NUP37

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Red NUP37 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Nephrotic syndrome Microcephaly 24, primary, autosomal recessive, MIM# 618179
Red NUP37 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.269	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Microcephaly 24, primary, autosomal recessive, MIM# 618179
Red NUP37 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 Red Expert list Phenotypes Nephrotic syndrome

3 panels