46, XX/XY
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46, XX/XY
Summary
46, XX/XY is a rare disease[1]. It is known by 3 alternative names across languages and contexts.[2]
Key Facts
- 46, XX/XY's instance of is recorded as rare disease[3].
- 46, XX/XY's instance of is recorded as intersex[4].
- 46, XX/XY's instance of is recorded as sex chromosome disorder[5].
- 46, XX/XY's instance of is recorded as developmental defect during embryogenesis[6].
- 46, XX/XY's instance of is recorded as class of disease[7].
- 46, XX/XY is a type of chimera[8].
- 46, XX/XY is a type of sex chromosome disorder of sex development[9].
- 46, XX/XY is a type of syndrome with disorder of sex development of gynecological interest[10].
- 46, XX/XY is a type of sex chromosome disorder[11].
- 46, XX/XY's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_199310[12].
Why It Matters
46, XX/XY is known by 3 alternative names across languages and contexts.[2]