COL25A1

collagen type XXV alpha 1 chain
OMIM: 610004
PanelMode of inheritanceDetails
2 panels
R-numbers: R83
Signed-off version 5.21
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arthrogryposis multiplex congenita with or without an ocular congenital cranial dysinnervation disorder
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5 616219