OMOP Concept 46272736
Autosomal dominant hypocalcemia
StandardConditionSNOMED711152006Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2015
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant hypocalcemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | E20.810 | Autosomal dominant hypocalcemia | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant hypocalcemia across source vocabularies.
- Autosomal dominant hypocalcaemia
- Autosomal dominant hypocalcemia (disorder)
- Autosomal dominant hypoparathyroidism
- Familial hypercalciuric hypocalcaemia
- Familial hypercalciuric hypocalcemia
- Familial hypocalcaemia
- Familial hypocalcemia
- hipocalcemia autosómica dominante
- hipocalcemia autosómica dominante (trastorno)
- hipocalcemia familiar
- hipocalcemia hipercalciúrica familiar
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Familial isolated hypoparathyroidism
- 1Hypocalcemia
- 2Autosomal hereditary disorder
- 2Disorder of calcium metabolism
- 2Hereditary disorder of endocrine system
- 2Hypoparathyroidism
- 3Decreased hormone secretion
- 3Disorder of endocrine system
- 3Disorder of parathyroid gland
- 3Disorder of phosphate, calcium and vitamin D metabolism
- 3Hereditary disease
- 3Hereditary disorder by system
- 4Decline in functional status
- 4Disorder of body system
- 4Disorder of mineral metabolism
- 4Disorder of neck
- 4Endocrine finding
- 4Genetic disease
- 5Clinical finding
- 5Disease
- 5Finding of neck region
- 5Functional finding
- 5Metabolic disease
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