SPTBN5

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

1 panel

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


Version 4.1
Latest signed off version: v4.0 (1 May 2024)

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