ONKI3 | Medical Subject Headings

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Coffin-Lowry Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome 8 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome 8 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome 8 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome 8 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome 8 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome 8 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome 8 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked ∟ Coffin-Lowry Syndrome Mental Retardation, X-Linked > Mental Retardation > Neurobehavioral Manifestations > Behavior and Behavior Mechanisms > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Genetic Diseases, X-Linked > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Heredodegenerative Disorders, Nervous System > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Mental Retardation > Mental Disorders Diagnosed in Childhood > Mental Disorders > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Nervous System Diseases > Medical Subject Headings (MeSH) Mental Retardation, X-Linked > Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Signs and Symptoms > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
History note:	Mental Retardation/genetics (1975-2002)X
historyNote*:	2003 X
publicMeSHNote*:	2003 X
Scope note:	A rare, X-linked mental retardation syndrome that results from mutations in the RIBOSOMAL PROTEIN S6 KINASE gene. Typical manifestations of the disease include an intelligence quotient of less than 50, facial anomalies, and other malformations. X
activeMeSHYear*:	2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	2002-07-03X
dateEstablished*:	2003-01-01X
Type:	Concept X
Coordinate terms:	Adrenoleukodystrophy \| Fragile X Syndrome \| Glycogen Storage Disease Type IIb \| Lesch-Nyhan Syndrome \| Menkes Kinky Hair Syndrome \| Mucopolysaccharidosis II \| Pyruvate Dehydrogenase Complex Deficiency Disease \| Rett Syndrome X
URI:	X
Labels and equivalent concepts:	Coffin-Lowryn oireyhtymä (fi) Coffin-Lowrys syndrom (sv) X
Share:	X