|
hereditary opalescent dentin
|
D003811 |
|
|
diabetes mellitus, deafness, nephropathy, and cerebral dysfunction photomyoclonus
|
C538113 |
|
|
ovarian mixed epithelial neoplasm
|
3811 |
|
|
ovarian mixed epithelial tumor
|
3811 |
|
|
congenital absence of insulin-producing beta cells with diabetes mellitus
|
C538111 |
|
|
opalescent dentin, hereditary
|
D003811 |
|
|
visceral, X-linked heterotaxy
|
C538116 |
|
|
neuroblastoma with hirschsprung disease
|
C538119 |
|
|
mixed epithelial neoplasm of ovary
|
3811 |
|
|
mixed epithelial neoplasm of the ovary
|
3811 |
|
|
combined oxidative phosphorylation defect type 9
|
13811 |
|
|
pigmentary abnormality of the anterior segment of the eye
|
C538115 |
|
|
dextrocardia with other cardiac malformations
|
C538116 |
|
|
MRPL3 combined oxidative phosphorylation deficiency
|
13811 |
|
|
combined oxidative phosphorylation deficiency 9
|
13811 |
|
