familial nonchromaffin paraganglioma

Genetics

• autosomal dominant non-chromaffin paraganglioma type 1 associated with defects in SDHD (penetrance is incomplete when transmitted through fathers; not transmitted maternally)
• autosomal dominant non-chromaffin paraganglioma type 3 associated with defect in SDHC

More general terms

• paraganglioma
• hereditary neoplastic syndrome; cancer susceptibility syndrome

More specific terms

• familial nonchromaffin paraganglioma 1 (PGL1)
• familial nonchromaffin paraganglioma 3 (PGL3)
• familial nonchromaffin paraganglioma 4 (PGL4)

Database

• OMIM: https://mirror.omim.org/entry/168000
• OMIM: https://mirror.omim.org/entry/602690
• OMIM: https://mirror.omim.org/entry/605373