Congenital Disorder

X-Linked Intellectual Disability

AMW:DIS:100489

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).

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X-Linked Intellectual Disability has parent Genetic Diseases, X-Linked

X-Linked Intellectual Disability has parent Heredodegenerative Disorders, Nervous System

X-Linked Intellectual Disability has parent Intellectual Disability

Adrenoleukodystrophy has parent X-Linked Intellectual Disability

Lesch-Nyhan Syndrome has parent X-Linked Intellectual Disability

Menkes Kinky Hair Syndrome has parent X-Linked Intellectual Disability

Pyruvate Dehydrogenase Complex Deficiency Disease has parent X-Linked Intellectual Disability

Classical Lissencephalies and Subcortical Band Heterotopias has parent X-Linked Intellectual Disability

Coffin-Lowry Syndrome has parent X-Linked Intellectual Disability

Fragile X Syndrome has parent X-Linked Intellectual Disability

Glycogen Storage Disease Type IIb has parent X-Linked Intellectual Disability

Mucopolysaccharidosis II has parent X-Linked Intellectual Disability

Rett Syndrome has parent X-Linked Intellectual Disability

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