SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Obesity  414916001

Childhood obesity  444862003

Genetic non-syndromic obesity   1260139006

SNOMED CT code


SNOMED code1260139006
nameGenetic non-syndromic obesity
statusactive
date introduced2022-12-31
fully specified name(s)Genetic non-syndromic obesity (disorder)
synonymsGenetic non-syndromic obesity
attributes - group1
InterpretsBody weight measure   363808001
Has interpretationAbove reference range   281302008
attributes - group2
OccurrenceChildhood   255398004
parents
children
  • Congenital leptin deficiency   700150001
  • Obesity due to CEP19 deficiency   783549006
  • Obesity due to SIM1 deficiency   783719006
  • Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency   783556000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Obesity   414916001
        Childhood obesity   444862003
          Genetic non-syndromic obesity   1260139006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic non-syndromic obesity   1260139006

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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