TMEM106B

transmembrane protein 106B
OMIM: 613413, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green TMEM106B in Leukodystrophy - paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Australian Genomcis Health Alliance Leukodystrophy Flagship
  • Expert Review Green
  • Royal Melbourne Hospital
  • Expert Review Green
Phenotypes
  • Leukodystrophy, hypomyelinating 16, MIM#617964