| NIEMANN-PICK DISEASE, TYPE C | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089 | | |
| NM | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00386 | | |
| NONAKA DISTAL MYOPATHY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00386 | | |
| NPC | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089 | | |
| NPC1 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089 | | |
| Nevo症候群@ja | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00407 | | |
| Niemann-Pick病C1型@ja | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089 | | |
| OSTEOGENESIS IMPERFECTA WITH CONGENITAL JOINT CONTRACTURES | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00408 | | |
| Ocular colobomas, ichthyosis, brain malformations and endocrine abnormalities | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00622 | | |
| PAROXYSMAL NOCTURNAL HEMOGLOBINURIA | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00414 | | |
| PDS, DEFECTIVE BIOSYNTHESIS OF | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00388 | | |
| PHOSPHOMANNOMUTASE 2 DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00343 | | |
| PHPTC | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00402 | | |
| PNH | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00414 | | |
| PNH1 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00414 | | |
| PPCA DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00023 | | |
| PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00632 | | |
| PROTECTIVE PROTEIN/CATHEPSIN A DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00023 | | |
| PROTEIN-LOSING ENTEROPATHY-HEPATIC FIBROSIS SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 | | |
| PROTEODERMATAN SULFATE, DEFECTIVE BIOSYNTHESIS OF | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00388 | | |
| Progeroid variant of Ehlers-Danlos syndrome | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00388 | | |
| QSM | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | | |
| RAMBAM-HASHARON SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 | | |
| RHS | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 | | |
| Rambam Hasharon syndrome | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360 | | |
| SAGUENAY-LAC SAINT-JEAN SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 | | |
| SLSJ SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 | | |
| SULFATIDOSIS, JUVENILE, AUSTIN TYPE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00078 | | |
| TEUTSCHLAENDER DISEASE, FAMILIAL | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00402 | | |
| TNPS | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00401 | | |
