49,XXXYY syndrome

Summary

49,XXXYY syndrome is a developmental defect during embryogenesis^[1]. It draws 165 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #47 of 308).^[2]

Key Facts

• 49,XXXYY syndrome's image is recorded as XXXYY karyotype (hypothetical).png^[3].
• 49,XXXYY syndrome's instance of is recorded as developmental defect during embryogenesis^[4].
• 49,XXXYY syndrome's instance of is recorded as class of disease^[5].
• 49,XXXYY syndrome's subclass of is recorded as sex chromosome disorder^[6].
• 49,XXXYY syndrome's subclass of is recorded as Y chromosome number anomaly^[7].
• 49,XXXYY syndrome's subclass of is recorded as X chromosome number anomaly with male phenotype^[8].
• 49,XXXYY syndrome's has cause is recorded as developmental defect during embryogenesis^[9].
• 49,XXXYY syndrome's Orphanet ID is recorded as 261534^[10].
• 49,XXXYY syndrome's different from is recorded as XXXY syndrome^[11].
• 49,XXXYY syndrome's different from is recorded as XXYYY syndrome^[12].
• 49,XXXYY syndrome's different from is recorded as XXYY syndrome^[13].
• 49,XXXYY syndrome's different from is recorded as 49,XXXXY syndrome^[14].
• 49,XXXYY syndrome's health specialty is recorded as medical genetics^[15].
• 49,XXXYY syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_261534^[16].
• 49,XXXYY syndrome's ICD-10-CM is recorded as Q98.8^[17].
• 49,XXXYY syndrome's GARD rare disease ID is recorded as 10922^[18].
• 49,XXXYY syndrome's Mondo ID is recorded as MONDO_0016854^[19].
• 49,XXXYY syndrome's Fandom article ID is recorded as lgbta:XXXYY_Syndrome^[20].
• 49,XXXYY syndrome's Miraheze article ID is recorded as lgbta:XXXYY_Syndrome^[21].

Why It Matters

49,XXXYY syndrome draws 165 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #47 of 308).^[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.^[22] It is known by 3 alternative names across languages and contexts.^[23]