TNXB

PanelMode of inheritanceDetails
1 panel
R-numbers: R101
Signed-off version 2.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ehlers-Danlos syndrome due to tenascin X deficiency, 606408, Classical-like EDS, clEDS, Ehlers-Danlos syndrome, classic-like type