HOXB1

homeobox B1
OMIM: 142968, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green HOXB1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Facial paresis, hereditary congenital, 3, MIM# 614744
  • MONDO:0013880

Red HOXB1 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genomics England PanelApp
Phenotypes
  • Facial paresis, hereditary congenital, 3, MIM# 614744
  • MONDO:0013880