7p22.1 Microduplication Syndrome

7p22.1 Microduplication Syndrome(来自ICD-11)

别称:

Trisomy 7p22.1

Dup(7)(p22.1)

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

7p22.1 Microduplication Syndrome, also known as trisomy 7p22.1, is related to hypertelorism and cryptorchidism, unilateral or bilateral. Affiliated tissues include kidney and heart, and related phenotypes are macrocephaly and global developmental delay

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