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Results 1 - 10 of 49 for pd
  1. Parkinson's disease 
    ... the inheritance pattern is usually unknown. Parkinson disease PD Primary parkinsonism Genetic Testing Registry: Autosomal dominant Parkinson ... Disorders (NORD) ClinicalTrials.gov PARKINSON DISEASE, LATE-ONSET; PD PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1 PARKINSON DISEASE, ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. Prolidase deficiency 
    ... and symptoms of the condition. Hyperimidodipeptiduria Imidodipeptidase deficiency PD Peptidase deficiency Genetic Testing Registry: Prolidase deficiency Prolidase ...
    https://medlineplus.gov/genetics/condition/prolidase-deficiency - Genetics
  3. Factor XIII deficiency 
    Factor XIII deficiency is a rare bleeding disorder. Researchers have identified an inherited form and a less severe form that is acquired during a person's ...
    https://medlineplus.gov/genetics/condition/factor-xiii-deficiency - Genetics
  4. Spondylocostal dysostosis 
    ... WE, Lampl BS, Cornier AS, Ramirez N, Turnpenny PD, Vitale MG, Seimon LP, Cowles RA. Clinical and ... ES, Krumlauf R, Hattersley AT, Ellard S, Turnpenny PD. Mutations in the human delta homologue, DLL3, cause ...
    https://medlineplus.gov/genetics/condition/spondylocostal-dysostosis - Genetics
  5. Familial encephalopathy with neuroserpin inclusion bodies 
    ... PubMed Bradshaw CB, Davis RL, Shrimpton AE, Holohan PD, Rea CB, Fieglin D, Kent P, Collins GH. ... abstract available. Citation on PubMed Davis RL, Holohan PD, Shrimpton AE, Tatum AH, Daucher J, Collins GH, ...
    https://medlineplus.gov/...lopathy-with-neuroserpin-inclusion-bodies - Genetics
  6. Jacobsen syndrome 
    ... SYNDROME; JBS PubMed Akshoomoff N, Mattson SN, Grossfeld PD. Evidence for autism spectrum disorder in Jacobsen syndrome: ... LM, Mattson SN, Riley EP, Treier M, Grossfeld PD. Chromosomal microarray mapping suggests a role for BSX ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  7. Inherited thyroxine-binding globulin deficiency 
    ... thyroxine-binding globulin, and the partial form (TBG-PD), which reduces the amount of this protein or ... 15,000 newborns worldwide. The partial form, TBG-PD, affects about 1 in 4,000 newborns. These ...
    https://medlineplus.gov/...ted-thyroxine-binding-globulin-deficiency - Genetics
  8. Von Willebrand disease 
    ... SH, Ozelo MC, Tosetto A, Weyand AC, James PD, Kalot MA, Husainat N, Mustafa RA. ASH ISTH ... 7836.2007.02563.x. Citation on PubMed James PD, Connell NT, Ameer B, Di Paola J, Eikenboom ...
    https://medlineplus.gov/genetics/condition/von-willebrand-disease - Genetics
  9. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy 
    ... PubMed Ferre EM, Rose SR, Rosenzweig SD, Burbelo PD, Romito KR, Niemela JE, Rosen LB, Break TJ, ... J, Al-Muhsen S, Al-Owain M, Arkwright PD, Costigan C, McConnell V, Cant AJ, Abinun M, ...
    https://medlineplus.gov/...inopathy-candidiasis-ectodermal-dystrophy - Genetics
  10. Trisomy 13 
    ... Feb;24(2):137-43. doi: 10.1002/pd.814. Citation on PubMed Crider KS, Olney RS, ... Oct;23(10):856-60. doi: 10.1002/pd.707. Citation on PubMed Pont SJ, Robbins JM, ...
    https://medlineplus.gov/genetics/condition/trisomy-13 - Genetics
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