Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital total lipodystrophy (disorder) | Is a | Lipodystrophy | true | Inferred relationship | Some | ||
Congenital total lipodystrophy (disorder) | Finding site | Subcutaneous fatty tissue | false | Inferred relationship | Some | 2 | |
Congenital total lipodystrophy (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Congenital total lipodystrophy (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
Congenital total lipodystrophy (disorder) | Is a | Congenital connective tissue disorder | true | Inferred relationship | Some | ||
Congenital total lipodystrophy (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Congenital total lipodystrophy (disorder) | Associated morphology | dégénérescence | false | Inferred relationship | Some | 1 | |
Congenital total lipodystrophy (disorder) | Associated morphology | dégénérescence | false | Inferred relationship | Some | 1 | |
Congenital total lipodystrophy (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Congenital total lipodystrophy (disorder) | Finding site | Subcutaneous fatty tissue | false | Inferred relationship | Some | 1 | |
Congenital total lipodystrophy (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Congenital total lipodystrophy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital total lipodystrophy (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 2 | |
Congenital total lipodystrophy (disorder) | Finding site | Subcutaneous fatty tissue | true | Inferred relationship | Some | 2 | |
Congenital total lipodystrophy (disorder) | Is a | Fetal and/or neonatal disorder of integument | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A rare form of genetic lipodystrophy, reported in 3 patients from one family to date, characterized by generalized congenital lipodystrophy, low birth weight, progressive sensorineural deafness occurring in childhood, intellectual deficit, progressive osteopenia, delayed skeletal maturation, skeletal abnormalities described as slender, undermineralized tubular bones, and dense metaphyseal striations in the distal femur, ulna and radius of older patients. Autosomal recessive inheritance has been suggested. | Is a | True | Congenital total lipodystrophy (disorder) | Inferred relationship | Some | |
Generalized congenital lipodystrophy with myopathy (disorder) | Is a | True | Congenital total lipodystrophy (disorder) | Inferred relationship | Some |
This concept is not in any reference sets