|
MIM:614696 - MOVED TO 600795
Xenbase Genes: chmp2b
Human Disease Resource: MIM
| MONDO:0005144 - metanephric glomerular capillary |
| MONDO:0010936 - frontotemporal dementia and/or amyotrophic lateral sclerosis 7 |
| MONDO:0013861 - obsolete amyotrophic lateral sclerosis type 17 |
