Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3311230010 | Piebaldism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3311231014 | Piebaldism | en | Synonym | Active | Case insensitive | SNOMED CT core |
3311232019 | Piebaldism is a rare congenital pigmentation skin disorder with characteristic of the presence of hypopigmented and depigmented skin areas (leukoderma) on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock (poliosis), and in some cases with hypopigmented and depigmented eyebrows and eyelashes. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Piebaldism | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Piebaldism | Associated morphology | Hypopigmentation | true | Inferred relationship | Some | 1 | |
Piebaldism | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Piebaldism | Is a | Congenital deficiency of pigment of skin | true | Inferred relationship | Some | ||
Piebaldism | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Piebaldism | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Piebaldism | Associated morphology | Congenital hypopigmentation | false | Inferred relationship | Some | 1 | |
Piebaldism | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Piebaldism | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Piebaldism | Is a | Genetic disorder of skin pigmentation | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set