PLEKHN1

pleckstrin homology domain containing N1
Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red PLEKHN1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Sensory Neuropathy

Red PLEKHN1 in Pain syndromes


Level 2: Neurology and neurodevelopmental disorders
Version 0.34

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Sensory Neuropathy