FAM161A

family with sequence similarity 161 member A
OMIM: 613596
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
RETINITIS PIGMENTOSA 28 606068
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Eye Disorders, Retinitis pigmentosa 28, 606068, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive