1. Genes and Genomic Entities
  2. FAM160B1

FAM160B1

family with sequence similarity 160 member B1
OMIM: 617312, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red FAM160B1 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.7
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Central hypotonia
    • Global developmental delay
    • Intellectual disability
    • Abnormality of the face
    Tags
    • new-gene-name