Hypothyroidism due to mutation in transcription factor of pituitary development   718194004

SNOMED CT code


SNOMED code718194004
nameHypothyroidism due to mutation in transcription factor of pituitary development
statusactive
date introduced2016-07-31
fully specified name(s)Hypothyroidism due to mutation in transcription factor of pituitary development (disorder)
synonymsHypothyroidism due to mutation in transcription factor of pituitary development
attributes - group2
Due toCongenital anomaly of pituitary gland   74012004
attributes - group1
OccurrenceCongenital   255399007
Finding siteThyroid structure   69748006
parents
  • Congenital hypothyroidism   190268003
  • Hereditary disorder of endocrine system   363104002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hypothyroidism   190268003
          Hypothyroidism due to mutation in transcription factor of pituitary development   718194004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Hereditary disorder of endocrine system   363104002
            Hypothyroidism due to mutation in transcription factor of pituitary development   718194004

ancestors
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