OMOP Concept 4292707
Hypopigmentation-immunodeficiency disease
StandardConditionSNOMED37548006Disorder
Maps from
2
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Hypopigmentation-immunodeficiency disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138027 | Hypopigmentation-immunodeficiency disease | Non-standard |
| Nebraska Lexicon | 37548006 | Hypopigmentation-immunodeficiency disease | Non-standard |
Synonyms
Alternative names recorded for Hypopigmentation-immunodeficiency disease across source vocabularies.
- albinismo parcial con inmunodeficiencia
- Chediak-Higashi-like syndrome
- enfermedad de hipopigmentación - inmunodeficiencia
- enfermedad de hipopigmentación - inmunodeficiencia (trastorno)
- Griscelli syndrome
- Griscelli syndrome with immunodeficiency
- Hypopigmentation-immunodeficiency disease (disorder)
- Partial albinism with immunodeficiency
- síndrome de Griscelli
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Congenital immunodeficiency disease
- 1Congenital malformation
- 1Disorder of pigmentation
- 1Disorder of tyrosine metabolism
- 1Immunodeficiency associated with multiple organ system abnormalities
- 2Congenital disease
- 2Developmental disorder
- 2Disease
- 2Disorder of amino acid and organic acid metabolism
- 2Immunodeficiency disorder
- 2Immunodeficiency with major anomalies
- 3Clinical finding
- 3Disorder of amino acid metabolism
- 3Disorder of fetus and/or newborn
- 3Disorder of immune function
- 3Disorder of immune structure
- 3Primary immune deficiency disorder
- 4Disorder of body system
- 4Disorder of organic acid metabolism
- 5Metabolic disease
Narrower concepts
(2)Included automatically when you query with descendants.
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