ONKI3 | Medical Subject Headings

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Mental Retardation, X-Linked

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked 53 coordinate concepts 9 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Mental Retardation, X-Linked 53 coordinate concepts 9 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked 53 coordinate concepts 9 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Mental Retardation, X-Linked 53 coordinate concepts 9 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked 53 coordinate concepts 9 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked 53 coordinate concepts 9 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked 53 coordinate concepts 9 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Coffin-Lowry Syndrome \| ∟ Fragile X Syndrome \| ∟ Glycogen Storage Disease Type IIb \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mucopolysaccharidosis II \| ∟ Pyruvate Dehydrogenase Complex Deficiency Disease \| ∟ Rett Syndrome ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Cri-du-Chat Syndrome \| ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Mental Retardation, X-Linked Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Mental Retardation, X-Linked Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Mental Retardation, X-Linked Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Mental Retardation, X-Linked Mental Retardation > Neurobehavioral Manifestations > Behavior and Behavior Mechanisms > Medical Subject Headings (MeSH) Genetic Diseases, X-Linked > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Heredodegenerative Disorders, Nervous System > 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) Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System 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
Narrower terms:	Adrenoleukodystrophy \| Coffin-Lowry Syndrome \| 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
History note:	Mental Retardation/genetics (1971-2002)X
historyNote*:	2003 X
publicMeSHNote*:	2003 X
Scope note:	A class of genetic disorders resulting in mental retardation that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS). X
activeMeSHYear*:	2003 \| 2004 \| 2005 \| 2005A \| 2006 \| 2007X
dateCreated*:	2002-07-03X
dateEstablished*:	2003-01-01X
dateRevised*:	2004-07-28X
recordAuthorizer*:	jlsX
recordMaintainer*:	jlsX
recordOriginator*:	jmpX
Type:	Concept X
Coordinate terms:	Androgen-Insensitivity Syndrome \| Choroideremia \| Dyskeratosis Congenita \| Ectodermal Dysplasia 1, Anhidrotic \| Fabry Disease \| Focal Dermal Hypoplasia \| Glycogen Storage Disease Type IIb \| Glycogen Storage Disease Type VIII \| Granulomatous Disease, Chronic \| Hemophilia B \| Hyper-IgM Immunodeficiency Syndrome, Type 1 \| Hypophosphatemic Rickets, X-Linked Dominant \| Ichthyosis, X-Linked \| Muscular Dystrophy, Duchenne \| Muscular Dystrophy, Emery-Dreifuss \| Oculocerebrorenal Syndrome \| Pelizaeus-Merzbacher Disease \| Wiskott-Aldrich Syndrome \| X-Linked Combined Immunodeficiency Diseases \| Cri-du-Chat Syndrome \| D008607Q000193* \| De Lange Syndrome \| Down Syndrome \| Prader-Willi Syndrome \| Rubinstein-Taybi Syndrome \| WAGR Syndrome \| Williams Syndrome \| Alexander Disease \| Amyloid Neuropathies, Familial \| Canavan Disease \| Cockayne Syndrome \| Dystonia Musculorum Deformans \| Gerstmann-Straussler-Scheinker Disease \| Hallervorden-Spatz Syndrome \| Hepatolenticular Degeneration \| Hereditary Central Nervous System Demyelinating Diseases \| Hereditary Motor and Sensory Neuropathies \| Hereditary Sensory and Autonomic Neuropathies \| Huntington Disease \| Lafora Disease \| Lesch-Nyhan Syndrome \| Menkes Kinky Hair Syndrome \| Myotonia Congenita \| Myotonic Dystrophy \| Neurofibromatoses \| Neuronal Ceroid-Lipofuscinoses \| Optic Atrophies, Hereditary \| Rett Syndrome \| Spinal Muscular Atrophies of Childhood \| Spinocerebellar Degenerations \| Tourette Syndrome \| Tuberous Sclerosis \| Unverricht-Lundborg Syndrome X
URI:	X
Labels and equivalent concepts:	X-sidonnainen kehitysvammaisuus (fi) X-sidonnainen kehitysvamma (fi, replaced) X-sidonnainen jälkeenjääneisyys (fi, replaced) Psykisk utvecklingsstörning, X-bunden (sv) X-Linked Mental Retardation Syndromes (en, replaced) X-Linked Mental Retardation Disorders (en, replaced) X-Linked Mental Retardation (en, replaced) X
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