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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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progressive cardiac conduction defect
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C566873 |
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tumoral, with hyperphosphatemia calcinosis
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C566870 |
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encephalopathy, neonatal severe, due to mecp2 mutations
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C566878 |
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tumoral calcinosis, primary hyperphosphatemic
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C566870 |
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type ia progressive familial heart block
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C566873 |
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heart block, progressive familial, type i
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C566873 |
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heart block progressive, familial
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C566873 |
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type g-cockayne syndrome xeroderma pigmentosum
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C566879 |
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burning mouth syndrome
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6687 |
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x-linked, with spasticity mental retardation
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C566877 |
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weaver smith syndrome
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C536687 |
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mental retardation, x-linked 79
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C566876 |
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progressive familial, type 1 heart block
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C566873 |
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protoplasmic astrocytic tumor
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16687 |
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hyperphosphatemic, familial tumoral calcinosis
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C566870 |
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