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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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paternal del(14)(q32.2)
|
16780 |
|
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disease, heartwater
|
6780 |
|
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heartwater disease
|
6780 |
|
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familial, 8 atrial fibrillation
|
C567802 |
|
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GSD IXC
|
C567809 |
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paternal monosomy 14q32.2
|
16780 |
|
|
malaria, vivax
|
D016780 |
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glycogen storage disease IXC
|
C567809 |
|
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plasmodium vivax malaria
|
D016780 |
|
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polymorphic light eruption, hereditary
|
C566780 |
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primary t-cell immunodeficiency disorders
|
C536780 |
|
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t cell immunodeficiency primary
|
C536780 |
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hereditary polymorphic light eruption
|
C566780 |
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malaria, plasmodium vivax
|
D016780 |
|
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paternal 14q32.2 microdeletion syndrome
|
16780 |
|
