XYYY syndrome

Summary

XYYY syndrome is a developmental defect during embryogenesis^[1]. It draws 126 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #58 of 308).^[2]

Key Facts

• XYYY syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• XYYY syndrome's instance of is recorded as Q3618210^[4].
• XYYY syndrome's instance of is recorded as class of disease^[5].
• XYYY syndrome's subclass of is recorded as male infertility due to gonadal dysgenesis^[6].
• XYYY syndrome's subclass of is recorded as syndromic urogenital tract malformation^[7].
• XYYY syndrome's subclass of is recorded as Y chromosome number anomaly^[8].
• XYYY syndrome's subclass of is recorded as genetic syndromic intellectual disability^[9].
• XYYY syndrome's Commons category is recorded as XYYY syndrome^[10].
• XYYY syndrome's Orphanet ID is recorded as 99329^[11].
• XYYY syndrome's different from is recorded as 49,XYYYY syndrome^[12].
• XYYY syndrome's different from is recorded as XXYYY syndrome^[13].
• XYYY syndrome's different from is recorded as XYY syndrome^[14].
• XYYY syndrome's health specialty is recorded as medical genetics^[15].
• XYYY syndrome's Google Knowledge Graph ID is recorded as /g/11hzdqt3w4^[16].
• XYYY syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99329^[17].
• XYYY syndrome's ICD-10-CM is recorded as Q98.8^[18].
• XYYY syndrome's GARD rare disease ID is recorded as 11985^[19].
• XYYY syndrome's Mondo ID is recorded as MONDO_0020469^[20].
• XYYY syndrome's Fandom article ID is recorded as lgbta:XYYY_Syndrome^[21].
• XYYY syndrome's WikiProjectMed ID is recorded as XYYY syndrome^[22].
• XYYY syndrome's Miraheze article ID is recorded as lgbta:XYYY_Syndrome^[23].

Why It Matters

XYYY syndrome draws 126 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #58 of 308).^[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.^[24]