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| language |
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| license |
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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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cervix endometrioid carcinoma
|
3665 |
|
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l-xylulose reductase deficiency
|
C536652 |
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cervix uteri endometrioid adenocarcinoma
|
3665 |
|
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deafness, autosomal dominant 78
|
33665 |
|
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uterine cervix endometrioid adenocarcinoma
|
3665 |
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cervix uteri endometrioid carcinoma
|
3665 |
|
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uterine cervix endometrioid carcinoma
|
3665 |
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premature aging syndrome penttinen type
|
C536653 |
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endometrioid adenocarcinoma of uterine cervix
|
3665 |
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endometrioid carcinoma of uterine cervix
|
3665 |
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penttinen type premature aging syndrome
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C536653 |
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hibernian fever, familial
|
C536657 |
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endometrioid adenocarcinoma of cervix
|
3665 |
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endometrioid carcinoma of cervix
|
3665 |
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endometrioid adenocarcinoma of cervix uteri
|
3665 |
|
