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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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congenital disorder of glycosylation type 2o
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14789 |
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congenital disorder of glycosylation type IIo
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14789 |
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congenital disorder of glycosylation, type IIo
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14789 |
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microcephaly, short stature, and impaired glucose metabolism 2
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14785 |
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microcephaly, short stature, and impaired glucose metabolism 2; MSSGM2
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14785 |
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microcephaly, short stature, and impaired glucose metabolism caused by mutation in PPP1R15B
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14785 |
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microcephaly, short stature, and impaired glucose metabolism type 2
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14785 |
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carbohydrate deficient glycoprotein syndrome type IIo
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14789 |
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preimplantation embryonic lethality 1
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14783 |
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preimplantation embryonic lethality 1; PREMBL1
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14783 |
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preimplantation embryonic lethality caused by mutation in TLE6
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14783 |
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preimplantation embryonic lethality type 1
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14783 |
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hyperphosphatasia with mental retardation syndrome 6
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14780 |
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hyperphosphatasia with mental retardation syndrome type 6
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14780 |
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benign nasopharyngeal neoplasm
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21478 |
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