OMOP Concept 4185779
Hawkinsinuria
StandardConditionSNOMED414380008Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2005
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
4 source codes normalize to Hawkinsinuria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139095 | Hawkinsinuria | Non-standard |
| HPO | HP_0034457 | Hawkinsinuria | Non-standard |
| MeSH | C535845 | Hawkinsinuria | Non-standard |
| Nebraska Lexicon | 414380008 | Hawkinsinuria | Non-standard |
Synonyms
Alternative names recorded for Hawkinsinuria across source vocabularies.
- hawkinsinuria
- hawkinsinuria asociada al gen HPD
- Hawkinsinuria (disorder)
- hawkinsinuria (trastorno)
- HPD-gene related hawkinsinuria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 14-Hydroxyphenylpyruvate dioxygenase deficiency
- 1Autosomal dominant hereditary disorder
- 1Disorder of sulfur-bearing amino acid metabolism
- 2Autosomal hereditary disorder
- 2Disorder of amino acid and organic acid metabolism
- 2Disorder of tyrosine metabolism
- 2Enzymopathy
- 3Disorder of amino acid metabolism
- 3Hereditary disease
- 3Metabolic disease
- 4Disease
- 4Disorder of organic acid metabolism
- 4Genetic disease
- 5Clinical finding
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