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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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candidiasis, familial chronic mucocutaneous
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13140 |
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hereditary sensory and autonomic neuropathy type 2 caused by mutation in RETREG1
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13142 |
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hereditary sensory and autonomic neuropathy type 2B
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13142 |
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hereditary sensory and autonomic neuropathy type IIB
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13142 |
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Brugada syndrome caused by mutation in HCN4
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13148 |
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Brugada syndrome caused by mutation in KCNE3
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13145 |
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Brugada syndrome caused by mutation in SCN3B
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13146 |
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CLEC7A familial chronic mucocutaneous candidiasis
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13140 |
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AT III deficiency
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13144 |
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antithrombin 3 deficiency
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13144 |
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antithrombin III deficiency
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13144 |
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congenital AT-III deficiency
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13144 |
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hereditary antithrombin deficiency
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13144 |
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inherited antithrombin deficiency
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13144 |
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antithrombin III deficiency; AT3D
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http://purl.obolibrary.org/obo/MONDO_0013144 |
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