ZSWIM6

zinc finger SWIM-type containing 6
OMIM: 615951, Gene2Phenotype

15 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 15 panels
Green ZSWIM6 in Skeletal Dysplasia_Fetal Level 2: Skeletal disorders Version 0.223	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Acromelic frontonasal dysostosis - MIM#603671
Green ZSWIM6 in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.198	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES NEDMAGA
Green ZSWIM6 in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.356	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, OMIM #617865
Amber ZSWIM6 in Ciliopathies Level 2: Dysmorphic and congenital abnormality syndromes Version 1.54	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Expert Review Phenotypes Acromelic frontonasal dysostosis (MIM#603671) Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, MIM# 617865
Green ZSWIM6 in Frontonasal dysplasia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.1	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Acromelic frontonasal dysostosis, MIM# 603671
Amber ZSWIM6 in Joubert syndrome and other neurological ciliopathies Level 2: Neurology and neurodevelopmental disorders Version 1.27	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Expert Review Phenotypes Acromelic frontonasal dysostosis (MIM#603671) Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, MIM#617865
Green ZSWIM6 in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Victorian Clinical Genetics Services Phenotypes Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, MIM# 617865 Acromelic frontonasal dysostosis, MIM# 603671
Green ZSWIM6 in Polydactyly Level 2: Dysmorphic and congenital abnormality syndromes Version 0.276 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green
Green ZSWIM6 in Pierre Robin Sequence Level 2: Dysmorphic and congenital abnormality syndromes Version 0.47	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green ZSWIM6 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Progressive Neurological Conditions	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Literature Phenotypes Acromelic frontonasal dysostosis MIM#603671 Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features MIM#617865
Green ZSWIM6 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Phenotypes Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, MIM#617865
Green ZSWIM6 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert Review Green Other Victorian Clinical Genetics Services Phenotypes Acromelic frontonasal dysostosis 603671
Red ZSWIM6 in Pituitary hormone deficiency Level 2: Endocrine disorders Version 0.34	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Genomics England PanelApp Phenotypes Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features (617865) Acromelic frontonasal dysostosis (603671)
Green ZSWIM6 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.252	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Phenotypes AFND ACROMELIC FRONTONASAL DYSOSTOSIS
Green ZSWIM6 in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Expert Review Phenotypes Acromelic frontonasal dysostosis (MIM#603671)