Linked from

The 10 pages that link to 22q11.2 deletion syndrome, each with the reason it gives.

• HaploinsufficiencyBroader topic: Reduced dosage of genes in the deleted region contributes to the syndrome's features.

• DiGeorge syndromeNarrower topic: DiGeorge syndrome is one name used within this broader condition, which also includes other clinical presentations.

• CHARGE syndromeCompared with: Both conditions can involve heart defects and airway or feeding problems, but their usual genetic causes differ.

• Cleft palateRelated: Palatal differences, including cleft palate, are among its recognized features.

• HypoparathyroidismRelated: Parathyroid underdevelopment in this syndrome can cause hypoparathyroidism.

• Tetralogy of FallotRelated: This syndrome is a well-established genetic association with Tetralogy of Fallot.

• Williams syndromeCompared with: Both involve recurrent chromosomal deletions, but differ in region, typical features, and clinical risks.

• Cleft lip and cleft palateRelated: Palatal differences, including cleft palate, can occur as part of this syndrome.

• 22q13 deletion syndromeCompared with: Despite the shared chromosome, it involves a different region and a distinct clinical pattern.

• Jacobsen syndromeRelated: Like Jacobsen syndrome, it can affect multiple organ systems and vary widely in severity.