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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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Leber congenital amaurosis caused by mutation in CRB1
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13453 |
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Leber congenital amaurosis caused by mutation in IMPDH1
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13454 |
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Leber congenital amaurosis caused by mutation in TULP1
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13457 |
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Leber congenital amaurosis type 11
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13454 |
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Leber congenital amaurosis type 15
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13457 |
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Leber congenital amaurosis type 8
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13453 |
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constitutional megaloblastic anemia with severe neurologic disease
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13456 |
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subarachnoid hemorrhage, aneurysmal
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D013345 |
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subarachnoid hemorrhages, aneurysmal
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D013345 |
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coarctation of aorta
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7345 |
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unilateral or bilateral cryptorchidism
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D003456 |
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perihilar extrahepatic bile duct carcinoma
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3345 |
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paragangliomas, carotid body
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D002345 |
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tumor, carotid body
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D002345 |
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tumors, carotid body
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D002345 |
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