SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Degenerative disorder  362975008

Lipodystrophy  71325002

Genetic lipodystrophy   724841000

SNOMED CT code


SNOMED code724841000
nameGenetic lipodystrophy
statusactive
date introduced2017-07-31
fully specified name(s)Genetic lipodystrophy (disorder)
synonymsGenetic lipodystrophy
attributes - group1
Associated morphologyDystrophy   4720007
Finding siteSubcutaneous fatty tissue   67769002
parents
children
  • Familial partial lipodystrophy   49292002
  • Generalized congenital lipodystrophy with myopathy   1156814008
  • Keppen Lubinsky syndrome   1220589007
  • Lipodystrophy, intellectual disability, deafness syndrome   721973006
  • Progeroid and marfanoid aspect, lipodystrophy syndrome   773644000
  • Severe neurodegenerative syndrome with lipodystrophy   773555005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Lipodystrophy   71325002
          Genetic lipodystrophy   724841000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic lipodystrophy   724841000

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

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