Chromosome Xp11.3 Deletion Syndrome

Alias:

Mental Retardation, X-Linked, with Retinitis Pigmentosa

Aldred Syndrome

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Gene & Mutation

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Chromosome Xp11.3 Deletion Syndrome, is also known as mental retardation, x-linked, with retinitis pigmentosa. An important gene associated with Chromosome Xp11.3 Deletion Syndrome is DELXP11.3 (Chromosome Xp11.3 Deletion Syndrome). Related phenotypes are intellectual disability and global developmental delay

Related ID：

MALACARDS：CHR397

OMIM：300578