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Results 1 - 10 of 968 for 6S -"2-amino-6-(3'-methoxybiphenyl-3-yl)-3,6-dimethyl-5,6-dihydropyrimidin-4(3H)-one"
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  1. Glucose-6-phosphate dehydrogenase deficiency 
    Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that affects red blood cells, which carry oxygen from the lungs to tissues throughout the ...
    https://medlineplus.gov/...cose-6-phosphate-dehydrogenase-deficiency - Genetics
  2. Dystonia 6 
    Dystonia 6 is one of many forms of dystonia, which is a group of conditions characterized by involuntary movements, twisting (torsion) and tensing of various muscles, ...
    https://medlineplus.gov/genetics/condition/dystonia-6 - Genetics
  3. Spinocerebellar ataxia type 6 
    Spinocerebellar ataxia type 6 (SCA6) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  4. Glycogen storage disease type I 
    ... down a type of sugar molecule called glucose 6-phosphate. The breakdown of this molecule produces the ... SLC37A4 genes prevent the effective breakdown of glucose 6-phosphate. Glucose 6-phosphate that is not broken ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-i - Genetics
  5. Glucose phosphate isomerase deficiency 
    ... pathway; in this step, a molecule called glucose-6-phosphate is converted to another molecule called fructose-6-phosphate.When GPI remains a single molecule (a ...
    https://medlineplus.gov/.../glucose-phosphate-isomerase-deficiency - Genetics
  6. Hereditary fructose intolerance 
    ... Fructose aldolase B deficiency Fructose intolerance Fructose-1,6-biphosphate aldolase deficiency Fructose-1-phosphate aldolase deficiency ... to hereditary fructose intolerance. FEBS Lett. 2002 Nov 6;531(2):152-6. doi: 10.1016/s0014- ...
    https://medlineplus.gov/.../hereditary-fructose-intolerance - Genetics
  7. Permanent neonatal diabetes mellitus 
    ... of diabetes that first appears within the first 6 months of life and persists throughout the lifespan. ... common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by ...
    https://medlineplus.gov/.../permanent-neonatal-diabetes-mellitus - Genetics
  8. TUBB4A-related leukodystrophy 
    ... related hypomyelinating leukodystrophy Genetic Testing Registry: Hypomyelinating leukodystrophy 6 Hypomyelination with atrophy of basal ganglia and cerebellum ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  9. MPV17-related hepatocerebral mitochondrial DNA depletion syndrome 
    ... symptoms of the condition. Mitochondrial DNA depletion syndrome 6 MPV17-associated hepatocerebral MDS MTDPS6 Navajo familial neurogenic ... NNH Genetic Testing Registry: Mitochondrial DNA depletion syndrome 6 (hepatocerebral type) Navajo neurohepatopathy National Organization for Rare ...
    https://medlineplus.gov/...bral-mitochondrial-dna-depletion-syndrome - Genetics
  10. Dopa-responsive dystonia 
    ... usually appear during childhood, most commonly around age 6. The first signs of the condition are typically ... 77. doi: 10.1086/321970. Epub 2001 Jul 6. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/condition/dopa-responsive-dystonia - Genetics
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