Intellectual Developmental Disorder with Microcephaly and with or Without Ocular Malformations or Hypogonadotropic Hypogonadism (IDDMOH)

Intellectual Developmental Disorder with Microcephaly and with or Without Ocular Malformations or Hypogonadotropic Hypogonadism, also known as coffin-siris syndrome 9, is related to coffin-siris syndrome 1 and cryptorchidism, unilateral or bilateral. An important gene associated with Intellectual Developmental Disorder with Microcephaly and with or Without Ocular Malformations or Hypogonadotropic Hypogonadism is SOX11 (SRY-Box Transcription Factor 11). Affiliated tissues include uterus and kidney, and related phenotypes are microcephaly and short stature