Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5408780019 | A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5408781015 | A rare primary bone dysplasia characterised by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3775321017 | Osteopathia striata, pigmentary dermopathy, white forelock syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3775322012 | Osteopathia striata, pigmentary dermopathy, white forelock syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3775323019 | Whyte Murphy syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5593021000241119 | syndrome d'ostéopathie striée, hyperpigmentation et mèche blanche | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1053181000195113 | Osteopathia striata - Hyperpigmentierung - weisse Stirnlocke | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Is a | White forelock | true | Inferred relationship | Some | ||
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Is a | Osteopathia striata | true | Inferred relationship | Some | ||
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Finding site | Hair structure (body structure) | true | Inferred relationship | Some | 3 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 3 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Is a | Inherited cutaneous hyperpigmentation | true | Inferred relationship | Some | ||
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Is a | Congenital anomaly of hair | true | Inferred relationship | Some | ||
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Has interpretation | Above reference range | true | Inferred relationship | Some | 4 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Interprets | Bone density scan | true | Inferred relationship | Some | 4 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Associated morphology | Hyperpigmentation | true | Inferred relationship | Some | 2 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. | Occurrence | Congenital | 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)