DBX1

developing brain homeobox 1
OMIM: 619830, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red DBX1 in Central Hypoventilation


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • central hypoventilation syndrome, congenital MONDO:0800031

Red DBX1 in Mendeliome


Version 2.16

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • central hypoventilation syndrome, congenital MONDO:0800031

Red DBX1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.1

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • central hypoventilation syndrome, congenital MONDO:0800031