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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 adrenal hyperplasia due to 21 hydroxylase deficiency
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C535979 |
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peripheral dysostosis-nasal hypoplasia-intellectual disability (PNM) syndrome
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19797 |
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endove syndrome, limb-brain type
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30979 |
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ALPS (autoimmune lymphoproliferative syndrome)
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17979 |
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adult-onset vitelliform macular dystrophy
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11979 |
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familial chronic mucocutaneous, autosomal recessive candidiasis
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C537979 |
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inclusion body myopathy, sporadic
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D018979 |
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inclusion body myositides
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D018979 |
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inclusion body myositis, sporadic
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D018979 |
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myoclonus, intractable, neonatal
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14979 |
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myoclonus, intractable, neonatal; NEIMY
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14979 |
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multifocal motor neuropathy
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18979 |
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multifocal motor neuropathy with conduction block
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18979 |
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gyrate atrophy of choroid and retina
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9796 |
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hyperornithinemia-gyrate atrophy of choroid and retina syndrome
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9796 |
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