OMOP Concept 36713458
Pseudohypoparathyroidism type 1C
StandardConditionSNOMED717792007Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Pseudohypoparathyroidism type 1C via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C548076 | Pseudohypoparathyroidism Type 1C | Non-standard |
| Nebraska Lexicon | 717792007 | Pseudohypoparathyroidism type 1C | Non-standard |
Synonyms
Alternative names recorded for Pseudohypoparathyroidism type 1C across source vocabularies.
- pseudohipoparatiroidismo tipo 1C
- pseudohipoparatiroidismo tipo 1C (trastorno)
- Pseudohypoparathyroidism type 1C (disorder)
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
- 1Hereditary disorder of endocrine system
- 1Pseudohypoparathyroidism
- 2Autosomal hereditary disorder
- 2Disorder of endocrine system
- 2Hereditary disorder by system
- 2Hypocalcemia
- 2Hypoparathyroidism
- 3Decreased hormone secretion
- 3Disorder of body system
- 3Disorder of calcium metabolism
- 3Disorder of parathyroid gland
- 3Hereditary disease
- 4Decline in functional status
- 4Disease
- 4Disorder of neck
- 4Disorder of phosphate, calcium and vitamin D metabolism
- 4Endocrine finding
- 4Genetic disease
- 5Clinical finding
- 5Disorder of mineral metabolism
- 5Finding of neck region
- 5Functional finding
- 6Metabolic disease
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