- 1. Abelcet
- (UMLS (NCI) C0281209) =Organic Chemical; Antibiotic ;
| - 6. Aberrant Chromosome
- [irregularity in the number or structure of chromosomes that may alter the course of development. ( CSP )] (UMLS (NCI) C0008625) =Cell or Molecular Dysfunction =Pathologic Process;
DNA Alteration =aneuploidy;
Chromosomal Inversion;
nondisjunction;
polyploidy;
Chromosomal Translocation;
trisomy;
tissue mosaicism;
aneuploidy;
Chromosomal Deletion;
Chromosome Fragility;
Chromosomal Inversion;
nondisjunction;
r;
Chromosomal Translocation;
Isochromosome;
Chromosome Breakage;
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- 2. Abelson leukemia virus
- [replication defective strain of murine leukemia virus capable of transforming lymphoid cells and producing a rapidly progressing lymphoid leukemia after superinfection with Maloney, Friend or Rauscher murine leukemia virus. ( CSP )] (UMLS (CSP) C0000742) =Virus
| - 7. Aberrant Chromosome 1
- (UMLS (NCI) C1510712) =Cell or Molecular Dysfunction
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- 3. Abelson Murine Leukemia Viral Oncogene Homolog
- [Human v-abl Abelson murine leukemia viral oncogene homolog 1 (ABL1) gene, located at 9q34.1, encodes proto-oncogene tyrosine-protein kinase ABL1 protein. Alternative splicing of this gene produces two protein isoforms. A t(9;22) translocation, resulting in the fusion of the BCR and ABL1 genes, has been detected in many cases of chronic myelogeneous leukemia.. This BCR-ABL fusion gene is also present in acute myeloid leukemia and acute lymphoblastic leukemia. ( NCI )] (UMLS (NCI) C0080279) =Gene or Genome ;
| - 8. Aberrant Crypt Foci of the Mouse Intestinal Tract
- (UMLS (NCI) C1510713) =Disease or Syndrome
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- 4. Abenaki
- (UMLS (HL7) C1555616) Abenaqui;
=Language =Abenakian;
| - 9. Aberrant DNA Methylation
- (UMLS (NCI) C1510714) =Cell or Molecular Dysfunction
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- 5. Abenakian
- (UMLS (HL7) C1698046) =Language ;
=EasternAlgonquin;
=Malecite-Passamaquoddy;
Eastern Abenaki;
Abenaki;
| - 10. abetalipoproteinemia
- [disorder of lipid metabolism inherited as an autosomal recessive trait characterized by the near absence of apolipoprotein B and apoB containing lipoproteins in plasma; microsomal triglyceride transfer protein is deficient or absent in enterocytes; clinical and laboratory findings include acanthocytosis, hypocholesterolemia, peripheral neuropathy, posterior column degeneration, ataxia, and steatorrhea; intellectual abilities may also be impaired. ( CSP )] (UMLS (CSP) C0000744) =Disease or Syndrome
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