SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Isolated autosomal dominant hypomagnesemia Glaudemans type   722008003

SNOMED CT code


SNOMED code722008003
nameIsolated autosomal dominant hypomagnesemia Glaudemans type
statusactive
date introduced2017-01-31
fully specified name(s)Isolated autosomal dominant hypomagnesemia Glaudemans type (disorder)
synonyms
  • Isolated autosomal dominant hypomagnesemia Glaudemans type
  • Isolated autosomal dominant hypomagnesaemia Glaudemans type
parents
  • Autosomal dominant hereditary disorder   11164009
  • Primary hypomagnesemia   80710001
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
              Isolated autosomal dominant hypomagnesemia Glaudemans type   722008003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic disorder of transport   111394006
          Primary hypomagnesemia   80710001
            Isolated autosomal dominant hypomagnesemia Glaudemans type   722008003

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:
  • CPT® to SNOMED Crosswalks

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