ZNF496

zinc finger protein 496
OMIM: 613911, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red ZNF496 in Mendeliome


Version 1.3050

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ZNF496-related

Red ZNF496 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.288

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ZNF496-related