SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Perilipin 1 related familial partial lipodystrophy   783616005

SNOMED CT code


SNOMED code783616005
namePerilipin 1 related familial partial lipodystrophy
statusactive
date introduced2019-07-31
fully specified name(s)Perilipin 1 related familial partial lipodystrophy (disorder)
synonyms
  • PLIN1-related familial partial lipodystrophy
  • FPLD4 - familial partial lipodystrophy type 4
  • Perilipin 1 related familial partial lipodystrophy
attributes - group1
Associated morphologyDystrophy   4720007
Finding siteSubcutaneous fatty tissue   67769002
attributes - group3
Finding siteTrunk structure   22943007
attributes - group4
Finding siteLimb structure   66019005
attributes - group2
Finding siteEndocrine structure   113331007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Connective tissue hereditary disorder   363045008
  • Hereditary disorder of endocrine system   363104002
  • Hereditary disorder of the integument   363185004
  • Familial partial lipodystrophy   49292002
  • Insulin resistance   763325000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Perilipin 1 related familial partial lipodystrophy   783616005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Connective tissue hereditary disorder   363045008
          Perilipin 1 related familial partial lipodystrophy   783616005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Hereditary disorder of endocrine system   363104002
            Perilipin 1 related familial partial lipodystrophy   783616005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Perilipin 1 related familial partial lipodystrophy   783616005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of trunk structure   302292003
      Disorder of trunk   128121009
        Familial partial lipodystrophy   49292002
          Perilipin 1 related familial partial lipodystrophy   783616005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Insulin resistance   763325000
            Perilipin 1 related familial partial lipodystrophy   783616005

ancestors
sorted most to least specific
cpt crosswalks

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