Diseases [C] » Nervous System Diseases [C10] » Neurologic Manifestations » Neurobehavioral Manifestations » Intellectual Disability » Mental Retardation, X-Linked
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked » Mental Retardation, X-Linked
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Heredodegenerative Disorders, Nervous System » Mental Retardation, X-Linked
Description
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). MeSH
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Subtype Terms (10)
Adrenoleukodystrophy
40 drugs (24 approved, 16 experimental)
Classical Lissencephalies and Subcortical Band Heterotopias
Fragile X Syndrome
40 drugs (23 approved, 17 experimental)
Glycogen Storage Disease Type IIb
1 experimental drug
Lesch-Nyhan Syndrome
2 drugs (1 approved, 1 experimental)
Menkes Kinky Hair Syndrome
3 drugs (1 approved, 2 experimental)
Mucopolysaccharidosis II
26 drugs (13 approved, 13 experimental)
Pyruvate Dehydrogenase Complex Deficiency Disease
2 drugs (1 approved, 1 experimental)
Rett Syndrome
30 drugs (17 approved, 13 experimental)
Organization Involved with Phase 3 Indications (1)
Organization Involved with Phase 2 Indications (2)
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UMLS Data
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