | 2 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Is a | Hereditary disorder of musculoskeletal system | false | Inferred relationship | Some | ||
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Finding site | Bone structure of head | false | Inferred relationship | Some | 3 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Associated morphology | Developmental failure of fusion (morphologic abnormality) | false | Inferred relationship | Some | 3 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 3 | |
An exceedingly rare association characterized by cleft lip and progressive retinopathy. | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)