SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital hypothyroidism  190268003

Transient congenital hypothyroidism due to dual oxidase 2 mutation   1142106007

SNOMED CT code


SNOMED code1142106007
nameTransient congenital hypothyroidism due to dual oxidase 2 mutation
statusactive
date introduced2021-07-31
fully specified name(s)Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
synonymsTransient congenital hypothyroidism due to dual oxidase 2 mutation
attributes - group1
Finding siteThyroid structure   69748006
OccurrenceCongenital   255399007
attributes - group2
Due toChromosomal disorder   409709004
attributes - group3
Clinical courseTransitory   14803004
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hypothyroidism   190268003
          Transient congenital hypothyroidism due to dual oxidase 2 mutation   1142106007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Acute disease   2704003
        Transient hypothyroidism   2917005
          Transient congenital hypothyroidism due to dual oxidase 2 mutation   1142106007

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