OMOP Concept 1075448
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
StandardConditionSNOMED1304111007Disorder
Maps from
0
Descendants
2
Valid from
1 Mar 2024
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis across source vocabularies.
- Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (disorder)
- FHHNC - familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- FHHNC - familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- hipomagnesemia familiar primaria con hipercalciuria y nefrocalcinosis
- hipomagnesemia familiar primaria con hipercalciuria y nefrocalcinosis (trastorno)
- Michellis Castrillo syndrome
- Primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- Primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- síndrome de Michellis Castrillo
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(59)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Familial hypomagnesemia-hypercalciuria
- 1Hereditary nephropathy
- 1Nephrocalcinosis
- 2Autosomal hereditary disorder
- 2Calcinosis
- 2Disorder of calcium metabolism
- 2Disorder of renal parenchyma
- 2Hereditary disorder of the urinary system
- 2Hypercalciuria
- 2Kidney disease
- 2Kidney lesion
- 2Metabolic renal disease
- 2Primary hypomagnesemia
- 3Degenerative disorder
- 3Disorder of kidney and/or ureter
- 3Disorder of phosphate, calcium and vitamin D metabolism
- 3Disorder of retroperitoneum
- 3Disorder of urinary system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hypomagnesemia
- 3Kidney finding
- 3Metabolic disease
- 3Metabolic disorder of transport
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Narrower concepts
(2)Included automatically when you query with descendants.
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