MeSH 搜索器

Bardet-Biedl Syndrome

An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTYLY; OBESITY; MENTAL RETARDATION; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME. (From J Med Genet 1997 Feb;34(2):92-8)
推出的年份: 2000
副标题
树号: C10.228.140.617.200, C11.270.684.624, C16.131.077.245.125, C16.320.184.125
MeSH 单一 ID: D020788
进入的组:
  • Bardet Biedl Syndrome
  • Syndrome, Bardet-Biedl
  • Laurence-Moon-Bardet-Biedl Syndrome
  • Laurence Moon Bardet Biedl Syndrome
  • Syndrome, Laurence-Moon-Bardet-Biedl
早前的内容:
  • Bardet-Biedl Syndrome (1966-1999)

留言 (0)

沒有登入
gif