Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement   725033008

SNOMED CT code


SNOMED code725033008
nameFamilial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
statusactive
date introduced2017-07-31
fully specified name(s)Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)
synonyms
  • Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
  • Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
  • Renal hypomagnesemia type 3
  • Renal hypomagnesaemia type 3
attributes - group1
Finding siteStructure of parenchyma of kidney   29704000
Associated morphologyPathologic calcification   18115005
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Hereditary nephropathy   367591000119105
              Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement   725033008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic renal disease   106000008
          Nephrocalcinosis   48638002
            Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement   725033008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic disorder of transport   111394006
          Primary hypomagnesemia   80710001
            Familial hypomagnesemia-hypercalciuria   50029007
              Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement   725033008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement   725033008

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

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.