CYP21A2
| Deellabo: | PGD DNA |
| Gen (Gen Code): | CYP21A2 |
| Aliases Gen: | CAH1; CPS1; CA21H; CYP21; CYP21B; P450c21B; MGC150536; MGC150537; CYP21A2 |
| Gen ID (NCBI): | 1589 |
| OMIM Gen ID: | +201910 |
| Chromosomale locatie: | 6p21.3 |
| Genetische aandoening / Analyse: | Adrenogenitaal syndroom (21-hydroxylase deficiëntie) |
| OMIM aandoening ID: | 201910 |
| Overerving: | AR |
| Aliases aandoening: | ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY ADRENAL HYPERPLASIA III 21-@HYDROXYLASE DEFICIENCY CYP21 DEFICIENCY CONGENITAL ADRENAL HYPERPLASIA 1; CAH1 |