SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital hypothyroidism  190268003

Congenital central hypothyroidism   722938007

SNOMED CT code


SNOMED code722938007
nameCongenital central hypothyroidism
statusactive
date introduced2017-01-31
fully specified name(s)Congenital central hypothyroidism (disorder)
synonymsCongenital central hypothyroidism
attributes - group1
Finding siteThyroid structure   69748006
OccurrenceCongenital   255399007
parents
childrenCongenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency   725462002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hypothyroidism   190268003
          Congenital central hypothyroidism   722938007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of neck   118939000
        Disorder of thyroid gland   14304000
          Hypothyroidism   40930008
            Central hypothyroidism   26692000
              Congenital central hypothyroidism   722938007

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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