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Molecular Function
Extracellular Matrix Structural Constituent
Diseases Associated With Extracellular Matrix Structural Constituent
Disease
Liver Cirrhosis, Experimental
Abortion, Spontaneous
Liver Cirrhosis
Osteoarthritis
Endometriosis
Hypertension
Muscular Dystrophy, Facioscapulohumeral
Colorectal Cancer
Keloid
Rheumatoid Arthritis
Craniofacial Abnormalities
Prostatic Neoplasms
Pulmonary Fibrosis
Aortic Valve Insufficiency
Mammary Neoplasms, Animal
Mammary Neoplasms, Experimental
Schizophrenia
Melanoma
Left Ventricular Hypertrophy
Nephrotic Syndrome
Carcinoma
Fibrosis
Ehlers-Danlos Syndrome Type 1
Diabetic Nephropathy
Megaepiphyseal Dwarfism
Osteoporosis
Mesothelioma, Malignant
Hyperglycemia
Hyperinsulinism
Drug-Induced Liver Injury
Leiomyoma, Epithelioid
Breast Carcinoma
Glioblastoma Multiforme
Neoplasm Invasiveness
Osteogenesis Imperfecta, Type 2a
Osteogenesis Imperfecta, Type 3
Hearing Loss, Sensorineural
Alport Syndrome, Recessive Type
Heart Valve Diseases
Focal Segmental Glomerulosclerosis
Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
Osteochondrodysplasias
Intervertebral Disc Disease
Osteogenesis Imperfecta, Type 4
Oral Submucous Fibrosis
Marfan Syndrome
Varicose Veins
Ulcerative Colitis
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
Erythema
Fatty Liver
Femur Head Necrosis
Fractures, Bone
Glaucoma, Angle-Closure
Glioma
Glomerulopathy With Fibronectin Deposits
Hematuria, Benign Familial
Hernia, Diaphragmatic
Hyaloideoretinal Degeneration Of Wagner
Hypercholesterolemia
Hyperostosis, Cortical, Congenital
Hyperplasia
Inflammation
Intellectual Disability
Intervertebral Disc Displacement
Joint Instability
Kallmann Syndrome
Keutel Syndrome
Kniest Dysplasia
Legg-Calve-Perthes Disease
Leiomyomatosis, Esophageal And Vulval, With Nephropathy
Leukemia, Myeloid, Acute
Limb Deformities, Congenital
Alcoholic Liver Cirrhosis
Liver Diseases
Lung Injury
Marshall Syndrome
Mass Syndrome
Metaphyseal Chondrodysplasia Schmid Type
Mouth Neoplasms
Cardiomyopathy, Dilated, 3b
Myocardial Ischemia
Myopia
Neoplasm Metastasis
Alport Syndrome, X-Linked
Nephrogenic Fibrosing Dermopathy
Nerve Degeneration
Non-Alcoholic Fatty Liver Disease
Osteoarthritis With Mild Chondrodysplasia
Osteogenesis Imperfecta
Osteomalacia
Ovarian Cysts
Pancreatic Carcinoma
Pelvic Organ Prolapse
Pierre Robin Syndrome With Fetal Chondrodysplasia
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
Pleural Diseases
Pneumoconiosis
Porencephaly
Pseudoachondroplasia
Chronic Obstructive Pulmonary Disease
Pulmonary Emphysema
Retinal Detachment
Cone-Rod Dystrophy 2
Retinitis Pigmentosa 25
Rupture, Spontaneous
Systemic Scleroderma
Shprintzen Golberg Craniosynostosis
Small Cell Lung Carcinoma
Spondyloepimetaphyseal Dysplasia, Aggrecan Type
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
Spondyloepiphyseal Dysplasia, Congenita
Spondyloepiphyseal Dysplasia, Kimberley Type
Spondylometaphyseal Dysplasia, Kozlowski Type
Stickler Syndrome, Type 1
Stickler Syndrome, Type 2
Stickler Syndrome, Type 3
Stickler Syndrome, Type I, Nonsyndromic Ocular
Stiff Skin Syndrome
Stomach Neoplasms
Strudwick Syndrome
Synovitis
Synpolydactyly 2
Uremia
Ureteral Obstruction
Vascular Calcification
Weight Gain
Weight Loss
Weill-Marchesani Syndrome
Williams Syndrome
Wounds And Injuries
Achondrogenesis Type 2
Aids-Related Opportunistic Infections
Aneurysm, Dissecting
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
Thoracic Aortic Aneurysm
Aortic Diseases
Aortic Rupture
Aortic Stenosis, Supravalvular
Arachnodactyly
Arthritis
Arthritis, Experimental
Asthma
Autism
Autoimmune Disease
Brain Small Vessel Disease With Hemorrhage
Calcinosis
Hepatocellular Carcinoma
Squamous Cell Carcinoma
Cartilage Diseases
Cataract
Cell Transformation, Neoplastic
Cholangitis
Chondrosarcoma
Coloboma
Corneal Dystrophy, Fuchs' Endothelial, 1
Corneal Dystrophy, Posterior Polymorphous, 1
Corneal Dystrophy, Posterior Polymorphous, 2
Crohn's Disease
Cutis Laxa
Deafness, Autosomal Dominant 12
Deafness, Autosomal Dominant 13
Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
Deafness, Autosomal Recessive 21
Deafness, Autosomal Recessive 53
Dentinogenesis Imperfecta
Dentinogenesis Imperfecta, Shields Type 3
Diabetes Mellitus
Ectopia Lentis
Edema
Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome, Cardiac Valvular Form
Ehlers-Danlos Syndrome Type 2
Ehlers-Danlos Syndrome Type 3
Endomyocardial Fibrosis
Epiphyseal Dysplasia, Multiple, 1
Epiphyseal Dysplasia, Multiple, 3
Epiphyseal Dysplasia, Multiple, 5
Related Genes
ACAN
CD4
CHI3L1
COL11A1
COL14A1
COL15A1
COL19A1
COL1A1
COL1A2
COL24A1
COL27A1
COL3A1
COL4A1
COL4A2
COL4A3
COL4A4
COL4A6
COL5A1
COL5A2
COL8A2
COMP
DSPP
EFEMP2
ELN
FBLN1
FBLN2
FBN1
FBN2
FBN3
HAPLN1
HAPLN4
IMPG1
LAMA1
LAMB1
LAMC1
LUM
MATN1
MEPE
MGP
MUC3
MUC5AC
NCAN
OPTC
PRELP
VCAN
