COL2: Hypochondrogenesis • Achondrogenesis type 2 • Stickler syndrome • متلازمة مارشال • Spondyloepiphyseal dysplasia congenita • Spondyloepimetaphyseal dysplasia, Strudwick type • Kniest dysplasia (see also C2/11)
COL3: Ehlers–Danlos syndrome, types 3 & 4 (Sack–Barabas syndrome)
COL4: متلازمة ألپورت
COL5: Ehlers–Danlos syndrome, types 1 & 2
COL6: Bethlem myopathy • Ullrich congenital muscular dystrophy
COL7: Epidermolysis bullosa dystrophica • Recessive dystrophic epidermolysis bullosa • Bart syndrome • Transient bullous dermolysis of the newborn
COL8: Fuchs' dystrophy 1
COL9: Multiple epiphyseal dysplasia 2, 3, 6
COL10: Schmid metaphyseal chondrodysplasia
COL11: Weissenbacher–Zweymüller syndrome • Otospondylomegaepiphyseal dysplasia (see also C2/11)
