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 Kennedy disease
  1. Spinal and bulbar muscular atrophy 
    Spinal and bulbar muscular atrophy, also known as Kennedy disease, is a disorder of specialized nerve cells that ... their sons. Bulbospinal muscular atrophy, X-linked KD Kennedy disease Kennedy spinal and bulbar muscular atrophy Kennedy's ...
    https://medlineplus.gov/.../spinal-and-bulbar-muscular-atrophy - Genetics
  2. AR gene 
    ... 243. Citation on PubMed Zajac JD, Fui MN. Kennedy's disease: clinical significance of tandem repeats in the androgen ...
    https://medlineplus.gov/genetics/gene/ar - Genetics
  3. Cap myopathy 
    ... on PubMed Waddell LB, Kreissl M, Kornberg A, Kennedy P, McLean C, Labarre-Vila A, Monnier N, North KN, Clarke NF. Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3. Neuromuscul ...
    https://medlineplus.gov/genetics/condition/cap-myopathy - Genetics
  4. WRN gene 
    ... or Free article on PubMed Central Kudlow BA, Kennedy BK, Monnat RJ Jr. Werner and Hutchinson-Gilford progeria syndromes: mechanistic basis of human progeroid diseases. Nat Rev Mol Cell Biol. 2007 May;8( ...
    https://medlineplus.gov/genetics/gene/wrn - Genetics
  5. Werner syndrome 
    ... or Free article on PubMed Central Kudlow BA, Kennedy BK, Monnat RJ Jr. Werner and Hutchinson-Gilford progeria syndromes: mechanistic basis of human progeroid diseases. Nat Rev Mol Cell Biol. 2007 May;8( ...
    https://medlineplus.gov/genetics/condition/werner-syndrome - Genetics
  6. TPM3 gene 
    ... on PubMed Waddell LB, Kreissl M, Kornberg A, Kennedy P, McLean C, Labarre-Vila A, Monnier N, North KN, Clarke NF. Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3. Neuromuscul ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  7. MPZ gene 
    ... Olney RK, Johnson J, Berry K, Russo P, Kennedy S, Teebi AS, Scavina M, Williams LL, Mancias P, Butler IJ, Krajewski K, Shy M, Lupski JR. Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype ...
    https://medlineplus.gov/genetics/gene/mpz - Genetics
  8. Harlequin ichthyosis 
    ... Witt DR, Sprecher E, Taylor AE, Ilchyshyn A, Kennedy CT, Goodyear H, Moss C, Paige D, Harper JI, Young BD, Leigh IM, Eady RA, O'Toole EA. Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. Am J Hum Genet. 2005 May; ...
    https://medlineplus.gov/genetics/condition/harlequin-ichthyosis - Genetics
  9. ABCA12 gene 
    ... Witt DR, Sprecher E, Taylor AE, Ilchyshyn A, Kennedy CT, Goodyear H, Moss C, Paige D, Harper JI, Young BD, Leigh IM, Eady RA, O'Toole EA. Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. Am J Hum Genet. 2005 May; ...
    https://medlineplus.gov/genetics/gene/abca12 - Genetics
  10. Primary ciliary dyskinesia 
    ... on PubMed or Free article on PubMed Central Kennedy MP, Omran H, Leigh MW, Dell S, Morgan L, Molina PL, Robinson BV, Minnix SL, Olbrich H, Severin T, Ahrens P, Lange L, Morillas HN, Noone PG, Zariwala MA, Knowles MR. Congenital heart disease and other heterotaxic defects in a large cohort ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
previous · 1 · 2 · next