PTCH1
| Deellabo: | PGD DNA |
| Gen (Gen Code): | PTCH1 |
| Aliases Gen: | RP11-435O5.3, BCNS, HPE7, NBCCS, PTC, PTC1, PTCH, PTCH11 |
| Gen ID (NCBI): | 5727 |
| OMIM Gen ID: | 601309 |
| Chromosomale locatie: | 9q22.3 |
| Genetische aandoening / Analyse: | Basaalcel naevus syndroom (BCNS) |
| OMIM aandoening ID: | 109400 |
| Overerving: | AD |
| Aliases aandoening: | BASAL CELL NEVUS SYNDROME; BCNS GORLIN SYNDROME GORLIN-GOLTZ SYNDROME NEVOID BASAL CELL CARCINOMA SYNDROME; NBCCS MULTIPLE BASAL CELL NEVI, ODONTOGENIC KERATOCYSTS, AND SKELETAL ANOMALIES |