SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Hereditary hypercarotenemia and vitamin A deficiency   726079008

SNOMED CT code


SNOMED code726079008
nameHereditary hypercarotenemia and vitamin A deficiency
statusactive
date introduced2017-07-31
fully specified name(s)Hereditary hypercarotenemia and vitamin A deficiency (disorder)
synonyms
  • Hereditary hypercarotenemia and vitamin A deficiency
  • Hereditary hypercarotenaemia and vitamin A deficiency
attributes - group1
OccurrenceCongenital   255399007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Inborn error of metabolism   86095007
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
              Hereditary hypercarotenemia and vitamin A deficiency   726079008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Hereditary hypercarotenemia and vitamin A deficiency   726079008

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

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.