ZSWIM6

zinc finger SWIM-type containing 6
OMIM: 615951
PanelMode of inheritanceDetails
7 panels
R-numbers: R57
Signed-off version 1.137
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, 617865
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
ACROMELIC FRONTONASAL DYSOSTOSIS, AFND
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Acromelic frontonasal dysostosis, 603671, Includes mental retardation, acromelic frontonasal dysostosis with severe intellectual disability
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Acromelic frontonasal dysostosis 603671
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 1.5
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Acromelic frontonasal dysostosis 603671
Component of the following Super Panels:
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Acromelic frontonasal dysostosis 603671
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Acromelic frontonasal dysostosis 603671