FBXL3

F-box and leucine rich repeat protein 3
OMIM: 605653, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green FBXL3 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual developmental disorder with short stature, facial anomalies, and speech defects
  • OMIM #606220

Green FBXL3 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual developmental disorder with short stature, facial anomalies, and speech defects
  • OMIM #606220