SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Homozygous hemoglobinopathy   123772008

SNOMED CT code


SNOMED code123772008
nameHomozygous hemoglobinopathy
statusactive
date introduced2002-01-31
fully specified name(s)Homozygous hemoglobinopathy (disorder)
synonyms
  • Homozygous hemoglobinopathy
  • Homozygous haemoglobinopathy
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsHereditary hemoglobinopathy   427306008
children
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Homozygous hemoglobinopathy   123772008

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.