A rare chromosome Y structural anomaly, with a highly variable phenotype, mostly characterised by short stature, partial to total gonadal failure, sexual infantilism, genital anomalies (e.g. ambiguous genitalia, hypospadias, cryptorchidism), and azoo
syndrome du chromosome Y en anneau
SNOMEDCT-BE (e.g. ambiguous genitalia, hypospadias, cryptorchidism), and azoo / 763407008
SNOMEDCT-BE (disorder) / 763407008