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Rubinstein-Taybi Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Chromosome Disorders ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Musculoskeletal Abnormalities ∟ Craniofacial Abnormalities ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Chromosome Disorders ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dysostoses ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Musculoskeletal Abnormalities ∟ Craniofacial Abnormalities ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome 48 coordinate concepts ∟ Cleidocranial Dysplasia \| ∟ Craniofacial Dysostosis \| ∟ Craniosynostoses \| ∟ Holoprosencephaly \| ∟ LEOPARD Syndrome \| ∟ Maxillofacial Abnormalities \| ∟ Microcephaly \| ∟ Noonan Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Plagiocephaly, Nonsynostotic \| ∟ Platybasia \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ 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 \| ∟ Focal Dermal Hypoplasia \| ∟ Klippel-Feil Syndrome \| ∟ Synostosis X
Broader terms:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Chromosome Disorders ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Musculoskeletal Abnormalities ∟ Craniofacial Abnormalities ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Chromosome Disorders ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dysostoses ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Musculoskeletal Abnormalities ∟ Craniofacial Abnormalities ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Rubinstein-Taybi Syndrome Mental Retardation > Neurobehavioral Manifestations > Behavior and Behavior Mechanisms > Medical Subject Headings (MeSH) 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) Craniofacial Abnormalities > Musculoskeletal Abnormalities > 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) Mental Retardation > Mental Disorders Diagnosed in Childhood > Mental Disorders > Medical Subject Headings (MeSH) Dysostoses > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Craniofacial Abnormalities > Musculoskeletal Abnormalities > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Nervous System Diseases > Medical Subject Headings (MeSH) Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Signs and Symptoms > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
History note:	Abnormalities, Multiple (1968-1971) \| Mental Retardation (1966-1971)X
historyNote*:	91(72); was see under ABNORMALITIES, MULTIPLE 1972-90 X
publicMeSHNote*:	91; was see under ABNORMALITIES, MULTIPLE 1972-90 X
Scope note:	A chromosomal disorder characterized by MENTAL RETARDATION, broad thumbs, webbing of fingers and toes, beaked nose, short upper lip, pouting lower lip, agenesis of corpus callosum, large foramen magnum, keloid formation, pulmonary stenosis, vertebral anomalies, chest wall anomalies, sleep apnea, and megacolon. The disease has an autosomal dominant pattern of inheritance and is associated with deletions of the short arm of chromosome 16 (16p13.3). X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1991-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Related term:	Mental Retardation X
Type:	Concept X
Coordinate terms:	Cleidocranial Dysplasia \| Craniofacial Dysostosis \| Craniosynostoses \| Holoprosencephaly \| LEOPARD Syndrome \| Maxillofacial Abnormalities \| Microcephaly \| Noonan Syndrome \| Orofaciodigital Syndromes \| Plagiocephaly, Nonsynostotic \| Platybasia \| Cri-du-Chat Syndrome \| D008607Q000193* \| De Lange Syndrome \| Down Syndrome \| Mental Retardation, X-Linked \| Prader-Willi Syndrome \| WAGR Syndrome \| Williams Syndrome \| Angelman Syndrome \| Beckwith-Wiedemann Syndrome \| Branchio-Oto-Renal Syndrome \| Sex Chromosome Disorders \| Alagille Syndrome \| Bardet-Biedl Syndrome \| Basal Cell Nevus Syndrome \| Bloom Syndrome \| Cockayne Syndrome \| Ectodermal Dysplasia \| Gardner Syndrome \| Incontinentia Pigmenti \| Laurence-Moon Syndrome \| Marfan Syndrome \| Mobius Syndrome \| Nail-Patella Syndrome \| Oculocerebrorenal Syndrome \| 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 \| Focal Dermal Hypoplasia \| Klippel-Feil Syndrome \| Synostosis X
URI:	X
Labels and equivalent concepts:	Rubinstein-Taybin oireyhtymä (fi) Rubinstein Syndrome (en, replaced) Broad Thumb-Hallux Syndrome (en, replaced) Síndrome de Rubinstein-Taybi (es) σύνδρομο Rubinstein-Taybi (el) Rubinstein-Taybi-Syndrom (de) Rubinsteinův-Taybiův syndrom (cs) Síndrome de Pulgar y Hallux Ancho (es, replaced) X
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