Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3324386011 | Blepharonasofacial malformation syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3324387019 | Blepharonasofacial malformation syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3324388012 | Pashayan syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3324389016 | Pashayan Prozansky syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401631014 | Blepharonasofacial syndrome is a rare otorhinolaryngological malformation syndrome characterized by a distinctive mask-like facial dysmorphism, lacrimal duct obstruction, extrapyramidal features, digital malformations and intellectual disability. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401632019 | Blepharonasofacial syndrome is a rare otorhinolaryngological malformation syndrome characterised by a distinctive mask-like facial dysmorphism, lacrimal duct obstruction, extrapyramidal features, digital malformations and intellectual disability. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Blepharonasofacial malformation syndrome (disorder) | Is a | Hereditary disease | false | Inferred relationship | Some | ||
Blepharonasofacial malformation syndrome (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Blepharonasofacial malformation syndrome (disorder) | Is a | Mental retardation | false | Inferred relationship | Some | ||
Blepharonasofacial malformation syndrome (disorder) | Is a | Congenital anomaly of nose | true | Inferred relationship | Some | ||
Blepharonasofacial malformation syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
Blepharonasofacial malformation syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Blepharonasofacial malformation syndrome (disorder) | Finding site | Nasal structure | true | Inferred relationship | Some | 1 | |
Blepharonasofacial malformation syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Blepharonasofacial malformation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Blepharonasofacial malformation syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Blepharonasofacial malformation syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Blepharonasofacial malformation syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 2 | |
Blepharonasofacial malformation syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Blepharonasofacial malformation syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 3 | |
Blepharonasofacial malformation syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)