The following pages link to COL4
External toolsShowing 41 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Genetic disorder (links | edit)
- Ehlers–Danlos syndrome (links | edit)
- Weissenbacher–Zweymüller syndrome (links | edit)
- Alport syndrome (links | edit)
- Osteogenesis imperfecta (links | edit)
- Goodpasture syndrome (links | edit)
- Stickler syndrome (links | edit)
- Fuchs' dystrophy (links | edit)
- Spondyloperipheral dysplasia (links | edit)
- Collagenopathy, types II and XI (links | edit)
- Hypochondrogenesis (links | edit)
- Achondrogenesis type 2 (links | edit)
- Kniest dysplasia (links | edit)
- Otospondylomegaepiphyseal dysplasia (links | edit)
- Spondyloepiphyseal dysplasia congenita (links | edit)
- Spondyloepimetaphyseal dysplasia, Strudwick type (links | edit)
- Bullous pemphigoid (links | edit)
- Nonsyndromic deafness (links | edit)
- Platyspondylic lethal skeletal dysplasia, Torrance type (links | edit)
- Infantile cortical hyperostosis (links | edit)
- Sack–Barabas syndrome (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Pseudoachondroplasia (links | edit)
- Raine syndrome (links | edit)
- Dermatopathia pigmentosa reticularis (links | edit)
- Pachyonychia congenita (links | edit)
- Bethlem myopathy (links | edit)
- Epidermolysis bullosa dystrophica (links | edit)
- Collagen disease (links | edit)
- Urbach–Wiethe disease (links | edit)
- Marshall syndrome (links | edit)
- Bart syndrome (links | edit)
- Metaphyseal chondrodysplasia Schmid type (links | edit)
- Junctional epidermolysis bullosa (medicine) (links | edit)
- Transient bullous dermolysis of the newborn (links | edit)
- Ullrich congenital muscular dystrophy (links | edit)
- Collagen VI (links | edit)
- Congenital stromal corneal dystrophy (links | edit)
- Laryngo-onycho-cutaneous syndrome (links | edit)
- Knobloch syndrome (links | edit)
- Template:Scleroprotein disease (links | edit)