NOL10

nucleolar protein 10
OMIM: 616197, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NOL10 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • NOL10-related neurological disorder MONDO:0100545

Red NOL10 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • NOL10-related neurological disorder MONDO:0100545