ZNF469

zinc finger protein 469
OMIM: 612078
PanelMode of inheritanceDetails
2 panels
R-numbers: R262
Signed-off version 1.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Brittle cornea syndrome 1 229200
R-numbers: R101
Signed-off version 2.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Brittle cornea syndrome 1, 229200, BCS, EDSVIB, Connective Tissue Disorders, Ehlers-Danlos syndrome type VIB, Brittle cornea syndrome