PHIDSPublic Health Indicators Data System (Florida Department of Health)
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References in periodicals archive ?
This syndrome (named also PHID syndrome) is an autosomal-recessive autoinflammatory disorder due to mutations in the SLC29A3 gene, which codifies the human equilibrative nucleoside transporter-3 (hENT3), regulating apoptosis and macrophage recruitment [93].
Brogan et al., "Pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus (PHID) syndrome is associated with severe chronic inflammation and cardiomyopathy, and represents a new monogenic autoinflammatory syndrome," Journal of Pediatric Endocrinology and Metabolism, vol.