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284449005: Congenital total lipodystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
423109014 Berardinelli's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
423110016 Lawrence-Seip syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
423111017 Seip's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
423112012 Congenital total lipodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
678342011 Congenital total lipodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1495355018 Lipoatrophic diabetes mellitus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1495356017 Total lipoatrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3029639016 Berardinelli-Seip congenital lipodystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3029702014 Congenital generalised lipodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3029742016 Congenital generalized lipodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3029802015 Beradinelli-Seip syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6052721000241118 LCBS - lipodystrophie congénitale de Berardinelli-Seip fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6052731000241116 lipodystrophie généralisée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


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

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