ONKI3 | Medical Subject Headings

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Branchio-Oto-Renal Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Branchio-Oto-Renal Syndrome 35 coordinate concepts ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Holoprosencephaly \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ Sex Chromosome Disorders \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Chromosome Disorders ∟ Branchio-Oto-Renal Syndrome 35 coordinate concepts ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Holoprosencephaly \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ Sex Chromosome Disorders \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Chromosome Disorders ∟ Branchio-Oto-Renal Syndrome 35 coordinate concepts ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Holoprosencephaly \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ Sex Chromosome Disorders \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Branchio-Oto-Renal Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Chromosome Disorders ∟ Branchio-Oto-Renal Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Chromosome Disorders ∟ Branchio-Oto-Renal Syndrome Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Chromosome Disorders > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Chromosome Disorders > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) X
Annotation:	multiple abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: note short X ref X
History note:	Abnormalities, Multiple (1966-1996) \| Chromosome Abnormalities (1966-1996)X
historyNote*:	97 X
publicMeSHNote*:	97 X
Scope note:	An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1996-06-10X
dateEstablished*:	1997-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	JLSX
Type:	Concept X
Coordinate terms:	Angelman Syndrome \| Beckwith-Wiedemann Syndrome \| Cri-du-Chat Syndrome \| De Lange Syndrome \| Down Syndrome \| Holoprosencephaly \| Prader-Willi Syndrome \| Rubinstein-Taybi Syndrome \| Sex Chromosome Disorders \| WAGR Syndrome \| Williams Syndrome \| Alagille Syndrome \| Bardet-Biedl Syndrome \| Basal Cell Nevus Syndrome \| Bloom Syndrome \| Cockayne Syndrome \| Ectodermal Dysplasia \| Gardner Syndrome \| Incontinentia Pigmenti \| Laurence-Moon Syndrome \| LEOPARD Syndrome \| Marfan Syndrome \| Mobius Syndrome \| Nail-Patella Syndrome \| Oculocerebrorenal Syndrome \| Orofaciodigital Syndromes \| POEMS Syndrome \| Proteus Syndrome \| Prune Belly Syndrome \| Rubella Syndrome, Congenital \| Short Rib-Polydactyly Syndrome \| Smith-Lemli-Opitz Syndrome \| Waardenburg's Syndrome \| Wolfram Syndrome \| Zellweger Syndrome X
URI:	X
Labels and equivalent concepts:	Brankio-oto-renaalinen oireyhtymä (fi) Brankio-oto-renaalinen syndrooma (fi, replaced) Brankio-oto-renalsyndrom (sv) Branchio-Otorenal Syndrome (en, replaced) Branchio-Otorenal Dysplasia (en, replaced) BOR Syndrome (en, replaced) X
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