SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Congenital malformation  276654001

Congenital anomaly of the hematopoietic system   40888008

SNOMED CT code


SNOMED code40888008
nameCongenital anomaly of the hematopoietic system
statusactive
date introduced2002-01-31
fully specified name(s)Congenital anomaly of the hematopoietic system (disorder)
synonyms
  • Congenital anomaly of the haematopoietic system
  • Congenital anomaly of the hematopoietic system
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteHematopoietic system structure   57171008
parents
children
  • Amino acid deficiency anemia   65560000  removed: 2018-07-31
  • Congenital anomaly of spleen   57497006
  • Congenital anomaly of the thymus   38824008
  • Congenital asymmetry of tonsils   445554007
  • Congenital hypoplastic anemia   88854002
  • Congenital pulmonary lymphatic dysplasia syndrome   708022000
  • Congenital thrombocytopenia   10386005  removed: 2009-01-31
  • Constitutional aplastic anemia   28975000
  • HNSHA due to aldolase A deficiency   111578003  removed: 2022-01-31
  • Kernicterus due to isoimmunization   206433007  removed: 2002-07-31
  • Muscle phosphofructokinase deficiency   234406005  removed: 2015-01-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital anomaly of the hematopoietic system   40888008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of hematopoietic structure   414027002
          Congenital anomaly of the hematopoietic system   40888008

ancestors
sorted most to least specific
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