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Death Statistics for Types of Connective tissue disorders

Deaths and Connective tissue disorders:

This section presents information about the death rate statistics for the various types of Connective tissue disorders.

Death Statistics for Types of Connective tissue disorders

Disease

Death Rate Estimate

US deaths estimate

Statistic Used for Calculation

Scleroderma N/A N/A estimated 300,000 Americans (NWHIC)
SLE N/A N/A 1.4 million people in the United States, 1 in 85 (NWHIC)
Rheumatoid arthritis N/A N/A 2.5 million Americans (NWHIC); 1% of US population (NIAMS)
Sjögren's syndrome N/A N/A 1 to 4 million people with Sjogren’s Syndrome (NIAMS)
Heritable Disorders of Connective Tissue N/A N/A estimated 1 million people in USA with heritable connective tissue disorder (NIAMS)
Ehlers-Danlos syndrome N/A N/A estimated 1 per 250,000 people suffer from the vascular type of Ehlers-Danlos syndrome, Genetics Home Reference website
Epidermolysis bullosa N/A N/A No information
Marfan syndrome N/A N/A 1 per 5,000 people are affected by Marfan syndrome worldwide, Genetics Home Reference website
Osteogenesis imperfecta N/A N/A 6-7 per 100,000 people are affected by osteogenesis imperfecta worldwide, Genetics Home Reference website
Generalized connective tissue syndrome N/A N/A No information
Liposarcoma N/A N/A No information
Fibrosarcoma N/A N/A No information
Soft Tissue Sarcoma unavailable No information
Sarcoma N/A N/A No information
Leiomyosarcoma N/A N/A No information
Collagenopathy, COL3 N/A N/A No information
Collagenopathy, COL4 N/A N/A No information
Collagenopathy, COL5 N/A N/A No information
Collagenopathy, COL6 N/A N/A No information
Collagenopathy, COL7 N/A N/A No information
Collagenopathy, COL8 N/A N/A No information
Collagenopathy, COL9 N/A N/A No information
Collagenopathy, COL10 N/A N/A No information
Collagenopathy, COL11 N/A N/A No information
Collagenopathy, COL17 N/A N/A No information
Collagenopathy, COL1 N/A N/A No information
Collagenopathy, type 2 alpha 1 N/A N/A No information
Cutis laxa N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 12 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 11 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 10 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 9 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 8 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 7 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 6 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 5 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 4 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 3 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 2 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 1 N/A N/A No information
Systemic Lupus Erythematosus with Vitiligo, Susceptibility to, 1 N/A N/A No information
Systemic Lupus Erythematosus with Hemolytic Anemia, Susceptibility to, 1 N/A N/A No information
Systemic Lupus Erythematosus with Nephritis, Susceptibility to, 1 N/A N/A No information
Systemic Lupus Erythematosus, Susceptibility to, 13 N/A N/A No information
Scleroderma Associated with Thymus Hyperplasia N/A N/A No information
Localized Scleroderma N/A N/A No information
Morphea N/A N/A No information
Lupus N/A N/A 1.4 million people in the United States, 1 in 85 (NWHIC)
Discoid lupus erythematosus N/A N/A No information
Neonatal lupus N/A N/A very rare
Mixed connective tissue disease N/A N/A No information
Discoid Lupus N/A N/A No information
Chronic Discoid lupus N/A N/A No information
Subacute cutaneous lupus erythematosus N/A N/A No information
Systemic lupus erythematoses N/A N/A No information
Bullous systemic lupus erythematosus N/A N/A No information
Lupus erythematosus tumidus N/A N/A No information
Subcutaneous lupus erythematosus psoariasiform type N/A N/A No information
Lupus nephritis N/A N/A No information
Winchester Syndrome N/A N/A No information
Marfan Syndrome type 2 N/A N/A No information
Ehlers-Danlos syndrome, Beasley Cohen type N/A N/A No information
Ehlers-Danlos syndrome, progeroid form N/A N/A No information
Ehlers-Danlos syndrome with periventricular heterotopia N/A N/A No information
Osteogenesis imperfecta, type 2A N/A N/A No information
Osteogenesis imperfecta, type IIB N/A N/A No information
Osteogenesis imperfecta, type VIII N/A N/A No information
Weak bones similar to that of osteogenesis imperfecta N/A N/A No information
Ehlers-Danlos syndrome type V N/A N/A No information
Ehlers-Danlos syndrome type X N/A N/A No information
Ehlers-Danlos syndrome, 6B N/A N/A No information
Ehlers-Danlos syndrome, hypermobile type N/A N/A No information
Osteogenesis imperfecta, type 1A N/A N/A No information
Osteogenesis imperfecta, type 1B N/A N/A No information
Ehlers-Danlos syndrome, hypermobility type N/A N/A No information
Ehlers-Danlos syndrome, progeroid form 2 N/A N/A No information
Ehlers-Danlos syndrome type II N/A N/A No information
Ehlers-Danlos syndrome, arthrochalasic type N/A N/A No information
Ehlers-Danlos syndrome type VIII N/A N/A No information
Ehlers-Danlos syndrome type VI N/A N/A No information
Ehlers-Danlos syndrome type IV N/A N/A No information
Ehlers-Danlos syndrome type IX N/A N/A No information
Ehlers-Danlos syndrome, vascular type N/A N/A No information
Ehlers-Danlos syndrome, dermatospraxis type N/A N/A No information
Ehlers-Danlos syndrome, kyphoscoliosis type N/A N/A No information
Osteogenesis imperfecta Type I N/A N/A 3-4 per 100,000 people are affected by osteogenesis imperfecta type I worldwide, Genetics Home Reference website
Ehlers-Danlos syndrome, tenascin-X deficiency N/A N/A No information
Ehlers-Danlos syndrome, cardiac valvular form N/A N/A No information
Ehlers-Danlos syndrome type III N/A N/A No information
Ehlers-Danlos syndrome, classic type N/A N/A No information
Ehlers-Danlos syndrome Type I N/A N/A No information
Ehlers-Danlos syndrome, X-linked N/A N/A No information
Ehlers-Danlos syndrome, VIIB N/A N/A No information
Ehlers-Danlos Syndrome, Dysfibronectinemic type N/A N/A No information
Ehlers-Danlos syndrome with Platelet Dysfunction from Fibronectin Abnormality N/A N/A No information
Ehlers-Danlos syndrome type VII N/A N/A No information
Ehlers-Danlos syndrome caused by tenascin-X deficiency N/A N/A No information
Ehlers Danlos syndrome type 4, autosomal dominant N/A N/A No information
Ehlers-Danlos, syndrome, periodontitis type N/A N/A No information
Ehlers-Danlos syndrome type 3 N/A N/A No information
Ehlers-Danlos syndrome type 4 N/A N/A No information
Ehlers-Danlos syndrome, dermatosparaxis type N/A N/A No information
Osteogenesis imperfecta, Type VI N/A N/A No information
Osteogenesis imperfecta -- congenital joint contractures N/A N/A No information
Osteogenesis imperfecta, type 2 N/A N/A No information
Osteogenesis imperfecta, type 3 N/A N/A No information
Osteogenesis imperfecta, type 4 N/A N/A No information
Osteogenesis imperfecta, type 5 N/A N/A No information
Osteogenesis imperfecta, type 6 N/A N/A No information
Osteogenesis imperfecta, Levin type N/A N/A No information
Osteogenesis imperfecta type IIII N/A N/A 1-2 per 100,000 people are affected by osteogenesis imperfecta type IIII worldwide, Genetics Home Reference website
Osteogenesis imperfecta type IV N/A N/A 3-4 per 100,000 people are affected by osteogenesis imperfecta type IV worldwide, Genetics Home Reference website
Osteogenesis imperfecta, type 7 N/A N/A No information
CREST syndrome N/A N/A No information
Eosinophilic fasciitis N/A N/A No information
Fibrosis N/A N/A No information
Human adjuvant disease N/A N/A No information
Acute rheumatic fever unavailable No information
Plexosarcoma N/A N/A No information
Rhabdomyosarcoma, Botryoid type N/A N/A No information
Rheumatism N/A N/A No information
Infantile Fibrosarcoma N/A N/A No information
Synovial sarcoma N/A N/A No information
Adult Fibrosarcoma N/A N/A No information
Rhabdomyosarcoma of the orbit N/A N/A No information
Rhabdomyosarcoma N/A N/A No information
Acroosteolysis dominant type N/A N/A No information
Hajdu-Cheney Syndrome N/A N/A No information
Cutis laxa, recessive type 1 N/A N/A No information
Cutis laxa, recessive type 2 N/A N/A No information
Cutis laxa, recessive N/A N/A No information
Cutis laxa, dominant type N/A N/A No information
Cutis laxa -- osteoporosis N/A N/A No information
Cutis Laxa, Autosomal Dominant N/A N/A No information
Cutis Laxa with or without Congenital Disorder of Glycosylation N/A N/A No information
Cutis Laxa, Debre Type N/A N/A No information
Cutis Laxa with Bone Dystrophy N/A N/A No information
Cutis Laxa with Growth and Developmental Delay N/A N/A No information
Cutis Laxa, Autosomal Recessive, Type IIA N/A N/A No information
Cutis Laxa, Autosomal Recessive, Type IIB N/A N/A No information
Cutis laxa congenital N/A N/A No information
Rheumatic fever unavailable No information
Scleroderma, linear N/A N/A No information
Inheritable disorders of connective tissue N/A N/A No information
Myxoid liposarcoma N/A N/A No information
Dermatofibrosarcoma protuberans N/A N/A No information
SLE associated with Thymus Hyperplasia N/A N/A No information
Marfanoid syndrome, da Silva type N/A N/A No information
OI, Type I N/A N/A No information
Meigel Disease N/A N/A No information
Alport Syndrome N/A N/A 1 per 50,000 newborns suffer from Alport syndrome, Genetics Home Reference website
Juvenile Scleroderma N/A N/A No information
Arterial tortuosity syndrome N/A N/A No information
Larsen-like syndrome, lethal form N/A N/A No information
Pseudoxanthoma elasticum, recessive form N/A N/A No information
Larsen-like syndrome, lethal type N/A N/A No information
Pseudoxanthoma elasticum, dominant form N/A N/A No information
Pseudoxanthoma elasticum, forme fruste N/A N/A No information
Pseudoxanthoma elasticum N/A N/A 1 per 25,000 - 100,000 people are affected by pseudoxanthoma elasticum, Genetics Home Reference website
Marfanoid hypermobility N/A N/A No information
Osteogenesis imperfecta congenita, microcephaly, and cataracts N/A N/A No information
Connective tissue dysplasia, Spellacy type N/A N/A No information
Scleroderma, diffuse N/A N/A No information
Scleroderma, systemic N/A N/A No information
Scleroderma sine scleroderma N/A N/A No information
Gerodermia osteodysplastica N/A N/A No information
Gerodermia osteodysplasticum N/A N/A No information
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency N/A N/A No information
Leigh syndrome, Saguenay-Lac-St. Jean type N/A N/A No information
Scleromyxedema N/A N/A No information
Gronblad-Strandberg-Touraine syndrome N/A N/A No information
Gerodermia osteodysplastica hereditaria N/A N/A No information
Geroderma osteodysplastica N/A N/A No information
Fibronectin-Deficient EDS N/A N/A No information
Saguenay-Lac Saint Jean -- COX deficiency N/A N/A No information
Macrodactyly -- Hemihypertrophy -- Connective tissue nevi syndrome N/A N/A No information
REST syndrome N/A N/A No information
Macleod-Fraser syndrome N/A N/A No information
Marfan-like syndrome, Boileau type N/A N/A No information
Marphanoid syndrome, type De Silva N/A N/A No information
Marfan-Like syndrome N/A N/A No information
MASS syndrome N/A N/A No information
Brittle bone syndrome lethal type N/A N/A No information
Strudwick syndrome N/A N/A only a few cases of the condition have been reported, Genetics Home Reference website
Achard syndrome N/A N/A No information
Fibrosing Mediastinitis idiopathic N/A N/A No information
Loewenthal syndrome N/A N/A No information
Beals syndrome N/A N/A No information

Types of Connective tissue disorders

For more information about types of Connective tissue disorders, refer to our section on types of Connective tissue disorders. See also more information on death information for Connective tissue disorders.

 

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