ZFHX4

zinc finger homeobox 4
OMIM: 606940, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green ZFHX4 in Mendeliome


Version 1.4216

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • neurodevelopmental disorder, ZFHX4-related (MONDO:0700092)
Tags
  • SV/CNV

Green ZFHX4 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.638

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • neurodevelopmental disorder, ZFHX4-related (MONDO:0700092)
Tags
  • SV/CNV

Green ZFHX4 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.310

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • neurodevelopmental disorder, ZFHX4-related (MONDO:0700092)

Red ZFHX4 in Speech apraxia


Level 2: Neurology and neurodevelopmental disorders
Version 1.27

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