Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Syndromic disease · Hereditary disorder of connective tissue · Skeletal dysplasia · Collagenopathy
Type 2 collagenopathy
Any disease or disorder in which the cause of the disease is a mutation in the COL2A1 gene.
-
Dysplasia of the proximal femoral epiphyses 0 trials · 36 incl. sub-types Sub-types →
-
Stickler syndrome type 1 3 trials Sub-types →
-
Kniest dysplasia 0 trials
-
Achondrogenesis type II 0 trials
-
Hypochondrogenesis 0 trials
-
Spondyloperipheral dysplasia 0 trials