Mental Retardation, X-Linked

A class of genetic disorders resulting in INTELLECTUAL DISABILITY 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).

Year introduced: 2003

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Subheadings:

Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C10.597.606.360.455, C16.320.322.500, C16.320.400.525

MeSH Unique ID: D038901

Entry Terms:

• Mental Retardation, X Linked
• Retardation, X-Linked Mental
• X-Linked Mental Retardations
• X-Linked Mental Retardation Syndromes
• X Linked Mental Retardation Syndromes
• X-Linked Mental Retardation Disorders
• X Linked Mental Retardation Disorders
• X-Linked Mental Retardation
• X Linked Mental Retardation

Previous Indexing:

• Mental Retardation/genetics (1971-2002)

All MeSH Categories
Diseases Category
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
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

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Adrenoleukodystrophy
Classical Lissencephalies and Subcortical Band Heterotopias
Coffin-Lowry Syndrome
Fragile X Syndrome
Lesch-Nyhan Syndrome
Menkes Kinky Hair Syndrome
Mucopolysaccharidosis II
Pyruvate Dehydrogenase Complex Deficiency Disease
Rett Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Adrenoleukodystrophy
Coffin-Lowry Syndrome
Fragile X Syndrome
Lesch-Nyhan Syndrome
Menkes Kinky Hair Syndrome
Mucopolysaccharidosis II
Pyruvate Dehydrogenase Complex Deficiency Disease
Rett Syndrome