DISEASE-DISEASE ASSOCIATIONS Disease,Disease,Common genes Hypochondrogenesis,Otospondylomegaepiphyseal dysplasia,1 Hypochondrogenesis,Achondrogenesis type 2,1 Hypochondrogenesis,Autosomal dominant rhegmatogenous retinal detachment,1 Hypochondrogenesis,Czech dysplasia metatarsal type,1 Hypochondrogenesis,Dysspondyloenchondromatosis,1 Hypochondrogenesis,Familial avascular necrosis of femoral head,1 Hypochondrogenesis,Kniest dysplasia,1 Hypochondrogenesis,Legg-Calvé-Perthes disease,1 Hypochondrogenesis,Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis,1 Hypochondrogenesis,Multiple epiphyseal dysplasia Beighton type,1 Hypochondrogenesis,Platyspondylic dysplasia Torrance type,1 Hypochondrogenesis,Spondyloepimetaphyseal dysplasia congenita Strudwick type,1 Hypochondrogenesis,Spondyloepiphyseal dysplasia congenita,1 Hypochondrogenesis,Spondylometaphyseal dysplasia 'corner fracture' type,1 Hypochondrogenesis,Spondylometaphyseal dysplasia Schmidt type,1 Hypochondrogenesis,Spondyloperipheral dysplasia - short ulna,1 Hypochondrogenesis,Stickler syndrome type 1,1 Hypochondrogenesis,Autosomal recessive Stickler syndrome,(interactome association) Hypochondrogenesis,Multiple epiphyseal dysplasia due to collagen 9 anomaly,(interactome association) Hypochondrogenesis,Autosomal dominant nonsyndromic sensorineural deafness type DFNA,(interactome association) Hypochondrogenesis,Fibrochondrogenesis,(interactome association) Hypochondrogenesis,Autosomal dominant macrothrombocytopenia,(interactome association) Hypochondrogenesis,Camurati-Engelmann disease,(interactome association) Hypochondrogenesis,Cystic fibrosis,(interactome association) Hypochondrogenesis,Fetal and neonatal alloimmune thrombocytopenia,(interactome association) Hypochondrogenesis,Glanzmann thrombasthenia,(interactome association) Hypochondrogenesis,20p12.3 microdeletion syndrome,(interactome association) Hypochondrogenesis,Brachydactyly type A2,(interactome association) Hypochondrogenesis,Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis,(interactome association) Hypochondrogenesis,Ménière disease,(interactome association) Hypochondrogenesis,Bilateral striopallidodentate calcinosis,(interactome association) Hypochondrogenesis,Dermatofibrosarcoma protuberans,(interactome association) Hypochondrogenesis,Familial multiple meningioma,(interactome association) Hypochondrogenesis,Anaplastic ependymoma,(interactome association) Hypochondrogenesis,CARASIL,(interactome association) Hypochondrogenesis,Hyaluronidase deficiency,(interactome association) Hypochondrogenesis,Fibronectin glomerulopathy,(interactome association) Hypochondrogenesis,Granular corneal dystrophy type I,(interactome association) Hypochondrogenesis,Granular corneal dystrophy type II,(interactome association) Hypochondrogenesis,Lattice corneal dystrophy type I,(interactome association) Hypochondrogenesis,Microcystic corneal dystrophy,(interactome association) Hypochondrogenesis,Reis-Bücklers corneal dystrophy,(interactome association) Hypochondrogenesis,Thiel-Behnke corneal dystrophy,(interactome association) Hypochondrogenesis,Autosomal recessive nonsyndromic sensorineural deafness type DFNB,(interactome association) Hypochondrogenesis,Bethlem myopathy,(interactome association) Hypochondrogenesis,Congenital muscular dystrophy Ullrich type,(interactome association) Hypochondrogenesis,Immunodeficiency due to an early component of complement deficiency,(interactome association) Hypochondrogenesis,Marshall syndrome,(interactome association) Hypochondrogenesis,Metaphyseal anadysplasia,(interactome association) Hypochondrogenesis,Multiple epiphyseal dysplasia type 1,(interactome association) Hypochondrogenesis,Pseudoachondroplasia,(interactome association) Hypochondrogenesis,Severe generalized recessive dystrophic epidermolysis bullosa,(interactome association) Hypochondrogenesis,Spondyloepimetaphyseal dysplasia Missouri type,(interactome association) Hypochondrogenesis,Stickler syndrome type 2,(interactome association) Hypochondrogenesis,Stickler syndrome type 3,(interactome association) Hypochondrogenesis,Weissenbacher- Zweymuller syndrome,(interactome association) Hypochondrogenesis,Congenital stromal corneal dystrophy,(interactome association)