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Parent Node:
expanddisorder of magnesium transport (MONDO:0017765)
Parent Node:
expandinborn metal metabolism disorder (MONDO:0004689)
Parent Node:
expandinherited renal tubular disease (MONDO:0015962)
Parent Node:
expandrare renal tubular disease (MONDO:0019744)
..Starting node
..expandfamilial primary hypomagnesemia ()

       Child Nodes:
........expandfamilial primary hypomagnesemia with hypercalciuria and nephrocalcinosis ()
........expandfamilial primary hypomagnesemia with hypocalcuria ()
........expandfamilial primary hypomagnesemia with normocalcuria ()



 Sister Nodes: 
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..expanddominant hypophosphatemia with nephrolithiasis or osteoporosis ()
..expandEAST syndrome ()
..expandfamilial juvenile hyperuricemic nephropathy type 2 ()
..expandfamilial primary hypomagnesemia ()
..expandhereditary renal hypouricemia ()
..expandhyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome ()
..expandhypotonia-cystinuria syndrome type 1 ()
..expandidiopathic inherited hypercalciuria ()
..expandIgG4-related kidney disease ()
..expandJeune syndrome ()
..expandmitochondrial DNA depletion syndrome, hepatocerebrorenal form ()
..expandnephrogenic diabetes insipidus ()
..expandnephrogenic diabetes insipidus-intracranial calcification syndrome ()
..expandnephrogenic syndrome of inappropriate antidiuresis ()
..expandnephronophthisis (disease) ()
..expandoculocerebrorenal syndrome ()
..expandprimary renal tubular acidosis ()
..expandpseudohypoparathyroidism ()
..expandpsychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome ()
..expandrenal tubular transport disease ()
..expandRHYNS syndrome ()
..expandSenior-Boichis syndrome ()
..expandSenior-Loken syndrome ()
..expandtubulointerstitial nephritis and uveitis syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18100
Name:familial primary hypomagnesemia
Definition:A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.
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Synonyms:familial primary hypomagnesemia; HOMG; hypomagnesemia; primary familial hypomagnesemia
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Reference: MedGen:
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