persistent Müllerian duct syndrome
intersex variation where one has XY chromosomes, male-typical reproductive organs and external genitalia, and some component(s) of a female-typical reproductive tract
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persistent Müllerian duct syndrome
Summary
persistent Müllerian duct syndrome is a developmental defect during embryogenesis[1]. It draws 87 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #54 of 308).[2]
Key Facts
- persistent Müllerian duct syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- persistent Müllerian duct syndrome's instance of is recorded as rare disease[4].
- persistent Müllerian duct syndrome's instance of is recorded as class of disease[5].
- persistent Müllerian duct syndrome's instance of is recorded as intersex variation[6].
- persistent Müllerian duct syndrome is a type of pseudohermaphroditism[7].
- persistent Müllerian duct syndrome is a type of 46,XY disorder of sex development of endocrine origin[8].
- persistent Müllerian duct syndrome is a type of rare genetic urogenital disease[9].
- persistent Müllerian duct syndrome is a type of rare genetic developmental defect during embryogenesis[10].
- persistent Müllerian duct syndrome is a type of rare male fertility disorder with obstructive azoospermia[11].
- persistent Müllerian duct syndrome is a type of rare genetic disorder with obstructive azoospermia[12].
- persistent Müllerian duct syndrome is a type of rare genetic endocrine disease[13].
- persistent Müllerian duct syndrome is a type of Mullerian anomalies[14].
- persistent Müllerian duct syndrome's ICD-9-CM is recorded as 752.89[15].
- persistent Müllerian duct syndrome's NCI Thesaurus ID is recorded as C120188[16].
- persistent Müllerian duct syndrome's health specialty is recorded as medical genetics[17].
- persistent Müllerian duct syndrome's genetic association is recorded as AMHR2[18].
- persistent Müllerian duct syndrome's genetic association is recorded as AMH[19].
- persistent Müllerian duct syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050791[20].
- persistent Müllerian duct syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050791[21].
- persistent Müllerian duct syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2856[22].
- persistent Müllerian duct syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].
Why It Matters
persistent Müllerian duct syndrome draws 87 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #54 of 308).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[24] It is known by 27 alternative names across languages and contexts.[25]