Bardet-Biedl syndrome (Q94128)

From determinar.ia.br - Determine suas informações
Revision as of 09:14, 16 August 2026 by Determinaradmin (talk | contribs) (‎Changed an Item)
Bardet-Biedl syndrome is a ciliopathy with multisystem involvement that is characterised by a combination of clinical signs: obesity, pigmentary retinopathy, post-axial polydactyly, polycystic kidneys, hypogenitalism, and learning disabilities, many of which appear several years after disease onset.
Language Label Description Also known as
default for all languages
ID_255526264
    English
    Bardet-Biedl syndrome
    Bardet-Biedl syndrome is a ciliopathy with multisystem involvement that is characterised by a combination of clinical signs: obesity, pigmentary retinopathy, post-axial polydactyly, polycystic kidneys, hypogenitalism, and learning disabilities, many of which appear several years after disease onset.

      Statements

      CID11:ID_255526264
      0 references
      dki-india-ID_255526264
      0 references