OMOP Concept 36716112
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome
StandardConditionSNOMED721977007Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 721977007 | Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome | Non-standard |
Synonyms
Alternative names recorded for Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome across source vocabularies.
- Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)
- síndrome de fibrosis pulmonar, inmunodeficiencia y disgenesia gonadal 46,XX
- síndrome de fibrosis pulmonar, inmunodeficiencia y disgenesia gonadal 46,XX (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(88)Roll up to these when you need a wider cohort.
- 1Autosomal recessive SCID (severe combined immunodeficiency disease)
- 1Developmental hereditary disorder
- 1Fibrosis of lung
- 1Hereditary disorder of endocrine system
- 1Pure gonadal dysgenesis 46,XX
- 1Reproductive system hereditary disorder
- 1T-cell negative B-cell positive severe combined immunodeficiency
- 2Autosomal recessive hereditary disorder
- 2Developmental disorder
- 2Disorder of endocrine system
- 2Disorder of reproductive system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of lung
- 2Ovarian dysgenesis
- 2Pure gonadal dysgenesis
- 2Severe combined immunodeficiency disease
- 3Autosomal hereditary disorder
- 3Combined immunodeficiency disease
- 3Congenital anomaly of endocrine ovary
- 3Congenital immunodeficiency disease
- 3Disease
- 3Disorder of body system
- 3Disorder of lung
- 3Disorder of the genitourinary system
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