# New Improvements in Pediatric Disease Diagnosis and Treatment

**Authors:** Elena Țarcă

PMC · DOI: 10.3390/diagnostics16040542 · 2026-02-12

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, ESM1 (endothelial cell specific molecule 1) [NCBI Gene 11082] {aka endocan}
- **Diseases:** prematurity (MESH:C536271), cardiac or pulmonary anomalies (MESH:D006331), Meconium Ileus (MESH:D000074270), Plastic Bronchitis (MESH:D001991), congenital deformities (MESH:D006228), Cowden Syndrome (MESH:D006223), anterior abdominal wall defects (MESH:D046449), genetic and metabolic disorders (MESH:D030342), Celiac Disease (MESH:D002446), congenital disorders (MESH:D009358), Niemann-Pick disease (MESH:D009542), Neonatal Sepsis (MESH:D000071074), congenital and acquired (MESH:D000163), Congenital Adrenal Hyperplasia (MESH:D000312), Silver-Russell Syndrome (MESH:D056730), Chromosomal anomalies (MESH:D002869), Anorectal Malformations (MESH:D000071056), Cystic Fibrosis (MESH:D003550), Anomalies (MESH:D000013), Omphalocele (MESH:D006554), diseases (MESH:D004194), injury to (MESH:D014947), Congenital Malformations (OMIM:163000)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12940054