HOXA3

homeobox A3
OMIM: 142954, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list HOXA3 in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 9.111
Latest signed off version: v9.91 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Congenital athymia
  • Hypoplasia of the epiglottis
  • Dysphagia
  • Respiratory aspiration
  • Abnormality of the face
  • Abnormality of the neck
  • Severe combined immunodeficiency