OMOP Concept 37165519
Griscelli syndrome type 3
StandardConditionSNOMED1254947002Disorder
Maps from
1
Descendants
0
Valid from
31 Oct 2022
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Griscelli syndrome type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537303 | Griscelli syndrome type 3 | Non-standard |
Synonyms
Alternative names recorded for Griscelli syndrome type 3 across source vocabularies.
- enfermedad de hipopigmentación-inmunodeficiencia tipo 3
- enfermedad de hipopigmentación-inmunodeficiencia tipo 3 (trastorno)
- Hypopigmentation-immunodeficiency disease type 3
- Hypopigmentation-immunodeficiency disease type 3 (disorder)
- síndrome de Griscelli tipo 3
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Hypopigmentation-immunodeficiency disease
- 2Congenital immunodeficiency disease
- 2Congenital malformation
- 2Disorder of pigmentation
- 2Disorder of tyrosine metabolism
- 2Immunodeficiency associated with multiple organ system abnormalities
- 3Congenital disease
- 3Developmental disorder
- 3Disease
- 3Disorder of amino acid and organic acid metabolism
- 3Immunodeficiency disorder
- 3Immunodeficiency with major anomalies
- 4Clinical finding
- 4Disorder of amino acid metabolism
- 4Disorder of immune function
- 4Disorder of immune structure
- 4Fetal and/or neonatal disorder
- 4Primary immune deficiency disorder
- 5Disorder of body system
- 5Disorder of organic acid metabolism
- 6Metabolic disease
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