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Unable to recruit subjects due to disease rarity
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The primary study objective is to collect biospecimen samples (e.g., blood) from participants diagnosed with Chronic Granulomatous Disease (CGD). The biospecimens will be used to create a biorepository that can be used to identify disease associated biomarkers and potential targets with immune and multi-omics profiling. The disease sample collection and analysis will be the foundation for an extensive network of biospecimen access and linked datasets for future translational research.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CGD with p47phox phenotype |
| ||
| X-Linked CGD |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Specimen Donation | Diagnostic Test | blood donation |
|
| Measure | Description | Time Frame |
|---|---|---|
| Participants have been diagnosed with Chronic Granulomatous Disease (CGD) | Participants have been diagnosed with Chronic Granulomatous Disease (CGD) | 1 Year |
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Inclusion Criteria:
Exclusion Criteria:
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Participants have been diagnosed with Chronic Granulomatous Disease (CGD)
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sanguine BioSciences, Inc. | Woburn | Massachusetts | 01801 | United States |
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| ID | Term |
|---|---|
| D006105 | Granulomatous Disease, Chronic |
| ID | Term |
|---|---|
| D010585 | Phagocyte Bactericidal Dysfunction |
| D007960 | Leukocyte Disorders |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
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| D040181 | Genetic Diseases, X-Linked |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D007153 | Immunologic Deficiency Syndromes |
| D007154 | Immune System Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |