PLXNA2

plexin A2
OMIM: 601054, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber PLXNA2 in Intellectual disability


Level 2: Developmental disorders
Version 11.26
Latest signed off version: v11.0 (12 Aug 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Other
    • Literature
    Phenotypes
    • Intellectual disability, MONDO:0001071
    • Abnormality of the face
    • Failure to thrive
    • Abnormal heart morphology
    Tags
    • watchlist