Persistent Mullerian duct syndrome [Supplementary Concept]

An autosomal recessive congenital abnormality where mullerian derivatives, uterus and tubes, persist in otherwise normally virilized males. Mutations in the AMH gene and AMHR2 gene have been identified. OMIM: 261550

Date introduced: August 25, 2010

MeSH Unique ID: C536665

Heading Mapped to:

• Disorder of Sex Development, 46,XY

Entry Terms:

• Persistent Müllerian Duct Syndrome
• Persistent Mullerian Duct Syndrome, Types I And II
• Persistent mullerian duct syndrome, types 1 and 2
• Pseudohermaphroditism, male internal
• Hernia uteri inguinale
• Persistent oviduct syndrome
• Persistent Muellerian duct syndrome