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Results 1 - 10 of 558 for AA
  1. Secondary systemic amyloidosis 
    ... 2020:chap 179. Papa R, Lachmann HJ. Secondary, AA, amyloidosis. Rheum Dis Clin North Am . 2018;44( ...
    https://medlineplus.gov/ency/article/000585.htm - Medical Encyclopedia
  2. Cardiac amyloidosis 
    Cardiac amyloidosis is a disorder caused by deposits of an abnormal protein (amyloid) in the heart tissue. These deposits make it hard ...
    https://medlineplus.gov/ency/article/000193.htm - Medical Encyclopedia
  3. Amyloidosis and Kidney Disease From the National Institutes of Health (National Institute of Diabetes and Digestive and Kidney Diseases)  
    ... amyloidosis, AL amyloidosis, primary amyloidosis, amyloid A amyloidosis, AA amyloidosis, secondary amyloidosis, hereditary amyloidosis, dialysis-related amyloidosis, ...
    https://www.niddk.nih.gov/.../kidney-disease/amyloidosis - External Health Links
  4. 7q11.23 duplication syndrome 
    ... syndrome Dup(7)(q11.23) Somerville-Van der Aa syndrome Trisomy 7q11.23 WBS duplication syndrome Williams- ... or Free article on PubMed Central Van der Aa N, Rooms L, Vandeweyer G, van den Ende ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  5. MYH7 gene 
    ... MyHC-beta myhc-slow MYHCB myosin heavy chain (AA 1-96) Myosin heavy chain 7 Myosin heavy ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  6. COL6A1 gene 
    ... This Health Condition alpha 1 (VI) chain (61 AA) CO6A1_HUMAN collagen alpha-1(VI) chain collagen ...
    https://medlineplus.gov/genetics/gene/col6a1 - Genetics
  7. SERPINC1 gene 
    ... More About This Health Condition ANT3_HUMAN antithrombin (aa 375-432) antithrombin III AT3 ATIII coding sequence ...
    https://medlineplus.gov/genetics/gene/serpinc1 - Genetics
  8. Alopecia areata 
    ... to have family members with other autoimmune disorders. AA Alopecia circumscripta Genetic Testing Registry: Alopecia universalis Alopecia ...
    https://medlineplus.gov/genetics/condition/alopecia-areata - Genetics
  9. Severe congenital neutropenia 
    ... Citation on PubMed Makaryan V, Zeidler C, Bolyard AA, Skokowa J, Rodger E, Kelley ML, Boxer LA, ... BP, Link DC, Stein S, Rodger E, Bolyard AA, Aprikyan AA, Bonilla MA, Dror Y, Kannourakis G, ...
    https://medlineplus.gov/.../condition/severe-congenital-neutropenia - Genetics
  10. ADNP syndrome 
    ... intellectual disability-autism spectrum disorder Helsmoortel-van der Aa syndrome HVDAS Mental retardation, autosomal dominant 28 MRD28 ... Rare Disorders (NORD) ClinicalTrials.gov HELSMOORTEL-VAN DER AA SYNDROME; HVDAS PubMed Gozes I, Van Dijck A, ...
    https://medlineplus.gov/genetics/condition/adnp-syndrome - Genetics
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