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X-linked intellectual disability
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Medical condition
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Subclasses 15
Influences rating
Fragile X syndrome
X-linked dominant genetic disorder
Lujan–Fryns syndrome
Medical condition
Börjeson–Forssman–Lehmann syndrome
Medical condition
Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia
Rare X-linked dominant genetic disorder
Christianson syndrome
Medical condition
MECP2 duplication syndrome
Medical condition
Norrie disease
Genetic disorder that primarily affects the eye
syndromic X-linked intellectual disability Hedera type
syndromic X-linked intellectual disability characterized by mild to moderate mental retardation and epilepsy that has material basis in mutation in the ATP6AP2 gene on chromosome Xp11
syndromic X-linked intellectual disability 7
syndromic X-linked intellectual disability characterized by intellectual deficit, obesity, hypogonadism, and tapering fingers that has material basis in variation in the chromosome region Xp11.3-q22
syndromic X-linked intellectual disability 12
syndromic X-linked intellectual disability characterized by severe intellectual deficit, mutism, epilepsy, growth retardation or failure and recurrent infections that has material basis in variation in the chromosome region Xp11
Subject of 1
Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1.
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Wikipedia

X-linked intellectual disability refers to medical disorders associated with X-linked recessive inheritance that result in intellectual disability.

Instance of
Rare disease
class of disease
Subclass of
Intellectual disability
X-linked disease
syndromic intellectual disability
genetic syndromic intellectual disability
References
Wikidata