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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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paragangliomas, carotid body
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D002345 |
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tumor, carotid body
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D002345 |
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tumors, carotid body
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D002345 |
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adenofibroma of body of uterus
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3458 |
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non-familial restrictive cardiomyopathy
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16345 |
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disease of cochlea
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3452 |
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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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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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night blindness, congenital stationary, type 1D
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13450 |
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