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 118 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's subclass of is recorded as pseudohermaphroditism[7].
- persistent Müllerian duct syndrome's subclass of is recorded as 46,XY disorder of sex development of endocrine origin[8].
- persistent Müllerian duct syndrome's subclass of is recorded as rare genetic urogenital disease[9].
- persistent Müllerian duct syndrome's subclass of is recorded as rare genetic developmental defect during embryogenesis[10].
- persistent Müllerian duct syndrome's subclass of is recorded as rare male fertility disorder with obstructive azoospermia[11].
- persistent Müllerian duct syndrome's subclass of is recorded as rare genetic disorder with obstructive azoospermia[12].
- persistent Müllerian duct syndrome's subclass of is recorded as rare genetic endocrine disease[13].
- persistent Müllerian duct syndrome's subclass of is recorded as Mullerian anomalies[14].
- persistent Müllerian duct syndrome's MeSH descriptor ID is recorded as C536665[15].
- persistent Müllerian duct syndrome's OMIM ID is recorded as 261550[16].
- persistent Müllerian duct syndrome's ICD-10 ID is recorded as Q55.8[17].
- persistent Müllerian duct syndrome's DiseasesDB is recorded as 33868[18].
- persistent Müllerian duct syndrome's KEGG ID is recorded as H00609[19].
- persistent Müllerian duct syndrome's Disease Ontology ID is recorded as DOID:0050791[20].
- persistent Müllerian duct syndrome's Orphanet ID is recorded as 2856[21].
- persistent Müllerian duct syndrome's ICD-9-CM is recorded as 752.89[22].
- persistent Müllerian duct syndrome's NCI Thesaurus ID is recorded as C120188[23].
- persistent Müllerian duct syndrome's health specialty is recorded as medical genetics[24].
- persistent Müllerian duct syndrome's genetic association is recorded as AMHR2[25].
- persistent Müllerian duct syndrome's genetic association is recorded as AMH[26].
- persistent Müllerian duct syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050791[27].
Why It Matters
persistent Müllerian duct syndrome draws 118 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.[28] It is known by 27 alternative names across languages and contexts.[29]