Chromosome Xp11.22 Duplication Syndrome (MRX17)

Alias:

Xp11.22 Microduplication Syndrome

Mental Retardation, X-Linked 31

Mrx17

Mrx31

Microduplication Syndrome, Xp11.22

Mental Retardation, X-Linked 17

X-Linked Mental Retardation 31

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Chromosome Xp11.22 Duplication Syndrome, also known as xp11.22 microduplication syndrome, is related to non-syndromic x-linked intellectual disability and intellectual developmental disorder, x-linked 19. An important gene associated with Chromosome Xp11.22 Duplication Syndrome is DUPXP11.22 (Xp11.22 Microduplication Syndrome). Related phenotypes are intellectual disability and macrocephaly

Related ID：

MALACARDS：CHR639

OMIM：300705