ZFHX4:Ensemblv115

zinc finger homeobox 4
OMIM: 606940, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red ZFHX4 in Speech apraxia


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review
  • Expert Review Red
Phenotypes
  • Neurodevelopmental disorder (MONDO:0700092), ZFHX4-related