EFEMP1

EGF containing fibulin extracellular matrix protein 1
OMIM: 601548
PanelMode of inheritanceDetails
2 panels
R-numbers: R101
Signed-off version 3.21
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Cutis laxa, autosomal recessive, type ID, OMIM:620780, cutis laxa, MONDO:0016175
R-numbers: R32
Signed-off version 7.8
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Doyne honeycomb degeneration of retina, OMIM:126600