PLK4

polo like kinase 4
OMIM: 605031, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green PLK4 in Mendeliome Version 1.3512	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171
Green PLK4 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.357	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171
Green PLK4 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171
Green PLK4 in Syndromic Retinopathy Level 2: Ophthalmological disorders Version 0.234 Component of the following Super Panels: Retinal Disorders Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green RetNet Phenotypes Microcephaly and chorioretinopathy, autosomal recessive, 2, MIM# 616171
Green PLK4 in Growth failure Version 1.83	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Microcephaly and chorioretinopathy 2, MONDO:0014516 Microcephaly and chorioretinopathy, autosomal recessive, 2, #MIM:616171
Green PLK4 in Fetal anomalies Version 1.465	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Microcephaly and chorioretinopathy, autosomal recessive, 2, OMIM #616171