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| language |
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| license |
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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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malformations, cerebral cavernous
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D020786 |
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malformations, familial cavernous
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D020786 |
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congenital septal defect
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2078 |
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heart septal defect
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2078 |
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congenital septal defect of heart
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2078 |
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Cardiac septal defects
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2078 |
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NAD(P)HX epimerase deficiency
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20781 |
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vascular anomalies, central nervous system
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D020785 |
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vascular malformations, central nervous system
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D020785 |
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cavernous angioma, central nervous system
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D020786 |
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cavernous hemangioma, central nervous system
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D020786 |
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hemangioma, cavernous, central nervous system
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D020786 |
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angioma, venous, central nervous system
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D020787 |
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venous angioma, central nervous system
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D020787 |
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capillary malformation, cerebral
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D020786 |
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