SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Familial primary hypomagnesemia with normocalciuria  717788000

Familial primary hypomagnesemia with normocalciuria and normocalcemia   725031005

SNOMED CT code


SNOMED code725031005
nameFamilial primary hypomagnesemia with normocalciuria and normocalcemia
statusactive
date introduced2017-07-31
fully specified name(s)Familial primary hypomagnesemia with normocalciuria and normocalcemia (disorder)
synonyms
  • Familial primary hypomagnesemia with normocalciuria and normocalcemia
  • Familial primary hypomagnesaemia with normocalciuria and normocalcemia
  • FPHNN - familial primary hypomagnesemia with normocalciuria and normocalcemia
  • FPHNN - familial primary hypomagnesaemia with normocalciuria and normocalcemia
parentsFamilial primary hypomagnesemia with normocalciuria   717788000
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
            Familial primary hypomagnesemia with normocalciuria   717788000
              Familial primary hypomagnesemia with normocalciuria and normocalcemia   725031005

ancestors
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