- 1. Achaete-Scute Complex Homolog-Like 1 Protein
- [Encoded by human ACSL1 Gene (bHLH/ASC Family), 236-aa 25 kDa transcription activation factor Achaete-Scute Complex-Like 1 Protein binds efficiently to the E box (5 prime-CANNTG-3 prime) as a heterodimer with other bHLH proteins, such as E12/E47. ACSL1 regulates commitment and differentiation of specific olfactory and autonomic neuronal lineages. ( NCI )] (UMLS (NCI) C0083344) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
| - 10. achlorhydria
- [(a-klor-HY-dree-a) A lack of hydrochloric acid in the digestive juices in the stomach. Hydrochloric acid helps digest food. ( NCI )] (UMLS (CSP) C0001075) =Pathologic Function ;
|
- 2. Achaete-Scute Complex-Like 1 (Drosophila) Gene
- [This gene plays a role in neural development and regulation of transcription. ( NCI )] (UMLS (NCI) C1332009) ASCL1;
ASCL1 Gene;
=Gene or Genome ;
| - 11. Achlya
- [A genus of ALGAE in the family Saprolegniaceae. They are pathogens of FISHES and INSECTS. ( MSH )] (UMLS (CSP) C0599017) =Alga ;
|
- 3. Achalasia
- [Failure of the smooth muscle fibers of the gastrointestinal tract to relax at any one point of junction of one part with another. ( NCI )] (UMLS (NCI) C1321756) =Finding ;
| - 12. Achomawi
- (UMLS (HL7) C1555628) Achumawi;
=Language =Palaihnihan;
|
- 4. ACHALASIA & CARDIOSPASM
- [failure of normal relaxation of the lower esophageal sphincter associated with uncoordinated contractions of the thoracic esophagus, resulting in functional obstruction and difficulty swallowing. ( CSP )] (UMLS (ICD9CM) C0014848) =Disease or Syndrome ;
=Disease of esophagus;
DYSKINESIA OF ESOPHAGUS | - 13. Achondrogenesis, Type II
- (UMLS (NCI) C0220685) =Congenital Abnormality ;
|
- 5. Achard Syndrome
- (UMLS (NCI) C1332135) =Disease or Syndrome ;
| - 14. achondroplasia
- [autosomal dominant disorder that is the most frequent form of short-limb dwarfism; a disturbance of epiphyseal chondroblastic growth, causing inadequate enchondral bone formation. ( CSP )] (UMLS (CSP) C0001080) =Congenital Abnormality; Disease or Syndrome
|
- 6. Achenbach Syndrome
- (UMLS (NCI) C0473563) =Sign or Symptom
| - 15. ACHROMATOPSIA
- [Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy. ( MSH )] (UMLS (ICD9CM) C0152200) =Disease or Syndrome ;
|
- 7. Achilles
- (UMLS (HL7) C0001074) =Body Part, Organ, or Organ Component
| - 16. Achromobacteraceae
- [ ] (UMLS (CSP) C0597951) =Bacterium ;
|
- 8. Achilles bursitis or tendinitis
- (UMLS (ICD9CM) C0149846) =Disease or Syndrome
| - 17. Achromycin
- (UMLS (NCI) C0740484) =Organic Chemical; Antibiotic
|
- 9. ACHILLOTENOTOMY
- [ ] (UMLS (ICD9CM) C0188472) =Therapeutic or Preventive Procedure
| |
home
