Moderate steroid 21-hydroxylase deficiency   60045007

SNOMED CT code


SNOMED code60045007
nameModerate steroid 21-hydroxylase deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Moderate steroid 21-hydroxylase deficiency (disorder)
synonymsModerate steroid 21-hydroxylase deficiency
attributes - group1
OccurrenceCongenital   255399007
Finding siteAdrenal cortex structure   68594002
parents
  • Deficiency of steroid 21-monooxygenase   124221007
  • Hereditary disorder of endocrine system   363104002
  • Autosomal recessive hereditary disorder   85995004
  • Inborn error of metabolism   86095007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of steroid metabolism   28710006
          Deficiency of steroid 21-monooxygenase   124221007
            Moderate steroid 21-hydroxylase deficiency   60045007

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
            Moderate steroid 21-hydroxylase deficiency   60045007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Moderate steroid 21-hydroxylase deficiency   60045007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Moderate steroid 21-hydroxylase deficiency   60045007

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