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livedo reticularis
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Genetic Markers
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ADA2
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Pathway Enrichment
Most Correlated Biogroups
Adenosine/AMP deaminase N-terminal
Adenosine deaminase-related growth factor
Adenosine/AMP deaminase domain
adenosine deaminase activity
Metal-dependent hydrolase
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OMIM - Sneddon syndrome
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Primary hyperoxaluria type 1-a rare hereditary metabolic disorder as cause of livedo racemosa].
Livedo racemosa associated with central venous catheter use in a newborn.
Amantadine-induced livedo racemosa.
Hepatitis C Virus-associated Cryoglobulinemic Livedo Reticularis Improved with Direct-acting Antivir…
Livedo Reticularis After COVID-19 Vaccination.
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Clinical Study to Evaluate the Efficacy of Blood Purification Therapy on Cholesterol Crystal Embolis…
Determining Disease Activity Biomarkers in Individuals With Polyarteritis Nodosa
Clinical Evaluation of LightSheer Duet 805nm HS Handpiece
Clinical Evaluation of Hair Removal and Permanent Hair Reduction for Skin Types VI Using Intense Pul…
Hematopoietic Stem Cell Transplantation in Patients With Antiphospholipid Syndrome
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