SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary disorder of endocrine system  363104002

Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency   725462002

SNOMED CT code


SNOMED code725462002
nameCongenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
statusactive
date introduced2017-07-31
fully specified name(s)Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder)
synonyms
  • Resistance to thyrotropin-releasing hormone syndrome
  • TRH (thyrotropin-releasing hormone) resistance syndrome
  • Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
attributes - group1
Due toPituitary thyroid hormone resistance   360348000
attributes - group2
OccurrenceCongenital   255399007
Finding siteThyroid structure   69748006
parents
  • Hereditary disorder of endocrine system   363104002
  • Congenital central hypothyroidism   722938007
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary disorder of endocrine system   363104002
          Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency   725462002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hypothyroidism   190268003
          Congenital central hypothyroidism   722938007
            Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency   725462002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency   725462002

ancestors
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