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 |
| 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 |
| 8215911000146114 | syndroom van osteopathia striata, pigmentaire dermatopathie en poliosis circumscripta | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8215921000146116 | syndroom van osteopathia striata, pigmentaire dermatopathie en witte haarlok | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8215931000146119 | syndroom van osteopathia striata, pigmentaire dermatopathie en poliosis circumscripta (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3775324013 | Syndrome with characteristics of the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular hyperpigmented dermopathy and a white forelock. It has been observed in a woman and her two daughters, whereas her son is unaffected. X-linked or autosomal dominant inheritance is proposed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Is a | White forelock | true | Inferred relationship | Some | ||
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Is a | Osteopathia striata | true | Inferred relationship | Some | ||
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Finding site | Hair structure (body structure) | true | Inferred relationship | Some | 3 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Is a | Inherited cutaneous hyperpigmentation | true | Inferred relationship | Some | ||
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Is a | Congenital anomaly of hair | true | Inferred relationship | Some | ||
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Has interpretation | Above reference range | true | Inferred relationship | Some | 4 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Interprets | Bone density scan | true | Inferred relationship | Some | 4 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Associated morphology | Hyperpigmentation | true | Inferred relationship | Some | 2 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets