|
cervix endometrioid carcinoma
|
3665 |
|
|
l-xylulose reductase deficiency
|
C536652 |
|
|
cervix uteri endometrioid adenocarcinoma
|
3665 |
|
|
deafness, autosomal dominant 78
|
33665 |
|
|
uterine cervix endometrioid adenocarcinoma
|
3665 |
|
|
cervix uteri endometrioid carcinoma
|
3665 |
|
|
uterine cervix endometrioid carcinoma
|
3665 |
|
|
epilepsy, juvenile myoclonic, susceptibility to, 9
|
13665 |
|
|
hibernian fever, familial
|
C536657 |
|
|
periodic fever, familial, autosomal dominant
|
C536657 |
|
|
epilepsy, juvenile myoclonic, susceptibility to, 9; EJM9
|
http://purl.obolibrary.org/obo/MONDO_0013665 |
|
|
endometrioid adenocarcinoma of uterine cervix
|
3665 |
|
|
endometrioid adenocarcinoma of cervix
|
3665 |
|
