Chromosome 10q22.3-Q23.2 Deletion Syndrome

Alias:

10q22.3q23.3 Microdeletion Syndrome

Chromosome 10q23 Deletion Syndrome

Deletion 10q22.3q23.3

Monosomy 10q22.3q23.3

Del(10)(q22.3q23.3)

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Chromosome 10q22.3-Q23.2 Deletion Syndrome, also known as 10q22.3q23.3 microdeletion syndrome, is related to chromosome 10q23 deletion syndrome and cowden syndrome 1. Affiliated tissues include breast and eye, and related phenotypes are macrocephaly and intellectual disability

Related ID：

MALACARDS：CHR610

OMIM：612242