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Results 1 - 10 of 11 for Gallbladder disease 4
  1. ABCB4 gene 
    ... ABCB4 PubMed ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 4; ABCB4 GALLBLADDER DISEASE 1; GBD1 NCBI Gene ClinVar Bacq Y, Gendrot ...
    https://medlineplus.gov/genetics/gene/abcb4 - Genetics
  2. Congenital hepatic fibrosis 
    ... Testing Registry: Congenital hepatic fibrosis Polycystic kidney disease 4 with or without polycystic liver disease National Organization ... Rare Disorders (NORD) ClinicalTrials.gov POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD4 PubMed ...
    https://medlineplus.gov/.../condition/congenital-hepatic-fibrosis - Genetics
  3. Glucose phosphate isomerase deficiency 
    ... for Rare Disorders (NORD) ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4; CNSHA4 PubMed Baronciani L, Zanella A, Bianchi P, ... isomerase (GPI) deficiency. Hum Genet. 1998 Oct;103(4):450-4. doi: 10.1007/s004390050849. Citation on ...
    https://medlineplus.gov/.../glucose-phosphate-isomerase-deficiency - Genetics
  4. Intrahepatic cholestasis of pregnancy 
    ... intrahepatic cholestasis of pregnancy. Gut. 2009 Apr;58(4):537-44. doi: 10.1136/gut.2008.159541. ... based case-control study. Hepatology. 2014 Apr;59(4):1482-91. doi: 10.1002/hep.26617. Epub ...
    https://medlineplus.gov/.../intrahepatic-cholestasis-of-pregnancy - Genetics
  5. Metachromatic leukodystrophy 
    ... metachromatic leukodystrophy, onset occurs between the age of 4 and adolescence. In this juvenile form, the first ... S257-62. doi: 10.1007/s10545-010-9140-4. Epub 2010 Jul 2. Citation on PubMed Deconinck ...
    https://medlineplus.gov/.../condition/metachromatic-leukodystrophy - Genetics
  6. ABCG5 gene 
    ... SB, Steiner RD, Mymin D. Sitosterolemia. 2013 Apr 4 [updated 2020 Jul 16]. In: Adam MP, Feldman ... children. J Inherit Metab Dis. 2010 Aug;33(4):437-43. doi: 10.1007/s10545-010-9126- ...
    https://medlineplus.gov/genetics/gene/abcg5 - Genetics
  7. Pulmonary alveolar microlithiasis 
    ... 1007/s00431-012-1678-8. Epub 2012 Feb 4. Citation on PubMed Saito A, McCormack FX. Pulmonary ... Gene mutation of pulmonary alveolar microlithiasis: report of four cases and review of literatures. Respir Med. 2013 ...
    https://medlineplus.gov/.../pulmonary-alveolar-microlithiasis - Genetics
  8. Alagille syndrome 
    ... Alagille syndrome. Semin Ophthalmol. 2007 Oct-Dec;22(4):205-10. doi: 10.1080/08820530701745108. Citation on ... Alagille Syndrome. 2000 May 19 [updated 2024 Jan 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/genetics/condition/alagille-syndrome - Genetics
  9. PKLR gene 
    ... genotype-phenotype association. Blood Rev. 2007 Jul;21(4):217-31. doi: 10.1016/j.blre.2007. ...
    https://medlineplus.gov/genetics/gene/pklr - Genetics
  10. Pyruvate kinase deficiency 
    ... genotype-phenotype association. Blood Rev. 2007 Jul;21(4):217-31. doi: 10.1016/j.blre.2007. ...
    https://medlineplus.gov/.../condition/pyruvate-kinase-deficiency - Genetics