Amyotrophic lateral sclerosis 5
ALS5. A form of amyotrophic lateral sclerosis (ALS) inherited in an autosomal recessive manner due to mutation in a gene on chromosome 15q15.1-q21.1.
Read Also:
- Amyotrophic lateral sclerosis 6
ALS6. A form of amyotrophic lateral sclerosis (ALS) inherited in an autosomal dominant manner due to mutation in a gene on chromosome 16q12.
- Amyotrophic lateral sclerosis 7
ALS7. A form of amyotrophic lateral sclerosis (ALS) inherited in an autosomal dominant manner due to mutation in a gene on chromosome 20ptel.
- Amyotrophic lateral sclerosis 8
ALS8. A form of amyotrophic lateral sclerosis (ALS) inherited in an autosomal dominant manner due to mutation in a gene on chromosome 20ptel.
- AMA
AMA: The American Medical Association. The AMA’s mission statement proclaims: “We are the Voice of the American Medical Profession. “We are the partnership of physicians and their professional associations dedicated to promoting the art and science of medicine and the betterment of public health. “We serve the physicians and their patients by establishing and promoting […]
- Anal atresia
Anal atresia: Congenital absence of an opening at the bottom end of the intestinal tract. Also called imperforate anus. Occurs in about 1 in 5,000 births. It is corrected by surgery. Atresia refers here to the absence of a normal opening.