TBCB

tubulin folding cofactor B
OMIM: 601303, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber TBCB in Childhood onset hereditary spastic paraplegia


Level 2: Neurology
Version 8.30
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092
Tags
  • watchlist
  • founder-effect