Status: current, Not 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 |
5045345015 | Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5045346019 | Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5045347011 | Retinal dystrophy, juvenile cataract, short stature syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5399968011 | A rare, genetic, syndromic rod-cone dystrophy disorder characterized by psychomotor developmental delay from early childhood, intellectual disability, short stature, mild facial dysmorphism (e.g. upslanted palpebral fissures, hypoplastic alae nasi, malar hypoplasia, attached earlobes), excessive dental spacing and malocclusion, juvenile cataract and ophthalmologic findings of atypical retinitis pigmentosa (i.e. salt-and-pepper retinopathy, attenuated retinal arterioles, generalized rod-cone dysfunction, mottled macula, peripapillary sparing of retinal pigment epithelium). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399969015 | A rare, genetic, syndromic rod-cone dystrophy disorder characterised by psychomotor developmental delay from early childhood, intellectual disability, short stature, mild facial dysmorphism (e.g. upslanted palpebral fissures, hypoplastic alae nasi, malar hypoplasia, attached earlobes), excessive dental spacing and malocclusion, juvenile cataract and ophthalmologic findings of atypical retinitis pigmentosa (i.e. salt-and-pepper retinopathy, attenuated retinal arterioles, generalised rod-cone dysfunction, mottled macula, peripapillary sparing of retinal pigment epithelium). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Is a | Autosomal recessive retinitis pigmentosa | true | Inferred relationship | Some | ||
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Is a | Short stature disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Is a | Juvenile cataract (disorder) | true | Inferred relationship | Some | ||
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Interprets | Body height (observable entity) | true | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Has interpretation | Below reference range | true | Inferred relationship | Some | 4 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Finding site | Face structure | true | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Finding site | Lens clear | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Associated morphology | Opacity | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Finding site | Retinal structure | true | Inferred relationship | Some | 2 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Associated morphology | Dystrophy | true | Inferred relationship | Some | 2 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 5 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 6 | |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 6 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)