XYY syndrome
genetic condition in which a male has an extra Y chromosome
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XYY syndrome
Summary
XYY syndrome is a developmental defect during embryogenesis[1]. It ranks in the top 3% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (722 views/month).[2]
Key Facts
- XYY syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- XYY syndrome's instance of is recorded as class of disease[4].
- XYY syndrome's instance of is recorded as intersex variation[5].
- XYY syndrome is a type of sex chromosome disorder[6].
- XYY syndrome is a type of Y chromosome number anomaly[7].
- XYY syndrome's Commons category is recorded as XYY syndrome[8].
- XYY syndrome's prevalence is recorded as {'amount': '+0.0005'}[9].
- XYY syndrome's prevalence is recorded as {'amount': '+0.0001'}[10].
- XYY syndrome's NCI Thesaurus ID is recorded as C85237[11].
- XYY syndrome's different from is recorded as XYYY syndrome[12].
- XYY syndrome's different from is recorded as XXYY syndrome[13].
- XYY syndrome's health specialty is recorded as medical genetics[14].
Why It Matters
XYY syndrome ranks in the top 3% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (722 views/month).[2] It has Wikipedia articles in 25 language editions, a strong signal of global cultural recognition.[15] It is known by 22 alternative names across languages and contexts.[16]