Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 19 for Gilbert syndrome
  1. Gilbert syndrome 
    Gilbert syndrome is a relatively mild condition characterized by periods of elevated levels of a toxic substance called bilirubin in the blood (hyperbilirubinemia). ...
    https://medlineplus.gov/genetics/condition/gilbert-syndrome - Genetics
  2. Crigler-Najjar syndrome 
    ... cell have mutations. A less severe condition called Gilbert syndrome can occur when one copy of the UGT1A1 ... K, Miners JO. Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other ...
    https://medlineplus.gov/genetics/condition/crigler-najjar-syndrome - Genetics
  3. Rotor syndrome 
    ... HYPERBILIRUBINEMIA, ROTOR TYPE; HBLRR PubMed Strassburg CP. Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome). ...
    https://medlineplus.gov/genetics/condition/rotor-syndrome - Genetics
  4. Alagille syndrome 
    ... on PubMed Spinner NB, Loomes KM, Krantz ID, Gilbert MA. Alagille Syndrome. 2000 May 19 [updated 2024 Jan 4]. In: ...
    https://medlineplus.gov/genetics/condition/alagille-syndrome - Genetics
  5. Loeys-Dietz syndrome 
    ... or Free article on PubMed Central Kalra VB, Gilbert JW, Malhotra A. Loeys-Dietz syndrome: cardiovascular, neuroradiological and musculoskeletal imaging findings. Pediatr Radiol. ...
    https://medlineplus.gov/genetics/condition/loeys-dietz-syndrome - Genetics
  6. Tourette syndrome 
    ... JF, Dure LS 4th, Kurlan R, Singer HS, Gilbert DL, Farhi A, Louvi A, Lifton RP, Sestan N, State MW. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science. 2005 Oct 14;310(5746):317-20. ...
    https://medlineplus.gov/genetics/condition/tourette-syndrome - Genetics
  7. Wiedemann-Rautenstrauch syndrome 
    ... Jordan Z, Bruggemann N, Westenberger A, Espay AJ, Gilbert DL, Wu SW. Spectrum of Pediatric to Early Adulthood POLR3A-Associated Movement Disorders. Mov Disord Clin Pract. 2022 Dec 23;10(2):316-322. doi: 10.1002/mdc3.13635. eCollection 2023 Feb. Citation on PubMed
    https://medlineplus.gov/.../wiedemann-rautenstrauch-syndrome - Genetics
  8. Short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay 
    ... Temple IK, Reardon W, Mansour S, Haq MR, Gilbert R, Lehmann OJ, Vanstone MR, Beaulieu CL; FORGE Canada Consortium; Majewski J, Bulman DE, O'Driscoll M, Boycott KM, Innes AM. Mutations in PIK3R1 cause SHORT syndrome. Am J Hum Genet. 2013 Jul 11;93( ...
    https://medlineplus.gov/...ression-rieger-anomaly-and-teething-delay - Genetics
  9. Holt-Oram syndrome 
    ... He J, Lee JS, Aftimos S, Brueckner M, Gilbert F, Graham GE, Hannibal MC, Innis ... criteria for Holt-Oram syndrome. Pediatr Res. 2005 Nov;58(5):981-6. ...
    https://medlineplus.gov/genetics/condition/holt-oram-syndrome - Genetics
  10. Central core disease 
    ... Myopathy, central core Shy's disease Shy-Magee syndrome Central core disease ... Fusto A, Moyle LA, Gilbert PM, Pegoraro E. Cored in the act: the ...
    https://medlineplus.gov/genetics/condition/central-core-disease - Genetics
previous · 1 · 2 · next