PLXNC1

plexin C1
OMIM: 604259, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red PLXNC1 in Mendeliome


Version 2.1

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Disease associations
  • Malformations of cortical development

Red PLXNC1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Disease associations
    • Malformations of cortical development