SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Hereditary elliptocytosis due to beta spectrin defect in self-association   73073009

SNOMED CT code


SNOMED code73073009
nameHereditary elliptocytosis due to beta spectrin defect in self-association
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder)
synonymsHereditary elliptocytosis due to beta spectrin defect in self-association
attributes - group3
Has interpretationPresent   52101004
InterpretsHemolysis   404227002
attributes - group4
Pathological processPathological developmental process   308490002
Finding siteErythrocyte   41898006
Associated morphologyElliptocyte   45028007
OccurrenceCongenital   255399007
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsMeasurement of total hemoglobin concentration   441689006
attributes - group2
Has interpretationBelow reference range   281300000
InterpretsRed blood cell count   14089001
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary elliptocytosis   191169008
  • Anemia due to intrinsic red cell abnormality   323666000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Hereditary elliptocytosis due to beta spectrin defect in self-association   73073009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Hereditary elliptocytosis   191169008
            Hereditary elliptocytosis due to beta spectrin defect in self-association   73073009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Anemia   271737000
          Anemia due to intrinsic red cell abnormality   323666000
            Hereditary elliptocytosis due to beta spectrin defect in self-association   73073009

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

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