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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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hereditary, transthyretin-related amyloidosis
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C567782 |
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hereditary sensory and autonomic, type IIA neuropathy
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C567738 |
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hereditary sensory and autonomic, type IIB neuropathy
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C567738 |
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severe congenital, autosomal dominant 2 neutropenia
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C567748 |
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complete, cbx2-related 46,xy gonadal dysgenesis
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C567766 |
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autosomal dominant, 5 progressive external ophthalmoplegia
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C567768 |
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autosomal dominant, 5 progressive external ophthalmoplegia with mitochondrial dna deletions
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C567768 |
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brugada syndrome 6
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C567735 |
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early-onset hyperuricemia, anemia, and progressive kidney failure
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C567760 |
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primary open angle glaucoma-1o
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C567753 |
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familial transthyretin cardiac amyloidosis
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C567782 |
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familial, 1 candidiasis
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C567779 |
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dilated, 1DD cardiomyopathy
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C567725 |
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dilated, 1CC cardiomyopathy
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C567733 |
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central areolar choroidal dystrophy-2
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C567750 |
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