ONKI3 | Medical Subject Headings


Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Cutis Laxa 43 coordinate concepts ∟ alpha 1-Antitrypsin Deficiency \| ∟ Cartilage Diseases \| ∟ Cellulitis \| ∟ Collagen Diseases \| ∟ Dermatomyositis \| ∟ Dupuytren's Contracture \| ∟ Homocystinuria \| ∟ Lupus Erythematosus, Cutaneous \| ∟ Lupus Erythematosus, Systemic \| ∟ Marfan Syndrome \| ∟ Mixed Connective Tissue Disease \| ∟ Mucinoses \| ∟ Neoplasms, Connective Tissue \| ∟ Noonan Syndrome \| ∟ Osteopoikilosis \| ∟ Panniculitis \| ∟ Penile Induration \| ∟ Pseudoxanthoma Elasticum \| ∟ Rheumatic Diseases \| ∟ Scleroderma, Localized \| ∟ Scleroderma, Systemic \| ∟ Albinism \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Rothmund-Thomson Syndrome \| ∟ Sjogren-Larsson Syndrome \| ∟ Xeroderma Pigmentosum Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Cutis Laxa 43 coordinate concepts ∟ alpha 1-Antitrypsin Deficiency \| ∟ Cartilage Diseases \| ∟ Cellulitis \| ∟ Collagen Diseases \| ∟ Dermatomyositis \| ∟ Dupuytren's Contracture \| ∟ Homocystinuria \| ∟ Lupus Erythematosus, Cutaneous \| ∟ Lupus Erythematosus, Systemic \| ∟ Marfan Syndrome \| ∟ Mixed Connective Tissue Disease \| ∟ Mucinoses \| ∟ Neoplasms, Connective Tissue \| ∟ Noonan Syndrome \| ∟ Osteopoikilosis \| ∟ Panniculitis \| ∟ Penile Induration \| ∟ Pseudoxanthoma Elasticum \| ∟ Rheumatic Diseases \| ∟ Scleroderma, Localized \| ∟ Scleroderma, Systemic \| ∟ Albinism \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Rothmund-Thomson Syndrome \| ∟ Sjogren-Larsson Syndrome \| ∟ Xeroderma Pigmentosum Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Cutis Laxa 43 coordinate concepts ∟ alpha 1-Antitrypsin Deficiency \| ∟ Cartilage Diseases \| ∟ Cellulitis \| ∟ Collagen Diseases \| ∟ Dermatomyositis \| ∟ Dupuytren's Contracture \| ∟ Homocystinuria \| ∟ Lupus Erythematosus, Cutaneous \| ∟ Lupus Erythematosus, Systemic \| ∟ Marfan Syndrome \| ∟ Mixed Connective Tissue Disease \| ∟ Mucinoses \| ∟ Neoplasms, Connective Tissue \| ∟ Noonan Syndrome \| ∟ Osteopoikilosis \| ∟ Panniculitis \| ∟ Penile Induration \| ∟ Pseudoxanthoma Elasticum \| ∟ Rheumatic Diseases \| ∟ Scleroderma, Localized \| ∟ Scleroderma, Systemic \| ∟ Albinism \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Rothmund-Thomson Syndrome \| ∟ Sjogren-Larsson Syndrome \| ∟ Xeroderma Pigmentosum X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Cutis Laxa Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Cutis Laxa Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Cutis Laxa Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Connective Tissue 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
Annotation:	loose pendulous skin X
historyNote*:	68; was DERMATOLYSIS 1963-67 X
onlineNote*:	use CUTIS LAXA to search DERMATOLYSIS 1966-67 X
publicMeSHNote*:	68; was DERMATOLYSIS 1963-67 X
Scope note:	A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (From Dorland, 27th ed) X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1968-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Related term:	Ehlers-Danlos Syndrome X
Type:	Concept X
Coordinate terms:	alpha 1-Antitrypsin Deficiency \| Cartilage Diseases \| Cellulitis \| Collagen Diseases \| Dermatomyositis \| Dupuytren's Contracture \| Homocystinuria \| Lupus Erythematosus, Cutaneous \| Lupus Erythematosus, Systemic \| Marfan Syndrome \| Mixed Connective Tissue Disease \| Mucinoses \| Neoplasms, Connective Tissue \| Noonan Syndrome \| Osteopoikilosis \| Panniculitis \| Penile Induration \| Pseudoxanthoma Elasticum \| Rheumatic Diseases \| Scleroderma, Localized \| Scleroderma, Systemic \| Albinism \| Dermatitis, Atopic \| Dyskeratosis Congenita \| Ectodermal Dysplasia \| Ehlers-Danlos Syndrome \| Epidermolysis Bullosa \| Ichthyosiform Erythroderma, Congenital \| Ichthyosis Bullosa of Siemens \| Ichthyosis Vulgaris \| Ichthyosis, X-Linked \| Incontinentia Pigmenti \| Keratoderma, Palmoplantar \| Keratosis Follicularis \| Leukokeratosis, Hereditary Mucosal \| Lipoid Proteinosis of Urbach and Wiethe \| Pemphigus, Benign Familial \| Porokeratosis \| Porphyria, Erythropoietic \| Porphyrias, Hepatic \| Rothmund-Thomson Syndrome \| Sjogren-Larsson Syndrome \| Xeroderma Pigmentosum X
URI:	X
Labels and equivalent concepts:	Veltto iho (fi) Ihon velttous (fi, replaced) Ihon ryppyisyys (fi, replaced) Dermatokalaasi (fi, replaced) Dermatomegaly (en, replaced) Dermatolysis (en, replaced) Cutis laxa (la-FI, replaced) Dermmatochalasis (la-FI, replaced) X
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