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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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Del(2)(q33.1)
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16653 |
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FCHL1
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C566535 |
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HYPLIP1
|
C566535 |
|
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anthracosilicosis
|
6653 |
|
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monosomy 2q33.1
|
16653 |
|
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penttinen-aula syndrome
|
C536653 |
|
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rheumatoid vasculitides
|
D056653 |
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vasculitides, rheumatoid
|
D056653 |
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familial combined, 1 hyperlipidemia
|
C566535 |
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type 4a bartter syndrome
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C566530 |
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combined, 1 hyperlipidemia
|
C566535 |
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colobomatous, with microcornea macrophthalmia
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C566533 |
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penttinen type premature aging syndrome
|
C536653 |
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2q33.1 microdeletion syndrome
|
16653 |
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premature aging syndrome penttinen type
|
C536653 |
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