ADAMTS18

ADAM metallopeptidase with thrombospondin type 1 motif 18
OMIM: 607512
PanelMode of inheritanceDetails
2 panels
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Genetic Retinal Degeneration Conditions, Microcornea, myopic chorioretinal atrophy, and telecanthus, 615458
R-numbers: R36
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microcornea, myopic chorioretinal atrophy, and telecanthus, 615458