ZBTB7B

zinc finger and BTB domain containing 7B
OMIM: 607646, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list ZBTB7B in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 9.18
Latest signed off version: v9.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • CD4+ T-cell deficiency
  • Allergic disease
  • Interstitial lung disease
  • Corneal neovascularization
  • Corneal scarring
  • Global developmental delay
  • Growth failure