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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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stenosis, renal artery
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D012078 |
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cerebral embryonic artery, persistent
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D020785 |
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laurence moon bardet biedl syndrome
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D020788 |
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capillary telangiectasia, brain
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D020785 |
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capillary telangiectasias, brain
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D020785 |
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vascular malformation, brain
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D020785 |
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vascular malformations, brain
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D020785 |
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telangiectasia, brain capillary
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D020785 |
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telangiectasia, pontine capillary
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D020785 |
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telangiectasias, brain capillary
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D020785 |
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telangiectasias, pontine capillary
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D020785 |
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malformation, cerebral capillary
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D020786 |
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malformations, cerebral capillary
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D020786 |
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Joubert syndrome caused by mutation in AHI1
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12078 |
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angioma, familial cavernous
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D020786 |
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