WNT9B

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Amber WNT9B in Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic Level 2: Renal and urinary tract disorders Version 0.117 Component of the following Super Panels: Congenital abnormalities of the kidneys and urinary tract (CAKUT)_SuperPanel Kidneyome_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert Review Amber Literature Victorian Clinical Genetics Services Phenotypes Renal agenesis/hypoplasia/dysplasia, no OMIM #
Amber WNT9B in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Renal agenesis/hypoplasia/dysplasia
Amber WNT9B in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Renal agenesis/hypoplasia/dysplasia, no OMIM #

3 panels