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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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EBVaGC
|
17784 |
|
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PRTH
|
7784 |
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gelsolin-related amyloidosis
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C000657784 |
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kymenlaakso syndrome
|
C000657784 |
|
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HMGCS2 deficiency
|
C567784 |
|
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3-Hydroxy-3-Methylglutaryl-CoA synthase 2 deficiency
|
C567784 |
|
|
familial thoracic 4 aortic aneurysm
|
C537784 |
|
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lattice type II corneal dystrophy
|
C000657784 |
|
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EBV-associated gastric carcinoma
|
17784 |
|
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aortic aneurysm-aortic dissection and patent ductus arteriosus
|
C537784 |
|
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hyperthyroidism, familial, due to inappropriate thyrotropin secretion
|
7784 |
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lattice corneal dystrophy type ii
|
C000657784 |
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lattice corneal dystrophy, gelsolin type
|
C000657784 |
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lattice corneal dystrophy, type II
|
C000657784 |
|
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finnish type familial amyloidosis
|
C000657784 |
|
