C1QTNF5

C1q and TNF related 5
OMIM: 608752
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Eye Disorders, Retinal Degeneration, Retinitis pigmentosa, Retinal degeneration, late-onset, autosomal dominant, 605670