PanelApp (test)
  1. Genes and Genomic Entities
  2. ZMYND8

ZMYND8

zinc finger MYND-type containing 8
OMIM: 615713, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green ZMYND8 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ZMYND8-related
  • Delayed speech and language development
  • Motor delay
  • Intellectual disability
  • Abnormality of cardiovascular system morphology
  • Hearing abnormality
  • Abnormality of vision
  • Abnormality of the face
  • Seizures

Green ZMYND8 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ZMYND8-related
  • Delayed speech and language development
  • Motor delay
  • Intellectual disability
  • Abnormality of cardiovascular system morphology
  • Hearing abnormality
  • Abnormality of vision
  • Abnormality of the face
  • Seizures