SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Genetic non-syndromic obesity  1260139006

Obesity due to CEP19 deficiency   783549006

SNOMED CT code


SNOMED code783549006
nameObesity due to CEP19 deficiency
statusactive
date introduced2019-07-31
fully specified name(s)Obesity due to centrosomal protein 19 deficiency (disorder)
synonyms
  • Obesity due to centrosomal protein 19 deficiency
  • Obesity due to CEP19 deficiency
attributes - group1
InterpretsBody weight measure   363808001
Has interpretationAbove reference range   281302008
attributes - group2
OccurrenceChildhood   255398004
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic non-syndromic obesity   1260139006
          Obesity due to CEP19 deficiency   783549006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Obesity   414916001
        Morbid obesity   238136002
          Obesity due to CEP19 deficiency   783549006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Obesity due to CEP19 deficiency   783549006

ancestors
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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:
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