Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1770704014 | Genetic syndrome with hypermelanosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1781874019 | Genetic syndrome with hypermelanosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Genetic syndrome with hypermelanosis (disorder) | Is a | Hereditary hypermelanosis (disorder) | true | Inferred relationship | Some | ||
Genetic syndrome with hypermelanosis (disorder) | Associated morphology | Hyperpigmentation | false | Inferred relationship | Some | 1 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Structure of skin region | false | Inferred relationship | Some | 1 | |
Genetic syndrome with hypermelanosis (disorder) | Associated morphology | Melanosis | true | Inferred relationship | Some | 2 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Genetic syndrome with hypermelanosis (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Linear and whorled nevoid hypermelanosis (disorder) | Is a | True | Genetic syndrome with hypermelanosis (disorder) | Inferred relationship | Some | |
Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome is a rare, syndromic nail anomaly disorder characterized by the association of leukonychia totalis with acanthosis-nigricans-like lesions (occurring in the neck, axillae and abdomen regions) and hair dysplasia, manifesting with dry, brittle hair which presents an irregular pattern of complete or incomplete twists and an irregular surface with longitudinal furrows on electronic microscopy. | Is a | True | Genetic syndrome with hypermelanosis (disorder) | Inferred relationship | Some |
This concept is not in any reference sets