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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.
acrofacial dysostosis, Cincinnati type
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14651 |
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acrofacial dysostosis, Cincinnati type; AFDCIN
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http://purl.obolibrary.org/obo/MONDO_0014651 |
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skin infundibulocystic basal cell carcinoma
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11465 |
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vermiform appendix benign neoplasm
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21465 |
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basal cell carcinoma with follicular differentiation
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11465 |
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infundibulocystic basal cell carcinoma
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11465 |
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basal cell carcinoma, infundibulocystic
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11465 |
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RSPH3 primary ciliary dyskinesia
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14657 |
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acrofacial dysostosis caused by mutation in POLR1A
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14651 |
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exudative vitreoretinopathy caused by mutation in ZNF408
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14652 |
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retinitis pigmentosa caused by mutation in ZNF408
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14653 |
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primary ciliary dyskinesia 32
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14657 |
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COL12A1 Ullrich congenital muscular dystrophy
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14654 |
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severe achondroplasia-developmental delay-acanthosis nigricans syndrome
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14658 |
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primary ciliary dyskinesia 32 without situs inversus
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14657 |
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