ZMYND8

zinc finger MYND-type containing 8
OMIM: 615713
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
ZMYND8-related neurodevelopmental disorder
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Delayed speech and language development, Motor delay, Intellectual disability, Abnormality of cardiovascular system morphology, Hearing abnormality, Abnormality of vision, Abnormality of the face, Seizures