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Items: 2

1.

Partial androgen insensitivity syndrome

Individuals with androgen insensitivity have a 46,XY karyotype and testes that produce age-appropriate androgen levels but have undermasculinized external genitalia due to defects in androgen action. The phenotype in PAIS varies depending on residual androgen receptor function, ranging from severe undermasculinization presenting as female-like external genitalia to male-appearing genitalia. The typical presentation comprises micropenis, severe hypospadias, and bifid scrotum with or without cryptorchidism (summary by Mongan et al., 2015). [from OMIM]

MedGen UID:
82785
Concept ID:
C0268301
Disease or Syndrome
2.

Chromosome inversion disorder

A type of chromosome rearrangement in which a segment has been turned through 180 degrees (inverted), and inserted back into its original location on the chromosome. [from NCI]

MedGen UID:
7145
Concept ID:
C0021943
Cell or Molecular Dysfunction

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