SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital immunodeficiency disease  36138009

Severe combined immunodeficiency disease  31323000

SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation  3439009

Reticular dysgenesis   111584000

SNOMED CT code


SNOMED code111584000
nameReticular dysgenesis
statusactive
date introduced2002-01-31
fully specified name(s)Reticular dysgenesis (disorder)
synonyms
  • Reticular dysgenesis
  • De Vaal disease
  • Immunoerythromyeloid hypoplasia
  • Severe combined immunodeficiency, neutropaenia and thrombocytopaenia
  • SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia
  • Congenital aleukia
  • Reticular dysgenesia
  • Generalised haematopoietic hypoplasia
  • Generalized hematopoietic hypoplasia
  • SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia
  • Severe combined immunodeficiency, neutropenia and thrombocytopenia
attributes - group3
OccurrenceCongenital   255399007
attributes - group4
Pathological processAbnormal immune process   769247005
attributes - group2
Finding siteImmune system structure   116003000
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsNeutrophil count   30630007
parents
  • SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation   3439009
  • Disorder of immune structure   414030009
  • Hereditary white blood cell disorder   414395005
  • Congenital neutropenia   89655007
children
  • De Vaal's syndrome   350353007
  • Reticular dysgenesis with congenital aleukocytosis   351287008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital immunodeficiency disease   36138009
          Severe combined immunodeficiency disease   31323000
            SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation   3439009
              Reticular dysgenesis   111584000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of immune structure   414030009
          Reticular dysgenesis   111584000

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
            Reticular dysgenesis   111584000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital immunodeficiency disease   36138009
          Congenital neutropenia   89655007
            Reticular dysgenesis   111584000

ancestors
sorted most to least specific
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