FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

284449005: Congenital total lipodystrophy (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1495355018 Lipoatrophic diabetes mellitus en Synonym Active Case insensitive SNOMED CT core
1495356017 Total lipoatrophy en Synonym Active Case insensitive SNOMED CT core
3029639016 Berardinelli-Seip congenital lipodystrophy en Synonym Active Case sensitive SNOMED CT core
3029702014 Congenital generalised lipodystrophy en Synonym Active Case insensitive SNOMED CT core
3029742016 Congenital generalized lipodystrophy en Synonym Active Case insensitive SNOMED CT core
3029802015 Beradinelli-Seip syndrome en Synonym Active Case sensitive SNOMED CT core
423109014 Berardinelli's syndrome en Synonym Active Case sensitive SNOMED CT core
423110016 Lawrence-Seip syndrome en Synonym Active Case sensitive SNOMED CT core
423111017 Seip's syndrome en Synonym Active Case sensitive SNOMED CT core
423112012 Congenital total lipodystrophy en Synonym Active Case insensitive SNOMED CT core
678342011 Congenital total lipodystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital generalised lipodystrophy Is a Lipodystrophy true Inferred relationship Some
Congenital generalised lipodystrophy Is a Congenital connective tissue disorder true Inferred relationship Some
Congenital generalised lipodystrophy Occurrence Congenital false Inferred relationship Some
Congenital generalised lipodystrophy Associated morphology Degeneration false Inferred relationship Some 1
Congenital generalised lipodystrophy Associated morphology Degeneration false Inferred relationship Some 1
Congenital generalised lipodystrophy Finding site Skin structure false Inferred relationship Some 1
Congenital generalised lipodystrophy Finding site Subcutaneous fatty tissue false Inferred relationship Some 1
Congenital generalised lipodystrophy Associated morphology Dystrophy false Inferred relationship Some 1
Congenital generalised lipodystrophy Occurrence Congenital true Inferred relationship Some 2
Congenital generalised lipodystrophy Associated morphology Dystrophy true Inferred relationship Some 2
Congenital generalised lipodystrophy Finding site Subcutaneous fatty tissue true Inferred relationship Some 2
Congenital generalised lipodystrophy Finding site Subcutaneous fatty tissue false Inferred relationship Some 2
Congenital generalised lipodystrophy Finding site Skin structure false Inferred relationship Some 1
Congenital generalised lipodystrophy Associated morphology Dystrophy false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Generalised congenital lipodystrophy with myopathy Is a True Congenital generalised lipodystrophy Inferred relationship Some
Lipodystrophy, intellectual disability, deafness syndrome Is a True Congenital generalised lipodystrophy Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start