ARR3

arrestin 3
OMIM: 301770, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green ARR3 in Structural eye disease


Level 2: Ophthalmology
Version 4.40
Latest signed off version: v4.0 (7 Aug 2024)

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • Myopia 26, X-linked, female-limited, OMIM:301010
  • myopia 26, X-linked, female-limited, MONDO:0049221
Tags
  • x-linked-over-dominance