1 posterior polar cataract
|
C535339 |
|
1 rippling muscle disease
|
C535686 |
|
1 tremor familial essential
|
C536545 |
|
1 tremor hereditary essential
|
C536545 |
|
1, preeclampsia eclampsia
|
D011225 |
|
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine poisoning
|
D020267 |
|
1-alpha, 25-hydroxyvitamin d3 deficiency, selective
|
C562688 |
|
1-alpha-hydroxylase deficiency
|
C562688 |
|
1-pyrroline-5-carboxylate dehydrogenase deficiency
|
C538385 |
|
1.35-mb chromosome 1q21.1 deletion syndrome
|
C567291 |
|
10p deletion syndrome (partial)
|
C538288 |
|
10p- partial chromosome 10
|
C538288 |
|