ZBTB18

zinc finger and BTB domain containing 18
OMIM: 608433, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ZBTB18 in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Red
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 22, MIM#612337

Green ZBTB18 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Australian Genomics Health Alliance Epilepsy Flagship
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Mental retardation, autosomal dominant 22, MIM# 612337

Green ZBTB18 in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Mental retardation, autosomal dominant 22, MIM# 612337