PRDM15

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber PRDM15 in Holoprosencephaly and septo-optic dysplasia Level 2: Neurology and neurodevelopmental disorders Version 1.16	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Holoprosenephaly Steroid resistant nephrotic syndrome Multiple congenital anomalies
Amber PRDM15 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Steroid resistant nephrotic syndrome Holoprosencephaly
Amber PRDM15 in Proteinuria Level 2: Renal and urinary tract disorders Version 0.225 Component of the following Super Panels: Kidneyome_SuperPanel Renal Glomerular Disease_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Steroid resistant nephrotic syndrome
Amber PRDM15 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Holoprosenephaly Steroid resistant nephrotic syndrome Multiple congenital anomalies

4 panels