ONKI3 | Medical Subject Headings

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The way concept relations are shown: separately in hierarchy

Hippel-Lindau Disease

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Angiomatosis ∟ Hippel-Lindau Disease 6 coordinate concepts ∟ Angiomatosis, Bacillary \| ∟ Klippel-Trenaunay-Weber Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Ataxia Telangiectasia \| ∟ Neurofibromatoses \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease 6 coordinate concepts ∟ Angiomatosis, Bacillary \| ∟ Klippel-Trenaunay-Weber Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Ataxia Telangiectasia \| ∟ Neurofibromatoses \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease 6 coordinate concepts ∟ Angiomatosis, Bacillary \| ∟ Klippel-Trenaunay-Weber Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Ataxia Telangiectasia \| ∟ Neurofibromatoses \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease 6 coordinate concepts ∟ Angiomatosis, Bacillary \| ∟ Klippel-Trenaunay-Weber Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Ataxia Telangiectasia \| ∟ Neurofibromatoses \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease 6 coordinate concepts ∟ Angiomatosis, Bacillary \| ∟ Klippel-Trenaunay-Weber Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Ataxia Telangiectasia \| ∟ Neurofibromatoses \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease 6 coordinate concepts ∟ Angiomatosis, Bacillary \| ∟ Klippel-Trenaunay-Weber Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Ataxia Telangiectasia \| ∟ Neurofibromatoses \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease 6 coordinate concepts ∟ Angiomatosis, Bacillary \| ∟ Klippel-Trenaunay-Weber Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Ataxia Telangiectasia \| ∟ Neurofibromatoses \| ∟ Tuberous Sclerosis X
Broader terms:	Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Angiomatosis ∟ Hippel-Lindau Disease Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Neurocutaneous Syndromes ∟ Hippel-Lindau Disease Angiomatosis > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Neurocutaneous Syndromes > Ectodermal Dysplasia > Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Neurocutaneous Syndromes > Ectodermal Dysplasia > Skin Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Neurocutaneous Syndromes > Ectodermal Dysplasia > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Neurocutaneous Syndromes > Nervous System Diseases > Medical Subject Headings (MeSH) Neurocutaneous Syndromes > Ectodermal Dysplasia > Skin Abnormalities > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Neurocutaneous Syndromes > Ectodermal Dysplasia > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
historyNote*:	91(75); was see under ANGIOMATOSIS 1975-90 X
onlineNote*:	search ANGIOMATOSIS 1966-74 X
publicMeSHNote*:	91; was see under ANGIOMATOSIS 1975-90 X
Scope note:	An autosomal dominant disorder associated with various neoplasms including central nervous system (most often cerebellar) and retinal HEMANGIOBLASTOMA, endolymphatic sac tumors, renal cell carcinoma (see CARCINOMA, RENAL CELL), renal and pancreatic cysts, HEMANGIOMA of the spinal cord, and PHEOCHROMOCYTOMA. The most common presenting manifestations are neurologic deficits associated with intracranial hemangioblastomas which may HEMORRHAGE, causing ataxia, INTRACRANIAL HYPERTENSION, and other signs of neurologic dysfunction. (From Neurochirurgie 1998 Nov;44(4):258-66) X
activeMeSHYear*:	2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1991-01-01X
dateRevised*:	2003-07-09X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Angiomatosis, Bacillary \| Klippel-Trenaunay-Weber Syndrome \| Sturge-Weber Syndrome \| Ataxia Telangiectasia \| Neurofibromatoses \| Tuberous Sclerosis X
URI:	X
Labels and equivalent concepts:	Serebroretinaalinen angiomatoosi (fi) von Hippel-Lindaun tauti (fi, replaced) Hippel-Lindaun tauti (fi, replaced) Hippel-Lindaus sjukdom (sv) von Hippel-Lindaus sjukdom (sv, replaced) von Hippel-Lindau Syndrome (en, replaced) Familial Cerebello-Retinal Angiomatosis (en, replaced) Lindau Disease (en, replaced) Lindau's Disease (en, replaced) von Hippel-Lindau Disease (en, replaced) Cerebelloretinal Angiomatosis, Familial (en, replaced) Angiomatosis cerebroretinalis (la-FI, replaced) Morbus Hippel-Lindau (la-FI, replaced) X
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