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Concept information

disease > stomatology > dysmorphic facies > Robinow syndrome
... > disease > congenital disease > malformation > dysmorphia > dysmorphic facies > Robinow syndrome
disease > genetic disease > hereditary disease > mesomelic dwarfism > Robinow syndrome
... > disease > diseases of the osteoarticular system > osteochondrodysplasia > dwarfism > mesomelic dwarfism > Robinow syndrome
disease > genital diseases > genital hypoplasia > Robinow syndrome
disease > hypoplasia > genital hypoplasia > Robinow syndrome

Preferred term

Robinow syndrome  

Definition

  • Robinow syndrome is an extremely rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia, as well as vertebral segmentation. (Wikipedia)

Broader concept

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URI

http://data.loterre.fr/ark:/67375/VH8-M2HQ4HXN-Q

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