|
glutamate pyruvate transaminase 2 deficiency
|
14567 |
|
|
hereditary nonpolyposis, type 5 colorectal cancer
|
C563456 |
|
|
amelogenesis imperfecta type 1F
|
14560 |
|
|
amelogenesis imperfecta, type 1F
|
14560 |
|
|
3-Methylglutaconic aciduria, type 7
|
14561 |
|
|
simpson-golabi-behmel syndrome, type 2
|
C564567 |
|
|
Charcot-Marie-Tooth disease type 2 caused by mutation in MARS
|
14566 |
|
|
3-methylglutaconic aciduria type 7
|
14561 |
|
|
amelogenesis imperfecta type IF
|
14560 |
|
|
3-Hydroxyacyl-CoA dehydrogenase, type 2, deficiency
|
C564560 |
|
|
Hydroxyacyl-CoA dehydrogenase, type 2, deficiency
|
C564560 |
|
|
Charcot-Marie-Tooth neuropathy type 2U
|
14566 |
|
|
Charcot-Marie-Tooth neuropathy, type 2U
|
14566 |
|
|
amelogenesis imperfecta, type IF
|
14560 |
|
|
amelogenesis imperfecta, type IF; AI1F
|
http://purl.obolibrary.org/obo/MONDO_0014560 |
|
