49,XXXYY syndrome
chromosomal disorder
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49,XXXYY syndrome
Summary
49,XXXYY syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- 49,XXXYY syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- 49,XXXYY syndrome's instance of is recorded as class of disease[4].
- 49,XXXYY syndrome is a type of sex chromosome disorder[5].
- 49,XXXYY syndrome is a type of Y chromosome number anomaly[6].
- 49,XXXYY syndrome is a type of X chromosome number anomaly with male phenotype[7].
- 49,XXXYY syndrome's has cause is recorded as developmental defect during embryogenesis[8].
- 49,XXXYY syndrome's different from is recorded as XXXY syndrome[9].
- 49,XXXYY syndrome's different from is recorded as XXYYY syndrome[10].
- 49,XXXYY syndrome's different from is recorded as XXYY syndrome[11].
- 49,XXXYY syndrome's different from is recorded as 49,XXXXY syndrome[12].
- 49,XXXYY syndrome's health specialty is recorded as medical genetics[13].
- 49,XXXYY syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_261534[14].
Why It Matters
49,XXXYY syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 3 alternative names across languages and contexts.[15]