SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Hemoglobinopathy Toms River   782880001

SNOMED CT code


SNOMED code782880001
nameHemoglobinopathy Toms River
statusactive
date introduced2019-07-31
fully specified name(s)Hemoglobinopathy Toms River (disorder)
synonyms
  • Haemoglobinopathy Toms River
  • Hemoglobinopathy Toms River
  • Transient neonatal cyanosis and anemia due to Toms River Hemoglobin
  • Transient neonatal cyanosis and anaemia due to Toms River Haemoglobin
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary hemoglobinopathy   427306008
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
              Hemoglobinopathy Toms River   782880001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Hemoglobinopathy Toms River   782880001

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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