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persistent Mullerian duct syndrome

Genetics: - associated with defects a) mullerian-inhibitory factor (type 1) b) mullerian-inhibitory factor receptor 2 (AMHR2) (type 2) Clinical manifestations: - a form of male pseudohermaphroditism characterized by a failure of mullerian duct regression in otherwise normal males

Related

Mullerian (paramesonephric) duct

General

genetic syndrome (multisystem disorder) pseudohermaphroditism; indeterminate sex; gynandrism

Database Correlations

OMIM 261550

References

  1. UniProt :accession Q16671
  2. UniProt :accession P15514
  3. OMIM :accession 261550