Hypertension due to gain-of-function mutation in mineralocorticoid receptor   766937004

SNOMED CT code


SNOMED code766937004
nameHypertension due to gain-of-function mutation in mineralocorticoid receptor
statusactive
date introduced2018-07-31
fully specified name(s)Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
synonyms
  • Pseudohyperaldosteronism type 2
  • Early-onset hypertension with exacerbation in pregnancy
  • Hypertension due to gain-of-function mutation in mineralocorticoid receptor
attributes - group2
Finding siteSystemic circulatory system structure   51840005
attributes - group1
InterpretsBlood pressure   75367002
Has interpretationIncreased   35105006
parents
  • Autosomal dominant hereditary disorder   11164009
  • Secondary hypertension   31992008
  • Cardiovascular system hereditary disorder   363005004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Hypertension due to gain-of-function mutation in mineralocorticoid receptor   766937004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Cardiovascular measurement - finding   366157005
        Hypertensive disorder   38341003
          Secondary hypertension   31992008
            Hypertension due to gain-of-function mutation in mineralocorticoid receptor   766937004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Hypertension due to gain-of-function mutation in mineralocorticoid receptor   766937004

ancestors
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