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 |
3313331017 | Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3313332012 | Lissencephaly type 3 metacarpal bone dysplasia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401837010 | A rare syndromic form of lissencephaly characterized by severe microcephaly, agyria, agenesis of the corpus callosum, cerebellar hypoplasia, facial dysmorphology and epiphyseal stippling of the metacarpal bones. The syndrome may be an allelic variant of Neu-Laxova syndrome and Lissencephaly type III with cystic dilations of the cerebellum and fetal akinesia sequence. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401838017 | A rare syndromic form of lissencephaly characterised by severe microcephaly, agyria, agenesis of the corpus callosum, cerebellar hypoplasia, facial dysmorphology and epiphyseal stippling of the metacarpal bones. The syndrome may be an allelic variant of Neu-Laxova syndrome and Lissencephaly type III with cystic dilations of the cerebellum and fetal akinesia sequence. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Congenital anomaly of metacarpal bone (disorder) | true | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Lissencephaly | true | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Chondrodysplasia punctata | true | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 6 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 6 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Finding site | Structure of central nervous system (body structure) | false | Inferred relationship | Some | 6 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 5 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Finding site | Metacarpal bone structure (body structure) | false | Inferred relationship | Some | 5 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 4 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Finding site | Brain structure | false | Inferred relationship | Some | 4 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Finding site | Brain structure | true | Inferred relationship | Some | 2 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Finding site | Metacarpal bone structure (body structure) | true | Inferred relationship | Some | 1 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) | Is a | Congenital dysplasia of limb (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)