VSX2

visual system homeobox 2
OMIM: 142993
PanelMode of inheritanceDetails
4 panels
R-numbers: R31
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia, cataracts and iris abnormalities
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
MICROPHTHALMIA ISOLATED TYPE 2 610093, MICROPHTHALMIA ISOLATED WITH COLOBOMA TYPE 3 610092, MICROPHTHALMIA WITH CATARACTS AND IRIS ABNORMALITIES 610092
R-numbers: R21, R412
Signed-off version 3.122
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
MICROPHTHALMIA WITH CATARACTS AND IRIS ABNORMALITIES, MICROPHTHALMIA ISOLATED WITH COLOBOMA TYPE 3, MICROPHTHALMIA ISOLATED TYPE 2
R-numbers: R36
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia with coloboma 3, 610092