WNT7B

Wnt family member 7B
OMIM: 601967
PanelMode of inheritanceDetails
1 panel
R-numbers: R21, R412
Signed-off version 3.122
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Pulmonary hypoplasia, Diaphragmatic anomalies, Anophthalmia/Microphthalmia, Cardiac defects