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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.
adenofibroma of body of uterus
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3458 |
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pharyngeal throat cancer
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21345 |
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hilar cholangiocellular carcinoma
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3345 |
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MYOZ2 hypertrophic cardiomyopathy
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13455 |
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non-familial restrictive cardiomyopathy
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16345 |
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D-2-hydroxyglutaric aciduria caused by mutation in IDH2
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13345 |
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retinitis pigmentosa caused by mutation in KIZ
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14345 |
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hypertrophic cardiomyopathy caused by mutation in MYOZ2
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13455 |
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osteogenesis imperfecta caused by mutation in SERPINH1
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13459 |
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Oropouche virus caused disease or disorder
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345 |
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Schistosoma mansoni caused disease or disorder
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44345 |
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disease of cochlea
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3452 |
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disorder of cochlea
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3452 |
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CRB1 Leber congenital amaurosis
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13453 |
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IMPDH1 Leber congenital amaurosis
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13454 |
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