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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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pseudohypoaldosteronism type 2 caused by mutation in WNK1
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13778 |
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pseudohypoaldosteronism type 2C
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13778 |
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pseudohypoaldosteronism, type 2C
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13778 |
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familial thoracic 3 aortic aneurysm
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C537783 |
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aortic aneurysm-aortic dissection and patent ductus arteriosus
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C537784 |
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immune deficiency disorder
|
3778 |
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aphalangia syndactyly microcephaly
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C537787 |
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Aorta-pulmonary artery fistula
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C537782 |
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Aorto-pulmonary artery fistula
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C537782 |
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deficiency syndrome, immunologic
|
3778 |
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deficiency syndromes, immunologic
|
3778 |
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deficiency syndrome, immunological
|
3778 |
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deficiency syndromes, immunological
|
3778 |
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type 2b loeys-dietz syndrome
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C537783 |
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antibody deficiency syndrome
|
3778 |
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