SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Dominant beta-thalassemia   716682000

SNOMED CT code


SNOMED code716682000
nameDominant beta-thalassemia
statusactive
date introduced2016-07-31
fully specified name(s)Dominant beta-thalassemia (disorder)
synonyms
  • Dominant beta-thalassemia
  • Inclusion body beta-thalassemia
  • Dominant beta-thalassaemia
  • Inclusion body beta-thalassaemia
attributes - group2
InterpretsMeasurement of total hemoglobin concentration   441689006
Has interpretationBelow reference range   281300000
attributes - group3
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
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
              Dominant beta-thalassemia   716682000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Thalassemia   40108008
            Beta thalassemia   65959000
              Dominant beta-thalassemia   716682000

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.

Access to this feature is available in the following products:
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