| Fraccaro achondrogenesis | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00396 | | |
| Fukuyama CMD | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00378 | | |
| FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00378 | | |
| GALACTOSYLTRANSFERASE DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00401 | | |
| GALACTOSYLTRANSFERASE I DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00388 | | |
| GLUCOSIDASE I DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00359 | | |
| GLYCOASPARAGINASE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00005 | | |
| GLYCOSYLASPARAGINASE DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00005 | | |
| GM2-GANGLIOSIDOSIS, TYPE I | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00055 | | |
| GOLDBERG SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00023 | | |
| GROENOUW TYPE II CORNEAL DYSTROPHY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00391 | | |
| GSL | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00023 | | |
| HARD SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00376 | | |
| HEMPAS | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00373 | | |
| HEMPAS Anemia | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00373 | | |
| HEREDITARY ERYTHROBLASTIC MULTINUCLEARITY WITH POSITIVE ACIDIFIED-SERUM TEST | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00373 | | |
| Hereditary inclusion body myopathy type 2 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | | |
| HEXA DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00055 | | |
| HEXOSAMINIDASE A DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00055 | | |
| HFTC | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00402 | | |
| HHS | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00402 | | |
| HIBM2 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | | |
| HPMRS1 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00635 | | |
| HYDROCEPHALUS, AGYRIA, AND RETINAL DYSPLASIA | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00376 | | |
| HYPEROSTOSIS-HYPERPHOSPHATEMIA SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00402 | | |
| HYPEROSTOSIS WITH HYPERPHOSPHATEMIA | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00402 | | |
| IBM2 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | | |
| INCLUSION BODY MYOPATHY, AUTOSOMAL RECESSIVE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | | |
| INCLUSION BODY MYOPATHY, QUADRICEPS-SPARING | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | | |
| サルファティドーシス@ja | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00078 | | |