OMOP Concept 4029602
Disorder of phosphate, calcium and vitamin D metabolism
StandardConditionSNOMED237879001Disorder
Maps from
1
Descendants
116
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Disorder of phosphate, calcium and vitamin D metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 237879001 | Disorder of phosphate, calcium and vitamin D metabolism | Non-standard |
Synonyms
Alternative names recorded for Disorder of phosphate, calcium and vitamin D metabolism across source vocabularies.
- Disorder of phosphate, calcium and vitamin D metabolism (disorder)
- trastorno del metabolismo del fósforo, del calcio y de la vitamina D
- trastorno del metabolismo del fósforo, del calcio y de la vitamina D (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(116)Included automatically when you query with descendants.
- 1Acid phosphatase deficiency
- 1Disorder of calcium metabolism
- 1Disorder of phosphorus metabolism
- 1Hyperphosphatasemia with bone disease
- 1Hypophosphatasia
- 1Osteopetrosis with renal tubular acidosis
- 1Phosphorus and calcium disorders
- 1Pseudohyperparathyroidism
- 2Adult hypophosphatasia
- 2Childhood hypophosphatasia
- 2Hypercalcemia
- 2Hypercalciuria
- 2Hyperphosphatasemia with intellectual disability
- 2Hyperphosphatemia
- 2Hyperphosphaturia
- 2Hypocalcemia
- 2Hypocalciuria
- 2Hypophosphatemia
- 2Hypophosphaturia
- 2Infantile hypophosphatasia
- 2Inverted serum calcium to serum phosphorus ratio
- 2Nephrocalcinosis
- 2Odontohypophosphatasia
- 2Renal phosphaturia
- 2Tumoral calcinosis
- 3Acquired hypocalciuric hypercalcemia
- 3Acquired hypophosphatemia
- 3Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome
- 3Autosomal dominant hypocalcemia
- 3Autosomal dominant hypophosphatemic bone disease
- 3Autosomal dominant primary hypomagnesemia with hypocalciuria
- 3Autosomal recessive hypophosphatemic bone disease
- 3Bartter syndrome
- 3Drug-induced hypocalcemia
- 3Enamel-renal syndrome
- 3Exacerbation of hypercalcemia
- 3Familial hypocalciuric hypercalcemia
- 3Familial hypomagnesemia-hypercalciuria
- 3Familial idiopathic hypercalciuria
- 3Familial normophosphatemic tumoral calcinosis
- 3Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- 3Familial x-linked hypophosphatemic vitamin D refractory rickets
- 3Hereditary hypophosphatemic rickets with hypercalciuria
- 3Humoral hypercalcemia of malignancy
- 3Hungry bone syndrome
- 3Hypercalcemia associated with chronic dialysis
- 3Hypercalcemia caused by a drug
- 3Hypercalcemia caused by thiazide and/or retinol
- 3Hypercalcemia due to chronic kidney disease
- 3Hypercalcemia due to granulomatous disease
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