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 127 for AR
  1. Renal tubular acidosis with deafness 
    ... not show signs and symptoms of the condition. AR dRTA with deafness AR dRTA with hearing loss Autosomal recessive distal renal ...
    https://medlineplus.gov/.../renal-tubular-acidosis-with-deafness - Genetics
  2. Androgen insensitivity syndrome 
    ... less common. Variants (also called mutations) in the AR gene cause androgen insensitivity syndrome. This gene provides ... hair growth and sex drive. Variants in the AR gene prevent androgen receptors from working properly, which ...
    https://medlineplus.gov/.../androgen-insensitivity-syndrome - Genetics
  3. DOCK8 immunodeficiency syndrome 
    ... not show signs and symptoms of the condition. AR-HIES Autosomal recessive HIES Autosomal recessive hyper-IgE ... A, Kilic M, Reisli I, Camcioglu Y, Gennery AR, Cant AJ, Jones A, Gaspar BH, Arkwright PD, ...
    https://medlineplus.gov/.../dock8-immunodeficiency-syndrome - Genetics
  4. Axenfeld-Rieger syndrome 
    ... each cell is sufficient to cause the disorder. ARS Axenfeld and Rieger anomaly Axenfeld anomaly Axenfeld syndrome ...
    https://medlineplus.gov/genetics/condition/axenfeld-rieger-syndrome - Genetics
  5. Emery-Dreifuss muscular dystrophy 
    Emery-Dreifuss muscular dystrophy is a condition that primarily affects muscles used for movement (skeletal muscles) and the heart (cardiac muscle). Among the ...
    https://medlineplus.gov/.../emery-dreifuss-muscular-dystrophy - Genetics
  6. PGM3-congenital disorder of glycosylation 
    PGM3-congenital disorder of glycosylation (PGM3-CDG) is an inherited condition that primarily affects the immune system but can also involve other areas of ...
    https://medlineplus.gov/...pgm3-congenital-disorder-of-glycosylation - Genetics
  7. Type 2 diabetes 
    ... N, Shah S, Shera AS, Shu XO, Shuldiner AR, Sigurdsson G, Sijbrands E, Silveira A, Sim X, ... BF, Wang C, Wareham NJ, Wennauer R, Wickremasinghe AR, Wilsgaard T, Wilson JF, Wiltshire S, Winckler W, ...
    https://medlineplus.gov/genetics/condition/type-2-diabetes - Genetics
  8. Microvillus inclusion disease 
    ... Citation on PubMed Khubchandani SR, Vohra P, Chitale AR, Sidana P. Microvillous inclusion disease--an ultrastructural diagnosis: ... O, Utermann G, Ruemmele FM, Huber LA, Janecke AR. MYO5B mutations cause microvillus inclusion disease and disrupt ...
    https://medlineplus.gov/.../condition/microvillus-inclusion-disease - Genetics
  9. Androgenetic alopecia 
    ... confirmed only that variations in one gene, the AR gene, are involved in this condition. The AR gene provides instructions for making a protein called ...
    https://medlineplus.gov/genetics/condition/androgenetic-alopecia - Genetics
  10. Spinal and bulbar muscular atrophy 
    ... from a particular type of mutation in the AR gene. This gene provides instructions for making a ... as regulating hair growth and sex drive.The AR gene mutation that causes spinal and bulbar muscular ...
    https://medlineplus.gov/.../spinal-and-bulbar-muscular-atrophy - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next