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Ehlers-Danlos Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Vascular Hemostatic Disorders ∟ Ehlers-Danlos Syndrome 41 coordinate concepts ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Keloid \| ∟ Necrobiotic Disorders \| ∟ Nephritis, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Cryoglobulinemia \| ∟ Hemangioma, Cavernous \| ∟ Multiple Myeloma \| ∟ Purpura, Hyperglobulinemic \| ∟ Purpura, Schoenlein-Henoch \| ∟ Scurvy \| ∟ Shwartzman Phenomenon \| ∟ Telangiectasia, Hereditary Hemorrhagic \| ∟ Waldenstrom Macroglobulinemia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ehlers-Danlos Syndrome 41 coordinate concepts ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Keloid \| ∟ Necrobiotic Disorders \| ∟ Nephritis, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Cryoglobulinemia \| ∟ Hemangioma, Cavernous \| ∟ Multiple Myeloma \| ∟ Purpura, Hyperglobulinemic \| ∟ Purpura, Schoenlein-Henoch \| ∟ Scurvy \| ∟ Shwartzman Phenomenon \| ∟ Telangiectasia, Hereditary Hemorrhagic \| ∟ Waldenstrom Macroglobulinemia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ehlers-Danlos Syndrome 41 coordinate concepts ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Keloid \| ∟ Necrobiotic Disorders \| ∟ Nephritis, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Cryoglobulinemia \| ∟ Hemangioma, Cavernous \| ∟ Multiple Myeloma \| ∟ Purpura, Hyperglobulinemic \| ∟ Purpura, Schoenlein-Henoch \| ∟ Scurvy \| ∟ Shwartzman Phenomenon \| ∟ Telangiectasia, Hereditary Hemorrhagic \| ∟ Waldenstrom Macroglobulinemia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Vascular Hemostatic Disorders ∟ Ehlers-Danlos Syndrome 41 coordinate concepts ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Keloid \| ∟ Necrobiotic Disorders \| ∟ Nephritis, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Cryoglobulinemia \| ∟ Hemangioma, Cavernous \| ∟ Multiple Myeloma \| ∟ Purpura, Hyperglobulinemic \| ∟ Purpura, Schoenlein-Henoch \| ∟ Scurvy \| ∟ Shwartzman Phenomenon \| ∟ Telangiectasia, Hereditary Hemorrhagic \| ∟ Waldenstrom Macroglobulinemia Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Collagen Diseases ∟ Ehlers-Danlos Syndrome 41 coordinate concepts ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Keloid \| ∟ Necrobiotic Disorders \| ∟ Nephritis, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Cryoglobulinemia \| ∟ Hemangioma, Cavernous \| ∟ Multiple Myeloma \| ∟ Purpura, Hyperglobulinemic \| ∟ Purpura, Schoenlein-Henoch \| ∟ Scurvy \| ∟ Shwartzman Phenomenon \| ∟ Telangiectasia, Hereditary Hemorrhagic \| ∟ Waldenstrom Macroglobulinemia Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ehlers-Danlos Syndrome 41 coordinate concepts ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Keloid \| ∟ Necrobiotic Disorders \| ∟ Nephritis, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Cryoglobulinemia \| ∟ Hemangioma, Cavernous \| ∟ Multiple Myeloma \| ∟ Purpura, Hyperglobulinemic \| ∟ Purpura, Schoenlein-Henoch \| ∟ Scurvy \| ∟ Shwartzman Phenomenon \| ∟ Telangiectasia, Hereditary Hemorrhagic \| ∟ Waldenstrom Macroglobulinemia Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ehlers-Danlos Syndrome 41 coordinate concepts ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Keloid \| ∟ Necrobiotic Disorders \| ∟ Nephritis, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Cryoglobulinemia \| ∟ Hemangioma, Cavernous \| ∟ Multiple Myeloma \| ∟ Purpura, Hyperglobulinemic \| ∟ Purpura, Schoenlein-Henoch \| ∟ Scurvy \| ∟ Shwartzman Phenomenon \| ∟ Telangiectasia, Hereditary Hemorrhagic \| ∟ Waldenstrom Macroglobulinemia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Vascular Hemostatic Disorders ∟ Ehlers-Danlos Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ehlers-Danlos Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ehlers-Danlos Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Vascular Hemostatic Disorders ∟ Ehlers-Danlos Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Collagen Diseases ∟ Ehlers-Danlos Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ehlers-Danlos Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ehlers-Danlos Syndrome Vascular Hemostatic Disorders > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Skin Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Vascular Hemostatic Disorders > Hemorrhagic Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Collagen Diseases > Connective Tissue Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Skin Abnormalities > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Scope note:	A heterogeneous group of inherited COLLAGEN DISEASES. The most common manifestations of Ehlers-Danlos Syndrome are hyperextensible skin and joints, skin fragility and reduced wound healing capability. X
activeMeSHYear*:	2002 \| 2002A \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2001-09-07X
recordAuthorizer*:	sjnX
recordMaintainer*:	sjnX
recordOriginator*:	NLMX
Related term:	Reticulin X
Type:	Concept X
Coordinate terms:	Acrodermatitis \| Dyskeratosis Congenita \| Ectodermal Dysplasia \| Epidermolysis Bullosa \| Ichthyosis \| Incontinentia Pigmenti \| Port-Wine Stain \| Pseudoxanthoma Elasticum \| Rothmund-Thomson Syndrome \| Sclerema Neonatorum \| Xeroderma Pigmentosum \| Epidermolysis Bullosa Dystrophica \| Keloid \| Necrobiotic Disorders \| Nephritis, Hereditary \| Osteogenesis Imperfecta \| Albinism \| Cutis Laxa \| Dermatitis, Atopic \| Ichthyosiform Erythroderma, Congenital \| Ichthyosis Bullosa of Siemens \| Ichthyosis Vulgaris \| Ichthyosis, X-Linked \| Keratoderma, Palmoplantar \| Keratosis Follicularis \| Leukokeratosis, Hereditary Mucosal \| Lipoid Proteinosis of Urbach and Wiethe \| Pemphigus, Benign Familial \| Porokeratosis \| Porphyria, Erythropoietic \| Porphyrias, Hepatic \| Sjogren-Larsson Syndrome \| Cryoglobulinemia \| Hemangioma, Cavernous \| Multiple Myeloma \| Purpura, Hyperglobulinemic \| Purpura, Schoenlein-Henoch \| Scurvy \| Shwartzman Phenomenon \| Telangiectasia, Hereditary Hemorrhagic \| Waldenstrom Macroglobulinemia X
URI:	X
Labels and equivalent concepts:	Ehlers-Danlosin oireyhtymä (fi) Ehlers-Danlosin tauti (fi, replaced) Ehlers-Danlosin syndrooma (fi, replaced) Ehlers-Danlos syndrom (sv) Ehlers-Danlos Disease (en, replaced) Cutis Elastica (en, replaced) Morbus Ehlers-Danlos (la-FI, replaced) Syndroma Ehlers-Danlos (la-FI, replaced) X
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