Medical Encyclopedia: 0–9
50 entries under “0–9”, projected from the canonical Medical Encyclopedia inventory. Index entries are listed by name while their full article is prepared and reviewed.
Educational information only. This explains health information to discuss with a qualified clinician; it is not a diagnosis, prescription, or treatment. Medical Information & Safety.
Showing 50 of 50 — page 1 of 1
- 10q26 deletion syndromeDefinition and full article under review.
- 15q11-q13 duplication syndromeDefinition and full article under review.
- 15q13.3 microdeletionDefinition and full article under review.
- 15q24 microdeletionDefinition and full article under review.
- 16p11.2 deletion syndromeDefinition and full article under review.
- 16p11.2 duplicationDefinition and full article under review.
- 16p12.2 microdeletionDefinition and full article under review.
- 17 alpha-hydroxylase/17,20-lyase deficiencyDefinition and full article under review.
- 17-beta hydroxysteroid dehydrogenase 3 deficiencyDefinition and full article under review.
- 17-HydroxyprogesteroneDefinition and full article under review.
- 17q12 deletion syndromeDefinition and full article under review.
- 17q12 duplicationDefinition and full article under review.
- 18F-FDG PET scanDefinition and full article under review.
- 19p13.13 deletion syndromeDefinition and full article under review.
- 1p36 deletion syndromeDefinition and full article under review.
- 1q21.1 microdeletionDefinition and full article under review.
- 1q21.1 microduplicationDefinition and full article under review.
- 2-hydroxyglutaric aciduriaDefinition and full article under review.
- 21-hydroxylase deficiencyDefinition and full article under review.
- 22q11 Deletion SyndromeDefinition and full article under review.
- 22q11.2 deletion syndromeAn educational overview of 22q11.2 deletion syndrome, a genetic condition caused by a missing small piece of chromosome 22 that can affect several parts of the body.
- 22q11.2 duplicationDefinition and full article under review.
- 22q13.3 deletion syndromeDefinition and full article under review.
- 2q37 deletion syndromeDefinition and full article under review.
- 3-beta-hydroxysteroid dehydrogenase deficiencyDefinition and full article under review.
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyDefinition and full article under review.
- 3-hydroxyacyl-CoA dehydrogenase deficiencyDefinition and full article under review.
- 3-M syndromeDefinition and full article under review.
- 3-methylcrotonyl-CoA carboxylase deficiencyDefinition and full article under review.
- 3-methylglutaconyl-CoA hydratase deficiencyDefinition and full article under review.
- 3MC syndromeDefinition and full article under review.
- 3p deletion syndromeDefinition and full article under review.
- 3q29 microdeletion syndromeDefinition and full article under review.
- 3q29 microduplication syndromeDefinition and full article under review.
- 3T3 CellsDefinition and full article under review.
- 3T3-L1 CellsDefinition and full article under review.
- 46, XX Disorders of Sex DevelopmentDefinition and full article under review.
- 46, XX Testicular Disorders of Sex DevelopmentDefinition and full article under review.
- 46,XX testicular difference of sex developmentDefinition and full article under review.
- 47,XYY syndromeDefinition and full article under review.
- 48,XXXY syndromeDefinition and full article under review.
- 48,XXYY syndromeDefinition and full article under review.
- 49,XXXXY syndromeDefinition and full article under review.
- 5-alpha reductase deficiencyDefinition and full article under review.
- 5q minus syndromeDefinition and full article under review.
- 5q31.3 microdeletion syndromeDefinition and full article under review.
- 6q24-related transient neonatal diabetes mellitusDefinition and full article under review.
- 7q11.23 duplication syndromeDefinition and full article under review.
- 8p11 myeloproliferative syndromeDefinition and full article under review.
- 9q22.3 microdeletionDefinition and full article under review.