46, XX/XY
human disease
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46, XX/XY
Summary
46, XX/XY is a rare disease[1]. It draws 169 Wikipedia views per month (rare_disease category, ranking #118 of 627).[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's subclass of is recorded as chimera[8].
- 46, XX/XY's subclass of is recorded as sex chromosome disorder of sex development[9].
- 46, XX/XY's subclass of is recorded as syndrome with disorder of sex development of gynecological interest[10].
- 46, XX/XY's subclass of is recorded as sex chromosome disorder[11].
- 46, XX/XY's ICD-10 ID is recorded as Q99.0[12].
- 46, XX/XY's Orphanet ID is recorded as 199310[13].
- 46, XX/XY's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_199310[14].
- 46, XX/XY's UMLS CUI is recorded as C5679592[15].
- 46, XX/XY's ICD-10-CM is recorded as Q99.0[16].
- 46, XX/XY's Mondo ID is recorded as MONDO_0016045[17].
- 46, XX/XY's Microsoft Academic ID is recorded as 2777500643[18].
- 46, XX/XY's ICD-11 ID is recorded as LD56[19].
- 46, XX/XY's ICD-11 ID is recorded as 1262245334[20].
Why It Matters
46, XX/XY draws 169 Wikipedia views per month (rare_disease category, ranking #118 of 627).[2] It is known by 3 alternative names across languages and contexts.[21]