| MENTAL RETARDATION, GROWTH RETARDATION, PROMINENT COLUMELLA, AND OPEN MOUTH | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00358 | | |
| MOGS-CDG (CDG-IIb) | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00359 | | |
| MORBUS TEUTSCHLAENDER | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00402 | | |
| MPI DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00344 | | |
| MRT22 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00369 | | |
| MRT7 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00369 | | |
| MSD | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00078 | | |
| MUCOSULFATIDOSIS | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00078 | | |
| MULTIPLE EPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00398 | | |
| MULTIPLE EPIPHYSEAL DYSPLASIA WITH BILAYERED PATELLAE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00398 | | |
| MULTIPLE EPIPHYSEAL DYSPLASIA WITH CLUBFOOT | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00398 | | |
| MUSCULAR DYSTROPHY, CONGENITAL, 1C | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 | | |
| MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 | | |
| MUSCULAR DYSTROPHY, CONGENITAL, LARGE-RELATED | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | | |
| Muscular dystrophy, congenital, type 1C | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 | | |
| MUSCULAR DYSTROPHY, CONGENITAL, TYPE 1D | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | | |
| MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00382 | | |
| MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00382 | | |
| MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00379 | | |
| MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE TYPE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00384 | | |
| MYOPATHY, DISTAL, WITH RIMMED VACUOLES | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00386 | | |
| NEONATAL OSSEOUS DYSPLASIA I | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00397 | | |
| NEURAMINIDASE/BETA-GALACTOSIDASE EXPRESSION | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00023 | | |
| NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00023 | | |
| NEUROVISCERAL STORAGE DISEASE WITH VERTICAL SUPRANUCLEAR OPHTHALMOPLEGIA | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089 | | |
| NEVO SYNDROME | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00407 | | |
| Nevo症候群@ja | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00407 | | |
| NGBE | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00023 | | |
| NIEMANN-PICK DISEASE, CHRONIC NEURONOPATHIC FORM | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089 | | |
| NIEMANN-PICK DISEASE, SUBACUTE JUVENILE FORM | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089 | | |
