|
combined oxidative phosphorylation deficiency 9; COXPD9
|
http://purl.obolibrary.org/obo/MONDO_0013811 |
|
|
combined oxidative phosphorylation deficiency caused by mutation in MRPL3
|
13811 |
|
|
combined oxidative phosphorylation deficiency type 9
|
13811 |
|
|
dentinogenesis imperfecta, shields type 2
|
D003811 |
|
|
dentinogenesis imperfecta, shields type II
|
D003811 |
|
|
hernandez aguirre-negrete syndrome
|
C538112 |
|
|
hernández aguirre-negrete syndrome
|
C538112 |
|
|
asymmetry in the pigmentation of the irides
|
C538115 |
|
|
ovarian Seromucinous tumor
|
3811 |
|
|
ovarian seromucinous tumor
|
3811 |
|
|
mixed epithelial tumor of ovary
|
3811 |
|
|
mixed epithelial tumor of the ovary
|
3811 |
|
|
hersh podruch weisskopk syndrome
|
C538114 |
|
|
ehlers-danlos syndrome with progeroid facies and mild mental retardation
|
C538112 |
|
|
visceral, 1, x-linked heterotaxy
|
C538116 |
|
