VAX1

ventral anterior homeobox 1
OMIM: 604294, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red VAX1 in Anophthalmia_Microphthalmia_Coloboma


Level 2: Ophthalmological disorders
Version 1.39

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 11, MIM# 614402

Red VAX1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 11, MIM# 614402

Red VAX1 in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 0.522

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Microphthalmia, syndromic 11, MIM# 614402

Red VAX1 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.252

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • MCOPS11
  • MICROPHTHALMIA, SYNDROMIC 11