PLEKHN1

pleckstrin homology domain containing N1
Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
No list PLEKHN1 in Pain syndromes Level 3: Channelopathies Level 2: Neurology and neurodevelopmental disorders Version 1.12	review	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Phenotypes Sensory neuropathy

Panel

Reviews

Mode of inheritance

Details

Level 3: Channelopathies
Level 2: Neurology and neurodevelopmental disorders
Version 1.12

review

BIALLELIC, autosomal or pseudoautosomal