SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Disorder of immune function  414029004

Hereditary disorder of immune system  363138005

Hereditary white blood cell disorder   414395005

SNOMED CT code


SNOMED code414395005
nameHereditary white blood cell disorder
statusactive
date introduced2005-01-31
fully specified name(s)Hereditary white blood cell disorder (disorder)
synonymsHereditary white blood cell disorder
attributes - group2
Pathological processAbnormal immune process   769247005
attributes - group1
Finding siteBody system structure   91689009
parents
  • Hereditary disorder of immune system   363138005
  • Hereditary disorder of cellular element of blood   414393003
  • White blood cell disorder   54097007
children
  • Ataxia pancytopenia syndrome   768556005
  • Chédiak-Higashi syndrome   111396008
  • Combined immunodeficiency, enteropathy spectrum   1197428008
  • Congenital neutropenia, myelofibrosis, nephromegaly syndrome   775909002
  • Familial hemophagocytic lymphohistiocytosis   398250003
  • Fanconi's anemia   30575002
  • Glutathione synthetase deficiency   234589002
  • Hennekam Beemer syndrome   722453009
  • Hereditary eosinophilia   191358004
  • Hereditary hypersegmentation   234435002
  • Hereditary isolated aplastic anemia   783255002
  • Hereditary neutrophilia   129639005
  • Heritable disorder of neutrophil function   402794002
  • Heritable disorder of neutrophil production   402793008
  • Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome   1186654001
  • Leukocyte adhesion deficiency   1187233008
  • Onycho-tricho-dysplasia neutropenia syndrome   1003381002
  • Pancytopenia with developmental delay syndrome   774071007
  • Periodic fever, infantile enterocolitis, autoinflammatory syndrome   1197594000
  • Poikiloderma with neutropenia   772126000
  • Reticular dysgenesis   111584000
  • Revesz syndrome   723512008
  • Severe combined immunodeficiency with reticular dysgenesis   190996002
  • Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome   1237618009
  • Shwachman syndrome   89454001
  • Warts, hypogammaglobulinemia, infections, and myelokathexis   234571003
  • WT limb blood syndrome   719019000
  • X-linked dyserythropoietic anemia with abnormal platelets and neutropenia   782759001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Hereditary disorder of immune system   363138005
          Hereditary white blood cell disorder   414395005

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
          Hereditary white blood cell disorder   414395005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        White blood cell disorder   54097007
          Hereditary white blood cell disorder   414395005

ancestors
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