2771
|
|
|
Collagen type XI alpha 2 chain |
DFNA13, DFNB53, FBCG2, HKE5, OSMEDA, OSMEDB, PARP, STL3 |
Asthma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Otospondylomegaepiphyseal dysplasia, Carpal tunnel syndrome, Cartilage disease, Celiac disease, Interstitial cystitis, Cleft palate, Conductive hearing loss, Congenital cartilage disorder, Congenital ear anomaly, Congenital heart defects, Connective tissue disease, Craniofacial abnormalities, Deafness, Desbuquois syndrome, Down syndrome, Hearing impairment, Hearing loss, Hereditary hearing loss, Hypothyroidism, Inflammatory bowel disease, Intellectual developmental disorder, Congenital anomaly of limb, Lung cancer, Marshall syndrome, Multiple sclerosis, Osteoarthritis, Osteochondrodysplasias, Peptic ulcer disease, Psoriasis, Rheumatoid arthritis, Squamous cell carcinoma, Stickler syndrome, Diabetes mellitus type 1View all (21 more) |
2772
|
|
|
Collagen type XII alpha 1 chain |
BA209D8.1, BTHLM2, COL12A1L, DJ234P15.1, EDSMYP, UCMD2 |
Alzheimer disease, Asthma, Bethlem myopathy, Cataract, Central nervous system cancer, Color vision deficiency, Dementia, Ehlers-danlos syndrome, Endometriosis, Glioblastoma, Glioma, Global developmental delay, Hereditary motor and sensory neuropathies, Keratoconus, Melanoma, Mesothelioma, Neurodevelopmental disorder, Orofacial cleft, Hypertension, Ullrich congenital muscular dystrophyView all (5 more) |
2773
|
|
|
Collagen type XIII alpha 1 chain |
CMS19, COLXIIIA1 |
Liver cirrhosis, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Endometriosis, Migraine, Myasthenic syndrome, Nonalcoholic fatty liver disease, Parkinson disease, Postsynaptic congenital myasthenic syndrome, Presynaptic congenital myasthenic syndrome, Scoliosis, Sialolithiasis, Ulcerative colitis |
2774
|
|
|
Collagen type XIV alpha 1 chain |
UND |
|
2775
|
|
|
Collagen type XV alpha 1 chain |
- |
|
2776
|
|
|
Collagen type XVI alpha 1 chain |
447AA, FP1572 |
|
2777
|
|
|
Collagen type XVII alpha 1 chain |
BA16H23.2, BP180, BPA-2, BPAG2, ERED, JEB4, LAD-1 |
|
2778
|
|
|
Collagen type XVIII alpha 1 chain |
GLCC, KNO, KNO1, KS |
Alzheimer disease, Calcinosis, Cataract, Cervical cancer, Fuchs endothelial dystrophy, Glaucoma, Heart valve disease, Heart valve prolapse, Hemangiosarcoma, Intellectual developmental disorder, Knobloch syndrome, Macular dystrophy, Nystagmus, Primary angle closure glaucoma, Retinitis pigmentosa, MyopiaView all (1 more) |
2779
|
|
|
Collagen type XIX alpha 1 chain |
COL9A1L, D6S228E |
|
2780
|
|
|
Collagen type I alpha 1 chain |
CAFYD, EDSARTH1, EDSC, OI1, OI2, OI3, OI4 |
Ankylosing spondylitis, Aortic dissection, Aortic valve disease, Jeune syndrome, Autoimmune disease, Beta thalassemia, Bone fragility with contractures, arterial rupture, and deafness, Breast cancer, Caffey disease, Calcinosis, Dilated cardiomyopathy, Cervical disc degenerative disorder, Cholangitis, Cholelithiasis, Ehlers-danlos syndrome, Combined osteogenesis imperfecta and ehlers-danlos syndrome , Congenital heart disease, Connective tissue disease, Cortical congenital hyperostosis, Dentinogenesis imperfecta, Dermatofibrosarcoma protuberans, Desbuquois syndrome, Epiphyseal dysplasia, Thoracic aortic aneurysm and aortic dissection, Heart valve disease, Heart valve prolapse, Hypertension, Hypertrophic cardiomyopathy, Hypertrophy, Keratoconus, Left ventricular disease, Liver cirrhosis, Auricle malformation, Marfan syndrome, Maternal hypertension, Nephrosclerosis, Nephrotic syndrome, Oral submucous fibrosis, Osteogenesis imperfecta, Osteopenia, Osteoporosis, Osteoporosis-pseudoglioma syndrome, Rhizomelia, Skeletal dysplasia, Stickler syndromeView all (30 more) |
