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 syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • no OMIM number yet