Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency   717261006

SNOMED CT code


SNOMED code717261006
nameClassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
statusactive
date introduced2016-07-31
fully specified name(s)Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder)
synonymsClassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
attributes - group1
Finding siteAdrenal cortex structure   68594002
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyHyperplasia   76197007
attributes - group2
Due toDeficiency of steroid 21-monooxygenase   124221007
parentsCongenital adrenal hyperplasia   237751000
children
  • Steroid 21-monooxygenase deficiency, salt wasting type   71578002
  • Steroid 21-monooxygenase deficiency, simple virilizing type   52604008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Congenital adrenal hyperplasia   237751000
            Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency   717261006

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