SPTBN5

spectrin beta, non-erythrocytic 5
OMIM: 605916, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SPTBN5 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.10
Latest signed off version: v7.0 (6 May 2026)

review Unknown
Sources
  • Literature
Phenotypes
  • Multicystic kidney
  • Oligohydramnios
  • Sacral agenesis