SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Disorder of body system  362965005

Hereditary disorder by system  363137000

Hereditary disorder of cellular element of blood   414393003

SNOMED CT code


SNOMED code414393003
nameHereditary disorder of cellular element of blood
statusactive
date introduced2005-01-31
fully specified name(s)Hereditary disorder of cellular element of blood (disorder)
synonymsHereditary disorder of cellular element of blood
attributes - group1
Finding siteBody system structure   91689009
parents
  • Hereditary disorder by system   363137000
  • Disorder of cellular component of blood   414022008
children
  • Aase syndrome   71988008
  • CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation   1237417007
  • Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome   765327005
  • Ghosal hematodiaphyseal dysplasia   389214003
  • Hereditary red blood cell disorder   414394009
  • Hereditary white blood cell disorder   414395005
  • Inherited platelet disorder   234469001
  • Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness   237617006
  • Mitochondrial myopathy with sideroblastic anemia syndrome   724138007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Hereditary disorder by system   363137000
          Hereditary disorder of cellular element of blood   414393003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Hereditary disorder of cellular element of blood   414393003

ancestors
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