21q22.11q22.12 Microdeletion Syndrome

21q22.11q22.12 Microdeletion Syndrome(来自ICD-11)

别称:

Monosomy 21q22.11q22.12

Del(21)(q22.11q22.12)

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

21q22.11q22.12 Microdeletion Syndrome, is also known as monosomy 21q22.11q22.12. An important gene associated with 21q22.11q22.12 Microdeletion Syndrome is KIF15 (Kinesin Family Member 15). Affiliated tissues include brain and tongue, and related phenotypes are thrombocytopenia and intellectual disability

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