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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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craniosynostosis radial aplasia syndrome
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C536788 |
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bilateral radial aplasia with wilms tumor
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C536707 |
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say-barber-biesecker-young-simpson type blepharophimosis-intellectual deficit syndrome
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C536717 |
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ring 22, chromosome
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C536795 |
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complementation group c mucolipidosis III
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C565367 |
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trisomy 2q chromosome 2
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C535367 |
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tetrasomy 21q chromosome 21
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C536793 |
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monosome mosaic chromosome 22
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C536798 |
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obstructive, and chronic sinopulmonary infections azoospermia
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C536718 |
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nystagmus with congenital zonular cataract
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C536727 |
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spastic ataxia charlevoix-saguenay type
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C536787 |
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spastic ataxia, charlevoix-saguenay type
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C536787 |
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zap70-related severe combined immunodeficiency
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C536722 |
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athabaskan severe combined immunodeficiency
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C536786 |
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pachygyria joint contractures facial abnormalities
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C536712 |
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