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Concept information

... > disease > skin appendages disease > skin disease > dyskeratosis > hyperkeratosis > keratoderma > Richner-Hanhart’s syndrome
... > disease > genetic disease > hereditary disease > aminoacid disorder > tyrosinemia > Richner-Hanhart’s syndrome
disease > enzymopathy > aminoacid disorder > tyrosinemia > Richner-Hanhart’s syndrome

Terme préférentiel

Richner-Hanhart’s syndrome  

Définition

  • Tyrosinemia type II is an autosomal recessive condition with onset between ages 2 and 4 years, when painful circumscribed calluses develop on the pressure points of the palm of the hand and sole of the foot. (Wikipedia)

Concept générique

Synonyme(s)

  • oculocutaneous tyrosinemia
  • tyrosinemia type II

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-CT80X962-7

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