ZNF335

zinc finger protein 335
OMIM: 610827, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber ZNF335 in Severe microcephaly

Level 3: DNA repair disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.74

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Amber
  • Other
  • Literature
Phenotypes
  • Autosomal recessive primary microcephaly (MCPH)
  • ?Microcephaly 10, primary, autosomal recessive, 615095

Amber ZNF335 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 2.1102

Component of the following Super Panels:

  • Paediatric disorders v4.401
  • White matter disorders - childhood onset v4.233
  • Hypotonic infant with a likely central cause v3.1053
  • review Unknown
    Sources
    • Expert Review Amber
    • Expert Review Red
    • Other
    Phenotypes
    • ?Microcephaly 10, primary, autosomal recessive, 615095
    • developmental delay
    • intellectual disability
    Tags
    • watchlist