C1QTNF5

C1q and TNF related 5
OMIM: 608752
PanelMode of inheritanceDetails
1 panel
R-numbers: R32, R33, R34, R35
Signed-off version 2.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Eye Disorders, Retinal Degeneration, Retinitis pigmentosa, Retinal degeneration, late-onset, autosomal dominant, 605670