SLC35F1

solute carrier family 35 member F1
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SLC35F1 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Neruodevelopmental disorder, MONDO:0700092, SLC35F1-associated
    • Rett-like syndrome