FYCO1

FYVE and coiled-coil domain containing 1
OMIM: 607182
PanelMode of inheritanceDetails
3 panels
R-numbers: R31
Signed-off version 4.14
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital Cataract, Cataract 18, autosomal recessive, 610019, Cataract 18, autosomal recessive, CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 2
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 2 610019
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 2