OMOP Concept 4178116
Familial hypomagnesemia-hypercalciuria
StandardConditionSNOMED50029007Disorder
Maps from
3
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Familial hypomagnesemia-hypercalciuria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 140567 | Familial hypomagnesemia-hypercalciuria | Non-standard |
| MeSH | C535709 | Manz syndrome | Non-standard |
| Nebraska Lexicon | 50029007 | Familial hypomagnesaemia-hypercalciuria | Non-standard |
Synonyms
Alternative names recorded for Familial hypomagnesemia-hypercalciuria across source vocabularies.
- Familial hypomagnesaemia-hypercalciuria
- Familial hypomagnesemia-hypercalciuria (disorder)
- hipomagnesemia-hipercalciuria familiar
- hipomagnesemia-hipercalciuria familiar (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(37)Roll up to these when you need a wider cohort.
- 1Hypercalciuria
- 1Primary hypomagnesemia
- 2Disorder of calcium metabolism
- 2Disorder of urinary system
- 2Hypomagnesemia
- 2Metabolic disorder of transport
- 2Urine calcium above reference range
- 3Disorder of phosphate, calcium and vitamin D metabolism
- 3Disorder of the genitourinary system
- 3Magnesium disorder
- 3Metabolic disease
- 3Urinary system finding
- 3Urine calcium outside reference range
- 3Urine substance level above reference range
- 4Disease
- 4Disorder of abdominopelvic segment of trunk
- 4Disorder of body system
- 4Disorder of electrolytes
- 4Disorder of mineral metabolism
- 4Finding of urine substance level
- 4Measurement finding above reference range
- 4Urine electrolytes outside reference range
- 4Urogenital finding
- 5Clinical finding
- 5Disorder of fluid AND/OR electrolyte
Narrower concepts
(3)Included automatically when you query with descendants.
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