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 506 for ALS
  1. Amyotrophic lateral sclerosis 
    Amyotrophic lateral sclerosis (ALS) is a progressive disease that affects motor neurons, which are specialized nerve cells that control muscle movement. These nerve ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  2. SOD1 gene 
    ... the SOD1 gene have been found to cause amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, a ... dismutase enzyme. About half of all Americans with ALS caused by SOD1 gene mutations have a particular ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  3. ALS2 gene 
    ... of nerve impulses. MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition At least 20 ... About This Health Condition ALS2_HUMAN ALS2CR6 ALSJ amyotrophic lateral sclerosis 2 (juvenile) IAHSP KIAA1563 PLSJ Tests of ALS2 ...
    https://medlineplus.gov/genetics/gene/als2 - Genetics
  4. Multicentric osteolysis, nodulosis, and arthropathy 
    ... not show signs and symptoms of the condition. Al-Aqeel Sewairi syndrome Hereditary multicentric osteolysis MONA NAO ... gov MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA PubMed Al Aqeel A, Al Sewairi W, Edress B, Gorlin ...
    https://medlineplus.gov/...tric-osteolysis-nodulosis-and-arthropathy - Genetics
  5. Winchester syndrome 
    Winchester syndrome is a rare inherited disease characterized by a loss of bone tissue (osteolysis), particularly in the hands and feet. Winchester syndrome used ...
    https://medlineplus.gov/genetics/condition/winchester-syndrome - Genetics
  6. Primary localized cutaneous amyloidosis 
    Primary localized cutaneous amyloidosis (PLCA) is a condition in which clumps of abnormal proteins called amyloids build up in the skin, specifically in the wave- ...
    https://medlineplus.gov/.../primary-localized-cutaneous-amyloidosis - Genetics
  7. C9orf72 gene 
    ... the C9orf72 gene have been found to cause amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, a ... is repeated too many times, it can cause ALS. This type of mutation is called a hexanucleotide ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  8. SLC19A3 gene 
    ... Alfadhel M, Almuntashri M, Jadah RH, Bashiri FA, Al Rifai MT, Al Shalaan H, Al Balwi M, Al Rumayan A, Eyaid W, Al-Twaijri W. Biotin-responsive basal ganglia disease should ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  9. Biotin-thiamine-responsive basal ganglia disease 
    ... Alfadhel M, Almuntashri M, Jadah RH, Bashiri FA, Al Rifai MT, Al Shalaan H, Al Balwi M, Al Rumayan A, Eyaid W, Al-Twaijri W. Biotin-responsive basal ganglia disease should ...
    https://medlineplus.gov/...thiamine-responsive-basal-ganglia-disease - Genetics
  10. IRAK-4 deficiency 
    ... Good NK, Miller R, Takada H, Hara T, Al-Hajjar S, Al-Ghonaium A, Speert D, Sanlaville D, Li X, ... Elbim C, Hitchcock R, Lammas D, Davies G, Al-Ghonaium A, Al-Rayes H, Al-Jumaah S, ...
    https://medlineplus.gov/genetics/condition/irak-4-deficiency - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next