search

MeSH 搜索器

Kallmann Syndrome

A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait.
推出的年份: 1993
副标题
树号: C12.050.351.875.253.096.750, C12.200.706.316.096.750, C12.800.316.096.750, C16.131.939.316.096.750, C16.320.467, C19.391.119.096.750, C19.391.482.600
MeSH 单一 ID: D017436
进入的组:
  • Syndrome, Kallmann
  • Anosmic Idiopathic Hypogonadotropic Hypogonadism
  • Kallmann's Syndrome
  • Kallmanns Syndrome
  • Syndrome, Kallmann's
  • Hypogonadotropic Hypogonadism and Anosmia
  • Hypogonadotropic Hypogonadism-Anosmia Syndrome
  • Anosmic Hypogonadism
  • Anosmic Hypogonadisms
  • Hypogonadism, Anosmic
  • Hypogonadisms, Anosmic
  • Dysplasia Olfactogenitalis of De Morsier
  • Kallmann Syndrome 1
  • Kallmann Syndrome, Type 1, X-linked
  • Kallmann Syndrome 3
  • Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion)
  • Kallmann Syndrome, Type 3, Recessive
  • Autosomal Recessive Form of Kallmann Syndrome
  • Kallmann Syndrome 2
  • Autosomal Dominant Form of Kallmann Syndrome
早前的内容:
  • Hypogonadism (1966-1992)

留言 (0)

沒有登入
gif