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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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autosomal recessive hyper IgE syndrome
|
9478 |
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obsolete primary hyperoxaluria
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18478.0 |
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nystagmus 5, infantile periodic alternating
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C564478 |
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acute myocardial infarction
|
4781 |
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acute myocardial infarction (disease)
|
4781 |
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biliary tract infection
|
4789 |
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hyper-IgE recurrent infection syndrome, autosomal recessive
|
9478 |
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hyperphosphatasia with intellectual disability syndrome 6
|
14780 |
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hyperphosphatasia with intellectual disability syndrome 6; HPMRS6
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14780 |
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hyperphosphatasia with intellectual disability syndrome type 6
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14780 |
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renal, with intracerebral calcifications hypophosphatemia
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C565478 |
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tay-sachs disease, juvenile
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C564782 |
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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
|
14783 |
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