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 |
3316235018 | Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3316236017 | Leukoencephalopathy with metaphyseal chondrodysplasia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3789576010 | Leucoencephalopathy with metaphyseal chondrodysplasia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5402096016 | A rare genetic neurological disorder characterized by the association of hypomyelinating leukodystrophy with spondylometaphyseal dysplasia. Patients present in infancy with absent or delayed ability to walk independently, slowly progressive motor deterioration, spasticity, ataxia, proximal weakness, and joint contractures. Additional manifestations include mild cognitive impairment, short stature, scoliosis, enlarged and deformed joints, dysarthria, nystagmus, visual defects, and mildly dysmorphic features, among others. Mode of inheritance is X-linked recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402097013 | A rare genetic neurological disorder characterised by the association of hypomyelinating leucodystrophy with spondylometaphyseal dysplasia. Patients present in infancy with absent or delayed ability to walk independently, slowly progressive motor deterioration, spasticity, ataxia, proximal weakness, and joint contractures. Additional manifestations include mild cognitive impairment, short stature, scoliosis, enlarged and deformed joints, dysarthria, nystagmus, visual defects, and mildly dysmorphic features, among others. Mode of inheritance is X-linked recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Leukoencephalopathy | true | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Metaphyseal chondrodysplasia | true | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Finding site | Cerebral white matter structure | true | Inferred relationship | Some | 2 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 3 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 3 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Interprets | Height / growth measure | true | Inferred relationship | Some | 3 | |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Is a | Cerebral degeneration (disorder) | true | Inferred relationship | Some | ||
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)