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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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familial hypocalcemia
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C562783 |
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juvenile myofibromatosis
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C562978 |
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myofibromatosis, infantile
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C562978 |
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branchiogenic-deafness syndrome
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C563780 |
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aarau disease
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C563781 |
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reticular erythrokeratoderma
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C563781 |
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pseudohyperkalemia lille
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C563785 |
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hyperthyroidism, nonautoimmune
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C563786 |
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nonautoimmune hyperthyroidism
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C563786 |
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adolescent nephronophthisis
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C565780 |
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nephronophthisis, adolescent
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C565780 |
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SCT syndrome
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C535780 |
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synspondylism, congenital
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C535780 |
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whyte syndrome
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C535783 |
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humero-spinal dysostosis
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C535789 |
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