Ehlers-Danlos syndrome classic-like 1 (DOID:0080731)
Alliance: disease page
Alt IDs: OMIM:606408
Definition: An Ehlers-Danlos syndrome that is characterized by hyperextensible skin, hypermobile joints, and tissue fragility and that has_material_basis_in omozygous or heterozygous mutation in the tenascin-XB gene (TNXB) on chromosome 6p21.