OSBPL9

oxysterol binding protein like 9
OMIM: 606737, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red OSBPL9 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.5
Latest signed off version: v8.0 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • Fetal Cerebral Ventriculomegaly, Cerebellar Hypoplasia, and Arthrogryposis Multiplex